Mobile Colistin-Resistant Genes mcr-1, mcr-2, and mcr-3 Identified in Diarrheal Pathogens among Infants, Children, and Adults in Bangladesh: Implications for the Future

Author:

Sarker Shafiuzzaman1ORCID,Neeloy Reeashat Muhit1ORCID,Habib Marnusa Binte1ORCID,Urmi Umme Laila12ORCID,Al Asad Mamun1ORCID,Mosaddek Abu Syed Md.3ORCID,Khan Mohammad Rabiul Karim4ORCID,Nahar Shamsun1ORCID,Godman Brian56ORCID,Islam Salequl12ORCID

Affiliation:

1. Department of Microbiology, Jahangirnagar University, Savar, Dhaka 1342, Bangladesh

2. School of Optometry and Vision Science, UNSW Sydney, Sydney, NSW 2052, Australia

3. Department of Pharmacology, Uttara Adhunik Medical College, Dhaka 1230, Bangladesh

4. Sheikh Hasina National Institute of Burn and Plastic Surgery (SHNIBP), Dhaka 1000, Bangladesh

5. Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0RE, UK

6. Division of Public Health Pharmacy and Management, School of Pharmacy, Sefako Makgatho Health Sciences University, Pretoria 0204, South Africa

Abstract

Colistin is a last-resort antimicrobial for treating multidrug-resistant Gram-negative bacteria. Phenotypic colistin resistance is highly associated with plasmid-mediated mobile colistin resistance (mcr) genes. mcr-bearing Enterobacteriaceae have been detected in many countries, with the emergence of colistin-resistant pathogens a global concern. This study assessed the distribution of mcr-1, mcr-2, mcr-3, mcr-4, and mcr-5 genes with phenotypic colistin resistance in isolates from diarrheal infants and children in Bangladesh. Bacteria were identified using the API-20E biochemical panel and 16s rDNA gene sequencing. Polymerase chain reactions detected mcr gene variants in the isolates. Their susceptibilities to colistin were determined by agar dilution and E-test by minimal inhibitory concentration (MIC) measurements. Over 31.6% (71/225) of isolates showed colistin resistance according to agar dilution assessment (MIC > 2 μg/mL). Overall, 15.5% of isolates carried mcr genes (7, mcr-1; 17, mcr-2; 13, and mcr-3, with co-occurrence occurring in two isolates). Clinical breakout MIC values (≥4 μg/mL) were associated with 91.3% of mcr-positive isolates. The mcr-positive pathogens included twenty Escherichia spp., five Shigella flexneri, five Citrobacter spp., two Klebsiella pneumoniae, and three Pseudomonas parafulva. The mcr-genes appeared to be significantly associated with phenotypic colistin resistance phenomena (p = 0.000), with 100% colistin-resistant isolates showing MDR phenomena. The age and sex of patients showed no significant association with detected mcr variants. Overall, mcr-associated colistin-resistant bacteria have emerged in Bangladesh, which warrants further research to determine their spread and instigate activities to reduce resistance.

Funder

Bangladesh Medical Research Council

Publisher

MDPI AG

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