AEM
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 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 Jones, L. F.
Right arrow Articles by Farmer, J. J.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Jones, L. F.
Right arrow Articles by Farmer, J. J., III
Agricola
Right arrow Articles by Jones, L. F.
Right arrow Articles by Farmer, J. J.

 Previous Article  |  Next Article 

Appl Environ Microbiol. 1974 February; 27(2): 400-406
Copyright © 1974 American Society for Microbiology. All Rights Reserved.

Pyocin Typing of Pseudomonas aeruginosa: a Simplified Method

Lois Faye Jones, J. P. Zakanycz, Evan T. Thomas and J. J. Farmer III1

a Department of Microbiology, The University of Alabama, University, Alabama 35486

ABSTRACT

A simplified method has been devised for typing Pseudomonas aeruginosa by pyocin production. Pyocins are produced as strains grow overnight in Trypticase soy broth (without glucose) plus 1% potassium nitrate. Because P. aeruginosa can use nitrate instead of oxygen as a terminal electron acceptor, mechanical shaking is not necessary, nor is induction by mitomycin C. Pyocins can now be produced in screw-cap tubes in a water bath or incubator. A total of 250 strains were tested as possible pyocin indicators, which included 60 strains already used in pyocin-typing systems. The final set contained 18 indicators which were chosen because (i) they had clear positive or clear negative reactions, thus eliminating reactions difficult to read, (ii) they had few zones due to bacteriophage lysis, and (iii) they were most sensitive in differentiating clinical isolates of P. aeruginosa. The final typing method was tested in several studies and the results were clear; thus definitive epidemiological conclusions could be made. Because it is simple to perform and easily automated, the new method should have application in many hospitals; however, it should be used only in carefully planned epidemiological studies. The method and its application are described in detail, and some pitfalls are discussed.


FOOTNOTES

1 Present address: Bacteriophage-Bacteriocin Laboratory, Enteric Unit, Center for Disease Control, Atlanta, Georgia 30333.


Appl Environ Microbiol. 1974 February; 27(2): 400-406
Copyright © 1974 American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 1974 by the American Society for Microbiology. All rights reserved.