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Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean

A large amount of bacterial biomass is transferred from land to ocean annually. Most transferred bacteria should not survive, but undoubtedly some do. It is unclear what mechanisms these bacteria use in order to survive and even thrive in a new marine environment. Myroides profundi D25(T), a member...

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Autores principales: Zhang, Yu-Zhong, Li, Yi, Xie, Bin-Bin, Chen, Xiu-Lan, Yao, Qiong-Qiong, Zhang, Xi-Ying, Kempher, Megan L., Zhou, Jizhong, Oren, Aharon, Qin, Qi-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725012/
https://www.ncbi.nlm.nih.gov/pubmed/26758181
http://dx.doi.org/10.1128/mBio.01946-15
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author Zhang, Yu-Zhong
Li, Yi
Xie, Bin-Bin
Chen, Xiu-Lan
Yao, Qiong-Qiong
Zhang, Xi-Ying
Kempher, Megan L.
Zhou, Jizhong
Oren, Aharon
Qin, Qi-Long
author_facet Zhang, Yu-Zhong
Li, Yi
Xie, Bin-Bin
Chen, Xiu-Lan
Yao, Qiong-Qiong
Zhang, Xi-Ying
Kempher, Megan L.
Zhou, Jizhong
Oren, Aharon
Qin, Qi-Long
author_sort Zhang, Yu-Zhong
collection PubMed
description A large amount of bacterial biomass is transferred from land to ocean annually. Most transferred bacteria should not survive, but undoubtedly some do. It is unclear what mechanisms these bacteria use in order to survive and even thrive in a new marine environment. Myroides profundi D25(T), a member of the Bacteroidetes phylum, was isolated from deep-sea sediment of the southern Okinawa Trough near the China mainland and had high genomic sequence identity to and synteny with the human opportunistic pathogen Myroides odoratimimus. Phylogenetic and physiological analyses suggested that M. profundi recently transitioned from land to the ocean. This provided an opportunity to explore how a bacterial genome evolved to survive in a novel environment. Changes in the transcriptome were evaluated when both species were cultured under low-salinity conditions and then transferred to high-salinity conditions. Comparative genomic and transcriptomic analyses showed that M. profundi altered transcription regulation in the early stages of survival. In these stages, vertically inherited genes played a key role in the survival of M. profundi. The contribution of M. profundi unique genes, some possibly acquired by horizontal gene transfer (HGT), appeared relatively small, and expression levels of unique genes were diminished under the high-salinity conditions. We postulate that HGT genes might play an important role in longer-term adaptation. These results suggested that some human pathogens might have the ability to survive in and adapt to the marine environment, which may have important implications for public health control in coastal regions.
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spelling pubmed-47250122016-01-28 Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean Zhang, Yu-Zhong Li, Yi Xie, Bin-Bin Chen, Xiu-Lan Yao, Qiong-Qiong Zhang, Xi-Ying Kempher, Megan L. Zhou, Jizhong Oren, Aharon Qin, Qi-Long mBio Research Article A large amount of bacterial biomass is transferred from land to ocean annually. Most transferred bacteria should not survive, but undoubtedly some do. It is unclear what mechanisms these bacteria use in order to survive and even thrive in a new marine environment. Myroides profundi D25(T), a member of the Bacteroidetes phylum, was isolated from deep-sea sediment of the southern Okinawa Trough near the China mainland and had high genomic sequence identity to and synteny with the human opportunistic pathogen Myroides odoratimimus. Phylogenetic and physiological analyses suggested that M. profundi recently transitioned from land to the ocean. This provided an opportunity to explore how a bacterial genome evolved to survive in a novel environment. Changes in the transcriptome were evaluated when both species were cultured under low-salinity conditions and then transferred to high-salinity conditions. Comparative genomic and transcriptomic analyses showed that M. profundi altered transcription regulation in the early stages of survival. In these stages, vertically inherited genes played a key role in the survival of M. profundi. The contribution of M. profundi unique genes, some possibly acquired by horizontal gene transfer (HGT), appeared relatively small, and expression levels of unique genes were diminished under the high-salinity conditions. We postulate that HGT genes might play an important role in longer-term adaptation. These results suggested that some human pathogens might have the ability to survive in and adapt to the marine environment, which may have important implications for public health control in coastal regions. American Society of Microbiology 2016-01-12 /pmc/articles/PMC4725012/ /pubmed/26758181 http://dx.doi.org/10.1128/mBio.01946-15 Text en Copyright © 2016 Zhang et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhang, Yu-Zhong
Li, Yi
Xie, Bin-Bin
Chen, Xiu-Lan
Yao, Qiong-Qiong
Zhang, Xi-Ying
Kempher, Megan L.
Zhou, Jizhong
Oren, Aharon
Qin, Qi-Long
Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean
title Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean
title_full Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean
title_fullStr Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean
title_full_unstemmed Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean
title_short Nascent Genomic Evolution and Allopatric Speciation of Myroides profundi D25 in Its Transition from Land to Ocean
title_sort nascent genomic evolution and allopatric speciation of myroides profundi d25 in its transition from land to ocean
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725012/
https://www.ncbi.nlm.nih.gov/pubmed/26758181
http://dx.doi.org/10.1128/mBio.01946-15
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