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Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome

BACKGROUND: The Central Indian gut microbiome remains grossly understudied. Herein, we sought to investigate the burden of antimicrobial resistance and diarrheal diseases, particularly Clostridioides difficile, in rural-agricultural and urban populations in Central India, where there is widespread u...

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Autores principales: Monaghan, Tanya M., Sloan, Tim J., Stockdale, Stephen R., Blanchard, Adam M., Emes, Richard D., Wilcox, Mark, Biswas, Rima, Nashine, Rupam, Manke, Sonali, Gandhi, Jinal, Jain, Pratishtha, Bhotmange, Shrejal, Ambalkar, Shrikant, Satav, Ashish, Draper, Lorraine A., Hill, Colin, Kashyap, Rajpal Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781581/
https://www.ncbi.nlm.nih.gov/pubmed/32459982
http://dx.doi.org/10.1080/19490976.2020.1752605
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author Monaghan, Tanya M.
Sloan, Tim J.
Stockdale, Stephen R.
Blanchard, Adam M.
Emes, Richard D.
Wilcox, Mark
Biswas, Rima
Nashine, Rupam
Manke, Sonali
Gandhi, Jinal
Jain, Pratishtha
Bhotmange, Shrejal
Ambalkar, Shrikant
Satav, Ashish
Draper, Lorraine A.
Hill, Colin
Kashyap, Rajpal Singh
author_facet Monaghan, Tanya M.
Sloan, Tim J.
Stockdale, Stephen R.
Blanchard, Adam M.
Emes, Richard D.
Wilcox, Mark
Biswas, Rima
Nashine, Rupam
Manke, Sonali
Gandhi, Jinal
Jain, Pratishtha
Bhotmange, Shrejal
Ambalkar, Shrikant
Satav, Ashish
Draper, Lorraine A.
Hill, Colin
Kashyap, Rajpal Singh
author_sort Monaghan, Tanya M.
collection PubMed
description BACKGROUND: The Central Indian gut microbiome remains grossly understudied. Herein, we sought to investigate the burden of antimicrobial resistance and diarrheal diseases, particularly Clostridioides difficile, in rural-agricultural and urban populations in Central India, where there is widespread unregulated antibiotic use. We utilized shotgun metagenomics to comprehensively characterize the bacterial and viral fractions of the gut microbiome and their encoded functions in 105 participants. RESULTS: We observed distinct rural-urban differences in bacterial and viral populations, with geography exhibiting a greater influence than diarrheal status. Clostridioides difficile disease was more commonly observed in urban subjects, and their microbiomes were enriched in metabolic pathways relating to the metabolism of industrial compounds and genes encoding resistance to 3(rd) generation cephalosporins and carbapenems. By linking phages present in the microbiome to their bacterial hosts through CRISPR spacers, phage variation could be directly related to shifts in bacterial populations, with the auxiliary metabolic potential of rural-associated phages enriched for carbon and amino acid energy metabolism. CONCLUSIONS: We report distinct differences in antimicrobial resistance gene profiles, enrichment of metabolic pathways and phage composition between rural and urban populations, as well as a higher burden of Clostridioides difficile disease in the urban population. Our results reveal that geography is the key driver of variation in urban and rural Indian microbiomes, with acute diarrheal disease, including C. difficile disease exerting a lesser impact. Future studies will be required to understand the potential role of dietary, cultural, and genetic factors in contributing to microbiome differences between rural and urban populations.
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spelling pubmed-77815812021-01-13 Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome Monaghan, Tanya M. Sloan, Tim J. Stockdale, Stephen R. Blanchard, Adam M. Emes, Richard D. Wilcox, Mark Biswas, Rima Nashine, Rupam Manke, Sonali Gandhi, Jinal Jain, Pratishtha Bhotmange, Shrejal Ambalkar, Shrikant Satav, Ashish Draper, Lorraine A. Hill, Colin Kashyap, Rajpal Singh Gut Microbes Research Paper BACKGROUND: The Central Indian gut microbiome remains grossly understudied. Herein, we sought to investigate the burden of antimicrobial resistance and diarrheal diseases, particularly Clostridioides difficile, in rural-agricultural and urban populations in Central India, where there is widespread unregulated antibiotic use. We utilized shotgun metagenomics to comprehensively characterize the bacterial and viral fractions of the gut microbiome and their encoded functions in 105 participants. RESULTS: We observed distinct rural-urban differences in bacterial and viral populations, with geography exhibiting a greater influence than diarrheal status. Clostridioides difficile disease was more commonly observed in urban subjects, and their microbiomes were enriched in metabolic pathways relating to the metabolism of industrial compounds and genes encoding resistance to 3(rd) generation cephalosporins and carbapenems. By linking phages present in the microbiome to their bacterial hosts through CRISPR spacers, phage variation could be directly related to shifts in bacterial populations, with the auxiliary metabolic potential of rural-associated phages enriched for carbon and amino acid energy metabolism. CONCLUSIONS: We report distinct differences in antimicrobial resistance gene profiles, enrichment of metabolic pathways and phage composition between rural and urban populations, as well as a higher burden of Clostridioides difficile disease in the urban population. Our results reveal that geography is the key driver of variation in urban and rural Indian microbiomes, with acute diarrheal disease, including C. difficile disease exerting a lesser impact. Future studies will be required to understand the potential role of dietary, cultural, and genetic factors in contributing to microbiome differences between rural and urban populations. Taylor & Francis 2020-05-27 /pmc/articles/PMC7781581/ /pubmed/32459982 http://dx.doi.org/10.1080/19490976.2020.1752605 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Monaghan, Tanya M.
Sloan, Tim J.
Stockdale, Stephen R.
Blanchard, Adam M.
Emes, Richard D.
Wilcox, Mark
Biswas, Rima
Nashine, Rupam
Manke, Sonali
Gandhi, Jinal
Jain, Pratishtha
Bhotmange, Shrejal
Ambalkar, Shrikant
Satav, Ashish
Draper, Lorraine A.
Hill, Colin
Kashyap, Rajpal Singh
Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome
title Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome
title_full Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome
title_fullStr Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome
title_full_unstemmed Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome
title_short Metagenomics reveals impact of geography and acute diarrheal disease on the Central Indian human gut microbiome
title_sort metagenomics reveals impact of geography and acute diarrheal disease on the central indian human gut microbiome
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781581/
https://www.ncbi.nlm.nih.gov/pubmed/32459982
http://dx.doi.org/10.1080/19490976.2020.1752605
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