Insights into the genomic features and lifestyle of B1 subcluster mycobacteriophages

IF 3.5 4区 生物学 Q2 MICROBIOLOGY
Ritam Das, Ritu Arora, Kanika Nadar, Saroj Saroj, Amit K. Singh, Shripad A. Patil, Sunil K. Raman, Amit Misra, Urmi Bajpai
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引用次数: 0

Abstract

Bacteriophages infecting Mycobacterium smegmatis mc2155 are numerous and, hence, are classified into clusters based on nucleotide sequence similarity. Analyzing phages belonging to clusters/subclusters can help gain deeper insights into their biological features and potential therapeutic applications. In this study, for genomic characterization of B1 subcluster mycobacteriophages, a framework of online tools was developed, which enabled functional annotation of about 55% of the previously deemed hypothetical proteins in B1 phages. We also studied the phenotype, lysogeny status, and antimycobacterial activity of 10 B1 phages against biofilm and an antibiotic-resistant M. smegmatis strain (4XR1). All 10 phages belonged to the Siphoviridae family, appeared temperate based on their spontaneous release from the putative lysogens and showed antibiofilm activity. The highest inhibitory and disruptive effects on biofilm were 64% and 46%, respectively. This systematic characterization using a combination of genomic and experimental tools is a promising approach to furthering our understanding of viral dark matter.

洞察 B1 亚群噬菌体的基因组特征和生活方式。
感染烟曲霉分枝杆菌 mc2155 的噬菌体数量众多,因此根据核苷酸序列的相似性将其划分为多个噬菌体簇。分析属于簇/亚簇的噬菌体有助于深入了解它们的生物学特征和潜在的治疗应用。在这项研究中,为了描述 B1 亚簇噬菌体的基因组特征,我们开发了一个在线工具框架,该框架能够对 B1 噬菌体中约 55% 以前被认为是假定的蛋白质进行功能注释。我们还研究了 10 个 B1 噬菌体的表型、溶原状态以及对生物膜和抗生素耐药 M. smegmatis 菌株(4XR1)的抗分枝杆菌活性。所有 10 个噬菌体都属于 Siphoviridae 科,根据它们从假定溶原中自发释放的情况来看,它们似乎是温和的,并显示出了抗生物膜活性。对生物膜的最高抑制和破坏作用分别为 64% 和 46% 。这种结合基因组学和实验工具进行的系统特征描述是一种很有前途的方法,有助于我们进一步了解病毒暗物质。
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
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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