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Chinese Journal of Antituberculosis ›› 2021, Vol. 43 ›› Issue (9): 952-960.doi: 10.3969/j.issn.1000-6621.2021.09.016

• Original Articles • Previous Articles     Next Articles

Analysis and comparative study on the virulence of several drug-resistant Mycobacterium tuberculosis

ZHOU Ying-yu, FU Lei, ZHANG Wei-yan, WANG Bin, CHEN Xi, LU Yu(), CHEN Xiao-you()   

  1. Beijing Key Laboratory of Drug Resistance Tuberculosis Research, Department of Pharmacology, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing Chest Hospital, Capital Medical University,Beijing 101149,China
  • Received:2021-05-08 Online:2021-09-10 Published:2021-09-07
  • Contact: LU Yu,CHEN Xiao-you E-mail:luyu4876@hotmail.com;chenxy1998@hotmail.com

Abstract:

Objective To evaluate the virulence of clinical drug-resistant isolates and laboratory induced drug-resistant strains of Mycobacterium tuberculosis (MTB). Methods MTB standard strain H37Rv and attenuated strain H37Ra, four clinical drug-resistant isolates (15833, 16030, 17080 and 30744) and eight laboratory induced drug-resistant strains, including one pretomanid(PA-824)resistant strain (P1), one Lzd resistant strain (L1), three PBTZ-169 resistant strain (169-1, 169-2, 169-3), three PA-824 and Lzd dual resistant strains (PL1, PL2, PL3), were selected. The minimum inhibitory concentration (MIC) of clinical drug-resistant isolates against first-line and second-line anti-tuberculosis drugs and laboratory induced drug-resistant strains against Lzd, PA-824 and PBTZ-169 were measured. The in vitro growth curves of the studied strains and the intracellular colony forming units (CFU) of macrophages 2 days after infection were drawn, and the content of lactate dehydrogenase (LDH) released by macrophages 2 days after infection was measured.One hundred and sixty-eight BALB/c mice, 6-7 weeks old and 16-18 g/mouse, were randomly divided into 14 groups with 12 mice in each group. BALB/c mice were infected with drug-resistant strains by tail vein injection. The half survival time of mice was recorded and analyzed. Results In vitro experiments showed that the plateau phase of growth curve of MTB clinical drug-resistant isolate 30744 was earlier than that of the other drug-resistant strains, the adaptability of the strain in vitro was lower, and the growth curve trend of the other drug-resistant strains was basically identical. The intracellular CFU counts of clinical drug resistant isolates (15833, 16030, 30744, 17080) and laboratory induced drug resistant strains (PL1, PL2, PL3) resistant to Lzd and PA-824 were (5.180±0.074), (5.571±0.029), (5.550±0.073), (5.446±0.099), (5.763±0.197), (5.907±0.053), and (5.661±0.083) log10 CFU/ml, which was significantly lower than that of standard strain H37Rv ((6.207 ± 0.028) log10 CFU/ml), and the difference was statistically significant (t=17.932, 12.758, 12.034, 10.241, 4.796, 7.042, 9.113, Ps<0.05). In addition, the absorbance A490 values of LDH release from macrophages infected by strains 15833, 16030, 30744, 1708, P1, L1, PL1, PL2, PL3, 169-1, 169-2 and 169-3 were 0.252±0.039, 0.412±0.078, 0.247±0.022, 0.358±0.054, 0.329±0.015, 0.483±0.017, 0.328±0.046, 0.455±0.075, 0.283±0.041, 0.258±0.044, 0.374±0.080, and 0.311±0.097, which was significantly lower than that of standard strain H37Rv (0.958±0.025), and the difference was statistically significant (t=27.269, 16.788, 38.244, 24.238, 44.005, 32.698, 27.713, 15.171, 31.798, 31.472, 16.515, 15.570, Ps<0.01). In vivo virulence test showed that: (1) The half surviors’ alive time (≥15 days) of all strains infected mice was significantly longer than that of H37Rv (12 days). (2) The survival curve of mice showed that the survival time of mice infected with pre-XDR strain was longer than that of MDR strains, namely 30744>17080>16030>15833; (3)The survival time of mice in the dual drug-resistant strain LPDR group>PBTZ-169 drug-resistant strain group=single Lzd resistant group>single PA-824 resistant strain group. Conclusion The virulence of MTB resistant strains was lower than that of wild-type standard strains, and the virulence might be negatively correlated with the number of drug-resistance.

Key words: Mycobacterium tuberculosis, Virulence, Survival analysis, Evaluation studies