Survival of the Fittest: The Relationship of (p)ppGpp With Bacterial Virulence

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...

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Published inFrontiers in microbiology Vol. 11; p. 601417
Main Authors Kundra, Shivani, Colomer-Winter, Cristina, Lemos, José A.
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 03.12.2020
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ISSN1664-302X
1664-302X
DOI10.3389/fmicb.2020.601417

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Summary: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.
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Edited by: Katarzyna Potrykus, University of Gdańsk, Poland
Reviewed by: Shinji Masuda, Tokyo Institute of Technology, Japan; Robert E. W. Hancock, University of British Columbia, Canada
This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2020.601417