Cargando…

Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches

Based on studies from the poultry literature, all birds are hypothesized to require at least 4 weeks to develop circulating mature B-cell lineages that express functionally different immunoglobulin specificities. However, many altricial passerines fledge at adult size less than four weeks after the...

Descripción completa

Detalles Bibliográficos
Autores principales: Killpack, Tess L., Karasov, William H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467253/
https://www.ncbi.nlm.nih.gov/pubmed/23056621
http://dx.doi.org/10.1371/journal.pone.0047294
_version_ 1782245773536133120
author Killpack, Tess L.
Karasov, William H.
author_facet Killpack, Tess L.
Karasov, William H.
author_sort Killpack, Tess L.
collection PubMed
description Based on studies from the poultry literature, all birds are hypothesized to require at least 4 weeks to develop circulating mature B-cell lineages that express functionally different immunoglobulin specificities. However, many altricial passerines fledge at adult size less than four weeks after the start of embryonic development, and therefore may experience a period of susceptibility during the nestling and post-fledging periods. We present the first study, to our knowledge, to detail the age-related changes in adaptive antibody response in an altricial passerine. Using repeated vaccinations with non-infectious keyhole limpet hemocyanin (KLH) antigen, we studied the ontogeny of specific adaptive immune response in altricial zebra finches Taeniopygia guttata. Nestling zebra finches were first injected at 7 days (7d), 14 days (14d), or 21 days post-hatch (21d) with KLH-adjuvant emulsions, and boosted 7 days later. Adults were vaccinated in the same manner. Induced KLH-specific IgY antibodies were measured using ELISA. Comparisons within age groups revealed no significant increase in KLH-specific antibody levels between vaccination and boost in 7d birds, yet significant increases between vaccination and boost were observed in 14d, 21d, and adult groups. There was no significant difference among age groups in KLH antibody response to priming vaccination, yet KLH antibody response post-boost significantly increased with age among groups. Post-boost antibody response in all nestling age groups was significantly lower than in adults, indicating that mature adult secondary antibody response level was not achieved in zebra finches prior to fledging (21 days post-hatch in zebra finches). Findings from this study contribute fundamental knowledge to the fields of developmental immunology and ecological immunology and strengthen the utility of zebra finches as a model organism for future studies of immune ontogeny.
format Online
Article
Text
id pubmed-3467253
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-34672532012-10-10 Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches Killpack, Tess L. Karasov, William H. PLoS One Research Article Based on studies from the poultry literature, all birds are hypothesized to require at least 4 weeks to develop circulating mature B-cell lineages that express functionally different immunoglobulin specificities. However, many altricial passerines fledge at adult size less than four weeks after the start of embryonic development, and therefore may experience a period of susceptibility during the nestling and post-fledging periods. We present the first study, to our knowledge, to detail the age-related changes in adaptive antibody response in an altricial passerine. Using repeated vaccinations with non-infectious keyhole limpet hemocyanin (KLH) antigen, we studied the ontogeny of specific adaptive immune response in altricial zebra finches Taeniopygia guttata. Nestling zebra finches were first injected at 7 days (7d), 14 days (14d), or 21 days post-hatch (21d) with KLH-adjuvant emulsions, and boosted 7 days later. Adults were vaccinated in the same manner. Induced KLH-specific IgY antibodies were measured using ELISA. Comparisons within age groups revealed no significant increase in KLH-specific antibody levels between vaccination and boost in 7d birds, yet significant increases between vaccination and boost were observed in 14d, 21d, and adult groups. There was no significant difference among age groups in KLH antibody response to priming vaccination, yet KLH antibody response post-boost significantly increased with age among groups. Post-boost antibody response in all nestling age groups was significantly lower than in adults, indicating that mature adult secondary antibody response level was not achieved in zebra finches prior to fledging (21 days post-hatch in zebra finches). Findings from this study contribute fundamental knowledge to the fields of developmental immunology and ecological immunology and strengthen the utility of zebra finches as a model organism for future studies of immune ontogeny. Public Library of Science 2012-10-09 /pmc/articles/PMC3467253/ /pubmed/23056621 http://dx.doi.org/10.1371/journal.pone.0047294 Text en © 2012 Killpack, Karasov http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Killpack, Tess L.
Karasov, William H.
Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches
title Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches
title_full Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches
title_fullStr Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches
title_full_unstemmed Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches
title_short Ontogeny of Adaptive Antibody Response to a Model Antigen in Captive Altricial Zebra Finches
title_sort ontogeny of adaptive antibody response to a model antigen in captive altricial zebra finches
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467253/
https://www.ncbi.nlm.nih.gov/pubmed/23056621
http://dx.doi.org/10.1371/journal.pone.0047294
work_keys_str_mv AT killpacktessl ontogenyofadaptiveantibodyresponsetoamodelantigenincaptivealtricialzebrafinches
AT karasovwilliamh ontogenyofadaptiveantibodyresponsetoamodelantigenincaptivealtricialzebrafinches