2007 年至 2013 年中国耐多药结核分枝杆菌分离株中莫西沙星耐药率的大幅增加。
Strong Increase in Moxifloxacin Resistance Rate among Multidrug-Resistant Mycobacterium tuberculosis Isolates in China, 2007 to 2013.
机构信息
National Tuberculosis Reference Laboratory, National Center for Tuberculosis Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
Institute of Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People's Hospital, Shenzhen, China.
出版信息
Microbiol Spectr. 2021 Dec 22;9(3):e0040921. doi: 10.1128/Spectrum.00409-21. Epub 2021 Dec 1.
We designed this study to determine the trend of moxifloxacin resistance among multidrug-resistant tuberculosis (MDR-TB) patients from 2007 to 2013 in China to inform the composition of multidrug-resistant/rifampicin-resistant tuberculosis (MDR/RR-TB) treatment regimens. We assessed moxifloxacin resistance among MDR-TB isolates collected in national drug resistance surveys in 2007 and 2013 that included 3,634 smear-positive and 7,206 culture-positive pulmonary tuberculosis patients, respectively. Moxifloxacin susceptibility was examined by a Mycobacterium growth indicator tube (MGIT) 960 for the 2007 isolates, and by the minimum inhibitory concentration (MIC) method for the 2013 isolates, at both breakpoints 0.5 and 2.0 μg/mL. Risk factors were explored through multivariable log-binominal regression analysis. Mutations in and for part of the isolates were also studied through sequencing. Of 401 MDR strains isolated in 2007, moxifiloxacin resistance could be determined for 319 (79.6%): 41 (12.9%) and 10 (3.1%) were resistant at 0.5 and 2.0 μg/mL, respectively. Of 365 MDR strains isolated in 2013, 338 (92.6%) could be analyzed: 140 (41.4%) and 79 (23.4%) were resistant at 0.5 and 2.0 μg/mL. For patients in 2007, no characteristics were significantly associated with moxifloxacin resistance. For patients in 2013, patients aged ≥60 years (adjusted prevalence ratio [aPR], 1.46; 95% confidence interval [CI], 1.10 to 1.93) were more likely to have resistance at 0.5 μg/mL, whereas those residing in eastern China compared to those in central China had an increased risk of resistance at both 0.5 (aPR, 1.85; 95% CI, 1.38 to 2.48) and 2.0 μg/mL (aPR, 2.14; 95% CI, 1.35 to 3.40). Sequencing results were obtained for 245 and 266 MDR-TB isolates in 2007 and 2013, respectively. In total, 34 of 38 (89.5%) and 89 of 104 (85.6%) of 2007 and 2013 moxifloxacin-resistant (0.5 μg/mL) MDR-TB strains had mutations in the and gene, respectively. Asp94Gly was the most common mutation among 2007 (11 of 38, 28.9%) and 2013 isolates (24 of 104, 23.1%) and conferred high-level moxifloxacin resistance. Moxifloxacin resistance among MDR-TB patients in China increased from modest to high from 2007 to 2013. Moxifloxacin should be used carefully as a potentially effective drug for composing MDR/RR-TB regimens especially for elderly patients in China. Individual susceptibility testing especially rapid molecular-based assays should be conducted to confirm the susceptibility to moxifloxacin. China is one of the high-burden countries for multidrug-resistant/rifampicin-resistant tuberculosis (MDR/RR-TB). Moxifloxacin is one of the critical antituberculosis drugs for MDR/RR-TB treatment. Susceptibility to moxifloxacin is therefore very important to compose effective regimens and to provide protection against development of resistance of companion drugs such as bedaquiline and linezolid. There are, however, no nationally representative data on moxifloxacin resistance among MDR/RR-TB cases in China. Therefore, we assessed the resistance prevalence for moxifloxacin among MDR-TB strains isolated in national drug resistance surveys in 2007 and 2013 that covered 72 sites around the country. We demonstrate that the prevalence of moxifloxacin resistance in MDR-TB isolates increased from modest to high, which should prompt the national tuberculosis program to use moxifloxacin cautiously in second-line regimens to treat MDR/RR-TB unless susceptibility can be laboratory-confirmed.
我们设计了这项研究,以确定 2007 年至 2013 年期间中国耐多药结核病(MDR-TB)患者中莫西沙星耐药的趋势,以便为多药耐药/利福平耐药结核病(MDR/RR-TB)治疗方案的组成提供信息。我们评估了 2007 年和 2013 年全国耐药监测中收集的耐多药结核分枝杆菌分离株中的莫西沙星耐药性,分别包括 3634 例痰涂片阳性和 7206 例培养阳性肺结核患者。2007 年分离株的莫西沙星药敏性通过分枝杆菌生长指示管(MGIT)960 进行检测,2013 年分离株的最小抑菌浓度(MIC)方法在 0.5 和 2.0μg/mL 两个断点进行检测。通过多变量对数二项式回归分析探讨了危险因素。还通过测序研究了部分分离株中 和 基因的突变情况。在 2007 年分离的 401 株 MDR 菌株中,可确定 319 株(79.6%)莫西沙星耐药:分别有 41 株(12.9%)和 10 株(3.1%)在 0.5 和 2.0μg/mL 时耐药。在 2013 年分离的 365 株 MDR 菌株中,可分析 338 株(92.6%):分别有 140 株(41.4%)和 79 株(23.4%)在 0.5 和 2.0μg/mL 时耐药。对于 2007 年的患者,没有特征与莫西沙星耐药显著相关。对于 2013 年的患者,年龄≥60 岁的患者(调整后患病率比 [aPR],1.46;95%置信区间 [CI],1.10 至 1.93)在 0.5μg/mL 时更有可能耐药,而与中国中部地区相比,居住在中国东部地区的患者在 0.5μg/mL (aPR,1.85;95%CI,1.38 至 2.48)和 2.0μg/mL(aPR,2.14;95%CI,1.35 至 3.40)时耐药的风险增加。对 2007 年和 2013 年的 245 和 266 株 MDR-TB 分离株进行了测序。总共,2007 年和 2013 年莫西沙星耐药(0.5μg/mL)的 38 株和 104 株 MDR-TB 株中,分别有 34 株(89.5%)和 89 株(85.6%)在 和 基因中有突变。2007 年(11 株,28.9%)和 2013 年(24 株,23.1%)分离株中最常见的突变是天冬氨酸 94 甘氨酸,其导致高水平的莫西沙星耐药性。从 2007 年到 2013 年,中国耐多药结核病患者的莫西沙星耐药率从适度增加到高度。莫西沙星作为一种潜在有效的抗结核药物,应谨慎用于组成耐多药/利福平耐药结核病(MDR/RR-TB)方案,尤其是中国的老年患者。应进行个体药敏试验,尤其是快速分子检测,以确认对莫西沙星的敏感性。中国是耐多药/利福平耐药结核病(MDR/RR-TB)负担较高的国家之一。莫西沙星是治疗 MDR/RR-TB 的关键抗结核药物之一。因此,对莫西沙星的敏感性对于组成有效的方案和防止伴随药物如贝达喹啉和利奈唑胺耐药的发展非常重要。然而,中国 MDR/RR-TB 病例中莫西沙星耐药的全国代表性数据尚不存在。因此,我们评估了 2007 年和 2013 年全国耐药监测中收集的耐多药结核分枝杆菌分离株中莫西沙星耐药的流行率,这两个监测覆盖了全国 72 个地点。我们证明,耐多药结核分枝杆菌分离株中莫西沙星耐药的流行率从适度增加到高度,这应该促使国家结核病规划谨慎使用莫西沙星作为二线方案来治疗 MDR/RR-TB,除非可以通过实验室确认其敏感性。