Proteomics

Dataset Information

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Succinylome-controlled antibiotic resistance in MRSA - Succinylome


ABSTRACT: A sucC and a sucD mutant from the Nebraska Transposon Mutant Library (NTML, Strain NE569 and NE1770) were found to be susceptible to cefoxitin and oxacillin when other mutations in TCA cycle genes did not affect their resistance to these antibiotics. The SucC strain (Strain NE569) accumulated Succinyl CoA, which is known to result in higher succinylation rate. We compared the proteome of the sucC mutant in exponential and stationary stages to the one of the WT strain JE2. The global proteome of the following strains were analyzed by TMT-labelled proteomics: Early exponential JE2 (3Hrs), Exponential JE2 (4Hrs), Exponential SucC (4Hrs), Stationary JE2 (10Hrs), Stationary SucC (12Hrs). For each condition, the bacterial pellet was collected and washed twice with PBS. The proteins were extracted by bead beating, 1000 ug of proteins were reduced with DTT, alkylated with IAA and digested with 1:50 (trypsin:protein, w:w) for 3 Hr at 37 C. 100ug of peptides were labelled with TMT11Plex reagents. The samples were pooled and enriched for Succinyl-lysine containing peptides using the PTMScan Succinyl-Lysine Motif Enrichment Kit following the supplier's instructions. The retained fraction was cleaned-up by C18 solid phase extraction. The peptides were concentrated in 15 ul and 5 ul were analyzed by reverse-phase liquid chromatography-tandem mass spectrometry (LC-MS/MS) using a Waters nanoEquity UPLC system coupled with a QExactive HF-X mass spectrometer.

INSTRUMENT(S): Q Exactive HF-X

ORGANISM(S): Staphylococcus Aureus (ncbitaxon:1280)

SUBMITTER: James P. O'Gara   Geremy Clair  

PROVIDER: MSV000086971 | MassIVE | Tue Mar 02 11:38:00 GMT 2021

SECONDARY ACCESSION(S): PXD024470

REPOSITORIES: MassIVE

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Publications

Accumulation of Succinyl Coenzyme A Perturbs the Methicillin-Resistant <i>Staphylococcus aureus</i> (MRSA) Succinylome and Is Associated with Increased Susceptibility to Beta-Lactam Antibiotics.

Campbell Christopher C   Fingleton Claire C   Zeden Merve S MS   Bueno Emilio E   Gallagher Laura A LA   Shinde Dhananjay D   Ahn Jongsam J   Olson Heather M HM   Fillmore Thomas L TL   Adkins Joshua N JN   Razvi Fareha F   Bayles Kenneth W KW   Fey Paul D PD   Thomas Vinai C VC   Cava Felipe F   Clair Geremy C GC   O'Gara James P JP  

mBio 20210629 3


Penicillin binding protein 2a (PBP2a)-dependent resistance to β-lactam antibiotics in methicillin-resistant Staphylococcus aureus (MRSA) is regulated by the activity of the tricarboxylic acid (TCA) cycle via a poorly understood mechanism. We report that mutations in <i>sucC</i> and <i>sucD</i>, but not other TCA cycle enzymes, negatively impact β-lactam resistance without changing PBP2a expression. Increased intracellular levels of succinyl coenzyme A (succinyl-CoA) in the <i>sucC</i> mutant sig  ...[more]

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