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Characterization of plasmids carrying the bla(OXA-24/40) carbapenemase gene and the genes encoding the AbkA/AbkB proteins of a toxin/antitoxin system

Abstract: Background: Carbapenem-resistant Acinetobacter baumannii (CRAb) is a major source of nosocomial infections in Spain associated with the production of OXA-58-like or OXA-24/40-like b-lactamase enzymes. We analysed the plasmids carrying the blaOXA-24/40-like gene in CRAb isolates obtained a decade apart. Methods: The presence of b-lactamases was screened for by PCR (metallo-b-lactamases, carbapenem-hydrolysing class D b-lactamases, GES and KPC) in 101 CRAb isolates obtained in two multicentre studies (GEIH/REIPI-Ab2000 and GEIH/REIPI-Ab-2010; n¼493 Acinetobacter spp). We analysed the distribution and characterization of the plasmids carrying the blaOXA-24/40-like gene and sequenced two plasmids, AbATCC223p (2000) and AbATCC329p (2010) from A. baumannii ATCC 17978 transformants. Results: Acquisition of the blaOXA-24/40-like gene was the main mechanism underlying resistance to carbapenems (48.7% in 2000 compared with 51.6% in 2010). This gene was mainly isolated in ST2 A. baumannii strains in both studies, although some novel STs (ST79 and ST80) appeared in 2010. The gene was located in plasmids (8-12 kbp) associated with the repAci2 or repAci2/repGR12 types. The sequences of AbATCC223p (8840 bp) and AbATCC329p (8842 bp) plasmids were similar, particularly regarding the presence of the genes encoding the AbkA/AbkB proteins associated with the toxin/antitoxin system. Moreover, the abkA/abkB gene sequences (.96% identity) were also located in plasmids harbouring the blaOXA-58-like gene. Conclusions: The action of OXA-24/40 and OXA-58 b-lactamase-like enzymes represents the main mechanism underlying resistance to carbapenems in Spain in the last decade. AbkA/AbkB proteins in the toxin/antitoxin system may be involved in the successful dissemination of plasmids carrying the blaOXA-24/40-like gene, and probably also the blaOXA-58-like gene, thus contributing to the plasmid stability.

 Autoría: Mosqueda N., Gato E., Roca I., López M., de Alegría C.R., Cuenca F.F., Martínez-Martínez L., Pachón J., Cisneros J.M., Rodríguez-Baño J., Pascual Á., Vila J., Bou G., Tomás M., Garnacho J., Pizarraya A.G., Márquez Vácaro J.A., Cano M.E., Fariñas M.C., Porto A.S., Meruendano G.E., Vales L.B., Ciria J.C., Vallejo L., Pérez B.F., Chao J.C.V., Ortega B.P., Mansilla E.C., Irure J.J.G., Jiménez A.d.A., Cardona C.G., Valía J.C., Palop N.T.

 Fuente: Journal of Antimicrobial Chemotherapy, 2014, 69(10), 2629-33

 Editorial: Oxford University Press

 Año de publicación: 2014

 Nº de páginas: 5

 Tipo de publicación: Artículo de Revista

 DOI: 10.1093/jac/dku179

 ISSN: 0305-7453,1460-2091

Autoría

MOSQUEDA, NORAIDA

GATO, EVA

ROCA, IGNASI

LÓPEZ, MARÍA

DE ALEGRÍA, CARLOS RUIZ

FERNÁNDEZ CUENCA, FELIPE

LUIS MARTINEZ MARTINEZ

PACHÓN, JERÓNIMO

RODRIGUEZ BAÑOS, JESÚS

PASCUAL, ÁLVARO

VILA, JORDI

BOU, GERMÁN

TOMÁS, MARÍA