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克氏锥虫无鞭毛体表面蛋白2的免疫相关菌株多态性

Immunologically relevant strain polymorphism in the Amastigote Surface Protein 2 of Trypanosoma cruzi.

作者信息

Claser Carla, Espíndola Noeli Maria, Sasso Gisela, Vaz Adelaide José, Boscardin Silvia B, Rodrigues Mauricio M

机构信息

Centro Interdisciplinar de Terapia Gênica (CINTERGEN), Universidade Federal de São Paulo-Escola Paulista de Medicina, Rua Mirassol, 207, São Paulo-SP 04044-010, Brazil.

出版信息

Microbes Infect. 2007 Jul;9(8):1011-9. doi: 10.1016/j.micinf.2007.04.006. Epub 2007 Apr 19.

Abstract

Several evidences suggest that the Amastigote Surface Protein-2 (ASP-2) of Trypanosoma cruzi is an important target for immunity during infection. Based on this, we considered it important to evaluate its strain polymorphism. Initially, we observed the presence of conserved cross-reactive epitopes in amastigotes of all parasite strains tested. In addition, the predicted amino acid sequences of the genes isolated from the cDNA of amastigotes of CL-Brener, Tulahuen, Colombian and G strains displayed a high degree of identity (>80%) to the previously described genes of ASP-2. Unexpectedly, Sylvio X10/4 and G strains expressed a new isoform of ASP-2 with limited identity to the previously described genes, but with a high degree of identity when compared to each other. Immunological studies confirmed the presence of cross-reactive epitopes between recombinant proteins representing the different isoforms of ASP-2. However, the genetic vaccination of mice with the new isoform of asp-2 gene expressed by the G strain failed to provide the same degree of protective immunity to a challenge by parasites of the Y strain as did asp-2 genes of Y or CL-Brener strains. In summary, we found that few strains can express different isoforms of ASP-2 which may not share cross-protective epitopes.

摘要

多项证据表明,克氏锥虫的无鞭毛体表面蛋白2(ASP-2)是感染期间免疫的重要靶点。基于此,我们认为评估其菌株多态性很重要。最初,我们在所有测试的寄生虫菌株的无鞭毛体中观察到保守的交叉反应性表位的存在。此外,从CL-Brener、Tulahuen、哥伦比亚和G菌株的无鞭毛体cDNA中分离的基因的预测氨基酸序列与先前描述的ASP-2基因显示出高度同一性(>80%)。出乎意料的是,Sylvio X10/4和G菌株表达了一种新的ASP-2同工型,与先前描述的基因同一性有限,但相互比较时具有高度同一性。免疫学研究证实了代表ASP-2不同同工型的重组蛋白之间存在交叉反应性表位。然而,用G菌株表达的asp-2基因新同工型对小鼠进行基因疫苗接种,未能像Y或CL-Brener菌株的asp-2基因那样,为抵抗Y菌株寄生虫的攻击提供相同程度的保护性免疫。总之,我们发现很少有菌株能表达可能不共享交叉保护表位的不同ASP-2同工型。

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