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Multiplex PCR Assay for Typing of Staphylococcal Cassette Chromosome Mec Types I to V in Methicillin-resistant Staphylococcus aureus
Published on: September 5, 2013
A Novel MSCRAMM Subfamily in Coagulase Negative Staphylococcal Species
Srishtee Arora1, Anne-Catrin Uhlemann2, Franklin D Lowy2
1Center for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M University Health Science Center, Houston TX, USA.
Abstract:
Coagulase negative staphylococci (CoNS) are important opportunistic pathogens. Staphylococcus epidermidis, a coagulase negative staphylococcus, is the third leading cause of nosocomial infections in the US. Surface proteins like Microbial Surface Components Recognizing Adhesive Matrix Molecules (MSCRAMMs) are major virulence factors of pathogenic gram positive bacteria. Here, we identified a new chimeric protein in S. epidermidis, that we call SesJ. SesJ represents a prototype of a new subfamily of MSCRAMMs. Structural predictions show that SesJ has structural features characteristic of a MSCRAMM along with a N-terminal repeat region and an aspartic acid containing C-terminal repeat region, features that have not been previously observed in staphylococcal MSCRAMMs but have been found in other surface proteins from gram positive bacteria. We identified and analyzed structural homologs of SesJ in three other CoNS. These homologs of SesJ have an identical structural organization but varying sequence identities within the domains. Using flow cytometry, we also show that SesJ is expressed constitutively on the surface of a representative S. epidermidis strain, from early exponential to stationary growth phase. Thus, SesJ is positioned to interact with protein targets in the environment and plays a role in S. epidermidis virulence.
Insights
Researchers discovered SesJ, a novel chimeric protein in Staphylococcus epidermidis. This protein, a new type of Microbial Surface Components Recognizing Adhesive Matrix Molecules (MSCRAMM), is constitutively expressed and may play a role in S. epidermidis virulence.
Area of Science:
- Microbiology
- Structural Biology
- Pathogenesis
Background:
- Coagulase-negative staphylococci (CoNS) are significant opportunistic pathogens.
- Staphylococcus epidermidis is a leading cause of hospital-acquired infections.
- Microbial Surface Components Recognizing Adhesive Matrix Molecules (MSCRAMMs) are key virulence factors in Gram-positive bacteria.
Purpose of the Study:
- To identify and characterize novel surface proteins in S. epidermidis.
- To investigate the structural features and distribution of a newly identified protein, SesJ.
- To understand the potential role of SesJ in S. epidermidis virulence.
Main Methods:
- Bioinformatic analysis to identify and predict the structure of SesJ.
- Comparative analysis of SesJ homologs in other CoNS species.
- Flow cytometry to determine SesJ surface expression levels in S. epidermidis.
Main Results:
- A novel chimeric protein, SesJ, was identified in S. epidermidis, representing a new MSCRAMM subfamily.
- SesJ possesses unique structural features, including N-terminal and C-terminal repeat regions, not previously seen in staphylococcal MSCRAMMs.
- Structural homologs of SesJ were found in other CoNS, sharing identical organization but varying sequence identities.
- SesJ is constitutively expressed on the S. epidermidis surface throughout its growth phases.
Conclusions:
- SesJ is a novel MSCRAMM prototype with unique structural characteristics.
- The constitutive expression of SesJ suggests its importance in S. epidermidis-host interactions.
- SesJ likely contributes to the virulence of S. epidermidis by interacting with environmental targets.
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