Takiuchi E, Alfieri A F, Alfieri A A
Laboratório de Virologia Animal, Departamento de Medicina Veterinária Preventiva, Universidade Estadual de Londrina, Londrina, PR, Brasil.
Braz J Med Biol Res. 2008 Apr;41(4):277-82. doi: 10.1590/s0100-879x2008000400004.
Bovine coronavirus (BCoV) causes severe diarrhea in newborn calves, is associated with winter dysentery in adult cattle and respiratory infections in calves and feedlot cattle. The BCoV S protein plays a fundamental role in viral attachment and entry into the host cell, and is cleaved into two subunits termed S1 (amino terminal) and S2 (carboxy terminal). The present study describes a strategy for the sequencing of the BCoV S1 gene directly from fecal diarrheic specimens that were previously identified as BCoV positive by RT-PCR assay for N gene detection. A consensus sequence of 2681 nucleotides was obtained through direct sequencing of seven overlapping PCR fragments of the S gene. The samples did not undergo cell culture passage prior to PCR amplification and sequencing. The structural analysis was based on the genomic differences between Brazilian strains and other known BCoV from different geographical regions. The phylogenetic analysis of the entire S1 gene showed that the BCoV Brazilian strains were more distant from the Mebus strain (97.8% identity for nucleotides and 96.8% identity for amino acids) and more similar to the BCoV-ENT strain (98.7% for nucleotides and 98.7% for amino acids). Based on the phylogenetic analysis of the hypervariable region of the S1 subunit, these strains clustered with the American (BCoV-ENT, 182NS) and Canadian (BCQ20, BCQ2070, BCQ9, BCQ571, BCQ1523) calf diarrhea and the Canadian winter dysentery (BCQ7373, BCQ2590) strains, but clustered on a separate branch of the Korean and respiratory BCoV strains. The BCoV strains of the present study were not clustered in the same branch of previously published Brazilian strains (AY606193, AY606194). These data agree with the genealogical construction and suggest that at least two different BCoV strains are circulating in Brazil.
牛冠状病毒(BCoV)可导致新生犊牛严重腹泻,与成年牛的冬季痢疾以及犊牛和育肥牛的呼吸道感染有关。BCoV的S蛋白在病毒附着和进入宿主细胞过程中起关键作用,并被切割成两个亚基,分别称为S1(氨基末端)和S2(羧基末端)。本研究描述了一种直接从粪便腹泻标本中对BCoV S1基因进行测序的策略,这些标本先前通过针对N基因检测的RT-PCR分析被鉴定为BCoV阳性。通过对S基因的七个重叠PCR片段进行直接测序,获得了一个2681个核苷酸的共有序列。样本在进行PCR扩增和测序之前未经过细胞培养传代。结构分析基于巴西毒株与来自不同地理区域的其他已知BCoV之间的基因组差异。对整个S1基因的系统发育分析表明,巴西BCoV毒株与Mebus毒株的亲缘关系更远(核苷酸同一性为97.8%,氨基酸同一性为96.8%),而与BCoV-ENT毒株更相似(核苷酸同一性为98.7%,氨基酸同一性为98.7%)。基于对S1亚基高变区的系统发育分析,这些毒株与美国(BCoV-ENT、182NS)和加拿大(BCQ20、BCQ2070、BCQ9、BCQ571、BCQ1523)的犊牛腹泻毒株以及加拿大冬季痢疾(BCQ7373、BCQ2590)毒株聚类,但与韩国和呼吸道BCoV毒株聚类在一个单独的分支上。本研究中的BCoV毒株未与先前发表的巴西毒株(AY606193、AY606194)聚类在同一分支上。这些数据与谱系构建结果一致,并表明巴西至少有两种不同的BCoV毒株在传播。