[The preparation of P particle of the norovirus strain SZ9711 from China and its affinity analysis with human histo-blood group antigens in saliva]

Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2010 Feb;24(1):5-7.
[Article in Chinese]

Abstract

Objective: To study the binding profile of NV strain SZ9711 (GII-4) with human histo-blood group antigens (HBGAs).

Methods: The P domain-encoding fragment was amplified by RT-PCR from the stain SZ9711 and cloned into the pGEX-4T-1 vector. The recombinant fusion protein was expressed in E. coli and purified using the column Sepharose 4B. The P protein was released by thrombin cleavage. The binding of P particles of SZ9711 and VA387 with the HBGAs were measured by saliva-based EIA method.

Results: The expression of the recombinant fusion protein was shown by the SDS-PAGE, in which a 38 x 10(3)-P protein was obtained. Saliva-based EIA revealed that the P particle of SZ9711 bound to HBGAs in saliva similar to that of the strain VA387 reported previously. It bound strongly to saliva of type A, B and O(secretor) but did not interact with saliva of type O(non-secretor). Noteworthy, binding ability of SZ9711 P particle to type A saliva was lower than that of the VA387 P particle.

Conclusion: This is the first time that a P particle was prepared from a norovirus strain isolated in China and the binding ability of the P particle with HBGAs was analyzed. The result indicated the binding profile of the SZ9711 P particle was similar to that of VA387 reported previously. These data may be valuable in studying the relationship between noroviruses and their bindings to HGBA receptors.

Publication types

  • English Abstract

MeSH terms

  • Blood Group Antigens / metabolism*
  • Caliciviridae Infections / metabolism*
  • Caliciviridae Infections / virology
  • China
  • Humans
  • Norovirus / chemistry
  • Norovirus / genetics
  • Norovirus / metabolism*
  • Protein Binding
  • Saliva / chemistry
  • Saliva / metabolism*
  • Viral Proteins / genetics
  • Viral Proteins / isolation & purification
  • Viral Proteins / metabolism*

Substances

  • Blood Group Antigens
  • Viral Proteins