Evidence map›Paper›PMID 41749078›Full record

ArticleBMC microbiology2026

Phenotypic and genotypic characterization of carbapenem resistant Klebsiella pneumoniae clinical isolates from Damietta, Egypt.

Mohamed I Abou-Dobara, Ahmed K A El-Sayed, Radwa N Elmaghalawy, Hazem H Saleh

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Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Mohamed I Abou-DobaraBotany and Microbiology Department, Faculty of Science, Damietta University, New Damietta, 34517, Egypt.
Ahmed K A El-SayedBotany and Microbiology Department, Faculty of Science, Damietta University, New Damietta, 34517, Egypt.
Radwa N ElmaghalawyBotany and Microbiology Department, Faculty of Science, Damietta University, New Damietta, 34517, Egypt. radwanagy@du.edu.eg.
Hazem H SalehUrology and Nephrology Center, Mansoura University, Mansoura, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe notable emergence of carbapenemase production is a critical problem threatening human health worldwide. Hence, this study aimed to monitor the prevalence of carbapenemase-producing Klebsiella pneumoniae in Damietta, Egypt. Additionally, the study investigated the association of carbapenemase producers and certain virulence traits, including biofilm formation and colibactin genotoxin.

methodsThis study included 86 clinical isolates of Klebsiella pneumoniae collected from various clinical analytical laboratories and private clinics in Damietta, Egypt, between June 2023 and May 2024. Carbapenemase production was determined by various phenotypic assays (CarbaNP/mCIM/eCIM). Genotypic detection of carbapenemase-encoding genes (blaNDM, blaKPC, blaVIM, blaIMP, and blaOXA-48) and certain virulence genes (clbA, clbB, mrkD, and fimH) was performed using multiplex PCR. Chi-square and Fisher’s exact tests were used for statistical analysis.

resultsIn the current study, 44.2% (38/86) of Klebsiella pneumoniae were identified as carbapenemase producers. All carbapenemase-producing Klebsiella pneumoniae (38/38, 100%) were positive by mCIM, while 92.1% (35/38) were positive by CarbaNP, and 65.8% (25/38) were positive by eCIM. The blaNDM, blaOXA-48, and blaKPC genes were detected in 71%, 36.8%, and 5.2% of the tested isolates, respectively. No blaIMP or blaVIM were detected. Different biofilm formation capabilities were observed among carbapenemase producers: moderate (42.1%), strong (36.8%), weak (13.1%), and non-biofilm (7.8%). The capacity for biofilm formation differed significantly between carbapenemase-producing and non-producing Klebsiella pneumoniae. The mrkD gene was significantly associated with carbapenemase-producing Klebsiella pneumoniae in contrast to fimH and colibactin-encoding genes.

conclusionsThis study provides valuable insights into the continuous emergence of carbapenemase-producing Klebsiella pneumoniae, which poses a serious clinical and public health concern. A significant association was observed between carbapenemase producers and certain virulence factors. This emphasizes the urgent need for ongoing monitoring, effective stewardship programs, intensive surveillance, and strict infection control policies to control the spread of such highly resistant strains.

Indexed as

Bacterial Proteinsbeta-LactamasesKlebsiella InfectionsKlebsiella pneumoniaeAnti-Bacterial AgentsBiofilmsCarbapenemsEgyptGenotypeHumansMicrobial Sensitivity TestsPhenotypeVirulenceVirulence FactorsAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseCarbapenemsVirulence FactorsBiofilmblaNDMblaOXA-48Carbapenem-resistant Klebsiella pneumoniaeColibactinVirulence factors

Identifiers

PMID41749078
PMCPMC13049837

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