Archa Sharma, Deepti Chaurasia, Mili Tripathi, Jaya Lalwani, Garima Kapoor, Rakesh Kumar Srivastava, Mamta Meena, Priyanka Singh, Nagaraj Perumal
This study documents progressive escalation of carbapenem resistance and nosocomial transmission of K. oxytoca in a large Indian teaching hospital, driven by NDM-type carbapenemases and dual-gene co-carriage. These findings support strengthening of molecular surveillance, infection prevention, and antimicrobial stewardship at Indian tertiary care centres.
BACKGROUND: Klebsiella oxytoca is an underrecognised nosocomial pathogen with growing multidrug resistance (MDR). Longitudinal surveillance data from Indian tertiary care hospitals remain scarce. We characterised six-year resistance trends, nosocomial transmission dynamics, and carbapenemase gene profiles of K. oxytoca at a large teaching hospital in central India.
METHODS: A prospective longitudinal observational study was conducted at Gandhi Medical College and Associated Hamidia Hospital, Bhopal (January 2020-December 2025). Non-duplicate inpatient K. oxytoca isolates (n=1,203) were included. Antimicrobial susceptibility used Kirby-Bauer disk diffusion; MDR and extensively drug-resistant (XDR) phenotypes were classified per Magiorakos et al. Nosocomial clusters were identified by WHONET-SaTScan (Space-Time Permutation model). Antibiotic consumption was quantified as defined daily doses per 100 patient-days. Carbapenem resistance in 67 cluster-associated isolates was characterised by singleplex PCR for blaNDM, blaOXA-48, and blaKPC.
RESULTS: K. oxytoca comprised 2.8% of inpatient specimens (incidence density 0.38/1,000 bed-days). MDR and XDR rates were 85.1% and 76.0% respectively. Carbapenem resistance rose from 46.0-50.0% (2020) to 73.0-73.5% (2025); ICU isolates had higher MDR rates than ward isolates (89.6% vs. 83.3%; p=0.008). Colistin susceptibility was preserved in 99.6% of isolates. Six significant spatiotemporal clusters were identified; the largest (observed-to-expected ratio 7.4) involved medical ICUs in 2024. blaNDM was detected in 89.6% of carbapenem-resistant cluster isolates, with blaNDM/blaOXA-48 co-carriage in 41.8%.
CONCLUSIONS: This study documents progressive escalation of carbapenem resistance and nosocomial transmission of K. oxytoca in a large Indian teaching hospital, driven by NDM-type carbapenemases and dual-gene co-carriage. These findings support strengthening of molecular surveillance, infection prevention, and antimicrobial stewardship at Indian tertiary care centres.