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Analysis of putative recombination hot sites in the S gene of canine coronaviruses.

机译:犬冠状病毒S基因推定重组热点的分析。

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The S gene sequence of Canine coronavirus strain 1-71 (CCoV 1-71) was cloned, sequenced, and compared to those of other CCoVs, Transmissible gastroenteritis virus (TGEV), and Feline coronavirus (FCoV). The sequence analysis showed that CCoV 1-71 displayed a 98.8-99.8% identity with CCoVs strains V1, K378, and GP. Four putative recombination sites were found at the 5'-end of the S gene, namely at nt 53, 75, 425, 991. Both sequences flanking each site were significantly different. Three recombination hot regions were found on the S gene, namely at nt 337-437, 1545-3405, and 4203-4356, which shared a common recombination signal with Group 2 coronaviruses. The G/CTAAAAA/GT sequence downstream of the recombination site may represent a specific recombination signal in CCoVs. The CCoV 1-71 S protein sequence was found to be similar to those of other CCoVs except for several N-glycosylation sites at the N-terminus of the S protein, which could be related to the differences in virulence and cell tropism in individual CCoVs. This study indicated that the similarity of CCoVs in virulence and tropism was mostly acquired by the homologous RNA recombination and not only by simple mutation and selection.
机译:克隆,测序犬冠状病毒株1-71(CCoV 1-71)的S基因序列,并将其与其他CCoV,可传播性胃肠炎病毒(TGEV)和猫冠状病毒(FCoV)的S基因序列进行比较。序列分析表明,CCoV 1-71与CCoV菌株V1,K378和GP的同源性为98.8-99.8%。在S基因的5'末端发现了四个推定的重组位点,即在核苷酸53、75、425、991。每个位点侧翼的两个序列都有显着差异。在S基因上发现了三个重组热区,即nt 337-437、1545-3405和4203-4356,它们与第2组冠状病毒共享共同的重组信号。重组位点下游的G / CTAAAAA / GT序列可以代表CCoV中的特定重组信号。发现CCoV 1-71 S蛋白序列与其他CCoV相似,除了在S蛋白N端有多个N-糖基化位点外,这可能与单个CCoVs的毒力和细胞嗜性差异有关。 。这项研究表明,CCoVs在毒力和嗜性上的相似性主要是通过同源RNA重组获得的,而不仅仅是通过简单的突变和选择获得的。

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