Kwak Miri, Lee Won-Kyu, Lim Young Ju, Lee Seung Heon, Ryoo Sungweon
Hana Pharmaceutical Pangyo R&D Center, Innovally E-dong, 255, Pangyo-ro, Bundang-gu, Seongnam-si, Gyeonggi-do 13550, Republic of Korea.
Osong Medical Innovation Foundation, 123 Osongsaengmyeong-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do 28160, Republic of Korea.
J Microbiol Methods. 2017 Oct;141:1-9. doi: 10.1016/j.mimet.2017.07.001. Epub 2017 Jul 8.
Recently, the need for rapid, reliable, and low-cost drug susceptibility testing (DST) methods has increased due to the emergence of multidrug-resistant Mycobacterium tuberculosis. Colorimetric methods of DST provide results more quickly than standard culture methods and are inexpensive than molecular methods. Thus, colorimetric methods, such as the nitrate reductase assay (NRA), are being recommended. We searched Medline PubMed for reports on the NRA for DST of M. tuberculosis written in English and published within the last five years. We selected 20 reports on six major anti-TB drugs and conducted a meta-analysis using Meta-Disc software. The pooled sensitivities for isoniazid, rifampicin, streptomycin, ethambutol, ofloxacin, and kanamycin were 95.4%, 96.4%, 91.5%, 93.1%, 99.3%, and 88.4%, and the pooled specificities were 98.5%, 99.2%, 92.9%, 97.8%, 97.4%, and 99.4%, respectively. The area under the summary receiver operator curve for all drugs was 0.9723-0.9952. The time to results (TTR) for the direct and indirect NRAs was 7-28days and 6-15days, respectively. Quality assessments were conducted using the quality of diagnostic accuracy studies tool (QUADAS-2) items, and most reports showed good performance. However, ethambutol, streptomycin, and kanamycin showed relatively low sensitivity. We performed a quantitative NRA in liquid media at various inoculum concentrations. The TTR at 4.94×10, 1.67×10, and 2.27×10CFU/mL was 4, 14, and 14days, respectively. The minimum absorbance and nitrite concentration for positive samples were 0.8 and 168μM, respectively. We propose a quantitative standard to determine sample positivity to address the problems with the current standard NRA which is much less expensive than the conventional assay conducted on solid medium.
近年来,由于耐多药结核分枝杆菌的出现,对快速、可靠且低成本的药物敏感性检测(DST)方法的需求不断增加。比色法DST比标准培养方法能更快地提供结果,且比分子方法成本更低。因此,诸如硝酸盐还原酶测定(NRA)等比色法正被推荐使用。我们在Medline PubMed上搜索了过去五年内以英文发表的关于结核分枝杆菌DST的NRA报告。我们选取了20篇关于六种主要抗结核药物的报告,并使用Meta-Disc软件进行了荟萃分析。异烟肼、利福平、链霉素、乙胺丁醇、氧氟沙星和卡那霉素的合并敏感性分别为95.4%、96.4%、91.5%、93.1%、99.3%和88.4%,合并特异性分别为98.5%、99.2%、92.9%、97.8%、97.4%和99.4%。所有药物的汇总受试者工作特征曲线下面积为0.9723 - 0.9952。直接和间接NRA的结果报告时间(TTR)分别为7 - 28天和6 - 15天。使用诊断准确性研究质量工具(QUADAS - 2)项目进行质量评估,大多数报告显示性能良好。然而,乙胺丁醇、链霉素和卡那霉素的敏感性相对较低。我们在不同接种浓度的液体培养基中进行了定量NRA。在4.94×10、1.67×10和2.27×10CFU/mL时的TTR分别为4天、14天和14天。阳性样本的最小吸光度和亚硝酸盐浓度分别为0.8和168μM。我们提出了一种确定样本阳性的定量标准,以解决当前标准NRA存在的问题,该标准比在固体培养基上进行的传统检测便宜得多。