Cited by 122Antimicrobial Resistance in StaphylococcusBacterial Genetics and BiotechnologyBacterial biofilms and quorum sensing

Regulation of protein A synthesis by the sar and agr loci of Staphylococcus aureus

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Cheung, A L, Eberhardt, K, Heinrichs, J H·1997·Infection and Immunity

Abstract

The synthesis of protein A in Staphylococcus aureus is regulated by global regulatory loci such as sar and agr. Phenotypic data indicate that both sar and agr suppress protein A synthesis; like agr, sar also regulates protein A production at the transcriptional level. To determine the genetic requirement of sar in protein A suppression, we transformed shuttle plasmids containing various sar fragments into a sar mutant. Our results indicated that the 560-bp sarA transcript, or, more probably, the SarA protein (13.5 kDa), is sufficient for suppressing protein A gene transcription when introduced on a multicopy plasmid or as a single copy in the chromosome. Immunoblot analysis with a chicken anti-protein A antibody also confirmed the reduction in protein A expression in these sar mutant clones. Complementation studies revealed that the transcription of the protein A gene can be suppressed in a sar mutant background by a plasmid containing RNAIII. Surprisingly, in agr deletion mutant clones and in clones derived from the agr-sar double mutant, protein A gene transcription can also be suppressed by plasmids containing the sarA transcript plus additional upstream sequence but not the sarA transcript alone. These data suggest that the sar locus can down-modulate protein A gene transcription via both RNAIII-dependent and RNAIII-independent pathways. Consistent with the hypothesis of an RNAIII-independent pathway is an additional genetic requirement for protein A suppression in the agr deletion mutant RN6911 as well as the isogenic double sar-agr mutant, whereas in the sar mutant background, the sarA transcript encoding the SarA protein alone is sufficient. These data suggested that both sar and agr are coregulators of protein A synthesis in S. aureus.

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Crossref · 10.1128/iai.65.6.2243-2249.1997

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Authors
Cheung, A. L., Eberhardt, K., & Heinrichs, J. H.
Affiliations
Rockefeller University (US)
Corresponding author
  • Cheung, A L
  • Eberhardt, K
  • Heinrichs, J H
Venue
Infection and Immunity
Published
1997-06
Volume
65
Issue
6
Pages
2243-2249
ISSN
  • 0019-9567 (ISSN-L)
  • 1098-5522
OpenAlex
W2136672055
Cited by
122
References
22
Citations by year
2025: 1 · 2024: 1 · 2023: 3 · 2022: 3 · 2021: 5 · 2020: 1 · 2019: 3 · 2017: 1 · 2016: 2 · 2015: 5 · 2014: 2 · 2013: 7 · 2012: 2
FWCI
8.78
Type
journal article
Language
en
Open access
Locations
  • Infection and Immunity (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute of Allergy and Infectious Diseases (AI37142, AI30061, R01AI037142)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Antimicrobial Resistance in Staphylococcus
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
Keywords
Staphylococcus aureus, protein A, agr locus, RNAIII, transcriptional regulation, global gene regulation, complementation
MeSH terms
Base Sequence, Chromosome Mapping, Molecular Sequence Data, Staphylococcal Protein A, Staphylococcus aureus, Transcription, Genetic, Gene Expression Regulation, Bacterial

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