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Genetic Analysis of Pseudomonas aeruginosa by Enterobacterial Repetitive Intergenic Consensus Polymerase Chain Reaction (PCR) and Arbitrarily Primed PCR: Gel Analysis Compared with Microchip Gel Electrophoresis

Published online by Cambridge University Press:  02 January 2015

Roudabeh J. Jamasbi ,
Stephen J. Kennel ,
Larry C. Waters ,
Linda J. Foote  and
J. Michael Ramsey
Roudabeh J. Jamasbi*
Affiliation:
Department of Public and Allied Health, Bowling Green State University, Bowling Green, Ohio
Stephen J. Kennel
Affiliation:
Oak Ridge National Laboratory, Oak Ridge, Tennessee
Larry C. Waters
Affiliation:
Oak Ridge National Laboratory, Oak Ridge, Tennessee
Linda J. Foote
Affiliation:
Oak Ridge National Laboratory, Oak Ridge, Tennessee
J. Michael Ramsey
Affiliation:
Oak Ridge National Laboratory, Oak Ridge, Tennessee
*
Department of Public and Allied Health, 504 Life Sciences Building, Bowling Green State University, Bowling Green, OH 43403
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Abstract

Objectives:

To assess the applicability of a newly emerging microchip gel electrophoresis for rapid strain differentiation among clinical isolates of Pseudomonas aeruginosa, and to compare this technique with the traditional gel method for DNA separation.

Methods:

One hundred clinical strains of P. aeruginosa obtained from a hospital in northwestern Ohio were tested for reactivity to 3 serotype-specific monoclonal antibodies by enzyme-linked immunosorbent assay. Twelve strains (4 from each serogroup) were selected for DNA analysis by polymerase chain reaction (PCR)-based, single primer DNA fingerprinting methods with 3 different primers: 1 enterobacterial repetitive intergenic consensus PCR and 2 arbitrarily primed PCRs. The PCR products were analyzed by agarose slab gel and microchip gel electrophoresis.

Results:

Of the 100 clinical isolates tested, 39% (4%, 14%, and 21%) were found to be serotypes 0:3, 0:6, and 0:11, respectively. Twelve strains were chosen for DNA analysis by PCR. The PCR products were analyzed by agarose slab gel electrophoresis and on microchips to determine interspecies diversity. Both methods demonstrated that different serotypes exhibited different electrophoretic patterns. Two strains (clinical strains 6 and 7, serotype 0:6) showed identical patterns, indicating a high degree of relatedness.

Conclusion:

In all cases, there was concordance between the electrophoretic patterns detected by the two methods. The capability of conducting both PCR and microchip gel electrophoresis offers an opportunity for an automated and rapid method for genetic analysis and differentiation among strains of P. aeruginosa and other microorganisms.

Type
Original Articles
Information
Infection Control & Hospital Epidemiology , Volume 25 , Issue 1 , January 2004 , pp. 65 - 71
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2004

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