Bae I, Jackwood D J, Benfield D A, Saif L J, Wesley R D, Hill H
Ohio Agricultural Research and Development Center, Ohio State University, Wooster 44691.
J Clin Microbiol. 1991 Jan;29(1):215-8. doi: 10.1128/jcm.29.1.215-218.1991.
Two cDNA clones prepared from the virulent Miller strain of transmissible gastroenteritis virus (TGEV) were identified, and their nucleotide sequences were determined. The clones were nonoverlapping and located in the 5' region of the S glycoprotein gene. Their nucleotide and predicted amino acid sequences were compared with published sequences of the attenuated Purdue strain of TGEV and feline infectious peritonitis virus (FIPV). TGEV clone pE21 contained 381 bp of the S glycoprotein gene and had greater than 98% nucleotide and amino acid sequence homology with Purdue TGEV and over 87% nucleotide and amino acid sequence homology with FIPV. TGEV clone pD24 contained 267 bp of the S glycoprotein gene. It had greater than 98% nucleotide and amino acid sequence homology with Purdue TGEV but only 54% nucleotide sequence homology and 24% amino acid sequence homology with FIPV. A probe prepared from pD24 could differentiate TGEV from porcine respiratory coronavirus and other antigenically related coronaviruses, FIPV, feline enteric coronavirus, and canine coronavirus in a dot blot hybridization assay.
从传染性胃肠炎病毒(TGEV)的强毒株米勒株制备了两个cDNA克隆,并测定了它们的核苷酸序列。这些克隆不重叠,位于S糖蛋白基因的5'区域。将它们的核苷酸和预测的氨基酸序列与已发表的TGEV减毒株普渡株和猫传染性腹膜炎病毒(FIPV)的序列进行了比较。TGEV克隆pE21包含381bp的S糖蛋白基因,与普渡TGEV的核苷酸和氨基酸序列同源性大于98%,与FIPV的核苷酸和氨基酸序列同源性超过87%。TGEV克隆pD24包含267bp的S糖蛋白基因。它与普渡TGEV的核苷酸和氨基酸序列同源性大于98%,但与FIPV的核苷酸序列同源性仅为54%,氨基酸序列同源性为24%。从pD24制备的探针在斑点印迹杂交试验中可将TGEV与猪呼吸道冠状病毒及其他抗原相关的冠状病毒、FIPV、猫肠道冠状病毒和犬冠状病毒区分开来。