Cargando…

Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas

Bacteria of the genus Sulfurimonas within the class Campylobacteria are predominant in global deep-sea hydrothermal environments and widespread in global oceans. However, only few bacteria of this group have been isolated, and their adaptations for these extreme environments remain poorly understood...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Shasha, Jiang, Lijing, Hu, Qitao, Cui, Liang, Zhu, Bitong, Fu, Xiaoteng, Lai, Qiliang, Shao, Zongze, Yang, Suping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952632/
https://www.ncbi.nlm.nih.gov/pubmed/33717015
http://dx.doi.org/10.3389/fmicb.2021.626705
_version_ 1783663770189430784
author Wang, Shasha
Jiang, Lijing
Hu, Qitao
Cui, Liang
Zhu, Bitong
Fu, Xiaoteng
Lai, Qiliang
Shao, Zongze
Yang, Suping
author_facet Wang, Shasha
Jiang, Lijing
Hu, Qitao
Cui, Liang
Zhu, Bitong
Fu, Xiaoteng
Lai, Qiliang
Shao, Zongze
Yang, Suping
author_sort Wang, Shasha
collection PubMed
description Bacteria of the genus Sulfurimonas within the class Campylobacteria are predominant in global deep-sea hydrothermal environments and widespread in global oceans. However, only few bacteria of this group have been isolated, and their adaptations for these extreme environments remain poorly understood. Here, we report a novel mesophilic, hydrogen- and sulfur-oxidizing bacterium, strain NW10(T), isolated from a deep-sea sulfide chimney of Northwest Indian Ocean.16S rRNA gene sequence analysis showed that strain NW10(T) was most closely related to the vent species Sulfurimonas paralvinellae GO25(T) with 95.8% similarity, but ANI and DDH values between two strains were only 19.20 and 24.70%, respectively, indicating that strain NW10 represents a novel species. Phenotypic characterization showed strain NW10(T) is an obligate chemolithoautotroph utilizing thiosulfate, sulfide, elemental sulfur, or molecular hydrogen as energy sources, and molecular oxygen, nitrate, or elemental sulfur as electron acceptors. Moreover, hydrogen supported a better growth than reduced sulfur compounds. During thiosulfate oxidation, the strain can produce extracellular sulfur of elemental α-S(8) with an unknown mechanism. Polyphasic taxonomy results support that strain NW10(T) represents a novel species of the genus Sulfurimonas, and named as Sulfurimonas hydrogeniphila sp. nov. Genome analyses revealed its diverse energy metabolisms driving carbon fixation via rTCA cycling, including pathways of sulfur/hydrogen oxidation, coupled oxygen/sulfur respiration and denitrification. Comparative analysis of the 11 available genomes from Sulfurimonas species revealed that vent bacteria, compared to marine non-vent strains, possess unique genes encoding Type V Sqr, Group II, and Coo hydrogenase, and are selectively enriched in genes related to signal transduction and inorganic ion transporters. These phenotypic and genotypic features of vent Sulfurimonas may explain their thriving in hydrothermal environments and help to understand the ecological role of Sulfurimonas bacteria in hydrothermal ecosystems.
format Online
Article
Text
id pubmed-7952632
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-79526322021-03-13 Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas Wang, Shasha Jiang, Lijing Hu, Qitao Cui, Liang Zhu, Bitong Fu, Xiaoteng Lai, Qiliang Shao, Zongze Yang, Suping Front Microbiol Microbiology Bacteria of the genus Sulfurimonas within the class Campylobacteria are predominant in global deep-sea hydrothermal environments and widespread in global oceans. However, only few bacteria of this group have been isolated, and their adaptations for these extreme environments remain poorly understood. Here, we report a novel mesophilic, hydrogen- and sulfur-oxidizing bacterium, strain NW10(T), isolated from a deep-sea sulfide chimney of Northwest Indian Ocean.16S rRNA gene sequence analysis showed that strain NW10(T) was most closely related to the vent species Sulfurimonas paralvinellae GO25(T) with 95.8% similarity, but ANI and DDH values between two strains were only 19.20 and 24.70%, respectively, indicating that strain NW10 represents a novel species. Phenotypic characterization showed strain NW10(T) is an obligate chemolithoautotroph utilizing thiosulfate, sulfide, elemental sulfur, or molecular hydrogen as energy sources, and molecular oxygen, nitrate, or elemental sulfur as electron acceptors. Moreover, hydrogen supported a better growth than reduced sulfur compounds. During thiosulfate oxidation, the strain can produce extracellular sulfur of elemental α-S(8) with an unknown mechanism. Polyphasic taxonomy results support that strain NW10(T) represents a novel species of the genus Sulfurimonas, and named as Sulfurimonas hydrogeniphila sp. nov. Genome analyses revealed its diverse energy metabolisms driving carbon fixation via rTCA cycling, including pathways of sulfur/hydrogen oxidation, coupled oxygen/sulfur respiration and denitrification. Comparative analysis of the 11 available genomes from Sulfurimonas species revealed that vent bacteria, compared to marine non-vent strains, possess unique genes encoding Type V Sqr, Group II, and Coo hydrogenase, and are selectively enriched in genes related to signal transduction and inorganic ion transporters. These phenotypic and genotypic features of vent Sulfurimonas may explain their thriving in hydrothermal environments and help to understand the ecological role of Sulfurimonas bacteria in hydrothermal ecosystems. Frontiers Media S.A. 2021-02-26 /pmc/articles/PMC7952632/ /pubmed/33717015 http://dx.doi.org/10.3389/fmicb.2021.626705 Text en Copyright © 2021 Wang, Jiang, Hu, Cui, Zhu, Fu, Lai, Shao and Yang. http://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
Wang, Shasha
Jiang, Lijing
Hu, Qitao
Cui, Liang
Zhu, Bitong
Fu, Xiaoteng
Lai, Qiliang
Shao, Zongze
Yang, Suping
Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas
title Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas
title_full Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas
title_fullStr Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas
title_full_unstemmed Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas
title_short Characterization of Sulfurimonas hydrogeniphila sp. nov., a Novel Bacterium Predominant in Deep-Sea Hydrothermal Vents and Comparative Genomic Analyses of the Genus Sulfurimonas
title_sort characterization of sulfurimonas hydrogeniphila sp. nov., a novel bacterium predominant in deep-sea hydrothermal vents and comparative genomic analyses of the genus sulfurimonas
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952632/
https://www.ncbi.nlm.nih.gov/pubmed/33717015
http://dx.doi.org/10.3389/fmicb.2021.626705
work_keys_str_mv AT wangshasha characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT jianglijing characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT huqitao characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT cuiliang characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT zhubitong characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT fuxiaoteng characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT laiqiliang characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT shaozongze characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas
AT yangsuping characterizationofsulfurimonashydrogeniphilaspnovanovelbacteriumpredominantindeepseahydrothermalventsandcomparativegenomicanalysesofthegenussulfurimonas