Evidence map›Paper›PMID 42026492›Full record

ArticleBMC infectious diseases2026

Detection of hypervirulence genes in carbapenem resistant Klebsiella pneumoniae from cancer patients at a tertiary referral hospital in Nepal.

Archana Katuwal Chhetri, Hari Prasad Dhakal, Banita Gurung, Sanjib Adhikari, Supriya Sharma, Megha Raj Banjara, Komal Raj Rijal, Prakash Ghimire

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Article in BMC infectious diseases, 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

8 authors.

Archana Katuwal ChhetriCentral Department of Microbiology, Tribhuvan University, Kirtipur, Nepal. archana.chhetri@trc.tu.edu.np.
Hari Prasad DhakalNepal Cancer Hospital and Research Center (NCHRC), Lalitpur, Nepal.
Banita GurungNepal Cancer Hospital and Research Center (NCHRC), Lalitpur, Nepal.
Sanjib AdhikariCentral Department of Microbiology, Tribhuvan University, Kirtipur, Nepal.
Supriya SharmaCentral Department of Microbiology, Tribhuvan University, Kirtipur, Nepal.
Megha Raj BanjaraCentral Department of Microbiology, Tribhuvan University, Kirtipur, Nepal.
Komal Raj RijalCentral Department of Microbiology, Tribhuvan University, Kirtipur, Nepal.
Prakash GhimireCentral Department of Microbiology, Tribhuvan University, Kirtipur, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarbapenem-resistant Klebsiella pneumoniae (CRKP) are a serious public health threat and is linked to high mortality, particularly in immunocompromised and critically ill patients. In addition, hyper-virulent K. pneumoniae (hvKP) variants contributing to severe clinical outcomes in cancer patients. This study aims to identify carbapenem-resistant K. pneumoniae isolates from cancer patients and detect associated hypervirulence genes.

methodsClinical specimens were collected from cancer patients and processed for bacterial isolation and identification by conventional method. The antibiotic susceptibility testing was performed using Kirby Bauer disk diffusion method following CLSI guideline. All carbapenem-resistant K. pneumoniae isolates were further analyzed for carbapenemase production using the modified carbapenem inactivation method (mCIM) and metallo-β-lactamase (MBL) production using the EDTA-modified carbapenem inactivation method (eCIM). The presence of carbapenemase and hypervirulence encoding genes in CRKP were confirmed by polymerase chain reaction (PCR). All data were analyzed using SPSS. The chi-square test was applied to assess associations, and a p-value < 0.05 was considered statistically significant at a 95% confidence interval.

resultsOut of 4273 samples, bacterial growth was observed in 23% (987/4273) with a total of 1016 bacterial isolates, including polymicrobial growth. A total of 23.7% (241/1016) of K. pneumoniae isolates were retrieved from 241 cancer patients. Carbapenem-resistant K. pneumoniae (CRKP) isolates were detect in 53.5% (129/241), with 38% (49/129) of blaNDM−1 as predominant carbapenemase gene. Among hypervirulence markers, iucA (66.7%, 86/129) was the most prevalent. Co-occurrence of carbapenem resistance genes and hypervirulence genes was detected in 21% (27/129) among CRKP.

conclusionEffective intervention strategies are crucial to enhance the timely clinical recognition and optimal management of CRKP and hvKP infections.

Indexed as

Carbapenem-Resistant EnterobacteriaceaeKlebsiella InfectionsKlebsiella pneumoniaeNeoplasmsAdultAgedAged, 80 and overAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesCarbapenemsFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseCarbapenemsVirulence Factorsbla NDM−1CancerCarbapenem resistanceHypervirulent geneiucAK. pneumoniae

Identifiers

PMID42026492
PMCPMC13255225

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