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Prevalence of genes for enterotoxins,toxic shock syndrome toxin 1 and exfoliative toxin among clinical isolates of Staphylococcus pseudintermedius from canine origin
Authors:Jang W Yoon  Gi‐Jong Lee  So‐Young Lee  Chul Park  Jong‐Hyun Yoo  Hee‐Myung Park
Institution:1. Advanced Human Resource and Research Group for Medical Science (BK21), Konkuk University School of Medicine, Seoul 143‐701, Korea;2. Both authors contributed equally to this work.Sources of Funding The Korea Science and Engineering Foundation (KOSEF) grant funded by the Korea government (MEST) (R11‐2002‐103) and the Second‐Phase of the BK (Brain Korea 21) Project to J.W.Y.;3. Department of Veterinary Internal Medicine, College of Veterinary Medicine, Konkuk University, Seoul 143‐701, Korea;4. Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California Davis, Davis, CA 95616, USA;5. BK21 Basic & Diagnostic Veterinary Specialist Program for Animal Diseases, Konkuk University, Seoul 143‐701, Korea
Abstract:A total of 74 Staphylococcus pseudintermedius strains were isolated from the 99 clinical cases of canine pyoderma or chronic otitis in our veterinary teaching hospital during May 2006–February 2008. In this study, we examined the genetic distribution of staphylococcal pyogenic toxins such as staphylococcal enterotoxins A (sea), B (seb), C (sec), D (sed), E (see), and toxic shock syndrome toxin 1 (tst) as well as the previously characterized S. intermedius exfoliative toxin (siet) among those isolates. The polymerase chain reaction analyses with the toxin gene‐specific primers revealed that 18 (24.3%) of 74 S. pseudintermedius isolates carried the sec genes, but none of the sea, seb, sed, see and tst genes. Further DNA sequencing analysis of the amplified sec genes revealed that they all belonged to the canine type C staphylococcal enterotoxin (SECcanine) whose superantigenic activity has been demonstrated. In addition to the seccanine genes, our polymerase chain reaction results showed that all the 74 isolates carried the siet gene. Since both SECcanine and SIET toxins are known to be biologically active, it would be interesting to investigate how those toxins are involved in the pathogenesis of the canine diseases by S. pseudintermedius such as pyoderma or chronic otitis.
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