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睡眠嗜血杆菌免疫显性表面抗原的特性分析

Characterization of immunodominant surface antigens of Haemophilus somnus.

作者信息

Corbeil L B, Kania S A, Gogolewski R P

机构信息

Department of Pathology 8416, University of California San Diego Medical Center 92103.

出版信息

Infect Immun. 1991 Dec;59(12):4295-301. doi: 10.1128/iai.59.12.4295-4301.1991.

Abstract

An immunodominant Haemophilus somnus outer membrane protein with an apparent molecular mass of 40 kDa on Western blots (immunoblots) of gradient sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels was characterized because a monospecific antibody against this antigen was protective. This monospecific antibody was used for immunoaffinity purification of the antigen. The immunoaffinity-purified antigen reacted with a polyclonal antibody to the 40-kDa antigen but not with a monoclonal antibody (3G9) which reacted with the 40-kDa antigen in gradient gels. On 8 or 10% gels, the approximately 40-kDa antigen was resolved as two bands, a 40-kDa band which reacted with the protective monospecific polyclonal antibody (p40) and a band of lower molecular mass which reacted with monoclonal antibody 3G9. The latter antigen was designated p39. Both antigens were conserved in all H. somnus isolates tested. The specific antibodies were also used to detect cross-reacting antigens in other gram-negative bacteria. Antibody to p40 reacted with proteins of 55 to 28 kDa, with the greatest intensity shown among proteins from other members of the family Pasteurellaceae. Antibody to p40 was reduced by absorption with live H. somnus or other members of the family Pasteurellaceae, so the antigen appears to be surface exposed. Antibody to p39 only cross-reacted with a broad band (38 to 40 kDa) in Haemophilus agni. Since H. agni is not a bovine pathogen and since convalescent-phase serum from H. somnus-infected animals did recognize p39, the latter may be a good immunodiagnostic antigen, if the lack of cross-reactivity with antigens in other gram-negative bacteria is confirmed with a polyclonal antibody to p39. The cross-reactivity of antiserum to p40 with antigens of members of the family Pasteurellaceae and the ability of this antiserum to protect against H. somnus pneumonia indicate that p40 may be a useful vaccine antigen for H. somnus disease and perhaps even diseases caused by other members of the family Pasteurellaceae.

摘要

在梯度十二烷基硫酸钠-聚丙烯酰胺凝胶电泳凝胶的蛋白质免疫印迹(免疫印迹法)上,一种明显分子量为40 kDa的睡眠嗜血杆菌免疫显性外膜蛋白得到了鉴定,因为针对该抗原的单特异性抗体具有保护性。这种单特异性抗体被用于该抗原的免疫亲和纯化。免疫亲和纯化的抗原与针对40 kDa抗原的多克隆抗体发生反应,但不与在梯度凝胶中与40 kDa抗原发生反应的单克隆抗体(3G9)发生反应。在8%或10%的凝胶上,约40 kDa的抗原被分离为两条带,一条40 kDa的带与保护性单特异性多克隆抗体(p40)发生反应,另一条分子量较低的带与单克隆抗体3G9发生反应。后一种抗原被命名为p39。在所有测试的睡眠嗜血杆菌分离株中,这两种抗原都是保守的。特异性抗体也被用于检测其他革兰氏阴性菌中的交叉反应抗原。针对p40的抗体与55至28 kDa的蛋白质发生反应,在巴斯德菌科其他成员的蛋白质中反应强度最大。针对p40的抗体通过与活的睡眠嗜血杆菌或巴斯德菌科其他成员进行吸收而减少,因此该抗原似乎暴露于表面。针对p39的抗体仅与羊嗜血杆菌中的一条宽带(38至40 kDa)发生交叉反应。由于羊嗜血杆菌不是牛病原体,并且由于来自感染睡眠嗜血杆菌动物的恢复期血清确实识别p39,如果用针对p39的多克隆抗体证实其与其他革兰氏阴性菌中的抗原缺乏交叉反应性,那么后者可能是一种良好的免疫诊断抗原。针对p40的抗血清与巴斯德菌科成员的抗原的交叉反应性以及该抗血清预防睡眠嗜血杆菌肺炎的能力表明,p40可能是用于睡眠嗜血杆菌疾病甚至可能是由巴斯德菌科其他成员引起的疾病的有用疫苗抗原。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16ec/259040/563a6fb8f07d/iai00048-0017-a.jpg

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