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SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance

SXT/R391 integrative and conjugative elements (ICEs) are self-transmissible mobile genetic elements that are found in most members of Enterobacteriaceae. Here, we determined fifteen SXT/R391 ICEs carried by Proteus isolates from food (4.2%) and diarrhoea patients (17.3%). BLASTn searches against Gen...

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Autores principales: Li, Xinyue, Du, Yu, Du, Pengcheng, Dai, Hang, Fang, Yujie, Li, Zhenpeng, Lv, Na, Zhu, Baoli, Kan, Biao, Wang, Duochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124997/
https://www.ncbi.nlm.nih.gov/pubmed/27892525
http://dx.doi.org/10.1038/srep37372
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author Li, Xinyue
Du, Yu
Du, Pengcheng
Dai, Hang
Fang, Yujie
Li, Zhenpeng
Lv, Na
Zhu, Baoli
Kan, Biao
Wang, Duochun
author_facet Li, Xinyue
Du, Yu
Du, Pengcheng
Dai, Hang
Fang, Yujie
Li, Zhenpeng
Lv, Na
Zhu, Baoli
Kan, Biao
Wang, Duochun
author_sort Li, Xinyue
collection PubMed
description SXT/R391 integrative and conjugative elements (ICEs) are self-transmissible mobile genetic elements that are found in most members of Enterobacteriaceae. Here, we determined fifteen SXT/R391 ICEs carried by Proteus isolates from food (4.2%) and diarrhoea patients (17.3%). BLASTn searches against GenBank showed that the fifteen SXT/R391 ICEs were closely related to that from different Enterobacteriaceae species, including Proteus mirabilis. Using core gene phylogenetic analysis, the fifteen SXT/R391 ICEs were grouped into six distinct clusters, including a dominant cluster and three clusters that have not been previously reported in Proteus isolates. The SXT/R391 ICEs shared a common structure with a set of conserved genes, five hotspots and two variable regions, which contained more foreign genes, including drug-resistance genes. Notably, a class A β-lactamase gene was identified in nine SXT/R391 ICEs. Collectively, the ICE-carrying isolates carried resistance genes for 20 tested drugs. Six isolates were resistant to chloramphenicol, kanamycin, streptomycin, trimethoprim-sulfamethoxazole, sulfisoxazole and tetracycline, which are drug resistances commonly encoded by ICEs. Our results demonstrate abundant genetic diversity and multidrug resistance of the SXT/R391 ICEs carried by Proteus isolates, which may have significance for public health. It is therefore necessary to continuously monitor the antimicrobial resistance and related mobile elements among Proteus isolates.
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spelling pubmed-51249972016-12-08 SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance Li, Xinyue Du, Yu Du, Pengcheng Dai, Hang Fang, Yujie Li, Zhenpeng Lv, Na Zhu, Baoli Kan, Biao Wang, Duochun Sci Rep Article SXT/R391 integrative and conjugative elements (ICEs) are self-transmissible mobile genetic elements that are found in most members of Enterobacteriaceae. Here, we determined fifteen SXT/R391 ICEs carried by Proteus isolates from food (4.2%) and diarrhoea patients (17.3%). BLASTn searches against GenBank showed that the fifteen SXT/R391 ICEs were closely related to that from different Enterobacteriaceae species, including Proteus mirabilis. Using core gene phylogenetic analysis, the fifteen SXT/R391 ICEs were grouped into six distinct clusters, including a dominant cluster and three clusters that have not been previously reported in Proteus isolates. The SXT/R391 ICEs shared a common structure with a set of conserved genes, five hotspots and two variable regions, which contained more foreign genes, including drug-resistance genes. Notably, a class A β-lactamase gene was identified in nine SXT/R391 ICEs. Collectively, the ICE-carrying isolates carried resistance genes for 20 tested drugs. Six isolates were resistant to chloramphenicol, kanamycin, streptomycin, trimethoprim-sulfamethoxazole, sulfisoxazole and tetracycline, which are drug resistances commonly encoded by ICEs. Our results demonstrate abundant genetic diversity and multidrug resistance of the SXT/R391 ICEs carried by Proteus isolates, which may have significance for public health. It is therefore necessary to continuously monitor the antimicrobial resistance and related mobile elements among Proteus isolates. Nature Publishing Group 2016-11-28 /pmc/articles/PMC5124997/ /pubmed/27892525 http://dx.doi.org/10.1038/srep37372 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Li, Xinyue
Du, Yu
Du, Pengcheng
Dai, Hang
Fang, Yujie
Li, Zhenpeng
Lv, Na
Zhu, Baoli
Kan, Biao
Wang, Duochun
SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance
title SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance
title_full SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance
title_fullStr SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance
title_full_unstemmed SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance
title_short SXT/R391 integrative and conjugative elements in Proteus species reveal abundant genetic diversity and multidrug resistance
title_sort sxt/r391 integrative and conjugative elements in proteus species reveal abundant genetic diversity and multidrug resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124997/
https://www.ncbi.nlm.nih.gov/pubmed/27892525
http://dx.doi.org/10.1038/srep37372
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