Abstract

The bactericidal effect of dioctadecyldimethylammonium bromide (DODAB), a liposome forming synthetic amphiphile, is further evaluated for Escherichia coli, Salmonella typhimurium, Pseudomonas aeruginosa, and Staphylococcus aureus in order to establish susceptibilities of different bacteria species towards DODAB at a fixed viable bacteria concentration (2.5 × 107 viable bacteria/mL). For the four species, susceptibility towards DODAB increases from E. coli to S. aureus in the order above. Typically, cell viability decreases to 5% over 1 h of interaction time at DODAB concentrations equal to 50 and 5 μm for E. coli and S. aureus, respectively. At charge neutralization of the bacterial cell, bacteria flocculation by DODAB vesicles is shown to be a diffusion-controlled process. Bacteria flocculation does not yield underestimated counts of colony forming units possibly because dilution procedures done before plating cause deflocculation. The effect of vesicle size on cell viability demonstrates that large vesicles, due to their higher affinity constant for the bacteria (45.20 m-1) relative to the small vesicles (0.14 m-1), kill E. coli at smaller DODAB concentrations. For E. coli and S. aureus, simultaneous determination of cell viability and electrophoretic mobility as a function of DODAB concentration yields a very good correlation between cell surface charge and cell viability. Negatively charged cells are 100% viable whereas positively charged cells do not survive.▪The results show a clear correlation between simple adsorption of entire vesicles generating a positive charge on the cell surfaces and cell death.—Campanhã, M. T. N., E. M. Mamizuka, and A. M. Carmona-Ribeiro. Interactions between cationic liposomes and bacteria: the physical-chemistry of the bactericidal action. J. Lipid Res. 1999. 40: 1495–1500.

Highlights

  • The bactericidal effect of dioctadecyldimethylammonium bromide (DODAB), a liposome forming synthetic amphiphile, is further evaluated for Escherichia coli, Salmonella typhimurium, Pseudomonas aeruginosa, and Staphylococcus aureus in order to establish susceptibilities of different bacteria species towards DODAB at a fixed viable bacteria concentration (2.5 ؋ 107 viable bacteria/mL)

  • We determine: 1) dose and time effects on four different bacteria species of clinical importance at a fixed bacteria concentration; 2) effect of vesicle size on E. coli viability; and 3) simultaneous effect of DODAB vesicles on bacteria electrophoretic mobility and viability

  • As cell concentration is the same for the 4 species, all other experimental conditions being the same, susceptibilities of the 4 bacteria towards DODAB can be compared for 50% and 5% viability (Table 1)

Read more

Summary

Introduction

The bactericidal effect of dioctadecyldimethylammonium bromide (DODAB), a liposome forming synthetic amphiphile, is further evaluated for Escherichia coli, Salmonella typhimurium, Pseudomonas aeruginosa, and Staphylococcus aureus in order to establish susceptibilities of different bacteria species towards DODAB at a fixed viable bacteria concentration (2.5 ؋ 107 viable bacteria/mL). For E. coli and S. aureus, simultaneous determination of cell viability and electrophoretic mobility as a function of DODAB concentration yields a very good correlation between cell surface charge and cell viability. We determine: 1) dose and time effects on four different bacteria species of clinical importance at a fixed bacteria concentration; 2) effect of vesicle size on E. coli viability; and 3) simultaneous effect of DODAB vesicles on bacteria electrophoretic mobility and viability. An interesting correlation between sign of the cell surface charge and cell viability is found: negatively charged cells are 100% viable whereas positively charged cells do not survive (ca. 0% viability)

Objectives
Methods
Results
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.