Cheetham S, Souza M, McGregor R, Meulia T, Wang Q, Saif L J
Food Animal Health Research Program, Ohio Agricultural Research and Development Center, The Ohio State University, 1680 Madison Avenue, Wooster, OH 44691, USA.
J Virol. 2007 Apr;81(7):3535-44. doi: 10.1128/JVI.01306-06. Epub 2007 Jan 10.
Histo-blood group antigen (HBGA) phenotypes have been associated with susceptibility to human noroviruses (HuNoVs). Our aims were: (i) to determine the patterns of A/H HBGA expression in buccal and intestinal tissues of gnotobiotic (Gn) pigs; (ii) to determine if virus-like particles (VLPs) of HuNoV genogroup I (GI) and GII bind to A- or H-type tissues; (iii) to compare A/H expression and VLP binding patterns and confirm their binding specificities by blocking assays; (iv) to develop a hemagglutination inhibition test using buccal cells from live pigs to determine the Gn pig's A/H phenotype and to match viral strains with previously determined HuNoV VLP binding specificities; and (v) to determine the A/H phenotypes and compare these data to the infection outcomes of a previous study of 65 Gn pigs inoculated with HuNoV GII/4 strain HS66 and expressing A and/or H or neither antigen on their buccal and intestinal tissues (S. Cheetham, M. Souza, T. Meulia, S. Grimes, M. G. Han, and L. J. Saif, J. Virol. 80:10372-10381, 2006). We found that the HuNoV GI/GII VLPs of different clusters bound to tissues from four pigs tested (two A+ and two H+). The GI/1 and GII/4 VLPs bound extensively to duodenal and buccal tissues from either A+ or H+ pigs, but surprisingly, GII/1 and GII/3 VLPs bound minimally to the duodenum of an A+ pig. The VLP binding was partially inhibited by A-, H1-, or H2-specific monoclonal antibodies, but was completely blocked by porcine mucin. Comparing the A/H phenotypes of 65 HS66-inoculated Gn pigs from our previous study, we found that significantly more A+ and H(+) pigs (51%) than non-A+ and non-H+ pigs (12.5%) shed virus. From the 22 convalescent pigs, significantly more A+ or H+ pigs (66%) than non-A+ or H+ pigs (25%) seroconverted.
组织血型抗原(HBGA)表型与人类诺如病毒(HuNoV)易感性相关。我们的目的是:(i)确定无菌(Gn)猪颊部和肠道组织中A/H HBGA的表达模式;(ii)确定HuNoV基因组I(GI)和GII的病毒样颗粒(VLP)是否与A或H型组织结合;(iii)比较A/H表达和VLP结合模式,并通过阻断试验确认其结合特异性;(iv)利用活猪颊部细胞开发血凝抑制试验,以确定Gn猪的A/H表型,并将病毒株与先前确定的HuNoV VLP结合特异性相匹配;(v)确定A/H表型,并将这些数据与先前一项对65只接种HuNoV GII/4株HS66且颊部和肠道组织表达A和/或H抗原或均不表达抗原的Gn猪的感染结果进行比较(S. Cheetham、M. Souza、T. Meulia、S. Grimes、M. G. Han和L. J. Saif,《病毒学杂志》80:10372 - 10381,2006年)。我们发现,不同簇的HuNoV GI/GII VLP与4只受试猪(2只A + 和2只H + )的组织结合。GI/1和GII/4 VLP广泛结合A + 或H + 猪的十二指肠和颊部组织,但令人惊讶的是,GII/1和GII/3 VLP与一只A + 猪的十二指肠结合最少。VLP结合被A、H1或H2特异性单克隆抗体部分抑制,但被猪黏蛋白完全阻断。比较我们先前研究中65只接种HS66的Gn猪的A/H表型,我们发现排出病毒的A + 和H(+)猪(51%)显著多于非A + 和非H + 猪(12.5%)。在22只康复猪中,血清转化的A + 或H + 猪(66%)显著多于非A + 或H + 猪(2%)。