Lin Xu
Xuan-Lei Zhong
Zhi-Chao Xi
Yang Li
Hong-Xi Xu- 1School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, China
- 2Engineering Research Center of Shanghai Colleges for TCM New Drug Discovery, Shanghai, China
- 3Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
Herpes simplex virus (HSV), an alphaherpesvirus, is highly prevalent in the human population and is known to cause oral and genital herpes and various complications. Represented by acyclovir (ACV), nucleoside analogs have been the main clinical treatment against HSV infection thus far. However, due to prolonged and excessive use, HSV has developed ACV-resistant strains. Therefore, effective treatment against ACV-resistant HSV strains is urgently needed. In this review, we summarized the plant extracts and natural compounds that inhibited ACV-resistant HSV infection and their mechanism of action.
Introduction
Herpes simplex virus (HSV) is an alphaherpesvirus belonging to the Herpesviridae family. The virion is made up of large double-stranded DNA, an icosapentahedral capsid, a tegument, and a glycoprotein-filled envelope (Whitley and Roizman, 2001). The viral entry into the host cells begins with the interaction between viral glycoproteins, gB, and gC with cell surface receptors. The fusion of the viral envelope is mediated by glycoproteins, gD, gB, and the heterodimer gH/gL, allowing the viral entry into the host cells (Kukhanova et al., 2014). After the entry of the viral particle, the capsid is trafficked to the nuclear pores along a network of microtubules and subsequently into the nucleus (Mues et al., 2015). VP16 triggers the transcription of six immediate early (IE) genes (ICP0, ICP4, ICP22, ICP27, ICP47, and US1.5) and the activation of early (E) and late (L) genes. With the help of the helicase-primase complex and some viral proteins, such as UL9 and ICP8, the viral DNA unwinds and replicates. The capsid is initially assembled in the nucleus and then transported into the cytoplasm. The virion is trafficked intracellularly, during which the virion forms an outer shell, package, and assemble. Finally, the virion is egressed to infect other cells, resulting in cell-to-cell spread. The replication cycle lasts for 18–20 h, which has been briefly illustrated in Figure 1. After primary infection, HSV virions replicate in large numbers in neuronal cells, enter sensory neuron axons, and hide in the neuronal cell nucleus (Kukhanova et al., 2014). The viruses establish latent infections, which are reactivated by persistent psychological stress and other stimuli (Cohen et al., 1999). HSV infections have become a major public health concern. According to a WHO investigation, more than one billion people worldwide are infected with HSV-1-caused oral herpes, and an estimated 500 million are infected with HSV-2-caused genital herpes (Kushch et al., 2021).
Figure 1. HSV replication cycle and the steps that were targeted by the phytomedicines mentioned in this review. (1) Plant extracts such as peppermint oil, P. vulgaris extract as well as the phytochemicals such as baicalein, caffeic acid showed virucidal effect. (2) HSV virions requires a set of viral glycoproteins to mediate host cell attachment and entry, which could be suppressed by V. nilotica extract, M. piperita extract, harringtonine and etc. (3) Then the capsids are transported into the nucleus, which could be inhibited by Amentoflavone. (4) The biosynthesis process produced viral DNA, which could be blocked by amentoflavone, R430 and IPAD. The phytomedicines suppressed the helicase-primase complex, Immediate Early genes (ICP0, ICP4, ICP27), Early genes (ICP6, ICP8) and Late genes (UL19, UL27, UL44, US6). (5) Glucoevatromonoside and 4′-phenylflavone exerted the inhibitory effect on virion egression. (6) The cell-to-cell spread could be interfered by glucoevatromonoside.
Acyclovir (ACV) is widely used to treat HSV infections and inhibits HSV-specific DNA polymerase and impedes HSV replication and further infection (Brigden and Whiteman, 1983). Since HSV infection is incurable and recurrent and prolonged, the excessive use of nucleoside analogs such as ACV causes severe side effects, including neurotoxicity and renal impairment (Paluch et al., 2021) and the emergence of drug resistance. ACV resistance was reported to be 7% in immunocompromised patients, but was only 0.27% in healthy immunocompetent adults. The emergence of drug-resistant HSV strains restricts therapeutic options, preventing timely treatment and causing a variety of diseases (Stranska et al., 2005). The mutant of HSV-induced TK led to ACV resistance in 95% of cases, and the mutant of DNA polymerase (DNA-pol) enzymes also accounted for resistance (Field, 2001; Morfin and Thouvenot, 2003). The resources and mechanism of resistance of ACV-resistant HSV strains mentioned in this review were organized in Table 1.
Table 1. Review of the ACV-resistant strains used in the collected literature.
This review summarizes a number of ACV-resistant HSV strains that have been genetically engineered or isolated from patients (Table 1), medicinal extracts (Table 2), and phytochemicals (Table 3) that exert antiviral effects and mechanisms of action.
Table 2. Review of the plants that show anti-herpes simplex virus activities with their prospective family, part, type of extract, and mode of action.
Table 3. A review of the bioactive natural products reported to have potent anti-HSV properties.
Medicinal plant extracts with anti-herpes simplex virus activities
The crude hydroethanolic extract (RCE40) from the leaves of Cecropia glaziovii Senthl. inhibited the replication of HSV-1 ACVr strain 29R, with an EC50 of 40 μg/ml and a selectivity index (SI) of 50. The antiherpes properties of RCE40 might be attributed to their phenolic composition (Petronilho et al., 2012).
The water extract of Cocos nucifera L. husk fiber that is rich in catechin exhibited inhibitory activity against HSV-1 ACVr. The fraction exhibited higher antiviral activity than the crude extract. Mechanistically, the antiviral activity has been attributed to inactivating the extracellular virus with a vircidual effect (Esquenazi et al., 2002). Furthermore, extracts containing catechin and condensed tannins have been reported to inhibit HSV adsorption and replication (De Bruyne et al., 1999; Serkedjieva and Ivancheva, 1999).
Peppermint oil, an essential oil extracted from the leaves of Mentha piperita L., mainly consists of methanol (42.8%), menthone (14.6%), isomenthone (5.9%), menthylacetate (4.4%), cineole (3.8%), limonene (1.2%) and carvone (0.6%). Peppermint oil inhibited HSV-1, HSV-2, and HSV-1 ACVr infection in a dose- and time-dependent manner. It showed an obvious virucidal effect when mixed with HSV prior to infection, which implies its direct interaction with the viral envelope and glycoproteins (Schuhmacher et al., 2003). This finding suggests that peppermint oil might be used topically as a virucidal agent in the treatment of recurrent herpes infections.
Viracea, a proprietary formula, is a blend of benzalkonium chloride and phytochemicals derived from the aerial parts of Echinacea purpurea, which was found to have significant antiviral activity against 25 different ACV-susceptible strains (13 strains of HSV-1 and 12 strains of HSV-2) and 15 ACV-resistant strains (5 strains of HSV-1 and 10 strains of HSV-2), with a therapeutic index in the range of 50–100. Instead of benzalkonium chloride, which was speculated to be a stabilizer, the phytochemicals had anti-HSV activity after the adsorption and penetration step (Thompson, 1998).
Lamiaceae ethanolic extracts from Prunella vulgaris L., dried leaves of Mentha × piperita L., Rosmarinus officinalis L., and dried herbs of Thymus vulgaris L. inhibited the infectivity of ACV-susceptible strains and HSV-1 ACVr strain Angelotti (ACV-resistant with a single point mutant in the DNA polymerase gene) and 1246/99 (ACV-resistant patient isolate with a single point mutant in the coding sequence of the TK gene) with 50% inhibitory concentrations (IC50) of 0.05–0.82 μg/ml, which exerted the potential topical antiviral effect in the treatment of recurrent herpes labialis. Time-on-addition assays suggested that 80% prunella and peppermint ethanolic extracts had direct inactivation of free HSV particles and suppression of virus attachment to host cells. Additionally, the antiherpetic activity of the extracts was thought to be related to the amount and composition of phenolics in the plants (Reichling et al., 2008).
The polysaccharide from Eucheuma gelatinae (EGP) had comprehensive antiviral activity not only for standard experimental strains but also for clinical HSV-1 ACVr strains 106 (ACV-resistant with TK mutant), 153 (ACV-resistant with TK mutant), and Blue (ACV-resistant with TK deletion). EGP exerted its antiviral activities mainly in the early stages of HSV-1 infection, involving direct inactivation of the virions and interference in virus adsorption as a consequence of interactions between EGP and viral glycoproteins. The PCR results showed that the RNA synthesis of the HSV-1 early gene UL52 and the late gene UL27 was suppressed by EGP. In addition, the intracellular genome copy number in the EGP-treated group significantly declined, indicating that EGP inhibited viral DNA synthesis. In addition, EGP not only suppressed the synthesis of HSV-1 capsid protein VP5 but also affected cellular localization through indirect immunofluorescence and Western blot assays (Jin et al., 2015).
Essential oils from ginger (Zingiber officinale), thyme (Thymus vulgaris), hyssop (Hyssopus officinalis), and sandalwood (Santalum album) are complex mixtures of low-molecular-weight molecules and the active components of lipophilic carbohydrates. EO inhibited the infection of HSV-1 ACVr strains 1246/99, Angelotti, and 496/02 (ACV-resistant patient isolate with a single point mutant in the coding sequence of the TK gene). The essential oils prior to infection caused significant reductions in infectivity and proved their virucidal activity by adding the oils at different times during the HSV infection cycle (Schnitzler et al., 2007). In addition, the essential oil from Salvia desoleana Atzei & V. Picci, which contains linalyl acetate and alpha terpinyl acetate, suppressed both HSV-2 and HSV-2 ACVr in the postinfection stage. It revealed that the EO might interfere with later steps of the virus replication cycle (e.g., uncoating, genome replication, virus assembly or exit, cell-to-cell spread) by virus inactivation and time-of-addition assays (Cagno et al., 2017). The antiviral effect of EO was totally due to the active fraction SD1, which was characterized by mono- and sesquiterpene hydrocarbons. Considering the limitation that short-term systemic bioavailability of the essential oils and high effective dosage might lead to cytotoxicity, other anti-HSV agents should be added alongside topical treatment against recurrent infection.
Acacia nilotica (L.) has been used as a traditional healer to treat sexually transmitted infections (STIs), such as syphilis, gonorrhea, and other HIV/AIDS-related diseases (Kambizi and Afolayan, 2001; Chinsembu, 2016). The methanolic extract of Vachellia nilotica, known by the taxonomic synonym A. nilotica, exerted antiviral activity against HSV-2 and HSV-2 ACVr. The methanolic bark extract, which was mostly composed of saponins and flavonoids with traces of tannins, exerted a dual-mode of action against HSV-2 infection, which interfered with early steps of the virus replication cycle instead of targeting the cell surface, including inactivation of virus extracellular particles and inhibition of virus attachment (Donalisio et al., 2018).
Vitex polygama Cham. is used as a diuretic in traditional medicine. The flavonoid-rich ethyl acetate extract of Vitex polygama Cham. possessed potential activity against HSV-1 ACVr, the leaf extract possessed the most pronounced antiviral ability by inhibiting intracellular spread, and the fruit extract exhibited a virucidal effect. VPAF-1, the fraction further extracted with organic reagents, was proven to reduce viral propagation by preventing HSV-1 ACVr from attaching to cellular receptors (Goncalves et al., 2001).
Ficus religiosa L. belongs to the genus Moraceae and is used to treat diabetes, inflammation, and sexually transmitted infections (Singh et al., 2011; Choudhari et al., 2013). The water bark extract of this plant effectively exhibited a virucidal effect against both HSV-2 MS (ACV-sensitive) and HSV-2 ACVr strain replication. The chloroform extract inhibited the early stage of the HSV-2 replicative cycle and interfered with viral attachment and penetration through the time-of-addition assay and attachment assay. In addition, the chloroform extract limited the production of viral progeny based on the result of the viral yield reduction assay (Ghosh et al., 2016). These findings suggest that bioactive metabolites of F. religiosa were identified as natural therapeutic substances for genital herpes, especially in HSV-2 ACVr strains.
The sulfated polysaccharide fraction, which is isolated from the hot water extract of Caulerpa racemose (HWE), has a molecular weight of 5–10 kDa and more than two SO3− groups for each sugar residue. HWE exhibited anti-herpetic activity against HSV-1/F, HSV-2/G, and HSV-1 ACVr strain B2006 (ACV-resistant with TK deficient) and field (ACV-resistant with TK deficient), with EC50 values in the range of 2.2–4.2 μg/ml, without any cytotoxic effects (Ghosh et al., 2004).
The Prunella vulgaris polysaccharide fraction (PPV) significantly reduced the antigen expression of both ACV-sensitive HSV and HSV-1 ACVr strain DM2.1 (ACV-resistant with TK deficiency) according to immunostaining and flow cytometric analyses of HSV-1 and HSV-2 antigens (Chiu et al., 2004). An anionic polysaccharide from Prunella vulgaris (PVP), which was isolated by hot water extraction, ethanol precipitation, and gel permeation column chromatography, was reported to possess anti-HSV activity against HSV-1 ACVr strain DM2.1 and PAAr (ACV-resistant with DNA polymerase mutant) and HSV-2 ACVr strain Kost (ACV-resistant with TK altered). According to the viral binding assay, PVP could compete with cell receptors to exert its inhibitory effect (Xu et al., 1999). These investigations provide the possibility that P. vulgaris developed as a self-applicable ointment for cold sores and genital herpes.
Houttuynia cordata is an herbal medicine of the family Saururaceae that shows anti-inflammatory, anticancer, and antioxidative activities (Chen et al., 2003; Lu et al., 2006), as well as antiviral activity against influenza virus, SARS-CoV, and HSV (Lau et al., 2008; Choi et al., 2009; Chen et al., 2011). The water extracts of H. cordata (HCWEs) showed low cytotoxicity in Vero cells and inhibited HSV-1 ACVr strain AR (ACV-resistant with TK mutant) infection. The molecular mechanisms of HCWEs involve anti-HSV activity through inhibition of viral entry, interfering with viral replication by suppressing viral late genes, and inhibiting HSV-induced NF-κB activation (Hung et al., 2015).
The study investigated the antiviral activity of the extract of Arisaema tortuosum (Wall.) Schott leaves, which have a medicinal history in India to treat piles, snake bites, and parasitic infections. Comparing seven fractions extracted by different solvents, chloroform extract (CE) exhibited the greatest antiviral activity against HSV-2 ACVr strains by inhibiting viral attachment and entry as well as the late steps in the replication cycle. The main components identified by HPLC-PDA-MS/MS analysis are apigenin and luteolin, which inhibit cell-to-cell virus spread and the production of viral progeny (Ritta et al., 2020).
Table 2 concluded the medicinal plant extracts mentioned in this review with their families, extract solvent, and antiviral efficacy (including the IC50, EC50, and mode of action).
Bioactive components that show anti-herpes simplex virus activities
Terpenes
Andrographolide and its derivatives were confirmed to have antiviral activities against HIV, HBV, and HSV by interacting with viral receptors, coreceptors, and enzymes related to viral replication (Jadhav and Karuppayil, 2021). 3,19-isopropylideneandrographolide (IPAD) is an andrographolide analog isolated from Andrographis paniculata Nees. IPAD exerted an inhibitory effect against both HSV wild types (HSV-1 and HSV-2) and HSV-1 ACVr strain ACGr4 (ACV-resistant with TK deficiency), dlsptk (ACV-resistant with TK deletion), and dxpIII (phosphonoacetic acid and phosphonoformate resistance). The inhibitory effects of IPAD are involved in the replication cycle by inhibiting the synthesis of viral DNA and the late protein gD. Furthermore, the synergistic effects of ACV and IPAD on HSV wild types and HSV-1 ACVr were determined by CPE reduction assay (Priengprom et al., 2015). The triterpene extract (TE) of birch bark and its major pentacyclic triterpenes (betulin, lupeol, and betulinic acid) were found to be active in suppressing HSV-1 strain KOS and two clinical isolates HSV-1 ACVr in a dose-dependent manner using plaque reduction assays. Unlike ACV, TE, and triterpenes achieved minor virucidal activity and antiviral effects in the early phase of infection (Heidary Navid et al., 2014).
Oleanolic acid, a pentacyclic triterpenoid that widely exists in natural products, possesses antitumor, anti-inflammatory, and hepatoprotective activities (Baer-Dubowska et al., 2021; Hosny et al., 2021; Zhang et al., 2021). Oleanolic acid exerted potent antiviral activity against the ACV-sensitive strain HSV-1/F and three HSV-1 ACVr strains (Blue, 106 and 153). Mechanistic studies demonstrated that oleanolic acid suppressed viral replication by downregulating the mRNA expression of the viral helicase-primase complex that is composed of UL5, UL52, and UL8. The in vivo study carried out on the HSV-1-infected zosteriform model suggested that oleanolic acid relieved skin lesions (Shan et al., 2021), which indicated that oleanolic acid could be a promising therapeutic target for HSV-1-related skin lesions, particularly in ACV-resistant individuals.
Phenolics
The essential oil of Lippia graveolens (Mexican oregano) inhibited the infection of ACV-sensitive HSV-1 and HSV-1 ACVr strains at different time points of viral replication. The main component carvacrol exhibited more significant antiviral activity only when the cells were post-treated, with a different mode of action as essential oil (Pilau et al., 2011).
Melissa officinalis (lemon balm), belonging to the Lamiaceae family, is reported to exert antioxidant and antibacterial effects (Canadanović-Brunet et al., 2008). The aqueous extract of Melissa officinalis interfered with the early steps of virus replication against both HSV-1 KOS and two clinical isolates of HSV-1 ACVr strains. Among the phenolic compounds isolated from Melissa leaves, caffeic acid, p-coumaric acid, and rosmarinic acid were the main contributors by inactivating the virus and inhibiting virus attachment and penetration (Astani et al., 2014).
Ellagitannins are plant-derived polyphenol compounds with pharmacological activities, including antitumor and antibacterial activities (Ismail et al., 2016; Puljula et al., 2020). Three ellagitannins (castalagin, vescalagin, and grandinin) were proven to exhibit antiviral effects against HSV-1 ACVr strain R-100 (ACV-resistant with a TK enzyme-encoding gene mutant) and HSV-2 ACVr strain PU (ACV-resistant with TK deficiency) through the focus forming units (FFU) reduction test and CPE inhibition test. In addition, the tested ellagitannins had combined effects with ACV on the replication of HSV-1 ACVr and HSV-2 ACVr strains, and the inhibitory mechanism was different from ACV (Vilhelmova-Ilieva et al., 2014).
Xanthones
Mangiferin, a polyphenol with a C-glycosylxanthone structure, can be discovered in mango trees (Mangifera indica) and is used as a treatment for burns and pruritus and exerts neuroprotective effects (Lee et al., 2009; Liu T. et al., 2021). Mangiferin was reported to have great in vitro and in vivo antiviral activity against HSV-1 ACVr strain AR-29 and HSV-1 strain KOS with low toxicity. Further mechanistic studies showed that mangiferin exerted its antiherpetic effect mainly by exerting a virucidal effect and inhibiting viral adsorption (Rechenchoski et al., 2020).
Cardenolides
Cardiac glycosides are naturally derived compounds and are widely used in the treatment of heart failure (Kelly, 1990). After screening 65 cardenolide derivatives, the natural cardenolide compound glucoevatromonoside, which was isolated from the Brazilian cultivar of Digitalis lanata, exhibited potent anti-HSV activity against the HSV-1 strain KOS, HSV-2 strain 333, and HSV-1 ACVr strain 29R with low IC50 values of 0.13 ± 0.01, 0.04 ± 0.00, and 0.06 ± 0.01 μM, respectively. It reduced the expression of the viral proteins ICP27, UL42, gB, and gD by downregulating the K+ concentration into cells that is essential for viral protein synthesis, thus interfering with virus release and viral spread (Bertol et al., 2011).
Flavonoids
Amentoflavone (AF), a naturally existing biflavonoid, was proven to exert antiviral activity against HSV-1 strain F and three HSV-1 ACVr strains (Blue, 106 and 153) through CPE and plaque assays. Mechanistically, AF completely reduced viral gene production (UL54, UL52, and UL27) and protein levels (ICP0, gD, and VP5) of HSV-1 strain F and three HSV ACVr strains. Furthermore, AF affected cofilin-mediated F-actin remodeling, which was essential for HSV-1 viral entry and reduction of viral nuclear transport (Li et al., 2019).
4’-Phenylflavone is a synthetic flavonoid that exerted antiviral activity against HSV-1 strain KOS, HSV-2 strain UW 268, and HSV-1 ACVr strain A4-3 (ACV-resistant with TK deletion) in vitro and in vivo by interfering with late stages in viral replication and reducing the release of progeny viruses. Synergistic therapy with 4′-phenylflavone and ACV remarkably improved the lesion scores and survival rates of HSV-infected mice, indicating the antiherpetic effect of the drug combination (Hayashi et al., 2012).
Soybean (Glycine max) isoflavonoids have great biological activity related to estrogenic responses. Genistein and coumestrol inhibited the infection of HSV-1 strain KOS, HSV-2 strain 333, and HSV-1 ACVr strain 29R. Coumestrol affected multiple steps in the HSV replication cycle, including adsorption and penetration, by reducing the expression of the viral proteins UL42 and gD. In comparison, genistein showed no effect on early stages but reduced the expression of viral proteins UL42, gD, and ICP27 (Argenta et al., 2015).
Baicalein is a flavonoid isolated from the root of Scutellaria baicalensis Georgi with biological activity against cancer and inflammatory diseases. Baicalein inhibited the replication of both HSV-1 strain F and HSV-1 ACVr strain Blue in Vero and HaCaT cells. Further mechanistic analysis elucidated that baicalein inactivated viral particles and suppressed NF-κB activation, which contributed to the protective effect of baicalein on HSV-1 infection. Furthermore, oral administration of baicalein also reduced HSV-1-induced lethality and viral loads and ameliorated symptoms in both the nose and trigeminal ganglia in an HSV-1 intranasal infection model (Luo et al., 2020).
Proteins
MAP30 and GAP31 were derived from the Himalayan tree Gelonium multiflorum and Chinese bitter melon Momordica charantia. These two proteins were found to be effective in inhibiting the HSV-1 ACVr strain DM21 and PAAr and the HSV-2 ACVr strain Kost (ACV-resistant with TK altered) and 8,708 (ACV-resistant with TK altered) without toxicity to human embryonic cells. However, the detailed mechanism remains to be defined (Bourinbaiar and Lee-Huang, 1996).
Cyanovirin-N (CV-N), the cyanobacterial protein isolated from Nostoc ellipsosporum, and its two chemically modified derivatives LCV-N and PEG10k-LCV-N were reported to possess antiviral activity against HSV-1 ACVr strains 153, Blue, and 106. According to the WST-8 assay, PEG10k-LCV-N had the lowest cytotoxicity, but it showed reduced activity against ACV-resistant HSV strains compared with CV-N and LCV-N, and the detailed mechanism still needs to be explored. However, the anti-HSV-1 potency of CV-N was confirmed due to the presence of an intact sugar binding site on the BM domain for viral glycoprotein interaction, which suggests that it is a viral entry inhibitor of HSV-1 and HIV (Barrientos et al., 2006; Xiong et al., 2010; Lei et al., 2019).
Alkaloids
Caffeine inhibited the plaque formation of HSV-2 and HSV-1 ACVr strain B2006 (TK deficient) and PAAv in vitro. Caffeine gel treatment decelerated the development of skin lesions in mice caused by HSV-2 and reduced the virus yield of the skin infected with ACV-resistant HSV-1 strains in vivo (Yoshida et al., 1996).
Harringtonine (HT), a natural alkaloid isolated from Cephalotaxus harringtonia, possessed antiviral effects against two HSV-1 ACVr strains (Blue and 153) and three ACV-sensitive strains. A further study showed that HT reduced the expression of HVEM, thereby affecting viral membrane fusion and viral entry (Liu Y. et al., 2021).
Transdihydrolycoricidine (R430) is a lycorane-type alkaloid derivative from the Amaryllidaceae family that showed more potent antiviral activity against HSV-1 ACVr strains TK mutant and PAAr compared to ACV. R430 influenced the early stages of the HSV-1 lytic phase principally by reducing the transcription and translation of the viral immediate early (IE) gene ICP4 and DNA polymerase, which may be a consequence of upregulation of STAT3 (D'Aiuto et al., 2018).
Steroids
Artocarpus lakoocha is used to treat HSV and varicella-zoster virus infection (Sangkitporn et al., 1995). Oxyresveratrol obtained from the heartwood of Artocarpus lakoocha Roxburgh exhibited antiherpes activity against HSV-1 strain 7401H and HSV-1 ACVr strain B2006 (ACV-resistant with TK deficiency) and PAAv by inhibiting the early gene products ICP6 and ICP8 as well as the late viral proteins gC and gD. The combination of oxyresveratrol and ACV showed a synergistic effect against HSV-1 according to isobologram analysis. In addition, 30% oxyresveratrol ointment treatment prolonged the survival rate and delayed mouse skin lesion development in HSV-1-infected mice (Chuanasa et al., 2008).
Peptides
Aspergillipeptide D is a cyclic pentapeptide isolated from the fungal strain Aspergillus SCSIO 41501. Aspergillipeptide D exerted a significant antiviral effect against three HSV-1 ACVr strains, Blue, 153, and 106, by reducing the mRNA expression of UL27 and the late viral gB protein encoded by UL27. Furthermore, Aspergillipeptide D interfered with the expression and localization of gB in the endoplasmic reticulum and Golgi apparatus, suggesting that it mainly affected gB in viral intercellular spread instead of viral entry (Wang et al., 2020).
Table 3 summarized phytochemicals mentioned in this review with their chemical class, structure and activity against ACV-resistant HSV strains (including the IC50, EC50 and the mode of action).
Conclusion
HSV infection is an urgent public health issue. The nucleoside analog ACV is the most effective clinical treatment that interferes with viral replication and alleviates HSV infection. However, excessive and prolonged use of ACV has led to the emergence of ACV-resistant HSV strains. Thus, it is urgent to develop an effective antiviral therapy with low toxicity to handle ACV-resistant strains (Li et al., 2022). In this review, medicinal plant extracts from 13 families, including Araceae, Asteraceae, Caulerpaceae, Cecropiaceae, Fabaceae, Lamiaceae, and Moraceae, and phytochemicals such as alkaloids, flavonoids, phenolics, terpenes and others, were concluded to exert antiviral properties against ACV-resistant HSV infection, and the mechanism of action were summarized in Figure 1. Most plant extracts that can inhibit ACV-resistant HSV infection are classified into heat-clearing and detoxifying drugs in Traditional Chinese Medicine, with a history of external use to treat sores. The majority of the active components exerted virucidal effects and viral entry inhibition, including blocking viral attachment and fusion. In addition, some phytomedicines prevented the intranuclear biosynthesis of viral proteins and cellular reinfection by progeny viruses. Nevertheless, only a few substances interfered with nuclear transportation and virion egress. In contrast to ACV, these natural products mainly interfered with the early stages of the HSV replication cycle rather than the later stages, demonstrating their potential to treat ACV-resistant HSV infection. Unfortunately, there is no candidate in clinical development or in clinical use against ACV-resistant HSV infection.
Overall, the medicinal plant and phytomedicines mentioned in this review might be promising options for treating ACV-resistant HSV infection, although further studies are needed to exploit sufficient theoretical support for antiviral therapy, such as structure optimization, the synergistic effect of medicinal plants and ACV, and confirmation of the evidence from in vitro and animal-based studies.
Author contributions
LX and X-LZ equally contributed to the development of this manuscript. Z-CX assisted to revise the manuscript. All authors wrote the manuscript and designed the tables in the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This work was financially supported by the National Natural Science Foundation of China (No. 82204437), NSFC-Joint Foundation of Yunnan Province (No. U1902213), Shanghai science and technology innovation action plan (No. 22YF1445100), and Key-Area Research and Development Program of Guangdong Province (No. 2020B1111110003).
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
Argenta, D. F., Silva, I. T., Bassani, V. L., Koester, L. S., Teixeira, H. F., and Simoes, C. M. (2015). Antiherpes evaluation of soybean isoflavonoids. Arch. Virol. 160, 2335–2342. doi: 10.1007/s00705-015-2514-z
Astani, A., Navid, M. H., and Schnitzler, P. (2014). Attachment and penetration of acyclovir-resistant herpes simplex virus are inhibited by Melissa officinalis extract. Phytother. Res. 28, 1547–1552. doi: 10.1002/ptr.5166
Baer-Dubowska, W., Narożna, M., and Krajka-Kuźniak, V. (2021). Anti-cancer potential of synthetic Oleanolic acid derivatives and their conjugates with NSAIDs. Molecules (Basel, Switzerland) 26:4957. doi: 10.3390/molecules26164957
Barrientos, L. G., Matei, E., Lasala, F., Delgado, R., and Gronenborn, A. M. (2006). Dissecting carbohydrate-Cyanovirin-N binding by structure-guided mutagenesis: functional implications for viral entry inhibition. Protein Eng. Des. Sel. 19, 525–535. doi: 10.1093/protein/gzl040
Bertol, J. W., Rigotto, C., de Padua, R. M., Kreis, W., Barardi, C. R., Braga, F. C., et al. (2011). Antiherpes activity of glucoevatromonoside, a cardenolide isolated from a Brazilian cultivar of Digitalis lanata. Antivir. Res. 92, 73–80. doi: 10.1016/j.antiviral.2011.06.015
Bourinbaiar, A. S., and Lee-Huang, S. (1996). The activity of plant-derived antiretroviral proteins MAP30 and GAP31 against herpes simplex virus in vitro. Biochem. Biophys. Res. Commun. 219, 923–929. doi: 10.1006/bbrc.1996.0334
Brigden, D., and Whiteman, P. (1983). The mechanism of action, pharmacokinetics and toxicity of acyclovir--a review. J. Infect. 6, 3–9, The mechanism of action, pharmacokinetics and toxicity of acyclovir — a review, doi: 10.1016/S0163-4453(83)94041-0.
Cagno, V., Sgorbini, B., Sanna, C., Cagliero, C., Ballero, M., Civra, A., et al. (2017). In vitro anti-herpes simplex virus-2 activity of salvia desoleana Atzei & V. Picci essential oil. PLoS One 12:e0172322. doi: 10.1371/journal.pone.0172322
Canadanović-Brunet, J., Cetković, G., Djilas, S., Tumbas, V., Bogdanović, G., Mandić, A., et al. (2008). Radical scavenging, antibacterial, and antiproliferative activities of Melissa officinalis L. extracts. J. Med. Food 11, 133–143. doi: 10.1089/jmf.2007.580
Chen, X., Wang, Z., Yang, Z., Wang, J., Xu, Y., Tan, R. X., et al. (2011). Houttuynia cordata blocks HSV infection through inhibition of NF-kappa B activation. Antivir. Res. 92, 341–345. doi: 10.1016/j.antiviral.2011.09.005
Chen, Y. Y., Liu, J. F., Chen, C. M., Chao, P. Y., and Chang, T. J. (2003). A study of the antioxidative and antimutagenic effects of Houttuynia cordata Thunb. Using an oxidized frying oil-fed model. J. Nutr. Sci. Vitaminol. (Tokyo) 49, 327–333. doi: 10.3177/jnsv.49.327
Chinsembu, K. C. (2016). Ethnobotanical study of plants used in the management of HIV/AIDS-related diseases in Livingstone, Southern Province, Zambia. Evid. Based Complement. Alternat. Med. 2016, 4238625–4238614. doi: 10.1155/2016/4238625
Chiu, L. C., Zhu, W., and Ooi, V. E. (2004). A polysaccharide fraction from medicinal herb Prunella vulgaris downregulates the expression of herpes simplex virus antigen in Vero cells. J. Ethnopharmacol. 93, 63–68. doi: 10.1016/j.jep.2004.03.024
Choi, H. J., Song, J. H., Park, K. S., and Kwon, D. H. (2009). Inhibitory effects of quercetin 3-rhamnoside on influenza a virus replication. Eur. J. Pharm. Sci. 37, 329–333. doi: 10.1016/j.ejps.2009.03.002
Choudhari, A. S., Suryavanshi, S. A., and Kaul-Ghanekar, R. (2013). The aqueous extract of Ficus religiosa induces cell cycle arrest in human cervical cancer cell lines SiHa (HPV-16 positive) and apoptosis in HeLa (HPV-18 positive). PLoS One 8:e70127. doi: 10.1371/journal.pone.0070127
Chuanasa, T., Phromjai, J., Lipipun, V., Likhitwitayawuid, K., Suzuki, M., Pramyothin, P., et al. (2008). Anti-herpes simplex virus (HSV-1) activity of oxyresveratrol derived from Thai medicinal plant: mechanism of action and therapeutic efficacy on cutaneous HSV-1 infection in mice. Antivir. Res. 80, 62–70. doi: 10.1016/j.antiviral.2008.05.002
Cohen, F., Kemeny, M. E., Kearney, K. A., Zegans, L. S., Neuhaus, J. M., and Conant, M. A. (1999). Persistent stress as a predictor of genital herpes recurrence. Arch. Intern. Med. 159, 2430–2436. doi: 10.1001/archinte.159.20.2430
D'Aiuto, L., McNulty, J., Hartline, C., Demers, M., Kalkeri, R., Wood, J., et al. (2018). R430: a potent inhibitor of DNA and RNA viruses. Sci. Rep. 8:16662. doi: 10.1038/s41598-018-33904-y
De Bruyne, T., Pieters, L., Witvrouw, M., De Clercq, E., Vanden Berghe, D., and Vlietinck, A. J. (1999). Biological evaluation of proanthocyanidin dimers and related polyphenols. J. Nat. Prod. 62, 954–958. doi: 10.1021/np980481o
Donalisio, M., Cagno, V., Civra, A., Gibellini, D., Musumeci, G., Ritta, M., et al. (2018). The traditional use of Vachellia nilotica for sexually transmitted diseases is substantiated by the antiviral activity of its bark extract against sexually transmitted viruses. J. Ethnopharmacol. 213, 403–408. doi: 10.1016/j.jep.2017.11.039
Donalisio, M., Nana, H. M., Ngane, R. A., Gatsing, D., Tchinda, A. T., Rovito, R., et al. (2013). In vitro anti-herpes simplex virus activity of crude extract of the roots of Nauclea latifolia smith (Rubiaceae). BMC Complement. Altern. Med. 13:266. doi: 10.1186/1472-6882-13-266
Dubbs, D. R., and Kit, S. (1964). Mutant strains of herpes simplex deficient in thymidine kinase-inducing activity. Virology 22, 493–502. doi: 10.1016/0042-6822(64)90070-4
Efstathiou, S., Kemp, S., Darby, G., and Minson, A. C. (1989). The role of herpes simplex virus type 1 thymidine kinase in pathogenesis. J. Gen. Virol. 70, 869–879. doi: 10.1099/0022-1317-70-4-869
Esquenazi, D., Wigg, M. D., Miranda, M. M., Rodrigues, H. M., Tostes, J. B., Rozental, S., et al. (2002). Antimicrobial and antiviral activities of polyphenolics from Cocos nucifera Linn. (Palmae) husk fiber extract. Res. Microbiol. 153, 647–652. doi: 10.1016/s0923-2508(02)01377-3
Field, H. J. (2001). Herpes simplex virus antiviral drug resistance--current trends and future prospects. Journal of Clinical Virology : the Official Publication of the Pan American Society For Clinical Virology 21, 261–269. doi: 10.1016/S1386-6532(00)00169-4
Ghosh, M., Civra, A., Ritta, M., Cagno, V., Mavuduru, S. G., Awasthi, P., et al. (2016). Ficus religiosa L. bark extracts inhibit infection by herpes simplex virus type 2 in vitro. Arch. Virol. 161, 3509–3514. doi: 10.1007/s00705-016-3032-3
Ghosh, P., Adhikari, U., Ghosal, P. K., Pujol, C. A., Carlucci, M. J., Damonte, E. B., et al. (2004). In vitro anti-herpetic activity of sulfated polysaccharide fractions from Caulerpa racemosa. Phytochemistry 65, 3151–3157. doi: 10.1016/j.phytochem.2004.07.025
Goncalves, J. L., Leitao, S. G., Monache, F. D., Miranda, M. M., Santos, M. G., Romanos, M. T., et al. (2001). In vitro antiviral effect of flavonoid-rich extracts of Vitex polygama (Verbenaceae) against acyclovir-resistant herpes simplex virus type 1. Phytomedicine 8, 477–480. doi: 10.1078/S0944-7113(04)70069-0
Hayashi, K., Hayashi, T., Otsuka, H., and Takeda, Y. (1997). Antiviral activity of 5,6,7-trimethoxyflavone and its potentiation of the antiherpes activity of acyclovir. J. Antimicrob. Chemother. 39, 821–824. doi: 10.1093/jac/39.6.821
Hayashi, K., Iinuma, M., Sasaki, K., and Hayashi, T. (2012). In vitro and in vivo evaluation of a novel antiherpetic flavonoid, 4′-phenylflavone, and its synergistic actions with acyclovir. Arch. Virol. 157, 1489–1498. doi: 10.1007/s00705-012-1335-6
Heidary Navid, M., Laszczyk-Lauer, M. N., Reichling, J., and Schnitzler, P. (2014). Pentacyclic triterpenes in birch bark extract inhibit early step of herpes simplex virus type 1 replication. Phytomedicine 21, 1273–1280. doi: 10.1016/j.phymed.2014.06.007
Honess, R. W., and Watson, D. H. (1977). Herpes simplex virus resistance and sensitivity to phosphonoacetic acid. J. Virol. 21, 584–600. doi: 10.1128/jvi.21.2.584-600.1977
Hosny, S., Sahyon, H., Youssef, M., and Negm, A. (2021). Oleanolic acid suppressed DMBA-induced liver carcinogenesis through induction of mitochondrial-mediated apoptosis and autophagy. Nutr. Cancer 73, 968–982. doi: 10.1080/01635581.2020.1776887
Hung, P. Y., Ho, B. C., Lee, S. Y., Chang, S. Y., Kao, C. L., Lee, S. S., et al. (2015). Houttuynia cordata targets the beginning stage of herpes simplex virus infection. PLoS One 10:e0115475. doi: 10.1371/journal.pone.0115475
Ismail, T., Calcabrini, C., Diaz, A. R., Fimognari, C., Turrini, E., Catanzaro, E., et al. (2016). Ellagitannins in cancer chemoprevention and therapy. Toxins 8:151. doi: 10.3390/toxins8050151
Jadhav, A. K., and Karuppayil, S. M. (2021). Andrographis paniculata (Burm. F) Wall ex Nees: antiviral properties. Phytother. Res. 35, 5365–5373. doi: 10.1002/ptr.7145
Jin, F., Zhuo, C., He, Z., Wang, H., Liu, W., Zhang, R., et al. (2015). Anti-herpes simplex virus activity of polysaccharides from Eucheuma gelatinae. World J. Microbiol. Biotechnol. 31, 453–460. doi: 10.1007/s11274-015-1798-1
Jofre, J. T., Schaffer, P. A., and Parris, D. S. (1977). Genetics of resistance to phosphonoacetic acid in strain KOS of herpes simplex virus type 1. J. Virol. 23, 833–836. doi: 10.1128/JVI.23.3.833-836.1977
Kambizi, L., and Afolayan, A. J. (2001). An ethnobotanical study of plants used for the treatment of sexually transmitted diseases (njovhera) in Guruve District. Zimbabwe. J Ethnopharmacol 77, 5–9. doi: 10.1016/s0378-8741(01)00251-3
Kelly, R. A. (1990). Cardiac glycosides and congestive heart failure. Am. J. Cardiol. 65, E10–E16. doi: 10.1016/0002-9149(90)90245-V
Kost, R. G., Hill, E. L., Tigges, M., and Straus, S. E. (1993). Brief report: recurrent acyclovir-resistant genital herpes in an immunocompetent patient. N. Engl. J. Med. 329, 1777–1782. doi: 10.1056/NEJM199312093292405
Kukhanova, M. K., Korovina, A. N., and Kochetkov, S. N. (2014). Human herpes simplex virus: life cycle and development of inhibitors. Biochemistry (Mosc) 79, 1635–1652. doi: 10.1134/S0006297914130124
Kushch, A. A., Kisteneva, L. B., Klimova, R. R., and Cheshik, S. G. (2021). The role of herpesviruses in development of diseases of the urogenital tract and infertility in women. Vopr. Virusol. 65, 317–325. doi: 10.36233/0507-4088-2020-65-6-2
Lau, K. M., Lee, K. M., Koon, C. M., Cheung, C. S., Lau, C. P., Ho, H. M., et al. (2008). Immunomodulatory and anti-SARS activities of Houttuynia cordata. J. Ethnopharmacol. 118, 79–85. doi: 10.1016/j.jep.2008.03.018
Lee, B., Trung Trinh, H., Bae, E.-A., Jung, K., and Kim, D.-H. (2009). Mangiferin inhibits passive cutaneous anaphylaxis reaction and pruritus in mice. Planta Med. 75, 1415–1417. doi: 10.1055/s-0029-1185773
Lei, Y., Chen, W., Liang, H., Wang, Z., Chen, J., Hong, H., et al. (2019). Preparation of a monoPEGylated derivative of cyanovirin-N and its virucidal effect on acyclovir-resistant strains of herpes simplex virus type 1. Arch. Virol. 164, 1259–1269. doi: 10.1007/s00705-018-04118-4
Li, F., Song, X., Su, G., Wang, Y., Wang, Z., Jia, J., et al. (2019). Amentoflavone inhibits HSV-1 and ACV-resistant strain infection by suppressing viral early infection. Viruses 11:466. doi: 10.3390/v11050466
Li, H., Wei, W., and Xu, H. (2022). Drug discovery is an eternal challenge for the biomedical sciences. Acta Materia Medica. 1, 1–3. doi: 10.15212/AMM-2022-1001
Liu, T., Song, Y., and Hu, A. (2021). Neuroprotective mechanisms of mangiferin in neurodegenerative diseases. Drug Dev. Res. 82, 494–502. doi: 10.1002/ddr.21783
Liu, Y., You, Q., Zhang, F., Chen, D., Huang, Z., and Wu, Z. (2021). Harringtonine inhibits herpes simplex virus type 1 infection by reducing herpes virus entry mediator expression. Front. Microbiol. 12:722748. doi: 10.3389/fmicb.2021.722748
Lu, H. M., Liang, Y. Z., Yi, L. Z., and Wu, X. J. (2006). Anti-inflammatory effect of Houttuynia cordata injection. J. Ethnopharmacol. 104, 245–249. doi: 10.1016/j.jep.2005.09.012
Luo, Z., Kuang, X. P., Zhou, Q. Q., Yan, C. Y., Li, W., Gong, H. B., et al. (2020). Inhibitory effects of baicalein against herpes simplex virus type 1. Acta Pharm. Sin. B 10, 2323–2338. doi: 10.1016/j.apsb.2020.06.008
McNulty, J., D'Aiuto, L., Zhi, Y., McClain, L., Zepeda-Velazquez, C., Ler, S., et al. (2016). iPSC neuronal assay identifies Amaryllidaceae pharmacophore with multiple effects against herpesvirus infections. ACS Med. Chem. Lett. 7, 46–50. doi: 10.1021/acsmedchemlett.5b00318
Morfin, F., and Thouvenot, D. (2003). Herpes simplex virus resistance to antiviral drugs. Journal of Clinical Virology : the Official Publication of the Pan American Society For Clinical Virology 26, 29–37. doi: 10.1016/S1386-6532(02)00263-9
Mues, M. B., Cheshenko, N., Wilson, D. W., Gunther-Cummins, L., and Herold, B. C. (2015). Dynasore disrupts trafficking of herpes simplex virus proteins. J. Virol. 89, 6673–6684. doi: 10.1128/JVI.00636-15
Ott, A., Fohring, B., and Kaerner, H. C. (1979). Herpes simplex virus type 1 Angelotti and a defective viral genotype: analysis of genome structures and genetic relatedness by DNA-DNA reassociation kinetics. J. Virol. 29, 423–430. doi: 10.1128/JVI.29.2.423-430.1979
Palu, G., Summers, W. P., Valisena, S., and Tognon, M. (1988). Preliminary characterization of a mutant of herpes simplex virus type 1 selected for acycloguanosine resistance in vitro. J. Med. Virol. 24, 251–262. doi: 10.1002/jmv.1890240303
Paluch, Z., Trojanek, M., Veliskova, Z., Mlichova, J., Chrbolka, P., Gregorova, J., et al. (2021). Neurotoxic side effects of acyclovir: two case reports. Neuro Endocrinol. Lett. 42, 375–382.
Parris, D. S., Courtney, R. J., and Schaffer, P. A. (1978). Temperature-sensitive mutants of herpes simplex virus type 1 defective in transcriptional and post-transcriptional functions required for viral DNA synthesis. Virology 90, 177–186. doi: 10.1016/0042-6822(78)90301-x
Petronilho, F., Dal-Pizzol, F., Costa, G. M., Kappel, V. D., de Oliveira, S. Q., Fortunato, J., et al. (2012). Hepatoprotective effects and HSV-1 activity of the hydroethanolic extract of Cecropia glaziovii (embauba-vermelha) against acyclovir-resistant strain. Pharm. Biol. 50, 911–918. doi: 10.3109/13880209.2011.643902
Pilau, M. R., Alves, S. H., Weiblen, R., Arenhart, S., Cueto, A. P., and Lovato, L. T. (2011). Antiviral activity of the Lippia graveolens (Mexican oregano) essential oil and its main compound carvacrol against human and animal viruses. Braz. J. Microbiol. 42, 1616–1624. doi: 10.1590/S1517-838220110004000049
Priengprom, T., Ekalaksananan, T., Kongyingyoes, B., Suebsasana, S., Aromdee, C., and Pientong, C. (2015). Synergistic effects of acyclovir and 3, 19-isopropylideneandrographolide on herpes simplex virus wild types and drug-resistant strains. BMC Complement. Altern. Med. 15:56. doi: 10.1186/s12906-015-0591-x
Puljula, E., Walton, G., Woodward, M. J., and Karonen, M. (2020). Antimicrobial activities of Ellagitannins against,, and. Molecules (Basel, Switzerland) 25:3714. doi: 10.3390/molecules25163714
Rechenchoski, D. Z., Agostinho, K. F., Faccin-Galhardi, L. C., Lonni, A., da Silva, J. V. H., de Andrade, F. G., et al. (2020). Mangiferin: a promising natural xanthone from Mangifera indica for the control of acyclovir - resistant herpes simplex virus 1 infection. Bioorg. Med. Chem. 28:115304. doi: 10.1016/j.bmc.2020.115304
Reichling, J., Nolkemper, S., Stintzing, F. C., and Schnitzler, P. (2008). Impact of ethanolic lamiaceae extracts on herpesvirus infectivity in cell culture. Forsch. Komplementmed. 15, 313–320. doi: 10.1159/000164690
Ritta, M., Marengo, A., Civra, A., Lembo, D., Cagliero, C., Kant, K., et al. (2020). Antiviral activity of a Arisaema Tortuosum leaf extract and some of its constituents against herpes simplex virus type 2. Planta Med. 86, 267–275. doi: 10.1055/a-1087-8303
Sangkitporn, S., Chaiwat, S., Balachandra, K., Na-Ayudhaya, T. D., Bunjob, M., and Jayavasu, C. (1995). Treatment of herpes zoster with Clinacanthus nutans (bi phaya yaw) extract. J. Med. Assoc. Thail. 78, 624–627.
Schnitzler, P., Koch, C., and Reichling, J. (2007). Susceptibility of drug-resistant clinical herpes simplex virus type 1 strains to essential oils of ginger, thyme, hyssop, and sandalwood. Antimicrob. Agents Chemother. 51, 1859–1862. doi: 10.1128/AAC.00426-06
Schuhmacher, A., Reichling, J., and Schnitzler, P. (2003). Effect of peppermint oil on the enveloped viruses herpes simplex virus type 1 and type 2 in vitro. Phytomedicine 10, 504–510. doi: 10.1078/094471103322331467
Serkedjieva, J., and Ivancheva, S. (1999). Antiherpes virus activity of extracts from the medicinal plant Geranium sanguineum L. J. Ethnopharmacol. 64, 59–68. doi: 10.1016/s0378-8741(98)00095-6
Shan, T., Ye, J., Jia, J., Wang, Z., Jiang, Y., Wang, Y., et al. (2021). Viral UL8 is involved in the antiviral activity of Oleanolic acid against HSV-1 infection. Front. Microbiol. 12:689607. doi: 10.3389/fmicb.2021.689607
Singh, D., Singh, B., and Goel, R. K. (2011). Traditional uses, phytochemistry and pharmacology of Ficus religiosa: a review. J. Ethnopharmacol. 134, 565–583. doi: 10.1016/j.jep.2011.01.046
Stranska, R., Schuurman, R., Nienhuis, E., Goedegebuure, I. W., Polman, M., Weel, J. F., et al. (2005). Survey of acyclovir-resistant herpes simplex virus in the Netherlands: prevalence and characterization. J. Clin. Virol. 32, 7–18. doi: 10.1016/j.jcv.2004.04.002
Su, C. T., Hsu, J. T., Hsieh, H. P., Lin, P. H., Chen, T. C., Kao, C. L., et al. (2008). Anti-HSV activity of digitoxin and its possible mechanisms. Antivir. Res. 79, 62–70. doi: 10.1016/j.antiviral.2008.01.156
Thompson, K. D. (1998). Antiviral activity of Viracea against acyclovir susceptible and acyclovir resistant strains of herpes simplex virus. Antivir. Res. 39, 55–61. doi: 10.1016/s0166-3542(98)00027-8
Valyi-Nagy, T., Gesser, R. M., Raengsakulrach, B., Deshmane, S. L., Randazzo, B. P., Dillner, A. J., et al. (1994). A thymidine kinase-negative HSV-1 strain establishes a persistent infection in SCID mice that features uncontrolled peripheral replication but only marginal nervous system involvement. Virology 199, 484–490. doi: 10.1006/viro.1994.1150
Vilhelmova-Ilieva, N., Jacquet, R., Quideau, S., and Galabov, A. S. (2014). Ellagitannins as synergists of ACV on the replication of ACV-resistant strains of HSV 1 and 2. Antivir. Res. 110, 104–114. doi: 10.1016/j.antiviral.2014.07.017
Wang, Y., Wang, Q., Zhu, Q., Zhou, R., Liu, J., and Peng, T. (2011). Identification and characterization of acyclovir-resistant clinical HSV-1 isolates from children. J. Clin. Virol. 52, 107–112. doi: 10.1016/j.jcv.2011.06.009
Wang, Z., Jia, J., Wang, L., Li, F., Wang, Y., Jiang, Y., et al. (2020). Anti-HSV-1 activity of Aspergillipeptide D, a cyclic pentapepetide isolated from fungus aspergillus sp. SCSIO 41501. Virol. J. 17:41. doi: 10.1186/s12985-020-01315-z
Whitley, R. J., and Roizman, B. (2001). Herpes simplex virus infections. Lancet 357, 1513–1518. doi: 10.1016/S0140-6736(00)04638-9
Xiong, S., Fan, J., and Kitazato, K. (2010). The antiviral protein cyanovirin-N: the current state of its production and applications. Appl. Microbiol. Biotechnol. 86, 805–812. doi: 10.1007/s00253-010-2470-1
Xu, H. X., Lee, S. H., Lee, S. F., White, R. L., and Blay, J. (1999). Isolation and characterization of an anti-HSV polysaccharide from Prunella vulgaris. Antivir. Res. 44, 43–54. doi: 10.1016/s0166-3542(99)00053-4
Yoshida, Y., Yamamura, J., Sato, H., Koyasu, M., Obara, Y., Sekiguchi, H., et al. (1996). Efficacy of Cafon gel on cutaneous infection with herpes simplex virus (HSV)-2 and acyclovir-resistant HSV in mice. J. Dermatol. Sci. 13, 237–241. doi: 10.1016/s0923-1811(97)89474-1
Keywords: herpes simplex virus, antiviral herbs, natural products, acyclovir-resistant, mode of action
Citation: Xu L, Zhong X-L, Xi Z-C, Li Y and Xu H-X (2022) Medicinal plants and natural compounds against acyclovir-resistant HSV infections. Front. Microbiol. 13:1025605. doi: 10.3389/fmicb.2022.1025605
Edited by:
Maria Teresa Sciortino, University of Messina, ItalyReviewed by:
Qinchang Zhu, Shenzhen Technology University, ChinaXun Song, Shenzhen University, China
Copyright © 2022 Xu, Zhong, Xi, Li and Xu. 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: Yang Li, eWFuZ2xAc2h1dGNtLmVkdS5jbg==; Hong-Xi Xu, aHh4dUBzaHV0Y20uZWR1LmNu
†These authors have contributed equally to this work