畜牧兽医学报 ›› 2016, Vol. 47 ›› Issue (8): 1635-1644.doi: doi: 10.11843/j.issn.0366-6964.2016.08.014

• 预防兽医 • 上一篇    下一篇

马立克病病毒超强毒株GX0101感染宿主部分病毒基因表达水平及致病阶段分析

马圣明1,2,滕蔓2,余祖华1,党露2,李会珍3,丁轲1,邓瑞广2,罗俊1,2*   

  1. (1.河南科技大学动物科技学院,动物疫病与公共安全重点实验室,洛阳 471003;2.河南省农业科学院动物免疫学重点实验室,农业部动物免疫学重点实验室,河南省动物免疫学重点实验室,郑州 450002;3.河南农业大学牧医工程学院,郑州450002)
  • 收稿日期:2016-03-21 出版日期:2016-08-23 发布日期:2016-08-23
  • 通讯作者: 罗俊,E-mail:luojun593@aliyun.com
  • 作者简介:马圣明(1991-),男,河南罗山人,硕士生,主要从事动物病毒分子致病机制研究,Tel:0371-65756056,E-mail:mashengming66@163.com
  • 基金资助:

    国家自然科学基金(31372445);国家重点研发计划(2016YFD0500802)

The Viral Gene Expression Profiles and Pathogenic Phases of the Disease Caused by Very Virulent MDV Strain GX0101

MA Sheng-ming 1,2,TENG Man 2,YU Zu-hua 1,DANG Lu 2,LI Hui-zhen 3,DING Ke 1,DENG Rui-guang 2,LUO Jun 1,2*   

  1. (1.Key Laboratory of Animal Disease and Public Safety,College of Animal Science and Technology,
    Henan University of Science and Technology,Luoyang 471003,China;2.Key Laboratory of Animal
    Immunology of the Ministry of Agriculture,Henan Provincial Key Laboratory of Animal Immunology,
    Henan Academy of Agricultural Sciences,Zhengzhou 450002,China;3.College of Animal Science
    and Veterinary Medicine,Henan Agricultural University,Zhengzhou 450002,China)
  • Received:2016-03-21 Online:2016-08-23 Published:2016-08-23

摘要:

旨在探讨马立克病病毒(MDV)超强毒株GX0101对宿主的感染过程及致病阶段,即“Cornell模型”,为进一步使用该毒株研究MDV的致病或致瘤机制奠定基础。用GX0101接种1日龄SPF鸡,建立了感染宿主的动物模型;然后用RT-qPCR分析10个具有代表性的MDV蛋白编码基因在感染不同时间点的动态基因转录水平。结果显示,GX0101感染发病鸡的临床症状及剖检病变与典型的马立克病一致;MDV编码的结构蛋白基因gB、gEUL6、非结构蛋白基因UL42和UL52、立早期基因ICP4、水平传播相关基因UL13以及磷酸化蛋白基因pp38具有相似的转录水平和趋势,均在GX0101感染后7 d上升至第一个峰值,10 d降至低谷,14 d又逐渐升高并在21 d达到第二个峰值,30~60 d逐渐下降并处于较低的转录水平;MDV编码的原癌基因meq和毒力相关基因RLORF6在GX0101感染7 d即持续升高,并在14~60 d的试验周期内较长时间处于高转录水平。结合作者此前研究及本文结果分析,GX0101感染宿主的“Cornell模型”:早期增殖性-限制性感染期为1~7 d,潜伏感染期约为10 d前后,晚期溶细胞性感染及免疫抑制期发生于14~21 d,而T细胞转化及淋巴瘤形成阶段可能在14 d前后就已经开始。

Abstract:

The present work was performed to study the infection phases of Marek’s disease (MD),namely ‘Cornell Model’,caused by the very virulent (vv) Marek’s disease virus (MDV) strain GX0101.For the first step,one-day-old specific pathogen free (SPF) chickens were challenged by GX0101 to establish the animal model of MD.Then,the kinetic transrption levels of 10 representative MDV protein-coding genes at different days post-infection (dpi) were determined by real-time quantitative PCR (RT-qPCR).The results showed that the onset of clinical symptoms and autopsy lesions of GX0101-infected birds was consistent with the typical MD cases.Some of the MDV protein-coding genes,including the structural protein-coding genes of gB,gE and UL6,the nonstructural protein-coding genes of UL42 and UL52,the immediate early infected cell protein 4 gene (ICP4),the horizontal transmission associated gene of UL13 and the 38 kD phosphorylated protein gene (pp38),demonstrated a similar transcription pattern,which increased to a first peak at 7 dpi,fell to a bottom level at 10 dpi,increased again at 14 dpi and reached to a second peak at 21 dpi,and then gradually declined to low levels from 30 to 60 dpi.However,both of the unique MDV oncogene meq and virulence related gene RLORF6 represented a persistent increasing transcription trend from 7 dpi,and then kept at a higher transcription level from 14 to 60 dpi.Our previous and present data indicates that the ‘Cornell Model’ of MD caused by GX0101 are as blow:the early cytolytic phase occurs at 1-7 dpi,the latent phase establishes at about 10 dpi and the late cytolytic and immunosuppressive phase appears at 14-21 dpi,while the T cell transformation and lymphomagenesis possibly starts at about 14 dpi.

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