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Surface hydrophobicity of Staphylococcus intermedius and Staphylococcus hyicus
R T Greene1, C Lämmler, M Schmitt
1Institut für Bakteriologie und Immunologie Justus-Liebig-Universität Giessen, Germany.
Research in Veterinary Science
|January 1, 1992
Summary
Surface hydrophobicity in Staphylococcus isolates was measured using two methods, revealing no correlation between them. Treatments like pronase and trypsin affected hexadecane adherence, but not always ammonium sulphate aggregation.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Surface Chemistry
Background:
- Staphylococcus intermedius and Staphylococcus hyicus are important veterinary pathogens.
- Bacterial surface hydrophobicity influences adhesion and colonization.
- Understanding surface properties is crucial for controlling staphylococcal infections.
Purpose of the Study:
- To evaluate and compare two assays for measuring surface hydrophobicity in Staphylococcus intermedius and Staphylococcus hyicus.
- To investigate the effect of enzymatic and heat treatments on bacterial surface hydrophobicity.
- To determine the relationship between surface hydrophobicity and other bacterial characteristics.
Main Methods:
- Hexadecane adherence assay was used to measure hydrocarbon adherence.
- Ammonium sulphate salt aggregation test assessed bacterial aggregation.
- Enzymatic (pronase, trypsin) and heat treatments were applied to bacterial cells.
Main Results:
- No statistical correlation was found between the hexadecane adherence assay and the ammonium sulphate salt aggregation test.
- Hexadecane adherence was reduced by pronase and trypsin, but enhanced by heat.
- Ammonium sulphate aggregation was reduced by pronase and heat, but unaffected by trypsin.
Conclusions:
- The two hydrophobicity assays measure different surface properties.
- Surface hydrophobicity in these Staphylococcus species is influenced by protein components and heat-labile factors.
- Surface hydrophobicity did not correlate with slime production, serum soft agar growth, or receptor activity for fibrinogen, fibronectin, or IgG.