Lu Jun, Jiang Shan, Ye Song, Deng Yun, Ma Shuai, Li Chao-Pin
Department of Pathogen Biology and Immunology, Anhui University of Science and Technology, Huainan, Anhui 232001, P.R. China.
Department of Mining Engineering, Huainan Vocational Technical College, Huainan, Anhui 23200, P.R. China.
Mol Med Rep. 2014 Apr;9(4):1325-30. doi: 10.3892/mmr.2014.1948. Epub 2014 Feb 13.
The aim of the present study was to investigate the mutational characteristics of the drug‑resistant Mycobacterium tuberculosis L‑form of the rpoB gene isolated from patients with pneumoconiosis complicated by tuberculosis, in order to reduce the occurrence of the drug resistance of patients and gain a more complete information on the resistance of the Mycobacterium tuberculosis L‑form. A total of 42 clinically isolated strains of Mycobacterium tuberculosis L‑form were collected, including 31 drug‑resistant strains. The genomic DNA was extracted, then the target genes were amplified by polymerase chain reaction and the hot mutational regions of the rpoB gene were analyzed by direct sequencing. The results revealed that no rpoB gene mutation was present in 11 rifampicin (RFP)‑sensitive strains, while conformational changes were identified in 31 RFP‑resistant strains. The mutation rate was 93.55% (29/31) in the resistant strains, and was frequently concentrated in codons 531 (51.61%; 16/31) and 526 (32.26%; 10/31), mainly occurring by case substitutions, including 27 unit point mutations and two two‑point mutations. The novel mutation identified in codon 516 had not been previously reported. The substitution of highly‑conserved amino acids encoded by the rpoB gene resulted in the molecular mechanism responsible for RFP resistance in the Mycobacterium tuberculosis L‑form. This also demonstrated that the rpoB gene is diversiform.
本研究旨在探讨从尘肺病合并肺结核患者中分离出的耐药结核分枝杆菌L型rpoB基因的突变特征,以降低患者耐药性的发生,并更全面地了解结核分枝杆菌L型的耐药情况。共收集42株临床分离的结核分枝杆菌L型菌株,其中31株为耐药菌株。提取基因组DNA,然后通过聚合酶链反应扩增靶基因,并通过直接测序分析rpoB基因的热点突变区域。结果显示,11株对利福平(RFP)敏感的菌株未出现rpoB基因突变,而31株RFP耐药菌株中发现了构象变化。耐药菌株的突变率为93.55%(29/31),且突变常集中在密码子531(51.61%;16/31)和526(32.26%;10/31),主要为碱基替换,包括27个单位点突变和2个双位点突变。密码子516中鉴定出的新突变此前未见报道。rpoB基因编码的高度保守氨基酸的替换导致了结核分枝杆菌L型对RFP耐药的分子机制。这也表明rpoB基因具有多样性。