JCM Figure table search 04
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Daly, J A
Right arrow Articles by Matsen, J M
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Daly, J A
Right arrow Articles by Matsen, J M

 Previous Article  |  Next Article 

J Clin Microbiol. 1984 June; 19(6): 742-743

Differential primary plating medium for enhancement of pigment production by Pseudomonas aeruginosa.

J A Daly, R Boshard and J M Matsen

ABSTRACT

A cost-effective and more rapid means of detection of Pseudomonas aeruginosa in cultures from clinical specimens would be very advantageous. We have developed a modified MacConkey agar (MMA), which enhances pigment production of P. aeruginosa and which, if pyocyanin pigment is present, provides a relatively rapid and very cost-effective identification. The MMA medium inhibits the gram-positive organisms, while lactose- and non-lactose-fermenting gram-negative rods are easily distinguishable from pigment-producing pseudomonads. Organisms that produce pyocyanin, pyoverdin, or pyorubin, or both pyocyanin and pyoverdin, are easily recognized on the medium. Pyocyanin production is clearly distinguishable from other Pseudomonas pigments on MMA. In a comparative study, MMA identified 97% of the P. aeruginosa strains 24 h earlier than routine laboratory biochemical methods. Highly mucoid strains which did not produce detectable pigments on standard biochemicals produced detectable pigments on the MMA within 48 h. This medium can provide a very practical, reliable, and cost-effective means for early characterization of P. aeruginosa.


J Clin Microbiol. 1984 June; 19(6): 742-743







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Antimicrob. Agents Chemother. Clin. Microbiol. Rev.
Clin. Vaccine Immunol. ALL ASM JOURNALS

Copyright © 1984 by the American Society for Microbiology. All rights reserved.