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[抗结核药物诱导的结核分枝杆菌L型特性观察]

[Observations of properties of the L-form of M. tuberculosis induced by the antituberculosis drugs].

作者信息

Wang H, Chen Z

机构信息

Department of Microbiology, Guiyang Medical College, Guiyang 550004, China.

出版信息

Zhonghua Jie He He Hu Xi Za Zhi. 2001 Jan;24(1):52-5.

Abstract

OBJECTIVES

To investigate the mechanism of generation of L-form of M. tuberculosis and its significance on the development, diagnosis and treatment of tuberculosis.

METHODS

M. tuberculosis was inoculated into the non-high osmotic medium with rifampin, isoniazid or ethambutol and then the L-form was observed by microscopy daily. The cultures were filtrated to get the pure cultures of stable L-form by subculture with the non-high osmotic medium and characteristics of morphology, growth, susceptibilities to the antibacterial drugs and the special gene of M. tuberculosis were observed when the pure subcultures of the L-form were isolated.

RESULTS

L-form of M. tuberculosis was induced by the concentrations of routine inhibition test of rifampin, isoniazid or ethambutol. The L-form would not be susceptible to the above mentioned antituberculosis drugs but susceptible to streptomycin, erythromycin, ofloxacin, norfloxacin and others. The morphologies of L-form were irregular or spherical with single, paired or chain form, and growth under the bottom of the medium but not movement or adhere to the glass. The L-form was negative by acid-fast stain and negative or positive by Gram stain. The gene of L-form reacted with the PCR kit for the M. tuberculosis and showed the same band.

CONCLUSIONS

M. tuberculosis could be killed by rifampin, isoniazid or ethambutol but also could be induced to become the L-form by these antituberculosis drugs, and it is one of the important factor that affecting the effect of treatment of the tuberculosis. The cell wall deficient variants of M. tuberculosis could be determined by the PCR of M. tuberculosis. It is recommended that the L-forms should be noticed during the treatment with the antituberculosis drugs and combination treatment with antituberculous drugs to which the L-forms were susceptible, is also very important.

摘要

目的

探讨结核分枝杆菌L型产生的机制及其在结核病发生、诊断和治疗中的意义。

方法

将结核分枝杆菌接种于含利福平、异烟肼或乙胺丁醇的非高渗培养基中,每日显微镜观察L型的形成情况。通过用非高渗培养基传代培养进行滤菌,获得稳定L型的纯培养物,分离出L型纯培养物后,观察其形态、生长、对抗菌药物的敏感性及结核分枝杆菌特异基因情况。

结果

利福平、异烟肼或乙胺丁醇常规抑菌试验浓度可诱导结核分枝杆菌形成L型。L型对上述抗结核药物不敏感,但对链霉素、红霉素、氧氟沙星、诺氟沙星等敏感。L型形态不规则或呈球形,有单个、成对或链状排列,在培养基底部生长,不运动或不黏附于玻璃。L型抗酸染色阴性,革兰染色阴性或阳性。L型基因与结核分枝杆菌PCR试剂盒反应显示相同条带。

结论

结核分枝杆菌可被利福平、异烟肼或乙胺丁醇杀灭,但也可被这些抗结核药物诱导成为L型,这是影响结核病治疗效果的重要因素之一。结核分枝杆菌细胞壁缺陷变异株可用结核分枝杆菌PCR法检测。建议在抗结核药物治疗过程中注意L型的存在,联合使用L型敏感的抗结核药物进行治疗也非常重要。

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