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Transferable mechanisms of quinolone resistance from 1998 onward

*Corresponding author for this work
Research Output:
Contribution to journal
Review article
Peer-review

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Publication Information

Output type

Research Output:
Contribution to journal
Review article
Peer-review

Original language

English

Article number

e00007-19

Journal (Volume, Issue Number)

Clinical Microbiology Reviews (Volume 32, Issue 4)

Publication milestones

  • Published - 10/2019

Publication status

Published - 10/2019

ISSN

0893-8512

Publication IDs

  • Scopus: 85071281910
  • PubMed: 31413045

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 explo-sion 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.

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