Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5684
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dc.contributor.authorMulu Lemlemen_US
dc.contributor.authorErkihun Akliluen_US
dc.contributor.authorMaizan Mohameden_US
dc.contributor.authorNor Fadhilah Kamaruzzamanen_US
dc.contributor.authorZunita Zakariaen_US
dc.contributor.authorAzian Harunen_US
dc.contributor.authorSusmita Seenu Devanen_US
dc.contributor.authorIntan Noor Aina Kamaruzamanen_US
dc.contributor.authorMohd Farhan Hanif Reduanen_US
dc.contributor.authorMuthupandian Saravananen_US
dc.date.accessioned2024-01-21T06:34:26Z-
dc.date.available2024-01-21T06:34:26Z-
dc.date.issued2023-
dc.identifier.issn14712180-
dc.identifier.urihttp://hdl.handle.net/123456789/5684-
dc.descriptionWeb of Science / Scopusen_US
dc.description.abstractBackground: Colistin is an antibiotic used as a last-resort to treat multidrug-resistant Gram-negative bacterial infections. Colistin had been used for a long time in veterinary medicine for disease control and as a growth promoter in food-producing animals. This excessive use of colistin in food animals causes an increase in colistin resistance. This study aimed to determine molecular characteristics of colistin-resistant Escherichia coli in broiler chicken and chicken farm environments. Results: Four hundred fifty-three cloacal and farm environment samples were collected from six different commercial chicken farms in Kelantan, Malaysia. E. coli was isolated using standard bacteriological methods, and the isolates were tested for antimicrobial susceptibility using disc diffusion and colistin minimum inhibitory concentration (MIC) by broth microdilution. Multiplex PCR was used to detect mcr genes, and DNA sequencing was used to confirm the resistance genes. Virulence gene detection, phylogroup, and multilocus sequence typing (MLST) were done to further characterize the E. coli isolates. Out of the 425 (94%; 425/453) E. coli isolated from the chicken and farm environment samples, 10.8% (48/425) isolates were carrying one or more colistin-resistance encoding genes. Of the 48 colistin-resistant isolates, 54.2% (26/48) of the mcr positive isolates were genotypically and phenotypically resistant to colistin with MIC of colistin ≥ 4 μg/ml. The most prominent mcr gene detected was mcr-1 (47.9%; 23/48), followed by mcr-8 (18.8%; 9/48), mcr-7 (14.5%; 7/48), mcr-6 (12.5%; 6/48), mcr-4 (2.1%; 1/48), mcr-5 (2.1%; 1/48), and mcr-9 (2.1%; 1/48) genes. One E. coli isolate originating from the fecal sample was found to harbor both mcr-4 and mcr-6 genes and another isolate from the drinking water sample was carrying mcr-1 and mcr-8 genes. The majority of the mcr positive isolates were categorized under phylogroup A followed by phylogroup B1. The most prevalent sequence typing (ST) was ST1771 (n = 4) followed by ST206 (n = 3). 100% of the mcr positive E. coli isolates were multidrug resistant. The most frequently detected virulence genes among mcr positive E. coli isolates were ast (38%; 18/48) followed by iss (23%; 11/48). This is the first research to report the prevalence of mcr-4, mcr-5, mcr-6, mcr-7, and mcr-8 genes in E. coli from broiler chickens and farm environments in Malaysia. Conclusion: Our findings suggest that broiler chickens and broiler farm environments could be reservoirs of colistin-resistant E. coli, posing a risk to public health and food safety.en_US
dc.language.isoenen_US
dc.publisherBioMed Central Ltden_US
dc.relation.ispartofBMC Microbiologyen_US
dc.subjectAMRen_US
dc.subjectColistin resistanceen_US
dc.subjectEscherichia colien_US
dc.subjectBroiler chickenen_US
dc.titlePhenotypic and genotypic characterization of colistin‑resistant Escherichia Coli with mcr‑4, mcr‑5, mcr‑6, and mcr‑9 genes from broiler chicken and farm environmenten_US
dc.typePrinteden_US
dc.identifier.doi10.1186/s12866-023-03118-y-
dc.description.page392en_US
dc.volume23(1)en_US
dc.description.articleno392en_US
dc.description.typeArticleen_US
dc.description.impactfactor0.94en_US
dc.description.quartileQ2en_US
dc.contributor.correspondingauthorerkihun@umk.edu.myen_US
item.fulltextWith Fulltext-
item.openairetypePrinted-
item.languageiso639-1en-
item.grantfulltextopen-
crisitem.author.deptFaculty of Veterinary Medicine UMK-
crisitem.author.deptUniversiti Malaysia Kelantan-
crisitem.author.deptUniversiti Malaysia Kelantan-
crisitem.author.deptUniversity Malaysia Kelantan, Malaysia-
Appears in Collections:Faculty of Veterinary Medicine - Journal (Scopus/WOS)
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