Department of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN, United States.
Front Cell Infect Microbiol. 2020 Oct 15;10:585791. doi: 10.3389/fcimb.2020.585791. eCollection 2020.
Highly successful invasive pathogens exploit host vulnerabilities by adapting tools to co-opt highly conserved host features. This is especially true when pathogens develop ligands to hijack trafficking routes or signaling patterns of host receptors. In this context, highly successful pathogens can be grouped together by the patterns of organs infected and diseases they cause. In the case of this perspective, the focus is on the historically most successful invasive bacterial pathogens of children that cause pneumonia, sepsis and meningitis: , and . This triad shares a ligand to bind to PAF receptor to enter host cells despite early defenses by innate immunity. All three also target laminin receptor to cross endothelial barriers using a common set of molecular tools that may prove to be a design for a cross-protective vaccine.
高度成功的侵袭性病原体通过适应工具来利用宿主的弱点,从而篡夺宿主高度保守的特征。当病原体开发配体来劫持宿主受体的运输途径或信号模式时,尤其如此。在这种情况下,可以根据感染的器官和引起的疾病将高度成功的病原体分组。在这种情况下,重点是引起肺炎、败血症和脑膜炎的历史上最成功的侵袭性儿童细菌病原体: 、 和 。尽管先天免疫存在早期防御,但三联体都有一个配体与 PAF 受体结合以进入宿主细胞。这三种病原体也都以层粘连蛋白受体为靶点,使用一组共同的分子工具穿过内皮屏障,这些分子工具可能被证明是交叉保护性疫苗的设计。