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感染表达萤火虫荧光素酶基因的重组牛3型腺病毒后棉鼠(棉鼠属棉鼠)模型中的病理学和免疫原性

Pathology and immunogenicity in the cotton rat (Sigmodon hispidus) model after infection with a bovine adenovirus type 3 recombinant virus expressing the firefly luciferase gene.

作者信息

Mittal S K, Middleton D M, Tikoo S K, Prevec L, Graham F L, Babiuk L A

机构信息

Veterinary Infectious Disease Organization, University of Saskatchewan, Saskatoon, Canada.

出版信息

J Gen Virol. 1996 Jan;77 ( Pt 1):1-9. doi: 10.1099/0022-1317-77-1-1.

Abstract

The histopathology of adenovirus pneumonia in cotton rats (Sigmodon hispidus) due to bovine adenovirus type 3-luciferase recombinant virus (BAd3-Luc), which has a 0.7 kb deletion from the early region 3 (E3) replaced with the firefly luciferase gene, was compared with that produced by the parental wild-type (wt) bovine adenovirus type 3 (BAd3). After intranasal inoculation of cotton rats with 3 x 10(7) p.f.u. of BAd3-Luc, the infectious virus titres in the lungs at various times post-infection were similar to those of animals infected with the parental virus. Quantitative analysis of histopathological changes and immunohistochemical staining showed that the character and severity of the lesions were indistinguishable in the two infections. Luciferase activity was detected in the lungs of BAd3-Luc-inoculated animals until 4 days post-infection (p.i.). Antibodies to both BAd3 and luciferase were detected in sera collected from BAd3-Luc-infected animals until at least 6 weeks p.i. These results show that Bad3-Luc produces pulmonary lesions in cotton rats similar to those of wt BAd3 and suggest that BAd3-based vectors may be suitable for the development of live recombinant virus vaccines.

摘要

将牛腺病毒3型荧光素酶重组病毒(BAd3-Luc)接种到棉鼠(棉鼠属)后引发的腺病毒肺炎的组织病理学,与亲本野生型(wt)牛腺病毒3型(BAd3)所引发的进行了比较。BAd3-Luc的早期区域3(E3)缺失了0.7 kb并用萤火虫荧光素酶基因进行了替换。在用3×10⁷ 蚀斑形成单位(p.f.u.)的BAd3-Luc经鼻接种棉鼠后,感染后不同时间肺中的感染性病毒滴度与感染亲本病毒的动物相似。组织病理学变化的定量分析和免疫组织化学染色表明,两种感染中病变的特征和严重程度没有区别。在接种BAd3-Luc的动物肺中,直到感染后4天(p.i.)都检测到了荧光素酶活性。在从感染BAd3-Luc的动物收集的血清中,直到感染后至少6周都检测到了针对BAd3和荧光素酶的抗体。这些结果表明,BAd3-Luc在棉鼠中产生的肺部病变与wt BAd3相似,并表明基于BAd3的载体可能适合用于开发重组活病毒疫苗。

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