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Journal of Clinical Microbiology, March 1999, p. 694-699, Vol. 37, No. 3
The Second Department of Internal Medicine,
Oita Medical University, Hasama-machi, Oita 879-5593, Japan
Received 17 June 1998/Returned for modification 20 July
1998/Accepted 18 December 1998
Deep-seated trichosporonosis is a lethal opportunistic infection
that disseminates rapidly and widely in immunocompromised patients, and
early diagnosis is crucial for the treatment of this infection. We
developed a novel nested-PCR assay that detects DNA specific for
clinically important strains of Trichosporon in serum
samples from patients with disseminated trichosporonosis. In this
assay, two sets of oligonucleotide primers were derived from the
sequence of 26S rRNA genes of Trichosporon asahii. The specific fragment was amplified from T. asahii and T. mucoides, but not from other microorganisms, including some other
basidiomycetous fungi (Cryptococcus, Malassezia,
Rhodotorula, and Sporobolomyces). Target DNA
was detected by the nested PCR with as little as 5 fg of the extracted
DNA of T. asahii. In a study using 11 clinical samples, the
specific fragment was detected by the nested PCR in 64% (7 of 11) of
sera from patients with histologically diagnosed disseminated
trichosporonosis, while glucuronoxylomannan antigen was detected in
only 54% (6 of 11) of the samples. Our new nested-PCR assay using
serum samples can be performed repeatedly throughout the course of the
disease. In addition, not only can it be used for early diagnosis of
trichosporonosis, but it may also be beneficial for monitoring its
progress or response to therapy.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
PCR Detection of DNA Specific for
Trichosporon Species in Serum of Patients with
Disseminated Trichosporonosis
*
Corresponding author. Mailing address: The Second
Department of Internal Medicine, Oita Medical University, Hasama-machi, Oita 879-5593, Japan. Phone: 81 (97) 586-5804. Fax: 81 (97) 549-4245.
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