Sharma Kusum, Appannanavar Suma B, Modi Manish, Singh Malkit, Sharma Aman, Varma Subhash
Department of Medical Microbiology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Indian J Pathol Microbiol. 2015 Jan-Mar;58(1):27-30. doi: 10.4103/0377-4929.151164.
Prompt and accurate diagnosis of extra-pulmonary tuberculosis (TB) is highly challenging. Current conventional techniques lack sensitivity and are time-consuming. Here, we report our experience with multiplex polymerase chain reaction (MPCR) using two targets namely IS6110 and protein antigen b in the diagnosis of extra-pulmonary TB.
A total of 150 patients of extra-pulmonary TB visiting tertiary care center in north India between September 2008 and December 2009 were included in the study. Sixty-six biopsy samples and 84 were body fluids from these patients were subjected for microscopy (Ziehl-Neelsen), culture on LJ medium and for Multiplex PCR using IS6110 and Protein b antigen.
Smear positivity was noted in 11 samples (7.33%), and LJ culture yielded Mycobacterium tuberculosis in 8 biopsies and 9 body fluids with overall positivity of 11.3%. The multi-targeted PCR could detect M. tuberculosis in a total of 112 samples. Of 112 positive samples, only Protein b band was detected in 7 samples and only IS6110 was detected in 5 samples. Overall Protein b, PCR could detect 71.33% of the cases, whereas IS6110 was positive in 66.6% of the cases. Overall the sensitivities of microscopy, culture, IS6110 PCR, Protein b PCR and MPCR were 7.33%, 11.3%, 66.67%, 71.3% and 74.6%, respectively. Thus by using more than two targets the sensitivity increased from 66.67% of IS6110 to 74.6% in MPCR.
Multiplex polymerase chain reaction using IS6110 and Protein b antigen is a highly sensitive and specific tool in the diagnosis of pauci-bacillary conditions like extra-pulmonary TB.
肺外结核病(TB)的及时准确诊断极具挑战性。当前的传统技术缺乏敏感性且耗时。在此,我们报告使用两个靶标即IS6110和蛋白抗原b的多重聚合酶链反应(MPCR)在肺外结核病诊断中的经验。
2008年9月至2009年12月期间,印度北部一家三级护理中心的150例肺外结核病患者被纳入研究。对这些患者的66份活检样本和84份体液进行显微镜检查(萋尼氏染色)、在罗-琴培养基上培养以及使用IS6110和蛋白b抗原进行多重聚合酶链反应。
11份样本(7.33%)涂片阳性,8份活检样本和9份体液的罗-琴培养培养出结核分枝杆菌,总体阳性率为11.3%。多靶标聚合酶链反应共能在112份样本中检测到结核分枝杆菌。在112份阳性样本中,仅在7份样本中检测到蛋白b条带,仅在5份样本中检测到IS6110。总体而言,蛋白b聚合酶链反应能检测到71.33%的病例,而IS6110在66.6%的病例中呈阳性。总体而言,显微镜检查、培养、IS6110聚合酶链反应、蛋白b聚合酶链反应和多重聚合酶链反应的敏感性分别为7.33%、11.3%、66.67%、71.3%和74.6%。因此,通过使用两个以上靶标,多重聚合酶链反应的敏感性从IS6110的66.67%提高到了74.6%。
使用IS6110和蛋白b抗原的多重聚合酶链反应是诊断肺外结核病等少菌型疾病的高度敏感和特异的工具。