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绵羊疱疹病毒2糖蛋白B的互补作用恢复了牛疱疹病毒4 gB基因缺失突变体的感染性。

Ovine Herpesvirus 2 Glycoprotein B Complementation Restores Infectivity to a Bovine Herpesvirus 4 gB-Null Mutant.

作者信息

Moré Daniela D, Baker Katherine N, Shringi Smriti, Bastos Reginaldo G, O'Toole Donal, Donofrio Gaetano, Cunha Cristina W

机构信息

Animal Disease Research Unit, Agricultural Research Service, United States Department of Agriculture, Pullman, WA 99164, USA.

Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164, USA.

出版信息

Pathogens. 2024 Mar 1;13(3):219. doi: 10.3390/pathogens13030219.

Abstract

Ovine herpesvirus 2 (OvHV-2) and bovine herpesvirus 4 (BoHV-4) are gamma herpesviruses that belong to the genera and , respectively. As with all herpesviruses, both OvHV-2 and BoHV-4 express glycoprotein B (gB), which plays an essential role in the infection of host cells. In that context, it has been demonstrated that a BoHV-4 gB-null mutant is unable to infect host cells. In this study, we used homologous recombination to insert OvHV-2 ORF 8, encoding gB, into the BoHV-4 gB-null mutant genome, creating a chimeric BoHV-4 virus carrying and expressing OvHV-2 gB (BoHV-4∆gB/OvHV-2-gB) that was infectious and able to replicate in vitro. We then evaluated BoHV-4∆gB/OvHV-2-gB as a potential vaccine candidate for sheep-associated malignant catarrhal fever (SA-MCF), a fatal disease of ungulates caused by OvHV-2. Using rabbits as a laboratory model for MCF, we assessed the safety, immunogenicity, and efficacy of BoHV-4∆gB/OvHV-2-gB in an immunization/challenge trial. The results showed that while BoHV-4∆gB/OvHV-2-gB was safe and induced OvHV-2 gB-specific humoral immune responses, immunization conferred only 28.5% protection upon challenge with OvHV-2. Therefore, future studies should focus on alternative strategies to express OvHV-2 proteins to develop an effective vaccine against SA-MCF.

摘要

绵羊疱疹病毒2(OvHV - 2)和牛疱疹病毒4(BoHV - 4)是γ疱疹病毒,分别属于 属和 属。与所有疱疹病毒一样,OvHV - 2和BoHV - 4都表达糖蛋白B(gB),它在宿主细胞感染中起关键作用。在这方面,已证明BoHV - 4 gB缺失突变体无法感染宿主细胞。在本研究中,我们利用同源重组将编码gB的OvHV - 2开放阅读框8插入BoHV - 4 gB缺失突变体基因组中,构建了一种携带并表达OvHV - 2 gB的嵌合BoHV - 4病毒(BoHV - 4∆gB/OvHV - 2 - gB),该病毒具有传染性且能够在体外复制。然后,我们评估了BoHV - 4∆gB/OvHV - 2 - gB作为绵羊相关恶性卡他热(SA - MCF)潜在疫苗候选物的可能性,SA - MCF是一种由OvHV - 2引起的有蹄类动物致命疾病。我们使用兔子作为MCF的实验模型,在免疫/攻毒试验中评估了BoHV - 4∆gB/OvHV - 2 - gB的安全性、免疫原性和有效性。结果表明,虽然BoHV - 4∆gB/OvHV - 2 - gB是安全的,并能诱导OvHV - 2 gB特异性体液免疫反应,但在接受OvHV - 2攻毒时,免疫仅提供了28.5%的保护。因此,未来的研究应集中在表达OvHV - 2蛋白的替代策略上,以开发一种针对SA - MCF的有效疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f46/10974308/1d6fbeed7b58/pathogens-13-00219-g001.jpg

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