J Med Microbiol Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zarnowski, R.
Right arrow Articles by Woods, J. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zarnowski, R.
Right arrow Articles by Woods, J. P.
Agricola
Right arrow Articles by Zarnowski, R.
Right arrow Articles by Woods, J. P.
J Med Microbiol 56 (2007), 788-797; DOI: 10.1099/jmm.0.47067-0
© 2007 Society for General Microbiology
ISSN 1473-5644

Typing of Histoplasma capsulatum strains by fatty acid profile analysis

Robert Zarnowski1, Makoto Miyazaki2, Agnieszka Dobrzyn2,{dagger}, James M. Ntambi2,3 and Jon P. Woods1

1 Department of Medical Microbiology and Immunology, University of Wisconsin, Madison, WI, USA

2 Department of Biochemistry, University of Wisconsin, Madison, WI, USA

3 Department of Nutritional Sciences, University of Wisconsin, Madison, WI, USA

Correspondence
Robert Zarnowski
rzarnowski{at}wisc.edu

Received 11 November 2006
Accepted 5 March 2007


The performance of fatty acid profiling for strain differentiation of Histoplasma capsulatum was assessed. Total fatty acids were isolated from the yeast-phase cells of seven stock and two previously unreported clinical strains of H. capsulatum var. capsulatum, as well as from one unreported clinical strain and one stock strain of H. capsulatum var. duboisii, and one strain of each of three other dimorphic zoopathogenic fungal species, Blastomyces dermatitidis, Paracoccidioides brasiliensis and Sporothrix schenckii. Different colony morphology and pigmentation types of the H. capsulatum strains were also included. The most frequently occurring fatty acids were oleic, palmitic, stearic and linoleic acids. There were variations in the relative percentage fatty acid contents of H. capsulatum strains that could be used for strain identification and discrimination. Differentiation between H. capsulatum strains was achieved by the comparison of detected fatty acids accompanied by principal component analysis using calculated Varimax-rotated principal component loadings. Statistical analysis yielded three major principal components that explained over 94 % of total variance in the data. All the strains of H. capsulatum var. capsulatum RFLP classes II and III were grouped into two distinct clusters: the heterogenic RFLP class I formed a large, but also well-defined group, whereas the outgroup strains of H. capsulatum var. duboisii, B. dermatitidis, P. brasiliensis and S. schenckii were shifted away. These data suggest that fatty acid profiling can be used in H. capsulatum strain classification and epidemiological studies that require strain differentiation at the intraspecies level.


Abbreviations: BHT, butylated hydroxytoluene; FAME, fatty acid methyl ester; PC, principal component; PCA, principal component analysis.

{dagger}Present address: Nencki Institute of Experimental Biology, Warsaw, Poland.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL J MED MICROBIOL MICROBIOLOGY J GEN VIROL ALL SGM JOURNALS
Copyright © 2007 Society for General Microbiology.