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Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members

β-lactamases are enzymes which are commonly produced by bacteria and which degrade the β-lactam ring of β-lactam antibiotics, namely penicillins, cephalosporins, carbapenems, and monobactams, and inactivate these antibiotics. We performed a rational and comprehensive investigation of β-lactamases in...

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Autores principales: Keshri, Vivek, Panda, Arup, Levasseur, Anthony, Rolain, Jean-Marc, Pontarotti, Pierre, Raoult, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905574/
https://www.ncbi.nlm.nih.gov/pubmed/29672703
http://dx.doi.org/10.1093/gbe/evy028
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author Keshri, Vivek
Panda, Arup
Levasseur, Anthony
Rolain, Jean-Marc
Pontarotti, Pierre
Raoult, Didier
author_facet Keshri, Vivek
Panda, Arup
Levasseur, Anthony
Rolain, Jean-Marc
Pontarotti, Pierre
Raoult, Didier
author_sort Keshri, Vivek
collection PubMed
description β-lactamases are enzymes which are commonly produced by bacteria and which degrade the β-lactam ring of β-lactam antibiotics, namely penicillins, cephalosporins, carbapenems, and monobactams, and inactivate these antibiotics. We performed a rational and comprehensive investigation of β-lactamases in different biological databases. In this study, we constructed hidden Markov model profiles as well as the ancestral sequence of four classes of β-lactamases (A, B, C, and D), which were used to identify potential β-lactamases from environmental metagenomic (1206), human microbiome metagenomic (6417), human microbiome reference genome (1310), and NCBI’s nonredundant databases (44101). Our analysis revealed the existence of putative β-lactamases in the metagenomic databases, which appeared to be similar to the four different molecular classes (A–D). This is the first report on the large-scale phylogenetic diversity of new members of β-lactamases, and our results revealed that metagenomic database dark-matter contains β-lactamase-like antibiotic resistance genes.
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spelling pubmed-59055742018-04-23 Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members Keshri, Vivek Panda, Arup Levasseur, Anthony Rolain, Jean-Marc Pontarotti, Pierre Raoult, Didier Genome Biol Evol Research Article β-lactamases are enzymes which are commonly produced by bacteria and which degrade the β-lactam ring of β-lactam antibiotics, namely penicillins, cephalosporins, carbapenems, and monobactams, and inactivate these antibiotics. We performed a rational and comprehensive investigation of β-lactamases in different biological databases. In this study, we constructed hidden Markov model profiles as well as the ancestral sequence of four classes of β-lactamases (A, B, C, and D), which were used to identify potential β-lactamases from environmental metagenomic (1206), human microbiome metagenomic (6417), human microbiome reference genome (1310), and NCBI’s nonredundant databases (44101). Our analysis revealed the existence of putative β-lactamases in the metagenomic databases, which appeared to be similar to the four different molecular classes (A–D). This is the first report on the large-scale phylogenetic diversity of new members of β-lactamases, and our results revealed that metagenomic database dark-matter contains β-lactamase-like antibiotic resistance genes. Oxford University Press 2018-03-05 /pmc/articles/PMC5905574/ /pubmed/29672703 http://dx.doi.org/10.1093/gbe/evy028 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Keshri, Vivek
Panda, Arup
Levasseur, Anthony
Rolain, Jean-Marc
Pontarotti, Pierre
Raoult, Didier
Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members
title Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members
title_full Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members
title_fullStr Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members
title_full_unstemmed Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members
title_short Phylogenomic Analysis of β-Lactamase in Archaea and Bacteria Enables the Identification of Putative New Members
title_sort phylogenomic analysis of β-lactamase in archaea and bacteria enables the identification of putative new members
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905574/
https://www.ncbi.nlm.nih.gov/pubmed/29672703
http://dx.doi.org/10.1093/gbe/evy028
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