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Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis

BACKGROUND: Early diagnosis and treatment of Mycobacterium tuberculosis infection can prevent most deaths resulting from this pathogen; however, multidrug-resistant strains present serious threats to global tuberculosis control and prevention efforts. In this study, we identified antigens that could...

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Autores principales: Zhang, Lu, Wang, Qingzhong, Wang, Wenjie, Liu, Yanyan, Wang, Jie, Yue, Jun, Xu, Ying, Xu, Wenxi, Cui, ZhenLing, Zhang, Xuelian, Wang, Honghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305424/
https://www.ncbi.nlm.nih.gov/pubmed/22364187
http://dx.doi.org/10.1186/1477-5956-10-12
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author Zhang, Lu
Wang, Qingzhong
Wang, Wenjie
Liu, Yanyan
Wang, Jie
Yue, Jun
Xu, Ying
Xu, Wenxi
Cui, ZhenLing
Zhang, Xuelian
Wang, Honghai
author_facet Zhang, Lu
Wang, Qingzhong
Wang, Wenjie
Liu, Yanyan
Wang, Jie
Yue, Jun
Xu, Ying
Xu, Wenxi
Cui, ZhenLing
Zhang, Xuelian
Wang, Honghai
author_sort Zhang, Lu
collection PubMed
description BACKGROUND: Early diagnosis and treatment of Mycobacterium tuberculosis infection can prevent most deaths resulting from this pathogen; however, multidrug-resistant strains present serious threats to global tuberculosis control and prevention efforts. In this study, we identified antigens that could be used for the serodiagnosis of drug-resistant M. tuberculosis strains, using a proteomics-based analysis. RESULTS: Serum from patients infected with drug-resistant or drug-susceptible M. tuberculosis strains and healthy controls was subjected to two-dimensional gel electrophoresis using a western blot approach. This procedure identified nine immunoreactive proteins, which were subjected to MALDI-TOF-MS analysis. Six recombinant proteins, namely rRv2031c, rRv0444c, rRv2145c, rRv3692, rRv0859c, and rRv3040, were expressed and used to determine the immuno-reactivity of 100 serum samples. Antibody reactivity against rRv2031c, rRv3692, and rRv0444c was consistently observed. Among them, the best sensitivity and specificity of rRv3692 were 37% and 95% respectively. Furthermore, when rRv2031c and rRv3692 or rRv2031c, rRv3692, and rRv0444c were combined in 2:1 or equal amounts, the assay sensitivity and specificity were improved to 56.7% and 100% respectively. CONCLUSIONS: These results suggest that Rv2031c, Rv3692, and Rv0444c are possible candidate biomarkers for effective use in the serodiagnosis of drug-resistant tuberculosis infections, and a combined formula of these antigens should be considered when designing a subunit assay kit.
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spelling pubmed-33054242012-03-16 Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis Zhang, Lu Wang, Qingzhong Wang, Wenjie Liu, Yanyan Wang, Jie Yue, Jun Xu, Ying Xu, Wenxi Cui, ZhenLing Zhang, Xuelian Wang, Honghai Proteome Sci Research BACKGROUND: Early diagnosis and treatment of Mycobacterium tuberculosis infection can prevent most deaths resulting from this pathogen; however, multidrug-resistant strains present serious threats to global tuberculosis control and prevention efforts. In this study, we identified antigens that could be used for the serodiagnosis of drug-resistant M. tuberculosis strains, using a proteomics-based analysis. RESULTS: Serum from patients infected with drug-resistant or drug-susceptible M. tuberculosis strains and healthy controls was subjected to two-dimensional gel electrophoresis using a western blot approach. This procedure identified nine immunoreactive proteins, which were subjected to MALDI-TOF-MS analysis. Six recombinant proteins, namely rRv2031c, rRv0444c, rRv2145c, rRv3692, rRv0859c, and rRv3040, were expressed and used to determine the immuno-reactivity of 100 serum samples. Antibody reactivity against rRv2031c, rRv3692, and rRv0444c was consistently observed. Among them, the best sensitivity and specificity of rRv3692 were 37% and 95% respectively. Furthermore, when rRv2031c and rRv3692 or rRv2031c, rRv3692, and rRv0444c were combined in 2:1 or equal amounts, the assay sensitivity and specificity were improved to 56.7% and 100% respectively. CONCLUSIONS: These results suggest that Rv2031c, Rv3692, and Rv0444c are possible candidate biomarkers for effective use in the serodiagnosis of drug-resistant tuberculosis infections, and a combined formula of these antigens should be considered when designing a subunit assay kit. BioMed Central 2012-02-25 /pmc/articles/PMC3305424/ /pubmed/22364187 http://dx.doi.org/10.1186/1477-5956-10-12 Text en Copyright ©2012 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhang, Lu
Wang, Qingzhong
Wang, Wenjie
Liu, Yanyan
Wang, Jie
Yue, Jun
Xu, Ying
Xu, Wenxi
Cui, ZhenLing
Zhang, Xuelian
Wang, Honghai
Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis
title Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis
title_full Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis
title_fullStr Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis
title_full_unstemmed Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis
title_short Identification of putative biomarkers for the serodiagnosis of drug-resistant Mycobacterium tuberculosis
title_sort identification of putative biomarkers for the serodiagnosis of drug-resistant mycobacterium tuberculosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305424/
https://www.ncbi.nlm.nih.gov/pubmed/22364187
http://dx.doi.org/10.1186/1477-5956-10-12
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