He Xiangyun, McDaniel Larry S
Department of Microbiology, The University of Mississippi Medical Center, Jackson, MS 39216, USA.
FEMS Microbiol Lett. 2007 Apr;269(2):189-95. doi: 10.1111/j.1574-6968.2006.00516.x. Epub 2007 Mar 13.
Anti-PspA antibodies are less efficient at protecting mice against certain pneumococcal strains. Immunization with PspA from EF5668 provided better protection against WU2 (a different capsular serotype and PspA family) than against EF5668. To understand the role of the pneumococcal genetic background in anti-PspA-mediated protection, we constructed a mutant of WU2 expressing pspA from EF5668. Both passive and active immunization demonstrated that the genetic background impacted the protection mediated by anti-PspA antibodies. We localized the protection-eliciting region to the first 122 amino acid residues of the N-terminus of the alpha-helical domain of PspA/EF5668.
抗肺炎球菌表面蛋白A(PspA)抗体在保护小鼠抵御某些肺炎球菌菌株方面效率较低。用来自EF5668的PspA进行免疫,对WU2(一种不同的荚膜血清型和PspA家族)的保护作用比对EF5668的保护作用更好。为了了解肺炎球菌遗传背景在抗PspA介导的保护中的作用,我们构建了一个表达来自EF5668的pspA的WU2突变体。被动免疫和主动免疫均表明,遗传背景影响了抗PspA抗体介导的保护作用。我们将引发保护作用的区域定位到PspA/EF5668α螺旋结构域N端的前122个氨基酸残基。