Complete genome constellation of a dominant Bovine rotavirus genotype circulating in Bangladesh reveals NSP4 intragenic recombination with human strains
Shama Ranjan Barua , Tridip Das , Tofazzal Md Rakib , Babu Kanti Nath , Suman Das Gupta , Subir Sarker , Sharmin Chowdhury , Shane R. Raidal , Shubhagata Das
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引用次数: 0
Abstract
Rotavirus A is a leading cause of non-bacterial gastroenteritis in humans and domesticated animals. Despite the vast diversity of bovine Rotavirus A strains documented in South Asian countries, there are very few whole genomes available for phylogenetic study. A cross-sectional study identified a high prevalence of the G6P[11] genotype of bovine Rotavirus A circulating in the commercial cattle population in Bangladesh. Next-generation sequencing and downstream phylogenetic analysis unveiled all 11 complete gene segments of this strain (BD_ROTA_CVASU), classifying it under the genomic constellation G6P[11]-I2-R2-C2-M2-A13-N2-T6-E2-H3, which belongs to a classical DS-1-like genomic backbone. We found strong evidence of intragenic recombination between human and bovine strains in the Non-structural protein 4 (NSP4) gene, which encodes a multifunctional enterotoxin. Our analyses highlight frequent zoonotic transmissions of rotaviruses in diverse human-animal interfaces, which might have contributed to the evolution and pathogenesis of this dominant genotype circulating in the commercial cattle population in Bangladesh.
轮状病毒 A 是人类和驯养动物非细菌性肠胃炎的主要病因。尽管南亚国家记录的牛轮状病毒 A 株系种类繁多,但可用于系统发育研究的全基因组却很少。一项横断面研究发现,G6P[11] 基因型的牛轮状病毒 A 在孟加拉国的商业牛群中流行率很高。下一代测序和下游系统发育分析揭示了该毒株(BD_ROTA_CVASU)的全部 11 个完整基因片段,将其归入 G6P[11]-I2-R2-C2-M2-A13-N2-T6-E2-H3 基因组群,该基因组群属于经典的 DS-1 样基因组骨架。我们在编码多功能肠毒素的非结构蛋白 4(NSP4)基因中发现了人和牛菌株之间基因内重组的有力证据。我们的分析凸显了轮状病毒在不同的人-动物界面中频繁的人畜共患传播,这可能是导致这种在孟加拉国商业牛群中流行的优势基因型进化和致病的原因。
期刊介绍:
Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.