Novel allelic variants of blaOXA-48-like carried on IncN2 and IncC2 plasmids isolated from clinical cases in Argentina: In vivo emergence of blaOXA-567

Both isolates were found to be resistant to carbapenems and susceptible to ceftriaxone. bla<sub>OXA-438</sub> was located on a 69-kb IncN<sub>2</sub> plasmid, while bla<sub>OXA-567</sub> was found on a 175-Kb IncC<sub>2</sub> plasmid, both transferable by biparental conjugation. The close genetic environment of the bla<sub>OXA</sub> genes suggests a common origin likely involving mobile genetic elements. Finally, the clinical case of M21014 revealed that the patient had previous infections with two genetically related K. pneumoniae ST6838 that carried bla<sub>OXA-163</sub> on an IncC<sub>2</sub> plasmid with equal size and genetic hallmarks to that of M21014, providing strong evidence for the intra-patient emergence of bla<sub>OXA-567.</sub> CONCLUSIONS: This research underscores the need for ongoing surveillance and integral studies to understand the emergence, biochemistry and dissemination capacity of OXA enzymes with the overarching aim to halt their spread.

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Publication Details

Journal
Journal of Global Antimicrobial Resistance
Published
2024-12-25
DOI
https://doi.org/10.1016/j.jgar.2024.12.008
Citations
1
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
0.17

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article

Novel allelic variants of blaOXA-48-like carried on IncN2 and IncC2 plasmids isolated from clinical cases in Argentina: In vivo emergence of blaOXA-567

Fernando Pasterán, Alejandra Corso, Melina Rapoport, Nathalie Tijet et al.
1 citations
Journal of Global Antimicrobial Resistance
Antibiotic Resistance in Bacteria
0.17
article

Novel allelic variants of blaOXA-48-like carried on IncN2 and IncC2 plasmids isolated from clinical cases in Argentina: In vivo emergence of blaOXA-567

Fernando Pasterán, Alejandra Corso, Melina Rapoport, Nathalie Tijet, Bárbara Ghiglione, P.P. Power, E. Biondi, Denise De Belder, Juan Manuel de Mendieta, Roberto G. Melano, Adriana Di Bella, Gomez A Sonia
article en
1 citations

Abstract

Both isolates were found to be resistant to carbapenems and susceptible to ceftriaxone. bla<sub>OXA-438</sub> was located on a 69-kb IncN<sub>2</sub> plasmid, while bla<sub>OXA-567</sub> was found on a 175-Kb IncC<sub>2</sub> plasmid, both transferable by biparental conjugation. The close genetic environment of the bla<sub>OXA</sub> genes suggests a common origin likely involving mobile genetic elements. Finally, the clinical case of M21014 revealed that the patient had previous infections with two genetically related K. pneumoniae ST6838 that carried bla<sub>OXA-163</sub> on an IncC<sub>2</sub> plasmid with equal size and genetic hallmarks to that of M21014, providing strong evidence for the intra-patient emergence of bla<sub>OXA-567.</sub> CONCLUSIONS: This research underscores the need for ongoing surveillance and integral studies to understand the emergence, biochemistry and dissemination capacity of OXA enzymes with the overarching aim to halt their spread.

Journal of Global Antimicrobial ResistanceVol. 41
Toronto Public Health (CA), Universidad de Buenos Aires (AR), Administración Nacional de Laboratorios e Institutos de Salud (AR), Public Health Ontario (CA), Hospital de Niños Superiora Sor María Ludovica (AR), Instituto de Química y Fisicoquímica Biológicas (AR), Hospital General de Niños Ricardo Gutierrez (AR)
Ministry of Health, Agencia Nacional de Promoción Científica y Tecnológica, Fondo para la Investigación Científica y Tecnológica
Openalex Percentile: Top 53%
Antibiotic Resistance in Bacteria
0.17
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