4.7 Article

Melatonin prevents conjugative transfer of plasmid-mediated antibiotic resistance genes by disrupting proton motive force

Journal

PHARMACOLOGICAL RESEARCH
Volume 175, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2021.105978

Keywords

Melatonin; Horizontal gene transfer; Plasmids; Proton motive force

Funding

  1. National Natural Science Foundation of China [32172907, 32002331, 31872526]
  2. National Key Research and Development Program of China [2018YFA0903400]
  3. Natural Sci-ence Foundation of Jiangsu Province of China [BK20190893]
  4. Agricul-tural Science and Technology Independent Innovation Fund of Jiangsu Province [CX (20) 3091, CX (21) 2010]
  5. China Postdoctoral Science Foundation [2019M651984, 2021T140579]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD) [2020QNRC001]
  7. Young Elite Scientists Sponsorship Program by CAST

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Melatonin has been found to effectively inhibit the transmission of antibiotic resistance genes, providing a potential strategy to prevent the spread of antibiotic resistance. It achieves this by reducing bacterial membrane permeability, inhibiting oxidative stress, and disrupting bacterial proton motive force.
The widespread dissemination of antibiotic resistance genes (ARGs) is a serious problem and constitutes a threat for public health. Plasmid-mediated conjugative transfer of ARGs is recognized as one of the most important pathways accounting for this global crisis. Inhibiting the conjugative transfer of resistant gene-bearing plasmids provides a feasible strategy to prevent the spread of antibiotic resistance. Here we found that melatonin, a neurohormone secreted from pineal gland, substantially inhibited the horizontal transfer of RP4-7 plasmid in a dose-dependent manner. Furthermore, melatonin could also suppress the conjugal frequency of different types of clinical plasmids that carrying colistin resistance gene mcr-1 rather than blaNDM or tet(X) genes. Next, we investigated the mechanisms underlying the inhibitory effect of melatonin on conjugation. As a result, we showed that the addition of melatonin markedly reduced bacterial membrane permeability and inhibited the oxidative stress. In line with these observations, the conjugative transfer-related genes were regulated accordingly. Most importantly, we uncovered that melatonin disrupted bacterial proton motive force (PMF), which is an essential bacterial energy metabolism substance and is important for conjugative process. Collectively, these results provide implications that some non-antibiotics such as melatonin are effective inhibitors of transmission of ARGs and raise a promising strategy to confront the increasing resistant infections.

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