Identification of mycobacterial MPT-64 and ESAT-6 proteins in urogenital tuberculosis patients by real-time immuno-PCR

Author:

Kamra Ekta1ORCID,Sharma Suman2,Sheoran Abhishek3,Singh Vishwajeet4,Chauhan Meenakshi5,Pawar Devendra S6,Yadav Aparna2,Mehta Promod K1ORCID

Affiliation:

1. Centre for Biotechnology, Maharshi Dayanand University, Rohtak, 124001, India

2. Department of Microbiology, Pt. B. D. Sharma University of Health Sciences (UHS), Rohtak, 124001, India

3. Department of Statistics, Ramanujan College, University of Delhi, Delhi, 110019, India

4. Department of Geriatric Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India

5. Department of Obstetrics & Gynecology, UHS, Rohtak, 124001, India

6. Department of Urology, UHS, Rohtak, 124001, India

Abstract

Aim: Diagnosis of urogenital tuberculosis (UGTB) is difficult and there is an immediate need to develop a reliable diagnostic test. Methods: A real-time immuno-PCR (RT-I-PCR) was developed to identify a cocktail of MPT-64 + ESAT-6 in both male/female UGTB patients comprising five confirmed cases, 40 clinically suspected cases and 37 non-TB controls, from whom mid-stream urine specimens were collected, while endometrial biopsies of female patients were obtained on day 1 of their menstrual cycle. Results obtained by RT-I-PCR were compared with I-PCR/ELISA and GeneXpert. Results: A wide range (500 fg/ml–10 ng/ml) of MPT-64 + ESAT-6 was detected in UGTB specimens by RT-I-PCR, although ELISA showed a narrow range (2.5–11 ng/ml). Sensitivities of 80% and 82.2% were obtained by RT-I-PCR in clinically suspected and total UGTB cases, respectively, whereas 94.6% specificity was obtained. Concurrently, RT-I-PCR revealed significantly higher (p < 0.05–0.001) sensitivity than I-PCR/ELISA and GeneXpert. Conclusion: After improving the specificity, the authors may develop RT-I-PCR into a diagnostic kit.

Funder

Indian Council of Medical Research

Publisher

Future Medicine Ltd

Subject

Microbiology (medical),Microbiology

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