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Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes

Using phage display and IgG of a goat infected with Caprine Arthritis Encephalitis Virus (CAEV) we obtained families of 7 mer constrained peptides with consensus motifs LxSDPF/Y and SWN/KHWSY and mapped the epitopes mimicked by them at the Env 6-LISDPY-11 and 67-WNTYHW-72 sites of the mature gp135 a...

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Autores principales: Gazarian, Karlen, Setién, Alvaro Aguilar, Gazarian, Tatiana, Pierle, Sebastian Aguilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162499/
https://www.ncbi.nlm.nih.gov/pubmed/21781322
http://dx.doi.org/10.1186/1297-9716-42-87
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author Gazarian, Karlen
Setién, Alvaro Aguilar
Gazarian, Tatiana
Pierle, Sebastian Aguilar
author_facet Gazarian, Karlen
Setién, Alvaro Aguilar
Gazarian, Tatiana
Pierle, Sebastian Aguilar
author_sort Gazarian, Karlen
collection PubMed
description Using phage display and IgG of a goat infected with Caprine Arthritis Encephalitis Virus (CAEV) we obtained families of 7 mer constrained peptides with consensus motifs LxSDPF/Y and SWN/KHWSY and mapped the epitopes mimicked by them at the Env 6-LISDPY-11 and 67-WNTYHW-72 sites of the mature gp135 amino acid sequence. The first epitope fell into the N-terminal immunogenic aa1-EDYTLISDPYGFS- aa14 site identified previously with a synthetic peptide approach; the second epitope has not been described previously. The first epitope is mostly conserved across CAEV isolates whereas the second newly described epitope is extremely conserved in Small Ruminant Lentiviruses env sequences. As being immunodominant, the epitopes are candidate targets for mimotope-mediated diagnosis and/or neutralization.
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spelling pubmed-31624992011-08-27 Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes Gazarian, Karlen Setién, Alvaro Aguilar Gazarian, Tatiana Pierle, Sebastian Aguilar Vet Res Short Report Using phage display and IgG of a goat infected with Caprine Arthritis Encephalitis Virus (CAEV) we obtained families of 7 mer constrained peptides with consensus motifs LxSDPF/Y and SWN/KHWSY and mapped the epitopes mimicked by them at the Env 6-LISDPY-11 and 67-WNTYHW-72 sites of the mature gp135 amino acid sequence. The first epitope fell into the N-terminal immunogenic aa1-EDYTLISDPYGFS- aa14 site identified previously with a synthetic peptide approach; the second epitope has not been described previously. The first epitope is mostly conserved across CAEV isolates whereas the second newly described epitope is extremely conserved in Small Ruminant Lentiviruses env sequences. As being immunodominant, the epitopes are candidate targets for mimotope-mediated diagnosis and/or neutralization. BioMed Central 2011 2011-07-22 /pmc/articles/PMC3162499/ /pubmed/21781322 http://dx.doi.org/10.1186/1297-9716-42-87 Text en Copyright ©2011 Gazarian 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 Short Report
Gazarian, Karlen
Setién, Alvaro Aguilar
Gazarian, Tatiana
Pierle, Sebastian Aguilar
Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes
title Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes
title_full Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes
title_fullStr Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes
title_full_unstemmed Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes
title_short Phage display identifies two Caprine Arthritis Encephalitis Virus env epitopes
title_sort phage display identifies two caprine arthritis encephalitis virus env epitopes
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162499/
https://www.ncbi.nlm.nih.gov/pubmed/21781322
http://dx.doi.org/10.1186/1297-9716-42-87
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