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Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes
BACKGROUND: Hospital wastewaters contain fecal material from a large number of individuals, of which many are undergoing antibiotic therapy. It is, thus, plausible that hospital wastewaters could provide opportunities to find novel carbapenemases and other resistance genes not yet described in clini...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598227/ https://www.ncbi.nlm.nih.gov/pubmed/31248462 http://dx.doi.org/10.1186/s40168-019-0710-x |
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author | Marathe, Nachiket P. Berglund, Fanny Razavi, Mohammad Pal, Chandan Dröge, Johannes Samant, Sharvari Kristiansson, Erik Larsson, D. G. Joakim |
author_facet | Marathe, Nachiket P. Berglund, Fanny Razavi, Mohammad Pal, Chandan Dröge, Johannes Samant, Sharvari Kristiansson, Erik Larsson, D. G. Joakim |
author_sort | Marathe, Nachiket P. |
collection | PubMed |
description | BACKGROUND: Hospital wastewaters contain fecal material from a large number of individuals, of which many are undergoing antibiotic therapy. It is, thus, plausible that hospital wastewaters could provide opportunities to find novel carbapenemases and other resistance genes not yet described in clinical strains. Our aim was therefore to investigate the microbiota and antibiotic resistome of hospital effluent collected from the city of Mumbai, India, with a special focus on identifying novel carbapenemases. RESULTS: Shotgun metagenomics revealed a total of 112 different mobile antibiotic resistance gene types, conferring resistance against almost all classes of antibiotics. Beta-lactamase genes, including encoding clinically important carbapenemases, such as NDM, VIM, IMP, KPC, and OXA-48, were abundant. NDM (0.9% relative abundance to 16S rRNA genes) was the most common carbapenemase gene, followed by OXA-58 (0.84% relative abundance to 16S rRNA genes). Among the investigated mobile genetic elements, class 1 integrons (11% relative abundance to 16S rRNA genes) were the most abundant. The genus Acinetobacter accounted for as many as 30% of the total 16S rRNA reads, with A. baumannii accounting for an estimated 2.5%. High throughput sequencing of amplified integron gene cassettes identified a novel functional variant of an IMP-type (proposed IMP-81) carbapenemase gene (eight aa substitutions) along with recently described novel resistance genes like sul4 and bla(RSA1). Using a computational hidden Markov model, we detected 27 unique metallo-beta-lactamase (MBL) genes in the shotgun data, of which nine were novel subclass B1 genes, one novel subclass B2, and 10 novel subclass B3 genes. Six of the seven novel MBL genes were functional when expressed in Escherichia coli. CONCLUSION: By exploring hospital wastewater from India, our understanding of the diversity of carbapenemases has been extended. The study also demonstrates that the microbiota of hospital wastewater can serve as a reservoir of novel resistance genes, including previously uncharacterized carbapenemases with the potential to spread further. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0710-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6598227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65982272019-07-11 Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes Marathe, Nachiket P. Berglund, Fanny Razavi, Mohammad Pal, Chandan Dröge, Johannes Samant, Sharvari Kristiansson, Erik Larsson, D. G. Joakim Microbiome Short Report BACKGROUND: Hospital wastewaters contain fecal material from a large number of individuals, of which many are undergoing antibiotic therapy. It is, thus, plausible that hospital wastewaters could provide opportunities to find novel carbapenemases and other resistance genes not yet described in clinical strains. Our aim was therefore to investigate the microbiota and antibiotic resistome of hospital effluent collected from the city of Mumbai, India, with a special focus on identifying novel carbapenemases. RESULTS: Shotgun metagenomics revealed a total of 112 different mobile antibiotic resistance gene types, conferring resistance against almost all classes of antibiotics. Beta-lactamase genes, including encoding clinically important carbapenemases, such as NDM, VIM, IMP, KPC, and OXA-48, were abundant. NDM (0.9% relative abundance to 16S rRNA genes) was the most common carbapenemase gene, followed by OXA-58 (0.84% relative abundance to 16S rRNA genes). Among the investigated mobile genetic elements, class 1 integrons (11% relative abundance to 16S rRNA genes) were the most abundant. The genus Acinetobacter accounted for as many as 30% of the total 16S rRNA reads, with A. baumannii accounting for an estimated 2.5%. High throughput sequencing of amplified integron gene cassettes identified a novel functional variant of an IMP-type (proposed IMP-81) carbapenemase gene (eight aa substitutions) along with recently described novel resistance genes like sul4 and bla(RSA1). Using a computational hidden Markov model, we detected 27 unique metallo-beta-lactamase (MBL) genes in the shotgun data, of which nine were novel subclass B1 genes, one novel subclass B2, and 10 novel subclass B3 genes. Six of the seven novel MBL genes were functional when expressed in Escherichia coli. CONCLUSION: By exploring hospital wastewater from India, our understanding of the diversity of carbapenemases has been extended. The study also demonstrates that the microbiota of hospital wastewater can serve as a reservoir of novel resistance genes, including previously uncharacterized carbapenemases with the potential to spread further. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-019-0710-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-27 /pmc/articles/PMC6598227/ /pubmed/31248462 http://dx.doi.org/10.1186/s40168-019-0710-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Marathe, Nachiket P. Berglund, Fanny Razavi, Mohammad Pal, Chandan Dröge, Johannes Samant, Sharvari Kristiansson, Erik Larsson, D. G. Joakim Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes |
title | Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes |
title_full | Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes |
title_fullStr | Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes |
title_full_unstemmed | Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes |
title_short | Sewage effluent from an Indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes |
title_sort | sewage effluent from an indian hospital harbors novel carbapenemases and integron-borne antibiotic resistance genes |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598227/ https://www.ncbi.nlm.nih.gov/pubmed/31248462 http://dx.doi.org/10.1186/s40168-019-0710-x |
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