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本文引用的文献

1
The structural biology of type IV secretion systems.IV型分泌系统的结构生物学
Nat Rev Microbiol. 2009 Oct;7(10):703-14. doi: 10.1038/nrmicro2218.
2
An anomalous type IV secretion system in Rickettsia is evolutionarily conserved.立克次氏体中一种异常的IV型分泌系统在进化上是保守的。
PLoS One. 2009;4(3):e4833. doi: 10.1371/journal.pone.0004833. Epub 2009 Mar 12.
3
Structure of a type IV secretion system core complex.IV型分泌系统核心复合物的结构
Science. 2009 Jan 9;323(5911):266-8. doi: 10.1126/science.1166101.
4
Agrobacterium VirB10 domain requirements for type IV secretion and T pilus biogenesis.农杆菌VirB10在IV型分泌和T菌毛生物合成中的结构域要求。
Mol Microbiol. 2009 Feb;71(3):779-94. doi: 10.1111/j.1365-2958.2008.06565.x. Epub 2008 Dec 1.
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Whole genome transcription profiling of Anaplasma phagocytophilum in human and tick host cells by tiling array analysis.通过平铺阵列分析对嗜吞噬细胞无形体在人类和蜱宿主细胞中的全基因组转录谱进行分析。
BMC Genomics. 2008 Jul 31;9:364. doi: 10.1186/1471-2164-9-364.
6
Cloning, sequencing and antigenic characterization of rVirB9 of Anaplasma marginale isolated from Paraná State, Brazil.从巴西巴拉那州分离出的边缘无形体rVirB9的克隆、测序及抗原特性分析
Genet Mol Res. 2008;7(2):460-6. doi: 10.4238/vol7-2gmr416.
7
VirB3 to VirB6 and VirB8 to VirB11, but not VirB7, are essential for mediating persistence of Brucella in the reticuloendothelial system.VirB3至VirB6以及VirB8至VirB11(而非VirB7)对于介导布鲁氏菌在网状内皮系统中的持续存在至关重要。
J Bacteriol. 2008 Jul;190(13):4427-36. doi: 10.1128/JB.00406-08. Epub 2008 May 9.
8
IgG and IgG2 antibodies from cattle naturally infected with Anaplasma marginale recognize the recombinant vaccine candidate antigens VirB9, VirB10, and elongation factor-Tu.来自自然感染边缘无形体的牛的IgG和IgG2抗体识别重组疫苗候选抗原VirB9、VirB10和延伸因子-Tu。
Mem Inst Oswaldo Cruz. 2008 Mar;103(2):186-90. doi: 10.1590/s0074-02762008000200010.
9
Composition of the surface proteome of Anaplasma marginale and its role in protective immunity induced by outer membrane immunization.边缘无形体表面蛋白质组的组成及其在外膜免疫诱导的保护性免疫中的作用。
Infect Immun. 2008 May;76(5):2219-26. doi: 10.1128/IAI.00008-08. Epub 2008 Mar 3.
10
High-throughput identification of T-lymphocyte antigens from Anaplasma marginale expressed using in vitro transcription and translation.利用体外转录和翻译对边缘无形体表达的T淋巴细胞抗原进行高通量鉴定。
J Immunol Methods. 2008 Mar 20;332(1-2):129-41. doi: 10.1016/j.jim.2007.12.018. Epub 2008 Jan 28.

边缘无浆体 IV 型分泌系统蛋白 VirB2、VirB7、VirB11 和 VirD4 是保护性细菌膜疫苗的免疫原性成分。

Anaplasma marginale type IV secretion system proteins VirB2, VirB7, VirB11, and VirD4 are immunogenic components of a protective bacterial membrane vaccine.

机构信息

Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164-7040, USA.

出版信息

Infect Immun. 2010 Mar;78(3):1314-25. doi: 10.1128/IAI.01207-09. Epub 2010 Jan 11.

DOI:10.1128/IAI.01207-09
PMID:20065028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2825951/
Abstract

Anaplasma and related Ehrlichia spp. are important tick-borne, Gram-negative bacterial pathogens of livestock and humans that cause acute infection and disease and can persist. Immunization of cattle with an Anaplasma marginale fraction enriched in outer membranes (OM) can provide complete protection against disease and persistent infection. Serological responses of OM vaccinees to the OM proteome previously identified over 20 antigenic proteins, including three type IV secretion system (T4SS) proteins, VirB9-1, VirB9-2, and VirB10. Subsequent studies showed that these three proteins also stimulated CD4(+) T-cell responses in OM vaccinees. The T4SS, composed of a complex of proteins spanning the inner and outer membranes of certain bacteria, is an important virulence factor but is relatively unexplored as a vaccine target. The goal of this study was to determine if additional T4SS proteins are immunogenic for animals immunized with the protective OM fraction of A. marginale. T4SS proteins expressed by in vitro transcription and translation were screened for stimulating proliferation of T cells from OM vaccinees, and immunogenic proteins were expressed as recombinant proteins in Escherichia coli and their immunogenicity was verified. VirB2, a putative VirB7, VirB11, and VirD4 were immunogenic for OM vaccinees expressing several common major histocompatibility complex (MHC) class II haplotypes. VirB2 is encoded by multiple genes that share a conserved central region, and epitope mapping revealed T-cell epitopes in this region. The discovery of novel immunogenic T4SS proteins recognized by outbred individuals with common MHC haplotypes further justifies evaluating the T4SS as a potential vaccine candidate for pathogenic bacteria.

摘要

无形体属和相关埃立克体属是重要的蜱传革兰氏阴性细菌病原体,可感染家畜和人类,引起急性感染和疾病,并能持续存在。用富含外膜(OM)的边缘无形体(Anaplasma marginale)片段对牛进行免疫接种,可以提供针对疾病和持续性感染的完全保护。OM 疫苗接种者对 OM 蛋白质组的血清学反应以前已经确定了超过 20 种抗原蛋白,包括三种 IV 型分泌系统(T4SS)蛋白,VirB9-1、VirB9-2 和 VirB10。随后的研究表明,这三种蛋白也刺激了 OM 疫苗接种者的 CD4(+)T 细胞反应。T4SS 由一组跨越某些细菌的内膜和外膜的蛋白质组成,是一种重要的毒力因子,但作为疫苗靶点相对未被探索。本研究的目的是确定是否有其他 T4SS 蛋白对用边缘无形体(A. marginale)的保护性 OM 部分免疫的动物具有免疫原性。通过体外转录和翻译表达的 T4SS 蛋白被筛选用于刺激 OM 疫苗接种者的 T 细胞增殖,并且免疫原性蛋白在大肠杆菌中作为重组蛋白表达,并验证了其免疫原性。VirB2、一种假定的 VirB7、VirB11 和 VirD4 对表达几种常见主要组织相容性复合体(MHC)II 类单倍型的 OM 疫苗接种者具有免疫原性。VirB2 由多个基因编码,这些基因共享一个保守的中心区域,并且表位作图显示该区域存在 T 细胞表位。在具有常见 MHC 单倍型的杂种个体中发现的新型免疫原性 T4SS 蛋白进一步证明了将 T4SS 作为潜在的疫苗候选物用于致病性细菌的合理性。