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PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection
Latent tuberculosis infection (LTBI) is a clinically distinct category of Mycobacterium tuberculosis (Mtb) infection that needs to be diagnosed at the initial stage. We have reported earlier that one of the Mtb proline-proline-glutamic acid (PPE) proteins, PPE17 (Rv1168c) is associated with stronger...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261109/ https://www.ncbi.nlm.nih.gov/pubmed/30475863 http://dx.doi.org/10.1371/journal.pone.0207787 |
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author | Abraham, Philip Raj Devalraju, Kamakshi Prudhula Jha, Vishwanath Valluri, Vijaya Lakshmi Mukhopadhyay, Sangita |
author_facet | Abraham, Philip Raj Devalraju, Kamakshi Prudhula Jha, Vishwanath Valluri, Vijaya Lakshmi Mukhopadhyay, Sangita |
author_sort | Abraham, Philip Raj |
collection | PubMed |
description | Latent tuberculosis infection (LTBI) is a clinically distinct category of Mycobacterium tuberculosis (Mtb) infection that needs to be diagnosed at the initial stage. We have reported earlier that one of the Mtb proline-proline-glutamic acid (PPE) proteins, PPE17 (Rv1168c) is associated with stronger B-cell and T-cell responses and could be used to diagnose different clinical categories of active TB patients with higher specificity and sensitivity than PPD and ESAT-6. Based on these observations we further tested the potential of PPE17 for the diagnosis of LTBI. We tested 198 sera samples collected from LTBI individuals (n = 61), QFT-negative (n = 58) and active TB patients (n = 79). Individuals were defined as LTBI by QuantiFERON-TB Gold In-Tube test (QFT–GIT) positive results, while active TB patients were confirmed based on the guidelines of the Revised National TB Control Programme of India. The antibody responses against PPE17, ESAT-6:CFP-10 and PPD were compared in these subjects by enzyme-linked immunosorbent assay. We observed that LTBI individuals show a higher sero-reactivity to PPE17 as compared to currently used latent TB diagnostic antigens like ESAT-6, CFP-10 and PPD. The LTBI and active TB patients display almost similar sensitivity. Interestingly, PPE17 could discriminate LTBI positive subjects from the QFT-negative subjects (P < 0.001). Our study hints that PPE17 may be used as a novel serodiagnostic marker to screen the latently infected subjects and may also be used as a complimentary tool to the QFT–GIT. |
format | Online Article Text |
id | pubmed-6261109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62611092018-12-06 PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection Abraham, Philip Raj Devalraju, Kamakshi Prudhula Jha, Vishwanath Valluri, Vijaya Lakshmi Mukhopadhyay, Sangita PLoS One Research Article Latent tuberculosis infection (LTBI) is a clinically distinct category of Mycobacterium tuberculosis (Mtb) infection that needs to be diagnosed at the initial stage. We have reported earlier that one of the Mtb proline-proline-glutamic acid (PPE) proteins, PPE17 (Rv1168c) is associated with stronger B-cell and T-cell responses and could be used to diagnose different clinical categories of active TB patients with higher specificity and sensitivity than PPD and ESAT-6. Based on these observations we further tested the potential of PPE17 for the diagnosis of LTBI. We tested 198 sera samples collected from LTBI individuals (n = 61), QFT-negative (n = 58) and active TB patients (n = 79). Individuals were defined as LTBI by QuantiFERON-TB Gold In-Tube test (QFT–GIT) positive results, while active TB patients were confirmed based on the guidelines of the Revised National TB Control Programme of India. The antibody responses against PPE17, ESAT-6:CFP-10 and PPD were compared in these subjects by enzyme-linked immunosorbent assay. We observed that LTBI individuals show a higher sero-reactivity to PPE17 as compared to currently used latent TB diagnostic antigens like ESAT-6, CFP-10 and PPD. The LTBI and active TB patients display almost similar sensitivity. Interestingly, PPE17 could discriminate LTBI positive subjects from the QFT-negative subjects (P < 0.001). Our study hints that PPE17 may be used as a novel serodiagnostic marker to screen the latently infected subjects and may also be used as a complimentary tool to the QFT–GIT. Public Library of Science 2018-11-26 /pmc/articles/PMC6261109/ /pubmed/30475863 http://dx.doi.org/10.1371/journal.pone.0207787 Text en © 2018 Abraham et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Abraham, Philip Raj Devalraju, Kamakshi Prudhula Jha, Vishwanath Valluri, Vijaya Lakshmi Mukhopadhyay, Sangita PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection |
title | PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection |
title_full | PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection |
title_fullStr | PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection |
title_full_unstemmed | PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection |
title_short | PPE17 (Rv1168c) protein of Mycobacterium tuberculosis detects individuals with latent TB infection |
title_sort | ppe17 (rv1168c) protein of mycobacterium tuberculosis detects individuals with latent tb infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261109/ https://www.ncbi.nlm.nih.gov/pubmed/30475863 http://dx.doi.org/10.1371/journal.pone.0207787 |
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