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Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis

The genus Vibrio is ubiquitous in marine environments and uses numerous evolutionary characteristics and survival strategies in order to occupy its niche. Here, a newly identified species, Vibrio fujianensis, was deeply explored to reveal a unique environmental adaptability. V. fujianensis type stra...

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Autores principales: Huang, Zhenzhou, Yu, Keyi, Fang, Yujie, Dai, Hang, Cai, Hongyan, Li, Zhenpeng, Kan, Biao, Wei, Qiang, Wang, Duochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232310/
https://www.ncbi.nlm.nih.gov/pubmed/32294952
http://dx.doi.org/10.3390/microorganisms8040555
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author Huang, Zhenzhou
Yu, Keyi
Fang, Yujie
Dai, Hang
Cai, Hongyan
Li, Zhenpeng
Kan, Biao
Wei, Qiang
Wang, Duochun
author_facet Huang, Zhenzhou
Yu, Keyi
Fang, Yujie
Dai, Hang
Cai, Hongyan
Li, Zhenpeng
Kan, Biao
Wei, Qiang
Wang, Duochun
author_sort Huang, Zhenzhou
collection PubMed
description The genus Vibrio is ubiquitous in marine environments and uses numerous evolutionary characteristics and survival strategies in order to occupy its niche. Here, a newly identified species, Vibrio fujianensis, was deeply explored to reveal a unique environmental adaptability. V. fujianensis type strain FJ201301(T) shared 817 core genes with the Vibrio species in the population genomic analysis, but possessed unique genes of its own. In addition, V. fujianensis FJ201301(T) was predicated to carry 106 virulence-related factors, several of which were mostly found in other pathogenic Vibrio species. Moreover, a comparative transcriptome analysis between the low-salt (1% NaCl) and high-salt (8% NaCl) condition was conducted to identify the genes involved in salt tolerance. A total of 913 unigenes were found to be differentially expressed. In a high-salt condition, 577 genes were significantly upregulated, whereas 336 unigenes were significantly downregulated. Notably, differentially expressed genes have a significant association with ribosome structural component and ribosome metabolism, which may play a role in salt tolerance. Transcriptional changes in ribosome genes indicate that V. fujianensis may have gained a predominant advantage in order to adapt to the changing environment. In conclusion, to survive in adversity, V. fujianensis has enhanced its environmental adaptability and developed various strategies to fill its niche.
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spelling pubmed-72323102020-05-22 Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis Huang, Zhenzhou Yu, Keyi Fang, Yujie Dai, Hang Cai, Hongyan Li, Zhenpeng Kan, Biao Wei, Qiang Wang, Duochun Microorganisms Article The genus Vibrio is ubiquitous in marine environments and uses numerous evolutionary characteristics and survival strategies in order to occupy its niche. Here, a newly identified species, Vibrio fujianensis, was deeply explored to reveal a unique environmental adaptability. V. fujianensis type strain FJ201301(T) shared 817 core genes with the Vibrio species in the population genomic analysis, but possessed unique genes of its own. In addition, V. fujianensis FJ201301(T) was predicated to carry 106 virulence-related factors, several of which were mostly found in other pathogenic Vibrio species. Moreover, a comparative transcriptome analysis between the low-salt (1% NaCl) and high-salt (8% NaCl) condition was conducted to identify the genes involved in salt tolerance. A total of 913 unigenes were found to be differentially expressed. In a high-salt condition, 577 genes were significantly upregulated, whereas 336 unigenes were significantly downregulated. Notably, differentially expressed genes have a significant association with ribosome structural component and ribosome metabolism, which may play a role in salt tolerance. Transcriptional changes in ribosome genes indicate that V. fujianensis may have gained a predominant advantage in order to adapt to the changing environment. In conclusion, to survive in adversity, V. fujianensis has enhanced its environmental adaptability and developed various strategies to fill its niche. MDPI 2020-04-13 /pmc/articles/PMC7232310/ /pubmed/32294952 http://dx.doi.org/10.3390/microorganisms8040555 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Huang, Zhenzhou
Yu, Keyi
Fang, Yujie
Dai, Hang
Cai, Hongyan
Li, Zhenpeng
Kan, Biao
Wei, Qiang
Wang, Duochun
Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis
title Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis
title_full Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis
title_fullStr Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis
title_full_unstemmed Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis
title_short Comparative Genomics and Transcriptomics Analyses Reveal a Unique Environmental Adaptability of Vibrio fujianensis
title_sort comparative genomics and transcriptomics analyses reveal a unique environmental adaptability of vibrio fujianensis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232310/
https://www.ncbi.nlm.nih.gov/pubmed/32294952
http://dx.doi.org/10.3390/microorganisms8040555
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