| Literature DB >> 34071703 |
Yunxing Fu1,2, Chunqing Leng3, Yuan Fan4, Xia Ma1,2, Xianghui Li1,2, Xuefei Wang1,2, Zhenghuan Guo1,2, Xiujun Wang1,2, Ruofeng Shang4.
Abstract
Staphylococcus aureus (S. aureus) is a major human pathogen that requires new antibiotics with unique mechanism. A new pleuromutilin derivative, 14-O-[(4,6-Diamino-pyrimidine-2-yl) thioacetyl] mutilin (DPTM), has been synthesized and proved as a potent antibacterial agent using in vitro and in vivo assays. In the present study, DPTM was further in vitro evaluated against methicillin-resistant Staphylococcus aureus (MRSA) isolated from dairy farms and outperformed tiamulin fumarate, a pleuromutilin drug used for veterinary. Moreover, a murine skin wound model caused by MRSA infection was established, and the healing effect of DPTM was investigated. The results showed that DPTM could promote the healing of MRSA skin infection, reduce the bacterial burden of infected skin MRSA and decrease the secretion of IL-6 and TNF-α inflammatory cytokines in plasma. These results provided the basis for further in-depth drug targeted studies of DPTM as a novel antibacterial agent.Entities:
Keywords: DPTM; MIC; antibacterial activity; methicillin-resistant Staphylococcus aureus (MRSA); murine skin wound model
Year: 2021 PMID: 34071703 DOI: 10.3390/molecules26113277
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411