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Journal of Clinical Microbiology, April 2003, p. 1673-1680, Vol. 41, No. 4
0095-1137/03/$08.00+0 DOI: 10.1128/JCM.41.4.1673-1680.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
likowski,1* Dobros
awa Gradecka,2 Magdalena Mielczarek,2 and Wies
aw Kaca1,2
Centre of Microbiology and Virology, Polish Academy of Sciences,1
Institute of Microbiology and Immunology, University of
ód
,
ód
, Poland2
Received 25 July 2002/ Returned for modification 15 October 2002/ Accepted 7 January 2003
Two microsatellite tandem repeated tetramers, (GACA)4 and (CAAT)4, were used for Proteus mirabilis strain differentiation. The microsatellite-based PCR tests were applied for the examination of interstrain diversity for 87 P. mirabilis strains. Forty-six of the investigated strains were clinical isolates (5 were hospital isolates and 39 were outpatient clinic isolates); 42 strains were derived from the Kauffmann-Perch collection of laboratory strains. Fingerprinting done with the tetramers had a high discrimination ability [0.992 and 0.940 for (GACA)4 and (CAAT)4, respectively]. The distributions of clinical isolates among well-defined laboratory strains, determined by numerical analysis (unweighted pair-group method with arithmetic averages; Dice similarity coefficient), proved their genetic similarity to reference strains in the Kauffmann-Perch collection. This analysis also indicated that it is possible to estimate some phenotypic properties of P. mirabilis clinical isolates solely on the basis of microsatellite fingerprinting.
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ód
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