Staphylococci are the leading cause of hospital-acquired infections, especially nosocomial bacteremia. The two most effective and widely used anti-staphylococcal therapeutic agents are glycopeptides and beta-lactams, both of which target cell wall biosynthesis. However, therapy with these agents is becoming less effective as resistance has developed, first to beta-lactams and, more recently, to glycopeptides. The most important mechanism of resistance to beta-lactams is the acquisition of a new target, a cell wall transpeptidase or penicillin binding protein (PBP2a) that is not inactivated by the antibiotic. This type is called methicillin or oxacillin resistance (OR) and the gene that mediates this resistance, mecA, is encoded within a pathogenicity island called SCCmec. The following proposal seeks to continue studies that explore the origin, dissemination and regulation of genes that mediate OR and genomic adaptations required for staphylococci to become resistant to agents that damage their cell walls. The First Specific Aim will be to investigate the transfer of SCCmec between strains of Staphylococcus aureus (SA) and from a different staphylococcal species, S. epidermidis (SE), to SA. There is evidence that a new SCCmec type, Type IV, has recently moved into SA isolates prevalent in the community and it is present in the majority of SE isolates. The excision, transfer (by plasmid and phage) and reinsertion of this element will be investigated. The Second Specific Aim will be to continue studies on the induction of mecA transcription through the sensor/transducer, MecR1, resulting in the release of the transcriptional repressor, Mecl, from its DNA binding site. The basis of signal transduction and role of proteolytic cleavage of inducer and repressor will be assessed by constructing chimeric molecules, determining the crystal structure of repressors and identifying additional chromosomal genes required for induction. The Third Specific Aim will be to confirm and expand observations made by microarray transcriptional profiling that purine biosynthesis is altered in strains that develop high level resistance to vancomycin and oxacillin, but in opposite directions (increased and decreased respectively). These two phenotypes appear to be mutually exclusive. The purine biosynthetic operons will be genetically manipulated and correlated with development of VR and OR. In addition, microarray and proteomic studies will be pursued on other agents that perturb the cell wall.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI035705-13
Application #
7009305
Study Section
Special Emphasis Panel (ZRG1-BM-1 (01))
Program Officer
Peters, Kent
Project Start
1994-04-01
Project End
2008-12-31
Budget Start
2006-01-01
Budget End
2006-12-31
Support Year
13
Fiscal Year
2006
Total Cost
$485,011
Indirect Cost
Name
Virginia Commonwealth University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
105300446
City
Richmond
State
VA
Country
United States
Zip Code
23298
Ray, M D; Boundy, S; Archer, G L (2016) Transfer of the methicillin resistance genomic island among staphylococci by conjugation. Mol Microbiol 100:675-85
Wang, Lei; Ahmed, Mostafa H; Safo, Martin K et al. (2015) A Plasmid-Borne System To Assess the Excision and Integration of Staphylococcal Cassette Chromosome mec Mediated by CcrA and CcrB. J Bacteriol 197:2754-61
Boundy, Sam; Safo, Martin K; Wang, Lei et al. (2013) Characterization of the Staphylococcus aureus rRNA methyltransferase encoded by orfX, the gene containing the staphylococcal chromosome Cassette mec (SCCmec) insertion site. J Biol Chem 288:132-40
Boundy, Sam; Zhao, Qixun; Fairbanks, Carly et al. (2012) Spontaneous staphylococcal cassette chromosome mec element excision in Staphylococcus aureus nasal carriers. J Clin Microbiol 50:469-71
Wang, Lei; Safo, Martin; Archer, Gordon L (2012) Characterization of DNA sequences required for the CcrAB-mediated integration of staphylococcal cassette chromosome mec, a Staphylococcus aureus genomic island. J Bacteriol 194:486-98
Kleiner, Elizabeth; Monk, Alastair B; Archer, Gordon L et al. (2010) Clinical significance of Staphylococcus lugdunensis isolated from routine cultures. Clin Infect Dis 51:801-3
Wang, Lei; Archer, Gordon L (2010) Roles of CcrA and CcrB in excision and integration of staphylococcal cassette chromosome mec, a Staphylococcus aureus genomic island. J Bacteriol 192:3204-12
Noto, Michael J; Fox, Paige M; Archer, Gordon L (2008) Spontaneous deletion of the methicillin resistance determinant, mecA, partially compensates for the fitness cost associated with high-level vancomycin resistance in Staphylococcus aureus. Antimicrob Agents Chemother 52:1221-9
Noto, Michael J; Kreiswirth, Barry N; Monk, Alastair B et al. (2008) Gene acquisition at the insertion site for SCCmec, the genomic island conferring methicillin resistance in Staphylococcus aureus. J Bacteriol 190:1276-83
Monk, Alastair B; Boundy, Sam; Chu, Vivian H et al. (2008) Analysis of the genotype and virulence of Staphylococcus epidermidis isolates from patients with infective endocarditis. Infect Immun 76:5127-32

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