Shared clusters between phylogenetic trees for genomic segments of Rotavirus A with distinct genotype constellations

IF 1 Q4 GENETICS & HEREDITY Gene Reports Pub Date : 2024-06-18 DOI:10.1016/j.genrep.2024.101956
Yoshiyuki Suzuki, Masaya Yaeshiro, Daiki Uehara, Ren Ishihara
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Abstract

Rotavirus A (RVA) possesses a genome of 11-segmented, double-stranded RNAs, each of which is classified into genotypes. A variety of genotype constellations have been generated through reassortment, but reassortment does not appear to occur randomly. Here genomic sequences for 281 RVA strains with distinct genotype constellations retrieved from the International Nucleotide Sequence Database were analyzed to identify shared clusters between phylogenetic trees for genomic segments. The largest numbers of shared clusters were observed between the genomic segments encoding viral protein 1 (VP1) and VP2 as well as VP2 and VP3, suggesting that not only VP1 but also VP3 may interact with VP2 inside the core. Larger numbers were also associated with the segment encoding non-structural protein 5/6 (NSP5/6), which may be a hub for bundling genomic segments. Although VP7 and VP4 segments were associated with smaller numbers, reassortments between these segments as well as VP7 and VP6 segments appeared to be restricted due to interactions in constructing the virion. For VP4 segment, the number with NSP1 segment was significantly greater than those with other segments, possibly reflecting that specificities in receptor binding and interferon antagonism may define host range restriction. Overall, no cluster was shared by all genomic segments, supporting that RVA constituted a single species.

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基因型不同的轮状病毒 A 基因组片段的系统发生树之间的共享集群
轮状病毒 A(RVA)的基因组由 11 段双链 RNA 组成,每段 RNA 可分为不同的基因型。通过重配产生了多种基因型组合,但重配似乎不是随机发生的。本文分析了从国际核苷酸序列数据库(International Nucleotide Sequence Database)检索到的 281 个具有不同基因型组合的 RVA 株系的基因组序列,以确定基因组片段的系统发生树之间的共享群。在编码病毒蛋白 1(VP1)和 VP2 以及 VP2 和 VP3 的基因组片段之间观察到的共享簇数量最多,这表明不仅 VP1,VP3 也可能在核心内与 VP2 相互作用。编码非结构蛋白 5/6(NSP5/6)的片段数量也较多,这可能是基因组片段捆绑的枢纽。虽然 VP7 和 VP4 区段的数量较少,但这些区段以及 VP7 和 VP6 区段之间的重新组合似乎受到限制,原因是在构建病毒体时发生了相互作用。就 VP4 片段而言,与 NSP1 片段相关的数量明显多于与其他片段相关的数量,这可能反映了受体结合和干扰素拮抗的特异性可能决定了宿主范围的限制。总体而言,所有基因组片段没有共享的聚类,这证明 RVA 是一个单一的物种。
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来源期刊
Gene Reports
Gene Reports Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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