2002
DOI: 10.1099/0022-1317-51-1-50
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Effects of silver sulphadiazine on the production of exoproteins by Staphylococcus aureus

Abstract: The effects of subinhibitory concentrations of silver sulphadiazine (AgSD) on exoprotein production in Staphylococcus aureus strains T1, T4, RN4282 and RN 4282agr were studied. AgSD markedly increased levels of toxic shock syndrome toxin (TSST)-1 in strains T4 and RN4282. This effect was independent of agr and AgSD restored TSST-1 production to the wild-type level in RN 4282agr. AgSD had no effect on enterotoxin A or coagulase activity in strains T1 or T4. Strain T4 produced enterotoxin C at high levels and no… Show more

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Cited by 6 publications
(3 citation statements)
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“…In this study, an attempt was made to determine the pathogenicity of obtained Salmonella isolates by CR binding assay and hemolysin assays which yielded results in acceptance with [ 26 - 28 ]. Findings on the hemolytic strains of Salmonella observed is in agreement with a study of hemolysin pattern of Salmonella gallinarum in poultry reporting multiplicity in the hemolysin production among the pathogenic strain [ 26 ].…”
Section: Discussionmentioning
confidence: 99%
“…In this study, an attempt was made to determine the pathogenicity of obtained Salmonella isolates by CR binding assay and hemolysin assays which yielded results in acceptance with [ 26 - 28 ]. Findings on the hemolytic strains of Salmonella observed is in agreement with a study of hemolysin pattern of Salmonella gallinarum in poultry reporting multiplicity in the hemolysin production among the pathogenic strain [ 26 ].…”
Section: Discussionmentioning
confidence: 99%
“…This mode of suppression has been reported to include the production of proteins such as ␣-and ␥-hemolysin, enterotoxins A and B, coagulase, and TSST-1 (5,13,17,20). These antibiotics are recommended for the treatment of severe staphylococcal illnesses associated with the secretion of these toxins.…”
Section: Discussionmentioning
confidence: 99%
“…The proteolytic activity analysis was performed as described by Edwards‐Jones & Foster (2002). In brief, 100 μL of the supernatant from postexponential‐phase (OD 600 nm of 2.5) cultures was added to 1 mL of azocasein (Sigma‐Aldrich) and incubated at 37 °C for 1 h. One millilitre of 5% w/v trichloroacetic acid was used to stop the reaction; undigested azocasein was allowed to precipitate for 30 min.…”
Section: Methodsmentioning
confidence: 99%