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假定的脑膜炎球菌疫苗抗原中存在正向达尔文选择的证据。

Evidence of positive Darwinian selection in putative meningococcal vaccine antigens.

作者信息

Fitzpatrick David A, Creevey Christopher J, McInerney James O

机构信息

Department of Biology, National University of Ireland, Maynooth, Co. Kildare, Ireland.

出版信息

J Mol Evol. 2005 Jul;61(1):90-8. doi: 10.1007/s00239-004-0290-6. Epub 2005 Jun 29.

Abstract

Meningococcal meningitidis is a life-threatening disease. In Europe and the United States the majority of cases are caused by virulent meningococcal strains belonging to serogroup B. Presently there is no effective vaccine against serogroup B strains, as traditional vaccine antigens such as polysaccharide capsules are unusable as they lead to autoimmunity. The year 2000 saw the publication of the complete genome of Neisseria meningitidis MC58, a virulent serogroup B bacterium. Working in conjunction with the sequencing project, researchers endeavored to locate highly conserved membrane-associated proteins that elicit an immune response. It is hoped that these proteins will provide a basis for novel vaccines against serogroup B strains. A number of potential vaccine antigens have been located and are presently in phase I clinical trials. Recently many reports pertaining to the evidence of positive Darwinian selection in membrane proteins of pathogens have been reported. This study utilized in silico methods to test for evidence of historical positive Darwinian selection in seven such vaccine candidates. We found that two of these proteins show signatures of adaptive evolution, while the remaining proteins show evidence of strong purifying selection. This has significant implications for the design of a vaccine against serogroup B strains, as it has been shown that vaccines that target epitopes that are under strong purifying selection are better than those that target variable epitopes.

摘要

脑膜炎奈瑟菌是一种危及生命的疾病。在欧洲和美国,大多数病例是由属于B血清群的强毒脑膜炎奈瑟菌菌株引起的。目前尚无针对B血清群菌株的有效疫苗,因为传统的疫苗抗原如多糖荚膜不可用,因为它们会导致自身免疫。2000年,强毒B血清群细菌脑膜炎奈瑟菌MC58的全基因组被公布。与测序项目合作,研究人员努力寻找能引发免疫反应的高度保守的膜相关蛋白。人们希望这些蛋白将为针对B血清群菌株的新型疫苗提供基础。一些潜在的疫苗抗原已被找到,目前正处于I期临床试验阶段。最近,有许多关于病原体膜蛋白中正向达尔文选择证据的报道。本研究利用计算机方法来测试七种此类候选疫苗中历史正向达尔文选择的证据。我们发现其中两种蛋白显示出适应性进化的特征,而其余蛋白则显示出强烈纯化选择的证据。这对针对B血清群菌株的疫苗设计具有重要意义,因为已表明针对处于强烈纯化选择下的表位的疫苗比针对可变表位的疫苗更好。

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