AI Article Synopsis

  • OXA-232 is a variant of OXA-48 found in carbapenem-resistant Klebsiella pneumoniae (CRKP), linked to infections in immunocompromised patients, and the study aimed to understand its characteristics and behavior under low-carbapenem levels.
  • The research involved isolating CRKP from neonate blood and stool samples, identifying the presence of blaOXA-232 along with other resistance genes, and examining its gene transfer ability and expression under specific conditions.
  • Results indicated that blaOXA-232 was commonly found alongside other resistance genes, its expression increased with sub-inhibitory carbapenem levels, and the study underscores the need for ongoing monitoring of this resistance variant to prevent further spread.

Article Abstract

Background & objectives OXA-232 is a five amino acid substitution variant of OXA-48 and is reported in carbapenem-resistant Klebsiella pneumoniae (CRKP), which is associated with nosocomial infections among immunocompromised patients in the intensive care unit. This study aimed to characterise blaOXA-232 in CRKP of clinical origin and investigate its transcriptional response against sub-inhibitory levels of carbapenems. Methods CRKP was isolated from blood (pathogens) and stool cultures (colonisers) of neonates and was characterized for blaOXA-232. Co-existing resistance determinants were investigated in blaOXA-232 positive isolates, followed by horizontal gene transferability assay and PCR-based replicon typing (PBRT). Cloning of blaOXA-232 was performed, and expression of blaOXA-232 in the isolates and their clones under sub-inhibitory concentrations of carbapenems was checked via RT-PCR. Mobile genetic elements associated with blaOXA-232 were investigated, followed by DNA fingerprinting through enterobacterial repetitive intergenic consensus (ERIC) PCR. Results blaOXA-232 with co-carriage of extended-spectrum beta-lactamases (ESBLs), sulphonamides and quinolones were identified in seven CRPK isolates recovered from blood samples of neonates. Transformation and cloning of blaOXA-232 was successful. The sub-inhibitory concentration of carbapenems induces elevated expression of this resistant determinant. ISEcp1 was associated with blaOXA-232 in the upstream region within two haplotypes of CRKP isolates of clinical origin. Interpretation & conclusions Selective carbapenem pressure resulted in higher expression of this gene, which could account for treatment failure. With frequent reports of occurrence among clinical isolates, monitoring and further investigation of this novel variant are necessary to understand its transmission dynamics and to thwart its further dissemination.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11463862PMC
http://dx.doi.org/10.25259/IJMR_1915_22DOI Listing

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