JAC Advance Access published online on April 8, 2004
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkh171
© 2004 by The British Society for Antimicrobial Chemotherapy
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Leading article
1 Welsh School of Pharmacy, Cardiff University, Cardiff CF10
3XF, UK
* Corresponding author. E-mail: russellD2{at}cardiff.ac.uk.
Triclosan has activity against many, but not all, types
of Gram-positive and Gram-negative bacteria. It is bacteriostatic
at low concentrations, but higher concentrations are bactericidal. Pseudomonas aeruginosa is highly resistant, whereas
methicillin-resistant Staphylococcus aureus strains
are inhibited over a range of
Keywords: mechanisms of action, mechanisms of resistance,
antibiotic resistance
Whither triclosan?
0.1-2
mg/L. Triclosan shows significant activity against some mycobacteria,
but is not sporicidal. Its growth-inhibitory properties result from
an inhibition of enoyl reductase, FabI. Membrane-destabilizing effects
are likely to be responsible for bacterial inactivation by higher
concentrations. Resistance can arise from mutations in, and/or overproduction
of, FabI, impermeability or efflux. Whilst triclosan resistance
in laboratory experiments may be associated with changes in antibiotic
susceptibility, comprehensive environmental surveys have not demonstrated
any association between triclosan usage and antibiotic resistance.
Triclosan has several important uses, and the future aim must be
to retain these applications whilst eliminating the more frivolous
and unnecessary ones.![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
L. Birosova and M. Mikulasova Development of triclosan and antibiotic resistance in Salmonella enterica serovar Typhimurium J. Med. Microbiol., April 1, 2009; 58(4): 436 - 441. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J. Stickler and G. L. Jones Reduced Susceptibility of Proteus mirabilis to Triclosan Antimicrob. Agents Chemother., March 1, 2008; 52(3): 991 - 994. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. F. Seaman, D. Ochs, and M. J. Day Small-colony variants: a novel mechanism for triclosan resistance in methicillin-resistant Staphylococcus aureus J. Antimicrob. Chemother., January 1, 2007; 59(1): 43 - 50. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. J. V. Piddock Clinically Relevant Chromosomally Encoded Multidrug Resistance Efflux Pumps in Bacteria Clin. Microbiol. Rev., April 1, 2006; 19(2): 382 - 402. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Ll. Jones, C. T. Muller, M. O'Reilly, and D. J. Stickler Effect of triclosan on the development of bacterial biofilms by urinary tract pathogens on urinary catheters J. Antimicrob. Chemother., February 1, 2006; 57(2): 266 - 272. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. Cholo, H. I. Boshoff, H. C. Steel, R. Cockeran, N. M. Matlola, K. J. Downing, V. Mizrahi, and R. Anderson Effects of clofazimine on potassium uptake by a Trk-deletion mutant of Mycobacterium tuberculosis J. Antimicrob. Chemother., January 1, 2006; 57(1): 79 - 84. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Sanchez, E. Moreno, and J. L. Martinez The Biocide Triclosan Selects Stenotrophomonas maltophilia Mutants That Overproduce the SmeDEF Multidrug Efflux Pump Antimicrob. Agents Chemother., February 1, 2005; 49(2): 781 - 782. [Abstract] [Full Text] [PDF] |
||||



