In vitro antifungal susceptibility and molecular identity of 99 clinical isolates of the opportunistic fungal genus Curvularia

被引:78
作者
da Cunha, Keith C. [1 ,2 ]
Sutton, Deanna A. [3 ]
Fothergill, Annette W. [3 ]
Gene, Josepa [1 ,2 ]
Cano, Josep [1 ,2 ]
Madrid, Hugo [4 ]
de Hoog, Sybren [4 ]
Crous, Pedro W. [4 ]
Guarro, Josep [1 ,2 ]
机构
[1] Univ Rovira & Virgili, Mycol Unit, Sch Med, E-43201 Reus, Spain
[2] Univ Rovira & Virgili, IISPV, E-43201 Reus, Spain
[3] Univ Texas Hlth Sci Ctr San Antonio, Fungus Testing Lab, San Antonio, TX 78229 USA
[4] CBS KNAW Fungal Biodivers Ctr, NL-3508 AD Utrecht, Netherlands
关键词
Curvularia; Antifungal susceptibility; Molecular identification; ITS region; GPDH gene; CUTANEOUS PHEOHYPHOMYCOSIS; LUNATA; INFECTION; KERATITIS; COCHLIOBOLUS; VORICONAZOLE; PERITONITIS; BIPOLARIS; DISEASE; PATIENT;
D O I
10.1016/j.diagmicrobio.2013.02.034
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The in vitro antifungal susceptibility of a set of 99 clinical isolates of Curvularia was tested against 9 drugs using a reference microdilution method. The isolates had been identified previously to species level by comparing their ITS rDNA and glyceraldehyde-3-phosphate dehydrogenase gene sequences with those of reference strains. We were able to reliably identify 73.2% of the isolates, the most frequent species being Curvularia aeria, Curvularia geniculata/Curvularia senegalensis, Curvularia lunata, Curvularia inaequalis, Curvularia verruculosa, and Curvularia borreriae. Most of these isolates had been recovered from nasal sinus, which is generally considered one of the most frequent sites of infection by these fungi. In addition, at least 3 phylogenetic species that have not yet been formally described were detected. The most active drugs were the echinocandins, amphotericin B, and posaconazole, whereas voriconazole and itraconazole showed poor activity. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:168 / 174
页数:7
相关论文
共 44 条
  • [1] 2 CASES OF CUTANEOUS PHEOHYPHOMYCOSIS CAUSED BY CURVULARIA-PALLESCENS
    AGRAWAL, A
    SINGH, SM
    [J]. MYCOSES, 1995, 38 (7-8) : 301 - 303
  • [2] Molecular phylogenetic diversity of the emerging mucoralean fungus Apophysomyces: Proposal of three new species
    Alvarez, Eduardo
    Stchigel, Alberto M.
    Cano, Josep
    Sutton, Deanna A.
    Fothergill, Annette W.
    Chander, Jagdish
    Salas, Valentina
    Rinaldi, Michael G.
    Guarro, Josep
    [J]. REVISTA IBEROAMERICANA DE MICOLOGIA, 2010, 27 (02): : 80 - 89
  • [3] Allergic fungal rhinosinusitis caused by Curvularia sp
    Alvarez, Veronica C.
    Guelfand, Liliana
    Carlos Pidone, Juan
    Soloaga, Rolando
    Ontivero, Paula
    Margari, Alejandra
    Lopez Daneri, Gabriela
    [J]. REVISTA IBEROAMERICANA DE MICOLOGIA, 2011, 28 (02): : 104 - 106
  • [4] [Anonymous], 1976, MORE DEMATIACEOUS HY, DOI DOI 10.1079/9780851983653.0000
  • [5] [Anonymous], 2008, Reference method for broth dilution antifungal susceptibility testing of yeasts
  • [6] Voriconazole versus natamycin as primary treatment in fungal corneal ulcers
    Arora, Ritu
    Gupta, Deepa
    Goyal, Jawaharlal
    Kaur, Ravinder
    [J]. CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2011, 39 (05) : 434 - 440
  • [7] Cochliobolus phylogenetics and the origin of known, highly virulent pathogens, inferred from ITS and glyceraldehyde-3-phosphate dehydrogenase gene sequences
    Berbee, ML
    Pirseyedi, M
    Hubbard, S
    [J]. MYCOLOGIA, 1999, 91 (06) : 964 - 977
  • [8] Curvularia lunata Endophthalmitis
    Berbel, Rodrigo Fabri
    Barbante Casella, Antonio Marcelo
    de Freitas, Denise
    Hoefling-Lima, Ana Luisa
    [J]. JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS, 2011, 27 (05) : 535 - 537
  • [9] CURVULARIA-LUNATA ENDOCARDITIS TREATED WITH TERBINAFINE - CASE-REPORT
    BRYAN, CS
    SMITH, CW
    BERG, DE
    KARP, RB
    [J]. CLINICAL INFECTIOUS DISEASES, 1993, 16 (01) : 30 - 32
  • [10] Fatal cerebral phaeohyphomycosis due to Curvularia lunata in an immunocompetent patient
    Carter, E
    Boudreaux, C
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (11) : 5419 - 5423