통영시 연안의 양식굴(Crassostrea gigas)에서 검출된 노로바이러스의 정량분석
Norovirus Quantification in Oysters Crassostrea gigas Collected from Tongyeoung, Korea
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초록
Norovirus (NoV) is a major cause of food poisoning outbreaks in Korea. Most NoV outbreaks originate from environmentalcontamination, but bivalves such as oysters are also important vectors. Oyster Crassostrea gigas contaminationby NoV has been reported in Korea, but no quantitative analyses of NoV have been performed. We investigatedthe NoV concentration in 21 oyster samples from a Korean commercial oyster-growing area with confirmedfecal contamination from January to December 2012, using real-time reverse transcription–polymerase chain reaction. Additionally, we assessed the NoV concentration after heating to investigate the effects of heat treatment onNoV-infected oysters. In NoV-positive samples, the cycle threshold (Ct) values were 37.43-39.41 and 36.77-39.30,while viral concentrations were 8.97×102–2.24×102 and 3.05×102–7.47×101 copies/g for genogroups I and II, respectively. After heat treatment, NoV genogroup I decreased by 83.4%, 88.0%, 89.4% and 100% at 60°C, 68°C, 70°C,and 100°C, respectively, for 15 min, while genogroup II respectively decreased by 67.3%, 76.3%, 80.1%, and 89.8%under the same conditions.
Abstract
Norovirus (NoV) is a major cause of food poisoning outbreaks in Korea. Most NoV outbreaks originate from environmentalcontamination, but bivalves such as oysters are also important vectors. Oyster Crassostrea gigas contaminationby NoV has been reported in Korea, but no quantitative analyses of NoV have been performed. We investigatedthe NoV concentration in 21 oyster samples from a Korean commercial oyster-growing area with confirmedfecal contamination from January to December 2012, using real-time reverse transcription–polymerase chain reaction. Additionally, we assessed the NoV concentration after heating to investigate the effects of heat treatment onNoV-infected oysters. In NoV-positive samples, the cycle threshold (Ct) values were 37.43-39.41 and 36.77-39.30,while viral concentrations were 8.97×102–2.24×102 and 3.05×102–7.47×101 copies/g for genogroups I and II, respectively. After heat treatment, NoV genogroup I decreased by 83.4%, 88.0%, 89.4% and 100% at 60°C, 68°C, 70°C,and 100°C, respectively, for 15 min, while genogroup II respectively decreased by 67.3%, 76.3%, 80.1%, and 89.8%under the same conditions.
참고문헌 (24)
- Alfano-Sobsey E, "Norovirus outbreak associated with undercooked oysters and secondary household transmission", Epidemiol Infect, 140, pp.276~282 (2012)
- Blackburn BG, "Surveillance for waterborne-disease outbreaks associated with drinking water-United States", MMWR Surveillance Summaries, 53, pp.23~45 (2004)
- Bozkurt H, "Determination of the thermal inactivation kinetics of the human norovirus surrogates, murine norovirus and feline calicivirus", J Food Prot, 76, pp.79~84 (2013)
- EFSA Panel on Biological Hazards, "Scientific opinion on norovirus (NoV) in oysters: methods, limits and control options", EFSA J, 10, pp.2500~2538 (2012)
- Fankhauser RL, "Epidemiologic and molecular trends of "Norwalk-like viruses" associated with outbreaks of gastroenteritis in the United States", J Infect Dis, 186, pp.1~7 (2002)
- Vital signs: Foodborne norovirus outbreaks - United States, 2009-2012, "Hall AJ", 491~495, pp.CDC morbidity and mortality weekly report 63 (2014)
- Iritani N, "Detection and genetic characterization of human enteric viruses in oyster-associated gastroenteritis outbreaks between 2001 and 2012 in Osaka City, Japan"[DOI]
- "Microbiology of food and animal feed - Horizontal method for determination of hepatitis A virus and norovirus in food using real-time RT-PCR - Part 1: Method for quantification" (2013)[URL]
- Jo SH, "Trends analysis of food-borne outbreaks in United States of America, Japan and Korea", Safe Food, 4, pp.3~14 (2009)
- Jothikumar N, "Rapid and sensitive detection of noroviruses by using TaqMan-based one-step reverse transcription- PCR assays and application to naturally contaminated shellfish samples", Appl Environ Microbiol, 71, pp.1870~1875 (2005)
- Kageyama T, "Broadly reactive and highly sensitive assay for Norwalk-like viruses based on real-time quantitative reverse transcription- PCR", J Clin Microbiol, 41, pp.1548~1557 (2003)
- Koopmans M, "Foodborne viruses", FEMS Microbiol, 26, pp.187~205 (2002)
- 이태식, "패류 양식장의 세균학적 수질에 미치는 강우의 영향", 한국수산과학회지, 43(5), pp.406~414 (2010), 한국수산과학회
- "Present condition of food-borne"[URL]
- Major statistics of oceans and fisheries, "MOF", ~, pp.Oceans and fisheries report, 1-395 (2013)
- 문애리, "Prevalence of Noroviruses in Oysters in Korea", Food Science and Biotechnology, 20(4), pp.1151~1154 (2011), 한국식품과학회
- Nims R, "Inactivation of caliciviruses", Pharmaceuticals, 6, pp.358~392 (2013)
- Nuanualsuwan S, "Pretreatment to avoid positive RT-PCR results with inactivated viruses", J Virol Methods, 104, pp.217~225 (2002)
- 오은경, "패류 중 자연정화 및 인공정화에 의한 위생지표세균의 변화", 한국수산과학회지, 45(1), pp.11~16 (2012), 한국수산과학회
- Park JH, "First norovirus outbreaks associated with consumption of green seaweed (Enteromorpha spp.) in South Korea", Epidemiol Infect, 27, pp.1~7 (2014)
- Patel MM, "Noroviruses: a comprehensive review", J Clin Virol, 44, pp.1~8 (2009)
- 신순범, "굴김치 숙성에 따른 노로바이러스 대체모델 Feline Calicivirus의 불활성화", 한국수산과학회지, 43(5), pp.415~420 (2010), 한국수산과학회
- 신순범, "Genetic Diversity of Noroviruses Detected in Oysters in Jinhae Bay,Korea", Food Science and Biotechnology, 22(5), pp.1453~1460 (2013), 한국식품과학회[DOI]
- 심길보, "자란만․사량도 패류생산해역의 위생학적 안전성 평가", 한국수산과학회지, 42(5), pp.442~448 (2009), 한국수산과학회
