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Thiazolidione derivatives targeting the histidine kinase YycG are effective against both planktonic and biofilm-associated Staphylococcus epidermidis

  
@article{APS7093,
	author = {Ren-zheng Huang and Li-kang Zheng and Hua-yong Liu and Bin Pan and Jian Hu and Tao Zhu and Wei Wang and Dan-bin Jiang and Yang Wu and You-cong Wu and Shi-qing Han and Di Qu},
	title = {Thiazolidione derivatives targeting the histidine kinase YycG are effective against both planktonic and biofilm-associated Staphylococcus epidermidis},
	journal = {Acta Pharmacologica Sinica},
	volume = {33},
	number = {3},
	year = {2016},
	keywords = {},
	abstract = {Aim:  To evaluate the efficacies of six derivatives of Compound 2, a novel YycG histidine kinase inhibitor with the thiazolidione core structure in the treatment of medical device-related biofilm infections.
Methods:  The minimal inhibitory concentration (MIC) of the derivatives was determined using the macrodilution broth method, and the minimal bactericidal concentration (MBC) was obtained via sub-culturing 100 μL from each negative tube from the MIC assay onto drug-free Mueller-Hinton agar plates. Biofilm-killing effect for immature (6 h-old) biofilms was examined using a semiquantitative plate assay, and the effect on mature (24 h-old) biofilms was observed under a confocal laser scanning microscope (CLSM).
Results:  The derivatives potently suppressed the growth of Staphylococcus epidermidis. The MIC values of the derivatives H2-10, H2-12, H2-20, H2-29, H2-27, and H2-28 on S epidermidis ATCC 35984 were 24.3, 6.5, 6.2, 3.3, 3.1, and 1.5 μg/mL, respectively. The MBC values of these derivatives were 48.6, 52.2, 12.4, 52.6, 12.4, and 6.2 μg/mL, respectively. The derivatives killed all bacteria in immature (6 h-old) biofilms and eliminated the biofilm proliferation. The derivatives also displayed strong bactericidal activities toward cells in mature (24 h-old) biofilms, whereas they showed low cytotoxicity and hemolytic activity toward Vero cells and human erythrocytes.
Conclusion:  The bactericidal and biofilm-killing activities of the new anti-YycG compounds were significantly better than the parent Compound 2.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/7093}
}