Osei-Wusu Stephen, Amo Omari Michael, Asante-Poku Adwoa, Darko Otchere Isaac, Asare Prince, Forson Audrey, Otu Jacob, Antonio Martin, Yeboah-Manu Dorothy
Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Ghana.
West Africa Centre for Cell Biology of Infectious Pathogens, University of Ghana, Legon, Ghana.
Infect Drug Resist. 2018 Feb 22;11:239-246. doi: 10.2147/IDR.S152720. eCollection 2018.
Drug resistance surveillance is crucial for tuberculosis (TB) control. Therefore, our goal was to determine the prevalence of second-line anti-TB drug resistance among diverse primary drug-resistant complex (MTBC) isolates in Ghana.
One hundred and seventeen MTBC isolates with varying first-line drug resistance were analyzed. Additional resistance to second-line anti-TB drugs (streptomycin [STR], amikacin [AMK] and moxifloxacin [MOX]) was profiled using the Etest and GenoType MTBDRsl version 2.0. Genes associated with resistance to AMK and MOX ( and ) were then analyzed for mutation.
Thirty-seven (31.9%) isolates had minimum inhibitory concentration (MIC) values ≥2 µg/mL against STR while 12 (10.3%) isolates had MIC values ≥1 µg/mL for AMK. Only one multidrug-resistant (MDR) isolate (Isolate ID: TB/Nm 919) had an MIC value of ≥0.125 µg/mL for MOX (MIC = 3 µg/mL). This isolate also had the highest MIC value for AMK (MIC = 16 µg/mL) and was confirmed as resistant to AMK and MOX by the line probe assay GenoType MTBDRsl version 2.0. Mutations associated with the resistance were: (G88C) and (A514C and A1401G).
Our findings suggest the need to include routine second-line anti-TB drug susceptibility testing of MDR/rifampicin-resistant isolates in our diagnostic algorithm.
耐药监测对于结核病(TB)控制至关重要。因此,我们的目标是确定加纳不同原发性耐药结核分枝杆菌复合群(MTBC)分离株中二线抗结核药物耐药的流行情况。
分析了117株具有不同一线耐药性的MTBC分离株。使用Etest和GenoType MTBDRsl 2.0版本对二线抗结核药物(链霉素[STR]、阿米卡星[AMK]和莫西沙星[MOX])的额外耐药性进行分析。然后分析与AMK和MOX耐药相关的基因(和)的突变情况。
37株(31.9%)分离株对STR的最低抑菌浓度(MIC)值≥2μg/mL,而12株(10.3%)分离株对AMK的MIC值≥1μg/mL。只有一株耐多药(MDR)分离株(分离株编号:TB/Nm 919)对MOX的MIC值≥0.125μg/mL(MIC = 3μg/mL)。该分离株对AMK的MIC值也最高(MIC = 16μg/mL),并通过线性探针检测GenoType MTBDRsl 2.0版本确认为对AMK和MOX耐药。与耐药相关的突变是:(G88C)和(A514C和A1401G)。
我们的研究结果表明,有必要在我们的诊断算法中纳入对MDR/耐利福平分离株进行常规二线抗结核药物敏感性检测。