Aggarwal Shifu, Kumaraswami Muthiah
Center for Molecular and Translational Human Infectious Diseases Research, Houston Methodist Research Institute, Houston, TX, United States.
Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, United States.
Front Cell Dev Biol. 2022 Jun 21;10:921920. doi: 10.3389/fcell.2022.921920. eCollection 2022.
Pathogenic streptococci require manganese for survival in the host. In response to invading pathogens, the host recruits nutritional immune effectors at infection sites to withhold manganese from the pathogens and control bacterial growth. The manganese scarcity impairs several streptococcal processes including oxidative stress defenses, DNA synthesis, bacterial survival, and virulence. Emerging evidence suggests that pathogens also encounter manganese toxicity during infection and manganese excess impacts streptococcal virulence by manganese mismetallation of non-cognate molecular targets involved in bacterial antioxidant defenses and cell division. To counter host-imposed manganese stress, the streptococcal species employ a sophisticated sensory system that tightly coordinates manganese stress-specific molecular strategies to negate host induced manganese stress and proliferate in the host. Here we review the molecular details of host-streptococcal interactions in the battle for manganese during infection and the significance of streptococcal effectors involved to bacterial pathophysiology.
致病性链球菌在宿主体内存活需要锰。作为对入侵病原体的反应,宿主在感染部位募集营养免疫效应分子,以阻止病原体获取锰并控制细菌生长。锰的缺乏会损害多种链球菌过程,包括氧化应激防御、DNA合成、细菌存活和毒力。新出现的证据表明,病原体在感染过程中也会遇到锰毒性,并且过量的锰会通过与参与细菌抗氧化防御和细胞分裂的非同源分子靶点发生锰错配来影响链球菌的毒力。为了应对宿主施加的锰胁迫,链球菌采用了一种复杂的传感系统,该系统紧密协调锰胁迫特异性分子策略,以消除宿主诱导的锰胁迫并在宿主体内增殖。在此,我们综述了感染期间在争夺锰的过程中宿主与链球菌相互作用的分子细节,以及所涉及的链球菌效应分子对细菌病理生理学的重要性。