School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology Brisbane, QLD, Australia.
The Wesley Research Institute, Wesley Hospital Auchenflower, QLD, Australia ; The Wesley Reproductive Medicine and Gynaecological Surgery Unit, The Wesley Hospital Auchenflower, QLD, Australia.
Front Cell Infect Microbiol. 2013 Dec 18;3:100. doi: 10.3389/fcimb.2013.00100. eCollection 2013.
The Chlamydia trachomatis serine protease HtrA (CtHtrA) has recently been demonstrated to be essential during the replicative phase of the chlamydial developmental cycle. A chemical inhibition strategy (serine protease inhibitor JO146) was used to demonstrate this essential role and it was found that the chlamydial inclusions diminish in size and are lost from the cell after CtHtrA inhibition without formation of viable elementary bodies. The inhibitor (JO146) was used in this study to investigate the role of CtHtrA for penicillin persistence and heat stress conditions for Chlamydia trachomatis. JO146 addition during penicillin persistence resulted in only minor reductions (~1 log) in the final viable infectious yield after persistent Chlamydia were reverted from persistence. However, JO146 treatment during the reversion and recovery from penicillin persistence was completely lethal for Chlamydia trachomatis. JO146 was completely lethal when added either during heat stress conditions, or during the recovery from heat stress conditions. These data together indicate that CtHtrA has essential roles during some stress environments (heat shock), recovery from stress environments (heat shock and penicillin persistence), as well as the previously characterized essential role during the replicative phase of the chlamydial developmental cycle. Thus, CtHtrA is an essential protease with both replicative phase and stress condition functions for Chlamydia trachomatis.
沙眼衣原体丝氨酸蛋白酶 HtrA(CtHtrA)最近被证明在衣原体发育周期的复制阶段是必不可少的。采用化学抑制策略(丝氨酸蛋白酶抑制剂 JO146)来证明这种必需作用,结果发现,在抑制 CtHtrA 后,衣原体包涵体的大小减小并从细胞中丢失,而没有形成有活力的始体。在这项研究中,抑制剂(JO146)用于研究 CtHtrA 在青霉素持续存在和沙眼衣原体热应激条件下的作用。在青霉素持续存在期间添加抑制剂(JO146)只会导致最终存活的感染性产量略有减少(约 1 个对数),即在从青霉素持续存在中恢复后持续存在的衣原体被逆转后。然而,在从青霉素持续存在中恢复和恢复期间,JO146 处理对沙眼衣原体是完全致命的。在热应激条件下或从热应激条件中恢复时添加抑制剂(JO146)也是完全致命的。这些数据表明,CtHtrA 在某些应激环境(热休克)、从应激环境中恢复(热休克和青霉素持续存在)以及以前在衣原体发育周期的复制阶段所描述的必需作用中都具有必需的作用。因此,CtHtrA 是一种必需的蛋白酶,对沙眼衣原体具有复制阶段和应激条件的功能。