http://orcid.org/0000-0002-6639-6058
Figures
Abstract
Background
Chromoblastomycosis (CBM) is a difficult-to-treat chronic subcutaneous mycosis. In Brazil, the main agent of this disease is Fonsecaea pedrosoi, which is phenotypically very similar to other Fonsecaea species, differing only genetically. The correct species identification is relevant since different species may differ in their epidemiologic aspects, clinical presentation, and treatment response.
Methodology/Principal findings
Partial sequencing of the internal transcribed spacer (ITS) was used to identify twenty clinical isolates of Fonsecaea spp. Their in vitro antifungal susceptibility was determined using the broth microdilution method, according to the M38-A2 protocol. Amphotericin B (AMB), flucytosine (5FC), terbinafine (TRB), fluconazole (FLC), itraconazole (ITC), ketoconazole (KTC), posaconazole (POS), voriconazole (VRC), ravuconazole (RVC), caspofungin (CAS), and micafungin (MFG) were tested. The association between ITC/TRB, AMB/5FC, and ITC/CAS was studied by the checkerboard method to check synergism. The available patients’ data were correlated with the obtained laboratory results. Fonsecaea monophora (n = 10), F. pedrosoi (n = 5), and F. nubica (n = 5) were identified as CBM’ agents in the study. TRB and VRC were the drugs with the best in vitro activity with minimal inhibitory concentrations (MIC) lower than 0.25 mg/L. On the other hand, FLC, 5FC, AMB, and MFG showed high MICs. The AMB/5FC combination was synergistic for three F. monophora strains while the others were indifferent. Patients had moderate or severe CBM, and ITC therapy was not sufficient for complete cure in most of the cases, requiring adjuvant surgical approaches.
Conclusions/Significance
F. monophora, the second most frequent Fonsecaea species in South America, predominated in patients raised and born in Rio de Janeiro, Brazil, without cerebral involvement in these cases. TRB, VRC, and the AMB/5FC combination should be further investigated as a treatment option for CBM.
Author summary
Chromoblastomycosis is a disfiguring disease usually occurring in rural workers from poor and remote communities. In Brazil, the most frequent agents of this neglected disease are the species belonging to the genus Fonsecaea. The disease occurs after traumatic inoculation during work. As the lesions progress, itching becomes severe, and scratching may result in further inoculation to other body sites. When patients seek medical help, the lesions are usually extensive and disfiguring. For this reason, a more effective and less time-consuming treatment is important. Oral antifungal therapy is not very effective, must be taken for months or years, it is costly for most patients and often unavailable. Hence, it is important to determine the in vitro antifungal susceptibility and correlate it with the isolated species. In this study, Fonsecaea monophora was the predominant species and, differently from some studies, dissemination to the central nervous system was not observed. In vitro analysis showed that the most effective antifungal drugs were terbinafine and voriconazole, followed by itraconazole, the most used drug in the treatment of this disease. The combination of amphotericin B and flucytosine may be synergistic, depending on the infective strain.
Citation: Coelho RA, Brito-Santos F, Figueiredo-Carvalho MHG, Silva JVdS, Gutierrez-Galhardo MC, do Valle ACF, et al. (2018) Molecular identification and antifungal susceptibility profiles of clinical strains of Fonsecaea spp. isolated from patients with chromoblastomycosis in Rio de Janeiro, Brazil. PLoS Negl Trop Dis 12(7): e0006675. https://doi.org/10.1371/journal.pntd.0006675
Editor: Todd B. Reynolds, University of Tennessee, UNITED STATES
Received: May 22, 2018; Accepted: July 9, 2018; Published: July 26, 2018
Copyright: © 2018 Coelho et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. The sequences obtained in this study have been deposited in GenBank under the accession numbers MF616485 – MF616504. All other relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by “Conselho Nacional de Desenvolvimento Científico e Tecnológico” [grant number 449184/2014-5 to RA-P] and “Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro” [grant number E-26/200.839/2017]. RA-P, RMZ-O and LT are partially supported by “Conselho Nacional de desenvolvimento Científico e Tecnológico” [grant numbers 305487/2015-9, 304976/2013-0 and 442837-2014-3]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Chromoblastomycosis (CBM) is a chronic fungal infection of cutaneous and subcutaneous tissues caused by traumatic implantation of several species of dematiaceous fungi [1]. In 2017, this mycosis was recognized as a neglected tropical disease by the World Health Organization [2].
The etiological agents of CBM belong mainly to the genera Cladophialophora, Phialophora, and Fonsecaea [3]. In the last decade, new species of the genus Fonsecaea have been described, based on molecular criteria: Fonsecaea monophora [4], Fonsecaea nubica [5], Fonsecaea multimorphosa [6], and Fonsecaea pugnacius [7]. These species can be found in nature, trace amounts in plant debris, thorns, and wood cortex, which provide microhabitats for these fungi [8]. In the Brazilian State of Maranhão, on the border of the Brazilian Amazon rainforest, several agricultural communities work on harvesting babassu (Orbignya phalerata), a wild palmacea specimen that was described as probable infection source in this area [9].
In the environment, all agents of CBM present in their mycelial form, which is composed by dematiaceous hyphae and conidia, which are specific for each genus. Infection usually follows a human trauma with a contaminated organic material such as plant thorns, wood, plant debris, grass, tree cortex among others, leading to the implantation of the fungus in the subcutaneous tissues, where the fungus changes to its parasitic form composed by muriform cells. These cells are heavily melanised and are extremely resistant to the harsh conditions imposed by the host immune system [10].
CBM can be caused by four Fonsecaea species: F. pedrosoi, F. nubica [4–6], F. monophora and F. pugnacius. The latter two show significant neurotropism, eventually leading to dissemination to the brain and other organs [4,7] or causing primary brain infection without skin lesions, which are classified as phaeohyphomycosis since no muriform cells are seen in tissues [10,11]. CBM may assume several clinical forms with different degrees of severity [10].
There is no treatment protocol to be followed, and antifungal therapy is often combined with physical methods such as cryosurgery or surgical excision for small lesions [12]. Itraconazole (ITC) and terbinafine (TRB) are the most used drugs in the treatment of CBM [10,13–15]. Other drugs used include posaconazole (POS), voriconazole (VRC), amphotericin B (AMB) and flucytosine (5FC) [10,16,17]. In addition, combined therapies of ITC with TRB [10,18], 5FC with AMB [17], or ITC with 5FC have been used [19].
It is important to determine the in vitro susceptibility of these isolates because of the difficulty found in the treatment of this mycosis and the frequency of refractory cases and relapses. The present study aimed to molecularly identify the species, to evaluate the in vitro susceptibility to antifungals, and to identify possible combinations of drugs with synergism against strains isolated from patients with CBM diagnosed in Rio de Janeiro state, Southeast Brazil, an area of low occurrence of this mycosis. Moreover, a clinical and laboratorial data association is provided for some patients.
Material and methods
Ethical statement
This study was approved by the Ethics Committee Board of the Evandro Chagas National Institute of Infectious Diseases (INI), Oswaldo Cruz Foundation (Fiocruz), under the number CAAE: 52247016.0.0000.5262.
Fungal isolates
Twenty isolates of dematiaceous fungi from skin lesions of 17 patients with CBM were included in this study. These isolates were stored from 1999 to 2015 at the INI Mycology Laboratory and identified phenotypically as Fonsecaea pedrosoi. From the total of 17 patients, 12 were treated at the INI's Infectious Dermatology Outpatient Clinic, 7 of which were previously studied by Mouchalouat et al.,[20] and the remaining 5 were followed up at other institutions after mycological diagnosis at the INI (Table 1). All stored fungi were recovered on Sabouraud Dextrose Agar (Difco Laboratories, Sparks, MD, USA) incubated at 25°C for 10 days. Microscopically, hyphae were septate, branched, and brown staining with the predominance of conidiophores with short chains of smooth, thin-walled dematiaceous conidia.
Molecular identification
Putative Fonsecaea spp. colonies were assessed on potato dextrose agar (PDA) (HiMedia Laboratories Pvt. Ltd., India) at 25°C after 7–14 days of inoculation. The DNA extraction and polymerase chain reaction (PCR) of the ITS1-5.8S-ITS2 region, the official Fungal DNA barcode, were performed according to Brito-Santos et al. [21]. PCR products were purified using the Wizard SV Gel and PCR Clean-Up System kit (Promega Corporation, Madison, USA) and sequenced at the Platform for DNA Sequencing PDTIS/Fiocruz. Sequences were edited using Sequencher 4.9 (Gene Codes Corporation, Ann Arbor, MI, USA), aligned and analyzed with MEGA 6.06 [22], and compared by BLAST with sequences available at the ISHAM ITS database (http://its.mycologylab.org). The molecular identification was considered valid when it presented more than 98.5% of identity, compared to the sequences available in the ISHAM-ITS database [23]. The evolutionary history was inferred by using the Maximum Likelihood method based on the Tamura-Nei model [24].
Antifungal susceptibility testing
In vitro antifungal susceptibility testing was performed according to the recommendations proposed in the Clinical and Laboratory Standards Institute (CLSI) M38-A2 protocol [25] with modifications. AMB, FLC, ketoconazole (KTC), POS, ITC, VRC, ravuconazole (RVC), 5FC, TRB, caspofungin (CAS) (all from Sigma-Aldrich Chemical Corporation, St. Louis, MO, USA) and micafungin (MFG) (Astellas Pharma Tech Corporation, Takaoka city, Toyama, Japan) were tested. The inoculum was prepared from a seven-day old PDA culture; the cells were harvested in RPMI medium and diluted to approximately 0.4–5 × 104 cells/mL. The plates were incubated at 35°C for five days [14]. The minimal inhibitory concentration (MIC) for AMB, FLC, KTC, POS, ITC, VRC, RVC, 5FC, and TRB; and the minimal effective concentration (MEC) for CAS and MFG were determined according to the CLSI M38-A2 protocol [25]. The reference strains Aspergillus flavus (ATCC 204304), Aspergillus fumigatus (ATCC 204305), Candida krusei (ATCC 6258) and Candida parapsilosis (ATCC 22019) were used for quality control.
Antifungal combination
The susceptibility test with antifungal combinations was performed by the checkerboard method, where two different drugs were applied at different concentrations in a single 96-well plate, so that in each well there were different concentrations of the antifungals in combination. The concentrations assayed in the combinations were ITC 0.0075–4 mg/L with TRB 0.015–1 mg/L; AMB 0.0075–4 mg/L with 5FC 0.06–4 mg/L; CAS 0.0075–4 mg/L with ITC 0.06–4 mg/L. Drug interaction, classified according to the fractional inhibitory concentration index (FICI), which defines the type of interaction between the antifungal agents in combination, was as follows: synergism if FICI ≤ 0.5; indifference if 0.5 < FICI ≤ 4 and antagonism if FICI > 4 [26,27]. The FICI was obtained by the sum of the fractional inhibitory concentrations (FIC) or by the formula: FICI ═ (A/MIC (a)) + (B/MIC (b)), where: A = MIC of the drug (a) in combination; MIC (a) = MIC of drug (a) alone; B = MIC of the drug (b) in combination; MIC (b) = MIC of drug (b) alone [28].
Statistical analyses
The geometric mean of MIC/MECs, MIC/MEC50, MIC/MEC90 and the MIC/MEC ranges were calculated using the Statistical Package for the Social Sciences v.17.0 (SPSS Inc, USA). Data analysis was performed in the GraphPad Prism 5 software. Kruskal-Wallis test was used to compare MIC of each antifungal drug between the different species. The Wilcoxon matched pairs test was used to compare MICs of two different drugs and the Friedman test to compare MICs of three or more antifungal drugs. P values lower than 0.05 were considered significant.
Results
Molecular identification
Ten isolates were identified as F. monophora (50%), five as F. pedrosoi (25%) and five as F. nubica (25%). The ITS sequencing alignment scores of the fungal isolates herein studied exhibited 99–100% identity compared with corresponding ITS sequences deposited in the ISHAM-ITS database (Fig 1). The ITS sequences obtained during this study were deposited in NCBI/GenBank under the accession numbers MF616485 –MF616504.
The percentage of trees in which the associated taxa clustered together is shown next to the branches. Initial tree(s) for the heuristic search were obtained automatically by applying Neighbor-Joining and BioNJ algorithms to a matrix of pairwise distances estimated using the Maximum Composite Likelihood (MCL) approach, and then selecting the topology with superior log likelihood value. The tree is drawn to scale, with branch lengths measured in the number of substitutions per site. The analysis involved 72 nucleotide sequences. All positions containing gaps and missing data were eliminated. Evolutionary analyses were conducted in MEGA 6 software [22]. Isolates of this study are marked with a filled circle. ITS Sequences of Fonsecaea brasiliensis, Fonsecaea erecta, and Fonsecaea multimorphosa were used as outgroups.
Antifungal susceptibility testing
Table 2 depicts the susceptibility profile of the strains included in this study. TRB (MIC range 0.015–0.25 mg/L) and VRC (MIC range 0.12–0.25 mg/L) were the antifungal drugs that showed the best in vitro activity against the Fonsecaea spp. isolates. FLC (MIC range 8–32 mg/L), 5FC (MIC range 2–32 mg/L), AMB (MIC range 4->16 mg/L) and echinocandins (MEC range 1–8 mg/L) showed higher MIC/MEC values. Overall, FLC was the azole with the poorest activity (P<0.0001) and among the echinocandins, CAS was more effective than MFG (P = 0.003). The susceptibility profile between the different species was very similar for the drugs tested. The few differences observed were as follows: F. pedrosoi presented MEC90 of 1 mg/L for MFG, while F. monophora and F. nubica presented both MEC90 of 8 mg/L (P = 0.0009) and F. monophora presented MIC50 and MIC90 of 8 mg/L for AMB, while F. pedrosoi and F. nubica presented MIC50 and MIC90 of 4mg/L for the same polyene drug (P = 0.0447). Although not significant (P = 0.0871), F. nubica presented MIC90 of 4 mg/L for 5FC, while for the other species the MIC90 was two-dilutions higher, that is, 16 mg/L.
Antifungal combination
According to the FICI, when 5FC and AMB were tested in combination, synergistic interaction (FICI ≤ 0.5) was observed in 3 F. monophora isolates (30%). For the combinations ITC/TRB and ITC/CAS, an indifferent interaction (0.5 < FICI ≤ 4.0) was observed for all isolates tested. S1 Table depicts the results of the three combinations of antifungal drugs herein studied.
Clinical and laboratorial correlation
It was possible to determine the probable site of infection for 9 out of the 12 patients with documented data, 8 of them in Rio de Janeiro and 1 in the Espírito Santo state. Among the patients infected in Rio de Janeiro, six were by F. monophora (75%) and two by F. nubica (25%). Regarding the geographic location, it is important to note that the three patients born and raised in Rio de Janeiro state were infected with F. monophora and all patients infected with F. pedrosoi were born outside the Rio de Janeiro state. In addition, two cases of F. pedrosoi without clinical data available (cases 13 and 14, Table 1) were diagnosed in patients from the Brazilian Amazon region.
Of the 12 patients followed up at INI, nine were cured; three of them used only antifungal drugs, two underwent surgical procedures, three used antifungal drugs associated with physical methods (cryosurgery and/or surgery) and one underwent surgery plus two sessions of cryosurgery (Table 3). The extension of treatment considering only the six patients who used antifungal drugs (ITC alone or in combination) ranged from 1 to 87 months (median = 9 months).
Regarding the severity of the disease, of the nine patients infected by F. monophora, clinical information was available for eight, five of which were characterized by the moderate form and three with the severe form. Moderate and severe CBM was also observed in patients infected with F. nubica, and moderate CBM was observed in the patient infected by F. pedrosoi with available clinical data. The only case of cutaneous disseminated CBM was observed in a patient with F. monophora. The only case with tumor lesion was observed in another patient with F. monophora. Of the patients infected by F. monophora, seven were cured and one had no outcome information. Regarding the five patients with no clinical data, three were infected with F. pedrosoi, one with F. monophora and one with F. nubica.
Extracutaneous manifestations of the disease were not observed in any case, regardless of the isolated species.
Discussion
This work represents a case series study of CBM for a period of 16 years in one of the main reference centers for infectious diseases in Rio de Janeiro. Studies on CBM in other Brazilian regions have been conducted in this decade by several groups [29–31], but in all these studies, data from Rio de Janeiro was missing. We believe that this study can be an important clinic-laboratorial contribution to the knowledge of the disease and an update to the actual Brazilian situation of CBM.
All four species of Fonsecaea up to now related to CBM are found in Brazil [5,7,32,33]. F. pedrosoi is the predominant species in South America, followed by F. monophora [34]. Rio de Janeiro, the geographic region where this study was conducted, is an area of low occurrence of CBM in Brazil [20], which explains the limited number of cases during the studied period. The high frequency of F. monophora in our study may indicate a reservoir for this species in this region. The fact that all patients born and raised in Rio de Janeiro were infected by F. monophora supports this hypothesis.
This is first study that evaluate in vitro antifungal susceptibility of CBM isolates in Rio de Janeiro. We found high MIC values for AMB corroborating other authors [35,36]. Treatment with AMB alone or combined with 5FC has not been used since the introduction of ITC during the 1980s. The frequent occurrence of nephrotoxicity, due to the drug characteristics and prolonged treatment [37,38], together with the reactivation of the infection with the drug discontinuation [10,34] are factors that hinder the use of AMB for CBM therapy.
The Fonsecaea strains included in this study presented low MIC values for KTC, similar to other studies [14,35,39]. This drug was the first systemic imidazole available, but it is rarely used due to serious hepatic reactions, as well as severe drug interactions [40,41]. Nowadays, ITC is considered the most commonly used drug for CBM treatment [10]. In this study, the MIC values for this drug indicate susceptibility of the isolates to the antifungal agent [42], and the schemes using ITC alone or associated with other antifungal or surgical modalities was able to lead 7 patients to cure.
POS, VRC and RVC represent the new generation of triazoles with a broad spectrum of activity and a favourable pharmacokinetic profile [43]. POS is known to have a better in vitro activity than ITC against clinical Fonsecaea isolates [44] in accordance with the results of this study. VRC has good in vitro activity against CBM agents, including Fonsecaea spp. [45]. However, in addition to its high cost [46], the prescription of VRC should be done with caution, since it presents risk of photo toxicity and cutaneous carcinoma in prolonged periods of treatment [47]. To the best of our knowledge, this is the first study on Fonsecaea spp. susceptibility to RVC using the CLSI M38-A2 protocol. González et al. [48] reported the in vitro activity of RVC against isolates of F. pedrosoi with MICs ranging between 0.125–0.5 mg/L using M38-A CLSI protocol. Despite the use of another protocol, this work reports MIC values ≤ 1 mg/L for the same drug against clinical Fonsecaea isolates. However, based on our results that showed POS and VRC with a better in vitro profile than RVC, the first two azoles should be considered in the treatment of CBM, instead of RVC.
The MIC values found for 5FC and FLC were compatible with other studies, showing that these drugs are ineffective in vitro against Fonsecaea spp., discouraging their use in CBM treatment [35,39,44]. As for 5FC, its use in the mid-1960s marked the beginning of chemotherapy approaches for CBM [45]. However, it was later observed that F. pedrosoi is able to develop in vitro resistance to 5FC [45,49–53]. Although not prohibited, the drug is not registered in the Brazilian regulatory agency (ANVISA) and is not commercialized on the Brazilian market [54], because there is no pharmaceutical industry that manufactures this antifungal drug in our country, which leads to a need to its import by tertiary hospitals.
Several studies have reported the susceptibility of Fonsecaea spp. to TRB, revealing its potent action against various filamentous fungi and in the treatment of CBM, demonstrating up to 80% of cure rate [14,39,55,56]. Our results were consistent with those studies showing low MIC values for this drug. In addition, TRB shows a potent antifibrotic effect in recent lesions [57]. This drug has little affinity for the cytochrome P450 enzyme system, resulting in less interaction with other substances [58] and in a general way, is well-tolerated, indicating an effective option for the treatment of CBM.
Echinocandins have a limited role in the treatment of CBM due to high MEC values for F. monophora and F. nubica, as observed in other studies [44,59]. Isolates of F. pedrosoi presented a better in vitro response to MFG. Nevertheless, due to the low number of analysed isolates, it is suggested that further studies will assess whether this echinocandin is specifically effective against F. pedrosoi.
According to some studies, in particular CBM cases, the best therapeutic strategy would be the association of two antifungals based on the results of previous susceptibility tests [17]. Some of the suggested combinations are AMB and 5FC [45,60] or ITC and TRB [61]. Our work showed a synergism between AMB and 5FC in three F. monophora isolates. This combination has two distinct mechanisms enhancing the antifungal action: AMB binds to ergosterol of the fungus membrane forming pores and 5FC acts inhibiting the synthesis of nucleic acids. This combination is widely used in cases of cryptococcal meningitis because it has a more effective penetration into the SNC [62]. In the past, the combination AMB/5FC had been used for CBM treatment [17,63,64], but now a days it is no longer considered due to the adverse side effects [10]. However, we believe that this association could be beneficial in severe cases of CBM, especially those with brain involvement. The synergism found for 100% of the isolates of Phialophora verrucosa by Li et al. [18] encouraged the use of ITC and CAS combination in our study. A single study [65] found synergism for isolates of F. monophora. An indifferent interaction was observed in all Fonsecaea isolates of this study, which is compatible with most studies [15,17,61].
There are few studies comparing in vitro susceptibility among clinical Fonsecaea isolates. Najafzadeh et al. [44] found no significant differences among species in the activity of eight antifungals (AMB, FLC, ITC, VRC, POS, CAS, anidulafungin and isavuconazole) against F. pedrosoi, F. monophora and F. nubica. However, in this study, F. monophora showed higher MIC values than F. nubica for AMB (P = 0.0447), and the species F. monophora and F. nubica (P = 0.0009) had higher MEC values for MFG when compared to F. pedrosoi.
CBM is known as a difficult-to-treat disease, there is no standard drug of choice and relapses are frequent [10,34,45,57,66]. There are many factors that can influence the patient outcome that can be related to the host or the fungal species. The host immune response, local lymphedema, and fibrosis become a barrier for a proper drug bioavailability at the site of infection. In addition, muriform cells are heavily pigmented and represent a resistant fungal form against antimicrobial compounds [67]. In the same vein, there is no clear correlation between in vitro susceptibility and clinical practice [45]. In general, MIC values ≤ 1 mg/L usually indicate a potential susceptibility of most drugs used in the treatment of infections by dematiaceous fungi [14,42], as occurred in this study. It is also possible that the broth microdilution test is not the best method to guide therapeutic management in CBM. In fact, in a correlation study between different antifungal susceptibility methodologies and clinical outcome of cryptococcosis patients treated with AMB showed that time-kill assays are more suitable to predict treatment failure than broth microdilution and gradient diffusion methods [68]. Further studies are necessary to check if a similar scenario occurs in CBM.
Due to the hardships to obtain the parasitic form of the CBM agents in vitro [67,69], most authors perform antifungal susceptibility testing using conidia. This is not an invalid strategy, since a similar scenario occurs in sporotrichosis, another deep mycosis, for what the official antifungal susceptibility testing guidelines suggest the use of conidia instead of the parasitic yeast-like form [25]. However, we are aware that this can be a bias in the correlation of in vitro and in vivo results.
We were not able to observe clear relationships between the treatment responses and the antifungal susceptibility of the isolates. ITC was used in almost all clinical cases, because it is distributed free of charge in our institution. However, most of patients only presented a slight improvement with this drug, despite the MIC observed. It is common the development of fibrosis in lesions of CBM [70], what hinders the action of the drugs, since it prevents their penetration [71]. In addition, ITC needs an acidic gastric environment to be properly absorbed [72]. A decrease in the production of gastric juice may result in a higher pH of the stomach, thus reducing the bioavailability of this drug and therefore its activity [73,74]. No synergism was observed between ITC and TRB in this study and the two cases treated with this drug combination required surgical approaches for complete cure. In a study with CBM cases, to which drugs were administered together for a long period of time, failure was observed. So, the authors chose to weekly alternate these drugs, with a positive outcome in some cases [61].
In summary, this study demonstrated that TRB and VRC exhibited better in vitro activity against Fonsecaea spp., while AMB, FLC, 5FC and echinocandins played a limited role in the CBM treatment because of their relatively high MICs. However, AMB and 5FC presented in vitro synergism for a few strains, which may be useful as a salvage therapy. ITC, although with higher MICs, were used alone or in association and lead to cure in moderate to severe clinical cases. Despite the fact that we did not use TRB as the sole therapeutic drug in the patients herein described, we believe that more attention should be given to this antifungal in the context of CBM treatment, due to the low MIC values observed in this study as well as safety and effectiveness in other studies [56].
Our work provides perspectives for future studies of clinical follow-up, treatment and outcome of patients with CBM, as well as the determination of in vitro susceptibility to antifungal and new compounds with fungicidal action, especially in melanized fungi.
Supporting information
S1 Table. Fractional inhibitory concentration index values of three antifungal combinations for clinical isolates of Fonsecaea spp.
https://doi.org/10.1371/journal.pntd.0006675.s001
(DOCX)
Acknowledgments
We are grateful for the technical contribution with patients’ data of the Evandro Chagas National Institute of Infectious Diseases (INI), Oswaldo Cruz Foundation (Fiocruz), to the sequencing platform team (PDTIS) at Fiocruz for automated nucleotide sequencing of the strains and to the students who helped in the mycological analyses.
References
- 1. Ameen M. Chromoblastomycosis: clinical presentation and management. Clin Exp Dermatol. 2009;34: 849–854. pmid:19575735
- 2.
WHO. Report of the Tenth Meeting of the WHO Strategic and Technical Advisory Group for Negleted Tropical Diseases [Internet]. World Health Organization, Geneva; 2017. Available: http://www.who.int/neglected_diseases/NTD_STAG_report_2017.pdf
- 3. Ameen M. Managing chromoblastomycosis. Trop Doct. 2010;40: 65–67. pmid:20305094
- 4. De Hoog G, Attili-Angelis D, Vicente V. Molecular ecology and pathogenic potential of Fonsecaea species. Med Mycol. 2004;42: 405–416. pmid:15552642
- 5. Najafzadeh MJ, Sun J, Vicente V, Xi L, van den Ende AHGG, de Hoog GS. Fonsecaea nubica sp. nov, a new agent of human chromoblastomycosis revealed using molecular data. Med Mycol. 2010;48: 800–806. pmid:20302550
- 6. Najafzadeh MJ, Sun J, Vicente VA, Klaassen C, Bonifaz A, Gerrits van den Ende A, et al. Molecular epidemiology of Fonsecaea species. Emerg Infect Dis. 2011;17: 464–469. pmid:21392438
- 7. de Azevedo CMPS Gomes RR, Vicente VA Santos DWCL, Marques SG, do Nascimento MMF, et al. Fonsecaea pugnacius, a Novel Agent of Disseminated Chromoblastomycosis. J Clin Microbiol. 2015;53: 2674–2685. pmid:26085610
- 8. Vicente VA, Najafzadeh MJ, Sun J, Gomes RR, Robl D, Marques SG, et al. Environmental siblings of black agents of human chromoblastomycosis. Fungal Divers. 2014;65: 47–63.
- 9. Marques SG, Silva C de MP, Saldanha PC, Rezende MA, Vicente VA, Queiroz-Telles F, et al. Isolation of Fonsecaea pedrosoi from the shell of the babassu coconut (Orbignya phalerata Martius) in the Amazon region of Maranhão Brazil. Nihon Ishinkin Gakkai Zasshi Jpn J Med Mycol. 2006;47: 305–311.
- 10. Queiroz-Telles F, de Hoog S, Santos DWCL, Salgado CG, Vicente VA, Bonifaz A, et al. Chromoblastomycosis. Clin Microbiol Rev. 2017;30: 233–276. pmid:27856522
- 11. Surash S, Tyagi A, De Hoog GS, Zeng JS, Barton RC, Hobson RP. Cerebral phaeohyphomycosis caused by Fonsecaea monophora. Med Mycol. 2005;43: 465–72. pmid:16178376
- 12. Torres-Guerrero E, Isa-Isa R, Isa M, Arenas R. Chromoblastomycosis. Clin Dermatol. 2012;30: 403–408. pmid:22682188
- 13. López Martínez R, Méndez Tovar LJ. Chromoblastomycosis. Clin Dermatol. 2007;25: 188–194. pmid:17350498
- 14. Daboit TC, Massotti Magagnin C, Heidrich D, Czekster Antochevis L, Vigolo S, Collares Meirelles L, et al. In vitro susceptibility of chromoblastomycosis agents to five antifungal drugs and to the combination of terbinafine and amphotericin B. Mycoses. 2014;57: 116–120. pmid:23895037
- 15. Daboit TC, Magagnin CM, Heidrich D, Castrillón MR, Mendes SDC, Vettorato G, et al. A Case of Relapsed Chromoblastomycosis Due to Fonsecaea monophora: Antifungal Susceptibility and Phylogenetic Analysis. Mycopathologia. 2013;176: 139–144. pmid:23645135
- 16. Lima AM de, Sacht GL, Paula LZP de, Aseka GK, Goetz HS, Gheller MF, et al. Response of chromoblastomycosis to voriconazole. An Bras Dermatol. 2016;91: 679–681. pmid:27828652
- 17. Poirriez J, Breuillard F, Francois N, Fruit J, Sendid B, Gross S, et al. A case of chromomycosis treated by a combination of cryotherapy, shaving, oral 5-fluorocytosine, and oral amphotericin B. Am J Trop Med Hyg. 2000;63: 61–63. pmid:11357997
- 18. Li Y, Wan Z, Li R. In vitro activities of nine antifungal drugs and their combinations against Phialophora verrucosa. Antimicrob Agents Chemother. 2014;58: 5609–5612. pmid:24982078
- 19. Antonello VS, Silva MCA da, Cambruzzi E, Kliemann DA, Santos BR, Queiroz-Telles F. Treatment of severe chromoblastomycosis with itraconazole and 5-flucytosine association. Rev Inst Med Trop São Paulo. 2010;52: 329–331. pmid:21225217
- 20. Mouchalouat M de F, Gutierrez Galhardo MC, Zancopé-Oliveira RM, Monteiro Fialho PC, de Oliveira Coelho JMC, Tavares S, et al. Chromoblastomycosis: a clinical and molecular study of 18 cases in Rio de Janeiro, Brazil. Int J Dermatol. 2011;50: 981–986. pmid:21781072
- 21. Brito-Santos F, Figueiredo-Carvalho MHG, Coelho RA, Sales A, Almeida-Paes R. Tinea Capitis by Microsporum audouinii: Case Reports and Review of Published Global Literature 2000–2016. Mycopathologia. 2017;182: 1053–1060. pmid:28736794
- 22. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0. Mol Biol Evol. 2013;30: 2725–2729. pmid:24132122
- 23. Irinyi L, Serena C, Garcia-Hermoso D, Arabatzis M, Desnos-Ollivier M, Vu D, et al. International Society of Human and Animal Mycology (ISHAM)-ITS reference DNA barcoding database—the quality controlled standard tool for routine identification of human and animal pathogenic fungi. Med Mycol. 2015;53: 313–337. pmid:25802363
- 24. Tamura K, Nei M. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol. 1993;10: 512–526. pmid:8336541
- 25.
CLSI—Clinical and Laboratory Standars Institute. Reference method for broth dilution antifungal susceptibility testing of filamentous fungi. Approved standard-second edition. Wayne, PA. USA: Clinical and Laboratory Standards Institute.; 2008.
- 26. Odds FC. Synergy, antagonism, and what the chequerboard puts between them. J Antimicrob Chemother. 2003;52: 1–1. pmid:12805255
- 27. Dannaoui E, Afeltra J, Meis JF, Verweij PE, Network E, others. In vitro susceptibilities of zygomycetes to combinations of antimicrobial agents. Antimicrob Agents Chemother. 2002;46: 2708–2711. pmid:12121963
- 28. Yu J, Li R, Zhang M, Liu L, Wan Z. In vitro interaction of terbinafine with itraconazole and amphotericin B against fungi causing chromoblastomycosis in China. Med Mycol. 2008;46: 745–747. pmid:18608889
- 29. Minotto R, Bernardi CDV, Mallmann LF, Edelweiss MIA, Scroferneker ML. Chromoblastomycosis: A review of 100 cases in the state of Rio Grande do Sul, Brazil. J Am Acad Dermatol. 2001;44: 585–592. pmid:11260530
- 30. de Bona E, Canton LM, Meneghello Fuentefria A. Chromoblastomycosis in Santa Catarina state, Brazil. Rev Cubana Med Trop. 2010;62: 254–256. pmid:23437557
- 31. Pires CAA, Xavier MB, Quaresma JAS, Macedo GMM de, Sousa BR de M, Brito AC de. Clinical, epidemiological and mycological report on 65 patients from the Eastern Amazon region with chromoblastomycosis. An Bras Dermatol. 2012; 555–560. pmid:22892768
- 32. Najafzadeh M, Gueidan C, Badali H, Van Den Ende AG, Xi L, Hoog G de. Genetic diversity and species delimitation in the opportunistic genus Fonsecaea. Med Mycol. 2009;47: 17–25. pmid:19107635
- 33. Gomes RR, Vicente VA, de Azevedo CM, Salgado CG, da Silva MB, Queiroz-Telles F, et al. Molecular Epidemiology of Agents of Human Chromoblastomycosis in Brazil with the Description of Two Novel Species. PLoS Negl Trop Dis. 2016;10: e0005102. pmid:27893750
- 34. Queiroz-Telles F, Santos DW de CL. Challenges in the therapy of chromoblastomycosis. Mycopathologia. 2013;175: 477–488. pmid:23636730
- 35. Bedout C de Gómez BL, Restrepo A. In vitro susceptibility testing of Fonsecaea pedrosoi to antifungals. Rev Inst Med Trop São Paulo. 1997; 145–148. pmid:9460254
- 36. Rasamoelina T, Raharolahy O, Rakotozandrindrainy N, Ranaivo I, Andrianarison M, Rakotonirina B, et al. Chromoblastomycosis and sporotrichosis, two endemic but neglected fungal infections in Madagascar. J Mycol Medicale. 2017;27: 312–324. pmid:28847419
- 37. Sawaya BP, Briggs JP, Schnermann J. Amphotericin B nephrotoxicity: the adverse consequences of altered membrane properties. J Am Soc Nephrol JASN. 1995;6: 154–164. pmid:7579079
- 38. Tonin FS, Steimbach LM, Borba HH, Sanches AC, Wiens A, Pontarolo R, et al. Efficacy and safety of amphotericin B formulations: a network meta-analysis and a multicriteria decision analysis. J Pharm Pharmacol. 2017; pmid:28815602
- 39. Andrade TS, Castro LG, Nunes RS, Gimenes VM, Cury AE. Susceptibility of sequential Fonsecaea pedrosoi isolates from chromoblastomycosis patients to antifungal agents. Mycoses. 2004;47: 216–221. pmid:15189187
- 40.
ANVISA. Anvisa alerta para o risco de reações hepáticas graves associadas ao uso oral do cetoconazol. [Internet]. Alerta SNVS/Anvisa/Nuvig/GFARM no 08; 2013. Available: http://portal.anvisa.gov.br/informacoes-tecnicas13/-/asset_publisher/FXrpx9qY7FbU/content/alerta-snvs-anvisa-nuvig-gfarm-n-08-de-7-de-novembro-de-2013/33868/pop_up?_101_INSTANCE_FXrpx9qY7FbU_viewMode=print&_101_INSTANCE_FXrpx9qY7FbU_languageId=en_US
- 41.
EMA EMA. European Medicines Agency recommends suspension of marketing authorisations for oral ketoconazole. [Internet]. London: European Medicines Agency; 2013. Available: http://www.ema.europa.eu/docs/en_GB/document_library/Referrals_document/Ketoconazole-containing_medicines/WC500146616.pdf
- 42. Revankar SG, Sutton DA. Melanized Fungi in Human Disease. Clin Microbiol Rev. 2010;23: 884–928. pmid:20930077
- 43. Blyth CC. Antifungal azoles: old and new. Pediatr Infect Dis J. 2011;30: 506–507. pmid:21587027
- 44. Najafzadeh MJ, Badali H, Illnait-Zaragozi MT, De Hoog GS, Meis JF. In Vitro Activities of Eight Antifungal Drugs against 55 Clinical Isolates of Fonsecaea spp. Antimicrob Agents Chemother. 2010;54: 1636–1638. pmid:20086140
- 45. Queiroz-Telles F, Esterre P, Perez-Blanco M, Vitale RG, Salgado CG, Bonifaz A. Chromoblastomycosis: an overview of clinical manifestations, diagnosis and treatment. Med Mycol. 2009;47: 3–15. pmid:19085206
- 46. Koo S, Klompas M, Marty FM. Fonsecaea monophora cerebral phaeohyphomycosis: case report of successful surgical excision and voriconazole treatment and review. Med Mycol. 2010;48: 769–774. pmid:20100141
- 47. Epaulard O, Leccia M-T, Blanche S, Chosidow O, Mamzer-Bruneel M-F, Ravaud P, et al. Phototoxicity and photocarcinogenesis associated with voriconazole. Med Mal Infect. 2011;41: 639–645. pmid:22055586
- 48. González GM, Fothergill AW, Sutton DA, Rinaldi MG, Loebenberg D. In vitro activities of new and established triazoles against opportunistic filamentous and dimorphic fungi. Med Mycol. 2005;43: 281–284. pmid:16010855
- 49. Bopp C. Terapia da Cromoblastomicose com um novo método. Med Cutan Ibero Lat Am. 1976;4: 285–292. pmid:798082
- 50.
Rippon JW. Medical mycology: the pathogenic fungi and the pathogenic actinomycetes. 3rd ed. Philadelphia, PA: WB Saunders; 1988.
- 51. Restrepo A. Treatment of tropical mycoses. J Am Acad Dermatol. 1994;31: S91–102. pmid:8077517
- 52. Attapattu MC. Chromoblastomycosis—a clinical and mycological study of 71 cases from Sri Lanka. Mycopathologia. 1997;137: 145–151. pmid:9368408
- 53. Bonifaz A, Paredes-Solís V, Saúl A. Treating chromoblastomycosis with systemic antifungals. Expert Opin Pharmacother. 2004;5: 247–254. pmid:14996622
- 54. Yamauti SM, Bonfim JR de A, Barberato-Filho S, Lopes LC. A essencialidade e racionalidade da lista nacional brasileira de medicamentos essenciais. Cienc Saude Coletiva. 2017;22: 975–986. pmid:28301004
- 55. McGinnis MR, Pasarell L. In vitro testing of susceptibilities of filamentous ascomycetes to voriconazole, itraconazole, and amphotericin B, with consideration of phylogenetic implications. J Clin Microbiol. 1998;36: 2353–2355. pmid:9666022
- 56. Esterre P, Inzan CK, Ramarcel ER, Andriantsimahavandy A, Ratsioharana M, Pecarrere JL, et al. Treatment of chromomycosis with terbinafine: preliminary results of an open pilot study. Br J Dermatol. 1996;134 Suppl 46: 33–36; discussion 40.
- 57. Esterre P, Queiroz-Telles F. Management of chromoblastomycosis: novel perspectives. Curr Opin Infect Dis. 2006;19: 148–152. pmid:16514339
- 58. Schmitt JV, Bombonatto G, Trierweiler SM, Fabri AB. General aspects of drug interactions with systemic antifungals in a retrospective study sample. An Bras Dermatol. 2013;88: 476–479. pmid:23793213
- 59. Badali H, Fernández-González M, Mousavi B, Illnait-Zaragozi MT, González-Rodríguez JC, de Hoog GS, et al. Chromoblastomycosis due to Fonsecaea pedrosoi and F. monophora in Cuba. Mycopathologia. 2013;175: 439–444. pmid:23471535
- 60. Bonifaz A, Martínez-Soto E, Carrasco-Gerard E, Peniche J. Treatment of chromoblastomycosis with itraconazole, cryosurgery, and a combination of both. Int J Dermatol. 1997;36: 542–547. pmid:9268758
- 61. Gupta AK, Taborda PR, Sanzovo AD. Alternate week and combination itraconazole and terbinafine therapy for chromoblastomycosis caused by Fonsecaea pedrosoi in Brazil. Med Mycol. 2002;40: 529–534. pmid:12462534
- 62. Perfect JR, Dismukes WE, Dromer F, Goldman DL, Graybill JR, Hamill RJ, et al. Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the infectious diseases society of america. Clin Infect Dis Off Publ Infect Dis Soc Am. 2010;50: 291–322. pmid:20047480
- 63. Lopes CF, Resende MA, Alvarenga RJ, Moreira YK. Combinação de 5-fluorocitosina e anfotericina B no tratamento de cromomicose. Med Cutan Ibero Lat Am. 1979;7: 1–7. pmid:398931
- 64. Astorga E, Bonilla E, Martínez C, Mura W. Treatment of chromoblastomycosis with amphotericin B and 5-fluorocytosine. Med Cutan Ibero Lat Am. 1981;9: 125–128. pmid:7026925
- 65. Zhang J, Xi L, Zhang H, Xie Z, Sun J, Li X, et al. Synergistic effects of terbinafine and itraconazole on clinical isolates of Fonsecaea monophora. Eur J Dermatol. 2009;19: 451–455. pmid:19502155
- 66. Queiroz-Telles F, McGinnis MR, Salkin I, Graybill JR. Subcutaneous mycoses. Subcutaneous Mycoses. 2003;17: 59–85. pmid:12751261
- 67. da Silva JP, Alviano DS, Alviano CS, de Souza W, Travassos LR, Diniz JAP, et al. Comparison of Fonsecaea pedrosoi sclerotic cells obtained in vivo and in vitro: ultrastructure and antigenicity. FEMS Immunol Med Microbiol. 2002;33: 63–69. pmid:11985971
- 68. Córdoba S, Vivot W, Szusz W, Isla G, Davel G. Comparison of different in vitro tests to detect Cryptococcus neoformans not susceptible to amphotericin B. Mycopathologia. 2015;179: 359–371. pmid:25700663
- 69. Mendoza L, Karuppayil SM, Szaniszlo PJ. Calcium regulates in vitro dimorphism in chromoblastomycotic fungi. Mycoses. 1993;36: 157–164. pmid:8264711
- 70. Uribe F, Zuluaga AI, Leon W, Restrepo A. Histopathology of chromoblastomycosis. Mycopathologia. 1989;105: 1–6. pmid:2739689
- 71. Yang Y, Hu Y, Zhang J, Li X, Lu C, Liang Y, et al. A refractory case of chromoblastomycosis due to Fonsecaea monophora with improvement by photodynamic therapy. Med Mycol. 2012;50: 649–653. pmid:22309458
- 72. Bae SK, Park S-J, Shim E-J, Mun J-H, Kim E-Y, Shin J-G, et al. Increased oral bioavailability of itraconazole and its active metabolite, 7-hydroxyitraconazole, when coadministered with a vitamin C beverage in healthy participants. J Clin Pharmacol. 2011;51: 444–451. pmid:20400647
- 73. Hof H. Mycoses in the elderly. Eur J Clin Microbiol Infect Dis Off Publ Eur Soc Clin Microbiol. 2010;29: 5–13. pmid:19911208
- 74. Allegra S, Fatiguso G, De Francia S, Favata F, Pirro E, Carcieri C, et al. Pharmacokinetic evaluation of oral itraconazole for antifungal prophylaxis in children. Clin Exp Pharmacol Physiol. 2017;44: 1083–1088. pmid:28744925