Cargando…

Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus

IgD is considered to be a recently-evolved Ig and a puzzling molecule, being previously found in all vertebrate taxa, except for birds. Although IgD likely plays an important role in vertebrate immune responses, the function of IgD in Nile tilapia (Oreochromis niloticus) is virtually unknown. In the...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Bei, Wang, Pei, Wu, Zao-He, Lu, Yi-Shan, Wang, Zhong-Liang, Jian, Ji-Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4813209/
https://www.ncbi.nlm.nih.gov/pubmed/27005611
http://dx.doi.org/10.3390/ijms17030348
_version_ 1782424264300822528
author Wang, Bei
Wang, Pei
Wu, Zao-He
Lu, Yi-Shan
Wang, Zhong-Liang
Jian, Ji-Chang
author_facet Wang, Bei
Wang, Pei
Wu, Zao-He
Lu, Yi-Shan
Wang, Zhong-Liang
Jian, Ji-Chang
author_sort Wang, Bei
collection PubMed
description IgD is considered to be a recently-evolved Ig and a puzzling molecule, being previously found in all vertebrate taxa, except for birds. Although IgD likely plays an important role in vertebrate immune responses, the function of IgD in Nile tilapia (Oreochromis niloticus) is virtually unknown. In the present study, a membrane form of IgD (mIgD) heavy chains were cloned from the GIFT strain of Nile tilapia (designated On-mIgD). The On-mIgD heavy chain’s cDNA is composed of 3347 bp with a 31 bp of 5′-UTR, 3015 bp open reading frame (ORF) and 301 bp 3′-UTR, encoding a polypeptide of 1004 amino acids (GenBank accession no: KF530821). Phylogenetic analysis revealed that On-mIgD heavy chains showed the highest similarity to Siniperca chuatsi. Quantitative real-time PCR (qRT-PCR) analysis showed that On-mIgD expression occurred predominately in head kidney, thymus, spleen, and kidney. After Streptococcus agalactiae infection, transcripts of On-mIgD increased and reached its peak at 48 h in the head kidney and thymus, and 72 h in the spleen, respectively. Taken together, these results collectively indicated that IgD could possibly have a key role to play in the immune response when bacterial infections in Nile tilapia.
format Online
Article
Text
id pubmed-4813209
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-48132092016-04-06 Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus Wang, Bei Wang, Pei Wu, Zao-He Lu, Yi-Shan Wang, Zhong-Liang Jian, Ji-Chang Int J Mol Sci Article IgD is considered to be a recently-evolved Ig and a puzzling molecule, being previously found in all vertebrate taxa, except for birds. Although IgD likely plays an important role in vertebrate immune responses, the function of IgD in Nile tilapia (Oreochromis niloticus) is virtually unknown. In the present study, a membrane form of IgD (mIgD) heavy chains were cloned from the GIFT strain of Nile tilapia (designated On-mIgD). The On-mIgD heavy chain’s cDNA is composed of 3347 bp with a 31 bp of 5′-UTR, 3015 bp open reading frame (ORF) and 301 bp 3′-UTR, encoding a polypeptide of 1004 amino acids (GenBank accession no: KF530821). Phylogenetic analysis revealed that On-mIgD heavy chains showed the highest similarity to Siniperca chuatsi. Quantitative real-time PCR (qRT-PCR) analysis showed that On-mIgD expression occurred predominately in head kidney, thymus, spleen, and kidney. After Streptococcus agalactiae infection, transcripts of On-mIgD increased and reached its peak at 48 h in the head kidney and thymus, and 72 h in the spleen, respectively. Taken together, these results collectively indicated that IgD could possibly have a key role to play in the immune response when bacterial infections in Nile tilapia. MDPI 2016-03-08 /pmc/articles/PMC4813209/ /pubmed/27005611 http://dx.doi.org/10.3390/ijms17030348 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Bei
Wang, Pei
Wu, Zao-He
Lu, Yi-Shan
Wang, Zhong-Liang
Jian, Ji-Chang
Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus
title Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus
title_full Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus
title_fullStr Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus
title_full_unstemmed Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus
title_short Molecular Cloning and Expression Analysis of IgD in Nile Tilapia (Oreochromis niloticus) in Response to Streptococcus agalactiae Stimulus
title_sort molecular cloning and expression analysis of igd in nile tilapia (oreochromis niloticus) in response to streptococcus agalactiae stimulus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4813209/
https://www.ncbi.nlm.nih.gov/pubmed/27005611
http://dx.doi.org/10.3390/ijms17030348
work_keys_str_mv AT wangbei molecularcloningandexpressionanalysisofigdinniletilapiaoreochromisniloticusinresponsetostreptococcusagalactiaestimulus
AT wangpei molecularcloningandexpressionanalysisofigdinniletilapiaoreochromisniloticusinresponsetostreptococcusagalactiaestimulus
AT wuzaohe molecularcloningandexpressionanalysisofigdinniletilapiaoreochromisniloticusinresponsetostreptococcusagalactiaestimulus
AT luyishan molecularcloningandexpressionanalysisofigdinniletilapiaoreochromisniloticusinresponsetostreptococcusagalactiaestimulus
AT wangzhongliang molecularcloningandexpressionanalysisofigdinniletilapiaoreochromisniloticusinresponsetostreptococcusagalactiaestimulus
AT jianjichang molecularcloningandexpressionanalysisofigdinniletilapiaoreochromisniloticusinresponsetostreptococcusagalactiaestimulus