Chlamydial Diseases Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Research Technologies Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
mBio. 2021 Jun 29;12(3):e0117921. doi: 10.1128/mBio.01179-21. Epub 2021 Jun 8.
Chlamydia are obligate intracellular Gram-negative bacteria distinguished by a unique developmental biology confined within a parasitophorous vacuole termed an inclusion. The chlamydial plasmid is a central virulence factor in the pathogenesis of infection. Plasmid gene protein 4 (Pgp4) regulates the expression of plasmid gene protein 3 (Pgp3) and chromosomal glycogen synthase (GlgA), virulence factors secreted from the inclusion to the host cytosol by an unknown mechanism. Here, we identified a plasmid-dependent secretion system for the cytosolic delivery of Pgp3 and GlgA. The secretion system consisted of a segregated population of globular structures originating from midcycle reticulate bodies. Globular structures contained the Pgp4-regulated proteins CT143, CT144, and CT050 in addition to Pgp3 and GlgA. Genetic replacement of Pgp4 with Pgp3 or GlgA negated the formation of globular structures, resulting in retention of Pgp3 and GlgA in chlamydial organisms. The generation of globular structures and secretion of virulence factors occurred independently of type 2 and type 3 secretion systems. Globular structures were enriched with lipopolysaccharide but lacked detectable major outer membrane protein and heat shock protein 60, implicating them as outer membrane vesicles. Thus, we have discovered a novel chlamydial plasmid-dependent secretion system that transports virulence factor cargo from the chlamydial inclusion to the host cytosol. The Chlamydia trachomatis plasmid regulates the expression and secretion of immune evasion virulence factors to the host cytosol by an unknown mechanism. In this study, we identified a novel plasmid gene protein 4 (Pgp4)-dependent secretion system. The system consists of globular structures distinct from typical chlamydial developmental forms that export Pgp3 and GlgA to the host cytosol. Globular structures emerged at mid-chlamydial growth cycle from distinct populations of reticulate bodies. The formation of globular structures occurred independently of known chlamydial secretion systems. These results identify a Pgp4-dependent secretory system required for exporting plasmid regulated virulence factors to the host cytosol.
衣原体是专性细胞内革兰氏阴性细菌,其独特的发育生物学特征是局限于称为包含体的寄生空泡内。衣原体质粒是感染发病机制中的主要毒力因子。质粒基因蛋白 4(Pgp4)调节质粒基因蛋白 3(Pgp3)和染色体糖基合成酶(GlgA)的表达,这些毒力因子通过未知机制从包含体分泌到宿主细胞质溶胶中。在这里,我们鉴定了一个依赖质粒的分泌系统,用于将 Pgp3 和 GlgA 细胞质内输送。该分泌系统由从中期网状体起源的分离的球状结构群体组成。球状结构包含 Pgp4 调节的蛋白 CT143、CT144 和 CT050 以及 Pgp3 和 GlgA。用 Pgp3 或 GlgA 替换 Pgp4 会消除球状结构的形成,导致 Pgp3 和 GlgA 在衣原体生物体内被保留。球状结构的形成和毒力因子的分泌与 2 型和 3 型分泌系统无关。球状结构富含脂多糖,但缺乏可检测到的主要外膜蛋白和热休克蛋白 60,暗示它们是外膜囊泡。因此,我们发现了一种新型的衣原体质粒依赖性分泌系统,它将毒力因子货物从衣原体包含体运输到宿主细胞质溶胶。沙眼衣原体质粒通过未知机制调节免疫逃避毒力因子的表达和分泌到宿主细胞质溶胶。在这项研究中,我们鉴定了一种新型的质粒基因蛋白 4(Pgp4)依赖性分泌系统。该系统由不同于典型衣原体发育形式的球状结构组成,将 Pgp3 和 GlgA 输出到宿主细胞质溶胶。球状结构在衣原体生长周期的中期从不同的网状体种群中出现。球状结构的形成独立于已知的衣原体分泌系统。这些结果鉴定了一种依赖 Pgp4 的分泌系统,该系统用于将质粒调节的毒力因子输出到宿主细胞质溶胶。