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Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis
BACKGROUND AND OBJECTIVES: Timely diagnosis of leptospirosis is essential for an effective treatment. Large diversity of clinical symptoms has led leptospirosis diagnosis difficult. Researchers have conducted many tests with wide-range of sensitivity and specificity to achieve novel diagnostic proce...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393495/ https://www.ncbi.nlm.nih.gov/pubmed/25870752 |
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author | Alizadeh, Safar Ali Abdolahpour, Gholamreza Pourmand, Mohammad Reza Naserpour, Taghi Najafipour, Reza Eshraghi, Seyyed Saeed |
author_facet | Alizadeh, Safar Ali Abdolahpour, Gholamreza Pourmand, Mohammad Reza Naserpour, Taghi Najafipour, Reza Eshraghi, Seyyed Saeed |
author_sort | Alizadeh, Safar Ali |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Timely diagnosis of leptospirosis is essential for an effective treatment. Large diversity of clinical symptoms has led leptospirosis diagnosis difficult. Researchers have conducted many tests with wide-range of sensitivity and specificity to achieve novel diagnostic procedures which have higher sensitivity and specificity compared with previous tests and which are more reliable and available to public laboratories. This study aimed to introduce Lsa63 and LipL32 proteins-based ELISA tests with more sensitivity, specificity, accuracy and convenience for public laboratories. MATERIALS AND METHODS: Recombinant forms of Lsa63 and LipL32 proteins were first generated. After coating these proteins, IgM and IgG ELISA tests were performed. 220 patients with suspicion of leptospirosis infection were selected for serum collection. The sera tests were carried out using MAT, IgM and IgG ELISA tests. In order to assess the performance of ELISA, the results of this test were compared with MAT. RESULTS: 30% of serum samples (n=65) in MAT were positive for leptospirosis infection, while ELISA tests including rLipL32- rLsa63-IgM and rLipL32-rLsa63-IgG showed 40.45% (n=89) and 38.63% (n=80) positive reaction, respectively. CONCLUSION: Our results demonstrated that new ELISA tests based on mixing LipL32 and Lsa63 proteins, a novel mixture of recombinant antigens, are valuable to detect specific antibodies against pathogenic Leptospira in human serum and could be considered as helpful techniques in leptospirosis diagnosis. |
format | Online Article Text |
id | pubmed-4393495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-43934952015-04-13 Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis Alizadeh, Safar Ali Abdolahpour, Gholamreza Pourmand, Mohammad Reza Naserpour, Taghi Najafipour, Reza Eshraghi, Seyyed Saeed Iran J Microbiol Medical Sciences BACKGROUND AND OBJECTIVES: Timely diagnosis of leptospirosis is essential for an effective treatment. Large diversity of clinical symptoms has led leptospirosis diagnosis difficult. Researchers have conducted many tests with wide-range of sensitivity and specificity to achieve novel diagnostic procedures which have higher sensitivity and specificity compared with previous tests and which are more reliable and available to public laboratories. This study aimed to introduce Lsa63 and LipL32 proteins-based ELISA tests with more sensitivity, specificity, accuracy and convenience for public laboratories. MATERIALS AND METHODS: Recombinant forms of Lsa63 and LipL32 proteins were first generated. After coating these proteins, IgM and IgG ELISA tests were performed. 220 patients with suspicion of leptospirosis infection were selected for serum collection. The sera tests were carried out using MAT, IgM and IgG ELISA tests. In order to assess the performance of ELISA, the results of this test were compared with MAT. RESULTS: 30% of serum samples (n=65) in MAT were positive for leptospirosis infection, while ELISA tests including rLipL32- rLsa63-IgM and rLipL32-rLsa63-IgG showed 40.45% (n=89) and 38.63% (n=80) positive reaction, respectively. CONCLUSION: Our results demonstrated that new ELISA tests based on mixing LipL32 and Lsa63 proteins, a novel mixture of recombinant antigens, are valuable to detect specific antibodies against pathogenic Leptospira in human serum and could be considered as helpful techniques in leptospirosis diagnosis. Tehran University of Medical Sciences 2014-06 /pmc/articles/PMC4393495/ /pubmed/25870752 Text en Copyright: © Iranian Journal of Microbiology & Tehran University of Medical Sciences This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Medical Sciences Alizadeh, Safar Ali Abdolahpour, Gholamreza Pourmand, Mohammad Reza Naserpour, Taghi Najafipour, Reza Eshraghi, Seyyed Saeed Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis |
title | Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis |
title_full | Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis |
title_fullStr | Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis |
title_full_unstemmed | Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis |
title_short | Evaluation of New ELISA based on rLsa63 – rLipL32 antigens for serodiagnosis of Human Leptospirosis |
title_sort | evaluation of new elisa based on rlsa63 – rlipl32 antigens for serodiagnosis of human leptospirosis |
topic | Medical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393495/ https://www.ncbi.nlm.nih.gov/pubmed/25870752 |
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