Proteomics

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The proteomic and transcriptomic landscapes altered by Rgg2/3 activity in Streptococcus pyogenes


ABSTRACT: Streptococcus pyogenes, otherwise known as Group A Streptococcus (GAS), is an important and highly adaptable human pathogen with the ability to cause both superficial and severe diseases. Understanding how S. pyogenes senses and responds to its environment will likely aid in determining how it causes a breadth of diseases. One regulatory network involved in GAS’s ability to sense and respond to the changing environment is the Rgg2/3 quorum sensing (QS) system, which responds to metal and carbohydrate availability and regulates changes to the bacterial surface. To better understand the impact of Rgg2/3 QS on S. pyogenes physiology, we performed RNA-seq and TMT (tandem mass tag)-LC-MS/MS analysis on cells in which this system was induced with SHP pheromone or disrupted. Primary findings confirmed that pheromone stimulation in wildtype cultures is limited to the induction of operons whose promoters contain previously determined Rgg2/3 binding sequences. However, a deletion mutant of rgg3, a strain that endogenously produces elevated amounts of pheromone, led to extended alterations of the transcriptome and proteome, ostensibly by stress-induced pathways. Under such exaggerated pheromone conditions, a connection was identified between Rgg2/3 and the stringent response. Mutation of relA, the bifunctional guanosine tetra- and penta-phosphate nucleoside synthetase/hydrolase, and alarmone synthase genes sasA and sasB, impacted culture doubling times and disabled induction of Rgg2/3 in response to mannose, while manipulation of Rgg2/3 signaling modestly altered nucleotide levels. Our findings indicate that excessive pheromone production or exposure places stress on GAS resulting in an indirect altered proteome and transcriptome beyond primary pheromone signaling.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Streptococcus Pyogenes Nz131

SUBMITTER: Britta Rued  

LAB HEAD: Michael Federle

PROVIDER: PXD033703 | Pride | 2022-10-04

REPOSITORIES: Pride

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mascot_daemon_merge__F005911_.mzid.gz Mzid
mascot_daemon_merge__F005911_.mzid_mascot_daemon_merge__F005911_.MGF Mzid
mascot_daemon_merge__F005914_1_.mzid.gz Mzid
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