Action of disinfectant quaternary ammonium compounds against Staphylococcus aureus

Ioannou, C.J., Hanlon, G.W. and Denyer, S.P. (2007) Action of disinfectant quaternary ammonium compounds against Staphylococcus aureus Antimicrobial Agents and Chemotherapy, 51 (1). pp. 296-306. ISSN 1098-6596

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Official URL: http://aac.asm.org/content/51/1/296

Abstract

Mode-of-action studies concluded that alkyldimethylbenzylammonium chloride (ADBAC) (a blend of C12, C14 and C16 alkyl homologues) and didecyldimethylammonium chloride (DDAC) are both membrane-active agents, possessing subtly different modes of action reflecting early cell interactions against Staphylococcus aureus. ADBAC and DDAC exhibited similar MIC behaviors from 0.4 ppm to 1.8 ppm over an inoculum range of 1 x 105 to 1 x 109 CFU/ml at 35°C. For ADBAC and DDAC, an increased rapidity of killing against S. aureus (final concentration, 2 x 109 CFU/ml) was observed at 35°C compared to 25°C. Concentration exponents () for killing were <2.5 for both agents, and temperature influenced the value. Examination of leakage and kill data suggested that a single leakage marker was not indicative of cell death. ADBAC and DDAC possessed Langmuir (L4) and high-affinity (H3/4) uptake isotherms, respectively. ADBAC molecules formed a single monolayer of coverage of cells at the end of primary uptake, and DDAC formed a double monolayer. Rapid cell leakage occurred at bactericidal concentrations, with total depletion of the intracellular potassium and 260-nm-absorbing pools released in this strict order. Autolysis was observed for ADBAC and DDAC at concentrations of 9 µg/ml (0.0278 mM and 0.0276 mM, respectively) and above, together with the depletion of approximately 30% of the internal potassium pool. Autolysis contributed to ADBAC and DDAC lethality, although high biocide concentrations may have inhibited autolytic enzyme activity.

Item Type:Journal article
Subjects:C000 Biological and Biomedical Sciences > C700 Molecular Biology, Biophysics and Biochemistry
DOI (a stable link to the resource):10.1128/AAC.00375-06
Faculties:Faculty of Science and Engineering > School of Pharmacy and Biomolecular Sciences > Biomedical Materials
ID Code:2642
Deposited By:editor spbs
Deposited On:08 Nov 2007
Last Modified:02 Jul 2013 12:19

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