Cargando…

The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis

Tuberculosis (TB) stays a major cause of death globally after COVID-19 and HIV. An early diagnosis to control TB effectively, needs a fast reliable diagnostic method with high sensitivity. Serodiagnosis involving polyclonal antibodies detection against an antigen of Mycobacterium tuberculosis (Mtb)...

Descripción completa

Detalles Bibliográficos
Autores principales: Mahmood, Nasir, Akhter, Mohsina, Hussain, Naveed, Shad, Mohsin, Nisa, Zaib un, Khan, Imran H., Akhtar, Muhammad Waheed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424118/
https://www.ncbi.nlm.nih.gov/pubmed/36067572
http://dx.doi.org/10.1016/j.tube.2022.102253
_version_ 1784778170216480768
author Mahmood, Nasir
Akhter, Mohsina
Hussain, Naveed
Shad, Mohsin
Nisa, Zaib un
Khan, Imran H.
Akhtar, Muhammad Waheed
author_facet Mahmood, Nasir
Akhter, Mohsina
Hussain, Naveed
Shad, Mohsin
Nisa, Zaib un
Khan, Imran H.
Akhtar, Muhammad Waheed
author_sort Mahmood, Nasir
collection PubMed
description Tuberculosis (TB) stays a major cause of death globally after COVID-19 and HIV. An early diagnosis to control TB effectively, needs a fast reliable diagnostic method with high sensitivity. Serodiagnosis involving polyclonal antibodies detection against an antigen of Mycobacterium tuberculosis (Mtb) in serum samples can be instrumental. In our study, Rv3874 and Rv3875 antigens were cloned, expressed, and purified individually and as a chimeric construct in Escherichia coli BL21. Enzyme-Linked Immunosorbent Assay (ELISA) based findings revealed that the Rv3874-Rv3875 chimeric construct was two-fold more sensitive (59.7%) than the individual sensitivities of Rv3874 (28.4%) and Rv3875 (24.9%) for 201 serum TB positive samples. Furthermore, the fusion construct was a little more sensitive (60.4%) for male subjects than that for females (58.8%). Lastly, our preliminary findings, molecular insights of secondary structure, and statistical and in silico analysis of each construct also advocate that CEP can be considered a better immunodiagnostic tool in addition to previously reported EC skin test.
format Online
Article
Text
id pubmed-9424118
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier Ltd.
record_format MEDLINE/PubMed
spelling pubmed-94241182022-08-30 The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis Mahmood, Nasir Akhter, Mohsina Hussain, Naveed Shad, Mohsin Nisa, Zaib un Khan, Imran H. Akhtar, Muhammad Waheed Tuberculosis (Edinb) Article Tuberculosis (TB) stays a major cause of death globally after COVID-19 and HIV. An early diagnosis to control TB effectively, needs a fast reliable diagnostic method with high sensitivity. Serodiagnosis involving polyclonal antibodies detection against an antigen of Mycobacterium tuberculosis (Mtb) in serum samples can be instrumental. In our study, Rv3874 and Rv3875 antigens were cloned, expressed, and purified individually and as a chimeric construct in Escherichia coli BL21. Enzyme-Linked Immunosorbent Assay (ELISA) based findings revealed that the Rv3874-Rv3875 chimeric construct was two-fold more sensitive (59.7%) than the individual sensitivities of Rv3874 (28.4%) and Rv3875 (24.9%) for 201 serum TB positive samples. Furthermore, the fusion construct was a little more sensitive (60.4%) for male subjects than that for females (58.8%). Lastly, our preliminary findings, molecular insights of secondary structure, and statistical and in silico analysis of each construct also advocate that CEP can be considered a better immunodiagnostic tool in addition to previously reported EC skin test. Elsevier Ltd. 2022-09 2022-08-30 /pmc/articles/PMC9424118/ /pubmed/36067572 http://dx.doi.org/10.1016/j.tube.2022.102253 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Mahmood, Nasir
Akhter, Mohsina
Hussain, Naveed
Shad, Mohsin
Nisa, Zaib un
Khan, Imran H.
Akhtar, Muhammad Waheed
The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis
title The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis
title_full The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis
title_fullStr The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis
title_full_unstemmed The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis
title_short The Rv3874-Rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis
title_sort rv3874-rv3875 chimeric protein shows a promiscuous serodiagnostic potential for tuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424118/
https://www.ncbi.nlm.nih.gov/pubmed/36067572
http://dx.doi.org/10.1016/j.tube.2022.102253
work_keys_str_mv AT mahmoodnasir therv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT akhtermohsina therv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT hussainnaveed therv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT shadmohsin therv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT nisazaibun therv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT khanimranh therv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT akhtarmuhammadwaheed therv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT mahmoodnasir rv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT akhtermohsina rv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT hussainnaveed rv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT shadmohsin rv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT nisazaibun rv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT khanimranh rv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis
AT akhtarmuhammadwaheed rv3874rv3875chimericproteinshowsapromiscuousserodiagnosticpotentialfortuberculosis