Medical Scientist Training Program, School of Medicine, University of Washington, Seattle, Washington, USA.
Molecular and Cellular Biology, School of Medicine, University of Washington, Seattle, Washington, USA.
Infect Immun. 2021 Feb 16;89(3). doi: 10.1128/IAI.00060-20.
Bacterial vaginosis (BV) is a vaginal dysbiotic condition linked to negative gynecological and reproductive sequelae. Flagellated bacteria have been identified in women with BV, including spp. and BV-associated bacterium-1 (BVAB1), an uncultivated, putatively flagellated species. The host response to flagellin mediated through Toll-like receptor 5 (TLR5) has not been explored in BV. Using independent discovery and validation cohorts, we examined the hypothesis that TLR5 deficiency-defined by a dominant negative stop codon polymorphism, rs5744168-is associated with an increased risk for BV and increased colonization with flagellated bacteria associated with BV (BVAB1, , and ). TLR5 deficiency was not associated with BV status, and TLR5-deficient women had decreased colonization with BVAB1 in both cohorts. We stimulated HEK-hTLR5-overexpressing NF-κB reporter cells with whole, heat-killed or and with partially purified flagellin from these species; as BVAB1 is uncultivated, we used cervicovaginal lavage (CVL) fluid supernatant from women colonized with BVAB1 for stimulation. While heat-killed and CVL fluid from women colonized with BVAB1 stimulate a TLR5-mediated response, heat-killed did not. In contrast, partially purified flagellin from both species stimulated a TLR5-mediated response We observed no correlation between vaginal interleukin 8 (IL-8) and flagellated BVAB concentrations among TLR5-sufficient women. Interspecies variation in accessibility of flagellin recognition domains may be responsible for these observations, as reflected in the potentially novel flagellin products encoded by species versus those encoded by BVAB1.
细菌性阴道病 (BV) 是一种与负面妇科和生殖后遗症相关的阴道生态失调状况。BV 患者中已鉴定出鞭毛菌,包括 spp. 和 BV 相关细菌-1 (BVAB1),一种未培养的、推测的鞭毛菌。宿主对鞭毛蛋白的反应尚未在 BV 中通过 Toll 样受体 5 (TLR5) 进行探索。使用独立的发现和验证队列,我们检验了以下假设:TLR5 缺陷 - 由显性负性终止密码子多态性 rs5744168 定义 - 与 BV 风险增加以及与 BV 相关的鞭毛菌(BVAB1、、和 )定植增加相关。TLR5 缺陷与 BV 状态无关,并且在两个队列中 TLR5 缺陷女性的 BVAB1 定植减少。我们用完整的、热灭活的 或 以及来自这些物种的部分纯化鞭毛蛋白刺激 HEK-hTLR5 过表达 NF-κB 报告细胞;由于 BVAB1 未培养,我们使用来自 BVAB1 定植的女性的宫颈阴道灌洗液 (CVL) 上清液进行刺激。虽然热灭活的 和 BVAB1 定植女性的 CVL 液刺激 TLR5 介导的反应,但热灭活的 不能。相比之下,来自两种 物种的部分纯化鞭毛蛋白均刺激 TLR5 介导的反应。我们在 TLR5 充足的女性中未观察到阴道白细胞介素 8 (IL-8) 与鞭毛 BVAB 浓度之间的相关性。鞭毛蛋白识别结构域的可及性的种间差异可能导致这些观察结果,这反映在 物种编码的潜在新型鞭毛蛋白产物与 BVAB1 编码的产物不同。