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Journal of Clinical Microbiology, February 1998, p. 367-374, Vol. 36, No. 2
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Rapid Differentiation of Closely Related
Candida Species and Strains by Pyrolysis-Mass Spectrometry
and Fourier Transform-Infrared Spectroscopy
Éadaoin M.
Timmins,1
Susan A.
Howell,2
Bjørn K.
Alsberg,1
William C.
Noble,2 and
Royston
Goodacre1,*
Institute of Biological Sciences, University
of Wales, Aberystwyth, Ceredigion SY23 3DA,1 and
Department of Microbial Diseases, St. John's Institute of
Dermatology, St. Thomas' Hospital, London SE1
7EH,2 United Kingdom
Received 19 June 1997/Returned for modification 18 August
1997/Accepted 17 October 1997
Two rapid spectroscopic approaches for whole-organism
fingerprinting of pyrolysis-mass spectrometry (PyMS) and Fourier
transform-infrared spectroscopy (FT-IR) were used to analyze a group of
29 clinical and reference Candida isolates. These strains
had been identified by conventional means as belonging to one of the
three species Candida albicans, C. dubliniensis
(previously reported as atypical C. albicans), and C. stellatoidea (which is also closely related to C. albicans). To observe the relationships of the 29 isolates as
judged by PyMS and FT-IR, the spectral data were clustered by
discriminant analysis. On visual inspection of the cluster analyses
from both methods, three distinct clusters, which were discrete for
each of the Candida species, could be seen. Moreover, these
phenetic classifications were found to be very similar to those
obtained by genotypic studies which examined the HinfI
restriction enzyme digestion patterns of genomic DNA and by use of the
27A C. albicans-specific probe. Both spectroscopic
techniques are rapid (typically, 2 min for PyMS and 10 s for
FT-IR) and were shown to be capable of successfully discriminating
between closely related isolates of C. albicans, C. dubliniensis, and C. stellatoidea. We believe that
these whole-organism fingerprinting methods could provide opportunities
for automation in clinical microbial laboratories, improving turnaround
times and the use of resources.
*
Corresponding author. Mailing address: Institute of
Biological Sciences, University of Wales, Aberystwyth, Ceredigion SY23 3DA, United Kingdom. Phone: 44 (0)1970 621947. Fax: 44 (0)1970 622354. E-mail: rrg{at}aber.ac.uk.
Journal of Clinical Microbiology, February 1998, p. 367-374, Vol. 36, No. 2
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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