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首页> 外文期刊>Microbial Pathogenesis >The effects of differences in pspA alleles and capsular types on the resistance of Streptococcus pneumoniae to killing by apolactoferrin
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The effects of differences in pspA alleles and capsular types on the resistance of Streptococcus pneumoniae to killing by apolactoferrin

机译:pspA等位基因和荚膜类型的差异对肺炎链球菌对无铁铁蛋白杀伤的抗性的影响

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Pneumococcal surface protein A (PspA) is the only pneumococcal surface protein known to strongly bind lactoferrin on the bacterial surface. In the absence of PspA Streptococcus pneumoniae becomes more susceptible to killing by human apolactoferrin (apo-hLf), the iron-free form of lactoferrin. In the present study we examined diverse strains of S. pneumoniae that differed by 2 logs in their susceptibility to apo-hLf. Among these strains, the amount of apo-hLf that bound to cell surface PspA correlated directly with the resistance of the strain to killing by apo-hLf. Moreover examination of different pspA alleles on shared genetic backgrounds revealed that those PspAs that bound more lactoferrin conferred greater resistance to killing by apo-hLf. The effects of capsule on killing of pneumococci by apo-hLf were generally small, but on one genetic background, however, the lack of capsule was associated with 4-times as much apo-hLf binding and 30-times more resistance to killing by apo-hLf. Overall these finding strongly support the hypothesis that most of the variation in the ability of apo-hLf is dependent on the variation in the binding of apo-hLf to surface PspA and this binding is dependent on variation in PspA as well as variation in capsule which may enhance killing by reducing the binding of apo-hLf to PspA. Published by Elsevier Ltd.
机译:肺炎球菌表面蛋白A(PspA)是已知的唯一能在细菌表面牢固结合乳铁蛋白的肺炎球菌表面蛋白。在缺乏PspA的情况下,肺炎链球菌变得更容易被人无铁乳铁蛋白(apo-hLf)杀死。在本研究中,我们检查了多种肺炎链球菌菌株,它们对apo-hLf的敏感性相差2个对数。在这些菌株中,结合至细胞表面PspA的apo-hLf的量与该菌株对apo-hLf杀死的抗性直接相关。此外,在共有的遗传背景下检查不同的pspA等位基因发现,那些结合更多乳铁蛋白的PspA赋予了更大的抗apo-hLf杀伤力的能力。胶囊对apo-hLf杀灭肺炎球菌的作用通常很小,但是在一种遗传背景下,缺乏胶囊与apo-hLf结合力高4倍,抗apo-hLf杀伤力高30倍-hLf。总体而言,这些发现强有力地支持了以下假设:载脂蛋白-hLf能力的大多数变化取决于载脂蛋白-hLf与表面PspA结合的变化,并且这种结合取决于PspA的变化以及胶囊的变化。可能通过减少apo-hLf与PspA的结合来增强杀伤力。由Elsevier Ltd.发布

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