Adam Muatsim Ahmed Mohammed, Ali Hamdan Mustafa Hamdan, Khalil Eltahir Awad Gasim
National Public Health Laboratory, National Tuberculosis Reference Laboratory, Federal Ministry of Health, Khartoum, Sudan.
National Tuberculosis Control Program, Federal Ministry of Health, Khartoum, Sudan.
Pan Afr Med J. 2019 Mar 15;32:124. doi: 10.11604/pamj.2019.32.124.12762. eCollection 2019.
hain GenoType MTBDRsl is nucleic acid amplification assay based on reverse hybridization with specific oligonucleotide probes on nitrocellulose strips. MTBDRsl identifies complex and detects resistance to fluoroquinolone, second line injectable drugs and ethambutol evident as mutations of genes respectively. This study aimed to evaluate the diagnostic performance of the Hain GenoType MTBDRsl Assay using 1% proportion method on LJ medium as gold standard.
a total of 52 rifampicin resistant (RR) isolates were tested for second line drug sensitivity by 1% proportion method and by MTBDRsl assay.
two strains were identified as mycobacteria other than tuberculosis MOTT and the rest were complex MTBC. Five of the MTBC isolates (5/50; 10%) showed resistance to at least one second line drug and one isolate (1/50; 2%) was XDR. XDR strain was concordantly detected by the two methods. One of two Kanamycin-resistant isolates showed discordant results. Ofloxacin showed one false positive and one false negative result. Most discrepancies were detected with Ethambutol. The sensitivity, specificity, positive and negative predictive values were respectively as follows: Ethambutol (63.3.4%, 85.7%, 94.4% and 62%), for Kanamycin (67%, 100%, 100% and 97.9%), for Amikacin and Capreomycin (100%, 100%, 100% and 100%), for Ofloxacin (75%, 97.5%, 75% and 97.8%). For XDR isolate the values were 100%, 100%, 100% and 100% respectively.
MTBDRsl showed high specificity and negative predictive values making it acceptable and time-saving for early presumptive detection of resistance to second-line drugs in Sudan.
海因基因分型MTBDRsl是一种基于与硝酸纤维素膜条上特定寡核苷酸探针进行反向杂交的核酸扩增检测方法。MTBDRsl可鉴定结核分枝杆菌复合群,并分别检测出因基因变异而导致的对氟喹诺酮类、二线注射用药物和乙胺丁醇的耐药性。本研究旨在以罗氏培养基上的1%比例法作为金标准,评估海因基因分型MTBDRsl检测方法的诊断性能。
采用1%比例法和MTBDRsl检测方法,对总共52株耐利福平(RR)菌株进行二线药物敏感性检测。
鉴定出2株非结核分枝杆菌(MOTT),其余为结核分枝杆菌复合群。5株结核分枝杆菌复合群菌株(5/50;10%)显示对至少一种二线药物耐药,1株菌株(1/50;2%)为广泛耐药。两种方法对广泛耐药菌株的检测结果一致。两株耐卡那霉素菌株中有一株结果不一致。氧氟沙星出现1例假阳性和1例假阴性结果。乙胺丁醇检测出的差异最多。其敏感性、特异性、阳性预测值和阴性预测值分别如下:乙胺丁醇(63.3%、85.7%、94.4%和62%),卡那霉素(67%、100%、100%和97.9%),阿米卡星和卷曲霉素(100%、100%、100%和100%),氧氟沙星(75%、97.5%、75%和97.8%)。对于广泛耐药菌株,相应的值分别为100%、100%、100%和100%。
MTBDRsl显示出高特异性和阴性预测值,使其在苏丹用于二线药物耐药性的早期初步检测是可接受且节省时间的。