Jamison Wendy P, Hackstadt Ted
Host-Parasite Interactions Section, Laboratory of Intracellular Parasites, Rocky Mountain Laboratories, 903 South Fourth Street, NIAID, NIH, Hamilton, MT 59840, USA.
Microb Pathog. 2008 Nov-Dec;45(5-6):435-40. doi: 10.1016/j.micpath.2008.10.002. Epub 2008 Oct 17.
Chlamydiae secrete type III effector proteins at two distinct stages of their developmental cycle. Elementary bodies (EBs) secrete at least one pre-formed effector protein, Tarp, across the host plasma membrane from an extracellular location. Once internalized, a set of newly transcribed proteins are secreted to modify the inclusion membrane. In an effort to better understand the triggers for chlamydial type III secretion and develop means to identify new effectors, we investigated various inducers of T3SS in other Gram-negative bacterial systems to determine if they were able to activate chlamydial type III secretion from EBs using Tarp secretion as an indicator of activation. Chlamydial EBs are induced to secrete Tarp by exposure to FBS, BSA, or sphingolipid and cholesterol-rich liposomes (SCRLs). The induction by FBS and BSA, but not SCRL, is enhanced in the presence of the calcium-chelator, EGTA. This secretion was temperature dependent and inhibited by paraformaldehyde fixation of the EBs.
衣原体在其发育周期的两个不同阶段分泌III型效应蛋白。原体(EBs)从细胞外位置通过宿主质膜分泌至少一种预先形成的效应蛋白Tarp。一旦内化,一组新转录的蛋白会被分泌出来以修饰包涵体膜。为了更好地理解衣原体III型分泌的触发因素并开发鉴定新效应器的方法,我们研究了其他革兰氏阴性细菌系统中III型分泌系统(T3SS)的各种诱导剂,以确定它们是否能够以Tarp分泌作为激活指标,从EBs激活衣原体III型分泌。通过暴露于胎牛血清(FBS)、牛血清白蛋白(BSA)或富含鞘脂和胆固醇的脂质体(SCRLs),衣原体EBs被诱导分泌Tarp。在钙螯合剂乙二醇双四乙酸(EGTA)存在的情况下,FBS和BSA而非SCRL的诱导作用增强。这种分泌是温度依赖性的,并且被EBs的多聚甲醛固定所抑制。