Type IV Secretion by Neisseria gonorrhoeae

描述（由申请人提供）：淋病奈瑟菌引起性传播疾病淋病以及盆腔炎、败血症、脑膜炎和关节炎。淋球菌产生了令人难以置信的遗传多样性和抗原多样性，使它们能够避免人类的免疫反应。大量的遗传多样性是通过自然转化产生的。自然转化是淋球菌的一种生存方式。它们组成型地具有转化能力，并且它们优先摄取来自其它淋球菌或其它奈瑟氏球菌的DNA，即，它们摄取最有可能用于与基因组重组的DNA。 我们发现了一个IV型分泌系统（T4SS）编码的基因组岛在淋球菌染色体。T4SS将细菌的染色体DNA分泌到周围环境中。分泌的DNA在附近的其他淋球菌的转化中是活跃的。我们证明了分泌的DNA是单链的，在5 '端被封闭，并且为了使其分泌，它必须首先被松弛酶加工， 作用于染色体上的一个位点，即转移的起点。T4SS对宿主细胞相互作用有影响。它还影响细菌彼此之间以及与细胞和表面的粘附。 该建议的重点是T4SS的表达如何调节。与许多其他T4SS一样，淋球菌IV型分泌基因在正常培养条件下受到抑制。许多T4SS蛋白不能通过蛋白质印迹法检测到，免疫金电子显微镜在细胞亚群上识别单个斑点。这些结果表明，每个细胞可能有一个T4SS装置，或者只有少数细胞在培养产生分泌系统。为了进一步研究分泌机制，鉴定其他分泌底物，并阐明感染期间IV型分泌的作用，将确定控制IV型分泌的机制。该建议的具体目标是：1）鉴定影响T4SS表达的调节剂和环境条件，2）确定traH调节区对T4SS转录、翻译和蛋白定位的机制和作用，以及3）使用模型底物和全基因组测序来检查DNA分泌的机制和后果。

DESCRIPTION (provided by applicant): Neisseria gonorrhoeae causes the sexually-transmitted disease gonorrhea as well as pelvic inflammatory disease, sepsis, meningitis, and arthritis. Gonococci generate an incredible degree of genetic diversity and antigenic diversity allowing them to avoid the human immune response. A significant amount of the genetic diversity is created through natural transformation. Natural transformation is a way of life for gonococci. They are constitutively competent for transformation, and they preferentially take up DNA from other gonococci or other Neisseria, i.e., they take up DNA that is most likely to be useful for recombination with the genome. We discovered a type IV secretion system (T4SS) encoded in a genomic island in the gonococcal chromosome. The T4SS secretes chromosomal DNA from the bacteria into their surroundings. The secreted DNA is active in the transformation of other gonococci in the vicinity. We demonstrated that the secreted DNA is single- stranded, blocked at the 5' end, and that for it to be secreted it must first be processed by a relaxase that acts at a single site in the chromosome, the origin of transfer. The T4SS has effects on host cell interactions. It also affects adherence of the bacteria to each other and to cells and surfaces. This proposal is focused on how expression of the T4SS is regulated. As is the case for many other T4SSs, the gonococcal type IV secretion genes are repressed under normal culture conditions. Many T4SS proteins are not detectable by western blot and immune-gold electron microscopy identifies a single spot on a subpopulation of cells. These results suggest that each cell might have one T4SS apparatus or that only a few cells in the culture produce the secretion system. To further study the mechanism of secretion, to identify additional secretion substrates, and to elucidate the effects of the type IV secretion during infection, the mechanism controlling type IV secretion will be determined. The specific aims of this proposal are: 1) to identify regulators and environmental conditions that affect T4SS expression, 2) to determine the mechanisms and effects of the traH regulatory region on T4SS transcription, translation, and protein localization, and 3) to use model substrates and whole genome sequencing to examine the mechanism and consequences of DNA secretion.