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Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain

Arr is an ADP-ribosyltransferase enzyme primarily reported in association with rifamycin resistance, which has been used to treat tuberculosis in addition to Gram-positive infections and, recently, pan-resistant Gram-negative bacteria. The arr gene was initially identified on the Mycolicibacterium s...

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Autores principales: Morgado, Sergio, Fonseca, Érica, Vicente, Ana Carolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492726/
https://www.ncbi.nlm.nih.gov/pubmed/34611248
http://dx.doi.org/10.1038/s41598-021-99255-3
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author Morgado, Sergio
Fonseca, Érica
Vicente, Ana Carolina
author_facet Morgado, Sergio
Fonseca, Érica
Vicente, Ana Carolina
author_sort Morgado, Sergio
collection PubMed
description Arr is an ADP-ribosyltransferase enzyme primarily reported in association with rifamycin resistance, which has been used to treat tuberculosis in addition to Gram-positive infections and, recently, pan-resistant Gram-negative bacteria. The arr gene was initially identified on the Mycolicibacterium smegmatis chromosome and later on Proteobacteria plasmids. This scenario raised concerns on the distribution and spread of arr, considering the Bacteria domain. Based on 198,082 bacterial genomes/metagenomes, we performed in silico analysis, including phylogenetic reconstruction of Arr in different genomic contexts. Besides, new arr alleles were evaluated by in vitro analysis to assess their association with rifampin resistance phenotype. The arr gene was prevalent in thousands of chromosomes and in hundreds of plasmids from environmental and clinical bacteria, mainly from the phyla Actinobacteria, Proteobacteria, Firmicutes, and Bacteroidetes. Furthermore, this gene was identified in other and new genomic contexts. Interestingly, Arr sequences associated with rifampin resistance were distributed across all phylogeny, indicating that, despite the diversity, their association with rifampin resistance phenotype were maintained. In fact, we found that the key residues were highly conserved. In addition, other analyzes have raised evidence of another Arr function, which is related to guanidine metabolism. Finally, this scenario as a whole also suggested the Actinobacteria phylum as a potential ancestral source of arr within the Bacteria domain.
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spelling pubmed-84927262021-10-07 Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain Morgado, Sergio Fonseca, Érica Vicente, Ana Carolina Sci Rep Article Arr is an ADP-ribosyltransferase enzyme primarily reported in association with rifamycin resistance, which has been used to treat tuberculosis in addition to Gram-positive infections and, recently, pan-resistant Gram-negative bacteria. The arr gene was initially identified on the Mycolicibacterium smegmatis chromosome and later on Proteobacteria plasmids. This scenario raised concerns on the distribution and spread of arr, considering the Bacteria domain. Based on 198,082 bacterial genomes/metagenomes, we performed in silico analysis, including phylogenetic reconstruction of Arr in different genomic contexts. Besides, new arr alleles were evaluated by in vitro analysis to assess their association with rifampin resistance phenotype. The arr gene was prevalent in thousands of chromosomes and in hundreds of plasmids from environmental and clinical bacteria, mainly from the phyla Actinobacteria, Proteobacteria, Firmicutes, and Bacteroidetes. Furthermore, this gene was identified in other and new genomic contexts. Interestingly, Arr sequences associated with rifampin resistance were distributed across all phylogeny, indicating that, despite the diversity, their association with rifampin resistance phenotype were maintained. In fact, we found that the key residues were highly conserved. In addition, other analyzes have raised evidence of another Arr function, which is related to guanidine metabolism. Finally, this scenario as a whole also suggested the Actinobacteria phylum as a potential ancestral source of arr within the Bacteria domain. Nature Publishing Group UK 2021-10-05 /pmc/articles/PMC8492726/ /pubmed/34611248 http://dx.doi.org/10.1038/s41598-021-99255-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Morgado, Sergio
Fonseca, Érica
Vicente, Ana Carolina
Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain
title Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain
title_full Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain
title_fullStr Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain
title_full_unstemmed Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain
title_short Genomic epidemiology of rifampicin ADP-ribosyltransferase (Arr) in the Bacteria domain
title_sort genomic epidemiology of rifampicin adp-ribosyltransferase (arr) in the bacteria domain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492726/
https://www.ncbi.nlm.nih.gov/pubmed/34611248
http://dx.doi.org/10.1038/s41598-021-99255-3
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