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J Med Microbiol 58 (2009), 13-25; DOI: 10.1099/jmm.0.005215-0
© 2009 Society for General Microbiology
ISSN 0022-2615

Associations between enterotoxin gene cluster types egc1, egc2 and egc3, agr types, enterotoxin and enterotoxin-like gene profiles, and molecular typing characteristics of human nasal carriage and animal isolates of Staphylococcus aureus

Mark M. Collery, Davida S. Smyth{dagger}, John J. G. Tumilty, Jane M. Twohig and Cyril J. Smyth

Department of Microbiology, Moyne Institute of Preventive Medicine, Trinity College Dublin, University of Dublin, Dublin 2, Republic of Ireland

Correspondence
Cyril J. Smyth
csmyth{at}tcd.ie

Received July 20, 2008
Accepted September 11, 2008

Twenty genes encoding enterotoxin and enterotoxin-like proteins have been described in Staphylococcus aureus strains. Five of these occur commonly in the enterotoxin gene cluster (egc: selo, selm, sei, seln and seg). In the sei–seln intergenic region, two pseudogenes, {psi}ent1 and {psi}ent2, can be present or an additional gene designated selu or a variant seluv. Whilst frequencies of loci bearing pseudogenes (egc1) or the selu gene (egc2) have been reported, the distinction between selu-bearing and seluv-bearing (egc3) loci has rarely been made. A PCR-RFLP procedure involving cleavage of the sei–seln intergenic region by restriction endonuclease BbvI or TseI was developed that allowed differentiation of selu+ and seluv+ loci. In addition, PCR primers were designed to yield a 203 bp amplimer for sequencing of a selu or seluv intragenic region, which encompassed ten signature nucleotide differences. A total of 43 egc+ human nasal isolates and 53 egc+ bovine, ovine, caprine, leporine and gallinaceous isolates were egc typed and agr typed. None of the animal isolates was of agr type III. A total of 12 out of 17 egc3+ human nasal isolates were of agr type III, the other 5 being agr type I. On the basis of representative multilocus sequence typing, agr type III/egc3+ strains belonged to CC30. Human nasal isolates bearing an egc1 locus were distributed evenly across agr types I, II and III. Only two nasal isolates had an egc2 locus. All 14 agr type IV isolates, only 1 of which was of human origin, possessed an egc2 locus. The agr IV nasal isolate was fusidic acid sensitive and was found to be ST123 (CC121). There were strong associations between bovine, leporine and gallinaceous S. aureus clonal types and egc locus types. The PCR-RFLP procedure was used to screen an additional 45 S. aureus isolates from dogs, cats, rats, pigs and horses for egc locus types. Of these, 33 were egc. Six equine isolates were selu+. One canine and three porcine isolates possessed pseudogenes {psi}ent1 and {psi}ent2. One porcine and one canine isolate each had the seluv gene. Putative relationships between disease-causing propensity and egc type need (re-)evaluation.


Abbreviations: MLEE, multilocus enzyme electrophoresis; MLST, multilocus sequence typing; RAPD, randomly amplified polymorphic DNA.

{dagger}Present address: New York Medical College, Department of Microbiology and Immunology, Valhalla, NY 10595, USA.

The GenBank/EMBL/DDBJ accession numbers for the sequences of the egc loci genes of S. aureus are EU885488–EU885496.







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