Babamahmoodi Farhang, Mahdavi Mohammad Reza, Jalali Hossein, Talebi Bita, Roshan Payam, Mahdavi Mehrad
Antimicrobial Resistance Research Center, Department of Infectious Diseases, Mazandaran University of Medical Sciences, Sari, Iran.
Thalassemia Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Int J Mol Cell Med. 2014 Summer;3(3):190-5.
Drug resistance (especially multiple drug resistance) in Mycobacterium tuberculosis makes global concerns in treatment and control of tuberculosis. Rapid diagnosis of drug resistant strains of the bacteria has vital importance in the prognosis of the disease. The aim of this study was to identify the mutations responsible for drug resistance in Mycobacterium tuberculosis strains derived from patients with tuberculosis using line probe assay (LPA) method which rapidly detect drug resistant strains and respective mutations. Sputum samples from tuberculosis patients were collected and cultured on Lowenstein- Jensen medium, and then the colonies of Mycobacterium tuberculosis from cultures of 54 bacterial positive cases were randomly chosen for DNA extraction. Bacterial DNA was extracted using standard Cetyl Trimethyl Ammonium Bromide (CTAB) method. In order to identify drug resistant strains and related mutations, LPA method was applied. Three subjects out of 54 investigated cases were resistant to quinolone (5.5%), and resistance to kanamycin/ amikacin, streptomycin, rifampin, and isoniazid were observed in 3 (5.5%), 4 (7.4%), 3 (5.5%), and 2 (3.7%) of the Mycobacterium tuberculosis strains, respectively. In the present study, 4 cases (7.4%) were detected to be resistant to more than one drug. Since LPA is a rapid method that simultaneously detects mutations involved in drug resistance, applying this method in the prediction of drug resistance and selecting appropriate treatment in tuberculosis patients is recommended.
结核分枝杆菌的耐药性(尤其是多重耐药性)引起了全球对结核病治疗和控制的关注。快速诊断该细菌的耐药菌株对疾病的预后至关重要。本研究的目的是使用线性探针分析法(LPA)来鉴定结核病患者来源的结核分枝杆菌菌株中导致耐药性的突变,该方法可快速检测耐药菌株及相应突变。收集结核病患者的痰液样本,接种于罗-琴培养基上培养,然后从54例细菌阳性培养物中随机选取结核分枝杆菌菌落进行DNA提取。采用标准的十六烷基三甲基溴化铵(CTAB)法提取细菌DNA。为鉴定耐药菌株及相关突变,应用了LPA法。在54例受调查病例中,有3例对喹诺酮耐药(5.5%),分别有3株(5.5%)、4株(7.4%)、3株(5.5%)和2株(3.7%)结核分枝杆菌菌株对卡那霉素/阿米卡星、链霉素、利福平及异烟肼耐药。在本研究中,有4例(7.4%)被检测出对不止一种药物耐药。由于LPA是一种可同时检测与耐药性相关突变的快速方法,建议将该方法应用于结核病患者的耐药性预测及选择合适的治疗方案。