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http://dx.doi.org/10.5657/KFAS.2014.0501

Norovirus Quantification in Oysters Crassostrea gigas Collected from Tongyeoung, Korea  

Shin, Soon Bum (Southwest Sea Fisheries Research Institute, National Fisheries Research and Development Institute)
Oh, Eun-Gyoung (West Sea Fisheries Research Institute, National Fisheries Research and Development Institute)
Lee, Hee-Jung (National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety)
Kim, Yeon Kye (Southwest Sea Fisheries Research Institute, National Fisheries Research and Development Institute)
Lee, Tae Seek (Food Safety Division, National Fisheries Research and Development Institute)
Kim, Ji-Hoe (Research and Development Planning Division, National Fisheries Research and Development Institute)
Publication Information
Korean Journal of Fisheries and Aquatic Sciences / v.47, no.5, 2014 , pp. 501-507 More about this Journal
Abstract
Norovirus (NoV) is a major cause of food poisoning outbreaks in Korea. Most NoV outbreaks originate from environmental contamination, but bivalves such as oysters are also important vectors. Oyster Crassostrea gigas contamination by NoV has been reported in Korea, but no quantitative analyses of NoV have been performed. We investigated the NoV concentration in 21 oyster samples from a Korean commercial oyster-growing area with confirmed fecal 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 on NoV-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 $8.97{\times}10^2-2.24{\times}10^2$ and $3.05{\times}10^2-7.47{\times}10^1$ 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 $60^{\circ}C$, $68^{\circ}C$, $70^{\circ}C$, and $100^{\circ}C$, respectively, for 15 min, while genogroup II respectively decreased by 67.3%, 76.3%, 80.1%, and 89.8% under the same conditions.
Keywords
Crassostrea gigas; Oyster; Norovirus; Quantitative analysis; Heat-treatment;
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1 Alfano-Sobsey E, Sweat D, Hall A, Breedlove F, Rodriguez R, Greene S, Pierce A, Sobsey M, Davies M and Ledford SL. 2012. Norovirus outbreak associated with undercooked oysters and secondary household transmission. Epidemiol Infect 140, 276-282. http://dx.doi.org/10.1017/S0950268811000665.   DOI   ScienceOn
2 Fankhauser RL, Monroe SS, Noel JS, Humphrey CD, Bresee JS, Parashar UD, Ando T and Glass RI. 2002. Epidemiologic and molecular trends of "Norwalk-like viruses" associated with outbreaks of gastroenteritis in the United States. J Infect Dis 186, 1-7. http://dx.doi.org/10.1086/341085.   DOI   ScienceOn
3 Blackburn BG, Craun GF, Yoder JS, Hill V, Calderon RL, Chen N, Lee SH, Levy DA, and Beach MJ. 2004. Surveillance for waterborne-disease outbreaks associated with drinking water-United States. MMWR Surveillance Summaries 53, 23-45.
4 Bozkurt H, D'Souza D and Davidson P.M. 2013. Determination of the thermal inactivation kinetics of the human norovirus surrogates, murine norovirus and feline calicivirus. J Food Prot 76, 79-84. http://dx.doi.org/10.4315/0362-028X.JFP-12-327.   DOI
5 EFSA Panel on Biological Hazards. 2012. Scientific opinion on norovirus (NoV) in oysters: methods, limits and control options. EFSA J 10, 2500-2538.   DOI
6 Hall AJ, Wikswo ME, Pringle K, Gould LH and Prashar UD. 2014. Vital signs: Foodborne norovirus outbreaks - United States, 2009-2012. CDC morbidity and mortality weekly report 63, 491-495. Retrieved from http://www.cdc.gov/mmwr on July 23.
7 Iritani N, Kaida A, Abe N, Kubo H, Sekiguchi JI, Yamamoto SP, Goto K, Tanaka T and Noda M. 2014. Detection and genetic characterization of human enteric viruses in oyster-associated gastroenteritis outbreaks between 2001 and 2012 in Osaka City, Japan. Retrieved from http://onlinelibrary.wiley.com on July 23. http://dx.doi.org/doi/10.1002/jmv.23883.   DOI   ScienceOn
8 ISO. 2013. 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. Retried from http://www.iso.orgon August 11.
9 Jo SH, Kim HJ, Choi EJ and Ha SD. 2009. Trends analysis of food-borne outbreaks in United States of America, Japan and Korea. Safe Food 4, 3-14.   과학기술학회마을
10 Jothikumar N, Lowther JA, Henshilwood K, Lees DN, Hill VR and Vinje J. 2005. 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, 1870-1875. http://dx.doi.org /doi/10.1128/AEM.71.4.1870-1875.2005.   DOI   ScienceOn
11 Kageyama T, Kojima S, Shinohara M, Uchida K, Fukushi S, Hoshino FB, Takeda N, and Katayama K. 2003. Broadly reactive and highly sensitive assay for Norwalk-like viruses based on real-time quantitative reverse transcription-PCR. J Clin Microbiol 41, 1548-1557. http://dx.doi.org/doi/10.1128/JCM.41.4.1548-1577.2003.   DOI   ScienceOn
12 MOF. 2013. Major statistics of oceans and fisheries. Oceans and fisheries report, 1-395.
13 Koopmans M, Bonsdor CH, Vinje J, Medici D and Monroe S. 2002. Foodborne viruses. FEMS Microbiol 26, 187-205. http://dx.doi.org /doi/10.1111/j.1574-6976.2002.   DOI
14 Nims R and Plavsic M. 2013. Inactivation of caliciviruses. Pharmaceuticals 6, 358-392. http://dx.doi. org/doi/10.3390/ph6030358.   DOI   ScienceOn
15 Lee TS, Oh EG, Yoo HD, Ha KS, Yu HS, Byun HS and Kim JH. 2010. Impact of rainfall events on the bacteriological water quality of the shellfish growing area in Korea. Kor J Fish Aquat Sci 43, 406-414.   과학기술학회마을   DOI   ScienceOn
16 MFDS. Present condition of food-borne. Retried from http://www.mfds.go.kr on July 23.
17 Moon A, Hwang IG and Choi WS. 2011. Prevalence of noroviruses in oyster in Korea. Food Sci Biotechnol 20. 1151-1154. http://dx.doi.org /doi/10.1007/s10068-011-0157-8.   DOI
18 Nuanualsuwan S and Cliver DO 2002. Pretreatment to avoid positive RT-PCR results with inactivated viruses. J Virol Methods 104, 217-225. http://dx.doi. org/doi/10.1016/S0166-0934(02)00089-7.   DOI   ScienceOn
19 Oh EG, Yoo HD, Yu HS, Ha KS, Shin SB, Lee TS, Lee HJ, Kim JH and Son KT. 2012. Removal of fecal indicator bacteria from bivalves under natural and electrolyzed water. Kor J Fish Aquat Sci 45, 11-16.   과학기술학회마을   DOI
20 Park JH, Jeong HS, Lee JS, Lee SW, Choi YH, Choi SJ, Joo IS, Kim YR, Park YK and Youn SK. 2014. First norovirus outbreaks associated with consumption of green seaweed (Enteromorpha spp.) in South Korea. Epidemiol Infect 27, 1-7. http://dx.doi.org/10.1017/S0950268814001332.   DOI   ScienceOn
21 Shin SB, Oh EG, Yu HS, Lee HJ, Kim JH, Park KBW, Kwon JY and Son KT. 2010. Inactivation of a norovirus surrogate (Feline calicivirus) during the ripening of oyster Kimch. Kor J Fish Aquat Sci 43, 415-420.   과학기술학회마을   DOI   ScienceOn
22 Patel MM, Hall AJ, Vinje J and Parashar UD. 2009. Noroviruses: a comprehensive review. J Clin Virol 44, 1-8. http://dx.doi.org/10.1016/j.jcv.2008.10.009.   DOI   ScienceOn
23 Shin SB, Oh EG, Yu HS, Son KT, Lee HJ, Park JY and Kim JH. 2013. Genetic diversity of noroviruses detected in oyster in Jinhae bay, Korea. Food Sci Biotechnol 22, 1453-1460. http://dx.doi.org/10.1007/s10068-013-0237-z.   DOI   ScienceOn
24 Shim KB, Ha KS, Yoo HD, Kim JH and Lee TS. 2009. Evaluation of the bacteriological safety for the shellfish growing area in Jaranman-Saryangdo area, Korea. Kor J Fish Aquat Sci 42, 442-448.   과학기술학회마을   DOI   ScienceOn