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Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria

Due to tetracycline abuse, the safe bifidobacteria in the human gastrointestinal intestinal tract (GIT) may serve as a reservoir of tetracycline resistance genes. In the present investigation of 92 bifidobacterial strains originating from the human GIT, tetracycline resistance in 29 strains was medi...

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Autores principales: Wang, Na, Hang, Xiaomin, Zhang, Min, Liu, Xianglong, Yang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524971/
https://www.ncbi.nlm.nih.gov/pubmed/28740169
http://dx.doi.org/10.1038/s41598-017-06595-0
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author Wang, Na
Hang, Xiaomin
Zhang, Min
Liu, Xianglong
Yang, Hong
author_facet Wang, Na
Hang, Xiaomin
Zhang, Min
Liu, Xianglong
Yang, Hong
author_sort Wang, Na
collection PubMed
description Due to tetracycline abuse, the safe bifidobacteria in the human gastrointestinal intestinal tract (GIT) may serve as a reservoir of tetracycline resistance genes. In the present investigation of 92 bifidobacterial strains originating from the human GIT, tetracycline resistance in 29 strains was mediated by the tet(W), tet(O) or tet(S) gene, and this is the first report of tet(O)- and tet(S)-mediated tetracycline resistance in bifidobacteria. Antibiotic resistance genes harbored by bifidobacteria are transferred from other bacteria. However, the characteristics of the spread and integration of tetracycline resistance genes into the human intestinal bifidobacteria chromosome are poorly understood. Here, conserved sequences were identified in bifidobacterial strains positive for tet(W), tet(O), or tet(S), including the tet(W), tet(O), or tet(S) and their partial flanking sequences, which exhibited identity with the sequences in multiple human intestinal pathogens, and genes encoding 23 S rRNA, an ATP transporter, a Cpp protein, and a membrane-spanning protein were flanking by the 1920-bp tet(W), 1920-bp tet(O), 1800-bp tet(O) and 252-bp tet(S) in bifidobacteria, respectively. These findings suggest that tetracycline resistance genes harbored by human intestinal bifidobacteria might initially be transferred from pathogens and that each kind of tetracycline resistance gene might tend to insert in the vicinity of specific bifidobacteria genes.
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spelling pubmed-55249712017-07-26 Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria Wang, Na Hang, Xiaomin Zhang, Min Liu, Xianglong Yang, Hong Sci Rep Article Due to tetracycline abuse, the safe bifidobacteria in the human gastrointestinal intestinal tract (GIT) may serve as a reservoir of tetracycline resistance genes. In the present investigation of 92 bifidobacterial strains originating from the human GIT, tetracycline resistance in 29 strains was mediated by the tet(W), tet(O) or tet(S) gene, and this is the first report of tet(O)- and tet(S)-mediated tetracycline resistance in bifidobacteria. Antibiotic resistance genes harbored by bifidobacteria are transferred from other bacteria. However, the characteristics of the spread and integration of tetracycline resistance genes into the human intestinal bifidobacteria chromosome are poorly understood. Here, conserved sequences were identified in bifidobacterial strains positive for tet(W), tet(O), or tet(S), including the tet(W), tet(O), or tet(S) and their partial flanking sequences, which exhibited identity with the sequences in multiple human intestinal pathogens, and genes encoding 23 S rRNA, an ATP transporter, a Cpp protein, and a membrane-spanning protein were flanking by the 1920-bp tet(W), 1920-bp tet(O), 1800-bp tet(O) and 252-bp tet(S) in bifidobacteria, respectively. These findings suggest that tetracycline resistance genes harbored by human intestinal bifidobacteria might initially be transferred from pathogens and that each kind of tetracycline resistance gene might tend to insert in the vicinity of specific bifidobacteria genes. Nature Publishing Group UK 2017-07-24 /pmc/articles/PMC5524971/ /pubmed/28740169 http://dx.doi.org/10.1038/s41598-017-06595-0 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Na
Hang, Xiaomin
Zhang, Min
Liu, Xianglong
Yang, Hong
Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria
title Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria
title_full Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria
title_fullStr Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria
title_full_unstemmed Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria
title_short Analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria
title_sort analysis of newly detected tetracycline resistance genes and their flanking sequences in human intestinal bifidobacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524971/
https://www.ncbi.nlm.nih.gov/pubmed/28740169
http://dx.doi.org/10.1038/s41598-017-06595-0
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