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REVIEW article

Front. Microbiol., 05 May 2023
Sec. Infectious Agents and Disease
This article is part of the Research Topic Zoonoses- A Rising Threat to Healthcare System View all 12 articles

Epidemiology, host range, and associated risk factors of monkeypox: an emerging global public health threat

  • 1State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China
  • 2Department of Clinical Studies, Faculty of Veterinary and Animal Sciences, PMAS-Arid Agriculture University Rawalpindi, Rawalpindi, Pakistan
  • 3College of Animal Husbandry and Veterinary Medicine, Southwest Minzu University, Chengdu, China
  • 4Department of Sociology, Allama Iqbal Open University Islamabad, Islamabad, Pakistan

Based on recent multiregional epidemiological investigations of Monkeypox (MPX), on 24 July 2022, the World Health Organization declared it a global public health threat. Retrospectively MPX was an ignored zoonotic endemic infection to tropical rainforest regions of Western and Central African rural communities until a worldwide epidemic in May 2022 verified the potential threat of monkeypox virus (MPXV) to be propagated across the contemporary world via transnational tourism and animal movements. During 2018–2022, different cases of MPX diagnosed in Nigerian travelers have been documented in Israel, the United Kingdom, Singapore, and the United States. More recently, on 27 September 2022, 66,000 MPX cases have been confirmed in more than 100 non-endemic countries, with fluctuating epidemiological footprinting from retrospective epidemics. Particular disease-associated risk factors fluctuate among different epidemics. The unpredicted appearance of MPX in non-endemic regions suggests some invisible transmission dynamic. Hence, broad-minded and vigilant epidemiological attention to the current MPX epidemic is mandatory. Therefore, this review was compiled to highlight the epidemiological dynamic, global host ranges, and associated risk factors of MPX, concentrating on its epidemic potential and global public health threat.

1. Introduction

The re-emergence of various transmissible infections, including Zika virus, swine flu (H1N1), Ebola virus, Nipah virus, avian influenza (H5N1), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Middle East respiratory syndrome coronaviruses (MERS-CoV), and recent regional outbreaks of monkeypox virus (MPXV) in the twentyfirst century, is alarming (Mourya et al., 2019). This spillover of viruses from animal origin to humans has predominantly been due to species barrier crossing (Bezerra-Santos et al., 2021). At a time when global health experts and world communities were awaiting the pandemic spread of coronavirus disease 2019 (COVID-19) to be diminished, contemporary global populations now face an unexpected MPX epidemic. In previous decades, irregular outbreaks, with thousands of MPX cases, have been predominantly limited to African countries. MPX is enzootic in several sub-Saharan states and has co-occurred in African inhabitants for several years but has not received sufficient consideration from global technical experts. Excitingly, MPX, for the first time, acquired worldwide consideration when it appeared in the USA in 2003 (Reed et al., 2004). Such sporadic and confined occurrences of MPX in the non-enzootic world have been associated with international travel and the importation of infected animals (Reed et al., 2004). Although MPXV spread among humans has been soundly investigated, its extensive concurrent appearance in non-enzootic nations has hit the globe with another shock. Additionally, MPX epidemics have been poorly inspected, irregularly reported, and poorly epidemiologically defined in the past, and, ultimately, the picture of this infection is incomplete. This menace can intensify with temporal patterns in the case where there is a rise in virulence naturally or through genomic rearrangement, a spillover into extra extensively dispersed taxa, or entrance and cluster epizootics in non-enzootic states (Sklenovská and Van Ranst, 2018). All these risks are further worsened by enhanced desforestation, increasing population density, large-scale international travel, immigration, invasion and damage of natural animal habitations, and poor epidemiological approaches toward emerging and re-emerging disease investigations (Adler et al., 2022). Lately, MPX is making headlines due to the worldwide surge in the occurrence of the infection in many countries and continents. On 24 July 2022, the World Health Organization (WHO) declared MPX a global public health threat. As per the US Centers for Disease Control and Prevention report of 2 August 2022, ~25,391 clinically confirmed MPX cases have been documented across 87 states globally (CDC, 2022b). This number has been ballooning prospectively in the USA, Brazil, Spain, the UK, and Germany (WHO, 2022d). More recently, on 27 September 2022, over 66,000 confirmed MPX cases have been documented in more than 100 non-endemic states, with fluctuating epidemiological footprinting from retrospective epidemics. In this scenario, when the global occurrence of MPX does not decline, the world might see another pandemic, which may be presently hanging over the head of the contemporary world and may easily become a global public health threat. Therefore, this review assembles updated literature on the different aspects of MPXV regarding disease epidemiology, host range, and associated risk factor, and also sheds light on its epizootic potential and global public health threat. Restoring public health setups and preparing for upcoming epidemics are required, particularly in underdeveloped countries with deprived healthcare delivery services.

2. MPX

Monkeypox (MPX) is a sporadic zoonotic viral infection caused by the MPXV, which belongs to the genus Orthopoxvirus of the family Poxviridae and is interrelated to the already eradicated smallpox virus. It is a large, enveloped virus comprising a dsDNA genome of 190 kbp and having a dumbbell-shaped core with horizontal figures (Kugelman et al., 2014). The MPXV has two distinct genomic groups, the West African clade and the Congo Basin clade. These genomic groups have been geologically isolated with diverse clinical and epizootological characteristics (WHO, 2022d). The Congo Basin clade is recognized to induce serious infection and can spread among humans with a fatality rate of ~11%. However, the West African clade displays a fatality rate of <1% and has never been known to exhibit human-to-human spread (Jezek et al., 1987). The early signs and symptoms of MPX are frequent pyrexia, vigorous headache, myalgia, lymphadenopathy, and lethargy. After fever, the dermal wounds characteristically burst within 1 to 3 days. The rash tends to be more confined to the facial region and extremities as compared with the trunk region of the body. MPX is frequently a self-determining disease, and symptoms last from 2 to 4 weeks. The clinical appearance and indications of MPX are exactly like those of smallpox; however, it is a mild and rarely fatal infection (Soheili and Nasseri, 2022).

Monkeypox virus (MPXV) continues to present challenges to public health and healthcare providers in areas with endemic disease, owing to inadequate capacity to diagnose and clinically manage patients and to accurately identify exposures (McCollum, 2023). Mostly, MPX cases in the African subcontinent are mainly misdiagnosed with other zoonotic infections such as cutaneous anthrax, chickenpox (Varicella), staphylococcal-associated rash, or fungal diseases in cases with human immunodeficiency virus (HIV) infection (Formenty et al., 2010). In addition to the current outbreak, there have been multiple reports of initial misdiagnosis of patients who were later confirmed to have MPX (Heskin et al., 2022; Minhaj et al., 2022) due to an atypical clinical manifestation that does not resemble the MPX observed in African outbreaks. Laboratory evaluations for monkeypox cases include electron microscopy, immunohistochemistry, culture of material from rash specimens, serological testing for specific antibodies, and real-time or conventional polymerase chain reaction (PCR) assays. Confirmation of specimens from suspected MPX cases is performed using nucleic acid amplification testing, such as real-time or conventional polymerase chain reaction. Restriction fragment length polymorphism (RFLP) of PCR-amplified genes or gene fragments is also used to detect monkeypox DNA. However, this method is time-consuming and requires a virus culture. Whole-genome sequencing, using next-generation sequencing technologies, is the gold standard for the characterization of MPXV and other orthopoxviruses. However, the use of most of the above diagnostic tools is limited due to their high cost and advanced technology, especially in developing countries and regions with limited healthcare resources (MacNeil et al., 2011; Radonić et al., 2014; Brown and Leggat, 2016; Petersen et al., 2019b; Alakunle et al., 2020; Cohen-Gihon et al., 2020; Altindis et al., 2022).

Another issue that may cause the disease to re-emerge is a failure to offer vaccination to susceptible persons in places where human immunodeficiency virus (HIV) infection is widespread. Insufficient studies have been devoted to producing a specialized vaccine to prevent the infection (Heymann et al., 1998), given the recent return of infectious illnesses during an epidemic. Moreover, routine vaccination is currently not available in endemic countries having limited healthcare resources (Damon, 2011). The extent of protection against the MPXV outbreak offered by vaccines remains unclear. Similarly, there is currently no specific treatment approved for MPXV infection, though there are several antivirals that have been developed and are being tested to treat smallpox, including tecovirimat, brincidofovir, and cidofovir (Adler et al., 2022). The present regionalized spatial distribution of MPX-confirmed cases is shown in Figure 1 (Kaler et al., 2022).

FIGURE 1
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Figure 1. The present regionalized spatial distribution of MPX-confirmed cases.

3. Epidemiological dynamics of MPX

Monkeypox (MPX) is an infection of global public health significance as it not only affects states in central and western African regions, but also the contemporary globe is under threat (Reynolds et al., 2007). In the previous era, the frequency of human monkeypox (HMPX) infection was sporadic, and irregular cases were investigated in several African states. The first HMPX case was recognized in the 1970s in the Democratic Republic of the Congo (DRC), associated with a 9-month-old child (Foster et al., 1972; Arita et al., 1985). This investigation was expanded to further irregular cases recorded in 11 other states of Africa including Gabon, Cameroon, Benin, the Central African Republic, DRC, the Republic of the Congo, South Sudan, Nigeria, Côte d'Ivoire, Sierra Leone, and Liberia (Durski et al., 2018; World Health Organization, 2022a). From February 1996 to February 1997, a huge outbreak of MPX was recorded in the DRC, and ~511 infected cases were investigated (Centers for Disease Control Prevention (CDC), 2022c). A systemic review and meta-analysis (Sham et al., 2022) explained details of suspected, confirmed, and fatal MPX cases by country and year-wise.

In 2003, an MPX epidemic occurred in the US, with 47 apparent or confirmed cases. Investigation showed that the affected individuals were exposed to the virus via pet prairie dogs retained with other mammals in a pet supply capacity, comprising the primary host and rodents from African Ghana (Bernard and Anderson, 2006). Petersen et al. (2019) investigated 116 clinically verified individuals with a death rate of 6.7%, and ~280 suspicious cases appeared in Nigerian territory in 2018, with the large majority of cases in individuals under 40 years of age.

The frequency of the infection has affectedly amplified, and the DRC recorded 20 times more cases between 1981 and 1986 (7.2 cases per 100,000 people) and 2006 and 2007 (144.2 cases per 100,000 people), and a 5-fold rise from 2001 (0.64 cases per 100,000 people) to 2012 (3.11 cases per100, 000 people) (Hoff et al., 2017). Bunge et al. (2022) collected data from 28 available manuscripts and 15 gray database studies on HMPX infection point out that the incidence rate has been amplified since 1970s, with a rise in the intermediate age of infected individuals from 4 years old in the 1970s to 21 years old from 2010 to 2019. Table 1 adopted from Brown and Leggat (2016), Beer and Rao (2019), Adegboye et al. (2022) and Hatmal et al. (2022) shows the incidence of MPX and the number of deaths from 1970 to 2021.

TABLE 1
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Table 1. Incidence of MPX and the number of deaths from 1970 to 2021.

In the retrospective outbreak investigations, MPX was recorded in youngsters and teenagers in the enzootic areas, with the same clinical picture and symptoms as observed in older individuals. The WHO has lately documented that serious cases of MPX more frequently occur among youngsters and are associated with the level of virus contact. Moreover, the severity of MPX cases may be associated with individual health conditions, the nature of complexities, and essential immune insufficiencies (WHO, 2022c). Individuals whose date of birth was after the 1980s are at greater risk because immunization for SPX stopped after its eradication, and this immunization can also defend people against MPX (Simpson et al., 2020). Additionally, it was thought that MPX infects women and men similarly, but, in the recent multi-country epidemic, several MPX cases have been reported in men who have sex with other men (MSM) (Bunge et al., 2022; Perez Duque et al., 2022; WHO, 2022c; Xiang and White, 2022). As per the CDC report on the 2022 outbreak, the majority of MPX cases are due to MSM, which puts bisexual, transgender, and gay individuals at a greater threat of MPX (CDC, 2022b). Further investigations are mandatory for a better understanding of risk factors regarding sexual transmission dynamics of MPXV among MSM. The multi-state 2022 epidemic of MPX cases and deaths recorded by WHO (2022e) is shows in Table 2.

TABLE 2
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Table 2. MPX cases and deaths recorded by the WHO during the multi-state 2022 epidemic (as of 8 June 2022) (World Health Organization, 2022e).

In some investigations, there is evidence of mixed infection of MPX with other blood-borne diseases and some sexually transmitted diseases (Liu et al., 2022), and people with HIV infection reflected a greater risk dynamic for MPX in the recent epidemic (Khaity et al., 2022; Bragazzi et al., 2023). In advanced cases of uncontrolled HIV infection, inappropriate immune response is significantly related to a weak prognosis, a longer period of disease signs, late curing of self-controlling MPX, and complex cures (Iñigo Martínez et al., 2022; Liu et al., 2022). Consequently, sorting MPX cases for HIV is extremely suggested in MSM (Liu et al., 2022). Recently, MPX has been accepted as a key factor that escalates the chance of contracting HIV (Davido et al., 2022; Patrocinio-Jesus and Peruzzu, 2022). A recent epidemiological study from Madrid, Spain reported that 44.3% (225 cases out of 508 totals) of MPX-confirmed cases were linked to HIV infection (Iñigo Martínez et al., 2022). An additional report from London, UK indicated that 35.9% (70 cases out of 195 totals) of MPX-confirmed cases were linked to HIV infection (Patel et al., 2022). Similarly, mild infections of MPX among individuals with HIV and AIDS have been documented in Italy and Portugal (Antinori et al., 2022; Perez Duque et al., 2022), particularly among people with enhanced T-helper cell count, untraceable HIV viral genomic substance, and weak anti-retroviral treatment (Ortiz-Martínez et al., 2022). Infected individuals with immunological suppression initiated by HIV presented a clear-cut, wide scale of clinical appearances and characteristic MPX wounds. Fever, exanthema, inguinal lymphadenopathy, and genital ulcers were major clinical appearances in MPX-infected individuals during the epidemic in Portugal (Perez Duque et al., 2022). Pustules, papules, and a necrotic centralized wound in the perianal region, trunk, genitals, mouth, and facial region were recorded in a 24 year old bisexual man with HIV infection (De Sousa et al., 2022). Moreover, throughout the 2017–2018 MPX outbreaks in Nigerian regions, the majority of mortalities related to MPX were in individuals with unrestrained HIV, with AIDS appearances, who were not receiving proper medication (Yinka-Ogunleye et al., 2019). Another study on Nigeria showed that mixed HIV-infected MPX cases had a more prolonged disorder, greater wounds, and greater frequency of both genital ulcers and bacterial skin diseases, compared with HIV-negative MPX-infected individuals (Ogoina et al., 2020). Mixed infection with other sexually transmitted diseases (STDs) was also documented among MPX and HIV cases. An infected individual with unidentified progressive HIV and syphilis presented with a severed penis, oral mucosal infection, nasal necrotic wound, and MPX lesions spread over the entire body (Boesecke et al., 2022).

Active surveillance of MPX was carried out in nine regions of central DRC during 2005–2007, and ~760 MPX confirmed cases were recorded, with an annual occurrence of 55.3 per 100,000 people. Male gender, age <15, a history of vaccination against SPX, and inhabitants of afforested regions were the main associated risk factors of MPX (Rimoin et al., 2010). In 2017, a huge incidence of MPX was recorded in the Nigerian regions, with over 500 suspicious, over 200 confirmed cases, and a death rate of 3% (World Health Organization, 2022b). In an additional study, Beer and Rao (2019) investigated 71 reports relating to MPX cases and local epidemics during 1970–2018. The rates of documented occurrences were amplified since 1970, with an overall of 35 recorded epidemics outside the DRC, with 20 between 2010 and 2018.

The CDC, from 1 January 2022 to 5 August 2022, documented 28,220 confirmed cases of MPX in 88 states of the world (CDC, 2022e). The majority of these cases (27,875) were documented in 81 states that have not retrospectively documented MPX (CDC, 2022e). Additionally, a few months ago, the WHO investigated various human MPX outbreaks in different regions of Europe, the Americas, the Eastern Mediterranean, and the Western Pacific, with a total of 1,285 MPX confirmed cases, while 59 confirmed and 1,536 suspicious MPX cases were recorded, with 72 deaths occurring in African territories from January 2022 to June 2022 (World Health Organization, 2022e). The host range and susceptibility to MPXV infection was detected during investigatory research in the laboratory by Silva et al. (2020) shown in Table 3. Several eco-bionomical, environmental, and geostrategic dynamics might have led to the regional and global appearance and re-appearance of MPX infection, including the misuse of rain timberlands, climate alteration, civil and military clashes in disease areas, highly mobile populations, declining herd immunity, and the ceasing of SPX immunization (Fauci, 2005; Liu et al., 2022). On the contrary, the reservoir host, natural history, and pathogenesis of MPXV are uncertain; hence, there are significant disputes in recognizing the epidemiological dynamics of MPX infection (Petersen et al., 2019).

TABLE 3
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Table 3. Host range and animals susceptible to MPXV infection (Silva et al., 2020).

3.1. Epidemiological dynamics of MPX retrospective to the global epidemic in 2022

Based on 50 years of retrospective analysis of MPX, the DRC has been the single state to constantly investigate HMPX patients, and, in the previous 30 years, the figure for documented infected individuals was over 1,000 per annum (Bunge et al., 2022; WHO, 2022f). During the year 2020, ~6,257 suspicious individuals of HMPX were investigated in the DRC (WHO, 2022f). In the initial 120 days of 2022, ~1,238 Central African clade-associated new MPX cases were documented in the DRC (Bunge et al., 2022; World Health Organization, 2022a).

Human monkeypox (HMPX) was only reported outside the African region when outbreaks linked to infected pet prairie dogs increased in the USA in 2003 (Brown and Leggat, 2016; Centers for Disease Control Prevention (CDC), 2020). None of the cases in this outbreak (a total of 81 recognized cases, 40% of which were confirmed cases) were attributed to secondary transmission, and the mortality rate was zero. The dogs acquired infections from infected exotic dormice and pouched rats, which were transported from Ghana.

Multiple factors are involved in the rise of HMPX since the 1970s. These include active, passive, and sentinel surveillance efforts, climatic dynamics, deforestation, and rapid demographic expansion of regions where the MPXV is retained in a huge population of host animals, with a surge in natural or incidental hosts. Furthermore, individuals aged 40–45 years or less lack immunity to the smallpox virus after the termination of immunization against smallpox in the 1980s. In summary, significantly associated dynamics also involve hominid behavior (for example, interaction with dead or live creatures, reservoir hosts, staying in tropically reforested or newly desforested ranges, hunting, close interaction with an infected individual, sharing a joint bedroom with an infected individual, sharing kitchenette kits with an infected individual, and preparation and intake of bush meat or monkeys), scarcity, military, and political conflicts, territorial movements, tourism, the trade of exotic animals, and public healthcare services (Hutin et al., 2001; Parker et al., 2007; Rimoin et al., 2010; Vaughan et al., 2020; Mauldin et al., 2022; Quarleri et al., 2022).

3.2. Epidemiological dynamics of MPX in the global epidemic in 2022

Since May 2022, many outbreaks of HMPX have been documented in European states for the first time, where the MPX infection is not prevalent (ECDC, 2022a; Sham et al., 2022; World Health Organization, 2022b,j). From 13 May 2022 to 16 May 2022, the UK documented six HMPX cases for the first time; these cases were investigated without any epidemiological associations with imported animals, travel to African countries, and with all cases self-distinguishing as men who have sex with other men, bisexual, or gay (WHO, 2022c). The majority of HMPX cases have a travel record to various states in Europe and America. Moreover, cases of HMPX in the enzootic world remain to be described.

Since early May and as of 19 September 2022, over 62,000 HMPX cases have been documented in the non-endemic world (Centers for Disease Control and Prevention (CDC), 2022d). As of 19 September 2022, ~44 European republics have documented 24,017 cases, demonstrating 38.5% of all the globally documented cases in the recent epidemic. The highest figure (n = 6947) was documented in Spain, followed by France (n = 3898), Germany (n = 3563), and the UK (n = 3552); however, one case each was documented in Ukraine and Turkey. In this epidemic, the largest number of cases (n = 23,892) was documented in the USA, comprising 38.3% of the globally reported MPX cases. Variations in the incidence rate of HMPX by state might be relatively described by dissimilarities in demography and density population at threat, social and economic circumstances, under-diagnosis, and/or improper reporting.

The person-to-person transmission dynamic of HMPX has been documented in the European region for the first time (ECDC, 2022a; Vivancos et al., 2022). In the recent occurrence, clinical features that differ from retrospective documentations were investigated, including the lack of prodromal or very minor prodromic symptoms, a rash that appears earlier than the prodromic stage, a rash that exhibits only an ulcer or some abrasions, a skin rash restricted only to the perineal or anogenital region, and mainly inguinal site lymphadenopathy (Bunge et al., 2022; Iñigo Martínez et al., 2022; Thornhill et al., 2022). Based on the severity, MPX is categorized as mild and moderate, with ~4 to 10% of patients admitted to hospitals (Centers for Disease Control and Prevention (CDC), 2022d; Girometti et al., 2022; WHO, 2022d). Due to encephalitis and comorbidities, ~20 deaths due to MPX have been documented in the current multiregional epidemic, a figure that matches that in Africa as well as in non-endemic states (Centers for Disease Control and Prevention (CDC), 2022d; ECDC, 2022a; European Centre for Disease Prevention Control (ECDC), 2022c). Though several documentations specified a small number of cases without symptoms (Centers for Disease Control and Prevention (CDC), 2022d), a UK-based cohort study investigation showed interactions with an individual with confirmed MPX infection were recorded in ~25% of cases (Patel et al., 2022). In this prospective epidemic, there has been no concrete evidence of animal-to-human or human-to-animal spread. In this occurrence, the investigated viruses were linked to the West African clade (Isidro et al., 2022; Kmiec and Kirchhoff, 2022).

An epidemiological study at 43 locations in 16 investigated states documented that ~99% of men were affected by MPX, among whom 98% self-distinguished as bisexual men or gay, or men who have sex with other men (Thornhill et al., 2022). In the current study, the 18–50 years of age range was reported as having an average of 38 years of age. Among them, 41% closely interacted with HIV patients, and in most of the cases, HIV was considerably controlled. Pre-exposure prevention protocol was adopted by 57% of HIV-negative individuals or those patients who were not aware of their HIV status. In 29% of examined individuals, there was evidence of associated sexually communicated infections. In this study, confirmation of sexual transmission of infection was impossible, sex-related history was investigated in 95% of5 patients, 20% reported engaging in “chem sex” (sex-linked with the practice of medicines), and 32% reported attending on-site-sex events (Thornhill et al., 2022).

In the Spanish outbreak (Iñigo Martínez et al., 2022), ~84.1% of MPX cases were documented as having a history of condomless sex or having sex with more than one sex partner within 3 weeks before the beginning of disease indications, 8.1% of infected persons confirmed having safe sexual activities, and 7.9% gave no response. Furthermore, in the present report, ~80.3% of individuals were not aware of MPX or had no interaction with a recognized MPX case. One month before MPX diagnosis, numerous individuals had an international travel history to Italy, the UK, Germany, Belgium, Portugal, Peru, etc., with no recorded cases of travel to African countries. Furthermore, at a sauna region in Madrid and at the Gay Pride festival on a Spanish island, some cases of MPX were reported, with various secret gatherings also having a major role; dating via social networks was recorded by 56.9% of individuals as well as sexual activities in bars, touring zones, and secret studios. In this occurrence, the MPXV was investigated in seminal fluid samples of the patients, with sexual interaction acts a significantly associated factor in the disease occurrence. More investigation is required to explain the sexual transmission dynamics of MPX via genital fluids (Antinori et al., 2022; Iñigo Martínez et al., 2022; Thornhill et al., 2022; Noe et al., 2023).

Remarkably, various reports show that data were registered as having a lack of immunization status (Benites-Zapata et al., 2022). Among the US MPX cases for whom immunization status was accessible, 14% testified retrospectively to being vaccinated against smallpox (with 23% receiving single instead of double doses, 23% receiving pre-exposure prevention at an unidentified stage before the current occurrence, and 54% of individuals not providing an answer about vaccination status) (Philpott et al., 2022). To date, 344 MPX cases have been recorded among medical staff, and among them, some cases of spread via job-related exposure have been described in this occurrence (Centers for Disease Control and Prevention (CDC), 2022d). Worldwide, youngsters are most vulnerable to MPX because of the termination of smallpox immunization after the eradication of smallpox (Factsheet for health professionals on monkeypox: European Centre for Disease, 2022d). To avoid MPX, two vaccines (JYNNEOS and ACAM2000) are applied as follows: JYNNEOS vaccine is applied to safeguard against both smallpox and MPX, whereas the ACAM2000 vaccine is applied to protect against smallpox (Centers for Disease Control Prevention (CDC), 2022c; Factsheet for health professionals on monkeypox: European Centre for Disease, 2022d). The feedback of the immune system after vaccination is mainly based on cross-defense among the orthopoxviruses and vaccinia virus (McCollum and Damon, 2014; ECDC, 2022a). In the ongoing occurrence of MPX in the USA, men who have sex with other men, gender-diverse individuals, or transgender individuals who had sex with men in the previous 14 days might get the vaccination if they had sex with numerous individuals, or had sex at commercial sex clubs or bathhouses, or had sexual activities at an occasion, site, or in a zone where MPX spread is happening (Centers for Disease Control Prevention (CDC), 2022c). As per the recommendations of the WHO, several states in Europe, including the UK, Germany, France, and Spain, were providing immunization during the 2022 MPX epidemic (ECDC, 2022b; Factsheet for health professionals on monkeypox: European Centre for Disease, 2022d).

The WHO measures the MPX threat as sensible worldwide, with the exemption of the European and American regions, where the threat is evaluated as high (Factsheet for health professionals on monkeypox: European Centre for Disease, 2022d; Zachary and Shenoy, 2022). The recent global occurrence differs from previous epidemics in a few ways: the infrequent degree of incidence; unusual rapid expansion globally; spreading in non-endemic countries; mostly spreading among younger men (aged 18–44 years), with over 97% of them self-recognizing as men who have sexual intercourse with other men or unsafe sex with several individuals; the role of different super spreading occasions associated with transnational get-togethers; while asymptomatic infections and lack of or mild signs throughout the prodromal period make easier the transmission dynamics of the virus; and the occurrence of minor cases (Bunge et al., 2022; Centers for Disease Control and Prevention (CDC), 2022d; Delaney et al., 2022; WHO, 2022d). In summary, an advanced investigation is required to properly recognize and advance the supervision of HMPX.

4. MPX host range

Monkeypox virus (MPXV) isolates based on phenotypic and genetic deviations are divided into two different clades, specifically the Congo Basin and the West African clades (Likos et al., 2005). In contrast to the variola virus, which affects only humans, the MPXV is among those orthopoxviruses that can infect numerous animal hosts and can spread to humans (Parker et al., 2007; Parker and Buller, 2013; Patrono et al., 2020; Kmiec and Kirchhoff, 2022). The fixed reservoir host of the MPXV can even be unrecognized, but some small mammalians such as giant pouched rats (Cricetomys spp.), rope squirrels (Funisciurus spp.), sun squirrels (Heliosciurus spp.), and African dormice (Graphiurus spp.) are assumed to transmit the virus to human beings in Central and West Africa (Alakunle et al., 2020). MPXV is communicated from animals to human beings during hunting, trapping, treating infected animals, and dealing with their secretory and excretory fluids.

Based on experimental analyses and field investigations, MPXV has been documented in a wide range of rodents, including Oryctolagus cuniculus (rabbits), Mus musculus (mice), Marmota monax (woodchucks), hamsters, Jaculus sp. (jerboas), and Atherurus africanus (porcupines). Similarly, based on techniques such as molecular assay, virus separation, or in vitro contamination, vulnerability to MPXV was investigated in black-tailed prairie dogs (Cynomys ludovicianus), anteaters, short-tailed opossums (Monodelphis domestica), giant anteater (Myrmecophaga tridactyla), African hedgehogs (Atelerix sp.), southern opossums (Didelphis marsupialis), and various non-human primate species (Parker et al., 2007; Doty et al., 2017). The host range and susceptibility to MPXV infection is also shown in Table 3 (Silva et al., 2020).

In Africa, Asia, and Europe, non-human primates, chimpanzees (Pan troglodytes), orangutans (Pongo pygmaeus), cynomolgus monkeys (Macaca fascicularis), and sooty mangabeys (Cercocebus atys) can be infected with MPXV. In the USA and the UK, non-human primates (Magnus et al., 1959; Wachtman and Mansfield, 2012; Alakunle et al., 2020) and common marmosets (Callithrix jacchus) were determined to be vulnerable to MPXV by intravenous injection (Mucker et al., 2015). Non-human primates may be affected by MPXV and show signs and symptoms, while small mammalians can be asymptomatic carriers of the virus (CDC, 2022a).

In 2003, HMPX infection in the USA was mainly linked with close interaction with ill pet prairie dogs introduced from the Ghana region of West Africa (Reed et al., 2004). This incident, as well as the rodent's infection, intensified alarms about the entry of MPX infection into the USA. In the meantime, the vulnerability of numerous African rodents to MPXV raised fear related to the spread of the virus to human beings, as these rodents are often maintained as pets (Centers for Disease Control Prevention (CDC), 2020; Sklenovská, 2020). Non-human primates, squirrels, and rodents have been observed to have MPXV based on sero-investigations in African territories. Wild animals are more susceptible to the disease. In 1985, MPXV was isolated from Thomas's rope squirrel (Funisciurus anerythrus) in the DRC and in 2012 from the sooty mangabey (Cercocebus atys) in Cote d Ivoire, signifying that these animal species might act as MPXV reservoirs hosts (Falendysz et al., 2017).

Human beings can also be accidental hosts (Parker et al., 2007) since the eradication of smallpox, based on MPXV morbidity and mortality, it is converted into the most significant infective zoonotic orthopoxvirus for humans. In 1970, the first human case of MPXV was documented in a 9-month-old child in the DRC, who presented with smallpox-like skin lesions (Arita and Henderson, 1968; Ladnyj et al., 1972). Numerous humanoid cases were investigated in subsequent years. During 1970–1999, the WHO documented almost 404 confirmed and 500 suspicious cases of human MPXV in various African states (Liberia, Gabon, Côte d'Ivoire, Central African Republic, and Cameroon, but predominantly in the DRC) (World Health Organization, 1997; Heymann et al., 1998; Sklenovská and Van Ranst, 2018). In May and June 2003, some MPX cases were reported to the Wisconsin Division of Public Health, with no mortality and no person-to-person spread observed (Centers for Disease Control Prevention (CDC), 2022c). The origin of this occurrence was traced back to the importation of exotic infected animals from Ghana (Khodakevich et al., 1986; Sklenovská and Van Ranst, 2018; CDC, 2022b). Luckily, the stage-wise episode of infected rodents in cages in the USA was temporary, and the pattern of spread in the country was destroyed (Petersen et al., 2019a). More recently, on 27 September 2022, 66,000 cases of MPX were confirmed in more than 100 non-endemic states, with fluctuating epidemiological footprinting from retrospective outbreaks (Li et al., 2022).

Human MPX cases have been snowballing globally with time, although they might have been miscalculated. Remarkably, diagnostic capacities in the affected states are mostly inadequate, while global healthcare personnel are mostly unaware of MPX disease. The emergence of the current MPX spread is linked with dynamics such as the growing invasion of hominids into wild habitations, the international and global travel of the public from enzootic regions to non-endemic areas, the introduction of pets and laboratory animals, lack of active disease surveillance, and improper prevention and control strategies (Essbauer et al., 2010). Furthermore, the termination of smallpox immunization and various reports of animals in captivity or experimental laboratories have made the global public susceptible to MPXV infection or other orthopoxvirus infection. As the MPX virus is an increasing global zoonotic threat with epidemic potential, and as most of its host range and life cycle in nature remains unclear, developments are immediately mandatory to recognize its biological cycle and host range for future prevention and control strategy.

5. Associated risk factors of MPX

Although the main associated risk factors fluctuate among different epidemics, the significance of obtaining the characteristics of particular individuals for calculating and predicting epidemic patterns cannot be ignored. Conventionally, MPX cases involving spread among human beings are more probable to be individuals who are women, non-vaccinated against smallpox, living in the same house, or providing cure to a primary case (JeŽek et al., 1988). Prominently, this information is based on clade 1-associated MPX in the DRC and did not represent other enzootic regions; outbreak investigations of different endemic states show that youngsters face the ample burden of the MPX infection. In an occurrence of clade 2B-associated MPX in Nigerian territory, mostly 21 to 40-year-old individuals were involved (Alakunle et al., 2020), although the index case was an 11-year-old teenager (Ogoina et al., 2019; Hobson et al., 2021). These associated risk factors specify the role of social and behavioral determining factors in helping the person-to-person spread of MPX infection. However, a systemic review and meta-analyses (Sham et al., 2022) explained the detailed associated risk factors for the primary introduction of MPX.

One of the serious associated risk factors for patients and healthcare workers is nosocomial MPXV infections (nosocomial infections, also referred to as healthcare-associated infections (HAI), are infection(s) acquired during the process of receiving healthcare that were not present at the time of admission) in both enzootic and non-enzootic areas. Smallpox was also mainly due to nosocomial occurrences (CDC, 1963), with the peak rate of spread occurring inside health centers (Kiang, 2003). Similarly, hospital-borne occurrences of MPX are mainly serious and long-term. These consistent multifactorial results include individuals who are susceptible to diseases, healthcare center sanitation patterns, and the usage of aerosol-producing measures (Judson, 2019). A total of six generations of MPXV spread were investigated in a public healthcare center in Impfondo, Republic of Congo, specifying MPXV's potential to spread if not rapidly handled in healthcare settings (Learned et al., 2005). On one occasion in the UK, a medical employee who had collected a blanket and dressing of an MPX-infected person was subsequently contracted MPXV (Vaughan et al., 2020).

Zoonotic transmission (transmission from animals to human beings) can arise from direct interaction with the blood, body fluids, or mucosal or cutaneous lesions of infected animals (Nigeria Centre for Disease (NCDC), 2022). In Africa, MPX has been reported in various hosts including tree squirrels, rope squirrels, dormice, Gambian poached rats, several types of monkeys, and other animals (Kile et al., 2005; Yinka-Ogunleye et al., 2019). The reservoir of MPX has not cleared yet; however, rodents are the main expected but not clear yet (Kile et al., 2005). The intake of uncooked meat and other foodstuffs of infected animal origin is a probable risk factor (Petersen et al., 2018). Individuals living in or near forested regions could have an incidental or low-degree of exposure to infected animals.

Human-to-human spread can result from close contact with respiratory discharges, dermal abrasions of an infected individual, or a newly infected entity (Nolen et al., 2015). MPXV spread via respiratory particles typically requires lengthy and close interactions, which put community health staff, families, and other close contacts of active cases at greater risk (Petersen et al., 2018). The predictable sequence of spread in the public has grown in the current era from six to nine repeated human-to-human contaminations, and this could indicate decreasing protection in humans due to the end of smallpox immunization (Meslin et al., 2000).

Human-to-animal transmission of MPXV has not been reported yet and it is believed that the outbreak may not have been caused by infection from animals (Diaz-Cánova et al., 2022). European health administrators firmly recommend that rodent pets, e.g., guinea pigs and hamsters, that belong to patients with HMPX should be quarantined and watched or even euthanized to stop the spread of the virus (Heskin et al., 2022). However, the most recent identifications in August 2022 were two cases of human-to-dog transmission reported in France and Brazil (Peters, 1966; Islam et al., 2023). In Paris, a pet dog (a healthy 4-year-old male Italian Greyhound) of two individuals who were suffering from MPX was also diagnosed with MPXV. The virus was found in the individuals, and the dog showed homology on DNA sequencing (Seang et al., 2022). This dog tested positive for MPXV after showing symptoms such as abdominal abscesses. Based on the sequencing results and symptoms of the two patients as well as the dog, the researchers concluded that MPXV was indeed transmitted between humans and dogs (Seang et al., 2022).

As per disease investigations, the main concern is more for youngsters and immunocompromised adults, such as persons who have HIV infection (De Sousa et al., 2022). The recent global MPXV occurrence in human beings increases the probability that the virus might have mutated genetically and that human behavior may have altered or collected. These mutations might have occurred due to decreasing smallpox immunity, diminishing COVID-19 protective policies, sexual connections, and the restart of intercontinental movements (Zhu et al., 2022). An additional factor recognized in the current topographical distribution of MPX spread is sexual interaction, in particular among men who have sex with other men (ECDC, 2022a). Table 4 shows the updated risk factors associated with MPX cases worldwide.

TABLE 4
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Table 4. Risk factors associated with MPX cases.

6. MPXV as a potential bioweapon

Monkeypox (MPX) is no longer a rare, self-limiting disease limited to endemic countries. The MPXV is a high-danger pathogen that can spread to various regions and poses a significant threat to public health. Its ever-changing epidemiology and transmission dynamics have increased the possibility of it evolving into a much deadlier pathogen that can be used as a bioweapon due to its unanticipated development in places with no known epidemiological linkages, which permits undetected transmission for a long period and raises concerns about the virus's evolution (Ferdous et al., 2023). Despite the potential of MPXV to be used as a global bioweapon, the possibility of biological warfare and bioterrorism cannot be completely ruled out due to modern molecular biological advances and the spread of the virus to various regions due to rising globalization and cross-border animal mobility. As a result of these factors, MPXV, along with the variola virus and many other poxviruses, is on the NIH's highest danger list. The CDC has categorized it as a “select agent.” Human travel is prevalent today, providing risk for the spread of MPX, and animals carried across borders represent an immediate danger of disease spread (Amir et al., 2023; Khattak et al., 2023).

7. Critical challenges associated with MPX research

To better understand the dynamics of MPX transmission and control, operational research is currently facing challenges, such as insufficient resources for detailed case investigations and contact follow-up in affected communities. A lack of adequate diagnostic facilities in laboratories is a serious problem. Owing to the lack of laboratory diagnosis capacity and access, as well as the difficulty of diagnosing MPX, it is difficult to discover any underlying etiology. A seroprevalence study would help to understand the epidemiology as well as subclinical infection among contacts in communities (Lederman et al., 2007). The currently available serological assays are generic orthopox tests; they do not specifically test for the MPXV. This is due to the fact that there is cross-reactivity between MPX and smallpox viruses, and therefore, we cannot distinguish between a MPXV infection and prior smallpox vaccinations or other orthopoxvirus infections. In addition, these assays are not currently available in the marketplace. It has been found that, according to data collected from Nigeria, ~20% of 70 MPX-negative patients presenting rash illness with similar antigens also had orthopox antibodies. To identify the transmission of other orthopoxviruses in human and animal populations, further research, including using molecular and genomic approaches, is needed (Ihekweazu et al., 2020).

Precautions such as avoiding close interaction with reservoir hosts and infected persons, proper handwashing and disinfection, avoiding non-important travel, usage of suitable personal protective equipment, appropriate practices of waste management, and quarantine, treatment, and immunization of infected individuals must be applied to reduce the spread of MPXV. It is necessary to enhance continuous active investigation and monitoring of the MPXV in community health services and in the general population, particularly in livestock populations such as animal farmhouses, marketplaces, and slaughterhouses. Individuals traveling from regions of the world where the infection is prevalent must be tested and declared free of disease before entry to another country. Infected persons must be supervised to stop the further spread of the virus to vulnerable populations. The public must be made aware of and educated on the threats of bushmeat intake, zoonotic spread, the significance of one's health, and the application of protective procedures and biosecurity against the MPXV. Finally, training public health facilitators on how to avoid the spread of the disease and how to protect themselves from the threat of infection is critical because they are at greater threat of being infected (Idris and Adesola, 2022).

8. Conclusion

The contemporary global public in the present era has already survived the COVID-19 pandemic and the extraordinary damages it produced. Due to globalization, communicable infections are becoming more widespread and pose a global public health threat. There is no method to determine subsequent emerging diseases, but one example, COVID-19, has re-taught the globe that what virus will arise as a major public health threat is somewhat unpredictable and that it is frequently too late to put in place counter-measures after the fact. The unpredicted appearance of MPX in the non-endemic world suggests some undetectable transmission dynamics. Hence, open-minded and vigilant epidemiological attention and global public awareness of the recent MPX epidemic are required, not only in developed economies but also in underdeveloped states that have been dominated by such viruses for several years. There is an urgent need for researchers and epidemiologists to participate more in this global public health threat, follow up on it, and conduct more molecular epidemiological research on the topic. Therefore, there is an urgent need for proper epidemiological approaches to be adopted to investigate the emergence of current MPX epidemics, as well as the true cause of the disease, transmission dynamics, identification of associated risk factors, and investigation of the global host range. Rapid documentation of new cases, active investigation, and syndromic observational surveillance approaches would provide insights into variations in epidemiological tendencies, particularly in situations where validating diagnostic techniques is challenging. Therefore, this review has been compiled to highlight the epidemiology, global host ranges, and associated risk factors of MPX, focusing on its epidemic potential and global public health threat.

Author contributions

Conceptualization: MU and ZZ. Methodology, investigation, data curation, and writing-original review draft preparation: MU, YL, and ZZ. Writing-review and editing and visualization: MU and KM. Funding acquisition: ZZ and YL. All authors have read and agreed to the published version of the manuscript.

Funding

This study was funded and supported by Southwest Mizu University Double World-Class Project (XM2023012), the Southwest Mizu University Research Startup Funds (16011211013), the Natural Science Foundation of Sichuan Province (2022NSFSC0073), and the Fundamental Research Funds for the Central Universities Southwest Minzu University (2021115).

Acknowledgments

We would like to thank ZZ and YL of the College of Animal Husbandry and Veterinary Medicine, Southwest Minzu University, Chengdu, China, for their support during the compilation of the review and providing the main idea for the manuscript. We are sincerely grateful to Prof. Dr. Arfan Yousaf and Dr. Muhammad Arif Zafar of the Pir Mehr Ali Shah Arid Agriculture University, Rawalpindi for their official support.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Adegboye, O. A., Eugenia Castellanos, M., Alele, F. O., Pak, A., Ezechukwu, H. C., Hou, K., et al. (2022). Travel-related monkeypox outbreaks in the era of COVID-19 pandemic: are we prepared?. Viruses 14, 1283. doi: 10.3390/v14061283

PubMed Abstract | CrossRef Full Text | Google Scholar

Adler, H., Gould, S., Hine, P., Snell, L. B., Wong, W., Houlihan, C. F., et al. (2022). Clinical features and management of human monkeypox: a retrospective observational study in the UK. Lancet Infect. Dis. 22, 1153–1162. doi: 10.1016/S1473-3099(22)00228-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Alakunle, E., Moens, U., Nchinda, G., and Okeke, M. I. (2020). Monkeypox virus in Nigeria: infection biology, epidemiology, and evolution. Viruses 12, 1257. doi: 10.3390/v12111257

PubMed Abstract | CrossRef Full Text | Google Scholar

Altindis, M., Puca, E., and Shapo, L. (2022). Diagnosis of monkeypox virus–An overview. Travel Med. Infect. Dis. 10, 2459. doi: 10.1016/j.tmaid.2022.102459

PubMed Abstract | CrossRef Full Text | Google Scholar

Amir, M., Vohra, M., Osoro, I., Sharma, A., and Kumar, R. (2023). Monkeypox (Mpox) re-emergence: prevalence, diagnostics, countermeasures, and its global effect. J. Zoon. Dis. 7, 199–206. doi: 10.22034/JZD.2023.16032

CrossRef Full Text | Google Scholar

Antinori, A., Mazzotta, V., Vita, S., Carletti, F., Tacconi, D., Lapini, L. E., et al. (2022). Epidemiological, clinical and virological characteristics of four cases of monkeypox support transmission through sexual contact, Italy, May 2022. Eurosurveillance 27, 2200421. doi: 10.2807/1560-7917.ES.2022.27.22.2200421

PubMed Abstract | CrossRef Full Text | Google Scholar

Arita, I., and Henderson, D. A. (1968). Smallpox and monkeypox in non-human primates. Bull. World Health Organiz. 39, 277.

Google Scholar

Arita, I., Jezek, Z., Khodakevich, L., and Ruti, K. (1985). Human monkeypox: a newly emerged orthopoxvirus zoonosis in the tropical rain forests of Africa. Am. J. Tropic. Med. Hygiene 34, 781–789. doi: 10.4269/ajtmh.1985.34.781

PubMed Abstract | CrossRef Full Text | Google Scholar

Beer, E. M., and Rao, V. B. (2019). A systematic review of the epidemiology of human monkeypox outbreaks and implications for outbreak strategy. PLoS Neglect. Tropic. Dis. 13, e0007791. doi: 10.1371/journal.pntd.0007791

PubMed Abstract | CrossRef Full Text | Google Scholar

Benites-Zapata, V. A., Ulloque-Badaracco, J. R., Alarcon-Braga, E. A., Hernandez-Bustamante, E. A., Mosquera-Rojas, M. D., Bonilla-Aldana, D. K., et al. (2022). Clinical features, hospitalisation and deaths associated with monkeypox: a systematic review and meta-analysis. Ann. Clinic. Microbiol. Antimicrob. 21, 36. doi: 10.1186/s12941-022-00527-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Bernard, S. M., and Anderson, S. A. (2006). Qualitative assessment of risk for monkeypox associated with domestic trade in certain animal species, United States. Emerg. Infect. Dis. 12, 1827–1833. doi: 10.3201/eid1212.060454

PubMed Abstract | CrossRef Full Text | Google Scholar

Berthet, N., Nakoun,é, E., Whist, E., Selekon, B., Burguière, A. M., Manuguerra, J. C., et al. (2011). Maculopapular lesions in the Central African Republic. The Lancet 378, 1354. doi: 10.1016/S0140-6736(11)61142-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Bezerra-Santos, M. A., Mendoza-Roldan, J. A., Thompson, R. A., Dantas-Torres, F., and Otranto, D. (2021). Illegal wildlife trade: a gateway to zoonotic infectious diseases. Trends Parasitol. 37, 181–184. doi: 10.1016/j.pt.2020.12.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Boesecke, C., Monin, M. B., van Bremen, K., Schlabe, S., and Hoffmann, C. (2022). Severe monkeypox-virus infection in undiagnosed advanced HIV infection. Infection 2, 1-2. doi: 10.1007/s15010-022-01901-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Bragazzi, N. L., Kong, J. D., Mahroum, N., Tsigalou, C., Khamisy-Farah, R., Converti, M., et al. (2023). Epidemiological trends and clinical features of the ongoing monkeypox epidemic: a preliminary pooled data analysis and literature review. J. Med. Virol. 95, e27931. doi: 10.1002/jmv.27931

PubMed Abstract | CrossRef Full Text | Google Scholar

Breman, J. G., Nakano, J. H., Coffi, E., Godfrey, H., and Gautun, J. C. (1977). Human poxvirus disease after smallpox eradication. Am. J. Tropic. Med. Hygiene 26, 273–281. doi: 10.4269/ajtmh.1977.26.273

PubMed Abstract | CrossRef Full Text | Google Scholar

Breman, J. G., Steniowski, M. V., Zanotto, E., Gromyko, A. I., and Arita, I. (1980). Human monkeypox, 1970–79. Bull. World Health Organizat. 58, 165–182.

Google Scholar

Brown, K., and Leggat, P. A. (2016). Human monkeypox: current state of knowledge and implications for the future. Tropic. Med. Infect. Dis. 1, 8. doi: 10.3390/tropicalmed1010008

PubMed Abstract | CrossRef Full Text | Google Scholar

Bunge, E. M., Hoet, B., Chen, L., Lienert, F., Weidenthaler, H., Baer, L. R., et al. (2022). The changing epidemiology of human monkeypox—a potential threat? a systematic review. PLoS Neglect. Tropic. Dis. 16, e0010141. doi: 10.1371/journal.pntd.0010141

PubMed Abstract | CrossRef Full Text | Google Scholar

CDC. (1963). “Smallpox–Stockholm, Sweden,” in Morbidity and Mortality Weekly Report, Centers for Disease Control and Prevention: Atlanta, GA.

Google Scholar

CDC. (1997). Human monkeypox – Kasai oriental, Democratic Republic of Congo, February 1996-October 1997. MMWR. 46, 1168–1171.

Google Scholar

CDC. (2022a). Monkeypox in animals. Atlanta, Georgia. Available online at: https://www.cdc.gov/poxvirus/monkeypox/veterinarian/monkeypox-in-animals.html (accessed August 9, 2022).

CDC. (2022b). Monkeypox outbreak global map. Centers for Disease Control and Prevention. Available online at: https://www.cdc.gov/poxvirus/monkeypox/response/2022/world-map.html (accessed August 2, 2022).

CDC. (2022e). Monkeypox Outbreak Global Map 2022. Available online at: https://www.cdc.gov/poxvirus/monkeypox/response/2022/world-map.html (accessed August 7, 2022).

Centers for Disease Control Prevention (CDC). (2020). Centers for Disease Control and Prevention. Update: Multistate Outbreak of Monkeypox-Illinois, Indiana, Missouri, Ohio, and Wisconsin. 2003. Available online at: https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5227a5.htm (accessed September 26, 2020).

Google Scholar

Centers for Disease Control and Prevention (CDC). (2022d) Monkeypox; CDC: Atlanta, GE, USA, 2022. Available online: https://www.cdc.gov/poxvirus/monkeypox/index.html. (accessed September 20, 2022).

Centers for Disease Control and Prevention (CDC). (2022c). Interim Clinical Considerations for Use of JYNNEOS and ACAM2000 Vaccines during the 2022 U.S. Monkeypox Outbreak; CDC: Atlanta, GE, USA. Available online: https://www.cdc.gov/poxvirus/monkeypox/health-departments/vaccine-considerations.html (accessed September 20, 2022).

Cohen-Gihon, I., Israeli, O., Shifman, O., Erez, N., Melamed, S., Paran, N., et al. (2020). Identification and whole-genome sequencing of a monkeypox virus strain isolated in Israel. Microbiol. Resour. Announc. 9, e01524–e01519. doi: 10.1128/MRA.01524-19

PubMed Abstract | CrossRef Full Text | Google Scholar

Damon, I. K. (2011). Status of human monkeypox: clinical disease, epidemiology and research. Vaccine 29, D54–D59. doi: 10.1016/j.vaccine.2011.04.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Davido, B., D'anglejan, E., Jourdan, J., Robinault, A., and Davido, G. (2022). Monkeypox 2022 outbreak: cases with exclusive genital lesions. J. Travel Med. 29, taac077. doi: 10.1093/jtm/taac077

PubMed Abstract | CrossRef Full Text | Google Scholar

De Sousa, D., Patrocínio, J., Frade, J., Correia, C., Borges-Costa, J., and Filipe, P. (2022). Human monkeypox coinfection with acute HIV: an exuberant presentation. Int. J. STD AIDS 33, 936–938. doi: 10.1177/09564624221114998

PubMed Abstract | CrossRef Full Text | Google Scholar

Delaney, K. P., Sanchez, T., Hannah, M., Edwards, O. W., Carpino, T., Agnew-Brune, C., et al. (2022). Strategies adopted by gay, bisexual, and other men who have sex with men to prevent monkeypox virus transmission - United States, August 2022. MMWR Morb. Mortal Wkly. Rep. 75, 1126–1130. doi: 10.15585/mmwr.mm7135e1

PubMed Abstract | CrossRef Full Text | Google Scholar

Diaz-Cánova, D., Moens, U. L., Brinkmann, A., Nitsche, A., and Okeke, M. I. (2022). Genomic sequencing and analysis of a novel human cowpox virus with mosaic sequences from North America and Old World Orthopoxvirus. Front Microbiol 13, 868887. doi: 10.3389/fmicb.2022.868887

PubMed Abstract | CrossRef Full Text | Google Scholar

Doty, J. B., Malekani, J. M., Kalemba, L. S. N., Stanley, W. T., Monroe, B. P., Nakazawa, Y. U., et al. (2017). Assessing monkeypox virus prevalence in small mammals at the human–animal interface in the Democratic Republic of the Congo. Viruses 9, 283. doi: 10.3390/v9100283

PubMed Abstract | CrossRef Full Text | Google Scholar

Durski, K. N., McCollum, A. M., Nakazawa, Y., Petersen, B. W., Reynolds, M. G., Briand, S., et al. (2018). Emergence of monkeypox—west and central Africa, 1970–2017. Morbidity Mortal. Weekly Rep. 67, 306–310. doi: 10.15585/mmwr.mm6710a5

PubMed Abstract | CrossRef Full Text | Google Scholar

ECDC. (2022a). Communicable Disease Threats Report; Week 31, 31 July−6 August 2022. ECDC: Stockholm, Sweden. Available online at: https://www.ecdc.europa.eu/sites/default/files/doc/Communicable-disease-threats-report-6-aug-2022-allusers.pdf (accessed August 31, 2022).

ECDC. (2022b). Factsheet for Health Professionals on Monkeypox. ECDC: Stockholm, Sweden. Available online at: https://www.ecdc.europa.eu/en/all-topics-z/monkeypox/factsheet-health-professionals. (accessed September 20, 2022)

Endo, A., Murayama, H., Abbott, S., Ratnayake, R., Pearson, C. A., Edmunds, W. J., et al. (2022). Heavy-tailed sexual contact networks and the epidemiology of monkeypox outbreak in non-endemic regions, May 2022. MedRxiv. 13, 6353. doi: 10.1101/2022.06.13.22276353

PubMed Abstract | CrossRef Full Text

Essbauer, S., Pfeffer, M., and Meyer, H. (2010). Zoonotic poxviruses. Vet. Microbiol. 140, 229–236. doi: 10.1016/j.vetmic.2009.08.026

PubMed Abstract | CrossRef Full Text | Google Scholar

European Centre for Disease Prevention and Control (ECDC). (2022c). Epidemiological update: Monkeypox outbreak [Internet]. Solna, Sweden: ECDC. [updated 2022 May 20; cited 2022 Jun 6]. Available online at: https://www.ecdc.europa.eu/en/news-events/epidemiological-updatemonkeypox-outbreak

Factsheet for health professionals on monkeypox: European Centre for Disease, Prevention, and Control. (2022d). Available online at: https://www.ecdc.europa.eu/en/all-topics-z/monkeypox/factsheet-health-professionals.

Falendysz, E. A., Lopera, J. G., Doty, J. B., Nakazawa, Y., Crill, C., Lorenzsonn, F., et al. (2017). Characterization of Monkeypox virus infection in African rope squirrels (Funisciurus sp.). PLoS Neglect. Tropic. Dis. 11, e0005809. doi: 10.1371/journal.pntd.0005809

PubMed Abstract | CrossRef Full Text | Google Scholar

Fauci, A. S. (2005). Emerging and reemerging infectious diseases: the perpetual challenge. Acad. Med. 80, 1079–1085. doi: 10.1097/00001888-200512000-00002

PubMed Abstract | CrossRef Full Text | Google Scholar

Ferdous, J., Barek, M. A., Hossen, M. S., Bhowmik, K. K., and Islam, M. S. (2023). A review on monkeypox virus outbreak: new challenge for world. Health Sci. Rep. 6, e1007. doi: 10.1002/hsr2.1007

PubMed Abstract | CrossRef Full Text | Google Scholar

Formenty, P., Muntasir, M. O., Damon, I., Chowdhary, V., Opoka, M. L., Monimart, C., et al. (2010). Human monkeypox outbreak caused by novel virus belonging to Congo Basin clade, Sudan, 2005. Emerg. Infect. Dis. 16, 1539–1545. doi: 10.3201/eid1610.100713

PubMed Abstract | CrossRef Full Text | Google Scholar

Foster, S. O., Brink, E. W., Hutchins, D. L., et al. (1972). Human monkeypox. Bull. World Health Organ. 46, 569–576.

Google Scholar

Girometti, N., Byrne, R., Bracchi, M., Heskin, J., McOwan, A., Tittle, V., et al. (2022). Demographic and clinical characteristics of confirmed human monkeypox virus cases in individuals attending a sexual health centre in London, UK: an observational analysis. Lancet Infect. Dis. 22, 1321–1328. doi: 10.1016/S1473-3099(22)00411-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Guagliardo, S. A. J., Monroe, B., Moundjoa, C., Athanase, A., Okpu, G., Burgado, J., et al. (2020). Asymptomatic orthopoxvirus circulation in humans in the wake of a monkeypox outbreak among chimpanzees in Cameroon. Am. J. Tropic. Med. Hygiene 102, 206–212. doi: 10.4269/ajtmh.19-0467

PubMed Abstract | CrossRef Full Text | Google Scholar

Hatmal, M. M. M., Al-Hatamleh, M. A., Olaimat, A. N., Ahmad, S., Hasan, H., Ahmad Suhaimi, N. A., et al. (2022). Comprehensive literature review of monkeypox. Emerg. Microb. Infect. 11, 2600–2631. doi: 10.1080/22221751.2022.2132882

PubMed Abstract | CrossRef Full Text | Google Scholar

Heskin, J., Belfield, A., Milne, C., Brown, N., Walters, Y., Scott, C., et al. (2022). Transmission of monkeypox virus through sexual contact - A novel route of infection. J. Infect. 85, 334–363. doi: 10.1016/j.jinf.2022.05.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Heymann, D. L., Szczeniowski, M., and Esteves, K. (1998). Re-emergence of monkeypox in Africa: a review of the past six years. Br. Med. Bull. 54, 693–702. doi: 10.1093/oxfordjournals.bmb.a011720

PubMed Abstract | CrossRef Full Text | Google Scholar

Hobson, G., Adamson, J., Adler, H., Firth, R., Gould, S., Houlihan, C., et al. (2021). Family cluster of three cases of monkeypox imported from Nigeria to the United Kingdom, May 2021. Eurosurveillance 26, 2100745. doi: 10.2807/1560-7917.ES.2021.26.32.2100745

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoff, N. A., Doshi, R. H., Colwell, B., Kebela-Illunga, B., Mukadi, P., Mossoko, M., et al. (2017). Evolution of a disease surveillance system: an increase in reporting of human monkeypox disease in the Democratic Republic of the Congo, 2001–2013. Int. J. Tropic. Dis. Health 25, 35885. doi: 10.9734/IJTDH/2017/35885

PubMed Abstract | CrossRef Full Text | Google Scholar

Hutin, Y. J., Williams, R. J., Malfait, P., Pebody, R., Loparev, V. N., Ropp, S. L., et al. (2001). Outbreak of human monkeypox, Democratic Republic of Congo, 1996 to 1997. Emerg. Infect. Dis. 7, 434–438. doi: 10.3201/eid0703.017311

PubMed Abstract | CrossRef Full Text | Google Scholar

Idris, I., and Adesola, R. O. (2022). Current efforts and challenges facing responses to Monkeypox in United Kingdom. Biomed. J. 7, 7. doi: 10.1016/j.bj.2022.07.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Ihekweazu, C., Yinka-Ogunleye, A., Lule, S., and Ibrahim, A. (2020). Importance of epidemiological research of monkeypox: is incidence increasing?. Exp. Rev. Anti-infect. Therapy 18, 389–392. doi: 10.1080/14787210.2020.1735361

PubMed Abstract | CrossRef Full Text | Google Scholar

Iñigo Martínez, J., Gil Montalbán, E., Jiménez Bueno, S., Martín Martínez, F., Nieto Juli,á, A., Sánchez Díaz, J., et al. (2022). Monkeypox outbreak predominantly affecting men who have sex with men, Madrid, Spain, 26 April to 16 June 2022. Eurosurveillance 27, 2200471. doi: 10.2807/1560-7917.ES.2022.27.27.2200471

PubMed Abstract | CrossRef Full Text | Google Scholar

Isidro, J., Borges, V., Pinto, M., Sobral, D., Santos, J. D., Nunes, A., et al. (2022). Phylogenomic characterization and signs of microevolution in the 2022 multi-country outbreak of monkeypox virus. Nat. Med. 28, 1569–1572. doi: 10.1038/s41591-022-01907-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Islam, M. M., Dutta, P., Rashid, R., Jaffery, S. S., Islam, A., Farag, E., et al. (2023). Monkeypox at the human-animal-ecology interface: a comprehensive review of viral characteristics, transmission, pathobiology, prevention, and control strategies. Virulence, (just-accepted) 2, 2186357. doi: 10.1080/21505594.2023.2186357

PubMed Abstract | CrossRef Full Text | Google Scholar

Jezek, Z., and Fenner, F. (1988). Human Monkeypox. Basel, Switzerland: Karger Publishers.

Google Scholar

JeŽek, Z., Grab, B., Szczeniowski, M., Paluku, K. M., and Mutombo, M. (1988). Clinico-epidemiological features of monkeypox patients with an animal or human source of infection. Bull. World Health Organiz. 66, 459.

PubMed Abstract | Google Scholar

Jezek, Z., Szczeniowski, M., Paluku, K. M., and Mutombo, M. (1987). Human monkeypox: clinical features of 282 patients. J. Infect. Dis. 156, 293–298. doi: 10.1093/infdis/156.2.293

PubMed Abstract | CrossRef Full Text | Google Scholar

Judson, S. M. V. (2019). Nosocomial transmission of emerging viruses via aerosol-generating medical procedures. Viruses. 11, 940. doi: 10.3390/v11100940

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaler, J., Hussain, A., Flores, G., Kheiri, S., and Desrosiers, D. (2022). Monkeypox: a comprehensive review of transmission, pathogenesis, and manifestation. Cureus. 14.

PubMed Abstract | Google Scholar

Kalthan, E., Tenguere, J., Ndjapou, S. G., Koyazengbe, T. A., Mbomba, J., Marada, R. M., et al. (2018). Investigation of an outbreak of monkeypox in an area occupied by armed groups, Central African Republic. Medecine et maladies infectieuses 48, 263–268. doi: 10.1016/j.medmal.2018.02.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Khaity, A., Hasan, H., Albakri, K., Elsayed, H., Abdelgawad, H. A. H., Islam, F., et al. (2022). Monkeypox from Congo 1970 to Europe 2022; is there a difference?. Int. J. Surg. 104, 106827. doi: 10.1016/j.ijsu.2022.106827

PubMed Abstract | CrossRef Full Text | Google Scholar

Khattak, S., Rauf, M. A., Ali, Y., Yousaf, M. T., Liu, Z., Wu, D. D., et al. (2023). The monkeypox diagnosis, treatments and prevention: a review. Front. Cell. Infect. Microbiol. 12, 2005. doi: 10.3389/fcimb.2022.1088471

PubMed Abstract | CrossRef Full Text | Google Scholar

Khodakevich, L., Jezek, Z., and Kinzanzka, K. (1986). Isolation of monkeypox virus from wild squirrel infected in nature. Lancet (London, England) 327, 98. doi: 10.1016/S0140-6736(86)90748-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Kiang, K. K. M. (2003). Rates and risks of transmission of smallpox and mechanisms of prevention. J. Lab. Clin. Med. 142, 229–238. doi: 10.1016/S0022-2143(03)00147-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Kile, J. C., Fleischauer, A. T., Beard, B., Kuehnert, M. J., Kanwal, R. S., Pontones, P., et al. (2005). Transmission of monkeypox among persons exposed to infected prairie dogs in Indiana in 2003. Archiv. Pediatr. Adolesc. Med. 159, 1022–1025. doi: 10.1001/archpedi.159.11.1022

PubMed Abstract | CrossRef Full Text | Google Scholar

Kmiec, D., and Kirchhoff, F. (2022). Monkeypox: a new threat?. Int. J. Mol. Sci. 23, 7866. doi: 10.3390/ijms23147866

PubMed Abstract | CrossRef Full Text | Google Scholar

Kugelman, J. R., Johnston, S. C., Mulembakani, P. M., Kisalu, N., Lee, M. S., Koroleva, G., et al. (2014). Genomic variability of monkeypox virus among humans, Democratic Republic of the Congo. Emerg. Infect. Dis. 20, 232–239. doi: 10.3201/eid2002.130118

PubMed Abstract | CrossRef Full Text | Google Scholar

Ladnyj, I. D., Ziegler, P., and Kima, E. (1972). A human infection caused by monkeypox virus in Basankusu Territory, Democratic Republic of the Congo. Bull. World Health Organiz. 46, 593–597.

PubMed Abstract | Google Scholar

Laudisoit, A., Komba, M., and Akonda, I. (2016). Scientific report research bushmeat and monkeypox Yahuma health zone–Aketi health zone-Bombongolo health area. DRC.

Google Scholar

Learned, L. A., Reynolds, M. G., Wassa, D. W., Li, Y., Olson, V. A., Karem, K., et al. (2005). Extended interhuman transmission of monkeypox in a hospital community in the Republic of the Congo, 2003. Am. J. Tropic. Med. Hyg. 73, 428–434. doi: 10.4269/ajtmh.2005.73.428

PubMed Abstract | CrossRef Full Text | Google Scholar

Lederman, E. R., Reynolds, M. G., Karem, K., Braden, Z., Learned-Orozco, L. A., Wassa-Wassa, D., et al. (2007). Prevalence of antibodies against orthopoxviruses among residents of Likouala region, Republic of Congo: evidence for monkeypox virus exposure. Am. J. Tropic. Med. Hygiene 77, 1150–1156. doi: 10.4269/ajtmh.2007.77.1150

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, H., Zhang, H., Ding, K., Wang, X. H., Sun, G. Y., Liu, Z. X., et al. (2022). The evolving epidemiology of monkeypox virus. Cytokine Growth Fact. Rev. 2, 102. doi: 10.1016/j.cytogfr.2022.10.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Likos, A. M., Sammons, S. A., Olson, V. A., Frace, A. M., Li, Y., Olsen-Rasmussen, M., et al. (2005). A tale of two clades: monkeypox viruses. Journal of General Virology 86, 2661–2672. doi: 10.1099/vir.0.81215-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, X., Zhu, Z., He, Y., Lim, J. W., Lane, B., Wang, H., et al. (2022). Monkeypox claims new victims: the outbreak in men who have sex with men. Infect. Dis. Pov. 11, 91–93. doi: 10.1186/s40249-022-01007-6

PubMed Abstract | CrossRef Full Text | Google Scholar

MacNeil, A., Abel, J., Reynolds, M. G., Lash, R. R., Fonnie, R., Kanneh, L. D., et al. (2011). Serologic evidence of human orthopoxvirus infections in Sierra Leone. BMC Res. Notes 4, 1–5. doi: 10.1186/1756-0500-4-465

PubMed Abstract | CrossRef Full Text | Google Scholar

Magnus, P. V., Andersen, E. K., Petersen, K. B., and Birch-Andersen, A. (1959). A pox-like disease in cynomolgus monkeys. Acta Pathologica Microbiologica Scandinavica 46, 156–176. doi: 10.1111/j.1699-0463.1959.tb00328.x

CrossRef Full Text | Google Scholar

Mauldin, M. R., McCollum, A. M., Nakazawa, Y. J., Mandra, A., Whitehouse, E. R., Davidson, W., et al. (2022). Exportation of monkeypox virus from the African continent. J. Infect. Dis. 225, 1367–1376. doi: 10.1093/infdis/jiaa559

PubMed Abstract | CrossRef Full Text | Google Scholar

McCollum, A. M. (2023). Epidemiology of Human Mpox—Worldwide, 2018–2021. MMWR. Morbidity and Mortality Weekly Report 72, 3. doi: 10.15585/mmwr.mm7203a4

PubMed Abstract | CrossRef Full Text | Google Scholar

McCollum, A. M., and Damon, I. K. (2014). Human monkeypox. Clinic. Infect. Dis. 58, 260–267. doi: 10.1093/cid/cit703

PubMed Abstract | CrossRef Full Text | Google Scholar

Meslin, F. X., Stöhr, K., and Heymann, D. (2000). Public health implications of emerging zoonoses. Revue scientifique et technique (International Office of Epizootics) 19, 310–317. doi: 10.20506/rst.19.1.1214

PubMed Abstract | CrossRef Full Text | Google Scholar

Minhaj, F. S., Ogale, Y. P., Whitehill, F., Schultz, J., Foote, M., Davidson, W., et al. (2022). Monkeypox outbreak—nine states, May 2022. Morbid. Mortal. Weekly Rep. 71, 764–769. doi: 10.15585/mmwr.mm7123e1

PubMed Abstract | CrossRef Full Text | Google Scholar

Mourya, D., Yadav, P., Ullas, P., Bhardwaj, S., Sahay, R., Chadha, M., et al. (2019). Emerging/re-emerging viral diseases and new viruses on the Indian horizon. Ind. J. Med. Res. 149, 447–467 doi: 10.4103/ijmr.IJMR_1239_18

PubMed Abstract | CrossRef Full Text | Google Scholar

Mucker, E. M., Chapman, J., Huzella, L. M., Huggins, J. W., Shamblin, J., Robinson, C. G., et al. (2015). Susceptibility of marmosets (Callithrix jacchus) to monkeypox virus: a low dose prospective model for monkeypox and smallpox disease. PloS one 10, e0131742. doi: 10.1371/journal.pone.0131742

PubMed Abstract | CrossRef Full Text | Google Scholar

Müller, G., Meyer, A., Gras, F., Emmerich, P., Kolakowski, T., and Esposito, J. J. (1988). Monkeypox virus in liver and spleen of child in Gabon. The Lancet 331, 769–770. doi: 10.1016/S0140-6736(88)91580-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Nakoune, E., Lampaert, E., Ndjapou, S. G., Janssens, C., Zuniga, I., Van Herp, M., et al. (2017). “A nosocomial outbreak of human monkeypox in the Central African Republic,” in Open forum infectious diseases (Vol. 4, No. 4, p. ofx168). US: Oxford University Press.

PubMed Abstract | Google Scholar

Nigeria Centre for Disease (NCDC). (2022). Monkeypox: Nigeria recorded 558 cases,eight deaths in five years. Premium Times; May 10,2022.

Google Scholar

Noe, S., Zange, S., Seilmaier, M., Antwerpen, M. H., Fenzl, T., Schneider, J., et al. (2023). Clinical and virological features of first human monkeypox cases in Germany. Infection 51, 265–270. doi: 10.1007/s15010-022-01874-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Nolen, L. D., Osadebe, L., Katomba, J., Likofata, J., Mukadi, D., Monroe, B., et al. (2015). Introduction of monkeypox into a community and household: risk factors and zoonotic reservoirs in the Democratic Republic of the Congo. Am. J. Tropic. Med. Hyg. 93, 410–415. doi: 10.4269/ajtmh.15-0168

PubMed Abstract | CrossRef Full Text | Google Scholar

Ogoina, D., Iroezindu, M., James, H. I., Oladokun, R., Yinka-Ogunleye, A., Wakama, P., et al. (2020). Clinical course and outcome of human monkeypox in Nigeria. Clinic. Infect. Dis. 71, e210–e214. doi: 10.1093/cid/ciaa143

PubMed Abstract | CrossRef Full Text | Google Scholar

Ogoina, D., Izibewule, J. H., Ogunleye, A., Ederiane, E., Anebonam, U., Neni, A., et al. (2019). The 2017 human monkeypox outbreak in Nigeria—report of outbreak experience and response in the Niger Delta University Teaching Hospital, Bayelsa State, Nigeria. PloS one 14, e0214229. doi: 10.1371/journal.pone.0214229

PubMed Abstract | CrossRef Full Text | Google Scholar

Ortiz-Martínez, Y., Zambrano-Sanchez, G., and Rodríguez-Morales, A. J. (2022). Monkeypox and HIV/AIDS: When the outbreak faces the epidemic. Int. J. STD and AIDS 33, 949–950. doi: 10.1177/09564624221114191

PubMed Abstract | CrossRef Full Text | Google Scholar

Parker, S., and Buller, R. M. (2013). A review of experimental and natural infections of animals with monkeypox virus between 1958 and 2012. Future Virol. 8, 129–157. doi: 10.2217/fvl.12.130

PubMed Abstract | CrossRef Full Text | Google Scholar

Parker, S., Nuara, A., Buller, R. M. L., and Schultz, D. A. (2007). Human monkeypox: an emerging zoonotic disease. Fut. Microbiol. 2, 17–34. doi: 10.2217/17460913.2.1.17

PubMed Abstract | CrossRef Full Text | Google Scholar

Patel, A., Bilinska, J., Tam, J. C., Fontoura, D. D. S., Mason, C. Y., Daunt, A., et al. (2022). Clinical features and novel presentations of human monkeypox in a central London centre during the 2022 outbreak: descriptive case series. bmj 378, e072410. doi: 10.1136/bmj-2022-072410

PubMed Abstract | CrossRef Full Text | Google Scholar

Patrocinio-Jesus, R., and Peruzzu, F. (2022). Monkeypox genital lesions. N. Engl. J. Med. 387, 66–66. doi: 10.1056/NEJMicm2206893

PubMed Abstract | CrossRef Full Text | Google Scholar

Patrono, L. V., Pléh, K., Samuni, L., Ulrich, M., Röthemeier, C., Sachse, A., et al. (2020). Monkeypox virus emergence in wild chimpanzees reveals distinct clinical outcomes and viral diversity. Nat. Microbiol. 5, 955–965. doi: 10.1038/s41564-020-0706-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Perez Duque, M., Ribeiro, S., Martins, J. V., Casaca, P., Leite, P. P., Tavares, M., et al. (2022). Ongoing monkeypox virus outbreak, Portugal, 29 April to 23 May 2022. Eurosurveillance 27, 2200424. doi: 10.2807/1560-7917.ES.2022.27.22.2200424

PubMed Abstract | CrossRef Full Text | Google Scholar

Peters, J. C. (1966). An epizootic of Monkeypox at Rotterdam Zoo. International Zoo Yearbook. 6:274–275. doi: 10.1111/j.1748-1090.1966.tb01794.x

CrossRef Full Text | Google Scholar

Petersen, B. W., Joelle Kabamba, J., McCollum, A. M., Lushima, R. S., Wemakoy, E. O., Tamfum, J. M., et al. (2018). Vaccinating against monkeypox in the Democratic Republic of the Congo. Antiviral Res. 162, 171–177.

PubMed Abstract | Google Scholar

Petersen, B. W., Kabamba, J., McCollum, A. M., Lushima, R. S., Wemakoy, E. O., Tamfum, J. J. M., et al. (2019). Vaccinating against monkeypox in the Democratic Republic of the Congo. Antivir. Res. 162, 171–177. doi: 10.1016/j.antiviral.2018.11.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Petersen, E., Abubakar, I., Ihekweazu, C., Heymann, D., Ntoumi, F., Blumberg, L., et al. (2019a). Monkeypox-Enhancing public health preparedness for an emerging lethal human zoonotic epidemic threat in the wake of the smallpox post-eradication era. Int. J. Infect. Dis. 78, 78–84. doi: 10.1016/j.ijid.2018.11.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Petersen, E., Kantele, A., Koopmans, M., Asogun, D., Yinka-Ogunleye, A., Ihekweazu, C., et al. (2019b). Human monkeypox: epidemiologic and clinical characteristics, diagnosis, and prevention. Infect. Dis. Clinics 33, 1027–1043. doi: 10.1016/j.idc.2019.03.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Philpott, D., Hughes, C. M., Alroy, K. A., Kerins, J. L., Pavlick, J., Asbel, L., Crawley, A., et al. (2022). CDC multinational monkeypox response team. epidemiologic and clinical characteristics of monkeypox cases—United States, May 17–July 22, 2022. MMWR Morb. Mortal. Wkly. Rep. 71, 1018–1022. doi: 10.15585/mmwr.mm7132e3

PubMed Abstract | CrossRef Full Text | Google Scholar

Quarleri, J., Delpino, M. V., and Galvan, V. (2022). Monkeypox: considerations for the understanding and containment of the current outbreak in non-endemic countries. Geroscience 44, 2095–2103. doi: 10.1007/s11357-022-00611-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Quiner, C. A., Moses, C., Monroe, B. P., Nakazawa, Y., Doty, J. B., Hughes, C. M., et al. (2017). Presumptive risk factors for monkeypox in rural communities in the Democratic Republic of the Congo. PloS one 12, e0168664. doi: 10.1371/journal.pone.0168664

PubMed Abstract | CrossRef Full Text | Google Scholar

Radonić, A., Metzger, S., Dabrowski, P. W., Couacy-Hymann, E., Schuenadel, L., Kurth, A., et al. (2014). Fatal monkeypox in wild-living sooty mangabey, Cote d'Ivoire, 2012. Emerg. Infect. Dis. 20, 1009–1329. doi: 10.3201/eid2006.131329

PubMed Abstract | CrossRef Full Text | Google Scholar

Reed, K. D., Melski, J. W., Graham, M. B., Regnery, R. L., Sotir, M. J., Wegner, M. V., et al. (2004). The detection of monkeypox in humans in the Western Hemisphere. New Engl. J. Med. 350, 342–350. doi: 10.1056/NEJMoa032299

PubMed Abstract | CrossRef Full Text | Google Scholar

Reynolds, M. G., Carroll, D. S., Olson, V. A., Hughes, C., Galley, J., Likos, A., et al. (2010). A silent enzootic of an orthopoxvirus in Ghana, West Africa: evidence for multi-species involvement in the absence of widespread human disease. Am. J. tropic. Med. Hygiene 82, 746–754. doi: 10.4269/ajtmh.2010.09-0716

PubMed Abstract | CrossRef Full Text | Google Scholar

Reynolds, M. G., Davidson, W. B., Curns, A. T., Conover, C. S., Huhn, G., Davis, J. P., et al. (2007). Spectrum of infection and risk factors for human monkeypox, United States, 2003. Emerg. Infect. Dis. 13, 1332–1339 doi: 10.3201/eid1309.070175

PubMed Abstract | CrossRef Full Text | Google Scholar

Reynolds, M. G., Emerson, G. L., Pukuta, E., Karhemere, S., Muyembe, J. J., Bikindou, A., et al. (2013). Detection of human monkeypox in the Republic of the Congo following intensive community education. Am. J. Trop. Med. Hygiene 88, 982–985. doi: 10.4269/ajtmh.12-0758

PubMed Abstract | CrossRef Full Text | Google Scholar

Rimoin, A. W., Mulembakani, P. M., Johnston, S. C., Lloyd Smith, J. O., Kisalu, N. K., Kinkela, T. L., et al. (2010). Major increase in human monkeypox incidence 30 years after smallpox vaccination campaigns cease in the Democratic Republic of Congo. Proceed. Nat. Acad. Sci. 107, 16262–16267. doi: 10.1073/pnas.1005769107

PubMed Abstract | CrossRef Full Text | Google Scholar

Salzer, J. S., Carroll, D. S., Rwego, I. B., Li, Y., Falendysz, E. A., Shisler, J. L., et al. (2013). Serologic evidence for circulating orthopoxviruses in peridomestic rodents from rural Uganda. J. Wildlife Dis. 49, 125–131. doi: 10.7589/2012-04-100

PubMed Abstract | CrossRef Full Text | Google Scholar

Seang, S., Burrel, S., Todesco, E., Leducq, V., Monsel, G., Le Pluart, D., et al. (2022). Evidence of human-to-dog transmission of monkeypox virus. Lancet 400, 658–659. doi: 10.1016/S0140-6736(22)01487-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Sejvar, J. J., Chowdary, Y., Schomogyi, M., Stevens, J., Patel, J., Karem, K., et al. (2004). Human monkeypox infection: a family cluster in the midwestern United States. J. Infect. Dis. 190, 1833–1840. doi: 10.1086/425039

PubMed Abstract | CrossRef Full Text | Google Scholar

Sham, S., Sapna, F. N. U., Anjali, F. N. U., Kumar, S., Podder, V., Jaladi, S., et al. (2022). The changing global epidemiology of re-emerging human monkeypox virus infection: a systematic review. medRxiv 20, 22–12. doi: 10.1101/2022.12.09.22283261

CrossRef Full Text | Google Scholar

Silva, N. I. O., de Oliveira, J. S., Kroon, E. G., Trindade, G. D. S., and Drumond, B. P. (2020). Here, there, and everywhere: the wide host range and geographic distribution of zoonotic orthopoxviruses. Viruses 13, 43. doi: 10.3390/v13010043

PubMed Abstract | CrossRef Full Text | Google Scholar

Simpson, K., Heymann, D., Brown, C. S., Edmunds, W. J., Elsgaard, J., Fine, P., et al. (2020). Human monkeypox–After 40 years, an unintended consequence of smallpox eradication. Vaccine 38, 5077–5081. doi: 10.1016/j.vaccine.2020.04.062

PubMed Abstract | CrossRef Full Text | Google Scholar

Sklenovská, N. (2020). “Monkeypox virus,” in Animal-origin viral zoonoses. Springer: Singapore, pp. 39–68.

Google Scholar

Sklenovská, N., and Van Ranst, M. (2018). Emergence of monkeypox as the most important orthopoxvirus infection in humans. Front. Public Health 6, 241. doi: 10.3389/fpubh.2018.00241

PubMed Abstract | CrossRef Full Text | Google Scholar

Soheili, M., and Nasseri, S. (2022). Monkeypox: virology, pathophysiology, clinical characteristics, epidemiology, vaccines, diagnosis, and treatments. J. Pharm. Pharmaceutic. Sci. 25, 322–297. doi: 10.18433/jpps33138

PubMed Abstract | CrossRef Full Text | Google Scholar

Tchokoteu, P. F., Kago, I., Tetanye, E., Ndoumbe, P., Pignon, D., and Mbede, J. (1991). “Variola or a severe case of varicella? a case of human variola due to monkeypox virus in a child from the Cameroon,” in Annales de la Societe Belge de Medecine Tropicale (Vol. 71, No. 2, pp. 123–128).

PubMed Abstract | Google Scholar

Thornhill, J. P., Barkati, S., Walmsley, S., Rockstroh, J., Antinori, A., Harrison, L. B., et al. (2022). Monkeypox virus infection in humans across 16 countries—April–June 2022. New Engl. J. Med. 387, 679–691. doi: 10.1056/NEJMoa2207323

PubMed Abstract | CrossRef Full Text | Google Scholar

UK, G. (2022). Monkeypox Cases Confirmed in England-Latest Updates.

Google Scholar

Vaughan, A., Aarons, E., Astbury, J., Brooks, T., Chand, M., Flegg, P., et al. (2020). Human-to-human transmission of monkeypox virus, United Kingdom, October 2018. Emerg. Infect. Dis. 26, 782–785. doi: 10.3201/eid2604.191164

PubMed Abstract | CrossRef Full Text | Google Scholar

Vivancos, R., Anderson, C., Blomquist, P., Balasegaram, S., Bell, A., Bishop, L., et al. (2022). Community transmission of monkeypox in the United Kingdom, April to May 2022. Eurosurveillance 27, 2200422. doi: 10.2807/1560-7917.ES.2022.27.22.2200422

PubMed Abstract | CrossRef Full Text | Google Scholar

Wachtman, L., and Mansfield, K. (2012). Viral diseases of nonhuman primates. Nonhum. Primates Biomed. Res. 1, 2012.doi: 10.1016/B978-0-12-381366-4.00001-8

CrossRef Full Text | Google Scholar

WHO (2022e). Multi-country monkeypox outbreak: situation update 2022. Available online at: https://www.who.int/emergencies/disease-outbreaknews/item/2022-DON392 (accessed July 5, 2022e).

WHO (2022f). Regional Office for Africa. Weekly Bulletin on Outbreak and Other Emergencies: Week 4: 18–24 January 2021. WHO: Geneva, Switzerland, 2021; Available online at: https://apps.who.int/iris/handle/10665/338891 (accessed August 31, 2022).

WHO. (2022c). Disease Outbreak News; Multi-Country Monkeypox Outbreak in Non-Endemic Countries. WHO: Geneva, Switzerland. Available online at: https://www.who.int/emergencies/disease-outbreak-news/item/2022-DON385 (accessed August 31, 2022).

WHO. (2022d). Monkeypox. World Health Organization. Available online at: https://www.who.int/news-room/fact-sheets/detail/monkeypox (accessed August 2, 2022).

WHO. (2022g). Monkeypox - Democratic Republic of the Congo. Available online at: http://www.who.int/emergencies/disease-outbreak-news/item/monkeypox-democratic-republic-of-the-congo (accessed July 5, 2022).

WHO. (2022h). Monkeypox—Central African Republic 2016. Available online at: https://www.who.int/emergencies/disease-outbreak-news/item/13-october-2016-monkeypox-caf-en (accessed July 5, 2022).

World Health Organization. (1997). Human monkeypox in Kasai Oriental, Democratic Republic of the Congo (former Zaire): Preliminary report of October, 1997 investigation. Wkly Epidemiol Rec. 72, 369–372.

Google Scholar

World Health Organization. (2022a). Monkeypox - United States of America. World Health Organization. Available online at: https://www.who.int/emergencies/disease-outbreak-news/item/2021-DON344 (accessed June 20, 2022).

World Health Organization. (2022b). Monkeypox – United States of America. Available online at: who.int/emergencies/disease-outbreak-news/item/2021-DON344 (accessed June 20, 2022).

World Health Organization. (2022e). Multi-Country Monkeypox Outbreak: Situation Update. World Health Organization. Available online at: https://www.who.int/emergencies/disease-outbreaknews/item/2022-DON392 (accessed July 5, 2022).

World Health Organization. (2022j). Disease Outbreak News; Multi-country monkeypox outbreak in non-endemic countries: Update; WHO: Geneva, Switzerland, 2022. Available online: https://www.who.int/emergencies/disease-outbreak-news/item/2022-DON396 (accessed September 20, 2022).

Xiang, Y., and White, A. (2022). Monkeypox virus emerges from the shadow of its more infamous cousin: family biology matters. Emerg. Microbes Infect. 11, 1768–1777. doi: 10.1080/22221751.2022.2095309

PubMed Abstract | CrossRef Full Text | Google Scholar

Yinka-Ogunleye, A., Aruna, O., Dalhat, M., Ogoina, D., McCollum, A., Disu, Y., et al. (2019). Outbreak of human monkeypox in Nigeria in 2017–18: a clinical and epidemiological report. Lancet Infectious Dis. 19, 872–879. doi: 10.1016/S1473-3099(19)30294-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Yong, S. E. F., Ng, O. T., Ho, Z. J. M., Mak, T. M., Marimuthu, K., Vasoo, S., et al. (2020). Imported Monkeypox, Singapore. Emerg. Infect. Dis. 26, 1826–1830. doi: 10.3201/eid2608.191387

PubMed Abstract | CrossRef Full Text | Google Scholar

Zachary, K. C., and Shenoy, E. S. (2022). Monkeypox transmission following exposure in healthcare facilities in nonendemic settings: low risk but limited literature. Infection Control Hosp. Epidemiol. 43, 920–924. doi: 10.1017/ice.2022.152

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, F., Li, L., and Che, D. (2022). Monkeypox virus under COVID-19: caution for sexual transmission—correspondence. Int. J. Surg, 104, 106768. doi: 10.1016/j.ijsu.2022.106768

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: epidemiology, monkeypox, host range, risk factors, global health, threat

Citation: Ullah M, Li Y, Munib K and Zhang Z (2023) Epidemiology, host range, and associated risk factors of monkeypox: an emerging global public health threat. Front. Microbiol. 14:1160984. doi: 10.3389/fmicb.2023.1160984

Received: 07 February 2023; Accepted: 27 March 2023;
Published: 05 May 2023.

Edited by:

Laurent Rénia, Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore

Reviewed by:

Vivek Podder, Bangladesh Institute of Research and Rehabilitation for Diabetes Endocrine and Metabolic Disorders (BIRDEM), Bangladesh
Emmanuel Couacy-Hymann, Laboratoire National d'Appui au Développement Agricole, Côte d'Ivoire

Copyright © 2023 Ullah, Li, Munib and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Zhidong Zhang, zhangzhidong@swun.edu.cn; Yanmin Li, Liyanmin@swun.edu.cn

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