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Differential contribution of Yersinia enterocolitica virulence factors to evasion of microbicidal action of neutrophils.

机译:耶尔森氏小肠结肠炎耶尔森氏菌毒力因子对中性粒细胞杀微生物作用的回避的不同贡献。

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摘要

The differential contribution of the virulence factors invasin, protein tyrosine phosphatase (YopH), cytotoxin (YopE), and adhesin (YadA) of Yersinia enterocolitica to evasion of the antibacterial activities of polymorphonuclear leukocytes (PMNs) (oxidative burst, phagocytosis, killing) was analyzed. We constructed virulence gene knockout mutants and a novel two-plasmid system allowing production and secretion of individual virulence factors. Wild-type Y. enterocolitica WA-314 harboring the virulence plasmid pYV08 resisted phagocytosis and killing by PMNs. Moreover, strain WA-314 was able to inhibit the neutrophil oxidative burst upon stimulation with opsonized zymosan independently on preincubation with normal human serum or YadA-specific serum. These phenotypic properties of strain WA-314 were differentially affected when mutants impaired in YadA production or Yop secretion were used. A more detailed analysis revealed that YopH plays the dominant role in suppression of the antibacterial action of PMNs without damaging the cells. The YopH suppressing effect could be enhanced by coproduction of YopE and YadA. The contribution of YadA is attributed to the adhesin function promoting interaction with PMNs under both opsonizing and nonopsonizing conditions. In contrast, invasin seems to mediate only opsonin-independent interaction with PMNs. Taken together, our results demonstrate that YopH, YopE, and YadA act in concert towards neutrophil attack to enable extracellular survival of Y. enterocolitica in host tissue.
机译:小肠结肠炎耶尔森氏菌毒力因子入侵素,蛋白酪氨酸磷酸酶(YopH),细胞毒素(YopE)和黏附素(YadA)对逃避多形核白细胞(PMNs)抗菌活性(氧化爆发,吞噬作用,杀伤力)的不同贡献。分析。我们构建了毒力基因敲除突变体和一个新型的两质粒系统,允许生产和分泌单个毒力因子。携带毒性质粒pYV08的野生型小肠结肠炎耶尔森氏菌WA-314抵抗吞噬作用并被PMN杀死。此外,菌株WA-314能够在用调理化酵母聚糖刺激后独立于与正常人血清或YadA特异性血清进行预温育而抑制中性粒细胞的氧化爆发。当使用YadA产量或Yop分泌受损的突变体时,WA-314菌株的这些表型特性受到不同的影响。更详细的分析表明,YopH在抑制PMN的抗菌作用而不损害细胞的过程中起着主导作用。 YopE和YadA的联合生产可以增强YopH抑制作用。 YadA的贡献归因于在调理和非调理条件下促进与PMN相互作用的粘附素功能。相反,入侵素似乎仅介导与调理素无关的调理素相互作用。两者合计,我们的结果表明,YopH,YopE和YadA协同作用于嗜中性粒细胞攻击,从而使宿主结肠炎耶尔森氏菌在细胞外存活。

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