Tadese Theodros, Fitzgerald Scott, Reed Willie M
Department of Pathobiology and Diagnostic Investigation and Diagnostic Center for Population and Animal Health, VMC A-19, Michigan State University, East Lansing, MI 48824, USA.
Vet Microbiol. 2008 Feb 5;127(1-2):39-49. doi: 10.1016/j.vetmic.2007.08.012. Epub 2007 Aug 17.
Current strains of fowlpox virus (FWPV) carrying circulating reticuloendotheliosis virus (FWPV-REV) sequence are becoming more pathogenic to poultry. This is evidenced by the fact that vaccination with current available FWPV vaccines provides limited protection against them. To characterize REV insertions in a collection of both older and more recent field isolates, we developed three different types of adjacent oligoprobes and primer sets from specific genomic locations of FWPV and REV: REV-ENV (accession no. K02537, 1382-2260), FWPV-REV integration site (accession no. AF006064, 86-1328), FWPV (accession no. AF198100, 232461-232670), and REV-LTR (accession no. V01204, 305-496). The data indicated that the primers from the REV-ENV region and the TaqMan probes specifically targeted REV-ENV sequences of FWPV-REV strains. Furthermore, the strains were differentiated based on quantitative melting temperature (T(m)) of their amplified products using FRET-based probes. The amplified products were further characterized by sequencing and multiple sequence alignment analysis. The results suggest that integrated REV-ENV sequences are both common and mostly conserved in field isolates. However, the minor variations found within the short-targeted ENV sequence from FWPV-REV strains suggest that these strains could have either undergone periodic point mutational changes or integration with different REV-ENV subtypes.
目前携带循环性网状内皮组织增生症病毒(FWPV-REV)序列的禽痘病毒(FWPV)毒株对家禽的致病性越来越强。现有FWPV疫苗接种后对这些毒株的保护作用有限,这一事实证明了这一点。为了对一系列较老和较新的野外分离株中的REV插入情况进行表征,我们从FWPV和REV的特定基因组位置开发了三种不同类型的相邻寡核苷酸探针和引物组:REV-ENV(登录号K02537,1382-2260)、FWPV-REV整合位点(登录号AF006064,86-1328)、FWPV(登录号AF198100,232461-232670)和REV-LTR(登录号V01204,305-496)。数据表明,来自REV-ENV区域的引物和TaqMan探针特异性靶向FWPV-REV毒株的REV-ENV序列。此外,利用基于荧光共振能量转移(FRET)的探针,根据扩增产物的定量熔解温度(T(m))对毒株进行区分。扩增产物通过测序和多序列比对分析进一步表征。结果表明,整合的REV-ENV序列在野外分离株中既常见又大多保守。然而,在FWPV-REV毒株的短靶向ENV序列中发现的微小变异表明,这些毒株可能经历了周期性的点突变变化或与不同的REV-ENV亚型整合。