Comparison of multiple typing methods for Aspergillus fumigatus

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Comparison of multiple typing methods for Aspergillus fumigatus L.M.E. Vanhee, F. Symoens, M.D. Jacobsen, H.J. Nelis, T. Coenye Clinical Microbiology and Infection Volume 15, Issue 7, Pages 643-650 (July 2009) DOI: 10.1111/j.1469-0691.2009.02844.x Copyright © 2009 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 1 Unweighted pair group method with arithmetic mean dendrograms of the isolates typed with short tandem repeat (STR) (left) and with a combination of four pattern-based methods (random amplified polymorphic DNA; MSP, microsatellite polymorphism, sequence-specific DNA polymorphism and multilocus enzyme electrophoresis) (right). The scale bar presents the genetic distance between the isolates. Clusters were delineated with a cut-off value of 0.1 genetic distance for both methods as indicated by the vertical lines. Clusters found in the STR dendrogram are designated with the numbers 1–10 and correspond to clusters 1–10′ in the right dendrogram. In both dendrograms the patient codes for the isolates in each cluster are shown. Clinical Microbiology and Infection 2009 15, 643-650DOI: (10.1111/j.1469-0691.2009.02844.x) Copyright © 2009 European Society of Clinical Infectious Diseases Terms and Conditions

FIG. 2 Unweighted pair group method with arithmetic mean dendrogram of the isolates typed with multilocus sequence typing. The scale bar presents the genetic distance between the isolates. Clusters were delineated with a cut-off value of 0.1 genetic distance as indicated by the vertical line. Clusters found in the dendrogram are designated with the letters A to F. Clinical Microbiology and Infection 2009 15, 643-650DOI: (10.1111/j.1469-0691.2009.02844.x) Copyright © 2009 European Society of Clinical Infectious Diseases Terms and Conditions