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Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken

Functional polymorphisms in pattern recognition receptors (PRRs) modulate innate immunity and play a crucial role in resistance or susceptibility to diseases. The present study was carried out to explore polymorphic patterns in the coding sequences of PRR genes TLR3, TLR1LA (TLRs), MDA5, LGP2 (RLRs)...

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Autores principales: Haunshi, Santosh, Burramsetty, Arun Kumar, Ramasamy, Kannaki, Chatterjee, Rudra Nath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Copernicus GmbH 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065405/
https://www.ncbi.nlm.nih.gov/pubmed/32175451
http://dx.doi.org/10.5194/aab-61-441-2018
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author Haunshi, Santosh
Burramsetty, Arun Kumar
Ramasamy, Kannaki
Chatterjee, Rudra Nath
author_facet Haunshi, Santosh
Burramsetty, Arun Kumar
Ramasamy, Kannaki
Chatterjee, Rudra Nath
author_sort Haunshi, Santosh
collection PubMed
description Functional polymorphisms in pattern recognition receptors (PRRs) modulate innate immunity and play a crucial role in resistance or susceptibility to diseases. The present study was carried out to explore polymorphic patterns in the coding sequences of PRR genes TLR3, TLR1LA (TLRs), MDA5, LGP2 (RLRs) and NOD1 (NLR) in chicken breeds of India, namely Ghagus (GH), Nicobari (NB) and the exotic White Leghorn (WLH) breed. Out of 209 SNPs observed in five genes among three breeds, 117 were synonymous (Syn) and 92 were non-synonymous (NS) SNPs. In TLR genes the highest polymorphism was observed in NB (16, 28) compared to GH (14, 16) and WLH (13, 19) breeds. In the MDA5 gene the highest polymorphism was observed in GH (12) compared to NB (eight) and WLH (four) breeds. However, an almost similar level of polymorphism was observed in the LGP2 gene among the three breeds. In the NOD1 gene, the highest polymorphism was observed in NB (27), followed by WLH (11) and GH (10) breeds. The overall highest number of SNPs was observed in NB (90), followed by GH (62) and the WLH (57) breed. With regard to variation in polymorphism among different classes of PRRs, the study revealed the highest polymorphism in TLRs compared to NOD1 and the RLR class of PRRs. Further, the domain locations of various Syn and NS SNPs in each PRR among the three breeds were identified. In silico analysis of NS SNPs revealed that most of them had a neutral effect on protein function. However, two each in TLR1LA and LGP2 and one in the MDA5 gene were predicted to be deleterious to protein function. The present study unravelled extensive polymorphism in the coding sequences of the TLR and NLR class of PRR genes, and the polymorphism was higher in indigenous chicken breeds.
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spelling pubmed-70654052020-03-13 Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken Haunshi, Santosh Burramsetty, Arun Kumar Ramasamy, Kannaki Chatterjee, Rudra Nath Arch Anim Breed Original Study Functional polymorphisms in pattern recognition receptors (PRRs) modulate innate immunity and play a crucial role in resistance or susceptibility to diseases. The present study was carried out to explore polymorphic patterns in the coding sequences of PRR genes TLR3, TLR1LA (TLRs), MDA5, LGP2 (RLRs) and NOD1 (NLR) in chicken breeds of India, namely Ghagus (GH), Nicobari (NB) and the exotic White Leghorn (WLH) breed. Out of 209 SNPs observed in five genes among three breeds, 117 were synonymous (Syn) and 92 were non-synonymous (NS) SNPs. In TLR genes the highest polymorphism was observed in NB (16, 28) compared to GH (14, 16) and WLH (13, 19) breeds. In the MDA5 gene the highest polymorphism was observed in GH (12) compared to NB (eight) and WLH (four) breeds. However, an almost similar level of polymorphism was observed in the LGP2 gene among the three breeds. In the NOD1 gene, the highest polymorphism was observed in NB (27), followed by WLH (11) and GH (10) breeds. The overall highest number of SNPs was observed in NB (90), followed by GH (62) and the WLH (57) breed. With regard to variation in polymorphism among different classes of PRRs, the study revealed the highest polymorphism in TLRs compared to NOD1 and the RLR class of PRRs. Further, the domain locations of various Syn and NS SNPs in each PRR among the three breeds were identified. In silico analysis of NS SNPs revealed that most of them had a neutral effect on protein function. However, two each in TLR1LA and LGP2 and one in the MDA5 gene were predicted to be deleterious to protein function. The present study unravelled extensive polymorphism in the coding sequences of the TLR and NLR class of PRR genes, and the polymorphism was higher in indigenous chicken breeds. Copernicus GmbH 2018-11-12 /pmc/articles/PMC7065405/ /pubmed/32175451 http://dx.doi.org/10.5194/aab-61-441-2018 Text en Copyright: © 2018 Santosh Haunshi et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/
spellingShingle Original Study
Haunshi, Santosh
Burramsetty, Arun Kumar
Ramasamy, Kannaki
Chatterjee, Rudra Nath
Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken
title Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken
title_full Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken
title_fullStr Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken
title_full_unstemmed Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken
title_short Polymorphisms in pattern recognition receptor genes of indigenous and White Leghorn breeds of chicken
title_sort polymorphisms in pattern recognition receptor genes of indigenous and white leghorn breeds of chicken
topic Original Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065405/
https://www.ncbi.nlm.nih.gov/pubmed/32175451
http://dx.doi.org/10.5194/aab-61-441-2018
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