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Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus
The objective of this study was to elucidate the kinetics and magnitudes of specific IgA antibody responses in intestines of turkey poults infected with turkey coronavirus (TCV). Turkey poults were orally inoculated with TCV at 10 days of age. Intestinal segment cultures were administered for duoden...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science B.V.
2002
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119794/ https://www.ncbi.nlm.nih.gov/pubmed/12088645 http://dx.doi.org/10.1016/S0165-2427(02)00135-6 |
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author | Loa, C.C Lin, T.L Wu, C.C Bryan, T Hooper, T Schrader, D |
author_facet | Loa, C.C Lin, T.L Wu, C.C Bryan, T Hooper, T Schrader, D |
author_sort | Loa, C.C |
collection | PubMed |
description | The objective of this study was to elucidate the kinetics and magnitudes of specific IgA antibody responses in intestines of turkey poults infected with turkey coronavirus (TCV). Turkey poults were orally inoculated with TCV at 10 days of age. Intestinal segment cultures were administered for duodenum, jejunum, and ileum and the IgA antibody responses were analyzed at 1, 2, 3, 4, 6, or 9 weeks post-infection (PI) in two different experiments. The kinetics of virus-specific IgA antibody responses in duodenum, jejunum, and ileum were similar: gradually increased from 1 week PI, reached the peak at 3 or 4 weeks PI, and declined afterward. The virus-specific IgA antibody responses in duodenum, jejunum, and ileum showed negative correlation with duration of TCV antigen in the corresponding locations of intestine with Spearman’s correlation coefficient of −0.85 (p=0.034), −0.74 (p=0.096), and −0.75 (p=0.084), respectively. Moreover, the virus-specific IgA antibody responses in serum were positively correlated with that of duodenum (coefficient=0.829, p=0.042), jejunum (coefficient=0.829, p=0.042), and ileum (coefficient=0.771, p=0.072) segment cultures, suggesting that the induction of specific IgA response in serum was predictive of an IgA response in intestine. The results indicate that intestinal mucosal IgA antibodies to TCV are elicited in turkeys following infection with TCV. The local mucosal antibodies may provide protective immunity for infected turkeys to recover from TCV infection. |
format | Online Article Text |
id | pubmed-7119794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Elsevier Science B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71197942020-04-08 Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus Loa, C.C Lin, T.L Wu, C.C Bryan, T Hooper, T Schrader, D Vet Immunol Immunopathol Article The objective of this study was to elucidate the kinetics and magnitudes of specific IgA antibody responses in intestines of turkey poults infected with turkey coronavirus (TCV). Turkey poults were orally inoculated with TCV at 10 days of age. Intestinal segment cultures were administered for duodenum, jejunum, and ileum and the IgA antibody responses were analyzed at 1, 2, 3, 4, 6, or 9 weeks post-infection (PI) in two different experiments. The kinetics of virus-specific IgA antibody responses in duodenum, jejunum, and ileum were similar: gradually increased from 1 week PI, reached the peak at 3 or 4 weeks PI, and declined afterward. The virus-specific IgA antibody responses in duodenum, jejunum, and ileum showed negative correlation with duration of TCV antigen in the corresponding locations of intestine with Spearman’s correlation coefficient of −0.85 (p=0.034), −0.74 (p=0.096), and −0.75 (p=0.084), respectively. Moreover, the virus-specific IgA antibody responses in serum were positively correlated with that of duodenum (coefficient=0.829, p=0.042), jejunum (coefficient=0.829, p=0.042), and ileum (coefficient=0.771, p=0.072) segment cultures, suggesting that the induction of specific IgA response in serum was predictive of an IgA response in intestine. The results indicate that intestinal mucosal IgA antibodies to TCV are elicited in turkeys following infection with TCV. The local mucosal antibodies may provide protective immunity for infected turkeys to recover from TCV infection. Elsevier Science B.V. 2002-09-06 2002-05-24 /pmc/articles/PMC7119794/ /pubmed/12088645 http://dx.doi.org/10.1016/S0165-2427(02)00135-6 Text en Copyright © 2002 Elsevier Science B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Loa, C.C Lin, T.L Wu, C.C Bryan, T Hooper, T Schrader, D Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus |
title | Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus |
title_full | Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus |
title_fullStr | Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus |
title_full_unstemmed | Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus |
title_short | Specific mucosal IgA immunity in turkey poults infected with turkey coronavirus |
title_sort | specific mucosal iga immunity in turkey poults infected with turkey coronavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119794/ https://www.ncbi.nlm.nih.gov/pubmed/12088645 http://dx.doi.org/10.1016/S0165-2427(02)00135-6 |
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