Emergence of plasmid-mediated mcr genes from Gram-negative bacteria at the human-animal interface.

Antibacterial profile Antimicrobial resistance Colistin resistance Mobile colistin resistance Plasmid-mediated resistance mcr genes

Journal

Gut pathogens
ISSN: 1757-4749
Titre abrégé: Gut Pathog
Pays: England
ID NLM: 101474263

Informations de publication

Date de publication:
20 Nov 2020
Historique:
received: 18 07 2020
accepted: 04 11 2020
entrez: 9 12 2020
pubmed: 10 12 2020
medline: 10 12 2020
Statut: epublish

Résumé

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. 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. 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 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.

Sections du résumé

BACKGROUND 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 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 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
CONCLUSIONS 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.

Identifiants

pubmed: 33292525
doi: 10.1186/s13099-020-00392-3
pii: 10.1186/s13099-020-00392-3
pmc: PMC7678191
doi:

Types de publication

Journal Article

Langues

eng

Pagination

54

Subventions

Organisme : Higher Education Commission, Pakistan
ID : NRPU 8557

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Auteurs

Humera Javed (H)

Department of Microbiology, University of Health Sciences, Lahore, Pakistan.
Department of Microbiology, The Children's Hospital & The Institute of Child Health, Lahore, Pakistan.

Sidrah Saleem (S)

Department of Microbiology, University of Health Sciences, Lahore, Pakistan.

Aizza Zafar (A)

Department of Microbiology, The Children's Hospital & The Institute of Child Health, Lahore, Pakistan.

Aamir Ghafoor (A)

University Diagnostic Laboratory, University of Veterinary and Animal Sciences, Lahore, Pakistan.

Ahmad Bin Shahzad (AB)

University Diagnostic Laboratory, University of Veterinary and Animal Sciences, Lahore, Pakistan.

Hasan Ejaz (H)

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Jouf University, Al Jouf, Saudi Arabia.

Kashaf Junaid (K)

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Jouf University, Al Jouf, Saudi Arabia.

Shah Jahan (S)

Department of Immunology, University of Health Sciences, Khayaban-e-Jamia Punjab, 54600, Lahore, Pakistan. shahjahan@uhs.edu.pk.

Classifications MeSH