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本文引用的文献

1
Molecular basis for vaccine development against the ehrlichial pathogen Anaplasma marginale.
Parasitol Today. 1999 Jul;15(7):281-6. doi: 10.1016/s0169-4758(99)01469-6.
2
Multiple p44 genes encoding major outer membrane proteins are expressed in the human granulocytic ehrlichiosis agent.编码主要外膜蛋白的多个p44基因在人粒细胞埃立克体病病原体中表达。
J Biol Chem. 1999 Jun 18;274(25):17828-36. doi: 10.1074/jbc.274.25.17828.
3
The map1 gene of Cowdria ruminantium is a member of a multigene family containing both conserved and variable genes.反刍兽考德里氏体的map1基因是一个多基因家族的成员,该家族包含保守基因和可变基因。
Biochem Biophys Res Commun. 1999 Apr 13;257(2):300-5. doi: 10.1006/bbrc.1999.0459.
4
Restriction of major surface protein 2 (MSP2) variants during tick transmission of the ehrlichia Anaplasma marginale.边缘无形体蜱传播过程中主要表面蛋白2(MSP2)变体的限制
Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):3171-6. doi: 10.1073/pnas.96.6.3171.
5
The repertoire of Anaplasma marginale antigens recognized by CD4(+) T-lymphocyte clones from protectively immunized cattle is diverse and includes major surface protein 2 (MSP-2) and MSP-3.来自经保护性免疫的牛的CD4(+) T淋巴细胞克隆所识别的边缘无浆体抗原库是多样的,包括主要表面蛋白2(MSP-2)和MSP-3。
Infect Immun. 1998 Nov;66(11):5414-22. doi: 10.1128/IAI.66.11.5414-5422.1998.
6
CD4(+) T-lymphocyte and immunoglobulin G2 responses in calves immunized with Anaplasma marginale outer membranes and protected against homologous challenge.用边缘无浆体(Anaplasma marginale)外膜免疫并对同源攻击具有抵抗力的犊牛的CD4(+) T淋巴细胞和免疫球蛋白G2反应
Infect Immun. 1998 Nov;66(11):5406-13. doi: 10.1128/IAI.66.11.5406-5413.1998.
7
Cloning and characterization of multigenes encoding the immunodominant 30-kilodalton major outer membrane proteins of Ehrlichia canis and application of the recombinant protein for serodiagnosis.犬埃立克体免疫显性30千道尔顿主要外膜蛋白多基因的克隆、特性分析及重组蛋白在血清学诊断中的应用
J Clin Microbiol. 1998 Sep;36(9):2671-80. doi: 10.1128/JCM.36.9.2671-2680.1998.
8
Major antigenic proteins of the agent of human granulocytic ehrlichiosis are encoded by members of a multigene family.人粒细胞埃立克体病病原体的主要抗原蛋白由一个多基因家族的成员编码。
Infect Immun. 1998 Aug;66(8):3711-8. doi: 10.1128/IAI.66.8.3711-3718.1998.
9
Molecular characterization of a 28 kDa surface antigen gene family of the tribe Ehrlichiae.埃立克体族28 kDa表面抗原基因家族的分子特征分析
Biochem Biophys Res Commun. 1998 Jun 29;247(3):636-43. doi: 10.1006/bbrc.1998.8844.
10
Cloning of the gene encoding the 44-kilodalton antigen of the agent of human granulocytic ehrlichiosis and characterization of the humoral response.人粒细胞埃立克体病病原体44千道尔顿抗原编码基因的克隆及体液免疫反应特征分析
Infect Immun. 1998 Jul;66(7):3264-9. doi: 10.1128/IAI.66.7.3264-3269.1998.

在持续性立克次体血症期间边缘无形体抗原变异体的出现。

Emergence of Anaplasma marginale antigenic variants during persistent rickettsemia.

作者信息

French D M, Brown W C, Palmer G H

机构信息

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

出版信息

Infect Immun. 1999 Nov;67(11):5834-40. doi: 10.1128/IAI.67.11.5834-5840.1999.

DOI:10.1128/IAI.67.11.5834-5840.1999
PMID:10531237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC96963/
Abstract

Anaplasma marginale is an ehrlichial pathogen of cattle, in the order Rickettsiales, that establishes persistent cyclic rickettsemia in the infected host. Within each rickettsemic cycle, A. marginale expressing antigenically variant major surface protein 2 (MSP2) emerge. By cloning 17 full-length msp2 transcripts expressed during cyclic rickettsemia, we determined that emergent variants have a single, central hypervariable region encoding variant B-cell epitopes. The N- and C-terminal regions are highly conserved among the expressed A. marginale variants, and similar sequences define the MSP2 homologues in the agent of human granulocytic ehrlichiosis (HGE). This is in contrast to the MSP2 homologues in ehrlichial genogroup I pathogens, Ehrlichia chaffeensis, Ehrlichia canis, and Cowdria ruminantium, that have multiple hypervariable regions. By defining the variable and conserved regions, we were able to show that the single hypervariable region of A. marginale MSP2 encodes epitopes that are immunogenic and induce variant-specific antibody responses during persistent infection. These findings demonstrate that the MSP2 structural variants that emerge during each cycle of persistent rickettsemia are true antigenic variants, consistent with MSP2 antigenic variation as a mechanism of A. marginale persistence.

摘要

边缘无形体是立克次氏体目下一种牛的埃立克体病原体,可在受感染宿主体内建立持续性循环立克次体血症。在每个立克次体血症循环中,都会出现表达抗原性可变主要表面蛋白2(MSP2)的边缘无形体。通过克隆在循环立克次体血症期间表达的17个全长msp2转录本,我们确定新出现的变体具有一个单一的中央高变区,该区域编码可变B细胞表位。N端和C端区域在表达的边缘无形体变体中高度保守,类似序列定义了人类粒细胞埃立克体病(HGE)病原体中的MSP2同源物。这与埃立克体基因组I病原体(查菲埃立克体、犬埃立克体和反刍兽考德里氏体)中的MSP2同源物形成对比,后者具有多个高变区。通过定义可变区和保守区,我们能够证明边缘无形体MSP2的单个高变区编码在持续性感染期间具有免疫原性并诱导变体特异性抗体反应的表位。这些发现表明,在持续性立克次体血症的每个循环中出现的MSP2结构变体是真正的抗原变体,这与MSP2抗原变异作为边缘无形体持续存在的一种机制相一致。