|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||



1 University of Dublin, Moyne Institute of Preventive Medicine, Department of Microbiology, School of Genetics and Microbiology, Trinity College, Dublin 2, Ireland
2 University of Bath, Department of Biology and Biochemistry, Bath BA2 7AY, UK
3 Teagasc, Dairy Production Research Centre, Cork, Ireland
4 University of Dublin, Department of Physiology, Trinity College, Dublin 2, Ireland
5 Department of Animal Health, National Veterinary Institute, Oslo, Norway
Correspondence
Davida S. Smyth
davida_smyth{at}nymc.edu
Received January 25, 2009
Accepted June 8, 2009
Staphylococcus aureus is an important pathogen of man, but is also able to colonize and cause disease in a wide variety of mammals and birds. An extended multilocus sequencing approach, involving multilocus sequence typing (MLST), sas typing, spa typing and agr typing, was used to examine the molecular diversity of 118 S. aureus isolates recovered from a range of host species and to compare these data with the known diversity of human-derived isolates. MLST revealed that the commonest animal-associated MLST types were ST133, ST5, ST71, ST97, ST126 and ST151. ST133 appears to be an ungulate-animal-specific genotype, as no evidence of ST133 associating with humans has yet been found in the literature. Novel and unique sas alleles were identified in the animal-associated strains that may represent animal-associated sas alleles. However, sas typing exhibited a lower typeability than MLST for the animal strains (91.3 %). Phylogenetic analyses using neighbour-joining and maximum-parsimony trees localized ruminant-associated MLST lineages to both previously identified S. aureus subspecies aureus subgroups, thus explaining the finding of all four agr types within the ruminant-associated strains. S. aureus isolates recovered from chickens and rabbits were genotypically more similar to known human genotypes than the ruminant-associated lineages.
Present address: New York Medical College, Department of Microbiology and Immunology, Valhalla, NY 10595, USA.
Present address: Centre for Infectious Diseases, The Chancellor's Building, New Royal Infirmary, University of Edinburgh, Edinburgh EH16 4SB, UK.
Present address: Department of Infectious Disease Epidemiology, Imperial College London, London W2 1P, UK.
Supplementary information is available with the online version of this paper.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | J MED MICROBIOL | MICROBIOLOGY | J GEN VIROL | ALL SGM JOURNALS |