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Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin
The emergence of tet(X) and carbapenemase genes in Enterobacterales pose significant challenges to the treatment of infectious diseases. Convergence of these two categories of genes in an individual pathogen would deteriorate the antimicrobial resistance (AMR) crisis furthermore. Here, tigecycline-r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457074/ https://www.ncbi.nlm.nih.gov/pubmed/32922378 http://dx.doi.org/10.3389/fmicb.2020.01940 |
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author | Li, Yan Wang, Qian Peng, Kai Liu, Yuan Li, Ruichao Wang, Zhiqiang |
author_facet | Li, Yan Wang, Qian Peng, Kai Liu, Yuan Li, Ruichao Wang, Zhiqiang |
author_sort | Li, Yan |
collection | PubMed |
description | The emergence of tet(X) and carbapenemase genes in Enterobacterales pose significant challenges to the treatment of infectious diseases. Convergence of these two categories of genes in an individual pathogen would deteriorate the antimicrobial resistance (AMR) crisis furthermore. Here, tigecycline-resistant Enterobacterales strains were isolated and detected with carbapenemase genes, characterized by antimicrobial susceptibility testing, PCR, conjugation assay, whole genome sequencing, and bioinformatics analysis. Three tigecycline-resistant isolates consisting of one plasmid-mediated tet(X4)-bearing Escherichia fergusonii and two chromosomal tet(X6)-bearing Proteus cibarius were recovered from chicken feces. The tet(X4) was located on a conjugative IncX1 plasmid pHNCF11W-tetX4 encoding the identical structure as reported tet(X4)-bearing IncX1 plasmids in Escherichia coli. Among two P. cibarius strains, tet(X6) was located on two similar chromosomal MDR regions with genetic contexts IS26-aac(3)-IVa-aph(4)-Ia-ISEc59-tnpA-tet(X6)-orf-orf-ISCR2-virD2-floR-ISCR2-glmM-sul2 and IS26-aac(3)-IVa-aph(4)-Ia-ISEc59-tnpA-tet(X6)-orf-orf-ISCR2-glmM-sul2. Apart from tet(X6), P. cibarius HNCF44W harbored a novel transposon Tn6450b positive for bla(NDM–)(1) on a conjugative plasmid. This study probed the genomic basis of three tet(X)-bearing, tigecycline-resistant strains, one of which coharbored bla(NDM–)(1) and tet(X6), and identified P. cibarius as the important reservoir of tet(X6) variants. Emergence of P. cibarius encoding both bla(NDM–)(1) and tet(X6) reveals a potential public health risk. |
format | Online Article Text |
id | pubmed-7457074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74570742020-09-11 Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin Li, Yan Wang, Qian Peng, Kai Liu, Yuan Li, Ruichao Wang, Zhiqiang Front Microbiol Microbiology The emergence of tet(X) and carbapenemase genes in Enterobacterales pose significant challenges to the treatment of infectious diseases. Convergence of these two categories of genes in an individual pathogen would deteriorate the antimicrobial resistance (AMR) crisis furthermore. Here, tigecycline-resistant Enterobacterales strains were isolated and detected with carbapenemase genes, characterized by antimicrobial susceptibility testing, PCR, conjugation assay, whole genome sequencing, and bioinformatics analysis. Three tigecycline-resistant isolates consisting of one plasmid-mediated tet(X4)-bearing Escherichia fergusonii and two chromosomal tet(X6)-bearing Proteus cibarius were recovered from chicken feces. The tet(X4) was located on a conjugative IncX1 plasmid pHNCF11W-tetX4 encoding the identical structure as reported tet(X4)-bearing IncX1 plasmids in Escherichia coli. Among two P. cibarius strains, tet(X6) was located on two similar chromosomal MDR regions with genetic contexts IS26-aac(3)-IVa-aph(4)-Ia-ISEc59-tnpA-tet(X6)-orf-orf-ISCR2-virD2-floR-ISCR2-glmM-sul2 and IS26-aac(3)-IVa-aph(4)-Ia-ISEc59-tnpA-tet(X6)-orf-orf-ISCR2-glmM-sul2. Apart from tet(X6), P. cibarius HNCF44W harbored a novel transposon Tn6450b positive for bla(NDM–)(1) on a conjugative plasmid. This study probed the genomic basis of three tet(X)-bearing, tigecycline-resistant strains, one of which coharbored bla(NDM–)(1) and tet(X6), and identified P. cibarius as the important reservoir of tet(X6) variants. Emergence of P. cibarius encoding both bla(NDM–)(1) and tet(X6) reveals a potential public health risk. Frontiers Media S.A. 2020-08-14 /pmc/articles/PMC7457074/ /pubmed/32922378 http://dx.doi.org/10.3389/fmicb.2020.01940 Text en Copyright © 2020 Li, Wang, Peng, Liu, Li and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Li, Yan Wang, Qian Peng, Kai Liu, Yuan Li, Ruichao Wang, Zhiqiang Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin |
title | Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin |
title_full | Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin |
title_fullStr | Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin |
title_full_unstemmed | Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin |
title_short | Emergence of Carbapenem- and Tigecycline-Resistant Proteus cibarius of Animal Origin |
title_sort | emergence of carbapenem- and tigecycline-resistant proteus cibarius of animal origin |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457074/ https://www.ncbi.nlm.nih.gov/pubmed/32922378 http://dx.doi.org/10.3389/fmicb.2020.01940 |
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