Invasive Trichosporon Infection: a Systematic Review on a Re-emerging Fungal Pathogen

被引:132
作者
Almeida Junior, Joao N. de [1 ,2 ]
Hennequin, Christophe [3 ,4 ,5 ]
机构
[1] Univ Sao Paulo, Fac Med, Cent Lab Div LIM03, Sao Paulo, Brazil
[2] Univ Sao Paulo, Inst Med Trop, Lab Med Mycol LIM53, Sao Paulo, Brazil
[3] Hop St Antoine, AP HP, Serv Parasitol Mycol, Paris, France
[4] UPMC, Sorbonne Univ, Ctr Natl Rech Sci ERL 8255, Inst Natl Sante & Rech Med UMR 1135, Paris, France
[5] Ctr Immunol & Malad Infect, Bd Hop, Paris, France
关键词
Trichosporon species; invasive infection; risk factors; prognosis; diagnosis; treatment; antifungal resistance; ACUTE MYELOID-LEUKEMIA; AMBULATORY PERITONEAL-DIALYSIS; LIPOSOMAL AMPHOTERICIN-B; BLOOD-STREAM INFECTIONS; INTENSIVE-CARE-UNIT; ANTIFUNGAL SUSCEPTIBILITY PROFILE; MULTIDRUG-RESISTANT TRICHOSPORON; ACUTE LYMPHOBLASTIC-LEUKEMIA; KIDNEY-TRANSPLANT RECIPIENT; OF-THE-LITERATURE;
D O I
10.3389/fmicb.2016.01629
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Objectives: This review aimed to better depict the clinical features and address the issue of therapeutic management of Trichosporon deep-seated infections. Methods: We comprehensively reviewed the cases of invasive Trichosporon infection reported in the literature from 1994 (date of taxonomic modification) to 2015. Data from antifungal susceptibility testing (AST) studies were also analyzed. Results: Two hundred and three cases were retained and split into four groups: homeopathy (n = 79), other immunodeficiency conditions (n = 41), miscellaneous (n = 58) and newborns (n = 25). Trichosporon asahii was the main causative species (46.7%) and may exhibit cross-resistance to different antifungal classes. The unfavorable outcome rate was at 44.3%. By multivariate analysis, breakthrough infection (OR 2.45) was associated with unfavorable outcome, whilst the use of an azole-based therapy improved the prognosis (OR 0.16). Voriconazole-based treatment was associated with favorable outcome in hematological patients (73.6 vs. 41.8%; p = 0.016). Compiled data from AST demonstrated that (i) T asahii exhibits the highest MICs to amphotericin B and (ii) voriconazole has the best in vitro efficacy against clinical isolates of Trichosporon spp. Conclusions: Trichosporon infection is not only restricted to hematological patients. Analysis of compiled data from AST and clinical outcome support the use of voriconazole as first line therapy.
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页数:18
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共 188 条
[1]   Trichosporon asahii fatal infection in a non-neutropenic patient after orthotopic liver transplantation [J].
Abdala, E ;
Lopes, RI ;
Chaves, CN ;
Heins-Vaccari, EM ;
Shikanai-Yasuda, MA .
TRANSPLANT INFECTIOUS DISEASE, 2005, 7 (3-4) :162-165
[2]   Identification of the first isolates of Trichosporon asahii var. asahii from disseminated trichosporonosis in China [J].
Abliz, P ;
Fukushima, K ;
Takizawa, K ;
Yang, RY ;
Li, RY ;
Nishimura, K .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 44 (01) :17-22
[3]   Breakthrough trichosporonosis in patients with acute myeloid leukemia receiving micafungin [J].
Akagi, Tomoaki ;
Yamaguti, Kohei ;
Kawamura, Tizuko ;
Nakumura, Toshihiko ;
Kubo, Komei ;
Takemori, Hiromitu .
LEUKEMIA & LYMPHOMA, 2006, 47 (06) :1182-1183
[4]   Invasive Trichosporon infection in solid organ transplant patients: a report of two cases identified using IGS1 ribosomal DNA sequencing and a review of the literature [J].
Almeida Junior, J. N. ;
Song, A. T. W. ;
Campos, S. V. ;
Strabelli, T. M. V. ;
Del Negro, G. M. ;
Figueiredo, D. S. Y. ;
Motta, A. L. ;
Rossi, F. ;
Guitard, J. ;
Benard, G. ;
Hennequin, C. .
TRANSPLANT INFECTIOUS DISEASE, 2014, 16 (01) :135-140
[5]   AZOLE THERAPY FOR TRICHOSPORONOSIS - CLINICAL-EVALUATION OF 8 PATIENTS, EXPERIMENTAL-THERAPY FOR MURINE INFECTION, AND REVIEW [J].
ANAISSIE, E ;
GOKASLAN, A ;
HACHEM, R ;
RUBIN, R ;
GRIFFIN, G ;
ROBINSON, R ;
SOBEL, J ;
BODEY, G .
CLINICAL INFECTIOUS DISEASES, 1992, 15 (05) :781-787
[6]   Fungemia due to Trichosporon asahii in a neutropenic child refractory to amphotericin B -: Clearance with voriconazole [J].
Antachopoulos, C ;
Papakonstantinou, E ;
Dotis, J ;
Bibashi, E ;
Tamiolaki, M ;
Koliouskas, D ;
Roilides, E .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2005, 27 (05) :283-285
[7]  
Anuradha S, 2000, J Assoc Physicians India, V48, P1022
[8]   Sequence-based identification, genotyping and EUCAST antifungal susceptibilities of Trichosporon clinical isolates from Greece [J].
Arabatzis, M. ;
Abel, P. ;
Kanellopoulou, M. ;
Adamou, D. ;
Alexandrou-Athanasoulis, H. ;
Stathi, A. ;
Platsouka, E. ;
Milioni, A. ;
Pangalis, A. ;
Velegraki, A. .
CLINICAL MICROBIOLOGY AND INFECTION, 2014, 20 (08) :777-783
[9]   ESCMID† and ECMM‡ joint clinical guidelines for the diagnosis and management of rare invasive yeast infections [J].
Arendrup, M. C. ;
Boekhout, T. ;
Akova, M. ;
Meis, J. F. ;
Cornely, O. A. ;
Lortholary, O. .
CLINICAL MICROBIOLOGY AND INFECTION, 2014, 20 :76-98
[10]   Comparison of NCCLS microdilution method and Etest in antifungal susceptibility testing of clinical Trichosporon asahii isolates [J].
Arikan, S ;
Hasçelik, G .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 43 (02) :107-111