Abstract:A total of 21 Trichosporon spp. isolates from blood over a period of 5 years (January 2009 to December 2013) were included in the study. The most common underlying diseases found were pancreatitis (33.3%) and cancer (33.3%). Trichosporon asahii (80.9%) was the commonest species followed by Trichosporon mycotoxinivorans (14.2%) and Trichosporon faecale (4.7%). On IGS1 region sequencing the most predominant T. asahii type in our region was genotype 1 (16/17 isolates; 94.1%) and one isolate belonged to genotype 4… Show more
“…A noteworthy finding of our study is that only a limited number of Trichosporon isolates (10.5% [14/133 isolates]) were isolated from patients with hematological malignances, which were earlier reported to be one of the major underlying conditions (4, 5). Dabas et al also found that the incidence rate for Trichosporon bloodstream infections was lower in patients with malignancies than in those with gastrointestinal manifestations (22). In a study conducted by the Invasive Fungal Infection Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group in cancer patients (5,23), involving 30 centers and lasting 2 years, 269 cases of fungemia were reported but only 3 were caused by Trichosporon spp.…”
A total of 133 clinical Trichosporon isolates were collected in the National China Hospital Invasive Fungal Surveillance Net (CHIF-NET) program in 2009 to 2016. Accurate identification was performed by sequencing of the intergenic spacer 1 (IGS1) region. Among these isolates, Trichosporon asahii (108 isolates [81.2%]) was the leading species, followed by Trichosporon dermatis (7 isolates [5.3%]), Trichosporon asteroides (5 isolates [3.8%]), Trichosporon inkin (5 isolates [3.8%]), Trichosporon dohaense (3 isolates [2.3%]), and 1 isolate (0.7%) each of Trichosporon faecale, Trichosporon jirovecii, Trichosporon mucoides, Trichosporon coremiiforme, and Trichosporon montevideense. Both the Vitek mass spectrometry (MS) (bioMérieux, Marcy l'Etoile, France) and Bruker Biotyper MS (Bruker Daltonics GmbH, Germany) platforms gave high levels (Ͼ97.5%) of correct identification when the species were present in the database. The geometric mean (GM) of amphotericin B MICs for T. asahii was 2-fold higher than that for non-asahii Trichosporon. High fluconazole MICs (Ն8 g/ml) were observed for 25% of T. asahii isolates (27/108 isolates) and 16% of non-asahii Trichosporon (4/25 isolates) isolates. Itraconazole MICs were Յ0.5 g/ml for 89.5% of the isolates. Voriconazole was the most potent antifungal agent in vitro, with a GM of 0.09 g/ml. Genotyping of the isolates using IGS1 sequence alignment revealed that genotype 1 was most common (41.7%), followed by genotype 4 (31.5%), genotype 3 (23.1%), genotype 5 (0.9%), genotype 6 (0.9%), and genotype 7 (1.8%). Our data on species distribution, genotypes, and antifungal susceptibilities may contribute to a better understanding of the epidemiology of invasive Trichosporon infections throughout China.
“…A noteworthy finding of our study is that only a limited number of Trichosporon isolates (10.5% [14/133 isolates]) were isolated from patients with hematological malignances, which were earlier reported to be one of the major underlying conditions (4, 5). Dabas et al also found that the incidence rate for Trichosporon bloodstream infections was lower in patients with malignancies than in those with gastrointestinal manifestations (22). In a study conducted by the Invasive Fungal Infection Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group in cancer patients (5,23), involving 30 centers and lasting 2 years, 269 cases of fungemia were reported but only 3 were caused by Trichosporon spp.…”
A total of 133 clinical Trichosporon isolates were collected in the National China Hospital Invasive Fungal Surveillance Net (CHIF-NET) program in 2009 to 2016. Accurate identification was performed by sequencing of the intergenic spacer 1 (IGS1) region. Among these isolates, Trichosporon asahii (108 isolates [81.2%]) was the leading species, followed by Trichosporon dermatis (7 isolates [5.3%]), Trichosporon asteroides (5 isolates [3.8%]), Trichosporon inkin (5 isolates [3.8%]), Trichosporon dohaense (3 isolates [2.3%]), and 1 isolate (0.7%) each of Trichosporon faecale, Trichosporon jirovecii, Trichosporon mucoides, Trichosporon coremiiforme, and Trichosporon montevideense. Both the Vitek mass spectrometry (MS) (bioMérieux, Marcy l'Etoile, France) and Bruker Biotyper MS (Bruker Daltonics GmbH, Germany) platforms gave high levels (Ͼ97.5%) of correct identification when the species were present in the database. The geometric mean (GM) of amphotericin B MICs for T. asahii was 2-fold higher than that for non-asahii Trichosporon. High fluconazole MICs (Ն8 g/ml) were observed for 25% of T. asahii isolates (27/108 isolates) and 16% of non-asahii Trichosporon (4/25 isolates) isolates. Itraconazole MICs were Յ0.5 g/ml for 89.5% of the isolates. Voriconazole was the most potent antifungal agent in vitro, with a GM of 0.09 g/ml. Genotyping of the isolates using IGS1 sequence alignment revealed that genotype 1 was most common (41.7%), followed by genotype 4 (31.5%), genotype 3 (23.1%), genotype 5 (0.9%), genotype 6 (0.9%), and genotype 7 (1.8%). Our data on species distribution, genotypes, and antifungal susceptibilities may contribute to a better understanding of the epidemiology of invasive Trichosporon infections throughout China.
“…mycotoxinivorans (formerly Trichosporon mycotoxinivorans) is now considered a relevant pathogen for patients with cystic fibrosis (16). Moreover, this microorganism has been related to deep-seated infections in immunocompromised patients with invasive disposals in India (17). The use of Bruker's MALDI-TOF MS as a reliable tool for A. mycotoxinivorans species identification has helped strengthen the epidemiologic link of T. mycotoxinivorans to cystic fibrosis (18,19).…”
Trichosporon species are relevant etiologic agents of hospital-acquired infections. High mortality rates are attributed to Trichosporon deep-seated infections in immunocompromised individuals, making fast and accurate species identification relevant for hastening the discovery of best-targeted therapy. Recently, Trichosporon taxonomy has been reassessed, and three genera have been proposed for the pathogenic species: Trichosporon, Cutaneotrichosporon, and Apiotrichum. Matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) has replaced old phenotypic methods for microorganism identification in clinical laboratories, but spectral profile databases have to be evaluated and improved for optimal species identification performance. Vitek MS (bioMérieux) is one of the commercially available MALDI-TOF MS platforms for pathogen identification, and its spectral profile databases remain poorly evaluated for Trichosporon, Cutaneotrichosporon, and Apiotrichum species identification. We herein evaluated and improved Vitek MS for the identification of the main clinical relevant species of Trichosporon, Cutaneotrichosporon, and Apiotrichum using a large set of strains and isolates belonging to different yeast collections in Brazil and France.KEYWORDS Trichosporon, Cutaneotrichosporon, Apiotrichum, Vitek M, MALDI-TOF mass spectrometry O pportunistic non-Candida yeasts, including Trichosporon spp., are emerging pathogens of deep-seated infections in the context of immunodepression and/or invasive procedures (1, 2). In addition, outbreaks of catheter-related fungemia by these pathogens have been described in neonatal intensive care units (3).Based on molecular phylogenetic analysis, Trichosporon pathogenic species were initially subdivided into three clades: clade Porosum, which included the species
“…A growing population of immunocompromised patients has resulted in frequent diagnoses of invasive fungal infections (IFIs), including those caused by unusual yeasts ( Dabas et al, 2017 ). Invasive candidiasis is a growing concern worldwide with high morbidity and mortality; it affects patients of all ages, including patients with malignancies, HIV-negative immunocompromised (IC) patients, and non-immunocompromised (NIC) patients among those who are critically ill, often admitted to an intensive care unit (ICU), or diagnosed with diabetes mellitus or uncontrolled hyperglycemia requiring invasive mechanical ventilation ( Berdal et al, 2014 ; Bitar et al, 2014 ; Epelbaum and Chasan, 2017 ; Alves et al, 2018 ; Ding et al, 2018 ; Mantadakis et al, 2018 ).…”
To determine the dynamic changes of pathogenic yeast prevalence and antifungal susceptibility patterns in tertiary hospitals in China, we analyzed 527 yeast isolates preserved in the
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