Antifungal susceptibility profile of Trichosporon isolates: correlation between CLSI and etest methodologies

MEDICAL MICROBIOLOGY

Antifungal susceptibility profile of Trichosporon isolates: correlation between CLSI and etest methodologies

Raquel M.L. Lemes^I; Juliana P. Lyon^II,*; Leonardo M. Moreira^III; Maria Aparecida de Resende^I

^IDepartamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brasil

^IIInstituto de Pesquisa e Desenvolvimento da Universidade do Vale do Paraíba, São José dos Campos, SP, Brasil

^IIIDepartamento de Engenharia Biomédica da Universidade Federal de São João Del Rei, São João Del Rei, MG, Brasil

ABSTRACT

The aim of the present study was to evaluate the antifungal susceptibility profile of Trichosporon species isolated from different sources employing the Clinical and Laboratory Standards Institute (CLSI) method and E-test method. Thirty-four isolates of Trichosporon spp. and six CBS reference samples were tested for their susceptibility to Amphotericin B, 5-flucytosine, Fluconazole, Itraconazole, Voriconazole and Terbinafine. All species showed high Minimun Inhibitory Concentrations (MIC) for Itraconazole and susceptibility to Fluconazole, The comparison among the results obtained by the CLSI method and E-test revealed larger discrepancies among 5-flucytosine and Itraconazole. The present work provides epidemiological data that could influence therapeutic choices. Furthermore, the comparison between different methodologies could help to analyze results obtained by different laboratories.

Key words: Trichosporon spp., antifungal drugs, CLSI, E-test

INTRODUCTION

Systemic fungal infections occur with increasing frequency in hospitalized patients. Although Candida species account for the majority of fungal systemic diseases, the number of yeasts that can cause infection continues to increase. In recent years, several reports of trichosporonosis have appeared (3, 6, 11, 16) Trichosporon infections are associated with a wide spectrum of clinical manifestations, ranging from superficial cutaneous involvement in immunocompetent individuals to severe systemic disease in immunocompromised patients (19).

Trichosporonosis is mainly caused by six species: T. asahii and T. mucoides are causative agents of deep-seated infection, T. cutaneum and T. asteroides cause superficial infections, and T. ovoides and T. inkin are involved in white piedra of the head and genital area, respectively (4, 17). Kustimur et al. (6) reported the first case of disseminated infection due to T. asteroides in an intensive care patient.). Carvalho et al. (2) reported a systemic infection involving T. cutaneum in a child with Wilm's tumour and Neves et al. (9) isolated T. pulullans from the oral cavity of an HIV positive patient.

The increase in the incidence and morbidity of fungal infections has caused interest in the development of new appropriate therapeutics (13). The CLSI method (8) for antifungal susceptibility testing includes the genera Candida and Cryptococcus, but not Trichosporon spp. According to Arikan and Hasçelik (1), it is unknown whether there is any species-related variation in the antifungal susceptibility profile of Trichosporon isolates. Additionally, the concordance between the methodologies used to delineate antifungal susceptibility profiles has not been extensively accessed for Trichosporn spp.

The present study was undertaken to determine the in vitro antifungal susceptibility profile of different species of Trichosporon isolates by using the CLSI reference method and E-test. The epidemiological data obtained could be helpful in the development of therapeutic strategies. Besides, the comparison between different methodologies is important to analyze results obtained by different laboratories.

MATERIAL AND METHODS

Isolates

Thirty-four isolates belonging to the collection of the laboratory of Mycology of the department of Microbiology of the Federal University of Minas Gerais were tested. The isolates were obtained from different sources: urine (12), oropharynx (8), blood (4), nail (3) skin (3), hair (1), bronchoalveolar lavage (1), fingers (1) and environment (1). The isolates were previously identified using morphological, physiological and biochemical proofs according with Kurtzman and Fell (4). The tests employed for identification were macroscopic appearance of the giant colony, microscopic features, susceptibility to cycloheximide, growth temperature, diazonium Blue color reaction, urease production and carbohydrate and nitrogen assimilation profiles. Six CBS reference samples (CENTRAALBUREAU VOOR SCHIMMELCULTURES, Baarn, The Netherlands) were included in susceptibility testing: T. asahii (CBS - 2479), T. coremiiforme (CBS -2482), T. asteroides (CBS -3481), T. inkin (CBS -5585), T. mucoides (CBS -7625) and T. ovoides (CBS - 7556). All the strains were maintained at 4º C on Sabouraud Dextrose Agar (SDA, Difco, Detroit, MI, USA) with 300 µg/ml of chloramphenicol and BHI broth (Brain Antifungal susceptibility profile of Trichosporon isolates Heart Infusion, Difco), until susceptibility tests were carried out. Transfers were done at 3-month intervals. The isolates were stored for three months.

Antifungal susceptibility testing

CLSI method-Susceptibility testing was performed according to the M27-A2 document of the CLSI (8). Amphotericin B (Sigma Chemical Co., St. Louis, USA), 5flucytosine (Hoffman La Roche, Bale, Switzerland), Fluconazole (Pfizer São Paulo, Brazil), Itraconazole (Janssen Pharmaceutica, São Paulo, Brazil), Voriconazole (Pfizer, São Paulo, Brazil), and Terbinafine (Novartis Biociências S.A., São Paulo, Brazil) were obtained as reagent grade powders from their respective manufacturers. Dilutions were made in RPMI 1640 medium (Sigma, St Louis, Mo, USA) buffered to pH 7 with 0,165M (3[N-morpholino] propanesulfonic acid) buffer (Sigma). The inoculum was prepared in a concentration of 1-5 x 10⁶ cells/ml. The final concentration of the inoculums was 1.0 × 10³ to 1.5 × 10³ cell/ml. The final concentration of the antifungal agents was 0.03 to 16 µg/ml for Itraconazole, 0.12 to 64.0 µg/ml for Amphotericin B, Voriconazole, Terbinafine, and Fluconazole and 0.25 to 128.0 fg/ml for 5-flucytosin. Trays were incubated at 35ºC and MIC (Minimum Inhibitory Concentration) endpoints were read after 48h of incubation. Drug free and yeast controls were included.

Following incubation, the MICs of Fluconazole, Terbinafine, Voriconazole and Itraconazole were read as the lowest concentration at which prominent decrease in turbidity relative to the growth control was observed (decrease of 80% in turbidity). For Amphotericin B and 5-flucytosine, MIC was considered as the complete inhibition of growth. Quality control was ensured by testing the CLSI recommended strain C. parapsilosis ATCC 22019. The isolate was considered to be susceptible if the MIC value was 2-8µg/ml for Fluconazole, < 0,125µg/ml for Itraconazole, 8-16µg/ml for 5-flucytosine, and < 1µg/ml for Amphotericin B, as suggested by Wolf et al (19) and < 1µg/ml for Voriconazole, as suggested by Pfaller et al (10). The isolate was considered to be susceptible if the MIC value for Terbinafine was s 1.4 µg/ml, as considered for Candida albicans by Ryder et al (13).

E-test

All the samples were tested by E-test for susceptibility profile. The test was performed according to the manufacturer's instructions (AB Biodisk, Solna, Sweden). Briefly, the inoculum concentration was adjusted to a 0.5 McFarland standard for Candida species (1-5 x 10⁶ cell/ml). Then, 0.5 ml of this suspension was inoculated onto plates containing RPMI 1640 agar (1.5%) with 2% glucose using a cotton swab. After a period of 15 minutes, the E-test strips Antifungal susceptibility profile of Trichosporon isolates were applied. The antifungal drugs Amphotericin B, Itraconazole, Fluconazole and 5-flucytosine were tested. The plates were incubated at 35º C and read after 24 and 48 hours.

RESULTS

MICs of Voriconazole, Terbinafine, Amphotericin B, 5 flucytosine, Fluconazole and Itraconazole for six CBS Trichosporon spp. strains are represented in Table 1. Amphotericin B, 5 - flucytosine, Fluconazole and Itraconazole were tested by both, CLSI and E-test methods.

Results shown in table 2 regarding MIC₅₀ and MIC₉₀ (MIC for 50 % and 90 % of the strains tested respectively) reveal that T. mucoides was susceptible to Amphotericin B (1/ 1µg/ ml), Terbinafine (0.5/ 1µg/ ml), and Voriconazole (0.25/ 0.5 µg/ml), while the other species were resistant to these drugs (8, 11, 16) All species showed resistance to Itraconazole and susceptibility to Fluconazole, according to the parameters suggested by Wolf et al (16). T. ovoides showed susceptibility to Fluconazole and 5-flucytoosine only.

The samples of Trichosporon spp. were submitted to comparison between the two methods (CLSI and E-test). Only one sample (T. ovoides) showed resistance to Amphotericin B by the CLSI method (2 µg/ ml) and susceptibility to this drug by E-test (0,75 µg/ ml). When the samples were compared for 5-flucytosine, two (T. mucoides, MIC_{50/ 90} > 250 / > 32 µg/ ml and T. asahii, MIC_{50/ 90} 16/ >32 µg/ ml) showed resistance in both methods. Regarding Itraconazole, two isolates showed susceptibility by the E-test and resistance by CLSI method. The parameters for resistance and susceptibility are those proposed by Wolf et al (16) and Pfaller et al (8).

DISCUSSION

The comparison of the susceptibility profile of CBS reference samples with the data available in the literature reveals that the results obtained for T. asahii (CBS 2479) in the present work were concordant with those obtained by Wolf et al. (19) for Amphotericin B and Fluconazole. When we compared the results obtained in the present work by the CLSI method of (2µg/ml), with those obtained by Ghého et al. (4), (0,019µg/ ml) the discrepancy among MICs obtained for Itraconazole against T. mucoides and T. ovoides reached 100 folds the dilution. The comparisons allowed the observation of the differences in MIC values obtained for different groups, even considering reference samples. These differences emphasize the importance of the standardized intra-laboratory conduct, since results obtained in our experiment were compatible with those obtained by Wolf et al. (19) that also used a visual system of evaluation, while Guého et al. (4) used an automatic system.

The presented data reveal a profile of high resistance of the genus Trichosporon to Amphotericin B and Itraconazole, high susceptibility to Fluconazole and moderate resistance to 5-flucytosine. Rodriguez-Tudela et al. (12) reported that the majority of the T. asahii, T. faecali and T. coremiiforme exhibited resistance to Amphotericin B in vitro. Li et al. (7) reported resistance to Amphotericin B among T. asahii, T. cutaneum and T. inkii strains. Differently, Uzun et al. (18), analyzing the in vitro susceptibility of eight samples of Trichosporon spp. reported that those samples were susceptible to Amphotericin B, but susceptible to Fluconazole. Silva, et al., (15) also evaluate the antifungal susceptibility profile of T. asahii clinical isolates. The isolates had reduced susceptibility in vitro to all drugs, showing 4-6 times higher MICs to itraconazole and 3-4 times to 5-flucytosine compared of MICs breakpoint values. In this study, Fluconazole exhibited the best activity in vitro against the majority of the isolates (90%), with MIC of 16 fg/ml and only one isolate with 32 fg/ml. Three isolates have MIC value for Amphotericin B above 2 fg/ml.

Variable susceptibility to Amphotericin B has been observed with samples of the genus Trichosporon, especially among isolates obtained from immunocompromised patients. This observation could result in a better conduct for antifungal therapy. On the other hand, Fluconazole was effective indicating that the azolic can be the valid option in the therapy of this infection, commonly difficult to treat.

Resistance to Itraconazole was observed in all of the Trichosporon species, as well as susceptibility to the Fluconazole. Only T. mucoides was susceptible to Amphotericin B, Terbinafine and Voriconazole, being the other species resistant to these drugs. The results obtained in this work with Voriconazole, when compared to those obtained by Uzun et al. (17) were surprisingly more than 30 times higher. On the other hand, Serena et al. (14) used a guinea pig model of systemic trichosporonosis to demonstrate a better efficacy of Voriconazole in comparison with Amphotericin B.

Regarding the comparison between the CLSI method and the E-test, the greater divergence from those reported in previous works were obtained for 5-flucytosine, while data obtained for Amphotericin B were considerably in agreement with other researchers. Although the number of samples analyzed is small, the correlation between the two methods for Amphotericin B is significant (1, 4, 19).

Trichosporon species has been increasingly involved in systemic infections and, despite this fact, there are relatively few studies about its antifungal susceptibility profile. Although these data do not correlate the susceptibility "in vitro/in vivo", the present work provides epidemiological data that could influence therapeutic choices. Furthermore, the comparison between different methodologies could help to analyze results obtained by different laboratories.

ACKNOWLEDGEMENTS

This work was supported by CNPq (Conselho Nacional de Pesquisa)

Submitted: April 08, 2009; Returned to authors for corrections: December 03, 2009; Approved: February 18, 2010.

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Publication Dates

• Publication in this collection
  16 Apr 2010
• Date of issue
  June 2010

History

• Reviewed
  03 Dec 2009
• Received
  08 Apr 2009
• Accepted
  18 Feb 2010