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Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection

INTRODUCTION: Human herpesvirus (HHV)-7 establishes a latent infection during the lifetime of the host and can reactivate after the primary infection, leading to lytic replication in immunosuppressed patients. METHODS: This study aimed to develop an enzyme-linked immunosorbent assay (ELISA) to ident...

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Autores principales: Puglia, Ana Lia Pradella, Peigo, Murilo de Freitas, Bomfim, Fernando Russo Costa, Thomasini, Ronaldo Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Medicina Tropical - SBMT 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094058/
https://www.ncbi.nlm.nih.gov/pubmed/32187333
http://dx.doi.org/10.1590/0037-8682-0181-2019
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author Puglia, Ana Lia Pradella
Peigo, Murilo de Freitas
Bomfim, Fernando Russo Costa
Thomasini, Ronaldo Luis
author_facet Puglia, Ana Lia Pradella
Peigo, Murilo de Freitas
Bomfim, Fernando Russo Costa
Thomasini, Ronaldo Luis
author_sort Puglia, Ana Lia Pradella
collection PubMed
description INTRODUCTION: Human herpesvirus (HHV)-7 establishes a latent infection during the lifetime of the host and can reactivate after the primary infection, leading to lytic replication in immunosuppressed patients. METHODS: This study aimed to develop an enzyme-linked immunosorbent assay (ELISA) to identify HHV-7 serum antibodies and compare its performance with that of an indirect immunofluorescence assay (IFA). RESULTS: Serum samples (n=102) were tested by IgG-IFA and by ELISA. IFA and ELISA showed IgG-positive results in 77 and 73 samples, respectively. Qualitative concordance of 96% was demonstrated between the two techniques. CONCLUSIONS: ELISA may be useful to diagnose HHV-7 infection.
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spelling pubmed-70940582020-03-25 Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection Puglia, Ana Lia Pradella Peigo, Murilo de Freitas Bomfim, Fernando Russo Costa Thomasini, Ronaldo Luis Rev Soc Bras Med Trop Short Communication INTRODUCTION: Human herpesvirus (HHV)-7 establishes a latent infection during the lifetime of the host and can reactivate after the primary infection, leading to lytic replication in immunosuppressed patients. METHODS: This study aimed to develop an enzyme-linked immunosorbent assay (ELISA) to identify HHV-7 serum antibodies and compare its performance with that of an indirect immunofluorescence assay (IFA). RESULTS: Serum samples (n=102) were tested by IgG-IFA and by ELISA. IFA and ELISA showed IgG-positive results in 77 and 73 samples, respectively. Qualitative concordance of 96% was demonstrated between the two techniques. CONCLUSIONS: ELISA may be useful to diagnose HHV-7 infection. Sociedade Brasileira de Medicina Tropical - SBMT 2020-03-16 /pmc/articles/PMC7094058/ /pubmed/32187333 http://dx.doi.org/10.1590/0037-8682-0181-2019 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Short Communication
Puglia, Ana Lia Pradella
Peigo, Murilo de Freitas
Bomfim, Fernando Russo Costa
Thomasini, Ronaldo Luis
Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection
title Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection
title_full Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection
title_fullStr Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection
title_full_unstemmed Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection
title_short Development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection
title_sort development of an enzyme-linked immunosorbent assay for diagnosis of human herpesvirus-7 infection
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094058/
https://www.ncbi.nlm.nih.gov/pubmed/32187333
http://dx.doi.org/10.1590/0037-8682-0181-2019
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