Hostname: page-component-7c8c6479df-995ml Total loading time: 0 Render date: 2024-03-28T16:50:08.867Z Has data issue: false hasContentIssue false

A brief review of foodborne zoonoses in China

Published online by Cambridge University Press:  23 May 2011

D. SHAO
Affiliation:
Animal Food-borne Safety Research Center, Chinese Academy of Agricultural Science, Shanghai, PR China
Z. SHI
Affiliation:
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, Shanghai, PR China
J. WEI
Affiliation:
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, Shanghai, PR China
Z. MA*
Affiliation:
Animal Food-borne Safety Research Center, Chinese Academy of Agricultural Science, Shanghai, PR China
*
*Author for correspondence: Dr Z. Ma, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Science, No. 518, Ziyue Road, Shanghai, 200241, PR China. (Email: zhiyongma@shvri.ac.cn)
Rights & Permissions [Opens in a new window]

Summary

Foodborne zoonoses have a major impact on public health in China. Its booming economy and rapid socioeconomic changes have affected food production, food supplies and food consumption habits, resulting in an increase in the number of outbreaks of foodborne zoonoses. Both emerging and re-emerging foodborne zoonoses have attracted increasing national and international attention in recent years. This paper briefly reviews the main foodborne zoonoses that have had a major impact on public health over the last 20 years in China. The major causative microorganisms, including foodborne bacteria, parasites and viruses, are discussed. The prevention and control of foodborne zoonoses are difficult challenges in China. The information provided here may aid the development of effective prevention and control strategies for foodborne zoonoses.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2011

INTRODUCTION

Foodborne zoonoses are defined as infections and diseases that are transmissible between animals and humans via foodstuffs [1]. They are caused by foodborne bacteria, parasites, viruses and prions, and have a major impact on global public health. In industrialized countries, up to 10% of the human population may annually suffer from foodborne zoonoses [Reference Fosse, Seegers and Magras2]. In China, the number of outbreaks of foodborne disease and the number of individuals affected has increased in the last two decades. During 1994–2005, 12 687 incidents of foodborne disease were reported to the Chinese authorities, in which 289 380 individuals were affected and 2297 individuals died [Reference Wang3]. Of the outbreaks for which the aetiology was determined, 40–50% were caused by predominantly zoonotic microorganisms [Reference Liu4, Reference Chen5]. This paper briefly reviews the main foodborne zoonoses that have had a major impact on public health over the last 20 years in China. The causative microorganisms include foodborne bacteria, parasites and viruses.

FOODBORNE BACTERIAL ZOONOSES

In China, foodborne bacterial diseases accounted for more than 28·25% of all cases of foodborne disease during 1994–2005, and more than 42·75% of cases annually [Reference Wang3]. Most bacteria that play a role in foodborne diseases have a zoonotic origin, with reservoirs in food animals. Salmonella and Campylobacter account for over 90% of all reported cases of bacteria-related food disease worldwide [Reference Thorns6]; however, in China, cases caused by Campylobacter are rare, although the rate of detection of Campylobacter is approximately 30% in fowl meat and milk in China [Reference Yang7]. Of the 57 612 cases reported in China during 1994–2005, Salmonella was the most frequently identified agent, accounting for 22·16% of illnesses, followed by Vibrio parahaemolyticus (18·73%), Proteus (11·56%), a mixture of bacteria (11·2%) and Bacillus cereus (9·97%) [Reference Wang3]. In this section, we review some of the most significant foodborne bacterial zoonoses in China, some of which have re-emerged.

Escherichia coli O157:H7 infection

E. coli O157:H7 is the main serotype of enterohaemorrhagic E. coli and a cause of foodborne zoonoses. Infection with E. coli O157:H7 often leads to bloody diarrhoea, haemorrhagic enteritis, haemolytic uraemic syndrome and acute kidney failure, especially in children. E. coli O157:H7 became well known to the public because of two outbreaks, which resulted in four fatalities in 1993 in the USA and over 10 fatalities in 1996 in Japan [Reference Fukushima, Hashizume and Morita8].

E. coli O157:H7 was first reported in 1990 in China, where five strains were isolated from 486 stool specimens collected during 1986–1988 from patients with diarrhoea in Jiangsu province [Reference Xu9]. An epidemiological survey revealed that the proportion of haemorrhagic colitis caused by E. coli O157:H7 was 0·98–5·89% in Xuzhou in Jiangsu province in June 2000, and in 27 isolates of E. coli O157:H7, 13 strains were identified as being Shiga toxin positive [Reference Li10]. In addition to infecting humans, E. coli O157:H7 was also detected in food animals. The overall detection rate of E. coli O157:H7 by an immunomagnetic separation technique in 1767 faecal samples collected from pigs, chickens, sheep and cattle in Jiangsu province in 1999 was 9·62%, and 56·47% of these strains carried the SLT2, eaeA and Hly toxin-encoding genes [Reference Ni11]. E. coli O157:H7 was not the dominant serotype of E. coli in food animals in China. A survey of the serotype distribution of E. coli in food animals in Hefei area of Anhui province indicated that E. coli O157:H7 was not detected by a slide agglutination test in 46 strains of E. coli isolated from diseased pigs and chickens, where serotype O127:K63 was most common, accounting for 33·33% (13/39) of identified isolates, followed by O142:K86 (15·38%), O125:K70 (12·82%), O111:K58 (10·26%) and O114:K90 (7·69%) [Reference Wang12]. The Chinese government has maintained a national network for the detection of E. coli O157:H7 since 1997, which involves over 30 public health laboratories in several provinces and municipalities [Reference Xu, Cheng and Jing13].

Salmonellosis (Salmonella infection)

Salmonellosis is a foodborne zoonosis caused by Salmonella, which infects humans and some warm-blooded animals, causing symptoms ranging from mild abdominal discomfort, to dehydration and vomiting, to death [Reference Benenson14]. Many Salmonella infections of humans are due to ingestion of contaminated food of animal origin. More than 2500 serotypes of Salmonella have been identified to date, with over 200 serotypes being detected in China [Reference Foley and Lynne15, Reference Zhang and Gu16]. China has submitted 268 strains to the WHO Global Salm-Surv Country Databank, a valuable resource for international Salmonella surveillance [Reference Galanis17]. Salmonella contamination in food of animal origin is relatively common in certain provinces of China. About 54% (276/515) of chicken, 31% (28/91) of pork, 17% (13/78) of beef and 20% (16/80) of lamb samples collected from markets in Shaanxi province during 2007–2008 were found to be positive for Salmonella, serotype S. Enteritidis was most common, accounting for 31·5% of the identified isolates, followed by S. Typhimurium (13·4%), S. Shubra (10·0%), S. Indiana (9·7%), S. Derby (9·5%) and S. Djugu (7·0%) [Reference Yang, Qu and Zhang18]. The contamination of food with Salmonella causes occasional outbreaks of S. Enteritidis. Liu et al. reported a massive outbreak of S. Enteritidis linked to Salmonella-contaminated eggs, where 197 of about 2000 workers became ill after eating cakes that had been in contact with raw eggs contaminated with Salmonella [Reference Liu19].

Vibrio parahaemolyticus infection

V. parahaemolyticus, a common bacterium in marine and estuarine environments, infects humans and is commonly associated with the consumption of raw or contaminated seafood, particularly molluscs, leading to clinical symptoms of acute gastroenteritis to septicaemia. V. parahaemolyticus accounted for a significant number of outbreaks (19·5%) and cases (18·73%) of foodborne illnesses during 1994–2005 in China [Reference Wang3]. The prevalence in suspected food samples of food poisoning outbreaks in Jiangsu province was 35·9%, while 24·9% of faecal samples from patients and outpatients with food poisoning were positive for V. parahaemolyticus [Reference Chao20]. An epidemiological survey indicated that 47·2% of aquatic products collected from retail markets and restaurants in Jiangsu province were positive for V. parahaemolyticus, with 8·5% and 1·5% of strains carrying the tdh and trh virulence genes, respectively [Reference Chao20]. Yang et al. reported that the isolation rates of V. parahaemolyticus from fresh, frozen/iced, dried, and salted seafood samples were 33·4%, 14·9%, 4·6%, and 4·3%, respectively, in Jiangsu province and Shanghai city [Reference Yang21].

Campylobacteriosis (Campylobacter infection)

Campylobacteriosis is an infection caused by the Campylobacter bacterium, most commonly C. jejuni, which has been recognized as an important zoonotic pathogen since the 1980s throughout the world. C. jejuni is found in the intestines of many wild and domestic animals. Human infection can be acquired via consumption of contaminated food and meats, especially chicken. In China, C. jejuni is most frequently detected in poultry with an average isolation rate of up to 18·61% and a flock contamination rate of 86·67%. The average incidence of C. jejuni in cattle, milk cows, heifers, and diarrhoea patients was 7·77%, 5·02%, 8·70%, and 4·84%, respectively, in Jiangsu province [Reference Huang22]. Yang et al. reported that 30·6% of chicken meat, 27·3% of milk, and 13·6% of water samples tested positive by a real-time polymerase chain reaction (PCR) assay for C. jejuni [Reference Yang7]. C. jejuni is associated with the development of Guillain–Barré syndrome (GBS) in humans. An outbreak with 36 cases of GBS was reported in Jilin province in 2007, serological and molecular analysis indicated that this outbreak was preceded by C. jejuni infection [Reference Zhang23].

In addition to C. jejuni, C. coli is also a causative agent of campylobacteriosis. Sun et al. reported that the prevalence of Campylobacter in chicken, duck, rabbit meat, pork, and beef collected from retail markets in Shenyang city were 94%, 96%, 97%, 31%, and 35%, respectively, and in 525 isolates of Campylobacter, 217 (41%) strains were identified as being C. coli by PCR analysis [Reference Sun24]. C. coli has been isolated from broiler chickens and pigs, with an isolation rate of 6·9% and 16·6%, respectively, in Shandong province [Reference Chen25, Reference Qin26].

Yersiniosis (Yersinia enterocolitica infection)

Yersiniosis is a zoonotic disease caused by Y. enterocolitica, a genus of Gram-negative rod-shaped bacteria of the family Enterobacteriaceae. Acute Y. enterocolitica infection causes diarrhoea, abdominal pain, fever and a number of other symptoms. Y. enterocolitica has a broad animal reservoir, with pigs being the most common source of infection for humans. Y. enterocolitica infection can be acquired by eating contaminated food, especially raw or undercooked pork products, and by drinking contaminated unpasteurized milk or untreated water.

In China, two outbreaks of Y. enterocolitica causing more than 500 infections were reported as early as the 1980s. Y. enterocolitica is distributed in a diverse range of animals in China, with strains being isolated from more than 10 kinds of animals including pigs, cattle, goats, dogs, and mice [Reference Wang27]. An epidemiological survey showed that 416/1295 (32%) strains isolated from diarrhoea patients, livestock, poultry, wild animals, insect vectors, food and the environment, were pathogenic. The main serotypes of Chinese isolates are O:3 and O:9, which are distributed mostly in the cold northern areas, whereas some serotype O:3 strains are detected in the warm southern areas [Reference Wang28].

Listeriosis (Listeria monocytogenes infection)

Listeriosis is a potentially serious infection caused by L. monocytogenes, a Gram-positive motile bacterium. Animals can carry L. monocytogenes and contaminate foods of animal origin. Human infection can be acquired via ingestion of food products contaminated with L. monocytogenes. An epidemiological survey indicated that the prevalence of L. monocytogenes in raw meat, fish, and poultry products collected from retail markets in Yangzhou city was 4·83%, 2·00%, and 1·55%, respectively [Reference Zhou and Jiao29]. Yan et al. reported that contamination by L. monocytogenes was detected in 4·13% (90/2177) of food samples (raw meats, cooked meats, rice products, bean products, seafood, vegetables) collected from nine cities in northern China during 2005–2007, with an average isolation rate of 6·28% (46/733) in raw meat products. The isolates of L. monocytogenes belonged to five serotypes (1/2a, 1/2b, 1/2c, 4b, 3a), with 1/2a being the dominant serotype (48·88%) [Reference Yan30].

Streptococcus (Str.) suis infection

Str. suis is a peanut-shaped, Gram-positive bacterium that is carried by pigs and generally does not cause illness, but can occasionally cause disease. Thirty-five serotypes have been identified and serotype 2 is the dominant pathogenic serotype in swine and humans. Infection of humans and pigs with Str. suis causes meningitis, septicaemia, endocarditis, arthritis and septic shock. Human infection can be acquired through exposure to Str. suis-contaminated pigs, pork or pork-derived products. The number of Str. suis infections in humans has increased significantly in recent years in South East Asia. Two massive outbreaks occurred in 1998 and 2005 in China. In the 2005 outbreak, a total of 215 cases of human Str. suis infection, 66 of which were laboratory confirmed, were reported in Sichuan province. All infections occurred in backyard farmers who were directly exposed to infection during the butchering process of pigs that had died of unknown causes. Sixty-one (28%) of the farmers exhibited streptococcal toxic shock syndrome and 38 (62%) died [Reference Yu31]. Analysis of the serotype of 421 strains of Str. suis that were isolated from clinically healthy sows from 10 provinces of China showed that the most common serotype was type 9 (26·6%), followed by type 3 (23·5%), type 7 (15·7%) and type 2 (7·4%) [Reference Zhang32].

FOODBORNE PARASITIC ZOONOSES

Foodborne parasitic zoonoses that are caused by helminths and (or) protozoans through the consumption of infected or contaminated meat and/or fish represent a significant health problem in China, where about 150 million people suffer from foodborne parasitic zoonoses and more people are at risk [Reference Zhou33]. The second national survey on the current status of important parasitic diseases in the human population, which was carried out from June 2001 to 2004, indicated that the total number of people suffering from clonorchiasis, trichinellosis, paragonimiasis, and angiostrongyliasis had increased compared to the first national survey carried out between 1988 and 1992. Some of these conditions cause significant public health problems [Reference Zhou33].

Clonorchiasis [Clonorchis (Cl.) sinensis infection]

Clonorchiasis is one of the major parasitic zoonosis in China, and is caused by Cl. sinensis. Human and animal reservoir hosts (dogs, pigs, cats, rats) acquire the infection via the ingestion of raw fish or shrimps containing infectious metacercariae of Cl. sinensis. It is estimated that 35 million people are infected globally, of which 15 million reside in China, with the largest incidence (5·5 million) in Guangdong province [Reference Lun34]. An epidemiological survey of the prevalence of Cl. sinensis in human populations in Hengxian county of Guangxi province indicated that 31·6% (491/1552) of faecal samples examined by the Kato-Katz thick smear technique were positive for Cl. sinensis, showing an increase from 18% to 31·6% in the past decade [Reference Yu35]. In the Shenzhen area of Guangdong province, 4·75% of people and 1·15% of snails examined were positive for Cl. sinensis, and the average infection rate in 15 species of freshwater fish was 16·97% [Reference Zhang36]. The increased prevalence of clonorchiasis in humans was proposed to be related to factors such as unhygienic practices, poor knowledge, inappropriate farming/fishery practices and eating raw fish [Reference Zhang36].

Trichinellosis (Trichinella infection)

Trichinellosis is caused mainly by the consumption of raw or undercooked pork or wild game that is infected with the larvae of a species of the Trichinella genus. Pork infected with T. spiralis is the main source of human infection, while dog meat contaminated with T. native also contributes to infections in China [Reference Liu37]. Swine trichinellosis has been reported in 26 provinces of China, with a prevalence rate varying from 0·0001% to 34·2%. Transmission to pigs by the consumption of contaminated garbage is the main factor in the epidemiology of swine trichinellosis. The rate of prevalence of T. spiralis in pigs varied from 1·98% to 15·06% in certain provinces and serves as an important reservoir in the domestic cycle of trichinellosis [Reference Wang and Cui38]. Trichinella larvae were detected in 0·29–5·6% of pork, 1·4% (3/215) of mutton and 2·1% (1/47) of beef sold at markets in certain provinces [Reference Wang, Cui and Shen39]. In addition to pork, dog meat has become an important source of Trichinella infection for humans. The average prevalence of the infection in dogs was 16·2%, ranging from 1·2% to 44·8%, with the highest prevalence located in northeast China. An outbreak caused by consumption of contaminated dog meat has been reported [Reference Cui and Wang40]. Trichinella infection has also been recorded in wildlife including wild rats, foxes, bears, wild boar, weasels, raccoon dogs, muntjak and bamboo rats [Reference Wang, Cui and Shen39].

Cysticercosis and taeniasis (Taenia infection)

Cysticercosis and taeniasis are, respectively, parasitic infections with the larval and adult stages of taeniid tapeworm. Human infection can be acquired via eating inadequately cooked pork that contains the larval stage of Taenia (Ta.) solium. Ta. solium is cyclically transmitted between humans and pigs, with pigs being the natural intermediate host. In China, cysticercosis was prevalent in northeastern areas several decades ago. Despite efforts to reduce transmission of cysticercosis over the last 30 years, it is still emerging as a serious public health problem in certain areas of China [Reference Li41]. Ta. solium infection is particularly prevalent in rural areas of 29 provinces, especially in minority populations, such as the Yi, Bai and Miao groups, where raw or undercooked pork is consumed, and scavenging pigs have access to human faeces [Reference Li41]. A survey of porcine cysticercosis performed via post-mortem inspection in nine districts of Guizhou province indicated that 328/4292 (7·6%) pigs harboured Ta. solium cysts and that 357/2599 (13·7%) samples collected from pigs were serologically positive for Ta. solium [Reference Qian, Peng and Zeng42]. In Liangshan prefecture of Sichuan province, porcine cysticercosis was highly endemic, with the prevalence in pigs ranging from 3·3% to 10·4%, with the highest rates being 25–30% [Reference Zhang43].

In addition to Ta. solium, Ta. saginata is also a causative agent for human Taenia infection. Human infection can be acquired via eating inadequately cooked beef infected with the larval form (Cysticercus bovis) of Ta. saginata. Ta. saginata infection is endemic in western China [Reference Bao and Mou44]. A survey of the prevalence of taeniasis/cysticercosis in Tibetan populations in Yajiang county of Sichuan province, where undercooked beef is consumed habitually, indicated that Ta. saginata was the dominant species causing human infection, where 30·5% of individuals reported proglottid expulsion (anamnesis) and 18/21 proglottids were identified as Ta. saginata by PCR [Reference Li45]. Shen et al. reported that Cysticercus bovis was detected in slaughterhouse cattle with prevalence rates ranging from 0% to 2·56% in Yili prefecture of Xinjiang uyghur autonomous region during 1991–2006 [Reference Shen, Hu and Zhang46].

Angiostrongyliasis (Angiostrongylus cantonensis infection)

A. cantonensis is a nematode parasite that causes angiostrongyliasis in humans. Snails and slugs are intermediate hosts. Of 32 wild molluscs screened for A. cantonensis, 22 (68·8%) were found to harbour the parasite in China. The highest rate and intensity of infections were recorded in giant African land snails (Achatina fulica), followed by slugs (Vaginulus spp.) and Pomacea canaliculata. Terrestrial snails and slugs showed higher rates and intensities of infection than freshwater molluscs [Reference Lv47]. Humans are incidental hosts of A. cantonensis. Human infection can be acquired mostly by consumption of raw or undercooked snails or slugs that contain the third-stage larvae of A. cantonensis. The first case of human angiostrongyliasis in China was diagnosed in 1984, and the number of cases has sharply increased during the past decade [Reference Lv47]. A large outbreak of A. cantonensis infection occurred in Beijing in 2006, where 160 people who had a history of eating raw freshwater snails became ill, 100 of whom were hospitalized. Of these patients, 81 were diagnosed with angiostrongyliasis [Reference Wang48].

FOODBORNE VIRAL ZOONOSES

In contrast to foodborne bacterial and parasitic zoonoses, only a few foodborne viral zoonoses have been identified. Although many different types of viruses, such as coronavirus and rotavirus, are present in the intestinal tracts of animals and are shed into the environment via faeces, awareness of the significance of these viruses with respect to food safety is generally poor. Severe acute respiratory syndrome (SARS) coronavirus spread to humans through the preparation and consumption of food animals, and the consumption of duck blood resulted in the infection of humans with H5N1 avian influenza virus. These cases have raised the question of whether foodborne introduction could be one of the routes by which these new viral diseases enter the human population [Reference Newell49].

Hepatitis E, caused by hepatitis E virus (HEV), is considered a foodborne viral zoonosis. Pigs, boars and deer have been identified as reservoirs, and their flesh and entrails as vehicles of HEV transmission to humans [Reference Teo50]. Hepatitis E infection of humans was first recognized after a large epidemic of non-A, non-B hepatitis in the Xinjiang region of China in 1986 [Reference Zhuang51]. Serological surveillance performed by an enzyme-linked immunosorbent assay (ELISA) to monitor the prevalence of HEV antibodies in animals revealed that 82·5% of sows, 55·7% of slaughterhouse pigs, 24% of goats, 16·3% of horses, 17·8% of pet dogs, 6% of cows, 12·8% of ducks, 4·4% of pigeons and 1·9% of chickens were positive for these antibodies in eastern China [Reference Zhang52]. Genotypes 3 and 4 of HEV are the most common in pigs in China. Swine and human HEV strains show extremely close genetic relatedness, which supports the hypothesis that hepatitis E is zoonotic in China [Reference Bihl and Negro53].

Hepatitis A is also considered a foodborne viral zoonosis, which is caused by hepatitis A virus (HAV), a faecal–oral pathogen. The transmission between individuals is associated with HAV-contaminated food and water. Shellfish contaminated with HAV is particularly notorious as a vehicle for the transmission of HAV. A major outbreak of hepatitis A, associated with consumption of HAV-contaminated raw clams, occurred in Shanghai city in 1988, in which over 300 000 cases were reported, 47 (0·015%) of which were fatal [Reference Cooksley54]. A total of 136 field oyster samples collected from seafood markets in Guangdong province in 2007 were screened by RT–PCR, seven (5·1%) of which were positive for HAV [Reference Wang55]. A survey of the contamination of HAV in aquatic products indicated that 13·83% of samples collected from aquatic product markets in Shanghai during 2002–2005 tested positive by an antibody capture RT–PCR for HAV [Reference Zhu56].

CONCLUSION

Since the transition to a market economy, the booming economy and rapid socioeconomic changes in China have affected food production, food supplies and food consumption habits. For example, the populations of livestock have increased exponentially in the last two decades. More Chinese have become used to eating raw or lightly cooked food and to demanding exotic foods, such as Japanese sashimi (fresh raw seafood). These changes have resulted in an increase in the number of outbreaks of foodborne zoonoses. However, the burden of disease caused by foodborne zoonotic pathogens remains largely unknown in China.

Foodborne zoonotic pathogens have developed efficient and effective strategies to exploit food as a vehicle for transmission from animals to humans. In addition, previously unknown foodborne zoonotic pathogens are constantly emerging. Therefore, the effective prevention and control of foodborne zoonoses presents a significant challenge in China, a country with more than 1·3 billion people of 56 nationalities with diverse food cultures, and millions of pigs and billions of poultry raised under a range of sanitary conditions. In the fight against foodborne zoonoses, efficient surveillance systems, and risk assessment and management systems should be established. Moreover, constructive dialogue and collaboration between public health workers, veterinarians and food-safety experts is essential to develop effective prevention and control strategies.

DECLARATION OF INTEREST

None.

References

REFERENCES

2.Fosse, J, Seegers, H, Magras, C. Foodborne zoonoses due to meat: a quantitative approach for a comparative risk assessment applied to pig slaughtering in Europe. Veterinary Research 2008; 39: 1.CrossRefGoogle ScholarPubMed
3.Wang, S, et al. Analysis of bacterial foodborne disease outbreaks in China between 1994 and 2005. FEMS Immunology and Medical Microbiology 2007; 51: 8183.CrossRefGoogle Scholar
4.Liu, XM, et al. Foodborne diseases occurred in 2003 – report of the National Foodborne Diseases Surveillance System, China. Journal of Hygiene Research 2006; 35: 201204.Google ScholarPubMed
5.Chen, Y, et al. Foodborne disease outbreaks in 2006 report of the National Foodborne Disease Surveillance Network, China. Journal of Hygiene Research 2010; 39: 331334.Google Scholar
6.Thorns, CJ. Bacterial food-borne zoonoses. International Office of Epizootics 2000; 19: 226239.Google ScholarPubMed
7.Yang, C, et al. Application of real-time PCR for quantitative detection of Campylobacter jejuni in poultry, milk and environmental water. FEMS Immunology and Medical Microbiology 2003; 38: 265271.CrossRefGoogle ScholarPubMed
8.Fukushima, H, Hashizume, T, Morita, Y. Clinical experiences in Sakai City Hospital during the massive outbreak of enterohemorrhagic Escherichia coli O157 infections in Sakai City, 1996. Pediatrics International 1999; 41: 213217.CrossRefGoogle ScholarPubMed
9.Xu, JG, et al. Isolation and characterization of Escherichia coli O157:H7 strains in China. Current Microbiology 1990; 20: 299303.CrossRefGoogle Scholar
10.Li, HW, et al. Study on diarrhea disease caused by enterohemorrhagic Escherichia coli O157:H7 in Xuzhou city, Jiangsu province in 2000. Chinese Journal of Epidemiology 2002; 23: 119122.Google Scholar
11.Ni, DX, et al. Surveillance of Escherichia coli O157:H7 among animals in Jiangsu province in 1999. Chinese Journal of Epidemiology 2002; 23: 102104.Google ScholarPubMed
12.Wang, PY, et al. Serotype distribution and drug resistance analysis of Escherichia coli isolated from different animal species in Hefei area. Chinese Journal of Microecology 2009; 21: 2022.Google Scholar
13.Xu, JG, Cheng, BK, Jing, HQ. Escherichia Coli O157:H7 and Shiga-like-toxinproducing Escherichia Coli in China. World Journal of Gastroenterology 1999; 5: 191194.CrossRefGoogle ScholarPubMed
14.Benenson, AS. Control of Communicable Diseases in Man. Washington, D.C.: American Public Health Association, 1990, pp. 532.Google Scholar
15.Foley, SL, Lynne, AM. Food animal-associated Salmonella challenges: pathogenicity and antimicrobial resistance. Journal of Animal Science 2008; 86: E173187.CrossRefGoogle ScholarPubMed
16.Zhang, HZ, Gu, QW. Classification and nomenclature of Salmonella and distribution of its serotypes in China. Progress in Microbiology and Immunology 2002; 30: 7476.Google Scholar
17.Galanis, E, et al. Web-based surveillance and global Salmonella distribution, 2000–2002. Emerging Infectious Diseases 2006; 12: 381388.CrossRefGoogle ScholarPubMed
18.Yang, B, Qu, D, Zhang, X. Prevalence and characterization of Salmonella serovars in retail meats of marketplace in Shaanxi, China. International Journal of Food Microbiology 2010; 141: 6372.CrossRefGoogle ScholarPubMed
19.Liu, LG, et al. Salmonellosis outbreak among factory workers – Huizhou, Guangdong Province, China, July 2004. Morbidity and Mortality Weekly Report 2006; 55 (Suppl. 1): 3538.Google ScholarPubMed
20.Chao, GX, et al. Distribution, prevalence, molecular typing, and virulence of Vibrio parahaemolyticus isolated from different sources in coastal province Jiangsu, China. Food Control 2009; 20: 907912.CrossRefGoogle Scholar
21.Yang, ZQ, et al. Isolation and molecular characterization of Vibrio parahaemolyticus from fresh, low-temperature preserved, dried, and salted seafood products in two coastal areas of eastern China. International Journal of Food Microbiology 2008; 125: 279285.CrossRefGoogle ScholarPubMed
22.Huang, JL, et al. Epidemiological surveillance of Campylobacter jejuni in chicken, dairy cattle and diarrhoea patients. Epidemiology and Infection 2009; 137: 11111120.CrossRefGoogle ScholarPubMed
23.Zhang, M, et al. Association study between an outbreak of Guillain-Barre syndrome in Jilin, China, and preceding Campylobacter jejuni infection. Foodborne Pathogens and Disease 2010; 7: 913919.CrossRefGoogle ScholarPubMed
24.Sun, Y, et al. Investigation on contamination by Campylobacter of retail raw meat in Shenyang. Chinese Journal of Public Health 2005; 21: 985987.Google Scholar
25.Chen, X, et al. Prevalence and antimicrobial resistance of Campylobacter isolates in broilers from China. Veterinary Microbiology 2010; 144: 133139.CrossRefGoogle ScholarPubMed
26.Qin, SS, et al. Antimicrobial resistance in Campylobacter coli isolated from pigs in two provinces of China. International Journal of Food Microbiology 2011; 146: 9498.CrossRefGoogle ScholarPubMed
27.Wang, X, et al. Pathogenic strains of Yersinia enterocolitica isolated from domestic dogs (Canis familiaris) belonging to farmers are of the same subtype as pathogenic Y. enterocolitica strains isolated from humans and may be a source of human infection in Jiangsu Province, China. Journal of Clinical Microbiology 2010; 48: 16041610.CrossRefGoogle ScholarPubMed
28.Wang, X, et al. Distribution of pathogenic Yersinia enterocolitica in China. European Journal of Clinical Microbiology & Infectious Diseases 2009; 28: 12371244.CrossRefGoogle ScholarPubMed
29.Zhou, X, Jiao, X. Prevalence and lineages of Listeria monocytogenes in Chinese food products. Letters in Applied Microbiology 2006; 43: 554559.CrossRefGoogle ScholarPubMed
30.Yan, H, et al. Prevalence and characterization of antimicrobial resistance of foodborne Listeria monocytogenes isolates in Hebei province of Northern China, 2005–2007. International Journal of Food Microbiology 2010; 144: 310316.CrossRefGoogle ScholarPubMed
31.Yu, H, et al. Human Streptococcus suis outbreak, Sichuan, China. Emerging Infectious Diseases 2006; 12: 914920.CrossRefGoogle ScholarPubMed
32.Zhang, P, et al. Distributions of pathogenic capsular types and in vitro antimicrobial susceptibility of different serotypes of Streptococcus suis isolated from clinically healthy sows from 10 provinces in China. Chinese Journal of Epidemiology 2009; 30: 235238.Google ScholarPubMed
33.Zhou, P, et al. Food-borne parasitic zoonoses in China: perspective for control. Trends in Parasitology 2008; 24: 190196.CrossRefGoogle Scholar
34.Lun, ZR, et al. Clonorchiasis: a key foodborne zoonosis in China. Lancet Infectious Diseases 2005; 5: 3141.CrossRefGoogle ScholarPubMed
35.Yu, SH, et al. Epidemiological investigation on Clonorchis sinensis in human population in an area of South China. Japanese Journal of Infectious Diseases 2003; 56: 168171.Google Scholar
36.Zhang, R, et al. Epidemiological study on Clonorchis sinensis infection in Shenzhen area of Zhujiang delta in China. Parasitology Research 2007; 101: 179183.CrossRefGoogle ScholarPubMed
37.Liu, MY. Trichinellosis in China and the updates on research advances. Meat Hygiene 2005; 6: 1416.Google Scholar
38.Wang, ZQ, Cui, J. Epidemiology of swine trichinellosis in China. Parasite 2001; 8: S6770.CrossRefGoogle ScholarPubMed
39.Wang, ZQ, Cui, J, Shen, LJ. The epidemiology of animal trichinellosis in China. Veterinary Journal 2007; 173: 391398.CrossRefGoogle ScholarPubMed
40.Cui, J, Wang, ZQ. Outbreaks of human trichinellosis caused by consumption of dog meat in China. Parasite 2001; 8: S7477.CrossRefGoogle ScholarPubMed
41.Li, TY, et al. Taeniasis/cysticercosis in China. Southeast Asian Journal of Tropical Medicine and Public Health 2007; 38: 131139.Google Scholar
42.Qian, DX, Peng, YH, Zeng, H. Epidemiological study on porcine cysticercosis in Guizhou Province. Chinese Journal of Veterinary Parasitology 1998; 6: 2930.Google Scholar
43.Zhang, C, et al. Review of cysticercosis in pigs in Liangshan Prefecture, Sichuan Province, China. Sichuan Animal Husbandry & Veterinary Sciences 2003; 30: 2425.Google Scholar
44.Bao, HE, Mou, R. Research progress on molecular identification and biologic behavior of Taenia saginata in Western China. Chinese Journal of Parasitology and Parasitic Diseases 2009; 27: 520526.Google ScholarPubMed
45.Li, T, et al. Taeniasis/cysticercosis in a Tibetan population in Sichuan Province, China. Acta Tropica 2006; 100: 223231.CrossRefGoogle Scholar
46.Shen, T, Hu, ZJ, Zhang, JY. Prevalence of Cysticercus bovis in slaughter cattle in Yili prefecture. Xinjiang Animal Husbandry 2007; 1: 4243.Google Scholar
47.Lv, S, et al. Emerging angiostrongyliasis in Mainland China. Emerging Infectious Diseases 2008; 14: 161164.CrossRefGoogle ScholarPubMed
48.Wang, J, et al. An outbreak of Angiostrongyliasis cantonensis in Beijing. Journal of Parasitology 2010; 96: 377381.CrossRefGoogle ScholarPubMed
49.Newell, DG, et al. Food-borne diseases – the challenges of 20 years ago still persist while new ones continue to emerge. International Journal of Food Microbiology 2010; 139: S315.CrossRefGoogle ScholarPubMed
50.Teo, CG. Much meat, much malady: changing perceptions of the epidemiology of hepatitis E. Clinical Microbiology and Infection 2010; 16: 2432.CrossRefGoogle ScholarPubMed
51.Zhuang, H, et al. Epidemiology of hepatitis E in China. Gastroenterologia Japonica 1991; 26: 135138.CrossRefGoogle ScholarPubMed
52.Zhang, W, et al. Hepatitis E virus infection among domestic animals in eastern China. Zoonoses and Public Health 2008; 55: 291298.CrossRefGoogle ScholarPubMed
53.Bihl, F, Negro, F. Hepatitis E virus: a zoonosis adapting to humans. Journal of Antimicrobial Chemotherapy 2010; 65: 817821.CrossRefGoogle ScholarPubMed
54.Cooksley, WG. What did we learn from the Shanghai hepatitis A epidemic? Journal of Viral Hepatitis 2000; 7: 13.CrossRefGoogle ScholarPubMed
55.Wang, D, et al. New target tissue for food-borne virus detection in oysters. Letters in Applied Microbiology 2008; 47: 405409.CrossRefGoogle Scholar
56.Zhu, ZK, et al. Study on detection of hepatitis A virus in aquatic products by transcription PCR approaches. Chinese Journal of Health Laboratory Technology 2005; 15: 677679.Google Scholar