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接种基于9型禽腺病毒左端缺失的重组病毒的鸡的抗体反应和病毒脱落情况

Antibody response and virus shedding of chickens inoculated with left end deleted fowl adenovirus 9-based recombinant viruses.

作者信息

Corredor Juan Carlos, Nagy Eva

机构信息

Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada N1G 2W1.

出版信息

Avian Dis. 2011 Sep;55(3):443-6. doi: 10.1637/9710-031311-Reg.1.

Abstract

The nonpathogenic fowl adenoviruses (FAdVs) are suitable recombinant virus vectors. Two different replication-competent FAdV-9-based recombinant viruses carrying the enhanced green fluorescent protein (EGFP) gene within a nonessential DNA sequence at the left end genomic region were tested in chickens to study the antibody response by enzyme-linked immunosorbent assay to both the foreign proteins, EGFP and FAdV-9, and virus shedding through the feces. All inoculations were done intramuscularly: groups 1 and 2 with the recombinant viruses and group 3 with the wild-type FAdV-9 virus. Group 4 was mock inoculated. Sentinel birds also were included in groups 1-3 to study virus transmission. Boosting inoculations were done in all groups at 2, 3, and 4 wk after the first inoculation. Antibodies to EGFP were detected at 3-7 wk postinoculation in groups 1 and 2 only. Antibody response to FAdV-9 in groups 1-3 did not differ significantly (P > 0.06). Virus was not detected in the feces of chickens in groups 1 and 2, including the sentinel birds, but virus was present in the feces of chickens in group 3, including the sentinel birds. These results further supported our previous findings regarding the suitability of the nonessential region at the left end of the viral genome as an insertion site for foreign genes and its importance in in vivo replication. In this work, we demonstrated the potential of FAdV-9-based recombinant viruses as vaccines for poultry.

摘要

非致病性禽腺病毒(FAdVs)是合适的重组病毒载体。在鸡中测试了两种不同的、基于复制能力强的FAdV-9的重组病毒,它们在基因组左端非必需DNA序列中携带增强型绿色荧光蛋白(EGFP)基因,以通过酶联免疫吸附测定法研究针对外源蛋白EGFP和FAdV-9的抗体反应以及通过粪便排出病毒的情况。所有接种均通过肌肉注射进行:第1组和第2组接种重组病毒,第3组接种野生型FAdV-9病毒。第4组进行 mock 接种。第1 - 3组还包括哨兵鸡以研究病毒传播。在首次接种后第2、3和4周对所有组进行加强接种。仅在第1组和第2组接种后3 - 7周检测到针对EGFP的抗体。第1 - 3组对FAdV-9的抗体反应无显著差异(P > 0.06)。在第1组和第2组的鸡(包括哨兵鸡)粪便中未检测到病毒,但在第3组的鸡(包括哨兵鸡)粪便中检测到病毒。这些结果进一步支持了我们之前关于病毒基因组左端非必需区域作为外源基因插入位点的适用性及其在体内复制中的重要性的发现。在这项工作中,我们证明了基于FAdV-9的重组病毒作为家禽疫苗的潜力。

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