Genome-wide expanding of genetic evolution and potential pathogenicity in Vibrio alginolyticus.

IF 8.4 2区 医学 Q1 IMMUNOLOGY Emerging Microbes & Infections Pub Date : 2024-12-01 Epub Date: 2024-05-26 DOI:10.1080/22221751.2024.2350164
Zhenzhou Huang, Yanjun Li, Keyi Yu, Lizhi Ma, Bo Pang, Qin Qin, Jie Li, Duochun Wang, He Gao, Biao Kan
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Abstract

Vibrio alginolyticus, an emergent species of Vibrio genus, exists in aquatic and marine environments. It has undergone genetic diversification, but its detailed genomic diversity is still unclear. Here, we performed a multi-dimensional comparative genomic analysis to explore the population phylogeny, virulence-related genes and potential drug resistance genes of 184 V. alginolyticus isolates. Although genetic diversity is complex, we analysed the population structure using three sub-datasets, including the subdivision for three lineages into sublineages and the distribution of strains in the marine ecological niche. Accessory genes, most of which reclassified V. alginolyticus genomes as different but with relatively close affinities, were nonuniformly distributed among these isolates. We demonstrated that the spread of some post-evolutionary isolates (mainly L3 strains isolated from Chinese territorial seas) was likely to be closely related to human activities, whereas other more ancestral strains (strains in the L1 and L2) tended to be locally endemic and formed clonal complex groups. In terms of pathogenicity, the potential virulence factors were mainly associated with toxin, adherence, motility, chemotaxis, and the type III secretion system (T3SS). We also found five types of antibacterial drug resistance genes. The prevalence of β-lactam resistance genes was 100%, which indicated that there may be a potential risk of natural resistance to β-lactam drugs. Our study reveals insights into genomic characteristics, evolution and potential virulence-associated gene profiles of V. alginolyticus.

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全基因组范围内藻类溶解弧菌基因进化和潜在致病性的扩展。
溶藻弧菌是弧菌属的一个新出现的物种,存在于水生和海洋环境中。它经历了基因多样化,但其详细的基因组多样性仍不清楚。在此,我们进行了多维比较基因组分析,以探索 184 个藻类弧菌分离物的种群系统发育、毒力相关基因和潜在耐药基因。虽然遗传多样性很复杂,但我们还是利用三个子数据集分析了种群结构,包括三个系的亚系细分和菌株在海洋生态位中的分布。附属基因在这些分离株中的分布并不均匀,其中大部分基因将溶藻病毒基因组重新分类为不同的基因组,但具有相对接近的亲缘关系。我们证明,一些进化后分离株(主要是分离自中国领海的 L3 株)的传播可能与人类活动密切相关,而其他更古老的菌株(L1 和 L2 株)则倾向于在当地流行并形成克隆复合群。在致病性方面,潜在的致病因子主要与毒素、粘附性、运动性、趋化性和 III 型分泌系统(T3SS)有关。我们还发现了五种抗菌药耐药基因。β-内酰胺类耐药基因的流行率为100%,这表明可能存在对β-内酰胺类药物产生天然耐药性的潜在风险。我们的研究揭示了溶藻病毒的基因组特征、进化和潜在的毒力相关基因谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Emerging Microbes & Infections
Emerging Microbes & Infections IMMUNOLOGY-MICROBIOLOGY
CiteScore
26.20
自引率
2.30%
发文量
276
审稿时长
20 weeks
期刊介绍: Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses. The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries. This journal addresses topics of critical biological and clinical importance, including but not limited to: - Epidemic surveillance - Clinical manifestations - Diagnosis and management - Cellular and molecular pathogenesis - Innate and acquired immune responses between emerging microbes and their hosts - Drug discovery - Vaccine development research Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.
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