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Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii

Bacteriophages function as a regulator of host communities and metabolism. Many phages have been isolated and sequenced in environments such as the ocean, but very little is known about hypersaline environments. Phages infecting members of the genus Chromohalobacter remain poorly understood, and no...

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Autores principales: Yi, Hao, Fu, Chaoqun, Diao, Kaixin, Li, Zhiying, Cui, Xiaolong, Xiao, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769972/
https://www.ncbi.nlm.nih.gov/pubmed/36569053
http://dx.doi.org/10.3389/fmicb.2022.1041471
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author Yi, Hao
Fu, Chaoqun
Diao, Kaixin
Li, Zhiying
Cui, Xiaolong
Xiao, Wei
author_facet Yi, Hao
Fu, Chaoqun
Diao, Kaixin
Li, Zhiying
Cui, Xiaolong
Xiao, Wei
author_sort Yi, Hao
collection PubMed
description Bacteriophages function as a regulator of host communities and metabolism. Many phages have been isolated and sequenced in environments such as the ocean, but very little is known about hypersaline environments. Phages infecting members of the genus Chromohalobacter remain poorly understood, and no Chromohalobacter phage genome has been reported. In this study, a halovirus infecting Chromohalobacter sp. F3, YPCBV-1, was isolated from Yipinglang salt mine. YPCBV-1 could only infect host strain F3 with burst size of 6.3 PFU/cell. It could produce progeny in 5%–20% (w/v) NaCl with an optimal concentration of 10% (w/v), but the optimal adsorption NaCl concentration was 5%–8% (w/v). YPCBV-1 is sensitive to pure water and depends on NaCl or KCl solutions to survive. YPCBV-1 stability increased with increasing salinity but decreased in NaCl saturated solutions, and it has a broader salinity adaptation than the host. YPCBV-1 has a double-stranded DNA of 36,002 bp with a G + C content of 67.09% and contains a total of 55 predicted ORFs and no tRNA genes. Phylogenetic analysis and genomic network analysis suggested that YPCBV-1 is a novel Mu-like phage under the class Caudoviricetes. Auxiliary metabolic gene, SUMF1/EgtB/PvdO family non-heme iron enzyme, with possible roles in antioxidant was found in YPCBV-1. Moreover, DGR-associated genes were predicted in YPCBV-1 genome, which potentially produce hypervariable phage tail fiber. These findings shed light on the halovirus-host interaction in hypersaline environments.
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spelling pubmed-97699722022-12-22 Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii Yi, Hao Fu, Chaoqun Diao, Kaixin Li, Zhiying Cui, Xiaolong Xiao, Wei Front Microbiol Microbiology Bacteriophages function as a regulator of host communities and metabolism. Many phages have been isolated and sequenced in environments such as the ocean, but very little is known about hypersaline environments. Phages infecting members of the genus Chromohalobacter remain poorly understood, and no Chromohalobacter phage genome has been reported. In this study, a halovirus infecting Chromohalobacter sp. F3, YPCBV-1, was isolated from Yipinglang salt mine. YPCBV-1 could only infect host strain F3 with burst size of 6.3 PFU/cell. It could produce progeny in 5%–20% (w/v) NaCl with an optimal concentration of 10% (w/v), but the optimal adsorption NaCl concentration was 5%–8% (w/v). YPCBV-1 is sensitive to pure water and depends on NaCl or KCl solutions to survive. YPCBV-1 stability increased with increasing salinity but decreased in NaCl saturated solutions, and it has a broader salinity adaptation than the host. YPCBV-1 has a double-stranded DNA of 36,002 bp with a G + C content of 67.09% and contains a total of 55 predicted ORFs and no tRNA genes. Phylogenetic analysis and genomic network analysis suggested that YPCBV-1 is a novel Mu-like phage under the class Caudoviricetes. Auxiliary metabolic gene, SUMF1/EgtB/PvdO family non-heme iron enzyme, with possible roles in antioxidant was found in YPCBV-1. Moreover, DGR-associated genes were predicted in YPCBV-1 genome, which potentially produce hypervariable phage tail fiber. These findings shed light on the halovirus-host interaction in hypersaline environments. Frontiers Media S.A. 2022-12-07 /pmc/articles/PMC9769972/ /pubmed/36569053 http://dx.doi.org/10.3389/fmicb.2022.1041471 Text en Copyright © 2022 Yi, Fu, Diao, Li, Cui and Xiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yi, Hao
Fu, Chaoqun
Diao, Kaixin
Li, Zhiying
Cui, Xiaolong
Xiao, Wei
Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii
title Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii
title_full Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii
title_fullStr Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii
title_full_unstemmed Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii
title_short Characterization and genomic analysis of a novel halovirus infecting Chromohalobacter beijerinckii
title_sort characterization and genomic analysis of a novel halovirus infecting chromohalobacter beijerinckii
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769972/
https://www.ncbi.nlm.nih.gov/pubmed/36569053
http://dx.doi.org/10.3389/fmicb.2022.1041471
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