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外膜而非宿主蛋白包被限制了毒力梅毒螺旋体的抗原性。

The outer membrane, not a coat of host proteins, limits antigenicity of virulent Treponema pallidum.

作者信息

Cox D L, Chang P, McDowall A W, Radolf J D

机构信息

Treponema Immunobiology Section, National Center for Infectious Diseases, Centers for Disease Control, Atlanta, Georgia 30333.

出版信息

Infect Immun. 1992 Mar;60(3):1076-83. doi: 10.1128/iai.60.3.1076-1083.1992.

DOI:10.1128/iai.60.3.1076-1083.1992
PMID:1541522
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC257596/
Abstract

Virulent Treponema pallidum reacts poorly with the specific antibodies present in human and rabbit syphilitic sera, a phenomenon often attributed to an outer coat of host serum proteins. Here we present additional evidence that the limited antigenicity of virulent organisms actually is due to a paucity of proteins in the outer membrane. Initially, we used electron microscopy to demonstrate that the outer membrane is highly susceptible to damage from physical manipulation (i.e., centrifugation and resuspension) and nonionic detergents. Organisms with disrupted outer membranes were markedly more antigenic than intact treponemes as determined by immunoelectron microscopy (IEM) with rabbit syphilitic and antiendoflagellar antisera. Data obtained with a new radioimmunoassay, designated the T. pallidum surface-specific radioimmunoassay, corroborated these IEM findings by demonstrating that the major T. pallidum immunogens are not surface exposed; the assay also was unable to detect serum proteins, including fibronectin, on the surfaces of intact organisms. Furthermore, IEM of T. pallidum on ultrathin cryosections with monospecific anti-47-kDa-immunogen antiserum confirmed the intracellular location of the 47-kDa immunogen. On the basis of these and previous findings, we proposed a new model for T. pallidum ultrastructure in which the outer membrane contains a small number of transmembrane proteins and the major membrane immunogens are anchored by lipids to the periplasmic leaflet of the cytoplasmic membrane. This unique ultrastructure explains the remarkable ability of virulent organisms to evade the humoral immune response of the T. pallidum-infected host.

摘要

毒力强的梅毒螺旋体与人类和兔梅毒血清中存在的特异性抗体反应较弱,这一现象通常归因于宿主血清蛋白的外层包膜。在此,我们提供了额外的证据,表明毒力强的生物体有限的抗原性实际上是由于外膜中蛋白质的缺乏。最初,我们使用电子显微镜证明外膜极易受到物理操作(即离心和重悬)和非离子去污剂的损伤。通过用兔梅毒血清和抗内鞭毛抗血清进行免疫电子显微镜(IEM)检测,发现外膜受损的生物体比完整的螺旋体具有明显更强的抗原性。用一种新的放射免疫测定法,即梅毒螺旋体表面特异性放射免疫测定法获得的数据,通过证明梅毒螺旋体的主要免疫原不暴露于表面,证实了这些IEM结果;该测定法也无法检测完整生物体表面的血清蛋白,包括纤连蛋白。此外,用单特异性抗47-kDa免疫原抗血清对超薄冷冻切片上的梅毒螺旋体进行IEM,证实了47-kDa免疫原的细胞内定位。基于这些及先前的发现,我们提出了一种梅毒螺旋体超微结构的新模型,其中外膜含有少量跨膜蛋白,主要膜免疫原通过脂质锚定在细胞质膜的周质小叶上。这种独特的超微结构解释了毒力强的生物体逃避梅毒螺旋体感染宿主体液免疫反应的显著能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/ffd7edf6ce4e/iai00027-0372-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/66e292c6aca3/iai00027-0371-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/96e65b86c1f8/iai00027-0371-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/30f6bf299e68/iai00027-0372-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/ffd7edf6ce4e/iai00027-0372-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/66e292c6aca3/iai00027-0371-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/96e65b86c1f8/iai00027-0371-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/30f6bf299e68/iai00027-0372-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2433/257596/ffd7edf6ce4e/iai00027-0372-b.jpg

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