实用医学杂志 ›› 2023, Vol. 39 ›› Issue (2): 198-203.doi: 10.3969/j.issn.1006⁃5725.2023.02.013

• 基础研究 • 上一篇    下一篇

结核分枝杆菌Rv3737抑制巨噬细胞自噬促进耻垢分枝杆菌在巨噬细胞内的存活

付雪峰 娄思玉 彭章丽   

  1. 遵义医科大学附属医院呼吸与危重症医学科结核病区(贵州遵义 563000)

  • 出版日期:2023-01-25 发布日期:2023-01-25
  • 通讯作者: 彭章丽 E⁃mail:pengzhangli1987@163.com

Mycobacterium tuberculosis Rv3737 suppresses macrophage autophagy to enhance bacterial survival in macrophages 

FU Xuefeng,LOU Siyu,PENG Zhangli.   

  1. Tuberculosis Division,Second Department of Respiratory and Critical Care Medicine,the Affiliated Hospital,Zunyi Medical University,Zunyi 563000,China

  • Online:2023-01-25 Published:2023-01-25
  • Contact: PENG Zhangli E⁃mail:pengzhangli1987@163.com
  • Supported by:
    国家自然科学基金地区基金(编号:81960004);贵州省科技计划项目课题(编号:黔科合基础⁃ZK[2021]一般 348);遵义市科技局课题(编号:遵市科合 HZ 字 2019(70)号);遵义医学院硕士启动基金(编号:2015(009))

摘要:

目的 了解结核分枝杆菌跨膜蛋白 Rv3737 对耻垢分枝杆菌感染巨噬细胞自噬的作用。方法 通过 PCR 扩增结核分枝杆菌 Rv3737 目的基因,T4 连接酶连接 Rv3737 及穿梭质粒 pMV261,构建pMV261⁃Rv3737,双酶切及测序验证pMV261⁃Rv3737,通过电转将pMV261⁃Rv3737及pMV261⁃Vector 电转至耻垢分枝杆菌感受态细胞中以构建过表达Rv3737的耻垢分枝杆菌菌株(MS::pMV261⁃Rv3737)和对照菌株(MS::pMV261),PCR 及 Western blot 验证过表达 Rv3737 的耻垢分枝杆菌菌株。利用分光光度计检测 OD600评估过表达 Rv3737 对耻垢分枝杆菌体外生长的影响。将 MS::pMV261⁃Rv3737 及 MS::pMV261 感染巨噬细胞,通过菌落形成单位(CFU)计数检测耻垢分枝杆菌在巨噬细胞内的存活,用 Western blot 及激光共聚焦检测自噬相关蛋白LC3II的变化。结果 Rv3737 不影响耻垢分枝杆菌的体外生长,但促进耻垢分枝杆菌在巨噬细胞内的存活,过表达 Rv3737 明显抑制 LC3II的表达,激光共聚焦结果显示过表达Rv3737后LC3II自噬点明显减少。结论 结核分枝杆菌跨膜蛋白Rv3737可能通过抑制巨噬细胞自噬来促进耻垢分枝杆菌在巨噬细胞内的存活,有望成为抗结核药物作用的靶点,为结核病的治疗提供一定的理论依据。

关键词:

text-indent:0pt, "> 结核分枝杆菌, Rv3737, 耻垢分枝杆菌, 自噬, 巨噬细胞

Abstract:

Objective To explore the effect of mycobacterium tuberculosis transmembrane protein Rv3737 on mycobacterium tuberculosis⁃infected macrophages autophagy. Methods The target gene of mycobacterium tubercu⁃ losis Rv3737 was amplified by PCR. Rv3737 and shuttle plasmid pMV261 were linked by T4 ligase to construct pMV261 ⁃ Rv3737,which was then verified by double enzyme digestion and sequencing. pMV261 ⁃ Rv3737 and pMV261⁃vector plasmids were electrically transferred into the mycobacterium smegmatis competent cells to construct over⁃expressed Rv3737 mycobacterium smegmatis strain(MS::RV3737)and control strain(MS::Vector). The over⁃ expressed Rv3737 in the mycobacterium smegmatis strains was verified by PCR and Western blot. The effect of Rv3737 on the growth of mycobacterium smegmatis in vitro was evaluated by detecting OD600 with a spectrophotome⁃ ter. MS::pMV261⁃RV3737 and MS::pMV261 infected macrophages,the survival of mycobacterium smegmatis in macrophages was detected by colony forming unit(CFU)count,and the effect of Rv3737 on the survival of mycobac⁃ terium smegmatis in macrophages was investigated through Western blot and laser confocal analysis,which were used to detect the changes of autophagy⁃related protein LC3 II. Results RV3737 did not affect the growth of myco⁃ bacterium smegmatis in vitro,but promoted its survival in macrophages. Over⁃expressed Rv3737 significantly inhibited the expression of LC3 II,and the laser confocal results showed that the autophagy sites of LC3 II were significantly reduced after over ⁃expression of Rv3737. Conclusion Mycobacterium tuberculosis transmembrane protein Rv3737 may promote the survival of mycobacterium in macrophages by inhibiting macrophages autophagy,and thus it is expected to be a target of anti⁃tuberculosis drugs and provide theoretical data for the treatment of tuberculosis.

Key words:

mycobacterium tuberculosis, Rv3737, mycobacterium smegmatis, autophagy, macro? phages