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Published on: September 5, 2013
Staphylococcus epidermidis MSCRAMM SesJ Is Encoded in Composite Islands
Srishtee Arora1, Xiqi Li2, Andrew Hillhouse3
1Center for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas, USA.
Staphylococcus epidermidis surface protein J (SesJ), a virulence factor, is found in mobile genetic elements (MGEs) like ACME and SCC, not just the core genome. This discovery impacts understanding of how this opportunistic pathogen adapts and causes infections.
Area of Science:
- Microbiology
- Genetics
- Infectious Diseases
Background:
- Staphylococcus epidermidis is a major cause of hospital-acquired infections, particularly in immunocompromised patients and those with medical devices.
- Most clinical isolates are methicillin-resistant and possess mobile genetic elements (MGEs) that can carry virulence and resistance genes.
- The microbial surface component recognizing adhesive matrix molecule (MSCRAMM) group includes key virulence factors in pathogenic bacteria.
Purpose of the Study:
- To investigate the genomic location and context of the sesJ gene, encoding a recently discovered S. epidermidis surface protein (SesJ).
- To determine if SesJ, an MSCRAMM, is located within MGEs in clinical isolates of S. epidermidis.
- To understand the implications of SesJ's presence in MGEs for pathogen adaptation and virulence.
Main Methods:
- Analysis of sesJ gene presence and its flanking regions in S. epidermidis clinical isolates.
- Identification of MGEs associated with the sesJ gene, specifically the arginine catabolic mobile element (ACME) and staphylococcal cassette chromosome (SCC) element.
- Characterization of the specific insertion sites (DR_B and DR_E) and associated genes within these MGEs.
Main Results:
- The sesJ gene is consistently found alongside glycosyltransferase genes (gtfA and gtfB) within two distinct MGEs: ACME and SCC.
- SesJ insertion into the SCC element occurs via DR_E, while insertion into ACME, along with a type 1 restriction-modification system, occurs via DR_B.
- The ACME and SCC elements encode different isoforms of the SesJ protein, indicating strain-specific variations.
Conclusions:
- This study reports, for the first time, the presence of an MSCRAMM (SesJ) within MGEs in S. epidermidis clinical isolates.
- The location of SesJ on MGEs suggests a mechanism for rapid dissemination of virulence factors, contributing to S. epidermidis's adaptability and pathogenicity.
- Understanding the role of MGEs in carrying virulence factors is crucial for developing strategies against emerging infectious diseases caused by adaptable pathogens.
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