4.6 Article

Acetylsalicylic acid (aspirin) reduces damage to reconstituted human tissues infected with Candida species by inhibiting extracellular fungal lipases

期刊

MICROBES AND INFECTION
卷 11, 期 14-15, 页码 1131-1139

出版社

ELSEVIER
DOI: 10.1016/j.micinf.2009.08.007

关键词

Candida; Acetylsalicylic acid; Lipases; Human fungal pathogen; Yeast; Inhibition; Pathogenesis

资金

  1. NIH [AI52733, AI056070-01A2]
  2. Center for AIDS Research at the Albert Einstein College of Medicine and Montefiore Medical Center [NIH AI-51519]
  3. Hirschl/Weill-Caulier Career Scientist Award
  4. OTKA [PD73250]
  5. EMBO [1813]
  6. Hungarian Academy of Sciences
  7. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI052733, P30AI051519, R01AI056070] Funding Source: NIH RePORTER

向作者/读者索取更多资源

A reconstituted human tissue model was used to mimic Candida albicans and Candida parapsilosis infection in order to investigate the protective effects of acetylsalicylic acid (aspirin, ASA). We found that therapeutic concentrations of ASA reduced tissue damage in the in vitro infection model. We further evaluated the lipase inhibitory effects of ASA by investigating the growth of C. albicans, C. parapsilosis and C. parapsilosis lipase negative (Delta cplip1-2/Delta cplip1-2) mutants in a lipid rich minimal medium supplemented with olive oil and found that a therapeutic concentration of ASA inhibited the growth of wild type fungi. The lipase inhibitors quinine and ebelactone B were also shown to reduce growth and protect against tissue damage from Candida species, respectively. A lipolytic activity assay also showed that therapeutic concentrations of ASA inhibited C. antarctica and C. cylindracea purified lipases obtained through a commercial kit. The relationship between ASA and lipase was characterized through a computed structural model of the Lipase-2 protein from C. parapsilosis in complex with ASA. The results suggest that development of inhibitors of fungal lipases could result in broad-spectrum therapeutics, especially since fungal lipases are not homologous to their human analogues. (C) 2009 Elsevier Masson SAS. All rights reserved.

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