4.5 Article

Antibiotic Adjuvant Activity Revealed in a Photoaffinity Approach to Determine the Molecular Target of Antipyocyanin Compounds

期刊

ACS INFECTIOUS DISEASES
卷 7, 期 3, 页码 535-543

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsinfecdis.0c00160

关键词

Pseudomonas aeruginosa; colistin; adjuvant; ArnA; PA14_30820

资金

  1. National Institutes of Health [5SC3GM118199, 5R25GM071381]
  2. California State University Program for Education and Research in Biotechnology (New Investigator Grant)
  3. Howard Hughes Medical Institute
  4. Merck (Merck Undergraduate Science Endeavor Grant)
  5. National Science Foundation [DUE-1258366, HRD-1302873]
  6. Organic Synthesis, Inc.
  7. Chancellor's Office of the California State University

向作者/读者索取更多资源

Newly developed antipyocyanin compounds not only have potential antivirulence effects, but may also act as antibiotic adjuvants to amplify bactericidal activity. These compounds could represent a first-in-class antibiotic adjuvant therapy, widening the therapeutic index and strengthening our arsenal against Pseudomonas aeruginosa infections.
Infections with Pseudomonas aeruginosa are a looming threat to public health. New treatment strategies are needed to combat this pathogen, for example, by blocking the production of virulence factors like pyocyanin. A photoaffinity analogue of an antipyocyanin compound was developed to interrogate the inhibitor's molecular mechanism of action. While we sought to develop antivirulence inhibitors, the proteomics results suggested that the compounds had antibiotic adjuvant activity. Unexpectedly, we found that these compounds amplify the bactericidal activity of colistin, a well-characterized antibiotic, suggesting they may represent a first-in-class antibiotic adjuvant therapy. Analogues have the potential not only to widen the therapeutic index of cationic antimicrobial peptides like colistin, but also to be effective against colistin-resistant strains, strengthening our arsenal to combat P. aeruginosa infections.

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