In vitro susceptibility of invasive isolates of Candida spp. to anidulafungin, caspofungin, and micafungin:: Six years of global surveillance

被引:301
作者
Pfaller, M. A. [1 ]
Boyken, L. [1 ]
Hollis, R. J. [1 ]
Kroeger, J. [1 ]
Messer, S. A. [1 ]
Tendolkar, S. [1 ]
Diekema, D. J. [2 ]
机构
[1] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Pathol, Iowa City, IA 52242 USA
[2] Univ Iowa, Roy J & Lucille A Carver Coll Med, Dept Med, Iowa City, IA 52242 USA
关键词
D O I
10.1128/JCM.01901-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The echinocandins are being used increasingly as therapy for invasive candidiasis. Prospective sentinel surveillance for the emergence of in vitro resistance to the echinocandins among invasive Candida sp. isolates is indicated. We determined the in vitro activities of anidulafungin, caspofungin, and micafungin against 5,346 invasive (bloodstream or sterile-site) isolates of Candida spp. collected from over 90 medical centers worldwide from I January 2001 to 31 December 2006. We performed susceptibility testing according to the CLSI M27-A2 method and used RPMI 1640 broth, 24-h incubation, and a prominent inhibition endpoint for determination of the MICs. Of 5,346 invasive Candida sp. isolates, species distribution was 54% C. albicans, 14% C. parapsilosis, 14% C. glabrata, 12% C. tropicalis, 3% C. krusei, 1% C. guilliermondii, and 2% other Candida spp. Overall, all three echinocandins were very active against Candida: anidulafungin (MIC50, 0.06 mu g/ml; MIC90, 2 mu g/ml), caspofungin (MIC50, 0.03 mu g/ml; MIC90, 0.25 mu g/ml), micafungin (MIC50, 0.015 mu g/ml; MIC90, 2 mu g/ml). More than 99% of isolates were inhibited by <= 2 mu g/ml of all three agents. Results by species (expressed as the percentages of isolates inhibited by <= 2 mu g/ml of anidulafungin, caspofungin, and micafungin, respectively) were as follows: for C. albicans, 99.6%, 100%, and 100%; for C. parapsilosis, 92.5%, 99.9%, and 100%; for C. glabrata, 99.9%,99.9%, and 100%; for C. tropicalis, 100%, 99.8%, and 100%; for C. krusei, 100%, 100%, and 100%; and for C. guilliermondii, 90.2%, 95.1%, and 100%. There was no significant change in the activities of the three echinocandins over the 6-year study period and no difference in activity by geographic region. All three echinocandins have excellent in vitro activities against invasive strains of Candida isolated from centers worldwide. Our prospective sentinel surveillance reveals no evidence of emerging echinocandin resistance among invasive clinical isolates of Candida spp.
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页码:150 / 156
页数:7
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共 43 条
  • [1] Efficacy of micafungin for the treatment of candidemia
    Andes, D
    Safdar, N
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2005, 24 (10) : 662 - 664
  • [2] Effects of caspofungin against Candida guilliermondii and Candida parapsilosis
    Barchiesi, Francesco
    Spreghini, Elisabetta
    Tomassetti, Serena
    Della Vittoria, Agnese
    Arzeni, Daniela
    Manso, Esther
    Scalise, Giorgio
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (08) : 2719 - 2727
  • [3] Echinocandins for candidemia in adults without neutropenia
    Bennett, John E.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (11) : 1154 - 1159
  • [4] The echinocandins
    Cappelletty, Diane
    Eiselstein-McKitrick, Kasi
    [J]. PHARMACOTHERAPY, 2007, 27 (03): : 369 - 388
  • [5] A randomized, double-blind, parallel-group, dose-response study of micafungin compared with fluconazole for the treatment of esophageal candidiasis in HIV-positive patients
    de Wet, N
    Llanos-Cuentas, A
    Suleiman, J
    Baraldi, E
    Krantz, EF
    Della Negra, M
    Diekmann-Berndt, H
    [J]. CLINICAL INFECTIOUS DISEASES, 2004, 39 (06) : 842 - 849
  • [6] Identification of the FKS1 gene of Candida albicans as the essential target of 1,3-beta-D-glucan synthase inhibitors
    Douglas, CM
    DIppolito, JA
    Shei, GJ
    Meinz, M
    Onishi, J
    Marrinan, JA
    Li, W
    Abruzzo, GK
    Flattery, A
    Bartizal, K
    Mitchell, A
    Kurtz, MB
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (11) : 2471 - 2479
  • [7] Espinel-Ingroff Ana, 2003, Revista Iberoamericana de Micologia, V20, P121
  • [8] Emergence of a Candida krusei isolate with reduced susceptibility to caspofungin during therapy
    Hakki, Morgan
    Staab, Janet F.
    Marr, Meren A.
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (07) : 2522 - 2524
  • [9] Hazen KC, 2007, MANUAL OF CLINICAL MICROBIOLOGY, 9TH ED, P1762
  • [10] Caspofungin resistance in Candida albicans:: Correlating clinical outcome with laboratory susceptibility testing of three is genic isolates serially obtained from a patient with progressive candida esophagitis
    Hernandez, S
    López-Ribot, JL
    Najvar, LK
    McCarthy, DI
    Bocanegra, R
    Graybill, JR
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (04) : 1382 - 1383