A novel, rapid (within hours) culture-free diagnostic method for detecting live Mycobacterium tuberculosis with high sensitivity

被引:28
|
作者
Wang, Wen-Hung [1 ]
Takeuchi, Rikiya [2 ]
Jain, Shu-Huei [1 ]
Jiang, Yong-Huang [2 ]
Watanuki, Sonoko [2 ]
Ohtaki, Yoshiharu [2 ]
Nakaishi, Kazunari [3 ,4 ]
Watabe, Satoshi [3 ,4 ]
Lu, Po-Liang [1 ,5 ]
Ito, Etsuro [4 ,6 ,7 ]
机构
[1] Kaohsiung Med Univ Hosp, Dept Internal Med, Div Infect Dis, 100 TzYou 1st Rd, Kaohsiung 80756, Taiwan
[2] TAUNS Labs Inc, R&D Dept, 761-1 Kamishima, Izunokuni, Shizuoka 4102325, Japan
[3] TAUNS Labs Inc, R&D Headquarters, 761-1 Kamishima, Izunokuni, Shizuoka 4102325, Japan
[4] Waseda Univ, Waseda Res Inst Sci & Engn, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
[5] Kaohsiung Med Univ, Coll Med, 100 Shih Chuan 1st Rd, Kaohsiung 80756, Taiwan
[6] Kaohsiung Med Univ, Grad Inst Med, 100 Shih Chuan 1st Rd, Kaohsiung 80756, Taiwan
[7] Waseda Univ, Dept Biol, Shinjuku Ku, 2-2 Wakamatsucho, Tokyo 1628480, Japan
来源
EBIOMEDICINE | 2020年 / 60卷
关键词
Mycobacterium tuberculosis; ELISA; thio-NAD cycling; MPT64; live bacilli detection; XPERT MTB/RIF ULTRA; ULTRASENSITIVE ELISA; COMPLEX; IDENTIFICATION; AMPLICOR; ASSAY; PERFORMANCE; RESISTANCE; ANTIGEN; PROTEIN;
D O I
10.1016/j.ebiom.2020.103007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Nucleic acid amplification tests (NAATs) are widely used to diagnose tuberculosis (TB), but cannot discriminate live bacilli from dead bacilli. Live bacilli can be isolated by culture methods, but this is time-consuming. We developed a de novo TB diagnostic method that detects only live bacilli with high sensitivity within hours. Methods: A prospective study was performed in Taiwan from 2017 to 2018. Sputum was collected consecutively from 1102 patients with suspected TB infection. The sputum was pretreated and heated at 46 degrees C for 1 h to induce the secretion of MPT64 protein from live Mycobacterium tuberculosis. MPT64 was detected with our ultrasensitive enzyme-linked immunosorbent assay (ELISA) coupled with thionicotinamide-adenine dinucleotide (thio-NAD) cycling. We compared our data with those obtained using a culture test (MGIT), a smear test (Kinyoun staining), and a NAAT (Xpert). Findings: The limit of detection for MPT64 in our culture-free ultrasensitive ELISA was 2.0 x 10(-19) moles/assay. When the criterion for a positive response was set as an absorbance value >= 17 mAbs, this value corresponded to ca. 330 CFU/mL in the culture method - almost the same high-detection sensitivity as the culture method. To confirm that MPT64 is secreted from only live bacilli, M. bovis BCG was killed using 8 mg/mL rifampicin and then heated. Following this procedure, our method detected no MPT64. Our rapid ultra-sensitive ELISA-based method required only 5 h to complete. Comparing the results of our method with those of culture tests for 944 specimens revealed a sensitivity of 86.9% (93/107, 95% CI: 79.0-92.7%) and a specificity of 92.0% (770/837, 95% CI: 89.9-93.7%). The performance data were not significantly different (McNemar's test, P = 0.887) from those of the Xpert tests. In addition, at a >= 1+ titer in the smear test, the positive predictive value of our culture-free ultrasensitive ELISA tests was in a good agreement with that of the culture tests. Furthermore, our culture-free ultrasensitive ELISA test had better validity for drug effectiveness examination than Xpert tests because our test detected only live bacilli. Interpretation: Our culture-free ultrasensitive ELISA method detects only live TB bacilli with high sensitivity within hours, allowing for rapid diagnosis of TB and monitoring drug efficacy. Funding: Matching Planner Program from JST (VP29117939087), the A-STEP Program from JST (AS3015096U), Waseda University grants for Specific Research Projects (2017A-015 and 2019C-123), the Precise Measurement Technology Promotion Foundation to E.I. (c) 2020 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
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