Cargando…
Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface
BACKGROUND: The global emergence of plasmid-mediated colistin resistance (Col-R) conferred by mcr genes in gram-negative rods (GNRs) has jeopardized the last treatment option for multidrug-resistant bacterial infections in humans. This study aimed to assess the emergence of mcr gene-mediated Col-R i...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678191/ https://www.ncbi.nlm.nih.gov/pubmed/33292525 http://dx.doi.org/10.1186/s13099-020-00392-3 |
_version_ | 1783612105997418496 |
---|---|
author | Javed, Humera Saleem, Sidrah Zafar, Aizza Ghafoor, Aamir Shahzad, Ahmad Bin Ejaz, Hasan Junaid, Kashaf Jahan, Shah |
author_facet | Javed, Humera Saleem, Sidrah Zafar, Aizza Ghafoor, Aamir Shahzad, Ahmad Bin Ejaz, Hasan Junaid, Kashaf Jahan, Shah |
author_sort | Javed, Humera |
collection | PubMed |
description | BACKGROUND: The global emergence of plasmid-mediated colistin resistance (Col-R) conferred by mcr genes in gram-negative rods (GNRs) has jeopardized the last treatment option for multidrug-resistant bacterial infections in humans. This study aimed to assess the emergence of mcr gene-mediated Col-R in GNRs isolated from humans and animals in Pakistan. METHODS: Animal and clinical specimens collected from various sources were prospectively analysed using standard microbiological procedures. Pathogens were identified using the API 20E and API 20NE systems (bioMerieux). Minimum inhibitory concentration (MIC) against colistin was determined using the MIC detection methods, and multiplex polymerase chain reaction (PCR) was used to amplify the mcr-1 to mcr-5 genes. RESULTS: We isolated 126 (88.1%) animal and 17 (11.9%) human Col-R phenotypes, among which there was a significant association (P < 0.01) of Escherichia coli and Proteus mirabilis with animals and of Acinetobacter baumannii with humans. Animal strains exhibited statistically significant (P < 0.05) resistance to co-trimoxazole, chloramphenicol, and moxifloxacin, and the human pathogens exhibited statistically significant (P < 0.05) antibiotic resistance to cephalosporins, carbapenems, and piperacillin-tazobactam. For Col-R strains, MIC(50) values were > 6 µg/mL and > 12 µg/mL for human and animal isolates, respectively. mcr genes were detected in 110 (76.9%) bacterial strains, of which 108 (98.2%) were mcr-1 and 2 (1.8%) were mcr-2. CONCLUSIONS: The detection of a considerable number of mcr-1 and mcr-2 genes in animals is worrisome, as they are now being detected in clinical pathogens. The acquisition of mcr genes by colistin-susceptible bacteria could leave us in a post-antibiotic era. |
format | Online Article Text |
id | pubmed-7678191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-76781912020-11-20 Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface Javed, Humera Saleem, Sidrah Zafar, Aizza Ghafoor, Aamir Shahzad, Ahmad Bin Ejaz, Hasan Junaid, Kashaf Jahan, Shah Gut Pathog Research BACKGROUND: The global emergence of plasmid-mediated colistin resistance (Col-R) conferred by mcr genes in gram-negative rods (GNRs) has jeopardized the last treatment option for multidrug-resistant bacterial infections in humans. This study aimed to assess the emergence of mcr gene-mediated Col-R in GNRs isolated from humans and animals in Pakistan. METHODS: Animal and clinical specimens collected from various sources were prospectively analysed using standard microbiological procedures. Pathogens were identified using the API 20E and API 20NE systems (bioMerieux). Minimum inhibitory concentration (MIC) against colistin was determined using the MIC detection methods, and multiplex polymerase chain reaction (PCR) was used to amplify the mcr-1 to mcr-5 genes. RESULTS: We isolated 126 (88.1%) animal and 17 (11.9%) human Col-R phenotypes, among which there was a significant association (P < 0.01) of Escherichia coli and Proteus mirabilis with animals and of Acinetobacter baumannii with humans. Animal strains exhibited statistically significant (P < 0.05) resistance to co-trimoxazole, chloramphenicol, and moxifloxacin, and the human pathogens exhibited statistically significant (P < 0.05) antibiotic resistance to cephalosporins, carbapenems, and piperacillin-tazobactam. For Col-R strains, MIC(50) values were > 6 µg/mL and > 12 µg/mL for human and animal isolates, respectively. mcr genes were detected in 110 (76.9%) bacterial strains, of which 108 (98.2%) were mcr-1 and 2 (1.8%) were mcr-2. CONCLUSIONS: The detection of a considerable number of mcr-1 and mcr-2 genes in animals is worrisome, as they are now being detected in clinical pathogens. The acquisition of mcr genes by colistin-susceptible bacteria could leave us in a post-antibiotic era. BioMed Central 2020-11-20 /pmc/articles/PMC7678191/ /pubmed/33292525 http://dx.doi.org/10.1186/s13099-020-00392-3 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Javed, Humera Saleem, Sidrah Zafar, Aizza Ghafoor, Aamir Shahzad, Ahmad Bin Ejaz, Hasan Junaid, Kashaf Jahan, Shah Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface |
title | Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface |
title_full | Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface |
title_fullStr | Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface |
title_full_unstemmed | Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface |
title_short | Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface |
title_sort | emergence of plasmid-mediated mcr genes from gram-negative bacteria at the human-animal interface |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678191/ https://www.ncbi.nlm.nih.gov/pubmed/33292525 http://dx.doi.org/10.1186/s13099-020-00392-3 |
work_keys_str_mv | AT javedhumera emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface AT saleemsidrah emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface AT zafaraizza emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface AT ghafooraamir emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface AT shahzadahmadbin emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface AT ejazhasan emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface AT junaidkashaf emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface AT jahanshah emergenceofplasmidmediatedmcrgenesfromgramnegativebacteriaatthehumananimalinterface |