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作 者:庄玉辉[1] 何秀云[1] 张小刚[1] 董恩军[1] 阎国蕊 胡忠义 王庆 翟秉祥 丁北川
机构地区:[1]解放军第三○九医院结核病研究室,北京100091 [2]河南省胸科医院参比实验室 [3]上海市疾病控制中心防痨科 [4]安徽省胸科医院检验科 [5]河北省胸科医院检验科 [6]北京市结核病控制研究所实验室
出 处:《中华结核和呼吸杂志》2000年第12期711-714,共4页Chinese Journal of Tuberculosis and Respiratory Diseases
基 金:国家重大基础研究发展规划(973);"严重传染病防治基础研究"课题资助(G1999054104)
摘 要:目的研究中国五省、市部分耐利福平(RFP)或含RFP的耐多药结核分支杆菌临床分离株rpoB基因突变的情况及抽提鉴定是否含有质粒,为评价耐RFP的分子机制,进而为结核病基础和临床研究提供分子遗传学依据。方法采用PCR-SSCP技术,对来自河南省、河北省、安徽省、北京市、上海市262株结核分支杆菌临床分离株(其中敏感株74株,耐RFP或含RFP耐多药株188株)rpoB基因突变的发生率进行研究;同时,对76株结核分支杆菌临床分离株按碱性溶菌法抽提分离并鉴定是否含有质粒。结果中国五省、市的部分耐RFP或含RFP耐多药结核分支杆菌临床分离株rpoB基因突变的发生率平均为92%,而各地分别为:河南省90%,河北省94%,安徽省91%,北京市91%,上海市92%,经统计学处理,五省、市之间差异元显著性意义(X2=0.42,P>0.05),所有受试74株对照敏感株rpoB基因均无突变;结核分支杆菌敏感株29株、耐RFP或含RFP耐多药株33株、耐INH、SM、EM 14株共76株均未提取分离与鉴定含有质粒。结论结核分支杆菌耐RFP与rpoB基因突变密切相关,rpoB基因突变是耐RFP结核分支杆菌耐药性的主要分子机制;Objective To evaluate the molecular mechanism of rifampin (RFP)-resistance of M.tuberculosis, and to provide evidence of molecular genetics for basic and clinical research of tuberculoois.Methods rpod gene mutation of M.tuberculosis was detected with PCR-SSCP from 262 clinical isolates, including 74 drug sensitive strains, and 188 RFP-resistant only or multiple drug-resistant strains of M.tuberculosis, collecting from Henan, Hebei and Anhui province, Beijing and Shanghai cities. Plasmids were extracted from 76 clinical isolates of M.tuberculosis with alkaline bacteriolytic methods. Results Mean mutation rate of rpoB gene was 92% in the RFP-resistant clinical isolates of M.tuberculosis. Respectively, the mutation rate was 90.0% in Henan province, 94% in Hebei province, 91% in Anhui province, 91% in Beijing city and 92% in Shanghai city. There was no significant difference between results from the provinces and the cities (X2 =0.42, P > 0.05). However, mutation of rpoB gene was not detected in 74 sensitive clinical isolates of M.tuberculosis. Moreover, in 76 clinical isolates of M.tuberculosis the plasmids were not found, including 29 sensitive strains, 33 RFP-resistant only or multiple drug-resistant strains and 14 RFP, isoniazid, steptomycin and ethambutol-resistant clinical isolates. Conclusions This study confirmed the strong correlation between the RFP-resistance and the mutation of the rpoB gene,which might be a major molecular mechanism of RFP-resistance in M.tuberculosis. No evidence shows that M.tuberculosis has the plasmid,which mediates RFP resistance to M.tuberculosis.
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