Publication:
Phenotypic and Genotypic Detection of Metallo-b Lactamase in Non-Fermenting Gram Negative Bacilli Obtained from Clinical Samples in a Tertiary Care Hospital in Nepal

creativeworkseries.issnISSN (Print) : 1993-2979 | ISSN (Online) : 1993-2987
dc.contributor.authorSapkota, Jyotshna
dc.contributor.authorGC, Divya Shree
dc.contributor.authorAdhikari, Ram Prasad
dc.contributor.authorKhadka, Shusila
dc.contributor.authorPandey, Ritu
dc.contributor.authorSah, Anil Kumar
dc.contributor.authorKhanal, Laxmi Kant
dc.date.accessioned2025-11-04T04:47:41Z
dc.date.available2025-11-04T04:47:41Z
dc.date.issued2025
dc.descriptionJyotshna Sapkota Department of Microbiology, Nepal Medical College Teaching Hospital, Kathmandu, Nepal Author Divya Shree GC Department of Microbiology, Nepal Medical College Teaching Hospital, Kathmandu, Nepal Author Ram Prasad Adhikari Department of Microbiology, Nepal Medical College Teaching Hospital, Kathmandu, Nepal Author Shusila Khadka Department of Microbiology, Nepal Medical College Teaching Hospital, Kathmandu, Nepal Author Ritu Pandey Department of Microbiology, Nepal Medical College Teaching Hospital, Kathmandu, Nepal Author Anil Kumar Sah Department of Microbiology, Nepal Medical College Teaching Hospital, Kathmandu, Nepal Author Laxmi Kant Khanal Department of Microbiology, Nepal Medical College Teaching Hospital, Kathmandu, Nepal Author
dc.description.abstractAbstract: Introduction Non-fermenting Gram-negative bacilli, including Pseudomonas aeruginosa and Acinetobacter baumannii, are significant nosocomial pathogens with limited treatment options due to their intrinsic and acquired resistance mechanisms. Among these, metallo-β-lactamases are of major concern which hydrolyze carbapenems and contribute to antimicrobial resistance. This study aimed to determine the prevalence of Metallo-β-Lactamase-producing non-fermenting gram negative bacilli in clinical specimens using both phenotypic and genotypic methods. Methods A descriptive cross-sectional study was conducted at Nepal Medical College Teaching Hospital from January 2024 to December 2024. A total of 16,954 clinical specimens were processed for culture and sensitivity testing. NFGNB were identified using standard microbiological methods. Antimicrobial susceptibility testing was conducted using the Kirby-Bauer disk diffusion method following Clinical and Laboratory Standards Institute guidelines. MBL production was detected phenotypically using the Imipenem-EDTA combined disc method. The presence of IMP and VIM genes was confirmed by conventional PCR. Results Among 16,954 specimens, 163 (0.96%) NFGNB isolates were identified, with Pseudomonas aeruginosa (52.1%) being the most prevalent, followed by Acinetobacter species (39.3%) and Burkholderia species (8.6%). MBL production was detected in 22 (13.5%) isolates: Pseudomonas aeruginosa (59.1%), and Acinetobacter species (40.9%). Genotypically IMP and VIM genes were found in 36.4% and 31.8% of MBL-positive isolates, respectively, while one isolate harbored both genes. Notably, 27.3% of phenotypic MBL producers tested negative for both IMP and VIM, suggesting the potential involvement of other MBL genes. Conclusion The significant prevalence of MBL-producing NLFGNB, particularly among Pseudomonas aeruginosa and Acinetobacter species, highlights a serious challenge for antimicrobial therapy and underscores an urgent need for robust infection control and antimicrobial stewardship strategies.
dc.identifierhttps://doi.org/10.59779/jiomnepal.1383
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3030
dc.language.isoen_US
dc.publisherInstitute of Medicine, Tribhuvan University
dc.subjectMetallo-β-lactamase
dc.subjectCarbapenem resistance
dc.subjectNon-fermenting Gram-negative bacilli
dc.subjectAcinetobacter species
dc.subjectPseudomonas aeruginosa
dc.subjectIMP gene
dc.subjectVIM gene
dc.titlePhenotypic and Genotypic Detection of Metallo-b Lactamase in Non-Fermenting Gram Negative Bacilli Obtained from Clinical Samples in a Tertiary Care Hospital in Nepal
dc.typeArticle
dspace.entity.typePublication
local.article.typeOriginal Article
oaire.citation.endPage113
oaire.citation.startPage108
relation.isJournalIssueOfPublication36785908-a57b-42f4-961a-9168ac067265
relation.isJournalIssueOfPublication.latestForDiscovery36785908-a57b-42f4-961a-9168ac067265
relation.isJournalOfPublicationa9ba45d9-ee33-4a6b-b1fc-6626b87eec6c

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