Tuboly Tamás, Nagy Éva
Veterinary Medical Research Institute of the Hungarian Academy of Sciences, Budapest, Hungary1.
Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, Ontario, CanadaN1G 2W12.
J Gen Virol. 2001 Jan;82(Pt 1):183-190. doi: 10.1099/0022-1317-82-1-183.
Five recombinant porcine adenoviruses of serotype 5 (PAdV-5) carrying the full-length or the 5' 2.2 kb half of the transmissible gastroenteritis virus (TGEV) spike (S) gene were generated by homologous recombination in E. coli strain BJ5183 cells and subsequent transfection of swine testicle cells. The foreign genes were inserted into the E3 region of PAdV-5. One recombinant virus had no deletion in the E3 region, whereas a 1.2 kb fragment was removed from the E3 region in the remainder of the recombinant viruses. One stable construct with a 4.4 kb insertion had a genome size of 109.6% of the wild-type genome, the largest reported for any recombinant adenovirus. Only those viruses that carried the S gene in the left to right orientation expressed the S gene. Three recombinant viruses were tested by oral immunization of pigs and both antibody response and virus shedding were monitored. None of the pigs showed clinical signs and the virus was recovered from rectal swabs until 6-7 days post-infection. Viruses expressing the S gene induced TGEV- and PAdV-5-specific virus-neutralizing antibodies. Moreover, TGEV-specific secretory IgA was detected in the small intestine and in the lungs of the immunized animals.
通过在大肠杆菌BJ5183细胞中进行同源重组并随后转染猪睾丸细胞,构建了5种携带传染性胃肠炎病毒(TGEV)刺突(S)基因全长或5' 2.2 kb片段的重组5型猪腺病毒(PAdV-5)。外源基因被插入到PAdV-5的E3区域。一种重组病毒在E3区域无缺失,而其余重组病毒的E3区域缺失了一个1.2 kb的片段。一个插入片段为4.4 kb的稳定构建体的基因组大小为野生型基因组的109.6%,这是报道的所有重组腺病毒中最大的。只有那些携带S基因且方向为从左到右的病毒才能表达S基因。通过对猪进行口服免疫对3种重组病毒进行了测试,并监测了抗体反应和病毒排毒情况。所有猪均未出现临床症状,直到感染后6 - 7天,仍可从直肠拭子中检测到病毒。表达S基因的病毒诱导了TGEV和PAdV-5特异性病毒中和抗体。此外,在免疫动物的小肠和肺中检测到了TGEV特异性分泌型IgA。