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可区分铜绿假单胞菌脂多糖内核、外核和脂质A区域的单克隆抗体。

Monoclonal antibodies that distinguish inner core, outer core, and lipid A regions of Pseudomonas aeruginosa lipopolysaccharide.

作者信息

de Kievit T R, Lam J S

机构信息

Department of Microbiology, College of Biological Science, University of Guelph, Ontario, Canada.

出版信息

J Bacteriol. 1994 Dec;176(23):7129-39. doi: 10.1128/jb.176.23.7129-7139.1994.

Abstract

In order to examine the immunochemistry of the core-lipid A region of Pseudomonas aeruginosa lipopolysaccharide (LPS), monoclonal antibodies (MAbs) specific for this region were produced in mice. Immunogen was prepared by coating a rough mutant of P. aeruginosa with column-purified core oligosaccharide fractions in order to enhance the immune response to the LPS core-lipid A region. Fourteen hybridoma clones were isolated, characterized, and further divided into three groups on the basis of their reactivities to rough LPS antigens in both enzyme-linked immunosorbent assays and Western immunoblots. In addition, another MAb, 18-19, designated group 1, was included in this study for defining core-lipid A epitopes. MAb 18-19 recognizes the LPS core-plus-one O-repeat unit of the serologically cross-reactive P. aeruginosa O2, O5, and O16. Group 2 MAbs are specific for the LPS outer core region and reacted with P. aeruginosa O2, O5, O7, O8, O10, O16, O18, O19, and O20, suggesting that these serotypes share a common outer core type. Group 3 MAbs recognize the inner core region and reacted with all 20 P. aeruginosa serotypes as well as with other Pseudomonas species, revealing the conserved nature of this region. Group 4 MAbs are specific for lipid A and reacted with all gram-negative organisms tested. Immunoassays using these MAbs and well-defined rough mutants, in addition to the recently determined P. aeruginosa core structures, have allowed us to precisely define immunodominant epitopes within the LPS core region.

摘要

为了研究铜绿假单胞菌脂多糖(LPS)核心脂质A区域的免疫化学性质,在小鼠体内制备了针对该区域的单克隆抗体(MAb)。通过用柱纯化的核心寡糖组分包被铜绿假单胞菌的粗糙突变体来制备免疫原,以增强对LPS核心脂质A区域的免疫反应。分离、鉴定了14个杂交瘤克隆,并根据它们在酶联免疫吸附测定和Western免疫印迹中对粗糙LPS抗原的反应性进一步分为三组。此外,本研究还纳入了另一种单克隆抗体18 - 19(指定为第1组)以确定核心脂质A表位。单克隆抗体18 - 19识别血清学交叉反应性铜绿假单胞菌O2、O5和O16的LPS核心加一个O重复单元。第2组单克隆抗体对LPS外核心区域具有特异性,并与铜绿假单胞菌O2、O5、O7、O8、O10、O16、O18、O19和O20反应,表明这些血清型共享一种常见的外核心类型。第3组单克隆抗体识别内核心区域,并与所有20种铜绿假单胞菌血清型以及其他假单胞菌属反应,揭示了该区域的保守性质。第4组单克隆抗体对脂质A具有特异性,并与所有测试的革兰氏阴性菌反应。除了最近确定的铜绿假单胞菌核心结构外,使用这些单克隆抗体和明确的粗糙突变体进行的免疫测定使我们能够精确确定LPS核心区域内的免疫显性表位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/154b/197099/7f8acd989220/jbacter00041-0016-a.jpg

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