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Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome

BACKGROUND: Hadal zone of the deep-sea trenches accommodates microbial life under extreme energy limitations and environmental conditions, such as low temperature, high pressure, and low organic matter down to 11,000 m below sea level. However, microbial pathogenicity, resistance, and adaptation the...

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Autores principales: He, Liuqing, Huang, Xinyu, Zhang, Guoqing, Yuan, Ling, Shen, Enhui, Zhang, Lu, Zhang, Xiao-Hua, Zhang, Tong, Tao, Liang, Ju, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036809/
https://www.ncbi.nlm.nih.gov/pubmed/35468809
http://dx.doi.org/10.1186/s40793-022-00413-5
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author He, Liuqing
Huang, Xinyu
Zhang, Guoqing
Yuan, Ling
Shen, Enhui
Zhang, Lu
Zhang, Xiao-Hua
Zhang, Tong
Tao, Liang
Ju, Feng
author_facet He, Liuqing
Huang, Xinyu
Zhang, Guoqing
Yuan, Ling
Shen, Enhui
Zhang, Lu
Zhang, Xiao-Hua
Zhang, Tong
Tao, Liang
Ju, Feng
author_sort He, Liuqing
collection PubMed
description BACKGROUND: Hadal zone of the deep-sea trenches accommodates microbial life under extreme energy limitations and environmental conditions, such as low temperature, high pressure, and low organic matter down to 11,000 m below sea level. However, microbial pathogenicity, resistance, and adaptation therein remain unknown. Here we used culture-independent metagenomic approaches to explore the virulence and antibiotic resistance in the hadal microbiota of the Mariana Trench. RESULTS: The results indicate that the 10,898 m Challenger Deep bottom sediment harbored prosperous microbiota with contrasting signatures of virulence factors and antibiotic resistance, compared with the neighboring but shallower 6038 m steep wall site and the more nearshore 5856 m Pacific basin site. Virulence genes including several famous large translocating virulence genes (e.g., botulinum neurotoxins, tetanus neurotoxin, and Clostridium difficile toxins) were uniquely detected in the trench bottom. However, the shallower and more nearshore site sediment had a higher abundance and richer diversity of known antibiotic resistance genes (ARGs), especially for those clinically relevant ones (e.g., fosX, sul1, and TEM-family extended-spectrum beta-lactamases), revealing resistance selection under anthropogenic stresses. Further analysis of mobilome (i.e., the collection of mobile genetic elements, MGEs) suggests horizontal gene transfer mediated by phage and integrase as the major mechanism for the evolution of Mariana Trench sediment bacteria. Notably, contig-level co-occurring and taxonomic analysis shows emerging evidence for substantial co-selection of virulence genes and ARGs in taxonomically diverse bacteria in the hadal sediment, especially for the Challenger Deep bottom where mobilized ARGs and virulence genes are favorably enriched in largely unexplored bacteria. CONCLUSIONS: This study reports the landscape of virulence factors, antibiotic resistome, and mobilome in the sediment and seawater microbiota residing hadal environment of the deepest ocean bottom on earth. Our work unravels the contrasting and unique features of virulence genes, ARGs, and MGEs in the Mariana Trench bottom, providing new insights into the eco-environmental and biological processes underlying microbial pathogenicity, resistance, and adaptative evolution in the hadal environment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40793-022-00413-5.
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spelling pubmed-90368092022-04-26 Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome He, Liuqing Huang, Xinyu Zhang, Guoqing Yuan, Ling Shen, Enhui Zhang, Lu Zhang, Xiao-Hua Zhang, Tong Tao, Liang Ju, Feng Environ Microbiome Research Article BACKGROUND: Hadal zone of the deep-sea trenches accommodates microbial life under extreme energy limitations and environmental conditions, such as low temperature, high pressure, and low organic matter down to 11,000 m below sea level. However, microbial pathogenicity, resistance, and adaptation therein remain unknown. Here we used culture-independent metagenomic approaches to explore the virulence and antibiotic resistance in the hadal microbiota of the Mariana Trench. RESULTS: The results indicate that the 10,898 m Challenger Deep bottom sediment harbored prosperous microbiota with contrasting signatures of virulence factors and antibiotic resistance, compared with the neighboring but shallower 6038 m steep wall site and the more nearshore 5856 m Pacific basin site. Virulence genes including several famous large translocating virulence genes (e.g., botulinum neurotoxins, tetanus neurotoxin, and Clostridium difficile toxins) were uniquely detected in the trench bottom. However, the shallower and more nearshore site sediment had a higher abundance and richer diversity of known antibiotic resistance genes (ARGs), especially for those clinically relevant ones (e.g., fosX, sul1, and TEM-family extended-spectrum beta-lactamases), revealing resistance selection under anthropogenic stresses. Further analysis of mobilome (i.e., the collection of mobile genetic elements, MGEs) suggests horizontal gene transfer mediated by phage and integrase as the major mechanism for the evolution of Mariana Trench sediment bacteria. Notably, contig-level co-occurring and taxonomic analysis shows emerging evidence for substantial co-selection of virulence genes and ARGs in taxonomically diverse bacteria in the hadal sediment, especially for the Challenger Deep bottom where mobilized ARGs and virulence genes are favorably enriched in largely unexplored bacteria. CONCLUSIONS: This study reports the landscape of virulence factors, antibiotic resistome, and mobilome in the sediment and seawater microbiota residing hadal environment of the deepest ocean bottom on earth. Our work unravels the contrasting and unique features of virulence genes, ARGs, and MGEs in the Mariana Trench bottom, providing new insights into the eco-environmental and biological processes underlying microbial pathogenicity, resistance, and adaptative evolution in the hadal environment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40793-022-00413-5. BioMed Central 2022-04-25 /pmc/articles/PMC9036809/ /pubmed/35468809 http://dx.doi.org/10.1186/s40793-022-00413-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
He, Liuqing
Huang, Xinyu
Zhang, Guoqing
Yuan, Ling
Shen, Enhui
Zhang, Lu
Zhang, Xiao-Hua
Zhang, Tong
Tao, Liang
Ju, Feng
Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome
title Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome
title_full Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome
title_fullStr Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome
title_full_unstemmed Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome
title_short Distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome
title_sort distinctive signatures of pathogenic and antibiotic resistant potentials in the hadal microbiome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036809/
https://www.ncbi.nlm.nih.gov/pubmed/35468809
http://dx.doi.org/10.1186/s40793-022-00413-5
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