Departament of Veterinary Sciences, Universidade Federal do Paraná-UFPR, Rua Pioneiro, 2153, Palotina, Paraná, 85950-000, Brazil.
Department of Preventive Veterinary Medicine, Universidade Estadual de Londrina-UEL, PO Box 6001, Londrina, Paraná, 86051-990, Brazil.
Braz J Microbiol. 2024 Jun;55(2):1967-1977. doi: 10.1007/s42770-024-01287-0. Epub 2024 Feb 21.
Bovine coronavirus (BCoV) has dual tropisms that can trigger enteric and respiratory diseases in cattle. Despite its global distribution, BCoV field strains from Brazil remain underexplored in studies investigating the virus's worldwide circulation. Another research gap involves the comparative analysis of S protein sequences in BCoV isolates from passages in cell lines versus direct sequencing from clinical samples. Therefore, one of the objectives of our study was to conduct a comprehensive phylogenetic analysis of BCoV strains identified from Brazil, including a respiratory strain obtained during this study, comparing them with global and ancestral BCoV strains. Additionally, we performed a comparative analysis between wild-type BCoV directly sequenced from the clinical sample (nasal secretion) and the cell culture-adapted strain, utilizing the Sanger method. The field strain and multiple cell passage in cell culture (HRT-18) adapted BCoV strain (BOV19 NS) detected in this study were characterized through molecular and phylogenetic analyses based on partial fragments of 1,448 nt covering the hypervariable region of the S gene. The analyses have demonstrated that different BCoV strains circulating in Brazil, and possibly Brazilian variants, constitute a new genotype (putative G15 genotype). Compared with the ancestral prototype (Mebus strain) of BCoV, 33 nt substitutions were identified of which 15 resulted in non-synonymous mutations (nine transitions and six transversions). Now, compared with the wild-type strain was identified only one nt substitution in nt 2,428 from the seventh passage onwards, which resulted in transversion, neutral-neutral charge, and one substitution of asparagine for tyrosine at aa residue 810 (N810Y).
牛冠状病毒(BCoV)具有双重嗜性,可引发牛的肠道和呼吸道疾病。尽管它在全球范围内分布,但巴西的 BCoV 田间毒株在研究病毒的全球传播时仍未得到充分探索。另一个研究空白涉及 BCoV 分离株 S 蛋白序列在细胞系传代与直接从临床样本测序之间的比较分析。因此,我们研究的目标之一是对从巴西鉴定的 BCoV 株进行全面的系统发育分析,包括本研究中获得的呼吸道株,将其与全球和原始 BCoV 株进行比较。此外,我们还利用桑格法对直接从临床样本(鼻分泌物)测序的野生型 BCoV 与细胞培养适应株进行了比较分析。本研究中检测到的田间株和在细胞培养中多次传代的适应株(HRT-18)通过基于 S 基因高变区的部分 1448 个核苷酸的分子和系统发育分析进行了特征描述。分析表明,在巴西循环的不同 BCoV 株,可能还有巴西变体,构成了一个新的基因型(假定的 G15 基因型)。与 BCoV 的原始原型(Mebus 株)相比,发现了 33 个核苷酸取代,其中 15 个导致非同义突变(9 个转换和 6 个颠换)。现在,与野生型株相比,只有在第 7 次传代后 nt2428 中的一个核苷酸取代,导致转换、中性中性电荷和天冬酰胺取代 aa 残基 810 处的酪氨酸(N810Y)。