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在对古代尔疫苗接种绵羊反应的转录组学研究中揭示的疫苗对亚种感染保护作用的相关因素。

Correlates of vaccine protection against sub-species infection revealed in a transcriptomic study of responses in Gudair vaccinated sheep.

作者信息

Purdie Auriol C, Plain Karren M, Pooley Hannah, Begg Douglas J, de Silva Kumudika, Whittington Richard J

机构信息

Sydney School of Veterinary Science, The University of Sydney, Sydney, NSW, Australia.

出版信息

Front Vet Sci. 2022 Nov 24;9:1004237. doi: 10.3389/fvets.2022.1004237. eCollection 2022.

Abstract

A critical hindrance in the development of effective vaccine strategies to combat infectious disease is lack of knowledge about correlates of protection and of the host responses necessary for successful adaptive immunity. Often vaccine formulations are developed by stepwise experimentation, with incomplete investigation of the fundamental mechanisms of protection. Gudair is a commercially available vaccine registered for use in sheep and goats for controlling spread of sub-species (MAP) infections and reduces mortality by up to 90%. Here, using an experimental infection model in sheep, we have utilized a transcriptomics approach to identify white blood cell gene expression changes in vaccinated, MAP-exposed Merino sheep with a protective response in comparison to those vaccinated animals that failed to develop immunity to MAP infection. This methodology facilitated an overview of gene-associated functional pathway adaptations using an analysis approach. We identified a group of genes that were activated in the vaccine-protected animals and confirmed stability of expression in samples obtained from naturally exposed commercially maintained sheep. We propose these genes as correlates of vaccine induced protection.

摘要

开发有效的传染病疫苗策略的一个关键障碍是缺乏对保护相关性以及成功的适应性免疫所需的宿主反应的了解。通常,疫苗配方是通过逐步实验开发的,对保护的基本机制的研究并不完整。古代尔(Gudair)是一种已注册用于绵羊和山羊的商业疫苗,用于控制亚种(MAP)感染的传播,并将死亡率降低多达90%。在这里,我们使用绵羊的实验感染模型,采用转录组学方法,来识别接种疫苗、接触MAP的美利奴绵羊中具有保护性反应的白细胞基因表达变化,并与那些未能对MAP感染产生免疫力的接种动物进行比较。这种方法通过一种分析方法促进了对基因相关功能途径适应性的概述。我们鉴定出一组在疫苗保护动物中被激活的基因,并证实了从自然接触的商业饲养绵羊获得的样本中表达的稳定性。我们提出这些基因作为疫苗诱导保护的相关性指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93d1/9729357/512e35500fe4/fvets-09-1004237-g0001.jpg

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