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Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b

BACKGROUND: Haemophilus influenzae type b (Hib) infection has high morbidity and mortality rate, especially in children under 5 years of age. Enzyme-linked immunosorbent assay (ELISA) technique is the most used method to detect antibodies against H. influenzae. Available commercial ELISA kits are ex...

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Autores principales: Mousavi, Seyed Fazlolah, Fatemi, Sara, Siadat, Seyed Davar, Zahraei, Seyed Mohsen, Nikanpour, Elnaz, Malekan, Mohamad Ali, Khabiri, Ali Reza, Janani, Ali Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976622/
https://www.ncbi.nlm.nih.gov/pubmed/27540453
http://dx.doi.org/10.5812/jjm.30629
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author Mousavi, Seyed Fazlolah
Fatemi, Sara
Siadat, Seyed Davar
Zahraei, Seyed Mohsen
Nikanpour, Elnaz
Malekan, Mohamad Ali
Khabiri, Ali Reza
Janani, Ali Reza
author_facet Mousavi, Seyed Fazlolah
Fatemi, Sara
Siadat, Seyed Davar
Zahraei, Seyed Mohsen
Nikanpour, Elnaz
Malekan, Mohamad Ali
Khabiri, Ali Reza
Janani, Ali Reza
author_sort Mousavi, Seyed Fazlolah
collection PubMed
description BACKGROUND: Haemophilus influenzae type b (Hib) infection has high morbidity and mortality rate, especially in children under 5 years of age. Enzyme-linked immunosorbent assay (ELISA) technique is the most used method to detect antibodies against H. influenzae. Available commercial ELISA kits are expensive and not always readily available, particularly for epidemiological studies. OBJECTIVES: This study was performed to develop and optimize a homemade ELISA kit for the detection of Hib anti-polyribosylribitol phosphate (PRP) antibodies in children. MATERIALS AND METHODS: To develop and optimize an indirect ELISA method, pure PRP was prepared. The PRP was coupled to bovine serum albumin, using sodium periodate. Then optimal conditions for ELISA, including coating antigen concentration and peroxidase labeled conjugate concentrations, incubation temperature and incubation time, were determined. To confirm the efficacy of optimized kit, 83 serum samples from non-vaccinated children, aged less than 6 years were collected and analyzed, using homemade and commercial ELISA. RESULTS: The optimal conditions were considered to perform ELISA. Comparison between results obtained from optimized ELISA kit and commercial ELISA kit showed a good agreement. CONCLUSIONS: Taking into account these data, we elaborated a homemade ELISA kit that is an efficacious and cost-effective substitute for commercial kit, in disease control and diagnosis.
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spelling pubmed-49766222016-08-18 Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b Mousavi, Seyed Fazlolah Fatemi, Sara Siadat, Seyed Davar Zahraei, Seyed Mohsen Nikanpour, Elnaz Malekan, Mohamad Ali Khabiri, Ali Reza Janani, Ali Reza Jundishapur J Microbiol Research Article BACKGROUND: Haemophilus influenzae type b (Hib) infection has high morbidity and mortality rate, especially in children under 5 years of age. Enzyme-linked immunosorbent assay (ELISA) technique is the most used method to detect antibodies against H. influenzae. Available commercial ELISA kits are expensive and not always readily available, particularly for epidemiological studies. OBJECTIVES: This study was performed to develop and optimize a homemade ELISA kit for the detection of Hib anti-polyribosylribitol phosphate (PRP) antibodies in children. MATERIALS AND METHODS: To develop and optimize an indirect ELISA method, pure PRP was prepared. The PRP was coupled to bovine serum albumin, using sodium periodate. Then optimal conditions for ELISA, including coating antigen concentration and peroxidase labeled conjugate concentrations, incubation temperature and incubation time, were determined. To confirm the efficacy of optimized kit, 83 serum samples from non-vaccinated children, aged less than 6 years were collected and analyzed, using homemade and commercial ELISA. RESULTS: The optimal conditions were considered to perform ELISA. Comparison between results obtained from optimized ELISA kit and commercial ELISA kit showed a good agreement. CONCLUSIONS: Taking into account these data, we elaborated a homemade ELISA kit that is an efficacious and cost-effective substitute for commercial kit, in disease control and diagnosis. Kowsar 2016-02-17 /pmc/articles/PMC4976622/ /pubmed/27540453 http://dx.doi.org/10.5812/jjm.30629 Text en Copyright © 2016, Ahvaz Jundishapur University of Medical Sciences. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Research Article
Mousavi, Seyed Fazlolah
Fatemi, Sara
Siadat, Seyed Davar
Zahraei, Seyed Mohsen
Nikanpour, Elnaz
Malekan, Mohamad Ali
Khabiri, Ali Reza
Janani, Ali Reza
Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b
title Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b
title_full Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b
title_fullStr Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b
title_full_unstemmed Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b
title_short Development and Optimization of a Homemade ELISA Kit for Detection of Antibodies Against Haemophilus influenzae Type b
title_sort development and optimization of a homemade elisa kit for detection of antibodies against haemophilus influenzae type b
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976622/
https://www.ncbi.nlm.nih.gov/pubmed/27540453
http://dx.doi.org/10.5812/jjm.30629
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