Kundra Shivani, Colomer-Winter Cristina, Lemos José A
Department of Oral Biology, UF College of Dentistry, Gainesville, FL, United States.
Front Microbiol. 2020 Dec 3;11:601417. doi: 10.3389/fmicb.2020.601417. eCollection 2020.
The signaling nucleotide (p)ppGpp has been the subject of intense research in the past two decades. Initially discovered as the effector molecule of the stringent response, a bacterial stress response that reprograms cell physiology during amino acid starvation, follow-up studies indicated that many effects of (p)ppGpp on cell physiology occur at levels that are lower than those needed to fully activate the stringent response, and that the repertoire of enzymes involved in (p)ppGpp metabolism is more diverse than initially thought. Of particular interest, (p)ppGpp regulation has been consistently linked to bacterial persistence and virulence, such that the scientific pursuit to discover molecules that interfere with (p)ppGpp signaling as a way to develop new antimicrobials has grown substantially in recent years. Here, we highlight contemporary studies that have further supported the intimate relationship of (p)ppGpp with bacterial virulence and studies that provided new insights into the different mechanisms by which (p)ppGpp modulates bacterial virulence.
在过去二十年中,信号核苷酸(p)ppGpp一直是深入研究的对象。(p)ppGpp最初被发现是严紧反应的效应分子,严紧反应是一种细菌应激反应,在氨基酸饥饿期间对细胞生理进行重新编程,后续研究表明,(p)ppGpp对细胞生理的许多影响发生在低于完全激活严紧反应所需的水平,并且参与(p)ppGpp代谢的酶种类比最初认为的更多样化。特别值得关注的是,(p)ppGpp调节一直与细菌的持留性和毒力相关,因此近年来,作为开发新型抗菌药物的一种方式,寻找干扰(p)ppGpp信号传导的分子的科学探索有了显著增长。在此,我们重点介绍了进一步支持(p)ppGpp与细菌毒力密切关系的当代研究,以及为(p)ppGpp调节细菌毒力的不同机制提供新见解的研究。