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首页|期刊导航|畜牧兽医学报|不同致病性H9N2亚型禽流感病毒诱导鸡TLR-7和Mx基因mRNA转录水平的差异

不同致病性H9N2亚型禽流感病毒诱导鸡TLR-7和Mx基因mRNA转录水平的差异

王建琳 曹志伟 王冬冬 尹燕博

畜牧兽医学报2017,Vol.48Issue(5):907-913,7.
畜牧兽医学报2017,Vol.48Issue(5):907-913,7.DOI:10.11843/j.issn.0366-6964.2017.05.015

不同致病性H9N2亚型禽流感病毒诱导鸡TLR-7和Mx基因mRNA转录水平的差异

Transcriptional Responses of TLR-7 and Mx mRNA in 3 Chicken Host Systems Infected with H9N2 Influenza Viruses with Different Pathogenicities

王建琳 1曹志伟 1王冬冬 1尹燕博1

作者信息

  • 1. 青岛农业大学动物科技学院,青岛266109
  • 折叠

摘要

Abstract

For a better understanding of the mechanism underlying the expression of type Ⅰ IFN induced by H9N2 influenza viruses with different pathogenicity,mRNA of TLR-7 and Mx were dynamically studied in 3 host systems of chicken which infected with strains SD/818 and SD/196 in this study.SPF chickens,SPF chicken embryos and primary chicken embryo fibroblasts were randomly divided into three groups,control group,SD/196-infected group and SD/818-infected group.The lungs,kidneys,duodenum,bursa of Fabricius,embryonic bodies and primary chicken embryo fibroblasts were collected at different time points after infection,and mRNA of TLR7 and Mx were dynamically studied using real-time quantitative reverse transcription PCR.The results showed that transcriptional level of TLR-7 and Mx in chicken host systems induced by SD/818 were significantly higher than those induced by SD/196 except expression of TLR-7 at chicken embryos.The results suggested that expression of TLR-7 and Mx mRNA in chicken host systems were induced by H9N2 influenza virus with different pathogenicity,and transcriptional level of TLR-7 and Mxc induced by SD/818 were higher than those induced by SD/196.

关键词

H9N2亚型禽流感病毒/致病性/SPF鸡/TLR-7/Mx

Key words

H9N2 influenza viruses/pathogenicity/SPF chicken/TLR-7/Mx/expression

分类

农业科技

引用本文复制引用

王建琳,曹志伟,王冬冬,尹燕博..不同致病性H9N2亚型禽流感病毒诱导鸡TLR-7和Mx基因mRNA转录水平的差异[J].畜牧兽医学报,2017,48(5):907-913,7.

基金项目

国家自然科学基金项目(31272535) (31272535)

山东省现代农业产业技术体系项目(SDAIT-11-03) (SDAIT-11-03)

山东省自然科学基金(ZR2013CL022) (ZR2013CL022)

畜牧兽医学报

OA北大核心CSCDCSTPCD

0366-6964

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