Department of Medicine, Section of Infectious Diseases, Louisiana State University Health Sciences Center, New Orleans, Louisiana, USA.
Infect Immun. 2012 Nov;80(11):3842-9. doi: 10.1128/IAI.00819-12. Epub 2012 Aug 20.
Infection with Mycoplasma genitalium has been associated with male and female urogenital disease syndromes, including urethritis, cervicitis, pelvic inflammatory disease (PID), and tubal factor infertility. Basic investigations of mucosal cytotoxicity, microbial persistence, and host immune responses are imperative to understanding these inflammatory urogenital syndromes, particularly in females, considering the potential severity of upper tract infections. Here, we report that M. genitalium can establish long-term infection of human endocervical epithelial cells that results in chronic inflammatory cytokine secretion and increased responsiveness to secondary Toll-like receptor (TLR) stimulation. Using a novel quantitative PCR assay, M. genitalium was shown to replicate from 0 to 80 days postinoculation (p.i.), during which at most time points the median ratio of M. genitalium organisms to host cells was ≤10, indicating that low organism burdens are capable of eliciting chronic inflammation in endocervical epithelial cells. This observation is consistent with clinical findings in women. Persistently secreted cytokines predominately consisted of potent chemotactic and/or activating factors for phagocytes, including interleukin-8 (IL-8), monocyte chemotactic protein 1 (MCP-1), and macrophage inflammatory protein 1β (MIP-1β). Despite persistent cytokine elaboration, no host cell cytotoxicity was observed except with superphysiologic loads of M. genitalium, suggesting that persistent infection occurs with minimal direct damage to the epithelium. However, it is hypothesized that chronic chemokine secretion with leukocyte trafficking to the epithelium could lead to significant inflammatory sequelae. Therefore, persistent M. genitalium infection could have important consequences for acquisition and/or pathogenesis of other sexually transmitted infections (STIs) and perhaps explain the positive associations between this organism and human immunodeficiency virus (HIV) shedding.
生殖道支原体感染与男性和女性泌尿生殖系统疾病综合征有关,包括尿道炎、宫颈炎、盆腔炎(PID)和输卵管因素不孕。了解这些炎症性泌尿生殖系统综合征,尤其是在女性中,需要对黏膜细胞毒性、微生物持续存在和宿主免疫反应进行基本研究,因为上生殖道感染的潜在严重程度。在这里,我们报告生殖道支原体能够建立人宫颈上皮细胞的长期感染,导致慢性炎症细胞因子分泌和对二次 Toll 样受体(TLR)刺激的反应性增加。使用新型定量 PCR 检测方法,我们发现生殖道支原体在接种后 0 至 80 天内复制,在此期间,大多数时间点生殖道支原体与宿主细胞的中位数比值≤10,表明低生物体负担能够在宫颈上皮细胞中引起慢性炎症。这一观察结果与女性的临床发现一致。持续分泌的细胞因子主要由吞噬细胞的趋化和/或激活因子组成,包括白细胞介素-8(IL-8)、单核细胞趋化蛋白 1(MCP-1)和巨噬细胞炎症蛋白 1β(MIP-1β)。尽管持续分泌细胞因子,但除了生殖道支原体的超生理负荷外,没有观察到宿主细胞毒性,这表明持续感染发生时上皮细胞的直接损伤最小。然而,据推测,慢性趋化因子分泌伴随着白细胞向上皮细胞的迁移可能导致严重的炎症后果。因此,生殖道支原体的持续感染可能对其他性传播感染(STI)的获得和/或发病机制有重要影响,并可能解释该微生物与人类免疫缺陷病毒(HIV)脱落之间的正相关关系。