Prevalence of Class 1 integron in disease-causing carbapenem-resistantEscherichia coliin a tertiary hospital in Kathmandu, Nepal

Author:

Thapa SuchitraORCID,Shrestha Basudha,Shrestha Manisha,Pokhrel Yojana,Tuladhar Reshma,Jauneikaite ElitaORCID,Joshi Dev RajORCID

Abstract

AbstractBackgroundHigh prevalence of carbapenem resistance genes have been abundantly reported within clinicalE. coliin Nepal but their co-prevalence with class-1 integron is poorly documented. These Class I Integrons play pivotal role in evolution and spread of antimicrobial resistance (AMR). Therefore, it is necessary to highlight their epidemiological significance, so this study determined the prevalence of Class 1 integrons within Carbapenem resistanceEscherichia coli(CREc) population.MethodsFifty-two clinicalE. coliwith confirmed resistance to Meropenem were collected between January 2020–April 2022 in Kathmandu Model Hospital, and undergone antimicrobial susceptibility testing for 11 antimicrobial classes. Carbapenemase production was confirmed by eCIM and mCIM methods. Presence of Class I integron and carbapenemase genes,blaNDM-1,blaKPC,blaIMP,blaVIM,blaOXA-23,blaOXA-48, was confirmed by PCR method.ResultsThe result revealed 92.3% (n=48/52) of the isolates harboredintI1gene. Among integron-positive population, 97.9% (n=47/48) were carbapenemase producers which were further identified as metallo β-lactamase (MBL) producers (82.9%, n=39/47) and serine β-lactamase (SBL) producer (17%, n=8/47). Carbapenemase geneblaNDM-1(79.2%, n=38/48) was highly prevalent within integron-positive isolates, followed byblaOXA-23(62.5%, n=30/48) andblaOXA-48(54.2%, n=26/48). All integron-positive CREc isolates were resistant to minimum 16 antibiotics tested, but were susceptible to Colistin, Polymixin B, and Tigecycline.ConclusionIn conclusion, Class 1 integrons were highly prevalent within clinical CREc in Nepal, and their co-prevalence with other CRE gene is concerning due to possibility of wider spread. Therefore, an in-depth genomic analysis of Class 1 integrons is needed to understand the integron mediated AMR in high risk clones like CREc and inform intervention measures to stop spread of such pathogens.

Publisher

Cold Spring Harbor Laboratory

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