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Quinolones: Mechanism, Lethality and Their Contributions to Antibiotic Resistance

期刊

MOLECULES
卷 25, 期 23, 页码 -

出版社

MDPI
DOI: 10.3390/molecules25235662

关键词

fluoroquinolones; DNA gyrase; topoisomerases; antibacterials; DNA topology; supercoiling; antibiotic resistance

资金

  1. Wellcome Trust [110072/Z/15/Z]
  2. BBSRC Institute Strategic Programme Grant [BB/P012523/1]
  3. DTP studentship - BBSRC [BB/M011216/1]
  4. BBSRC [1916136] Funding Source: UKRI
  5. Wellcome Trust [110072/Z/15/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

Fluoroquinolones (FQs) are arguably among the most successful antibiotics of recent times. They have enjoyed over 30 years of clinical usage and become essential tools in the armoury of clinical treatments. FQs target the bacterial enzymes DNA gyrase and DNA topoisomerase IV, where they stabilise a covalent enzyme-DNA complex in which the DNA is cleaved in both strands. This leads to cell death and turns out to be a very effective way of killing bacteria. However, resistance to FQs is increasingly problematic, and alternative compounds are urgently needed. Here, we review the mechanisms of action of FQs and discuss the potential pathways leading to cell death. We also discuss quinolone resistance and how quinolone treatment can lead to resistance to non-quinolone antibiotics.

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