| Literature DB >> 26700563 |
Xiaoran Zhao1, Hongen Li1, Jianfeng Wang1, Yan Guo1, Bowen Liu1, Xuming Deng2, Xiaodi Niu2.
Abstract
Pneumolysin (PLY), an essential virulence factor of Streptococcus pneumoniae (pneumococcus), can penetrate the physical defenses of the host and possesses inflammatory properties. The vital role PLY plays in pneumococcus pathogenesis makes this virulence factor one of the most promising targets for the treatment of pneumococcal infection. Verbascoside (VBS) is an agent that does not exhibit bacteriostatic activity but has been shown to inhibit PLY-mediated cytotoxicity. The results from molecular dynamics simulations and mutational analysis indicated that VBS binds to the cleft between domains 3 and 4 of PLY, thereby blocking PLY's oligomerization and counteracting its hemolytic activity. Moreover, VBS can effectively alleviate PLY-mediated human alveolar epithelial (A549) cell injury, and treatment with VBS provides significant protection against lung damage and reduces mortality in a pneumococcal pneumonia murine model. Our results demonstrate that VBS is a strong candidate as a novel therapeutic in the treatment of Streptococcus pneumoniae infection.Entities:
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Year: 2015 PMID: 26700563 DOI: 10.1124/mol.115.100610
Source DB: PubMed Journal: Mol Pharmacol ISSN: 0026-895X Impact factor: 4.436