Center for Global Infectious Disease Research, Seattle Children's Research Institute, Washington.
Department of Global Health, University of Washington, Seattle.
J Infect Dis. 2018 Apr 23;217(10):1626-1636. doi: 10.1093/infdis/jiy076.
Preterm birth is a leading cause of neonatal mortality and lacks an effective therapy. Ascending microbial infections from the lower genital tract lead to infection of the placenta, amniotic fluid, and fetus causing preterm birth or stillbirth. Directly in the path of an ascending infection is the cervical mucus plug (CMP), a dense mucoid structure in the cervical canal with potential antimicrobial properties. In this study, we aimed to define the components of CMP responsible for antimicrobial activity against a common lower genital tract organism associated with preterm birth and stillbirths, namely, group B streptococcus (GBS). Using a quantitative proteomic approach, we identified antimicrobial factors in CMPs that were collected from healthy human pregnancies. However, we noted that the concentration of antimicrobial peptides present in the human CMPs were insufficient to directly kill GBS, and antimicrobial activity, when observed, was due to antibiotics retained in the CMPs. Despite this insufficiency, CMP proteins were able to activate leukocytes in whole blood resulting in increased rates of bacterial killing, suggesting a role for the CMP in enhancing complement-mediated killing or leukocyte activation. This study provides new insight into how the human CMP may limit ascending bacterial infection.
早产是新生儿死亡的主要原因,目前缺乏有效的治疗方法。下生殖道的微生物上行感染会导致胎盘、羊水和胎儿感染,从而引发早产或死产。宫颈黏液栓(CMP)直接处于上行感染的路径中,它是宫颈管中一种具有潜在抗菌特性的致密黏液结构。在这项研究中,我们旨在确定 CMP 中负责针对与早产和死产相关的常见下生殖道病原体——B 族链球菌(GBS)产生抗菌活性的成分。我们使用定量蛋白质组学方法鉴定了从健康妊娠女性中收集的 CMP 中的抗菌因子。然而,我们注意到存在于人类 CMP 中的抗菌肽浓度不足以直接杀死 GBS,并且观察到的抗菌活性是由于 CMP 中保留的抗生素所致。尽管存在这种不足,但 CMP 蛋白能够激活全血中的白细胞,导致细菌杀伤率增加,这表明 CMP 在增强补体介导的杀伤或白细胞激活方面发挥作用。这项研究为人类 CMP 如何限制细菌上行感染提供了新的见解。