A novel virus potentially evolved from the N4-like viruses represents a unique viral family: Poorviridae.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2024-12-18 Epub Date: 2024-11-21 DOI:10.1128/aem.01559-24
Wei Wang, Hongmin Wang, Xiao Zou, Yundan Liu, Kaiyang Zheng, Xin Chen, Xinyi Wang, Shujuan Sun, Yang Yang, Min Wang, Hongbing Shao, Yantao Liang
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引用次数: 0

Abstract

Pseudoalteromonas are widely distributed in marine extreme habitats and exhibit diverse extracellular protease activity, which is essential for marine biogeochemical cycles. However, our understanding of viruses that infect Pseudoalteromonas remains limited. This study isolated a virus infecting Pseudoalteromonas nigrifaciens from Xiaogang in Qingdao, China. vB_PunP_Y3 comprises a linear, double-strand DNA genome with a length of 48,854 bp, encoding 52 putative open reading frames. Transmission electron microscopy demonstrates the short-tailed morphology of vB_PunP_Y3. Phylogenetic and genome-content-based analysis indicate that vB_PunP_Y3 represents a novel virus family named as Poorviridae, along with three high-quality uncultivated viral genomes. Biogeographical analyses show that Poorviridae is distributed across five viral ecological zones, and is predominantly detected in the Antarctic, Arctic, and bathypelagic zones. Comparative genomics analyses identified three of the seven hallmark proteins of N4-like viruses (DNA polymerase, major capsid protein, and virion-encapsulated RNA polymerase) from vB_PunP_Y3, combing with the protein tertiary structures of the major capsid protein, suggesting that vB_PunP_Y3 might evolve from the N4-like viruses.

Importance: vB_PunP_Y3 is a unique strain containing three of the seven hallmark proteins of N4-like viruses, but is grouped into a novel family-level viral cluster with three uncultured viruses from metagenomics, named Poorviridae. This study enhanced the understanding about the genetic diversity, evolution, and distribution of Pseudoalteromonas viruses and provided insights into the novel evolution mechanism of marine viruses.

一种可能由类似 N4 病毒进化而来的新型病毒代表了一个独特的病毒科:穷病毒科
假交替单胞菌广泛分布于海洋极端栖息地,具有多种胞外蛋白酶活性,对海洋生物地球化学循环至关重要。然而,我们对感染假交替单胞菌的病毒的了解仍然有限。vB_PunP_Y3 由线性双链 DNA 基因组组成,长度为 48,854 bp,编码 52 个推测开放阅读框。透射电子显微镜显示了 vB_PunP_Y3 的短尾形态。基于系统发育和基因组内容的分析表明,vB_PunP_Y3 代表了一个新的病毒科,被命名为 Poorviridae,同时还有三个高质量的未培养病毒基因组。生物地理学分析表明,Poorviridae 分布在五个病毒生态区,主要在南极、北极和深海区发现。比较基因组学分析从vB_PunP_Y3中发现了类N4病毒7种标志蛋白中的3种(DNA聚合酶、主要噬菌体蛋白和病毒包被的RNA聚合酶),结合主要噬菌体蛋白的蛋白质三级结构,表明vB_PunP_Y3可能是从类N4病毒进化而来。重要意义:vB_PunP_Y3是一个独特的毒株,含有N4样病毒7个标志蛋白中的3个,但与元基因组学中3个未培养的病毒组成了一个新的科级病毒集群,命名为Poorviridae。这项研究加深了对假交替单胞菌病毒的遗传多样性、进化和分布的认识,并为了解海洋病毒的新型进化机制提供了见解。
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
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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