Affiliation:
1. Program in Infectious Diseases, Fred Hutchinson Cancer Research Center
2. Department of Microbiology
3. Department of Medicine, University of Washington, Seattle, Washington
Abstract
ABSTRACT
In a prior study, we identified seven clinical isolates of an
Aspergillus
sp. that were slow to sporulate in multiple media and demonstrated decreased in vitro susceptibilities to multiple antifungals, including amphotericin B, itraconazole, voriconazole, and caspofungin. These isolates were initially considered to be variants of
Aspergillus fumigatus
because of differences in mitochondrial cytochrome
b
sequences and unique randomly amplified polymorphic DNA PCR patterns (S. A. Balajee, M. Weaver, A. Imhof, J. Gribskov, and K. A. Marr, Antimicrob. Agents Chemother. 48: 1197-1203, 2004). The present study was performed to clarify the taxonomic status of these organisms by phylogenetic analyses based on multilocus sequence typing of five genes (the β-tubulin gene, the rodlet A gene, the salt-responsive gene, the mitochondrial cytochrome
b
gene, and the internal transcribed spacer regions). Results revealed that four of the seven variant isolates clustered together in a clade very distant from
A. fumigatus
and distinct from other members of the
A. fumigatus
group. This new clade, consisting of four members, was monophyletic with strong bootstrap support when the protein-encoding regions were analyzed, indicating a new species status under the phylogenetic species concept. Phenotype studies revealed that the variant isolate has smaller conidial heads with diminutive vesicles compared to
A. fumigatus
and is not able to survive at 48°C. Our findings suggest the presence of a previously unrecognized, potentially drug-resistant
Aspergillus
species that we designate
A. lentulus
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
358 articles.
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