Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/20.500.12394/7755
Título: Transferable mechanisms of quinolone resistance from 1998 onward
Autor(es): Ruiz, J.
Palabras clave: Quimioterapia
Cáncer
Editorial: Universidad Continental
Fecha de publicación: oct-2019
Fecha disponible: 15-jul-2020
Cita bibliográfica: Ruiz, J., Transferable Mechanisms of Quinolone Resistance from 1998 Onward.Clinical Microbiology Reviews. 32(4), e00007-19,(2019). DOI: 10.1128/CMR.00007-19
Resumen/Abstract: While the description of resistance to quinolones is almost as old as these antimicrobial agents themselves, transferable mechanisms of quinolone resistance (TMQR) remained absent from the scenario for more than 36 years, appearing first as sporadic events and afterward as epidemics. In 1998, the first TMQR was soundly described, that is, QnrA. The presence of QnrA was almost anecdotal for years, but in the middle of the first decade of the 21st century, there was an explosion of TMQR descriptions, which definitively changed the epidemiology of quinolone resistance. Currently, 3 different clinically relevant mechanisms of quinolone resistance are encoded within mobile elements: (i) target protection, which is mediated by 7 different families of Qnr (QnrA, QnrB, QnrC, QnrD, QnrE, QnrS, and QnrVC), which overall account for more than 100 recognized alleles; (ii) antibiotic efflux, which is mediated by 2 main transferable efflux pumps (QepA and OqxAB), which together account for more than 30 alleles, and a series of other efflux pumps (e.g., QacBIII), which at present have been sporadically described; and (iii) antibiotic modification, which is mediated by the enzymes AAC(6′)Ib-cr, from which different alleles have been claimed, as well as CrpP, a newly described phosphorylase.
Notas: Cáncer, quimioterapia
Incluido en: https://cmr.asm.org/content/32/4/e00007-19
Acceso: Restringido
Fuente: Universidad Continental
Repositorio Institucional - Continental
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