Prostaglandin E2 attenuates synergistic bactericidal effects between COX inhibitors and antibiotics on Staphylococcus aureus. (June 2018)

• Record Type: Journal Article
• Authors: Cai, Jia-Yi; Hou, Yong-Na; Li, Jian; Ma, Kai; Yao, Guo-Dong; Liu, Wei-Wei; Hayashi, Toshihiko; Itoh, Kikuji; Tashiro, Shin-ichi; Onodera, Satoshi; Ikejima, Takashi
• Is Part Of: Prostaglandins, leukotrienes, and essential fatty acids. Volume 133(2018)
• Page Start: 16
• Page End: 22
• Publication Date: 2018-06
• Subjects: Antibiotic -- Biofilm formation -- COX inhibitors -- Efflux pump -- Prostaglandin E2; PGE2 prostaglandin -- COX cyclooxygenase -- MRSA methicillin-resistant Staphylococcus aureus -- CFU colony forming unit; Lipids -- Periodicals; Unsaturated fatty acids -- Periodicals; Prostaglandins -- Periodicals; Leukotrienes -- Periodicals; Fatty Acids, Unsaturated -- Periodicals; Acides gras insaturés -- Périodiques; Prostaglandines -- Périodiques; Leucotriènes -- Périodiques; Lipides -- Périodiques; 612.01577
• DOI: 10.1016/j.plefa.2018.04.005
• Languages: English
• ISSNs: 0952-3278

Abstract

Highlights: PGE2 attenuates the bactericidal effects of antibiotics in S. aureus and MRSA. PGE2 downregulates synergistic bactericidal effects between COX inhibitors and antibiotics. PGE2 restored the efflux pump activity and increased biofilm formation. Abstract: PGE2 is found to attenuate the bactericidal effects of kanamycin or ampicillin in Staphylococcus aureus, as well as the methicillin-resistant S. aureus (MRSA). Co-treatment with cyclooxygenase (COX) inhibitors (celecoxib, aspirin or naproxen) synergistically enhances kanamycin or ampicillin-induced cell death of S. aureus and MRSA. COX inhibitors repressed bacterial multidrug resistance through down-regulating efflux pump activity in antibiotics-treated S. aureus and MRSA. However, this synergistic bactericidal effects are reduced by the treatment with PGE2. PGE2 restores the efflux pump activity as well as increases biofilm formation in S. aureus and MRSA. Collectively, the enhancement of efflux pump activity and biofilm formation with PGE2 might partially explain the resistance to synergistic bactericidal effects between COX inhibitors and antibiotics in PGE2-treated S. aureus .