Cui Zhizhong, Zhuang Guoqin, Xu Xiaoyun, Sun Aijun, Su Shuai
College of Veterinary Medicine, Shandong Agricultural University, #61 Daizong Street, Taian 271018, China.
Virus Genes. 2010 Apr;40(2):236-43. doi: 10.1007/s11262-009-0437-z. Epub 2009 Dec 31.
A Marek's disease virus (MDV) field strain designated GX0101 was isolated from a layer flock and confirmed to be a recombinant virus with an insert of a long terminal repeat (LTR) from the reticuloendotheliosis virus (REV). A chimeric molecule containing an REV-LTR insert of 539 bp and its flanking sequences from MDV was amplified and sequenced. An REV-LTR downstream from the Internal Repeat Short (IRS) region has 77.4-98.6% homology to seven REV field strains isolated from different avian species in different parts of the world. The insertion site is located downstream of SORF 1 and upstream of SORF2 in the IRS region near the junction with the Unique Short (US) region in the MDV serotype 1 genome. Chicken experiments were conducted to determine the oncogenicity of the recombinant GX0101 virus and its transmissibility to contact chickens. Dot blot hybridization was used to detect the presence of the pp38 gene in feather tips from GX0101 or Md5 infected and contact birds. The pp38 was detected in GX0101 contact birds about 1-2 weeks earlier than in Md5 birds when both groups were vaccinated with HVT vaccine. Long term pathogenicity tests in specific pathogen free (SPF) chickens reveal that the recombinant GX0101 has a higher virulence than GA, but less virulence than Md5, the very virulent pathotype of MDV. This is the first report on an oncogenic serotype 1 MDV field strain with LTR insert and its pathogenicity.
一株名为GX0101的马立克氏病病毒(MDV)野毒株从一个蛋鸡群中分离得到,并被确认为是一种重组病毒,其插入了来自网状内皮组织增生症病毒(REV)的长末端重复序列(LTR)。扩增并测序了一个包含539 bp REV-LTR插入片段及其来自MDV的侧翼序列的嵌合分子。内部短重复序列(IRS)区域下游的REV-LTR与从世界不同地区不同禽类分离得到的7株REV野毒株具有77.4 - 98.6%的同源性。插入位点位于MDV 1型基因组中IRS区域与独特短区域(US)交界处附近的SORF 1下游和SORF2上游。进行了鸡实验以确定重组GX0101病毒的致瘤性及其对接触鸡的传播性。采用斑点杂交法检测来自感染GX0101或Md5的鸡及其接触鸡的羽毛尖端中pp38基因的存在情况。当两组都接种HVT疫苗时,在GX0101接触鸡中检测到pp38的时间比在Md5鸡中早约1 - 2周。在无特定病原体(SPF)鸡中进行的长期致病性试验表明,重组GX0携带的致瘤性MDV野毒株及其致病性。
这是关于一株带有LTR插入片段的致瘤性1型MDV野毒株及其致病性的首次报道。