Makafe Gaëlle Guiewi, Cao Yuanyuan, Tan Yaoju, Julius Mugweru, Liu Zhiyong, Wang Changwei, Njire Moses M, Cai Xingshan, Liu Tianzhou, Wang Bangxing, Pang Wei, Tan Shouyong, Zhang Buchang, Yew Wing Wai, Lamichhane Gyanu, Guo Jintao, Zhang Tianyu
State Key Laboratory of Respiratory Disease, Guangzhou Institutes of Biomedicine and Health (GIBH), Chinese Academy of Sciences (CAS), Guangzhou, China.
State Key Laboratory of Respiratory Disease, Guangzhou Institutes of Biomedicine and Health (GIBH), Chinese Academy of Sciences (CAS), Guangzhou, China School of Life Sciences, Anhui University, Hefei, China.
Antimicrob Agents Chemother. 2016 Apr 22;60(5):3202-6. doi: 10.1128/AAC.00152-16. Print 2016 May.
We expressed the wild-type rplC and mutated rplC (Cys154Arg) genes, respectively, in Mycobacterium tuberculosis H37Ra and H37Rv in an attempt to delineate the role of rplC (Cys154Arg) regarding oxazolidinone resistance. An increase of the MICs of linezolid (LZD) and sutezolid (PNU-100480, PNU) against the recombinant mycobacteria with overexpressed rplC mutation (Cys154Arg) was found, suggesting the rplC gene is a determinant of bacillary susceptibilities to LZD and PNU.
我们分别在结核分枝杆菌H37Ra和H37Rv中表达了野生型rplC基因和突变型rplC(Cys154Arg)基因,试图阐明rplC(Cys154Arg)在恶唑烷酮耐药性方面的作用。结果发现,利奈唑胺(LZD)和舒他唑胺(PNU-100480,PNU)对过表达rplC突变体(Cys154Arg)的重组分枝杆菌的最低抑菌浓度(MIC)有所增加,这表明rplC基因是细菌对LZD和PNU敏感性的一个决定因素。