Molecular analysis of an oyster-related norovirus outbreak

Journal of Clinical Virology

Volumn 45, Issue 2, 2009, Pages 105-108

  Nenonen, Nancy P ^a   Hannoun, Charles ^a   Olsson, Margareta B ^b   Bergström, Tomas ^a  

^a UNIVERSITY OF GOTHENBURG   (Sweden)

^b UDDEVALLA HOSPITAL   (Sweden)

Author keywords

Genome stability; Norovirus; Outbreak; Oysters; Phylogeny; RT PCR

Indexed keywords

ARTICLE; CLINICAL FEATURE; CONTAMINATED MUSSEL; CONTROLLED STUDY; EPIDEMIC; FECES ANALYSIS; FOOD CONTAMINATION; GENOMIC INSTABILITY; GENOTYPE; HUMAN; MOLECULAR EPIDEMIOLOGY; NONHUMAN; NOROVIRUS; NUCLEOTIDE SEQUENCE; OYSTER; PHYLOGENY; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; VIRUS DETECTION; VIRUS INFECTION; VIRUS STRAIN;

ANIMALS; CALICIVIRIDAE INFECTIONS; CLUSTER ANALYSIS; DISEASE OUTBREAKS; EPIDEMIOLOGY, MOLECULAR; FECES; FOOD POISONING; GASTROENTERITIS; HUMANS; MOLECULAR SEQUENCE DATA; NOROVIRUS; OSTREIDAE; PHYLOGENY; RNA, VIRAL; SEQUENCE ANALYSIS, DNA; SWEDEN;

EID: 66049092035     PISSN: 13866532     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcv.2009.04.011     Document Type: Article

References (35)

1. Kaplan J.E., Feldman R., Campbell D.S., Lookabaugh C., and Gary G.W. The frequency of a Norwalk-like pattern of illness in outbreaks of acute gastroenteritis. Am J Public Health 72 12 (1982) 1329-1332
2. Lees D. Viruses and bivalve shellfish. Int J Food Microbiol 59 1-2 (2000) 81-116
3. Le Guyader F.S., Bon F., DeMedici D., Parnaudeau S., Bertone A., Crudeli S., et al. Detection of multiple noroviruses associated with an international gastroenteritis outbreak linked to oyster consumption. J Clin Microbiol 44 11 (2006) 3878-3882
4. Le Guyader F., Neill F.H., Estes M.K., Monroe S.S., Ando T., and Atmar R.L. Detection and analysis of a small round-structured virus strain in oysters implicated in an outbreak of acute gastroenteritis. Appl Environ Microbiol 62 11 (1996) 4268-4272
5. Appleton H., Palmer S.R., and Gilbert R.J. Foodborne gastroenteritis of unknown aetiology: a virus infection?. Br Med J (Clin Res Ed) 282 6278 (1981) 1801-1802
6. Webby R.J., Carville K.S., Kirk M.D., Greening G., Ratcliff R.M., Crerar S.K., et al. Internationally distributed frozen oyster meat causing multiple outbreaks of norovirus infection in Australia. Clin Infect Dis 44 8 (2007) 1026-1031
7. Marionneau S., Ruvoen N., Le Moullac-Vaidye B., Clement M., Cailleau-Thomas A., Ruiz-Palacois G., et al. Norwalk virus binds to histo-blood group antigens present on gastroduodenal epithelial cells of secretor individuals. Gastroenterology 122 7 (2002) 1967-1977
8. Le Guyader F., Loisy F., Atmar R.L., Hutson A.M., Estes M.K., Ruvoen-Clouet N., et al. Norwalk virus-specific binding to oyster digestive tissues. Emerg Infect Dis 12 6 (2006) 931-936
9. Tian P., Bates A.H., Jensen H.M., and Mandrell R.E. Norovirus binds to blood group A-like antigens in oyster gastrointestinal cells. Lett Appl Microbiol 43 6 (2006) 645-651
10. Tian P., Engelbrektson A.L., Jiang X., Zhong W., and Mandrell R.E. Norovirus recognizes histo-blood group antigens on gastrointestinal cells of clams, mussels, and oysters: a possible mechanism of bioaccumulation. J Food Prot 70 9 (2007) 2140-2147
11. Schwab K.J., Neill F.H., Estes M.K., Metcalf T.G., and Atmar R.L. Distribution of Norwalk virus within shellfish following bioaccumulation and subsequent depuration by detection using RT-PCR. J Food Prot 61 12 (1998) 1674-1680
12. Berg D.E., Kohn M.A., Farley T.A., and McFarland L.M. Multi-state outbreaks of acute gastroenteritis traced to fecal-contaminated oysters harvested in Louisiana. J Infect Dis 181 Suppl. 2 (2000) S381-S386
13. Donaldson E.F., Lindesmith L.C., Lobue A.D., and Baric R.S. Norovirus pathogenesis: mechanisms of persistence and immune evasion in human populations. Immunol Rev 225 (2008) 190-211
14. Lindesmith L., Moe C., Marionneau S., Ruvoen N., Jiang X., Lindblad L., et al. Human susceptibility and resistance to Norwalk virus infection. Nat Med 9 5 (2003) 548-553
15. Tan M., and Jiang X. Norovirus-host interaction: implications for disease control and prevention. Expert Rev Mol Med 9 19 (2007) 1-22
16. Choi J.M., Hutson A.M., Estes M.K., and Prasad B.V. Atomic resolution structural characterization of recognition of histo-blood group antigens by Norwalk virus. Proc Natl Acad Sci USA 105 27 (2008) 9175-9180
17. Prasad B.V., Hardy M.E., Dokland T., Bella J., Rossmann M.G., and Estes M.K. X-ray crystallographic structure of the Norwalk virus capsid. Science 286 5438 (1999) 287-290
18. Kwok S., and Higuchi R. Avoiding false positives with PCR. Nature 339 6221 (1989) 237-238
19. Nenonen N.P., Hannoun C., Horal P., Hernroth B., and Bergstrom T. Tracing of norovirus outbreak strains in mussels collected near sewage effluents. Appl Environ Microbiol 74 8 (2008) 2544-2549
20. Nenonen N.P., Hernroth B., Chauque A.A., Hannoun C., and Bergstrom T. Detection of hepatitis A virus genotype IB variants in clams from Maputo Bay, Mozambique. J Med Virol 78 7 (2006) 896-905
21. Zheng D.P., Ando T., Fankhauser R.L., Beard R.S., Glass R.I., and Monroe S.S. Norovirus classification and proposed strain nomenclature. Virology 346 2 (2006) 312-323
22. Casas N., Amarita F., and de Maranon I.M. Evaluation of an extracting method for the detection of Hepatitis A virus in shellfish by SYBR-Green real-time RT-PCR. Int J Food Microbiol 120 1-2 (2007) 179-185
23. Shieh Y., Monroe S.S., Fankhauser R.L., Langlois G.W., Burkhardt III W., and Baric R.S. Detection of norwalk-like virus in shellfish implicated in illness. J Infect Dis 181 Suppl. 2 (2000) S360-S366
24. Sartorius B., Andersson Y., Velicko I., De Jong B., Lofdahl M., Hedlund K.O., et al. Outbreak of norovirus in Vastra Gotaland associated with recreational activities at two lakes during August 2004. Scand J Infect Dis 39 4 (2007) 323-331
25. Wang J., Jiang X., Madore H.P., Gray J., Desselberger U., Ando T., et al. Sequence diversity of small, round-structured viruses in the Norwalk virus group. J Virol 68 9 (1994) 5982-5990
26. Roos B. Hepatitis epidemic spread by oysters. Sv Läkartidningen 53 16 (1956) 989-1003
27. La Rosa G., Fontana S., Di Grazia A., Iaconelli M., Pourshaban M., and Muscillo M. Molecular identification and genetic analysis of Norovirus genogroups I and II in water environments: comparative analysis of different reverse transcription-PCR assays. Appl Environ Microbiol 73 13 (2007) 4152-4161
28. Rzezutka A., and Cook N. Survival of human enteric viruses in the environment and food. FEMS Microbiol Rev 28 4 (2004) 441-453
29. Maunula L., Miettinen I.T., and von Bonsdorff C.H. Norovirus outbreaks from drinking water. Emerg Infect Dis 11 11 (2005) 1716-1721
30. Boxman I.L., Tilburg J.J., Te Loeke N.A., Vennema H., Jonker K., de Boer E., et al. Detection of noroviruses in shellfish in the Netherlands. Int J Food Microbiol 108 3 (2006) 391-396
31. da Silva A.K., Le Saux J.C., Parnaudeau S., Pommepuy M., Elimelech M., and Le Guyader F.S. Evaluation of removal of noroviruses during wastewater treatment, using real-time reverse transcription-PCR: different behaviors of genogroups I and II. Appl Environ Microbiol 73 24 (2007) 7891-7897
32. Myrmel M., Berg E.M., Grinde B., and Rimstad E. Enteric viruses in inlet and outlet samples from sewage treatment plants. J Water Health 4 2 (2006) 197-209
33. Kageyama T., Shinohara M., Uchida K., Fukushi S., Hoshino F.B., Kojima S., et al. Coexistence of multiple genotypes, including newly identified genotypes, in outbreaks of gastroenteritis due to Norovirus in Japan. J Clin Microbiol 42 7 (2004) 2988-2995
34. Gallimore C.I., Cheesbrough J.S., Lamden K., Bingham C., and Gray J.J. Multiple norovirus genotypes characterised from an oyster-associated outbreak of gastroenteritis. Int J Food Microbiol 103 3 (2005) 323-330
35. Simmons G., Garbutt C., Hewitt J., and Greening G. A New Zealand outbreak of norovirus gastroenteritis linked to the consumption of imported raw Korean oysters. N Z Med J 120 1264 (2007) U2773