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Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis

BACKGROUND: Iran is one of the endemic areas of Mediterranean Visceral Leishmaniasis, a disease caused by Leishmania infantum. In this work, we examined whether Proteína quimérica 10 (PQ10) recombinant protein is suitable for immunological diagnosis of human visceral leishmaniasis. METHODS: The stud...

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Autores principales: JAMEIE, Farnoosh, DALIMI, Abdolhossein, PIRESTANI, Majid, MOHEBALI, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988677/
https://www.ncbi.nlm.nih.gov/pubmed/33786042
http://dx.doi.org/10.18502/ijpa.v16i1.5506
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author JAMEIE, Farnoosh
DALIMI, Abdolhossein
PIRESTANI, Majid
MOHEBALI, Mehdi
author_facet JAMEIE, Farnoosh
DALIMI, Abdolhossein
PIRESTANI, Majid
MOHEBALI, Mehdi
author_sort JAMEIE, Farnoosh
collection PubMed
description BACKGROUND: Iran is one of the endemic areas of Mediterranean Visceral Leishmaniasis, a disease caused by Leishmania infantum. In this work, we examined whether Proteína quimérica 10 (PQ10) recombinant protein is suitable for immunological diagnosis of human visceral leishmaniasis. METHODS: The study was carried out in Tarbiat Modares University during 2016–2018. The coding sequence of PQ10 recombinant protein was sub-cloned in pET28 expression vector and was commercially synthesized by GENERAY Biotechnology, China. Sequencing with proper primers was done, the expression, optimization of expression and protein purification were performed, and the purified recombinant protein was confirmed by western blot. The efficacy of PQ10 for serodiagnosis was evaluated with 50 positive and 50 negative serum samples, which confirmed by the direct agglutination test and collected from individuals living in the visceral leishmaniasis endemic areas of Iran. ELISA was performed with the PQ10 recombinant protein. RESULTS: The 95% CI sensitivity of ELISA that was evaluated with sera from naturally infected individuals was 84%. The 95% CI specificity value of the ELISA determined with sera from healthy individuals (50 serum samples) and from individuals with other infectious diseases was 82%. The 95% CI positive predictive value (PPV) and negative predictive value (NPV) were exterminated 82.35% and 83.67%, respectively. CONCLUSION: We have used a recombinant synthetic protein to improve serodiagnosis of human visceral leishmaniasis. PQ10 could be useful for diagnosis of asymptomatic cases, as well as in the early phase of infections.
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spelling pubmed-79886772021-03-29 Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis JAMEIE, Farnoosh DALIMI, Abdolhossein PIRESTANI, Majid MOHEBALI, Mehdi Iran J Parasitol Original Article BACKGROUND: Iran is one of the endemic areas of Mediterranean Visceral Leishmaniasis, a disease caused by Leishmania infantum. In this work, we examined whether Proteína quimérica 10 (PQ10) recombinant protein is suitable for immunological diagnosis of human visceral leishmaniasis. METHODS: The study was carried out in Tarbiat Modares University during 2016–2018. The coding sequence of PQ10 recombinant protein was sub-cloned in pET28 expression vector and was commercially synthesized by GENERAY Biotechnology, China. Sequencing with proper primers was done, the expression, optimization of expression and protein purification were performed, and the purified recombinant protein was confirmed by western blot. The efficacy of PQ10 for serodiagnosis was evaluated with 50 positive and 50 negative serum samples, which confirmed by the direct agglutination test and collected from individuals living in the visceral leishmaniasis endemic areas of Iran. ELISA was performed with the PQ10 recombinant protein. RESULTS: The 95% CI sensitivity of ELISA that was evaluated with sera from naturally infected individuals was 84%. The 95% CI specificity value of the ELISA determined with sera from healthy individuals (50 serum samples) and from individuals with other infectious diseases was 82%. The 95% CI positive predictive value (PPV) and negative predictive value (NPV) were exterminated 82.35% and 83.67%, respectively. CONCLUSION: We have used a recombinant synthetic protein to improve serodiagnosis of human visceral leishmaniasis. PQ10 could be useful for diagnosis of asymptomatic cases, as well as in the early phase of infections. Tehran University of Medical Sciences 2021 /pmc/articles/PMC7988677/ /pubmed/33786042 http://dx.doi.org/10.18502/ijpa.v16i1.5506 Text en Copyright © 2021 Jameie et al. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
JAMEIE, Farnoosh
DALIMI, Abdolhossein
PIRESTANI, Majid
MOHEBALI, Mehdi
Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis
title Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis
title_full Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis
title_fullStr Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis
title_full_unstemmed Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis
title_short Development of a Multi-Epitope Recombinant Protein for the Diagnosis of Human Visceral Leishmaniasis
title_sort development of a multi-epitope recombinant protein for the diagnosis of human visceral leishmaniasis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988677/
https://www.ncbi.nlm.nih.gov/pubmed/33786042
http://dx.doi.org/10.18502/ijpa.v16i1.5506
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