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Article

First Insight into the Seroepidemiology of Hepatitis E Virus (HEV) in Dogs, Cats, Horses, Cattle, Sheep, and Goats from Bulgaria

1
Department of Microbiology, Infectious and Parasitic Diseases, Faculty of Veterinary Medicine, Trakia University, 6000 Stara Zagora, Bulgaria
2
Department of Infectious Pathology, Hygiene, Technology and Control of Foods from Animal Origin, Faculty of Veterinary Medicine, University of Forestry, 1797 Sofia, Bulgaria
3
Department of Plant Physiology and Molecular Biology, University of Plovdiv, 4000 Plovdiv, Bulgaria
4
Department of Occupational Medicine, Faculty of Public Health, Medical University, 1527 Sofia, Bulgaria
5
Department of Technology Transfer and IP Management, Center of Plant Systems Biology and Biotechnology, 4000 Plovdiv, Bulgaria
6
Department of Infectious Diseases, Military Medical Academy, 1606 Sofia, Bulgaria
*
Author to whom correspondence should be addressed.
Submission received: 21 June 2023 / Revised: 17 July 2023 / Accepted: 19 July 2023 / Published: 21 July 2023
(This article belongs to the Special Issue Infectious Disease Epidemiology and Transmission Dynamics 2.0)

Abstract

:
In recent years, hepatitis E virus (HEV) infection has been found to be widespread among different animal species worldwide. In Bulgaria, high HEV seropositivity was found among pigs (60.3%), wild boars (40.8%), and East Balkan swine (82.5%). The aim of the present study was to establish the seroprevalence of HEV among dogs, cats, horses, cattle, sheep, and goats in Bulgaria. In total, 720 serum samples from six animal species were randomly collected: dogs—90 samples; cats—90; horses—180; cattle—180; sheep—90; and goats—90. The serum samples were collected from seven districts of the country: Burgas, Kardzhali, Pazardzhik, Plovdiv, Sliven, Smolyan, and Stara Zagora. The animal serum samples were tested for HEV antibodies using the commercial Wantai HEV-Ab ELISA kit (Beijing, China). The overall HEV seroprevalence among different animal species from Bulgaria was as follows: dogs—21.1%; cats—17.7%; horses—8.3%; cattle—7.7%; sheep—32.2%; and goats—24.4%. We found the lowest overall HEV seropositivity in Plovdiv district (6.2%; 4/64; p = 0.203) and Smolyan district (8.8%; 4/45; p = 0.129), vs. the highest in Pazardzhik district (21.6%; 29/134; p = 0.024) and Burgas district (28.8%; 26/90; p = 0.062). To the best of our knowledge, this is the first serological evidence of HEV infection in dogs, cats, horses, cattle, sheep, and goats from Bulgaria. We found high HEV seropositivity in small ruminants (sheep and goats), moderate seropositivity in pets (dogs and cats), and a low level of seropositivity in large animals (horses and cattle). Previous Bulgarian studies and the results of this research show that HEV infection is widespread among animals in our country. In this regard, the Bulgarian health authorities must carry out increased surveillance and control of HEV infection among animals in Bulgaria.

1. Introduction

Worldwide, the hepatitis E virus (HEV) is one of the leading causes of acute viral hepatitis, transmitted mainly via the fecal-oral route or by contact with infected animals and their products. In recent decades, the understanding of the HEV infection has changed considerably. HEV was first detected in June 1983 by a scientific team led by Mikhail S. Balayan [1]. According to the latest revision of the International Committee on Taxonomy of Viruses (ICTV), HEV belongs to the Hepeviridae family, which is divided into two subfamilies: Orthohepevirinae and Parahepevirinae [2,3]. Orthohepevirinae has four genera: Avihepevirus, Chirohepevirus, Paslahepevirus, and Rocahepevirus [2]. The hepeviruses from Paslahepevirus balayani and Rocahepevirus ratti include strains that cause acute hepatitis in humans of zoonotic origin [2,4,5,6]. The Paslahepevirus balayani species have been assigned to eight genotypes (gt): HEV gt 1 (Southern Asia; humans), HEV gt 2 (Africa and Mexico; humans), HEV gt 3 and HEV gt 4 (America, Asia, and Europe; humans, pigs, cattle, deer, goats, rabbits, rats, sheep, Tursiops truncatus, etc.), HEV gt 5 and HEV gt 6 (Japan; wild boars), HEV gt 7 (United Arab Emirates; Camelus dromedarius, humans), and HEV gt 8 (China; Camelus bactrianus) [7,8,9,10,11,12,13,14,15,16,17,18]. HEV gt 1 and HEV gt 2 cause hepatitis disease in humans and are transmitted by the fecal-oral route, mainly due to contaminated water and lower sanitary and hygienic standards. Worldwide, HEV gt 3 and HEV gt 4 are found primarily in domestic pigs and wild boar. They can be transferred to humans, usually through the consumption of raw or undercooked infected meat [19]. In addition, transmission to humans, specifically hunters, veterinarians, and forest workers, can also occur as a result of occupational exposure to the virus [20,21]. A patient from the United Arab Emirates was infected with HEV gt 7 as a result of regular consumption of camel milk [14]. Infection with rat HEV (Rocahepevirus ratti) was also observed in humans, and evidence of rat HEV was found in animals other than rodents [22,23].
The role and impact of other host species (wild and domestic) in HEV transmission are still under investigation, but a growing number of studies have shown that HEV infections of animals with close contact with humans, including dogs, cats, cattle, horses, goats, and sheep, are also possible [24,25,26,27]. In 2001, Arankalle et al. found IgG anti-HEV antibodies in dogs from Pune, India (22.7%) and cattle from Surat, India (4.4%) and Pune, India (6.9%) [28]. Okamoto et al. detected antibodies to HEV in 135 sera of Japanese pet cats (the A450 values of anti-HEV antibodies ranged from 0.026 to 2.917, and 33% of the samples had an A450 value of ≥0.600) [29]. The first evidence of HEV in horses was found in Egypt (13%, or 26/200 equine serum samples, were positive by HEV IgG serological assay) [30]. In 1994, Usmanov et al. conducted experimental inoculation of lambs with HEV (a pool of 10% HEV patient fecal suspension containing HEV isolates Osh-225 and Osh-228) and indicated the susceptibility of lambs to this virus [31]. HEV seropositivity in goats was first reported by Zhang et al. [32]. They found that 24.0% of the tested goats from Eastern China were positive for anti-HEV IgG antibodies [32].
Recent studies have shown the spread of HEV and the prevalent genotypes among humans and pigs in Bulgaria. HEV-specific antibodies were found in pigs from farrow-to-finish farms (36.0% and 60.3%) [33,34], wild boars (12.5% and 40.8%) [35,36] and East Balkan swine—the only aboriginal pig breed in Bulgaria (82.5%) [37]. The HEV seroprevalence among pigs and wild boars in Bulgaria is similar to the reported seroprevalence rate in European countries, which ranges between 30 and 100% [38,39,40,41,42,43]. Krumova-Valcheva et al. reported overall 10.8% HEV RNA-positive fecal samples among swine from Bulgarian farrow-to-finish pig farms [44]. HEV RNA detection studies in pigs, carried out in many other European countries, have shown similar results: Slovakia—13.7% [45]; Italy—42.2% [46]; the Netherlands—15.0% [47]; Belgium—7.0% [47]; Spain—18.8% [48]; and Hungary—21.0% [49]. Palombieri et al. reported that HEV gt 3 (subtype C) probably dominated among Bulgarian pigs [50]. Bruni et al. show that the acute hepatitis E human cases in Bulgaria are caused by HEV gt 3 (subtypes 3e, 3f, and 3c), which are usually found in pigs and wild boars, revealing the possible zoonotic transmission of the HEV infection to humans [51]. Until now, HEV has only been detected in pigs in Bulgaria, i.e., there are no data on the spread of the virus among other animal reservoirs in our country. The aim of the present study was to establish the seroprevalence of HEV among dogs, cats, horses, cattle, sheep, and goats in Bulgaria. To the best of our knowledge, this is the first seroepidemiological HEV survey on these animal reservoirs in Bulgaria. In addition, this is the first serological evidence of HEV infection in dogs, horses, cattle, sheep, and goats in Southeastern Europe (Balkan Peninsula).

2. Materials and Methods

2.1. Study Design and Data Collection

The current research was conducted between 1 June 2022 and 30 December 2022. In total, 720 serum samples from six animal species were randomly collected from randomly chosen farms and animals: dog (Canis lupus familiaris)—90 samples; cat (Felis silvestris catus)—90; horse (Equus ferus caballus)—180; cattle (Bos primigenius taurus)—180; sheep (Ovis aries)—90; and goat (Capra hircus)—90. The animals included in the present study were domestically bred. The samples from the dogs and cats were obtained at the University Veterinary Hospital on different occasions. These animals were pets and were most often kept in urban households. Horses were used as working animals and were bred by minority ethnic communities (with low education) in rural and suburban areas. Equine samples were collected by mobile veterinary teams that visited the minority ethnic communities in their place of residence. Cattle were raised on farms (100–200 animals in a herd). During the routine veterinary examination, the veterinarian took a sample from the cattle. Sheep and goats were kept in herds of 100–200 animals in the rural areas of the administrative districts. The sheep and goat samples were taken during the routine veterinary examination of these animals. For all animals, we received data on which administrative district they live in. Additionally, we collected sex and age information for dogs, cats, and horses.
The serum samples were collected from different administrative areas of the country: Burgas district (approximately 27°46′ E Longitude; 42°50′ N Latitude), Kardzhali district (approx. 25°37′ E Long; 41°63′ N Lat), Pazardzhik district (approx. 24°33′ E Long; 42°19′ N Lat), Plovdiv district (approx. 24°74′ E Long; 42°13′ N Lat), Sliven district (approx. 26°32′ E Long; 42°68′ N Lat), Smolyan district (approx. 24°70′ E Long; 41°57′ N Lat), and Stara Zagora district (approx. 25°63′ E Long; 42°42′ N Lat). The number of animals studied by districts is presented in Figure 1.
A blood sample of up to 5 mL was obtained from each animal species. The blood samples were kept in plain vacutainers (without anticoagulant reagent) at room temperature (20.0 °C) until visible clot retraction. After being centrifuged at 1500× g for 10 min., the sera were separated and stored at −20.0 °C until analysis. Sample testing and the analysis of serological results were performed at the Laboratory of Animal Infectious Diseases, Faculty of Veterinary Medicine, Trakia University, 6000 Stara Zagora, Bulgaria.

2.2. HEV Antibody Detection

The animal serum samples were tested for HEV antibodies using the commercial Wantai HEV-Ab ELISA kit (Beijing Wantai Biological Pharmacy Enterprise Co., Ltd., Beijing, China; Catalog number: WE-7396). The applied serological test was for the qualitative detection of total HEV antibodies in animal serum. It was intended for the diagnosis of HEV infection and seroprevalence studies among different animal species. This commercial ELISA test has been shown to be superior to other ELISA tests for detecting HEV antibodies in previous research (both the Wantai test and DiaPro, Milan, Italy, have shown the highest sensitivity) [52].

2.3. Ethical Considerations

Animals were treated humanely according to Bulgarian national legislation. The owners of the animals participating in this study provided “Five freedoms of animal welfare”: freedom from hunger and thirst; freedom from discomfort; freedom from pain, injury, and disease; freedom to express normal behavior; and freedom from fear and distress. Immobilization procedures during the blood collection rule out pain, fear, or agitation in the animals. Sampling was carried out by qualified personnel (veterinarians) who used protective equipment (masks, gloves, glasses, boots, etc.). Written informed consent for participation in the present study was obtained from all animal owners. The current study was permitted and approved by the Local Ethics Committee at Trakia University, Stara Zagora, Bulgaria (FVM-05/17 May 2022).

2.4. Statistical Analysis

Data analysis was performed with the help of SPSS Statistics 20.0 (IBM Corp., Armonk, NY, USA) and Excel 2007 (Microsoft, Redmond, WA, USA). The data were entered and arranged in MS Excel. HEV prevalence was estimated from the ratio of positive samples to the total number of samples analyzed, with confidence intervals of 95%. For all characteristics, the Z-test was used to test the hypothesis that the observed proportion is equal to a predetermined proportion. The samples (dogs, cats, and horses) were divided into three age groups and categorized according to sex. Univariate logistic regression was used to assess the risk regarding sex, age, animal species, HEV-positive result, and districts. Multivariate logistic regression was applied to assess the independent influence of animal species on sex and age. A p-value < 0.05 was considered statistically significant.

3. Results

In total, 15.9% (115/720) anti-HEV-positive samples were detected among all animals (Table 1). The overall HEV seroprevalence among different animal species from Bulgaria was as follows: dogs—21.1% (19/90); cats—17.7% (16/90); horses—8.3% (15/180); cattle—7.7% (14/180); sheep—32.2% (29/90); and goats—24.4% (22/90).
The samples from dogs, cats, and horses were categorized according to sex. Regarding sex, a higher HEV seropositivity was found in the female dogs (26.0%), followed by the male cats (20.4%), male dogs (15.9%), and female cats (15.2%), but the observed difference is not statistically significant (Table 2). In horses, we observed a statistically significantly lower rate of HEV antibodies in females (4.1%) compared to males (13.4%) (odds ratio, OR = 0.243; p = 0.029). Data on HEV seroprevalence were collected according to age groups that were each divided into three different age groups (animals < 2 years old; 2–6 years old; >6 years old). The research shows that the anti-HEV antibody prevalence percentage in age group <2 years old animal species was 14.5% (7/48); age group 2–6 years old—13.6% (19/139); and age group > 6 years old—13.8% (24/173) (p = 0.988) (Table 2). There was no significant difference among the age groups.
HEV seroprevalence distribution varies by region (Table 3 and Table 4). We detected the highest HEV-positive results for horses in the Sliven district (9.4%); cattle in the Stara Zagora district (13.3%); sheep in the Pazardzhik district (33.3%); and goats in the Burgas district (26.6%) (Table 3). In addition, we found that the districts with the highest HEV seropositivity were Burgas (28.8%) and Pazardzhik (21.6%); vice versa, the districts with the lowest HEV seropositivity were Kardzhali (0.0%) and Plovdiv (6.2%) (Table 4). The binary logistic regression showed that the risk of a HEV-positive result was 20.469 times higher for Stara Zagora district (p = 0.035), 25.446 times higher for Pazardzhik district (p = 0.024), and 14.660 times higher for Burgas district (p = 0.062) compared to the reference district of Kardzhali.

4. Discussion

Numerous studies have shown animal transmission of HEV disease to humans and have identified a wide variety of animal species that can act as HEV hosts [7,8,10,19]. Many of these studies are focused on HEV in pigs and wild boars [11,33,34,35,36,37,38,39,40]. However, it appears that other animal species, which are in much closer contact with humans, also have high HEV seropositive rate. In this research, we report HEV seropositivity among a wide group of animals (dogs, cats, horses, cattle, sheep, and goats), and it is the first seroepidemiological HEV survey of this kind in Bulgaria. The overall HEV seroprevalence was 21.1% in dogs, 17.7% in cats, 8.3% in horses, 7.7% in cattle, 32.2% in sheep, and 24.4% in goats.
The reported HEV seroprevalence in dogs in European countries varies widely. What we have observed fits somewhat in the middle. The HEV seropositivity in dogs in Bulgaria was slightly higher than that reported in the Netherlands (18.5%) [53] and significantly higher than those those reported in the United Kingdom (0.8%) [54], Italy (5.0%) [55], and Spain (9.9%) [24]. The HEV seroprevalence observed in Switzerland (38.0%) [56] and Germany (56.5%) [57], however, was significantly higher than what we observed. The seroprevalence found in our cats was 17.7%, which is approximately at a mean level compared to the results of other European countries: Spain (2.8%) [24], and (37.0%) [58]; Italy (3.1%) [59]; Turkey (5.4%) [60]; Netherlands (14.8%) [53]; and Germany (32.3%) [57]. Although it is difficult to make a comparison between different studies due to the use of different serological tests and a difference in the number of animals studied, we can state that the seroprevalence of HEV in cats and dogs in Bulgaria should be considered moderate.
Several studies have proposed HEV serological spread in animals according to sex and age. Caballero-Gomez et al. reported 12.4% HEV seropositivity in male urban dogs compared to 6.4% in females [24]. German authors showed 47.2% HEV-positive results in male cats from Brandenburg and 27.6% in female cats [57]. Capozza et al. reported 3.9% HEV seropositivity in male household cats compared to 2.0% in females [59]. Some surveys established an equable distribution of HEV seroprevalence among different age groups. Spanish authors found 11.1% and 0.0% HEV seropositivity in yearling dogs and cats, respectively. HEV seropositivity of 7.9% and 0.0% in sub-adult dogs and cats, respectively. Finally, in adult dogs and cats, the HEV seropositivity was 10.8% and 3.9%, respectively [24]. Bernardini et al. reported 0.0% HEV-positive results in dogs under 2 years old, 6.9% in dogs between 2 and 5 years old, and 3.7% in dogs over 5 years of age [55]. Italian researchers found 0.0% (<2 years old) HEV seropositivity in household cats; 4.4% in cats aged 2–8 years, 4.6% in cats aged 9–14 years, 0.0% in cats >14 years or of an undetermined age [59]. Cagirgan et al. reported 3.2% HEV positivity in domestic cats (0–2 age group); 1.09% in cats of the 2–8 age group, and 1.09% in those older than 8 years [60]. Our overall HEV seropositivity in dogs (21.1%) and cats (17.7%) is similar to that of Li et al. from the Netherlands, who reported 18.5% among dogs and 14.8% in cats [53].
There are various potential reasons for the moderate HEV seroprevalence among pets (dogs and cats) presented by our study. For example, the animals’ behavior could influence the seropositivity. During the walk, dogs like to sniff and dig in the bushes, grass, and garbage. So, this instinctual behavior could increase the risk of HEV contamination. In addition, cats love to hunt small mammals such as rats and mice, which could be a serious prerequisite for HEV transmission. In this regard, Caballero-Gomez et al. suggested that both HEV gt 3 (Paslahepevirus balayani) and rat HEV-C1 (Rocahepevirus ratti) genotypes circulate in urban cats and dogs in Spain, which hypothesis supports the above-mentioned ways for infection of pets [24]. Dogs and cats are carnivores and it is possible that they can become infected via the food chain by consuming raw meat contaminated with swine HEV gt 3 or rat HEV-C1. Furthermore, the moderate HEV seropositivity in our dogs (21.1%) and cats (17.7%) is similar to that found among Bulgarian blood donors (25.9%) [20] and individuals with Guillain-Barre syndrome (24.5%) [61].
Most equine HEV studies show low seropositivity. Saad et al. presented 13% HEV IgG ELISA positive results among privately owned work horses from suburban areas of Cairo (Egypt), particularly “Old Cairo” [30]. Low HEV seropositivity among horses was also found in other countries: China (11.0%) [62] and (16.3%) [32]; South Korea (12.4%) [63]; and the Netherlands (18.18%) [53]. Yoon et al. reported a higher HEV seroprevalence in male horses (16.7%) compared to females (11.7%) [63]. The same authors reported different results for different age groups: 1–2 years (20.0%); 3–10 years (9.9%); >10 years (13.1%) [63]. Our results in horses (8.3%) are similar to those of Fu et al. from Xinjiang, China, who reported 11.0% HEV-positive results in domestic horses [62].
The prevalence of HEV in cattle varies widely in different countries around the world. In Croatia, 0.0% HEV seropositivity was found among cattle (Bos taurus) [64]; Spain (0.0%) [58]; South Korea (0.0%) [65]; Brazil (1.42%) [66]; India (4.4%) in Surat and (6.9%) in Pune [28]; China (6.0%) [32], (6.3%) [67], (6.5%) [62], (18.7%) [68], (28.2%) [69], (29.35%) [70]; Jordan (14.5%) [71]; USA (20.4%) [72]; and Egypt (21.6%) [73]. Our overall HEV seropositivity in cattle (7.7%) is similar to that of Arankalle et al. from Pune, Western India, who reported (6.9%) in cattle [28].
We found low levels of HEV antibodies in large animals (horses (8.3%); cattle (7.7%)). The most likely reason could be the horse’s feeding by minority ethnic communities. Usually, these population groups have low education and low social status. They keep the horses alone (one or two horses per household). In addition, these horses are bred in rural and suburban areas. Their habitats do not interact with the habitats of the main HEV reservoirs, such as those of wild boar or deer. A potential reason for the low HEV seropositivity in cattle could be the controlled, balanced diet and the lack of contact with free pastures and meadows. These factors reduce the risk of HEV exposure and, consequently, high HEV seroprevalence.
The prevalence of HEV infection in sheep and goats varies widely between studies. Low seropositivity was found in sheep in Spain (2.1%) [74] and (2.6%) [58]—compared to high seropositivity reported in Portugal (16.6%) [75]; and Italy (21.3%) [76] and (21.6%) [77]. HEV antibodies were detected in goat sera from Spain (1.6%) [58] and (13.8%) [74]; Italy (11.4%) [77]; and the USA (16%) [78]. Our results for sheep (32.2%) and goats (24.4%) are similar to those of Palombieri et al. from Italy, who reported (21.6%) HEV-positive results in sheep serum samples [77], and Sanford et al. from the USA, who presented 16% HEV-positive results in serum samples of mature goats [78].
We found high HEV seropositivity among small ruminants (sheep, 32.2%; goats, 24.4%). These animals are bred in rural areas of our country. In most cases, these sheep and goats graze on free pastures and meadows in areas outside the settlements. Frequently, these animals drink water from natural springs and untested sources. These factors lead to an increased risk of HEV infection. On the other hand, the high HEV seropositivity among our small ruminants is similar to that found in Bulgarian wild boars (40.8%) [36] and East Balkan swine—the only aboriginal pig breed in Bulgaria (82.5%) [37].
The serological test used could be a potential reason for different HEV-positive results between different seroepidemiological surveys. We used the commercial Wantai HEV-Ab ELISA kit (Beijing Wantai Biological Pharmacy Enterprise Co., Ltd., Beijing, China). In fact, it is the most widely used serological test for HEV infection in animals [32,53,59,62,63,69,70,72,75,76,77]. Additionally, Norder et al. reported that this commercial ELISA test (produced by Wantai, Beijing, China) has been shown to be superior to other ELISA tests for detecting HEV antibodies [52]. In this regard, we could assume that our results are adequate to reality and in unison with our results from other animal and human studies.
It is well known from the scientific literature that male animals are more likely to be affected by HEV [24,57,59,63,73,79,80], and the incidence of HEV infection increased with age [13,24,79,81]. Unfortunately, in some studies, this information was missing. In this regard, in part of the studies on the prevalence of HEV infection in animal species, it is not possible to analyze the influence of sex and age. Furthermore, it is well known that there is an age-dependent trend for domestic pigs and wild boars—with increasing age = increasing HEV-positive results [33,34,37]. Therefore, it is good to have data on these two important indicators (sex and age).
The present study has some limitations that need to be addressed. First, we did not perform molecular analysis of HEV (HEV RNA testing) due to technical and financial reasons. Second, it was not a nationwide survey, i.e., the present research showed data on several districts in our country. Third, we had sex and age information only for some animals (dogs, cats, and horses). Fourth, information on herds (for cattle, sheep, and goats) was not collected. Fifth, the comparison of HEV seropositivity by administrative districts in our survey should be interpreted with care and kept in mind that individual districts include different animal species, i.e., comparison of different animal populations in different districts. Sixth, in the absence of a demonstration of HEV RNA, the epidemiological role of all investigated animal species in relation to the risk of transmission to humans remains to be clarified. In this regard, the results and conclusions should be interpreted with caution. Despite these limitations, this research has its merits. To the best of our knowledge, this is the first seroepidemiological HEV survey among dogs, cats, horses, cattle, sheep, and goats in Bulgaria. Furthermore, this is the first serological evidence of HEV infection in dogs, horses, cattle, sheep, and goats from Southeastern Europe (the Balkan Peninsula).

5. Conclusions

We conducted a seroepidemiological study on HEV infection in animal species from Bulgaria. We found high HEV seropositivity in small ruminants (sheep—32.2%; goats—24.4%); moderate in pets (dogs—21.1%; cats—17.7%); and lower in large animals (horses—8.3%; cattle—7.7%). These results enhance our knowledge about the prevalence of HEV infection in animals from Bulgaria. Both previous Bulgarian studies [33,34,35,36,37,44,50] and the current results of this research show that HEV infection is widespread among animals in our country. Furthermore, HEV seropositivity is widespread among some groups of the Bulgarian population: blood donors (25.9%) [20], general hunters (48.7%) [20], hunters of wild boars (51.6%) [20], and individuals with Guillain-Barre syndrome (24.5%) [61]. These facts are a serious reason for increasing surveillance and control of HEV infection among animals and humans in Bulgaria. In this regard, all Bulgarian health authorities and scientific organizations are recommended to improve their policies and programs for the prevention and control of HEV infection in our country.

Author Contributions

Conceptualization, I.T. and M.B.; methodology, I.T. and M.B.; data collection, I.T., R.P. and K.K.; data curation, I.T., K.T. and K.K.; data interpretation, I.T. and M.B.; laboratory analysis, K.G.; statistical analysis, T.K.; literature search, I.T. and M.B.; writing—original draft preparation, M.B.; writing—review and editing, I.T., T.K. and G.Z.; visualization, M.B.; supervision, I.T.; funding collection, I.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Bulgarian Ministry of Education and Science (MES) in the frames of the Bulgarian National Recovery and Resilience Plan, Component “Innovative Bulgaria”, Project No. BG-RRP-2.004-0006-C02 “Development of research and innovation at Trakia University in service of health and sustainable well-being”.

Institutional Review Board Statement

Ethical approval for this survey was obtained from the Local Ethics Committee of the Faculty of Veterinary Medicine, Trakia University, 6000 Stara Zagora, Bulgaria (FVM-05/17 May 2022). According to Bulgarian national legislation, animals were treated humanely.

Informed Consent Statement

Written informed consent for participation in the present study was obtained from all animal owners.

Data Availability Statement

Not applicable.

Acknowledgments

We thank our families for providing us with the time and support needed to write this survey in a timely manner.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Balayan, M.S.; Andjaparidze, A.G.; Savinskaya, S.S.; Ketiladze, E.S.; Braginsky, D.M.; Savinov, A.P.; Poleschuk, V.F. Evidence for a virus in non-A, non-B hepatitis transmitted via the fecal-oral route. Intervirology 1983, 20, 23–31. [Google Scholar] [CrossRef] [PubMed]
  2. International Committee on Taxonomy of Viruses (ICTV). Family: Hepeviridae. Available online: https://ictv.global/ (accessed on 21 June 2023).
  3. Purdy, M.A.; Drexler, J.F.; Meng, X.J.; Norder, H.; Okamoto, H.; Van der Poel, W.H.M.; Reuter, G.; de Souza, W.M.; Ulrich, R.G.; Smith, D.B. ICTV virus taxonomy profile: Hepeviridae 2022. J. Gen. Virol. 2022, 103, 001778. [Google Scholar] [CrossRef] [PubMed]
  4. Sridhar, S.; Yip, C.C.Y.; Wu, S.; Cai, J.; Zhang, A.J.; Leung, K.H.; Chung, T.W.H.; Chan, J.F.W.; Chan, W.M.; Teng, J.L.L.; et al. Rat hepatitis E virus as cause of persistent hepatitis after liver transplant. Emerg. Infect. Dis. 2018, 24, 2241–2250. [Google Scholar] [CrossRef] [Green Version]
  5. Andonov, A.; Robbins, M.; Borlang, J.; Cao, J.; Hatchette, T.; Stueck, A.; Deschambault, Y.; Murnaghan, K.; Varga, J.; Johnston, L. Rat hepatitis E virus linked to severe acute hepatitis in an immunocompetent patient. J. Infect. Dis. 2019, 220, 951–955. [Google Scholar] [CrossRef]
  6. Sridhar, S.; Yip, C.C.; Wu, S.; Chew, N.F.; Leung, K.H.; Chan, J.F.; Zhao, P.S.; Chan, W.M.; Poon, R.W.; Tsoi, H.W.; et al. Transmission of rat hepatitis E virus infection to humans in Hong Kong: A clinical and epidemiological analysis. Hepatology 2021, 73, 10–22. [Google Scholar] [CrossRef]
  7. Smith, D.B.; Izopet, J.; Nicot, F.; Simmonds, P.; Jameel, S.; Meng, X.J.; Norder, H.; Okamoto, H.; van der Poel, W.H.M.; Reuter, G.; et al. Update: Proposed reference sequences for subtypes of hepatitis E virus (species Orthohepevirus A). J. Gen. Virol. 2020, 101, 692–698. [Google Scholar] [CrossRef] [PubMed]
  8. Prpic, J.; Baymakova, M. Hepatitis E virus (HEV) infection among humans and animals: Epidemiology, clinical characteristics, treatment, and prevention. Pathogens 2023, 12, 931. [Google Scholar] [CrossRef]
  9. Lack, J.B.; Volk, K.; Van Den Bussche, R.A. Hepatitis E virus genotype 3 in wild rats, United States. Emerg. Infect. Dis. 2012, 18, 1268–1273. [Google Scholar] [CrossRef] [PubMed]
  10. Songtanin, B.; Molehin, A.J.; Brittan, K.; Manatsathit, W.; Nugent, K. Hepatitis E virus infections: Epidemiology, genetic diversity, and clinical considerations. Viruses 2023, 15, 1389. [Google Scholar] [CrossRef]
  11. Takahashi, M.; Nishizawa, T.; Nagashima, S.; Jirintai, S.; Kawakami, M.; Sonoda, Y.; Suzuki, T.; Yamamoto, S.; Shigemoto, K.; Ashida, K.; et al. Molecular characterization of a novel hepatitis E virus (HEV) strain obtained from a wild boar in Japan that is highly divergent from the previously recognized HEV strains. Virus Res. 2014, 180, 59–69. [Google Scholar] [CrossRef]
  12. Woo, P.C.; Lau, S.K.; Teng, J.L.; Tsang, A.K.; Joseph, M.; Wong, E.Y.; Tang, Y.; Sivakumar, S.; Xie, J.; Bai, R.; et al. New hepatitis E virus genotype in camels, the Middle East. Emerg. Infect. Dis. 2014, 20, 1044–1048. [Google Scholar] [CrossRef]
  13. Wu, J.; Si, F.; Jiang, C.; Li, T.; Jin, M. Molecular detection of hepatitis E virus in sheep from Southern Xinjiang, China. Virus Genes 2015, 50, 410–417. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Lee, G.H.; Tan, B.H.; Teo, E.C.; Lim, S.G.; Dan, Y.Y.; Wee, A.; Aw, P.P.; Zhu, Y.; Hibberd, M.L.; Tan, C.K.; et al. Chronic infection with camelid hepatitis E virus in a liver transplant recipient who regularly consumes camel meat and milk. Gastroenterology 2016, 150, 355–357.e3. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Huang, F.; Li, Y.; Yu, W.; Jing, S.; Wang, J.; Long, F.; He, Z.; Yang, C.; Bi, Y.; Cao, W.; et al. Excretion of infectious hepatitis E virus into milk in cows imposes high risks of zoonosis. Hepatology 2016, 64, 350–359. [Google Scholar] [CrossRef] [Green Version]
  16. Baymakova, M.; Popov, G.T.; Pepovich, R.; Tsachev, I. Hepatitis E virus infection in Bulgaria: A brief analysis of the situation in the country. Open Access Maced. J. Med. Sci. 2019, 7, 458–460. [Google Scholar] [CrossRef] [Green Version]
  17. Woo, P.C.; Lau, S.K.; Teng, J.L.; Cao, K.Y.; Wernery, U.; Schountz, T.; Chiu, T.H.; Tsang, A.K.; Wong, P.C.; Wong, E.Y.; et al. New hepatitis E virus genotype in Bactrian camels, Xinjiang, China, 2013. Emerg. Infect. Dis. 2016, 22, 2219–2221. [Google Scholar] [CrossRef]
  18. Montalvo Villalba, M.C.; Cruz Martinez, D.; Ahmad, I.; Rodriguez Lay, L.A.; Bello Corredor, M.; Guevara March, C.; Martinez, L.S.; Martinez-Campo, L.S.; Jameel, S. Hepatitis E virus in bottlenose dolphins Tursiops truncatus. Dis. Aquat. Organ. 2017, 123, 13–18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Pavio, N.; Doceul, V.; Bagdassarian, E.; Johne, R. Recent knowledge on hepatitis E virus in Suidae reservoirs and transmission routes to human. Vet. Res. 2017, 48, 78. [Google Scholar] [CrossRef] [Green Version]
  20. Baymakova, M.; Terzieva, K.; Popov, R.; Grancharova, E.; Kundurzhiev, T.; Pepovich, R.; Tsachev, I. Seroprevalence of hepatitis E virus infection among blood donors in Bulgaria. Viruses 2021, 13, 492. [Google Scholar] [CrossRef]
  21. Dremsek, P.; Wenzel, J.J.; Johne, R.; Ziller, M.; Hofmann, J.; Groschup, M.H.; Werdermann, S.; Mohn, U.; Dorn, S.; Motz, M.; et al. Seroprevalence study in forestry workers from Eastern Germany using novel genotype 3- and rat hepatitis E virus-specific immunoglobulin G ELISAs. Med. Microbiol. Immunol. 2012, 201, 189–200. [Google Scholar] [CrossRef]
  22. Rivero-Juarez, A.; Frias, M.; Perez, A.B.; Pineda, J.A.; Reina, G.; Fuentes-Lopez, A.; Freyre-Carrillo, C.; Ramirez-Arellano, E.; Alados, J.C.; Rivero, A.; et al. Orthohepevirus C infection as an emerging cause of acute hepatitis in Spain: First report in Europe. J. Hepatol. 2022, 77, 326–331. [Google Scholar] [CrossRef]
  23. Qian, Z.; Hao, X.; Xia, Y.; Yu, W.; Huang, F. Rat hepatitis E virus is a potential zoonotic pathogen to humans. J. Hepatol. 2022, 77, 868–870. [Google Scholar] [CrossRef] [PubMed]
  24. Caballero-Gomez, J.; Rivero-Juarez, A.; Jurado-Tarifa, E.; Jimenez-Martin, D.; Jimenez-Ruiz, E.; Castro-Scholten, S.; Ulrich, R.G.; Lopez-Lopez, P.; Rivero, A.; Garcia-Bocanegra, I. Serological and molecular survey of hepatitis E virus in cats and dogs in Spain. Transbound. Emerg. Dis. 2022, 69, 240–248. [Google Scholar] [CrossRef]
  25. Di Profio, F.; Sarchese, V.; Palombieri, A.; Fruci, P.; Lanave, G.; Robetto, S.; Martella, V.; Di Martino, B. Current knowledge of hepatitis E virus (HEV) epidemiology in ruminants. Pathogens 2022, 11, 1124. [Google Scholar] [CrossRef]
  26. Pepovich, R.; Baymakova, M.; Pishmisheva, M.; Marutsov, P.; Pekova, L.; Tsachev, I. Current knowledge on hepatitis E virus infection. Vojnosanit. Pregl. 2019, 76, 733–739. [Google Scholar] [CrossRef] [Green Version]
  27. Dziedzinska, R.; Krzyzankova, M.; Bena, M.; Vasickova, P. Evidence of hepatitis E virus in goat and sheep milk. Viruses 2020, 12, 1429. [Google Scholar] [CrossRef] [PubMed]
  28. Arankalle, V.A.; Joshi, M.V.; Kulkarni, A.M.; Gandhe, S.S.; Chobe, L.P.; Rautmare, S.S.; Mishra, A.C.; Padbidri, V.S. Prevalence of anti-hepatitis E virus antibodies in different Indian animal species. J. Viral. Hepat. 2001, 8, 223–227. [Google Scholar] [CrossRef] [PubMed]
  29. Okamoto, H.; Takahashi, M.; Nishizawa, T.; Usui, R.; Kobayashi, E. Presence of antibodies to hepatitis E virus in Japanese pet cats. Infection 2004, 32, 57–58. [Google Scholar] [CrossRef]
  30. Saad, M.D.; Hussein, H.A.; Bashandy, M.M.; Kamel, H.H.; Earhart, K.C.; Fryauff, D.J.; Younan, M.; Mohamed, A.H. Hepatitis E virus infection in work horses in Egypt. Infect. Genet. Evol. 2007, 7, 368–373. [Google Scholar] [CrossRef]
  31. Usmanov, R.K.; Balaian, M.S.; Dvoinikova, O.V.; Alymbaeva, D.B.; Zamiatina, N.A.; Kazachkov, I.A.; Belov, V.I. An experimental infection in lambs by the hepatitis E virus. Vopr. Virusol. 1994, 39, 165–168. (In Russian) [Google Scholar]
  32. Zhang, W.; Shen, Q.; Mou, J.; Gong, G.; Yang, Z.; Cui, L.; Zhu, J.; Ju, G.; Hua, X. Hepatitis E virus infection among domestic animals in Eastern China. Zoonoses Public Health 2008, 55, 291–298. [Google Scholar] [CrossRef] [PubMed]
  33. Tsachev, I.; Baymakova, M.; Dimitrov, K.K.; Gospodinova, K.; Marutsov, P.; Pepovich, R.; Kundurzhiev, T.; Ciccozzi, M.; Dalton, H.R. Serological evidence of hepatitis E virus infection in pigs from Northern Bulgaria. Vet. Ital. 2021, 57, 155–159. [Google Scholar] [CrossRef]
  34. Tsachev, I.; Baymakova, M.; Ciccozzi, M.; Pepovich, R.; Kundurzhiev, T.; Marutsov, P.; Dimitrov, K.K.; Gospodinova, K.; Pishmisheva, M.; Pekova, L. Seroprevalence of hepatitis E virus infection in pigs from Southern Bulgaria. Vector Borne Zoonotic Dis. 2019, 19, 767–772. [Google Scholar] [CrossRef] [PubMed]
  35. Takova, K.; Koynarski, T.; Minkov, I.; Ivanova, Z.; Toneva, V.; Zahmanova, G. Increasing hepatitis E virus seroprevalence in domestic pigs and wild boar in Bulgaria. Animals 2020, 10, 1521. [Google Scholar] [CrossRef]
  36. Tsachev, I.; Baymakova, M.; Marutsov, P.; Gospodinova, K.; Kundurzhiev, T.; Petrov, V.; Pepovich, R. Seroprevalence of hepatitis E virus infection among wild boars in Western Bulgaria. Vector Borne Zoonotic Dis. 2021, 21, 441–445. [Google Scholar] [CrossRef] [PubMed]
  37. Tsachev, I.; Baymakova, M.; Pepovich, R.; Palova, N.; Marutsov, P.; Gospodinova, K.; Kundurzhiev, T.; Ciccozzi, M. High seroprevalence of hepatitis E virus infection among East Balkan swine (Sus scrofa) in Bulgaria: Preliminary results. Pathogens 2020, 9, 911. [Google Scholar] [CrossRef]
  38. Breum, S.O.; Hjulsager, C.K.; de Deus, N.; Segales, J.; Larsen, L.E. Hepatitis E virus is highly prevalent in the Danish pig population. Vet. Microbiol. 2010, 146, 144–149. [Google Scholar] [CrossRef]
  39. Ivanova, A.; Tefanova, V.; Reshetnjak, I.; Kuznetsova, T.; Geller, J.; Lundkvist, A.; Janson, M.; Neare, K.; Velstrom, K.; Jokelainen, P.; et al. Hepatitis E virus in domestic pigs, wild boars, pig farm workers, and hunters in Estonia. Food Environ. Virol. 2015, 7, 403–412. [Google Scholar] [CrossRef]
  40. Lange, H.; Overbo, J.; Borgen, K.; Dudman, S.; Hoddevik, G.; Urdahl, A.M.; Vold, L.; Sjurseth, S.K. Hepatitis E in Norway: Seroprevalence in humans and swine. Epidemiol. Infect. 2017, 145, 181–186. [Google Scholar] [CrossRef]
  41. Salines, M.; Andraud, M.; Rose, N. From the epidemiology of hepatitis E virus (HEV) within the swine reservoir to public health risk mitigation strategies: A comprehensive review. Vet. Res. 2017, 48, 31. [Google Scholar] [CrossRef] [Green Version]
  42. Martinelli, N.; Luppi, A.; Cordioli, P.; Lombardi, G.; Lavazza, A. Prevalence of hepatitis E virus antibodies in pigs in Northern Italy. Infect. Ecol. Epidemiol. 2011, 1, 7331. [Google Scholar] [CrossRef]
  43. Seminati, C.; Mateu, E.; Peralta, B.; de Deus, N.; Martin, M. Distribution of hepatitis E virus infection and its prevalence in pigs on commercial farms in Spain. Vet. J. 2008, 175, 130–132. [Google Scholar] [CrossRef]
  44. Krumova-Valcheva, G.L.; Di Bartolo, I.; Smith, R.P.; Gyurova, E.; Mateva, G.; Milanov, M.; Dimitrova, A.; Burow, E.; Daskalov, H. Detection of HEV RNA using one-step real-time RT-PCR in farrow-to-finish pig farms in Bulgaria. Pathogens 2023, 12, 673. [Google Scholar] [CrossRef] [PubMed]
  45. Jackova, A.; Dudasova, K.; Salamunova, S.; Mandelik, R.; Novotny, J.; Vilcek, S. Identification and genetic diversity of hepatitis E virus in domestic swine from Slovakia. BMC Vet. Res. 2021, 17, 232. [Google Scholar] [CrossRef] [PubMed]
  46. Di Bartolo, I.; Martelli, F.; Inglese, N.; Pourshaban, M.; Caprioli, A.; Ostanello, F.; Ruggeri, F.M. Widespread diffusion of genotype 3 hepatitis E virus among farming swine in Northern Italy. Vet. Microbiol. 2008, 132, 47–55. [Google Scholar] [CrossRef] [Green Version]
  47. Hakze-van der Honing, R.W.; van Coillie, E.; Antonis, A.F.; van der Poel, W.H. First isolation of hepatitis E virus genotype 4 in Europe through swine surveillance in the Netherlands and Belgium. PLoS ONE 2011, 6, e22673. [Google Scholar] [CrossRef]
  48. Jimenez de Oya, N.; de Blas, I.; Blazquez, A.B.; Martin-Acebes, M.A.; Halaihel, N.; Girones, O.; Saiz, J.C.; Escribano-Romero, E. Widespread distribution of hepatitis E virus in Spanish pig herds. BMC Res. Notes 2011, 4, 412. [Google Scholar] [CrossRef] [Green Version]
  49. Forgach, P.; Nowotny, N.; Erdelyi, K.; Boncz, A.; Zentai, J.; Szucs, G.; Reuter, G.; Bakonyi, T. Detection of hepatitis E virus in samples of animal origin collected in Hungary. Vet. Microbiol. 2010, 143, 106–116. [Google Scholar] [CrossRef] [Green Version]
  50. Palombieri, A.; Tsachev, I.; Sarchese, V.; Fruci, P.; Di Profio, F.; Pepovich, R.; Baymakova, M.; Marsilio, F.; Martella, V.; Di Martino, B. A molecular study on hepatitis E virus (HEV) in pigs in Bulgaria. Vet. Sci. 2021, 8, 267. [Google Scholar] [CrossRef] [PubMed]
  51. Bruni, R.; Villano, U.; Equestre, M.; Chionne, P.; Madonna, E.; Trandeva-Bankova, D.; Peleva-Pishmisheva, M.; Tenev, T.; Cella, E.; Ciccozzi, M.; et al. Hepatitis E virus genotypes and subgenotypes causing acute hepatitis, Bulgaria, 2013–2015. PLoS ONE 2018, 13, e0198045. [Google Scholar] [CrossRef]
  52. Norder, H.; Karlsson, M.; Mellgren, A.; Konar, J.; Sandberg, E.; Lasson, A.; Castedal, M.; Magnius, L.; Lagging, M. Diagnostic performance of five assays for anti-hepatitis E virus IgG and IgM in a large cohort study. J. Clin. Microbiol. 2016, 54, 549–555. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Li, Y.; Qu, C.; Spee, B.; Zhang, R.; Penning, L.C.; de Man, R.A.; Peppelenbosch, M.P.; Fieten, H.; Pan, Q. Hepatitis E virus seroprevalence in pets in the Netherlands and the permissiveness of canine liver cells to the infection. Ir. Vet. J. 2020, 73, 6. [Google Scholar] [CrossRef] [Green Version]
  54. McElroy, A.; Hiraide, R.; Bexfield, N.; Jalal, H.; Brownlie, J.; Goodfellow, I.; Caddy, S.L. Detection of hepatitis E virus antibodies in dogs in the United Kingdom. PLoS ONE 2015, 10, e0128703. [Google Scholar] [CrossRef] [PubMed]
  55. Bernardini, A.; Pacini, M.I.; Fonti, N.; Forzan, M.; Marchetti, V.; Mazzei, M. Serological, virological investigation and hepatic injury evaluation for hepatitis E virus in hunting dogs. Pathogens 2022, 11, 1123. [Google Scholar] [CrossRef]
  56. Veronesi, R.; Morach, M.; Hubschke, E.; Bachofen, C.; Stephan, R.; Nuesch-Inderbinen, M. Seroprevalence of hepatitis E virus in dogs in Switzerland. Zoonoses Public Health 2021, 68, 8–11. [Google Scholar] [CrossRef] [PubMed]
  57. Dahnert, L.; Conraths, F.J.; Reimer, N.; Groschup, M.H.; Eiden, M. Molecular and serological surveillance of hepatitis E virus in wild and domestic carnivores in Brandenburg, Germany. Transbound. Emerg. Dis. 2018, 65, 1377–1380. [Google Scholar] [CrossRef]
  58. Peralta, B.; Casas, M.; de Deus, N.; Martin, M.; Ortuno, A.; Perez-Martin, E.; Pina, S.; Mateu, E. Anti-HEV antibodies in domestic animal species and rodents from Spain using a genotype 3-based ELISA. Vet. Microbiol. 2009, 137, 66–73. [Google Scholar] [CrossRef] [Green Version]
  59. Capozza, P.; Martella, V.; Lanave, G.; Beikpour, F.; Di Profio, F.; Palombieri, A.; Sarchese, V.; Marsilio, F.; La Rosa, G.; Suffredini, E.; et al. A surveillance study of hepatitis E virus infection in household cats. Res. Vet. Sci. 2021, 137, 40–43. [Google Scholar] [CrossRef] [PubMed]
  60. Cagirgan, A.A.; Yildirim, Y.; Okulmus, C. The first evidence of zoonotic hepatitis E virus (HEV) exposure in domestic cats in Turkiye. Comp. Immunol. Microbiol. Infect. Dis. 2022, 86, 101820. [Google Scholar] [CrossRef]
  61. Golkocheva-Markova, E.; Ismailova, C.; Kevorkyan, A.; Raycheva, R.; Zhelyazkova, S.; Kotsev, S.; Pishmisheva, M.; Rangelova, V.; Stoyanova, A.; Yoncheva, V.; et al. Age and gender trends in the prevalence of markers for hepatitis E virus exposure in the heterogeneous Bulgarian population. Life 2023, 13, 1345. [Google Scholar] [CrossRef]
  62. Fu, H.; Li, L.; Zhu, Y.; Wang, L.; Geng, J.; Chang, Y.; Xue, C.; Du, G.; Li, Y.; Zhuang, H. Hepatitis E virus infection among animals and humans in Xinjiang, China: Possibility of swine to human transmission of sporadic hepatitis E in an endemic area. Am. J. Trop. Med. Hyg. 2010, 82, 961–966. [Google Scholar] [CrossRef] [PubMed]
  63. Yoon, J.; Park, T.; Sohn, Y.; Lee, S.K.; Park, B.J.; Ahn, H.S.; Go, H.J.; Kim, D.H.; Lee, J.B.; Park, S.Y.; et al. Surveillance of hepatitis E virus in the horse population of Korea: A serological and molecular approach. Infect. Genet. Evol. 2022, 103, 105317. [Google Scholar] [CrossRef] [PubMed]
  64. Prpic, J.; Cerni, S.; Skoric, D.; Keros, T.; Brnic, D.; Cvetnic, Z.; Jemersic, L. Distribution and molecular characterization of hepatitis E virus in domestic animals and wildlife in Croatia. Food Environ. Virol. 2015, 7, 195–205. [Google Scholar] [CrossRef] [PubMed]
  65. Song, Y.J.; Jeong, H.J.; Kim, Y.J.; Lee, S.W.; Lee, J.B.; Park, S.Y.; Song, C.S.; Park, H.M.; Choi, I.S. Analysis of complete genome sequences of swine hepatitis E virus and possible risk factors for transmission of HEV to humans in Korea. J. Med. Virol. 2010, 82, 583–591. [Google Scholar] [CrossRef]
  66. Vitral, C.L.; Pinto, M.A.; Lewis-Ximenez, L.L.; Khudyakov, Y.E.; dos Santos, D.R.; Gaspar, A.M. Serological evidence of hepatitis E virus infection in different animal species from the Southeast of Brazil. Mem. Inst. Oswaldo Cruz 2005, 100, 117–122. [Google Scholar] [CrossRef] [Green Version]
  67. Wang, Y.C.; Zhang, H.Y.; Xia, N.S.; Peng, G.; Lan, H.Y.; Zhuang, H.; Zhu, Y.H.; Li, S.W.; Tian, K.G.; Gu, W.J.; et al. Prevalence, isolation, and partial sequence analysis of hepatitis E virus from domestic animals in China. J. Med. Virol. 2002, 67, 516–521. [Google Scholar] [CrossRef]
  68. Yu, Y.; Sun, J.; Liu, M.; Xia, L.; Zhao, C.; Harrison, T.J.; Wang, Y. Seroepidemiology and genetic characterization of hepatitis E virus in the northeast of China. Infect. Genet. Evol. 2009, 9, 554–561. [Google Scholar] [CrossRef]
  69. Geng, Y.; Wang, C.; Zhao, C.; Yu, X.; Harrison, T.J.; Tian, K.; Wang, Y. Serological prevalence of hepatitis E virus in domestic animals and diversity of genotype 4 hepatitis E virus in China. Vector Borne Zoonotic Dis. 2010, 10, 765–770. [Google Scholar] [CrossRef]
  70. Chang, Y.; Wang, L.; Geng, J.; Zhu, Y.; Fu, H.; Ren, F.; Li, L.; Wang, X.; Zhuang, H. Zoonotic risk of hepatitis E virus (HEV): A study of HEV infection in animals and humans in suburbs of Beijing. Hepatol. Res. 2009, 39, 1153–1158. [Google Scholar] [CrossRef]
  71. Obaidat, M.M.; Roess, A.A. Individual animal and herd level seroprevalence and risk factors of hepatitis E in ruminants in Jordan. Infect. Genet. Evol. 2020, 81, 104276. [Google Scholar] [CrossRef]
  72. Yugo, D.M.; Cossaboom, C.M.; Heffron, C.L.; Huang, Y.W.; Kenney, S.P.; Woolums, A.R.; Hurley, D.J.; Opriessnig, T.; Li, L.; Delwart, E.; et al. Evidence for an unknown agent antigenically related to the hepatitis E virus in dairy cows in the United States. J. Med. Virol. 2019, 91, 677–686. [Google Scholar] [CrossRef] [PubMed]
  73. El-Tras, W.F.; Tayel, A.A.; El-Kady, N.N. Seroprevalence of hepatitis E virus in humans and geographically matched food animals in Egypt. Zoonoses Public Health 2013, 60, 244–251. [Google Scholar] [CrossRef] [PubMed]
  74. Caballero-Gomez, J.; Garcia-Bocanegra, I.; Jimenez-Martin, D.; Cano-Terriza, D.; Risalde, M.A.; Lopez-Lopez, P.; Jimenez-Ruiz, S.; Rivero, A.; Rivero-Juarez, A. Epidemiological survey and risk factors associated with hepatitis E virus in small ruminants in Southern Spain. Zoonoses Public Health 2022, 69, 387–393. [Google Scholar] [CrossRef]
  75. Mesquita, J.R.; Santos-Ferreira, N.; Ferreira, A.S.; Albuquerque, C.; Nobrega, C.; Esteves, F.; Cruz, R.; Vala, H.; Nascimento, M.S.J. Increased risk of hepatitis E virus infection in workers occupationally exposed to sheep. Transbound. Emerg. Dis. 2020; Ahead of Print. [Google Scholar] [CrossRef] [PubMed]
  76. Sarchese, V.; Di Profio, F.; Melegari, I.; Palombieri, A.; Sanchez, S.B.; Arbuatti, A.; Ciuffetelli, M.; Marsilio, F.; Martella, V.; Di Martino, B. Hepatitis E virus in sheep in Italy. Transbound. Emerg. Dis. 2019, 66, 1120–1125. [Google Scholar] [CrossRef]
  77. Palombieri, A.; Robetto, S.; Di Profio, F.; Sarchese, V.; Fruci, P.; Bona, M.C.; Ru, G.; Orusa, R.; Marsilio, F.; Martella, V.; et al. Surveillance study of hepatitis E virus (HEV) in domestic and wild ruminants in Northwestern Italy. Animals 2020, 10, 2351. [Google Scholar] [CrossRef]
  78. Sanford, B.J.; Emerson, S.U.; Purcell, R.H.; Engle, R.E.; Dryman, B.A.; Cecere, T.E.; Buechner-Maxwell, V.; Sponenberg, D.P.; Meng, X.J. Serological evidence for a hepatitis E virus-related agent in goats in the United States. Transbound. Emerg. Dis. 2013, 60, 538–545. [Google Scholar] [CrossRef] [Green Version]
  79. Liang, H.; Chen, J.; Xie, J.; Sun, L.; Ji, F.; He, S.; Zheng, Y.; Liang, C.; Zhang, G.; Su, S.; et al. Hepatitis E virus serosurvey among pet dogs and cats in several developed cities in China. PLoS ONE 2014, 9, e98068. [Google Scholar] [CrossRef]
  80. Wang, L.; Zheng, Y.; Fu, C.; Huang, S.; Hong, M.; Yan, Z.; Jia, K.; Zhou, P.; Li, S. Seroprevalence of hepatitis E virus infection among dogs in several developed cities in the Guangdong province of China. J. Med. Virol. 2016, 88, 1404–1407. [Google Scholar] [CrossRef]
  81. Zeng, M.Y.; Gao, H.; Yan, X.X.; Qu, W.J.; Sun, Y.K.; Fu, G.W.; Yan, Y.L. High hepatitis E virus antibody positive rates in dogs and humans exposed to dogs in the South-West of China. Zoonoses Public Health 2017, 64, 684–688. [Google Scholar] [CrossRef]
Figure 1. The number of all animal species studied by districts (in gray).
Figure 1. The number of all animal species studied by districts (in gray).
Viruses 15 01594 g001
Table 1. Seroprevalence of hepatitis E virus (HEV) infection in different species from Bulgaria.
Table 1. Seroprevalence of hepatitis E virus (HEV) infection in different species from Bulgaria.
SpeciesInvestigated Animals, nHEV-Positive95% CI
NumberPercentLowerUpper
Dog901921.113.230.9
Cat901617.710.527.2
Horse180158.34.713.3
Cattle180147.74.312.6
Sheep902932.222.742.9
Goat902224.415.934.6
Total72011515.913.318.8
Note: CI—confidence interval.
Table 2. Univariate and multivariable analysis showing the association between HEV seropositivity and different variables (sex and age).
Table 2. Univariate and multivariable analysis showing the association between HEV seropositivity and different variables (sex and age).
Animal Species VariableTotalHEV-Positive, n (%)HEV-Negative, n (%)Univariate Logistic RegressionMultivariable Logistic Regression
OR95% CIp-ValueOR95% CIp-Value
DogSexMale447 (15.9)37 (84.1)1.00 1.00
Female4612 (26.0)34 (74.0)1.860.65–5.280.2412.090.71–6.140.177
Age<2 years old203 (15.0)17 (85.0)1.00 1.00
2–6 years old307 (23.3)23 (76.7)1.720.38–7.650.4741.950.43–8.870.385
>6 years old409 (22.5)31 (77.5)1.640.39–6.900.4962.050.46–9.060.339
CatSexMale449 (20.4)35 (79.6)1.00 1.00
Female467 (15.2)39 (84.8)0.690.23–2.070.5170.620.19–1.990.424
Age<2 years old143 (21.4)11 (78.6)1.00 1.00
2–6 years old376 (16.2)31 (83.8)0.710.15–3.330.6640.580.11–2.980.515
>6 years old397 (17.9)32 (82.1)0.800.17–3.650.7760.650.12–3.260.601
HorseSexMale8211 (13.4)71 (86.6)1.00 1.00
Female984 (4.1)94 (95.9)0.270.08–0.890.0330.240.06–0.860.029
Age<2 years old141 (7.1)13 (92.9)1.00 1.00
2–6 years old726 (8.3)66 (91.7)1.180.13–10.650.8820.670.06–6.780.739
>6 years old948 (8.5)86 (91.5)1.200.14–10.470.8630.530.05–5.440.593
Note: OR—odds ratio.
Table 3. Serological evidence of HEV infection in different districts of Bulgaria.
Table 3. Serological evidence of HEV infection in different districts of Bulgaria.
Species by DistrictInvestigated Animals, nHEV-Positive95% CI
NumberPercentLowerUpper
Stara Zagora district
Dog901921.113.230.9
Cat901617.710.527.2
Cattle45613.35.026.8
Pazardzhik district
Horse4449.02.921.6
Sheep451533.319.948.9
Goat451022.211.237.1
Burgas district
Sheep451431.118.246.6
Goat451226.614.641.9
Sliven district
Horse117119.44.816.2
Plovdiv district
Horse1900.0NANA
Cattle4548.82.421.1
Smolyan district
Cattle4548.82.421.1
Kardzhali district
Cattle4500.0NANA
Note: NA—not applicable.
Table 4. Binary logistic regression showing the association between HEV seropositivity and different districts in the country.
Table 4. Binary logistic regression showing the association between HEV seropositivity and different districts in the country.
DistrictInvestigated Animals, nHEV-Positive, n (%)HEV-Negative, n (%)Binary Logistic Regression
OR95% CIp-Value
Kardzhali450 (0.0)45 (100.0)1.00
Plovdiv644 (6.2)60 (93.8)6.760.35–128.930.203
Smolyan454 (8.8)41 (91.2)9.850.51–188.890.129
Sliven11711 (9.4)106 (90.6)9.820.56–170.330.116
Stara Zagora22541 (18.2)184 (81.8)20.461.23–339.070.035
Pazardzhik13429 (21.6)105 (78.4)25.441.52–425.520.024
Burgas9026 (28.8)64 (71.2)14.660.87–245.220.062
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Tsachev, I.; Gospodinova, K.; Pepovich, R.; Takova, K.; Kundurzhiev, T.; Zahmanova, G.; Kaneva, K.; Baymakova, M. First Insight into the Seroepidemiology of Hepatitis E Virus (HEV) in Dogs, Cats, Horses, Cattle, Sheep, and Goats from Bulgaria. Viruses 2023, 15, 1594. https://0-doi-org.brum.beds.ac.uk/10.3390/v15071594

AMA Style

Tsachev I, Gospodinova K, Pepovich R, Takova K, Kundurzhiev T, Zahmanova G, Kaneva K, Baymakova M. First Insight into the Seroepidemiology of Hepatitis E Virus (HEV) in Dogs, Cats, Horses, Cattle, Sheep, and Goats from Bulgaria. Viruses. 2023; 15(7):1594. https://0-doi-org.brum.beds.ac.uk/10.3390/v15071594

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Tsachev, Ilia, Krasimira Gospodinova, Roman Pepovich, Katerina Takova, Todor Kundurzhiev, Gergana Zahmanova, Kristin Kaneva, and Magdalena Baymakova. 2023. "First Insight into the Seroepidemiology of Hepatitis E Virus (HEV) in Dogs, Cats, Horses, Cattle, Sheep, and Goats from Bulgaria" Viruses 15, no. 7: 1594. https://0-doi-org.brum.beds.ac.uk/10.3390/v15071594

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