Stanley Browne Laboratory, The Leprosy Mission Community Hospital, Nand Nagari, Delhi, India, PIN 110093.
Diagn Microbiol Infect Dis. 2019 Nov;95(3):114855. doi: 10.1016/j.diagmicrobio.2019.06.007. Epub 2019 Jun 20.
Early diagnosis of leprosy is important for limiting the severity of disease, which may lead to disabilities and deformities if not treated timely. Multiplex PCR employing more than one gene, specific to target DNA, is more efficient detection tool. In the present study, slit skin scrapings, blood, nasal swabs and saliva from Paucibacillary (PB) and Multibacillary (MB) cases as well as household contacts of PB cases were tested by multiplex PCR using three different gene targets namely RLEP, 16SrRNA and sodA. We found an increase in overall diagnostic positivity for M. leprae DNA detection by M-PCR as compared to individual PCR. In case of nasal swabs using M-PCR the PPV, NPV were 0.5454, 0.8333 respectively. There is remarkable increase in PPV in SSS of PB cases and nasal swabs of HHCs using M-PCR. Conclusively, our finding suggests the utility of M-PCR for early diagnosis and household contact surveillance for leprosy.
麻风病的早期诊断对于限制疾病的严重程度很重要,如果不及时治疗,可能会导致残疾和畸形。采用多个针对特定 DNA 的基因的多重 PCR 是更有效的检测工具。在本研究中,采用多重 PCR 技术,使用三种不同的基因靶标(RLEP、16SrRNA 和 sodA),对少菌型(PB)和多菌型(MB)病例的皮肤划痕、血液、鼻拭子和唾液以及 PB 病例的家庭接触者进行了检测。与单独的 PCR 相比,我们发现 M-PCR 对麻风分枝杆菌 DNA 检测的总体诊断阳性率有所提高。对于鼻拭子,M-PCR 的 PPV、NPV 分别为 0.5454、0.8333。使用 M-PCR 检测 PB 病例的皮肤划痕和家庭接触者的鼻拭子时,PPV 显著增加。总之,我们的发现表明 M-PCR 可用于麻风病的早期诊断和家庭接触者监测。