基因型-Ia 牛冠状病毒肠道分离株的分离和分子鉴定,该分离株在尖峰糖蛋白的受体结合域有显著突变。

Abid Ullah Shah, Phillip Gauger, Maged Gomaa Hemida
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引用次数: 0

摘要

利用 MDBK 和 HRT-18 对新分离的 BCoV 进行了斑块纯化、分离和体外繁殖。该 BCoV 新分离株的全长基因组测序(31 Kbs)已经完成,并上传到 GenBank。基因组结构为(5'-UTR-Gene-1-32kDa-HE-S-4.9 kDa-4.8 kDa-12.7 kDa-E-M-N-UTR-3')。基于(全长基因组、S、HE 和 N)序列的系统发生分析表明,BCoV-13 与其他北美 BCoV 基因型 I 成员聚类。序列分析表明,S 糖蛋白的各个结构域,尤其是受体结合结构域中存在多个同义突变。我们发现紧靠核壳基因 RNA 结合域下游有 9 个明显的核苷酸缺失。我们鼓励进一步开展基因功能研究,研究这些突变对 BCoV 分子致病机理和免疫调节的作用。这项研究加深了我们对 BCoV 基因组学的了解,有助于改进牛 BCoV 感染的诊断和控制措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and molecular characterization of an enteric isolate of the genotype-Ia bovine coronavirus with notable mutations in the receptor binding domain of the spike glycoprotein.

BCoV new isolate was plaque purified, isolated, and propagated in vitro using MDBK and HRT-18. The full-length genome sequencing of this new BCoV isolate (31 Kbs) was drafted and deported in the GenBank. The genome organization is (5'-UTR-Gene-1-32kDa-HE-S-4.9 kDa-4.8 kDa-12.7 kDa-E-M-N-UTR-3'). Phylogenetic analysis based on the sequences of (the full-length genome, S, HE, and N) showed that the BCoV-13 clustered with other North American BCoV genotype I members. The sequence analysis shows several synonymous mutations among various domains of the S glycoprotein, especially the receptor binding domain. We found nine notable nucleotide deletions immediately downstream of the RNA binding domain of the nucleocapsid gene. Further gene function studies are encouraged to study the function of these mutations on the BCoV molecular pathogenesis and immune regulation. This research enhances our understanding of BCoV genomics and contributes to improved diagnostic and control measures for BCoV infections in cattle.

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