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伯氏疏螺旋体动物媒介循环中寡肽转运蛋白的宿主特异性功能区隔化。

Host-specific functional compartmentalization within the oligopeptide transporter during the Borrelia burgdorferi enzootic cycle.

机构信息

Department of Medicine, UConn Health, Farmington, Connecticut, United States of America.

Department of Pediatrics, UConn Health, Farmington, Connecticut, United States of America.

出版信息

PLoS Pathog. 2021 Jan 11;17(1):e1009180. doi: 10.1371/journal.ppat.1009180. eCollection 2021 Jan.

Abstract

Borrelia burgdorferi must acquire all of its amino acids (AAs) from its arthropod vector and vertebrate host. Previously, we determined that peptide uptake via the oligopeptide (Opp) ABC transporter is essential for spirochete viability in vitro and during infection. Our prior study also suggested that B. burgdorferi employs temporal regulation in concert with structural variation of oligopeptide-binding proteins (OppAs) to meet its AA requirements in each biological niche. Herein, we evaluated the contributions to the B. burgdorferi enzootic cycle of three of the spirochete's five OppAs (OppA1, OppA2, and OppA5). An oppA1 transposon (tn) mutant lysed in the hyperosmolar environment of the feeding tick, suggesting that OppA1 imports amino acids required for osmoprotection. The oppA2tn mutant displayed a profound defect in hematogenous dissemination in mice, yet persisted within skin while inducing only a minimal antibody response. These results, along with slightly decreased growth of the oppA2tn mutant within DMCs, suggest that OppA2 serves a minor nutritive role, while its dissemination defect points to an as yet uncharacterized signaling function. Previously, we identified a role for OppA5 in spirochete persistence within the mammalian host. We now show that the oppA5tn mutant displayed no defect during the tick phase of the cycle and could be tick-transmitted to naïve mice. Instead of working in tandem, however, OppA2 and OppA5 appear to function in a hierarchical manner; the ability of OppA5 to promote persistence relies upon the ability of OppA2 to facilitate dissemination. Structural homology models demonstrated variations within the binding pockets of OppA1, 2, and 5 indicative of different peptide repertoires. Rather than being redundant, B. burgdorferi's multiplicity of Opp binding proteins enables host-specific functional compartmentalization during the spirochete lifecycle.

摘要

伯氏疏螺旋体必须从其节肢动物载体和脊椎动物宿主中获取所有的氨基酸 (AAs)。此前,我们确定通过寡肽 (Opp) ABC 转运体摄取肽对于螺旋体在体外和感染期间的生存能力至关重要。我们之前的研究还表明,伯氏疏螺旋体采用时间调节与寡肽结合蛋白 (OppAs) 的结构变化相结合,以满足其在每个生物小生境中的 AA 需求。在此,我们评估了螺旋体的五个 OppA 中的三个(OppA1、OppA2 和 OppA5)对伯氏疏螺旋体的生态循环的贡献。OppA1 转座子 (tn) 突变体在取食蜱的高渗环境中裂解,表明 OppA1 输入了对渗透压保护所必需的氨基酸。OppA2tn 突变体在小鼠血源传播中表现出严重缺陷,但在皮肤内持续存在,同时仅诱导最小的抗体反应。这些结果,以及 OppA2tn 突变体在 DMC 中生长略有下降,表明 OppA2 起次要营养作用,而其传播缺陷指向尚未表征的信号功能。此前,我们确定了 OppA5 在螺旋体在哺乳动物宿主中的持续存在中的作用。我们现在表明,OppA5tn 突变体在循环的蜱阶段没有缺陷,并且可以通过蜱传播给未感染的小鼠。然而,OppA2 和 OppA5 似乎不是协同作用,而是以层次方式起作用;OppA5 促进持久性的能力依赖于 OppA2 促进传播的能力。结构同源模型显示,OppA1、2 和 5 的结合口袋内存在差异,表明肽库不同。伯氏疏螺旋体的多种 Opp 结合蛋白不是冗余的,而是在螺旋体生命周期中实现宿主特异性功能分区。

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