SarT, a Repressor of α-Hemolysin in Staphylococcus aureus
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In searching the Staphylococcus aureus genome, we found several homologs to SarA. One of these genes, sarT , codes for a basic protein with 118 residues and a predicted molecular size of 16,096 Da. Northern blot analysis revealed that the expression of sarT was repressed by sarA and agr . An insertion sarT mutant generated in S. aureus RN6390 and 8325-4 backgrounds revealed minimal effect on the expression of sarR and sarA . The RNAIII level was notably increased in the sarT mutant, particularly in postexponential-phase cells, while the augmentative effect on RNAII was less. SarT repressed the expression of α-hemolysin, as determined by Northern blotting, Western blotting, and a rabbit erythrocyte hemolytic assay. This repression was relieved upon complementation. Similar to agr and sarA mutants, which predictably displayed a reduction in hla expression, the agr sarT mutant exhibited a lower level of hla transcription than the sarT mutant. In contrast, hla transcription was enhanced in the sarA sarT mutant compared with the single sarA mutant. Collectively, these results indicated that the sarA locus, contrary to the regulatory action of agr , induced α-hemolysin production by repressing sarT , a repressor of hla transcription.
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Staphylococcal toxins are generally expressed during the stationary phase of bacterial growth and may not be present in vivo in sufficient concentration during the early stages of pulmonary infection to participate in staphylococcal invasion.
“However, staphylococcal toxins are generally expressed during the stationary phase of bacterial growth and may not be present in vivo in sufficient concentration during the early stages of pulmonary infection to participate in staphylococcal invasion (11).”
From Staphylococcus aureus protein A mediates invasion across airway epithelial cells through activation of RhoA GTPase signaling and proteolytic activity (2011) · cites this paper as [11]
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References 47 · Cited by 124
- Authors
- Schmidt, K. A., Manna, A. C., Gill, S., & Cheung, A. L.
- Affiliations
- Dartmouth College (US)
- <!--label omitted: 2-->TIGR, Rockville, Maryland 208502
- Venue
- Infection and Immunity
- Publisher
- American Society for Microbiology
- Published
- 2001-08
- Volume
- 69
- Issue
- 8
- Pages
- 4749-4758
- ISSN
- 0019-9567 (ISSN-L)
- 1098-5522
- PMC
- PMC98561
- OpenAlex
- W2144372579
- Cited by
- 124
- References
- 47
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 5 · 2023: 2 · 2022: 2 · 2021: 1 · 2020: 3 · 2019: 5 · 2018: 2 · 2017: 1 · 2016: 4 · 2015: 1 · 2014: 8 · 2013: 6 · 2012: 7
- FWCI
- 6.64
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Infection and Immunity (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Oklahoma
- National Institutes of Health
- U.S. Public Health Service (A107519-14)
- National Institute of Allergy and Infectious Diseases (AI37142, R01AI037142, AI43968)
- 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
- SART, alpha-hemolysin, Staphylococcus aureus, SARA, agr locus, RNAIII, transcriptional repression, gene expression regulation, complementation, hemolytic activity
- MeSH terms
- Amino Acid Sequence, Animals, Bacterial Proteins, Bacterial Toxins, Base Sequence, DNA, Bacterial, Hemolysin Proteins, Molecular Sequence Data, Phenotype, Rabbits, Repressor Proteins, Staphylococcus aureus, Transcription Factors, Blotting, Western, Trans-Activators, Gene Expression Regulation, Bacterial, Mutagenesis
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