Cargando…

Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines

Newcastle disease virus (NDV) causes substantial economic losses to smallholder farmers in low- and middle-income countries with high levels of morbidity and mortality in poultry flocks. Previous investigations have suggested differing levels of susceptibility to NDV between specific inbred lines an...

Descripción completa

Detalles Bibliográficos
Autores principales: Schilling, Megan A., Memari, Sahar, Cattadori, Isabella M., Katani, Robab, Muhairwa, Amandus P., Buza, Joram J., Kapur, Vivek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6596324/
https://www.ncbi.nlm.nih.gov/pubmed/31281305
http://dx.doi.org/10.3389/fmicb.2019.01432
_version_ 1783430493158506496
author Schilling, Megan A.
Memari, Sahar
Cattadori, Isabella M.
Katani, Robab
Muhairwa, Amandus P.
Buza, Joram J.
Kapur, Vivek
author_facet Schilling, Megan A.
Memari, Sahar
Cattadori, Isabella M.
Katani, Robab
Muhairwa, Amandus P.
Buza, Joram J.
Kapur, Vivek
author_sort Schilling, Megan A.
collection PubMed
description Newcastle disease virus (NDV) causes substantial economic losses to smallholder farmers in low- and middle-income countries with high levels of morbidity and mortality in poultry flocks. Previous investigations have suggested differing levels of susceptibility to NDV between specific inbred lines and amongst breeds of chickens, however, the mechanisms contributing to this remain poorly understood. Studies have shown that some of these differences in levels of susceptibility to NDV infection may be accounted for by variability in the innate immune response amongst various breeds of poultry to NDV infection. Recent studies, in inbred Fayoumi and Leghorn lines, uncovered conserved, breed-dependent, and subline-dependent responses. To better understand the role of innate immune genes in engendering a protective immune response, we assessed the transcriptional responses to NDV of three highly outbred Tanzanian local chicken ecotypes, the Kuchi, the Morogoro Medium, and the Ching’wekwe. Hierarchical clustering and principal coordinate analysis of the gene expression profiles of 21-day old chick embryos infected with NDV clustered in an ecotype-dependent manner and was consistent with the relative viral loads for each of the three ecotypes. The Kuchi and Morogoro Medium exhibit significantly higher viral loads than the Ching’wekwe. The results show that the outbred ecotypes with increased levels of expression of CCL4, NOS2, and SOCS1 also had higher viral loads. The higher expression of SOCS1 is inconsistent with the expression in inbred lines. These differences may uncover new mechanisms or pathways in these populations that may have otherwise been overlooked when examining the response in highly inbred lines. Taken together, our findings provide insights on the specific conserved and differentially expressed innate immune-related genes involved the response of highly outbred chicken lines to NDV. This also suggests that several of the specific innate immunity related genes identified in the current investigation may serve as markers for the selection of chickens with reduced susceptibility to NDV.
format Online
Article
Text
id pubmed-6596324
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-65963242019-07-05 Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines Schilling, Megan A. Memari, Sahar Cattadori, Isabella M. Katani, Robab Muhairwa, Amandus P. Buza, Joram J. Kapur, Vivek Front Microbiol Microbiology Newcastle disease virus (NDV) causes substantial economic losses to smallholder farmers in low- and middle-income countries with high levels of morbidity and mortality in poultry flocks. Previous investigations have suggested differing levels of susceptibility to NDV between specific inbred lines and amongst breeds of chickens, however, the mechanisms contributing to this remain poorly understood. Studies have shown that some of these differences in levels of susceptibility to NDV infection may be accounted for by variability in the innate immune response amongst various breeds of poultry to NDV infection. Recent studies, in inbred Fayoumi and Leghorn lines, uncovered conserved, breed-dependent, and subline-dependent responses. To better understand the role of innate immune genes in engendering a protective immune response, we assessed the transcriptional responses to NDV of three highly outbred Tanzanian local chicken ecotypes, the Kuchi, the Morogoro Medium, and the Ching’wekwe. Hierarchical clustering and principal coordinate analysis of the gene expression profiles of 21-day old chick embryos infected with NDV clustered in an ecotype-dependent manner and was consistent with the relative viral loads for each of the three ecotypes. The Kuchi and Morogoro Medium exhibit significantly higher viral loads than the Ching’wekwe. The results show that the outbred ecotypes with increased levels of expression of CCL4, NOS2, and SOCS1 also had higher viral loads. The higher expression of SOCS1 is inconsistent with the expression in inbred lines. These differences may uncover new mechanisms or pathways in these populations that may have otherwise been overlooked when examining the response in highly inbred lines. Taken together, our findings provide insights on the specific conserved and differentially expressed innate immune-related genes involved the response of highly outbred chicken lines to NDV. This also suggests that several of the specific innate immunity related genes identified in the current investigation may serve as markers for the selection of chickens with reduced susceptibility to NDV. Frontiers Media S.A. 2019-06-20 /pmc/articles/PMC6596324/ /pubmed/31281305 http://dx.doi.org/10.3389/fmicb.2019.01432 Text en Copyright © 2019 Schilling, Memari, Cattadori, Katani, Muhairwa, Buza and Kapur. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Schilling, Megan A.
Memari, Sahar
Cattadori, Isabella M.
Katani, Robab
Muhairwa, Amandus P.
Buza, Joram J.
Kapur, Vivek
Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines
title Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines
title_full Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines
title_fullStr Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines
title_full_unstemmed Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines
title_short Innate Immune Genes Associated With Newcastle Disease Virus Load in Chick Embryos From Inbred and Outbred Lines
title_sort innate immune genes associated with newcastle disease virus load in chick embryos from inbred and outbred lines
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6596324/
https://www.ncbi.nlm.nih.gov/pubmed/31281305
http://dx.doi.org/10.3389/fmicb.2019.01432
work_keys_str_mv AT schillingmegana innateimmunegenesassociatedwithnewcastlediseasevirusloadinchickembryosfrominbredandoutbredlines
AT memarisahar innateimmunegenesassociatedwithnewcastlediseasevirusloadinchickembryosfrominbredandoutbredlines
AT cattadoriisabellam innateimmunegenesassociatedwithnewcastlediseasevirusloadinchickembryosfrominbredandoutbredlines
AT katanirobab innateimmunegenesassociatedwithnewcastlediseasevirusloadinchickembryosfrominbredandoutbredlines
AT muhairwaamandusp innateimmunegenesassociatedwithnewcastlediseasevirusloadinchickembryosfrominbredandoutbredlines
AT buzajoramj innateimmunegenesassociatedwithnewcastlediseasevirusloadinchickembryosfrominbredandoutbredlines
AT kapurvivek innateimmunegenesassociatedwithnewcastlediseasevirusloadinchickembryosfrominbredandoutbredlines