Unbound MEDLINE

The arginine catabolic mobile element and staphylococcal chromosomal cassette mec linkage: convergence of virulence and resistance in the USA300 clone of methicillin-resistant Staphylococcus aureus. The Journal of infectious diseases [J Infect Dis] Journal article

 
TitleThe arginine catabolic mobile element and staphylococcal chromosomal cassette mec linkage: convergence of virulence and resistance in the USA300 clone of methicillin-resistant Staphylococcus aureus.
Author(s)Diep BA, Stone GG, Basuino L, Graber CJ, Miller A, des Etages SA, Jones A, Palazzolo-Ballance AM, Perdreau-Remington F, Sensabaugh GF, DeLeo FR, Chambers HF 
InstitutionDivision of Infectious Diseases, Department of Medicine, San Francisco General Hospital, University of California, San Francisco 94110, USA.
SourceJ Infect Dis 2008 Jun 1; 197(11):1523-30.
MeSHAnimals
Bacteremia
Chromosomes, Bacterial
DNA, Bacterial
Electrophoresis, Gel, Pulsed-Field
Genomic Islands
Interspersed Repetitive Sequences
Male
Methicillin Resistance
Phylogeny
Rabbits
Sequence Deletion
Staphylococcus aureus
Virulence
AbstractThe epidemic character of community-associated methicillin-resistant Staphylococcus aureus, especially the geographically widespread clone USA300, is poorly understood. USA300 isolates carry a type IV staphylococcal chromosomal cassette mec (SCCmec) element conferring beta-lactam antibiotic class resistance and a putative pathogenicity island, arginine catabolic mobile element (ACME). Physical linkage between SCCmec and ACME suggests that selection for antibiotic resistance and for pathogenicity may be interconnected. We constructed isogenic mutants containing deletions of SCCmec and ACME in a USA300 clinical isolate to determine the role played by these elements in a rabbit model of bacteremia. We found that deletion of type IV SCCmec did not affect competitive fitness, whereas deletion of ACME significantly attenuated the pathogenicity or fitness of USA300. These data are consistent with a model in which ACME enhances growth and survival of USA300, allowing for genetic "hitchhiking" of SCCmec. SCCmec in turn protects against exposure to beta-lactams.
Languageeng
Pub Type(s)Journal Article
Research Support, N.I.H., Extramural
Research Support, N.I.H., Intramural
Research Support, U.S. Gov't, P.H.S.
PubMed ID18700257
  
Advertise on this site.