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Journal of Clinical Microbiology, June 1998, p. 1625-1629, Vol. 36, No. 6
Immunocompromised Host Section, Pediatric
Oncology Branch, National Cancer Institute, National Institutes of
Health, Bethesda, Maryland
Received 6 October 1997/Returned for modification 30 October
1997/Accepted 17 March 1998
Current methods of DNA extraction from different fungal pathogens
are often time-consuming and require the use of toxic chemicals. DNA
isolation from some fungal organisms is difficult due to cell walls or
capsules that are not readily susceptible to lysis. We therefore
investigated a new and rapid DNA isolation method using high-speed cell
disruption (HSCD) incorporating chaotropic reagents and lysing matrices
in comparison to standard phenol-chloroform (PC) extraction protocols
for isolation of DNA from three medically important yeasts
(Candida albicans, Cryptococcus neoformans, and Trichosporon beigelii) and two filamentous fungi
(Aspergillus fumigatus and Fusarium solani).
Additional extractions by HSCD were performed on Saccharomyces
cerevisiae, Pseudallescheria boydii, and
Rhizopus arrhizus. Two different inocula (108
and 107 CFU) were compared for optimization of obtained
yields. The entire extraction procedure was performed on as many as 12 samples within 1 h compared to 6 h for PC extraction. In
comparison to the PC procedure, HSCD DNA extraction demonstrated
significantly greater yields for 108 CFU of C. albicans, T. beigelii, A. fumigatus, and
F. solani (P
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Rapid Extraction of Genomic DNA from Medically
Important Yeasts and Filamentous Fungi by High-Speed Cell
Disruption
0.005), 107
CFU of C. neoformans (P
0.05), and
107 CFU of A. fumigatus (P
0.01). Yields were within the same range for 108 CFU of
C. neoformans and 107 CFU of C. albicans for both HSCD extraction and PC extraction. For
107 CFU of T. beigelii, PC extraction resulted
in a greater yield than did HSCD (P
0.05). Yields
obtained from 108 and 107 CFU were
significantly greater for filamentous fungi than for yeasts by the HSCD
extraction procedure (P < 0.0001). By the PC extraction procedure, differences were not significant. For all eight
organisms, the rapid extraction procedure resulted in good yield,
integrity, and quality of DNA as demonstrated by restriction fragment
length polymorphism, PCR, and random amplified polymorphic DNA. We
conclude that mechanical disruption of fungal cells by HSCD is a safe,
rapid, and efficient procedure for extracting genomic DNA from
medically important yeasts and especially from filamentous fungi.
*
Corresponding author. Mailing address for Thomas J. Walsh: Immunocompromised Host Section, Pediatric Oncology Branch,
National Cancer Institute, Building 10, Room 13N240, Bethesda, MD
20892. Phone: (301) 402-0023. Fax: (301) 402-0575. E-mail:
walsht{at}pbmac.nci.nih.gov. Mailing address for
Frank-Michael C. Müller: Institut für Molekulare Infektionsbiologie, Universität Würzburg, Röntgenring
11, D-97070 Würzburg, Germany. Phone: 49-931-312575. Fax:
49-931-312578. E-mail: frank.mueller{at}mail.uni-wuerzburg.de.
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