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SYSTEMATIC REVIEW article

Front. Vet. Sci., 02 September 2020
Sec. Veterinary Infectious Diseases
This article is part of the Research Topic Emerging Zoonoses and Transboundary Infections View all 27 articles

ONE Health Approach to Address Zoonotic Brucellosis: A Spatiotemporal Associations Study Between Animals and Humans

\nKun Zhou&#x;Kun Zhou1Beibei Wu&#x;Beibei Wu2Hang Pan&#x;Hang Pan1Narayan PaudyalNarayan Paudyal3Jize JiangJize Jiang4Le ZhangLe Zhang4Yan Li,
Yan Li1,5*Min Yue,
Min Yue1,5*
  • 1Department of Veterinary Medicine & Institute of Veterinary Sciences, Zhejiang University College of Animal Sciences, Hangzhou, China
  • 2Zhejiang Province Center for Disease Control and Prevention, Hangzhou, China
  • 3Animal Health Research Division, Nepal Agricultural Research Council, Kathmandu, Nepal
  • 4College of Computer Science, Sichuan University, Chengdu, China
  • 5Zhejiang Provincial Laboratory of Preventive Veterinary Medicine, Hangzhou, China

Background: Brucellosis is one of the most significant zoonosis over the world, threatening both veterinary and human public health. However, few studies were focused on nationwide animal brucellosis and made association with human brucellosis.

Methodology and Principal Findings: We conducted a bilingual literature search on Brucella or brucellosis in China on the two largest databases (China National Knowledge Infrastructure and PubMed) and conducted a systematic review. A total of 1,383 Chinese and 81 English publications, published between 1958 and 2018 were identified. From them, 357 publications presenting 692 datasets were subjected to the meta-analysis. The overall prevalence rate is 1.70% (95% CI: 1.66–1.74), with a declining (until the late 1990s) and rising trend (starting the early 2000s). Interestingly, the animal with highest prevalence rate is canine (8.35%, 95% CI: 7.21–9.50), and lowest in cattle (1.22%, 95% CI: 1.17–1.28). The prevalence of Brucella in animals was unequally distributed among the 24 examined regions in China.

Conclusions: Brucellosis is a reemerging disease for both humans and animals in China. The observed data suggests that dogs and yaks are the leading reservoirs for Brucella, and the provinces with highest prevalence rates in animals are Hubei, Sichuan, Inner Mongolia, Fujian, and Guizhou. Accordingly targeted intervention policy should be implemented to break the Brucella transmission chain between animals and humans in China.

Introduction

Zoonotic diseases are capable of infecting humans from animals by direct contact, or via food, water and environment, representing a significant public health problem. Brucellosis, caused by multiple species of the genera Brucella, is a textbook example of zoonotic disease prevalent all over the world. Brucellosis, recognized as the leading neglected zoonotic diseases by World Health Organization (WHO), remains a major epidemic, particularly in low- and middle-income countries, including China (14). During the past decades, it was observed a significant increase in human brucellosis in China (5, 6). Given a broad range of animal reservoirs, and humans serving as an accidental host, the exact relationship between human brucellosis and its animal reservoirs remains elusive. This is one of the most pressing knowledge gaps to understand the dynamics of zoonotic Brucella in China.

The Brucella pathogens infect and invade the host via the mucous membranes, gastrointestinal tract, respiratory tract or abraded skin. In China, human infections are more often related to the occupation and consumption of foods of animal origin (7). Veterinary personnel, animal-farmers, and slaughterhouse workers are at the highest risk, usually acquiring infections through the mucous or abraded skin (8, 9). Respiratory tract infections are common in people inhaling contaminated air-borne droplets or dust, for example, those working in the fur processing environment (10). People with no exposure to farm animals or animal-products are usually infected by contaminated food or water via gastrointestinal tract infections (11). The disease burden of human brucellosis infections is dynamic with respect to the endemic areas and time. Despite this dynamism, the only static component in the transmission chain is that the human incidences of brucellosis are always linked to certain animal reservoirs. Here, for the first time, we can address these key questions by using a “One Health” approach in an interconnected manner (6).

Farm animals, companion animals, and wild animals are well-known reservoirs for human Brucella infections (10). Farm animal brucellosis, with a wide range of clinical signs, is dependent on the infected animal hosts, age, sex, routes of exposure and organs involved (12). The hallmarks of infection include spontaneous abortion, undulant fever, and sometimes mastitis. Generally, animal brucellosis is sub-clinical but causes significant economic losses in the livestock industry. In companion animals, most of the infection cases are usually asymptomatic or mild (13). Therefore, farm and companion animal brucellosis are usually underappreciated due to their obscure syndrome and clinical presentations. Nevertheless, a systematic understanding the burden of animal brucellosis is largely lacking in China.

In this study, we conducted a systematic review and meta-analysis of the spatiotemporal epidemiological feature of brucellosis in animals and humans from a nationwide One Health approach. A comprehensive review of animal brucellosis in China, with an integrated evidence-based result analysis of human brucellosis to address the parameters for potential transboundary infections, was also undertaken.

Materials and Methods

Search Strategy

This review and systematic analysis included studies published in Chinese or English languages, between 1958 and 2018. The Chinese Publications were retrieved from China National Knowledge Infrastructure, CNKI (https://www.cnki.net/) and English papers were from PubMed with the same search string composed using keywords “Brucella or Brucellosis” and “China.”

Selection Criteria

Publications were firstly screened based on their title and abstract followed by inclusion or exclusion criteria formulated by the authors (Table 1).

TABLE 1
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Table 1. Inclusion/exclusion criteria for publication screening.

Data Extraction

Selected publications were perused for data extraction. Information on the title, author, journal, publication year, province, host (sheep and goat were grouped into one category because they were referred to as one single entity in Chinese literature), sampling year, type of samples, number of total samples, number of positive samples and number of Brucella strains and species wherever available, were determined. That information was extracted and arranged in an MS Excel spreadsheet formatted especially for this purpose.

Descriptive Analysis

Descriptive analysis was undertaken to calculate an approximately accurate epidemiologic picture of the disease and its causative agent. We analyzed the spatiotemporal relationship between human and animal brucellosis, where possible. We identified dominant species of Brucella in humans and some common animals including cattle, dog, pig, sheep & goat, and pointed out potentially high-risk infectious sources toward the human.

Meta-Analysis

A second step quality control screening of each record used for the descriptive analysis was applied using the exclusion criteria (Table 2). This was used to revise the data necessary for a meta-analysis of the prevalence of animal brucellosis.

TABLE 2
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Table 2. Exclusion criteria for the second round of record screening.

The data extracted from hence selected publications were meta-analyzed in a binary random-effects model by DerSimonian-Laird method at 95% confidence level using OpenMeta-analysis, as described previously (14). The meta-analysis was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to ensure the quality of the writing and presentation of this review (15). Three subgroup meta-analysis on the host, sampling year, and province were conducted simultaneously. The results obtained as the forest plots were projected with GraphPad Prism 7.

Results

Literature Search and Data Extraction

A total of 1,464 bilingual publications, which included 1,383 in Chinese and 81 in English, were used for the descriptive analysis after a full-text screening of primary eligible studies. Only 357 publications, 350 in Chinese, and 7 in English, among the total of 692 eligible records, were deemed suitable for meta-analysis. A flow chart of literature research and data extraction is shown (Figure 1).

FIGURE 1
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Figure 1. A flow chart of literature research and data extraction.

Descriptive Analysis

All provinces or municipality cities in China except Macao had reported positively for the prevalence of brucellosis. In mainland China, the largest number of records were from Inner Mongolia (n = 431), while there were only a few records from Tianjin (n = 11). Rose-Bengal Plate Agglutination Test (RBPT), Standard Tube Agglutination Test (SAT), Polymerase Chain Reaction (PCR), and Enzyme-Linked Immunosorbent Assay (ELISA) were the most common assays used for the detection of positive samples which were mostly blood. A total of 70,035,273 samples were tested in all these eligible studies, while 2,339,773 samples turned out to be positive, considered as the confirmed brucellosis cases or separated strains in these studies. There were more records on Brucella and brucellosis in northern China than in southern China. The number of samples tested in northern China was also much higher. The details are shown in Table 3 below (Some data are not counted into the table because they are lacking information either on host or on sampling places).

TABLE 3
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Table 3. Characteristics of records from eligible studies.

We also calculated the number of specific Brucella species mentioned in all these studies in human, sheep & goat, cattle, yak, dog and pig. Only five species, B. melitensis, B. canis, B. abortus, B. suis, and B. ovis were detected (Figure 2). Humans are most likely to be infected by all the four Brucella species from all kinds of animal host albeit in varying proportions. The proportion of presence of these pathogens in humans and sheep & goat are highly similar, illustrating that sheep & goat may be the likely source of infection for human brucellosis. Brucella serovars infecting yak, dog and pig are apparently highly species-specific, for example, B. abortus for yak, B. canis for dog, and B. suis for pig.

FIGURE 2
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Figure 2. Prevalence of various species of Brucella on different hosts. Height of the column in different color shows the proportion of Brucella species. Hosts are specified as human, sheep & goat, cattle, yak, dog, and pig at the base of each bar. Number above the bars indicates the number of positive samples.

The average prevalence rates of all the records were calculated and the results are illustrated as the temporal (Figure 3) and spatial (Figure 4) prevalence rates in humans and animals in China. Prevalence rates of human and animal brucellosis both have a decreasing trend, until the late 1990s, followed by an increasing trend, starting the early 2000s. Interestingly, prevalence of brucellosis in animals was higher than that of humans before the year 1995, while after 1995 the prevalence of brucellosis in humans becomes higher.

FIGURE 3
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Figure 3. Temporal distribution of human and animal brucellosis in China between 1951 and 2018.

FIGURE 4
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Figure 4. Geographical distribution of brucellosis in animal reservoirs and humans. In two municipal cities Shanghai and Tianjin, only human cases were observed.

Provinces in southern China had a higher prevalence rate before 1990, and currently, central Chinese provinces make the lead. There is always a higher rate of prevalence in the animals than in humans in most littoral areas, while things are on the contrary in the inwards areas. Regarding the geographic distribution, except in two municipal cities of Shanghai and Tianjin where only human cases were recorded, all other provinces had recorded an almost simultaneous increase or decrease in the prevalence in human and animal subjects. The analysis also reveals that the prevalence in hosts was high before 1990, then it started a downhill trend from 1991 to 2000, but again climbing up with a gradual increase after the 2000s at multiple geographical regions in mainland China. This spatiotemporal dynamism for human and animal brucellosis in China from 1951 to 2018 has been clearly shown (Supplemental Figure 1).

Prevalence of Brucellosis in Animals and Humans

A total of 357 publications screened twice (using the criteria as given in Table 2) were put into a meta-analysis, followed by a subgroup analysis on three variables including sampling year, geographical regions and host was also undertaken. Subgroups with less than five records were also put into meta-analysis but were not showed in the results below.

The overall prevalence rate among all animals in China from 1951 to 2018 was estimated to be 1.70% (95% CI: 1.66–1.74) (Figure 5A). As a factor of time, the largest number of records were for years between 2011 and 2015 (n = 170), whereas the smallest was for 1961–1965 (n = 6). There was an insufficient number of records (less than five) for the years 1951–1955, 1956–1960, 1966–1970, and 1971–1975 so these time frames were not shown. The result of subgroup analysis on the sampling year showed declining followed by a rising trend. Period with the lowest prevalence rate, irrespective of the host was 0.24% during 1996–2000 (63 records, 95% CI: 0.20–0.27), while the one with the highest prevalence was 12.44% during 1961–1965 (6 records, 95% CI: 7.70–17.19). In recent years, 2016–2018 the prevalence rate was 2.91% (29 records, 95% CI: 2.57–3.26), ~10 times higher than the lowest one.

FIGURE 5
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Figure 5. Results of subgroup meta-analysis for different animal-related factors. Subgroup analysis on sampling year (A), subgroup analysis on the province (B), and subgroup analysis on the host (C). The broken vertical line indicates the pooled summary estimate of prevalence for the selected variable.

There were only 24 provinces/autonomous regions which had no less than five qualified datasets for meta-analysis (Figure 5B). Five provinces/autonomous with the highest rate were Hubei (5 records, 7.69%, 95% CI: 5.51–9.87), Sichuan (20 records, 6.86%, 95% CI: 5.68–8.04), Inner Mongolia (50 records, 4.44%, 95% CI: 4.04–4.85), Fujian (20 records, 4.25%, 95% CI: 3.58–4.92), and Guizhou (18 records, 3.89%, 95% CI: 3.18–4.59). In contrast, five lowest rates were for Jilin (16 records, 0.39%, 95% CI: 0.29–0.48), Gansu (55 records, 0.70%, 95% CI: 0.60–0.79), Jiangsu (15 records, 0.77%, 95% CI: 0.49–1.05), Shandong (37 records, 1.13%, 95% CI: 0.95–1.31), and Qinghai (112 records, 1.40%, 95% CI: 1.29–1.52).

Among the five different types of host groups analyzed (Figure 5C), dog possessed the highest prevalence rate (52 records, 8.35%, 95% CI: 7.21–9.50), followed by yak with 43 records and 8.22% prevalence rate (95% CI: 7.23–9.20), while cattle (228 records, 1.22%, 95% CI: 1.17–1.28), sheep & goat (277 records, 1.61%, 95% CI: 1.54–1.67), and lastly the pigs (63 records, 2.35%, 95% CI: 2.16–2.54). This preferably indicates that dogs and yaks could be the emerging host that possess some significant threat to Brucella transmission in China. The detailed results of subgroup analysis are shown as forest plots in Figures 5A–C.

Discussion

Brucellosis is one of the most common zoonotic diseases worldwide, with a bioweapon potential, posing a significant public health concern (16). It not only causes considerable damages to public health but also significantly impairs veterinary public health and animal welfare. For example, reduced milk yield and contaminated dairy products due to animal brucellosis in America alone worth ~400 million US dollars (17), and the annual economic losses of brucellosis in two counties in Jilin province, China was more than 2.3 million US dollars (18). Brucellosis had been well-controlled last century in China by a nationwide program for brucellosis control, as well as by a national campaign for preventing and controlling brucellosis (19). In China, it had been well-controlled by a national campaign for preventing and controlling brucellosis in the last century. However, the disease has reemerged during the last two decades (20). In certain regions of China, the number of cases of brucellosis reported is higher than that in the 1990s (21). Recently, a study on the epidemiology of human brucellosis was carried out with official data (6). Moreover, Ran and his group applied a meta-analysis on seroprevalence in dairy cows in China (22). Despite these interesting and novel studies, information on the dominant biotype of Brucella in multiple kinds of hosts and prevalence within other animals is ambiguous. To a general extension, our unique One Health approach, combined with evidence-based meta-analysis, could be readily scaled to other zoonotic agents with significant public health importance.

In China, brucellosis was first recorded as Malta fever in two foreigners in Shanghai in 1905 (6). Until the 1990s, there was a high incidence of animal brucellosis, with relatively few human incidence (Supplemental Figure 1). Then after the 1990s, it started an uphill climb in most of the regions of mainland China. Brucellosis, previously thought to be frequently detected in northern China, is now increasingly seen in highly cosmopolitan parts of southern China (23). Our findings are in line with an earlier study which, using the notifiable reporting data for 1955–2014 based on the magnitude and distribution of human brucellosis in mainland China, had emphasized its recent re-emergence (6). Similar to the findings of our analysis, a previous study focusing only on the human incidence of brucellosis, showed some distinct temporal patterns, such as high incidence during 1955–1978, low incidence during 1979–1994, and dramatic accumulation incidences from 1995 onwards is consistent with the trend in Brucella seroprevalence from animal and human sero-surveys conducted in China during 1950–2014 (6). In general, where human prevalence of brucellosis is higher than prevalence of brucellosis in animals are mainly in southern China, including Hainan, Guangxi, Guangdong, Fujian, Jiangxi, Zhejiang, and Hubei (Figure 4). This might be because (1) a lack of animal surveillance capabilities in southern regions as a result of small population of large livestock; (2) the imported animal food contaminated with Brucella are responsible for the infections, which further support the multiple routes for disease transmission (2428). These reasons might be lead to extreme cases in particular years and places where there is only human brucellosis without an indication of animal brucellosis (Supplemental Figure 1).

In China, 90% of brucellosis occurs in six northern agricultural provinces including Inner Mongolia, Shanxi, Heilongjiang, Hebei, Jilin, and Shaanxi. The Inner Mongolia Autonomous Region has the highest incidence rate of human and animal brucellosis throughout China (29). Human cases have been observed in those regions where animal farming is prevalent, particularly in areas with many poor rural farms and pastures in northwest China (30). However, it is suggested that there is a change in the epidemiology of brucellosis in China (23). Recent publications show that the areas of brucellosis endemicity gradually shifted from pasturing areas, i.e., Inner Mongolia, Xinjiang, Tibet, Qinghai, and Ningxia, to grassland and agricultural areas, i.e., Shanxi, Liaoning, Hebei, Shandong, and Jilin provinces, and the southern provinces became increasingly affected (6). Some analyses further revealed that patients from Guangdong province were more likely to have consumption of apparently exotic foods such as goat placenta (23), thereby manifesting as increased incidence of brucellosis. Although incidence appeared to increase in every province, Tibet seems to follow an inverse pattern and reported a few cases during the past 10 years (6). These hint on the probable movement of infected animals or contaminated food from northern to southern China and thus may explain the current change in the epidemiology of brucellosis in China (23).

Sheep and goats are the major herbivores in northwest China, and they are primarily kept by poor rural farmers in pastoral areas. In general, a considerable number of sheep and yaks are raised on the same grazing land on the Tibetan plateau, and these animals are considered to be the main hosts of Brucella (30). Brucellosis was recognized in Tibet in the 1980s as a disease of both livestock and humans. Some study indicates that bovine brucellosis is endemic among the yak population in the plateau region of China (31).

In the last 12 years, brucellosis has re-emerged in most regions of China, showing an annual accumulation in animal and human infections during this period (29). This is also evident in our meta-analysis which shows a general increasing trend in the prevalence, particularly for the recent past years. With regard to the geographic distribution, our investigation confirmed that sero-prevalence in eastern regions was higher than the central and western regions. This conclusion is also supported by the localized and dense clusters of small ruminants in those regions.

Our analysis has shown that most of the human cases of brucellosis were caused by B. melitensis. It is well-known that B. melitensis is a dominant epidemic strain in animal and B. abortus and B. suis can also infect sheep; B. suis biovar 3, especially emerged in Inner Mongolia (32). B. melitensis genotype ST8 was not only the predominant genotype in sheep but also responsible for human brucellosis (33). The results of seroprevalence assays have confirmed that Brucella spp. was mainly epidemic in sheep and dairy cows, whereas other animals had a very low incidence. These results also showed a strong host preference for certain Brucella species. Furthermore, this also indicates that small ruminants or cattle are the primary risk factors for human contagion. Human brucellosis in northwest China is closely related to infectious sheep. From an epidemiological perspective, the major causes of brucellosis in animals in China have been sheep infected by B. melitensis (34). Sheep and dairy cows with Brucella had higher infection trends, although the positive rates in dairy cows dipped to a downward trend between 2013 and 2014. Compared with this, in sheep and dairy cows, brucellosis in yellow cattle and dogs maintained sporadic onset, and no cases were found in swine (34).

A notable feature in our analysis is the presence of B. canis in all other hosts except for pig and yak. Human brucellosis caused by B. suis and B. canis in Guangxi, China (35) have also been reported earlier. An earlier study reports that B. canis is a rare source of human brucellosis in China (36), where B. melitensis has been the major pathogen associated with human brucellosis outbreaks. B. canis infection was first reported in China in 1983 (13), but now our data indicates that this has become the leading reservoir for emerging brucellosis. This scenario will be even more challenging, considering a significantly growing population in canine market. In a less frequent situation, B. suis can also be directly or indirectly transferred from swine to sheep, which could act as reservoirs for B. suis infection and later transmitted to humans (37). Therefore, an enhanced surveillance system for companion animals in the densely populated cities is urgently needed.

Our data and subsequent analysis have thus revealed that brucellosis was a major concern for study and research in Northern China as compared to Southern China over time, for around three-quarters publications on brucellosis were carried out in North China. However, the meta-analysis showed that some areas in Southern China had even higher prevalence rates than northern ones, suggesting that brucellosis in the south is as severe as the north. It can be inferred from these analyses that human is likely to get infected with Brucella from all available transmission pathways, and various kinds of animals, among which the sheep and goat are possibly the highest risks because the formation of Brucella species in sheep and goat is similar with that of human. More alarmingly, canine brucellosis could be a top public health concern imposing a greater threat to human because pet dogs are playing a more and more important role in the current days of Chinese life. According to statistics, there have been over 740 million domestic dogs in China in 2019 (38), relationships between pet dogs and human are getting more and more close, which emphasizes that canine brucellosis is a pressing concern. An earlier study had shown that Chinese isolates of B. suis strains had unique genetic lineages at the global level whereas the isolates of B. canis were closely homologous to strains from Korea (35). Despite this disease being the most widespread zoonosis globally, it is also true that it remains severely neglected as a potential cause for chronic, debilitating maladies for multiple reasons such as its non-descript clinical presentation in human populations and its varying degree of clinical presentations (11).

Despite our updated largest analysis, there are some limitations to our analysis. Firstly, we only used two databases for bilingual publication research, so we might have missed some literatures. Second, most publications chose RBPT and SAT to detect positive blood samples, which have lower specificity and sensitivity than other recommended methods such as ELISA. Only 24 provinces in China had sufficient qualified data and thus were eligible for meta-analysis, leaving a quite large leak of animal brucellosis in remaining regions in China. Despite these, owing to a large number in the examined dataset, we believe that our meta-analysis is able to unravel a general situation and trend of animal brucellosis in China over time, thus attracting more attention to prevention and control of brucellosis in China.

Conclusion

Brucellosis is an important zoonosis in China, which was controlled well in the late twentieth century but re-emerged in the past two decades. Human may get infected from various domesticated animals, and most possibly sheep and goat. Canine brucellosis deserves more attention for the prevalence rate in dogs are quite high and the relationship between human and dogs is more and more close. Studies on brucellosis and Brucella were gaining more attention at northern provinces than those of southern region. However, our findings suggests that brucellosis among animals in the south is as equally serious as that in the north. Therefore, a nationwide comprehensive monitoring program must be reinitiated for both human and animals. In this perspective, brucellosis being a zoonotic disease, the One Health approach would be an ideal tool for alleviating the other diseases impacts on both humans and animals with the public health concerns.

Author Summary

Brucellosis is a worldwide zoonosis caused by Brucella posing significant damage to both public health and agriculture. However, the report about animal brucellosis in China is scattered, unintegrated, and dominant species among each kind of animals remains unknown. Here, we aimed to present the nationwide evidence-based results by using the systematic review and meta-analytic approach.

Evidence Before This Study

After over 100 years in discovery of the agent of Malta fever by David Bruce, brucellosis remains one of the important zoonotic infections causing huge reproductive failure in livestock, and economic losses of the dairy industry in low and middle-income countries. Brucellosis is also a serious public health problem for humans, due to food-chain, and/or occupational exposure. It is estimated that over one-fifth of the 1.4 billion worldwide cattle population is currently infected by Brucella, and results in over half-million new human cases annually, representing the most common systemic bacterial zoonosis. As the world largest population (1.4 billion people and 500 million livestock units), even though numerous studies reported significant accumulation of human brucellosis in China, only scattered and unintegrated animal brucellosis datasets are available, leaving huge knowledge gap for the zoonotic control and measurement.

Added-Value of This Study

We used the evidence-based studies, a meta-analysis, to build the most updated and comprehensive picture of brucellosis in China, including humans, livestock, and companion animals. The One Health approach indicates that the trend of human and animal brucellosis are closely associated with each other in China, with significant expansion from traditional northern farming areas to southern China. Importantly, we found that canine and yak could serve as the emerging reservoirs for human infections in China.

Implications of All The Available Evidence

The surveillance measurement for human brucellosis should be shifted from traditional northern China to southern regions. Policymakers should consider regional epidemiological data and risk factors to mitigate the zoonotic transmission from animals to humans. Our unique One Health approach, combined with evidence-based meta-analysis, could be readily scaled to other zoonotic agents with significant public health importance.

Data Availability Statement

All datasets generated for this study are included in the article/Supplementary Material.

Author Contributions

MY: conceptualization. KZ and BW: data curation. KZ and NP: formal analysis and visualization. MY, NP, and HP: methodology. MY and YL: project administration, and writing—review and editing. NP, HP, and JJ: software. MY, YL, and LZ: supervision. KZ: writing—original draft. All authors contributed to the article and approved the submitted version.

Funding

This study was supported by the National Program on Key Research Project of China (2019YFE0103900; 2018YFD0500501; and 2017YFC1600103) as well as European Union's Horizon 2020 Research and Innovation Programme under Grant Agreement No. 861917—SAFFI, Zhejiang Provincial Natural Science Foundation of China (LR19C180001), Zhejiang Provincial Key R&D Program of China (2020C02032), and National Science and Technology Major Project of China (No. 2018ZX10201002).

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.

Acknowledgments

We would like to thank the Veterinary Medicine students from Class of 2018 at ZJU, who participate in this data collection.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets.2020.00521/full#supplementary-material

Supplemental Figure 1. Spatiotemporal prevalence of human and animal brucellosis in China from 1951 to 2018.

References

1. Rubach MP, Halliday JE, Cleaveland S, Crump JA. Brucellosis in low-income and middle-income countries. Curr Opin Infect Dis. (2013) 26:404–12. doi: 10.1097/QCO.0b013e3283638104

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Pappas G, Papadimitriou P, Akritidis N, Christou L, Tsianos EV. The new global map of human brucellosis. Lancet Infect Dis. (2006) 6:91–9. doi: 10.1016/S1473-3099(06)70382-6

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Musallam II, Abo-Shehada MN, Hegazy YM, Holt HR, Guitian FJ. Systematic review of brucellosis in the Middle East: disease frequency in ruminants and humans and risk factors for human infection. Epidemiol Infect. (2016) 144:671–85. doi: 10.1017/S0950268815002575

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Cárdenas L, Awada L, Tizzani P, Cáceres P, Casal J. Characterization and evolution of countries affected by bovine brucellosis (1996-2014). Transbound Emerg Dis. (2019) 66:1280–90. doi: 10.1111/tbed.13144

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Kong W. Brucellosis infection increasing in Southern China. Eur J Intern Med. (2018) 51:e16–8. doi: 10.1016/j.ejim.2018.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Lai S, Zhou H, Xiong W, Gilbert M, Huang Z, Yu J, et al. Changing epidemiology of human brucellosis, China, 1955-2014. Emerg Infect Dis. (2017) 23:184–94. doi: 10.3201/eid2302.151710

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Xiao Y, Zou G, Yin J, Tan W, Zhou J, Zhang H. Seroepidemiology of human Brucella infection in Yixing, China. Trop Doc. (2017) 47:165–7. doi: 10.1177/0049475516640191

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Krueger WS, Lucero NE, Brower A, Heil GL, Gray GC. Evidence for unapparent Brucella canis infections among adults with occupational exposure to dogs. Zoonoses Public Health. (2014) 61:509–18. doi: 10.1111/zph.12102

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Lytras T, Danis K, Dounias G. Incidence patterns and occupational risk factors of human brucellosis in Greece, 2004-2015. Int J Occup Environ Med. (2016) 7:221–6. doi: 10.15171/ijoem.2016.806

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Mangalgi SS, Sajjan AG, Mohite ST, Gajul S. Brucellosis in occupationally exposed groups. J Clin Diagn Res. (2016) 10: Dc24–7. doi: 10.7860/JCDR/2016/15276.7673

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Hull NC, Schumaker BA. Comparisons of brucellosis between human and veterinary medicine. Infect Ecol Epidemiol. (2018) 8:1500846. doi: 10.1080/20008686.2018.1500846

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Deng Y, Liu X, Duan K, Peng Q. Research progress on brucellosis. Curr Med Chem. (2019) 26:5598–608. doi: 10.2174/0929867325666180510125009

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Piao D, Wang H, Di D, Tian G, Luo J, Gao W, et al. MLVA and LPS characteristics of Brucella canis isolated from humans and dogs in Zhejiang, China. Front Vet Sci. (2017) 4:223. doi: 10.3389/fvets.2017.00223

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Paudyal N, Pan H, Liao X, Zhang X, Li X, Fang W, et al. A meta-analysis of major foodborne pathogens in Chinese food commodities between 2006 and 2016. Foodborne Pathog Dis. (2018) 15:187–97. doi: 10.1089/fpd.2017.2417

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Shamseer L, Moher D, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation. BMJ. (2015) 350:g7647. doi: 10.1136/bmj.g7647

PubMed Abstract | CrossRef Full Text

16. Ariza J, Bosilkovski M, Cascio A, Colmenero JD, Corbel MJ, Falagas ME, et al. Perspectives for the treatment of brucellosis in the 21st century: the ioannina recommendations. PLoS Med. (2007) 4:e317. doi: 10.1371/journal.pmed.0040317

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Seleem MN, Boyle SM, Sriranganathan N. Brucellosis: a re-emerging zoonosis. Vet Microbiol. (2010) 140:392–8. doi: 10.1016/j.vetmic.2009.06.021

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Liu F, Wang D, Wang J, Li T, Zhao Y, Jiang S. National brucellosis intervention pilot county survey on the economic losses. Chin J Control Endemic Dis. (2008) 23:424–5.

Google Scholar

19. Shang D. 50-Year research on prevention and control of brucellosis in China. Chin J Epidemiol. (2000) 21:55–57.

20. Jia P, Joyner A. Human brucellosis occurrences in Inner Mongolia, China: a spatio-temporal distribution and ecological niche modeling approach. BMC Infect Dis. (2015) 15:36. doi: 10.1186/s12879-015-0763-9

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Zhang J, Yin F, Zhang T, Yang C, Zhang X, Feng Z, et al. Spatial analysis on human brucellosis incidence in mainland China: 2004-2010. BMJ Open. (2014) 4:e004470. doi: 10.1136/bmjopen-2013-004470

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Ran X, Cheng J, Wang M, Chen X, Wang H, Ge Y, et al. Brucellosis seroprevalence in dairy cattle in China during 2008-2018: a systematic review and meta-analysis. Acta Trop. (2019) 189:117–23. doi: 10.1016/j.actatropica.2018.10.002

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Ye HY, Xing FF, Yang J, Lo SK, Lau RW, Chen JH, et al. High index of suspicion for brucellosis in a highly cosmopolitan city in southern China. BMC Infect Dis. (2020) 20:22. doi: 10.1186/s12879-019-4748-y

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Pan H, Paudyal N, Li X, Fang W, Yue M. Multiple food-animal-borne route in transmission of antibiotic-resistant salmonella newport to humans. Front Microbiol. (2018) 9:23. doi: 10.3389/fmicb.2018.00023

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Pan H, Zhou X, Chai W, Paudyal N, Li S, Zhou X, et al. Diversified sources for human infections by Salmonella enterica serovar newport. Transbound Emerg Dis. (2019) 66:1044–8. doi: 10.1111/tbed.13099

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Wang X, Biswas S, Paudyal N, Pan H, Li X, Fang W, et al. Antibiotic resistance in salmonella typhimurium isolates recovered from the food chain through national antimicrobial resistance monitoring system between 1996 and 2016. Front Microbiol. (2019) 10:985. doi: 10.3389/fmicb.2019.00985

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Elbediwi M, Pan H, Biswas S, Li Y, Yue M. Emerging colistin resistance in Salmonella enterica serovar Newport isolates from human infections. Emerg Microbes Infect. (2020) 9:535–8. doi: 10.1080/22221751.2020.1733439

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Paudyal N, Pan H, Wu B, Zhou X, Zhou X, Chai W, et al. Persistent asymptomatic human infections by Salmonella enterica serovar newport in China. mSphere. (2020) 5:e00163-20. doi: 10.1128/mSphere.00163-20

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Liu ZG, Wang M, Ta N, Fang MG, Mi JC, Yu RP, et al. Seroprevalence of human brucellosis and molecular characteristics of Brucella strains in Inner Mongolia autonomous region of China, from 2012 to 2016. Emerg Microbes Infect. (2020) 9:263–74. doi: 10.1080/22221751.2020.1720528

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Cao X, Li Z, Liu Z, Fu B, Liu Y, Shang Y, et al. Molecular epidemiological characterization of Brucella isolates from sheep and yaks in northwest China. Transbound Emerg Dis. (2018) 65:e425–e33. doi: 10.1111/tbed.12777

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Zeng J, Duoji C, Yuan Z, Yuzhen S, Fan W, Tian L, et al. Seroprevalence and risk factors for bovine brucellosis in domestic yaks (Bos grunniens) in Tibet, China. Trop Anim Health Prod. (2017) 49:1339–44. doi: 10.1007/s11250-017-1331-7

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Liu ZG, Di DD, Wang M, Liu RH, Zhao HY, Piao DR, et al. MLVA genotyping characteristics of human Brucella melitensis isolated from Ulanqab of Inner Mongolia, China. Front Microbiol. (2017) 8:6. doi: 10.3389/fmicb.2017.00006

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Piao DR, Liu X, Di DD, Xiao P, Zhao ZZ, Xu LQ, et al. Genetic polymorphisms identify in species/biovars of Brucella isolated in China between 1953 and 2013 by MLST. BMC Microbiol. (2018) 18:7. doi: 10.1186/s12866-018-1149-0

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Cao X, Li S, Li Z, Liu Z, Ma J, Lou Z, et al. Enzootic situation and molecular epidemiology of Brucella in livestock from 2011 to 2015 in Qingyang, China. Emerg Microb Infect. (2018) 7:58. doi: 10.1038/s41426-018-0060-y

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Liu ZG, Wang M, Zhao HY, Piao DR, Jiang H, Li ZJ. Investigation of the molecular characteristics of Brucella isolates from Guangxi Province, China. BMC Microbiol. (2019) 19:292. doi: 10.1186/s12866-019-1665-6

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Ferreira Vicente A, Girault G, Corde Y, Souza Ribeiro Mioni M, Borges Keid L, Jay M, et al. The study of worldwide Brucella canis of phylogenetic groups by comparative genomics-based approaches. China Biotechnol. (2020) 40, 38–47. doi: 10.13523/j.cb.1907053

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Liu ZG, Wang LJ, Piao DR, Wang M, Liu RH, Zhao HY, et al. Molecular investigation of the transmission pattern of Brucella suis 3 from inner Mongolia, China. Front Vet Sci. (2018) 5:271. doi: 10.3389/fvets.2018.00271

PubMed Abstract | CrossRef Full Text | Google Scholar

38. De-gui L. Current status, opportunities and challenges of pet industry in China. Chin J Comp Med. (2010) 20:13–6. doi: 10.3969/j.issn.1671/7856.2010.11.12.004

CrossRef Full Text | Google Scholar

Keywords: Brucella, brucellosis, China, spatial, temporal

Citation: Zhou K, Wu B, Pan H, Paudyal N, Jiang J, Zhang L, Li Y and Yue M (2020) ONE Health Approach to Address Zoonotic Brucellosis: A Spatiotemporal Associations Study Between Animals and Humans. Front. Vet. Sci. 7:521. doi: 10.3389/fvets.2020.00521

Received: 18 May 2020; Accepted: 07 July 2020;
Published: 02 September 2020.

Edited by:

Yashpal S. Malik, Indian Veterinary Research Institute (IVRI), India

Reviewed by:

Vassilis Papatsiros, University of Thessaly, Greece
Mohammed AbdelHameed AboElkhair, University of Sadat City, Egypt

Copyright © 2020 Zhou, Wu, Pan, Paudyal, Jiang, Zhang, Li and Yue. 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: Yan Li, yanli3@zju.edu.cn; Min Yue, myue@zju.edu.cn

These authors have contributed equally to this work

Disclaimer: 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.