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鉴定严格意义上的边缘无浆体菌株和活的边缘无浆体亚种中央疫苗之间保守的边缘无浆体外膜蛋白抗原。

Identification of Anaplasma marginale outer membrane protein antigens conserved between A. marginale sensu stricto strains and the live A. marginale subsp. centrale vaccine.

机构信息

Program in Vector-Borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164-7040, USA.

出版信息

Infect Immun. 2011 Mar;79(3):1311-8. doi: 10.1128/IAI.01174-10. Epub 2010 Dec 28.

DOI:10.1128/IAI.01174-10
PMID:21189322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3067503/
Abstract

Live vaccination with Anaplasma marginale subsp. centrale (synonym for Anaplasma centrale) induces protection against severe disease upon challenge with A. marginale sensu stricto strains. Despite over a century of field use, the targets of protective immunity remained unknown. Using a broad proteomic approach, we identified the proteins in a challenge sensu stricto strain that were bound by the relevant antibody isotype induced by live vaccination with Anaplasma marginale subsp. centrale. A core of 15 proteins was identified in vaccinated animals across multiple major histocompatibility complex (MHC) haplotypes. This core separated into two structural/functional classes: "housekeeping" proteins involved in replication and metabolism and outer membrane proteins (OMPs). Orthologous proteins of both classes were identified within the vaccine strain and among sensu stricto strains. In contrast to the broad conservation among strains in the sequences of the housekeeping proteins, there was significantly greater divergence in the OMPs and greater divergence in both OMP sequences and the encoding locus structure between the vaccine strain and the sensu stricto strains than among the sensu stricto strains. The OMPs bound by live vaccine-induced antibody overlapped with OMPs that were immunogenic in animals vaccinated with inactivated vaccines and subsequently protected against bacteremia and disease. The identification of this core set of OMPs is consistent with the hypothesis that "subdominant" immunogens are required for vaccine-induced protection against A. marginale and provides clear direction for development of a safer, more effective vaccine.

摘要

用中央绵羊无浆体亚种(同义名中央绵羊无形体)进行活疫苗接种,可在接种严格意义上的边缘无形体菌株时诱导对严重疾病的保护。尽管已经使用了一个多世纪,但保护性免疫的靶标仍然未知。我们使用广泛的蛋白质组学方法,鉴定了在严格意义上的挑战菌株中与由中央绵羊无形体亚种活疫苗接种诱导的相关抗体同种型结合的蛋白质。在多个主要组织相容性复合体(MHC)单倍型的接种动物中,鉴定出了 15 种核心蛋白。该核心分为两类结构/功能:参与复制和代谢的“管家”蛋白和外膜蛋白(OMP)。两类蛋白在疫苗株和严格意义上的菌株中都有同源蛋白。与管家蛋白序列在菌株间广泛保守形成对比的是,OMP 存在显著更大的差异,而且在疫苗株和严格意义上的菌株之间的 OMP 序列和编码基因座结构上都存在更大的差异,而严格意义上的菌株之间的差异则较小。活疫苗诱导的抗体结合的 OMP 与用灭活疫苗接种的动物中具有免疫原性的 OMP 重叠,并且随后可预防菌血症和疾病。鉴定出的这种核心 OMP 集与“亚显性”免疫原是疫苗接种保护边缘无形体所必需的假设一致,并为开发更安全、更有效的疫苗提供了明确的方向。

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