Keeler C L, Kingsley D H, Burton C R
Department of Animal Science and Agricultural Biochemistry, College of Agricultural Sciences, University of Delaware, Newark 19717-1303.
Avian Dis. 1991 Oct-Dec;35(4):920-9.
An an initial step in the development of a recombinant poultry infectious laryngotracheitis virus (ILTV) vaccine, we report on the identification, cloning, and sequencing of a thymidine kinase (tk) gene from a virulent U.S. field isolate of ILTV. Degenerate oligonucleotide primers for the consensus nucleotide (ATP) binding site and the nucleoside (thymidine) binding site of other herpesvirus tk genes were used in the polymerase chain reaction (PCR) to amplify a fragment of ILTV DNA. The 344-base-pair (bp) amplified fragment was cloned into plasmid pKSII and used in Southern hybridizations to locate the ILTV tk gene on a 2.4-kb HindIII fragment. Upon cloning and sequencing this fragment, a 1089-bp open reading frame was identified, which is predicted to encode a protein demonstrating 27.9% amino acid homology to the herpes simplex virus type 1 (HSV-1) thymidine kinase protein. Analysis of the sequence revealed one region of difference from that reported for the Thorne strain of ILTV. In addition, the portion of the TK protein corresponding to the nucleotide binding domain is highly conserved among the avian herpesviruses.
作为重组禽传染性喉气管炎病毒(ILTV)疫苗研发的第一步,我们报告了从一株美国ILTV强毒株中鉴定、克隆和测序胸苷激酶(tk)基因的情况。利用针对其他疱疹病毒tk基因的共有核苷酸(ATP)结合位点和核苷(胸苷)结合位点的简并寡核苷酸引物,通过聚合酶链反应(PCR)扩增ILTV DNA片段。将扩增得到的344个碱基对(bp)的片段克隆到质粒pKSII中,并用于Southern杂交,以将ILTV tk基因定位在一个2.4 kb的HindIII片段上。对该片段进行克隆和测序后,鉴定出一个1089 bp的开放阅读框,预计其编码的蛋白质与单纯疱疹病毒1型(HSV-1)胸苷激酶蛋白具有27.9%的氨基酸同源性。序列分析显示,该序列与已报道的ILTV Thorne株存在一个差异区域。此外,TK蛋白对应于核苷酸结合域的部分在禽疱疹病毒中高度保守。