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胸膜肺炎放线杆菌一种常见的48千道尔顿外膜蛋白的分子特征分析

Molecular characterization of a common 48-kilodalton outer membrane protein of Actinobacillus pleuropneumoniae.

作者信息

Cruz W T, Nedialkov Y A, Thacker B J, Mulks M H

机构信息

Department of Microbiology, Michigan State University, East Lansing 48824, USA.

出版信息

Infect Immun. 1996 Jan;64(1):83-90. doi: 10.1128/iai.64.1.83-90.1996.

Abstract

Previous studies have shown that a vaccine prepared from outer membranes of Actinobacillus pleuropneumoniae serotype 5 can elicit protective immunity in swine against challenge with either serotype 5 or serotype 1. These results suggest the presence of common subcapsular surface antigens, such as outer membrane proteins, that contribute to cross-protective immunity. We have identified a 48-kDa outer membrane protein that is common to all 12 capsular serotypes of A. pleuropneumoniae but is not present in the outer membranes of related species of gram-negative swine pathogens. This protein is immunogenic in swine infected with either A. pleuropneumoniae serotype 5 or 1A, as well as in swine vaccinated with A. pleuropneumoniae serotype 5 outer membranes. This 48-kDa protein is readily detected in outer membranes produced by sucrose density gradient centrifugation, but it is sarcosyl soluble and therefore not found in outer membranes prepared by detergent treatment. The gene encoding the 48-kDa outer membrane protein has been cloned from A. pleuropneumoniae serotype 5 and and has been designated aopA, for Actinobacillus outer membrane protein A. The gene is 1,347 bp in length and encodes a protein, designated AopA, of 449 amino acids with a predicted molecular weight of 48,603. Southern blot analysis under high-stringency conditions showed that strains of all 12 serotypes of A. pleuropneumoniae contain DNA homologous to this gene, as do strains of two closely related species, Actinobacillus suis and Pasteurella multocida. Whether antibodies against the AopA antigen contribute to cross-protective immunity against A. pleuropneumoniae infection remains to be determined.

摘要

先前的研究表明,由胸膜肺炎放线杆菌5型外膜制备的疫苗可使猪产生保护性免疫,抵抗5型或1型菌株的攻击。这些结果表明存在共同的荚膜下表面抗原,如外膜蛋白,它们有助于产生交叉保护性免疫。我们鉴定出一种48 kDa的外膜蛋白,它存在于胸膜肺炎放线杆菌的所有12种荚膜血清型中,但不存在于革兰氏阴性猪病原体的相关物种的外膜中。这种蛋白在感染胸膜肺炎放线杆菌5型或1A型的猪以及接种胸膜肺炎放线杆菌5型外膜的猪中具有免疫原性。这种48 kDa的蛋白很容易在通过蔗糖密度梯度离心产生的外膜中检测到,但它可溶于肌氨酸钠,因此在通过去污剂处理制备的外膜中找不到。编码48 kDa外膜蛋白的基因已从胸膜肺炎放线杆菌5型中克隆出来,并被命名为aopA,即放线杆菌外膜蛋白A。该基因长度为1347 bp,编码一种名为AopA的蛋白,由449个氨基酸组成,预测分子量为48603。在高严格条件下的Southern印迹分析表明,胸膜肺炎放线杆菌的所有12种血清型菌株都含有与该基因同源的DNA,两种密切相关的物种猪放线杆菌和多杀性巴氏杆菌的菌株也含有该基因。针对AopA抗原的抗体是否有助于抵抗胸膜肺炎放线杆菌感染的交叉保护性免疫仍有待确定。

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