Histo-blood group antigens in <italic style="font-style: italic">Crassostrea gigas</italic> and binding profiles with GII.4 Norovirus

Liping MA; Hui LIU; Laijin SU; Feng ZHAO; Deqing ZHOU; Delin DUAN

doi:10.1007/s00343-018-7024-x

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Histo-blood group antigens in Crassostrea gigas and binding profiles with GII.4 Norovirus

Biology | Updated：2023-05-19

- Histo-blood group antigens in Crassostrea gigas and binding profiles with GII.4 Norovirus
- Chinese Journal of Oceanology and Limnology Vol. 36, Issue 4, Pages: 1383-1391(2018)
- Affiliations：
  
  1.Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China
  2.Key Laboratory for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China
  3.Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, China
- Author bio：
  
  ZHOU Deqing, zhoudq@ysfri.ac.cn
  DUAN Delin, dlduan@qdio.ac.cn
- Funds：
- DOI：10.1007/s00343-018-7024-x
  CLC：
- Received：22 January 2017，
  
  Accepted：31 May 2017，
  
  Online First：24 July 2017，
  
  Published：2018-07
- Accepted：
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Liping MA, Hui LIU, Laijin SU, et al. Histo-blood group antigens in Crassostrea gigas and binding profiles with GII.4 Norovirus[J]. Chinese Journal of Oceanology and Limnology, 2018, 36(4): 1383-1391.
DOI：

Liping MA, Hui LIU, Laijin SU, et al. Histo-blood group antigens in Crassostrea gigas and binding profiles with GII.4 Norovirus[J]. Chinese Journal of Oceanology and Limnology, 2018, 36(4): 1383-1391. DOI： 10.1007/s00343-018-7024-x.

摘要

Abstract

Noroviruses (NoVs) are the main cause of viral gastroenteritis outbreaks worldwide

and oysters are the most common carriers of NoV contamination and transmission. NoVs bind specifically to oyster tissues through histo-blood group antigens (HBGAs)

and this facilitates virus accumulation and increases virus persistence in oysters. To investigate the interaction of HBGAs in Pacific oysters with GⅡ.4 NoV

we examined HBGAs with ELISAs and investigated binding patterns with oligosaccharide-binding assays using P particles as a model of five GⅡ.4 NoV capsids. The HBGAs in the gut and gills exhibited polymorphisms. In the gut

type A was detected (100%)

whereas type Leb (91.67%) and type A (61.11%) were both observed in the gills. Moreover

we found that seasonal NoV gastroenteritis outbreaks were not significantly associated with the specific HBGAs detected in the oyster gut and gills. In the gut

we found that strain-2006b and strain-96/96US bound to type A and H1 but only weakly bound to type Leb; in contrast

the Camberwell and Hunter strains exhibited weak binding to types H1 and Ley

and strain-Sakai exhibited no binding to any HBGA type. In the gills

strain-96/96US and strain-2006b bound to type Leb but only weakly bound to type H1; strains Camberwell

Hunter

and Sakai did not bind to oyster HBGAs. Assays for oligosaccharide binding to GⅡ.4 NoV P particles showed that strain-95/96US and strain-2006b strongly bound to type A

Leb

and Ley oligosaccharides

while strains Camberwell and Hunter showed weak binding ability to type H1 and Ley oligosaccharides and strain-Sakai showed weak binding ability to type Leb and Ley oligosaccharides. Our study presents new information and enhances understanding about the mechanism for NoV accumulation in oysters. Further studies of multiple NoV-tissue interactions might assist in identifying new or improved strategies for minimizing contamination

including HBGA-based attachment inhibition or depuration.

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references

Anbazhagi S, Kamatchiammal S. 2010. A comparative study for the efficient detection of norovirus from drinking water by RT-PCR and real-time PCR. Water Air Soil Poll., 213(1-4):71-84.

Chung H, Sobsey M D. 1993. Comparative survival of indicator viruses and enteric viruses in seawater and sediment. Water Sci. Technol., 27(3-4):425-428.

DePaola A, Jones J L, Woods J, Burkhardt Ⅲ W, Calci K R, Krantz J A, Bowers J C, Kasturi K, Byars R H, Jacobs E, Williams-Hill D, Nabe K. 2010. Bacterial and viral pathogens in live oysters:2007 United States market survey. Appl. Environ. Microbiol., 76(9):2 754-2 768.

Fankhauser R L, Monroe S S, Noel J S, Humphrey C D, Bresee J S, Parashar U D, Ando T, Glass R I. 2002. Epidemiologic and molecular trends of "Norwalk-like viruses" associated with outbreaks of gastroenteritis in the United States. J. Infect. Dis., 186(1):1-7.

Huang P W, Farkas T, Zhong W M, Tan M, Thornton S, Morrow A L, Jiang X. 2005. Norovirus and histo-blood group antigens:demonstration of a wide spectrum of strain specificities and classification of two major binding groups among multiple binding patterns. J. Virol., 79(11):6 714-6 722.

Le Guyader F S, Loisy F, Atmar R L, Hutson A M, Estes M K, Ruvoën-Clouet N, Pommepuy M, Le Pendu J. 2006.Norwalk virus-specific binding to oyster digestive tissues.Emerg. Infect. Dis., 12(6):931-936.

Lindesmith L, Moe C, Marionneau S, Ruvoen N, Jiang X, Lindblad L, Stewart P, LePendu J, Baric R. 2003. Human susceptibility and resistance to Norwalk virus infection.Nat. Med., 9(5):548-553.

Lipp E K, Kurz R, Vincent R, Rodriguez-Palacios C, Farrah S R, Rose J B. 2001. The effects of seasonal variability and weather on microbial fecal pollution and enteric pathogens in a subtropical estuary. Estuaries, 24(2):266-276.

Love D C, Lovelace G L, Sobsey M D. 2010. Removal of Escherichia coli , Enterococcus fecalis , coliphage MS2, poliovirus, and hepatitis A virus from oysters ( Crassostrea virginica ) and hard shell clams ( Mercinaria mercinaria )by depuration. Int. J. Food Microbiol., 143(3):211-217.

Lowther J A, Gustar N E, Hartnell R E, Lees D N. 2012.Comparison of norovirus RNA levels in outbreak-related oysters with background environmental levels. J. Food Protect., 75(2):389-393.

Ma L P, Su L J, Zhao F, Zhou D Q. 2015. Type-like of HBGAs in Crassostrea gigas and its binding properties with norovirus P particles. J. Food Saf. Qual., 6(10):3 970-3 975. (in Chinese with English abstract)

Ma L P, Zhao F, Yao L, Li X G, Zhou D Q, Zhang R L. 2013.The presence of genogroup Ⅱ norovirus in retail shellfish from seven coastal cities in China. Food Environ. Virol., 5(2):81-86.

Maalouf H, Schaeffer J, Parnaudeau S, Le Pendu J, Atmar R L, Crawford S E, Le Guyader F S. 2011. Strain-dependent norovirus bioaccumulation in oysters. Appl. Environ.Microbiol., 77(10):3 189-3 196.

Maalouf H, Zakhour M, Le Pendu J, Le Saux J C, Atmar R L, Le Guyader F S. 2010. Distribution in tissue and seasonal variation of norovirus genogroup Ⅰ and Ⅱ ligands in oysters. Appl. Environ. Microbiol., 76(16):5 621-5 630.

Myrmel M, Berg E M M, Rimstad E, Grinde B. 2004. Detection of enteric viruses in shellfish from the Norwegian coast.Appl. Environ. Microbiol., 70(5):2 678-2 684.

Nishida T, Nishio O, Kato M, Chuma T, Kato H, Iwata H, Kimura H. 2007. Genotyping and quantitation of noroviruses in oysters from two distinct sea areas in Japan. Microbiol. Immunol., 51(2):177-184.

Prasad B V V, Hardy M E, Dokland T, Bella J, Rossmann M G, Estes M K. 1999. X-ray crystallographic structure of the Norwalk virus capsid. Science, 286(5438):287-290.

Provost K, Dancho B A, Ozbay G, Anderson R S, Richards G P, Kingsley D H. 2011. Hemocytes are sites of enteric virus persistence within oysters. Appl. Environ. Microbiol., 77(23):8 360-8 369.

Rodriguez-Manzano J, Hundesa A, Calgua B, Carratala A, de Motes C M, Rusiñol M, Moresco V, Ramos A P, MartínezMarca F, Calvo M, Barardi C R M, Girones R, Bofill-Mas S. 2014. Adenovirus and norovirus contaminants in commercially distributed shellfish. Food Environ. Virol., 6(1):31-41.

Savini G, Casaccia C, Barile N B, Paoletti M, Pinoni C. 2009.Norovirus in bivalve molluscs:A study of the efficacy of the depuration system. Vet. Ital., 45(4):535-539.

Schaeffer J, Le Saux J C, Lora M, Atmar R L, Le Guyader F S. 2013. Norovirus contamination on French marketed oysters. Int. J. Food Microbiol., 166(2):244-248.

Siebenga J J, Vennema H, Zheng D P, Vinjé J, Lee B E, Pang X L, Ho E C M, Lim W, Choudekar A, Broor S, Halperin T, Rasool N B G, Hewitt J, Greening G E, Jin M, Duan Z J, Lucero Y, O'Ryan, M, Hoehne M, Schreier E, Ratcliff R M, White R A, Iritani N, Reuter G, Koopmans M. 2009. Norovirus illness is a global problem: emergence and spread of norovirus GⅡ. 4 variants, 2001-2007. J. Infect. Dis ., 200 (5): 802-812.

Sinton L W, Davies-Colley R J, Bell R G. 1994. Inactivation of enterococci and fecal coliforms from sewage and meatworks effluents in seawater chambers. Appl. Environ.Microbiol., 60(6):2 040-2 048.

Tan M, Jiang X. 2005a. Norovirus and its histo-blood group antigen receptors:an answer to a historical puzzle. Trends Microbiol., 13(6):285-293.

Tan M, Jiang X. 2005b. The P domain of norovirus capsid protein forms a subviral particle that binds to histo-blood group antigen receptors. J. Virol., 79(22):14 017-14 030.

Tan M, Jiang X. 2007. Norovirus-host interaction:implications for disease control and prevention. Expert Rev. Mol. Med., 9(19):1-22.

Tan M, Zhong W M, Song D, Thornton S, Jiang X. 2004. E.coli-expressed recombinant norovirus capsid proteins maintain authentic antigenicity and receptor binding capability. J. Med. Virol., 74(4):641-649.

Tian P, Bates A H, Jensen H M, Mandrell R E. 2006. Norovirus binds to blood group A-like antigens in oyster gastrointestinal cells. Lett. Appl. Microbiol., 43(6):645-651.

Tian P, Engelbrektson A L, Mandrell R E. 2008. Seasonal tracking of histo-blood group antigen expression and norovirus binding in oyster gastrointestinal cells. J. Food.Prot., 71(8):1 696-1 700.

Wang D P, Wu Q P, Kou X X, Yao L, Zhang J M. 2008.Distribution of norovirus in oyster tissues. J. Appl.Microbiol., 105(6):1 966-1 972.

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Histo-blood group antigens in Crassostrea gigas and binding profiles with GII.4 Norovirus

DOI：10.1007/s00343-018-7024-x

摘要

Abstract

关键词

Keywords

references