Feline sporotrichosis: associations between clinical-epidemiological profiles and phenotypic-genotypic characteristics of the etiological agents in the Rio de Janeiro epizootic area

BACKGROUND Sporotrichosis is caused by species of the genus Sporothrix. From 1998 to 2015, 4,703 cats were diagnosed at the Fundação Oswaldo Cruz (Fiocruz), Rio de Janeiro, Brazil. Even after the description of the Sporothrix species, the characterisation of feline isolates is not performed routinely. OBJECTIVES To characterise the clinical isolates from cats at the species level and correlate them with the clinical and epidemiological characteristics of the cats. METHODS Forty seven Sporothrix spp. isolates from cats assisted at Fiocruz from 2010 to 2011 were included. Medical records were consulted to obtain the clinical and epidemiological data. The isolates were identified through their morphological and physiological characteristics. T3B polymerase chain reaction (PCR) fingerprinting was used for molecular identification of the species. FINDINGS In phenotypic tests, 34 isolates were characterised as S. brasiliensis, one as S. schenckii and 12 as Sporothrix spp. PCR identified all isolates as S. brasiliensis. MAIN CONCLUSIONS S. brasiliensis is the only etiological agent of feline sporotrichosis in Rio de Janeiro to date. None association was found between the isolates and the clinical and epidemiological data. In addition, we strongly recommend the use of molecular techniques for the identification of isolates of Sporothrix spp.

S. brasiliensis has been described as an emerging species, highly pathogenic to humans and cats, which to date has a regional distribution in Brazil (Marimon et al. 2007, Arrillaga-Moncrieff et al. 2009, Oliveira et al. 2011a, Rodrigues et al. 2013b). S. schenckii sensu stricto is considered the second most pathogenic species (Arrillaga-Moncrieff et al. 2009), and has a worldwide distribution, with a greater preference for tropical and subtropical humid climate countries, so the highest incidence of this mycosis occurs in Americas, Africa, Australia and Asia (Marimon et al. 2007, Lopez-Romero et al. 2011, Oliveira et al. 2011a, Chakrabarti et al. 2015. The cases related to S. globosa occurred in humans in Europe, Asia and Americas (Marimon et al. 2007, Liu et al. 2014, including Brazil (Oliveira et al. 2011a, Rodrigues et al. 2013b. Regarding S. mexicana, it has been believed to be an environmental species restricted to Mexico, being isolated initially in plants from there (Marimon et al. 2007). However, this species was also isolated in a human case in Portugal (Dias et al. 2011) and in three human cases in Brazil (Rodrigues et al. 2013a). S. luriei is a rare species, the descriptions of human and animal sporotrichosis cases caused by this species are scarce, so far it has been reported as the causal agent of four human cases in Africa (Marimon et al. 2008) and one canine case in Brazil (Oliveira et al. 2011b). S. pallida is rarely described as a causal agent of sporotrichosis, with one human case described in the USA (Morrison et al. 2013) and one feline case in Brazil (Oliveira et al. 2011b). Although recently described, S. chilensis was isolated from a human case and environmental sample in Chile (Rodrigues et al. 2016a).
Since 1998, a large number of sporotrichosis cases in humans and cats have been described in the metropolitan region of Rio de Janeiro, Brazil, the first sporotrichosis epidemic in the form of zoonosis. Since then, the Evandro Chagas National Institute of Infectious Diseases (INI), Oswaldo Cruz Foundation (Fiocruz), a reference centre in the diagnosis of mycoses, diagnosed 4,188 human cases in the period from 1997 to 2011 (Silva et al. 2012) and 4,703 feline cases from 1998 to 2015 (Gremião et al. 2017).
Classically, the transmission of the etiological agent occurs through the skin by traumatic inoculation of the fungus present in vegetal or organic matter in the soil contaminated by conidia of Sporothrix spp. (Lopez-Romero et al. 2011). On rare occasions, infection can be acquired by inhalation of the conidia (Lopez-Romero et al. 2011). However, the epidemic in Rio de Janeiro has a particular profile due to the importance of zoonotic transmission, that occurs mainly through scratching and/or biting by naturally infected domestic cats (Silva et al. 2012), which transmit the yeast form of the fungus present in the nails and oral cavity of these animals (Schubach et al. 2004).
In recent years, the frequency of reported cases of sporotrichosis in cats has been increasing in Brazil, notably in Rio de Janeiro (Schubach et al. 2004, Gremião et al. 2017). Infection in cats may begin subclinically and progress to multiple skin lesions and fatal systemic form, associated or not with extracutaneous signs (Schubach et al. 2004).
A definitive diagnosis of sporotrichosis requires isolating the fungus in a culture medium (Lopez-Romero et al. 2011). The culture technique characterises the fungus as Sporothrix spp. or S. schenkii latu sensu, so, in order to characterise the species, polyphasic taxonomy has to be used (Oliveira et al. 2011a). The pathogenic species of the genus Sporothrix are very similar macroscopically; microscopically show very subtle differences and the carbohydrate assimilation pattern is very similar, which makes it difficult to identify them using only the taxonomic key initially proposed by previous study (Marimon et al. 2007).
Although there are clinical studies on feline sporotrichosis, the relationship between the clinical data of cats and the identification of the species of the genus Sporothrix has not been properly investigated. The aim of the present study was to characterise the clinical isolates of Sporothrix spp. from naturally infected cats from Rio de Janeiro, based on phenotypic and genotypic identification. In addition, the clinical-epidemiological profile of these cats and its correlation with the morphological, physiological and molecular aspects of fungal isolates were described.

MATERIALS AND METHODS
Forty-seven isolates of Sporothrix spp. from cats assisted at the INI/Fiocruz from 2010 to 2011 were includ-ed, which were obtained from skin and mucosal lesions of the cats before the beginning of antifungal treatment (ketoconazole at doses 9,2 to 38,5 mg/kg/day or itraconazole at doses 8,3 to 34,5 mg/kg/day). Twenty-five cats received itraconazole (Itraconazol 100 mg; Prati Donaduzzi) as treatment and the remaining 22 cats received ketoconazole (Cetoconazol 200 mg; Prati Donaduzzi). The isolates were subsequently stored in 10% skimmed milk (Fluka Analytical, Sigma-Aldrich, Switzerland) at -20ºC in the Mycology Laboratory of INI/Fiocruz. Clinical and epidemiological data were subsequently collected from the medical records of the cats.
To identify the fungal isolates at the species level, polyphasic taxonomy was used, with morphological, physiological and molecular studies, with the isolate in its filamentous form being used at all of these stages. For the phenotypic tests, the isolates were subcultured in potato dextrose agar (PDA -Difco TM ; Becton, Dickinson and Company, Sparks MD USA) and visually examined for DHN melanin production (Almeida-Paes et al. 2015). In order to study conidiogenesis, these isolates were subcultured on corn meal agar (BBL TM ; BD, Franklin Lakes NJ USA), and incubated at 30ºC in a dark environment. After 10 days, microscopic characteristics were evaluated (Marimon et al. 2007).
The growth of colonies at 30ºC and 37ºC in PDA medium was evaluated after 21 days of incubation, when the diameter of the colonies was measured, with this test being performed in triplicate at different times (Marimon et al. 2007, Oliveira et al. 2011a. Carbohydrate assimilation tests were performed in 96-well racks containing Yeast Nitrogen Base -YNB culture medium (Difco™; Becton, Dickinson and Company, Sparks, MD USA) supplemented with sucrose or raffinose in a 0.5% concentration (Marimon et al. 2007, Oliveira et al. 2011a. For the control, to check the stability of the carbon sources in the culture medium, was used a Rhodotorula mucilaginosa isolate (IPEC41978), which has the capacity to assimilate all the carbohydrates tested. Negative control wells were supplemented with sterile distilled water and positive controls were added with glucose. In the carbohydrate assimilation test, the reading was performed on the 10th day. After this time of incubation, the media containing sucrose and raffinose were analysed. The media with similar growth to the medium with glucose were considered positive, and negative were those similar to the medium without carbohydrate. After obtaining the results of the morphological and physiological tests, we interpreted them based on the taxonomic key proposed previously (Marimon et al. 2007(Marimon et al. , 2008. For the classification of the isolates for thermotolerance, the percentage inhibition of growth was calculated as previously reported (Almeida-Paes et al. 2015). For isolates whose growth at 37ºC was reduced by 50% or more were classified as having low thermotolerance, and the isolates whose growth was reduced by less than 50% were classified as having high thermotolerance.
Subsequently, all the isolates were identified by means of genotypic testing, the genomic DNA being extracted from the filamentous form with the use of chloroform/isoamyl alcohol (24:1) (Oliveira et al. 2011a). The molecular tool used was a polymerase chain reaction (PCR) fingerprinting using the universal T3B primer (5'-AGGTCGCGGGTTCGAATCC-3') to distinguish between the species of the genus Sporothrix . Strains of species of the genus Sporothrix associated with cases found in humans and animals, S. brasiliensis (IPEC16490), S. globosa (IPEC27135), S. mexicana (MUM11.02), and S. schenckii (IPEC27722) were used as controls for molecular identification. Succinctly, we used the PCR reaction mix 10x buffer with KCl, dNTP mix 0.2 mM, MgCl 2 50 mM, platinum Taq DNA polymerase 1.0 U and 10 mM T3B primer . The T3B fingerprinting profiles obtained were analysed with Bionumerics (version 5.1; Applied Maths BVBA, Sint-Martens Latem, Belgium). Similarity coefficients were calculated using the Dice algorithm and cluster analysis was performed by means of the unweighted paired group method using arithmetic averages (UPGMA).
Georeferencing was performed from the addresses of felines, residents of the capital and other municipalities in the state of Rio de Janeiro. For this, an individual search of the addresses was done in the animal records. The address was marked as a point in the free Google Earth Pro program, allowing the identification of latitude and longitude. LatLong designed coordinates system was used. The coordinates of each point identified in Google Earth Pro were inserted in a shapefile of Rio de Janeiro, resulting in a new digital mesh. The shapefile is a vector format of geospatial data that is used in Geographic Information System (GIS) environments.
The exploratory analysis of the data was performed by applying the simple frequencies of each isolate to the species level of the genus Sporothrix, as well as the clinical variables of the cats (distribution of skin lesions, occurrence of lymphadenomegaly, presence of respiratory signs, presence of mucosal lesions and therapeutic response). Also, the epidemiological variables (origin and possible form of cat infection), both described in individual clinical records from the study were evaluated. For the distribution of skin lesions, the cats were divided into three groups: L1 (skin lesions in one place), L2 (skin lesions in two noncontiguous places) and L3 (skin lesions in three or more nonadjacent places) (Schubach et al. 2004).
To check the association between categorical variables, Fisher's exact test or Pearson's chi-square test were used. For the correlation of related samples the Wilcoxon test was used. For evaluation of treatment time (in weeks) to favorable outcome (clinical cure) stratified by categorical variables, the Kaplan-Meier method (KM) and Log-rank test were used. Failure events (failure of treatment, abandonment of treatment, death by sporotrichosis and death by other causes) were considered censoring by KM analysis and its length of time considered the time until last follow-up date. P-values < 0.05 indicated significant associations in the statistical tests. The data obtained with the phenotypic tests were stored and analysed in the database using the software Statistical Package for Social Science (SPSS) version 16.0.
The procedures performed in these animals were approved by the Ethics in Research Committee of the Fiocruz (CEUA/Fiocruz), Rio de Janeiro, Brazil, under license number L-041/06.

RESULTS
Simple frequency distribution of clinical and epidemiological characteristics of the 47 cats included in this study were reported in Table I. Thirty-five cats (74.5%) lived in the municipality of Rio de Janeiro, seven (14.9%) in Nova Iguaçu, three (6.4%) in São João de Meriti and two (4.2%) in Duque de Caxias (Fig. 1).
As to the macromorphological aspect of the fungal colonies subcultured in PDA medium, all of them had a velvety (83%) or smooth (17%) appearance, of which 41 (87.2%) had a brown (85.1%), black (2.1%) coloration with some pigment production and in six (12.7%), no pigmentation was observed in some isolates [IPEC (6G); (8G); (47G); (48G); (57G); (58G)]. With respect to the micromorphology, all the colonies had thin hyaline, septate and ramified hyphae. Forty-six colonies (97.8%) showed hyaline and dematiaceous conidia and in one isolate (IPEC 53G) only the presence of hyaline conidia in AMC. How-  ever, macroscopically in PDA, this colony showed brown coloration, thus demonstrating melanin production by the fungus. The dematiaceous conidia had a globous or subglobous shape and the hyaline conidia were of a thin, elongated shape. No conidia with a triangular shape was found in our isolates. In the six colonies with no macroscopic pigmentation, it was possible to observe the presence of both dematiaceous conidia and hyaline conidia.
All the isolates showed excellent growth at 30ºC and were thermotolerant at 37ºC. The median diameter of the colonies incubated at 30ºC after 21 days was 33.75 mm (20-44 mm), while the median for colonies at 37ºC was 16.5 mm (5-23.5 mm). It was possible to observe that the growth of colonies at 30ºC was better than at 37ºC (p < 0.05).
For the classification of the isolates by thermotolerance, 31 (66%) isolates had their growth at 37ºC reduced by 50% or more and were classified as having low thermotolerance. Sixteen (34%) isolates had their growth reduced by less than 50% and were classified as having high thermotolerance.
After 10 days, assimilation of glucose occurred in all isolates including the controls, 35 (72.9%) isolates did not assimilate sucrose and raffinose, 11 (22.9%) assimilated sucrose, but did not assimilate raffinose and one isolate assimilated both sugars tested. With the results of the morphological and physiological tests, it was possible to perform the phenotypic characterisation of each isolate, according to the taxonomic key previously proposed (Marimon et al. 2007). Therefore, 12 isolates (23.4%) showed no phenotypic characteristics compatible with the species of the genus Sporothrix, and it was not possible to define what species they were. These isolates were classified as Sporothrix spp. One isolate was characterised as S. schenckii and the remaining 34 isolates were phenotypically characterised as S. brasiliensis (Table II). Subsequently, they were identified using the molecular tool T3B PCR fingerprinting, and all of the control strains showed profiles with very distinct bands, which allowed us to differentiate the main species with clinical association with the species of the genus Sporothrix: S. brasiliensis, S. globosa, S. mexicana and S. schenckii, and it was possible to identify the feline isolates from this study at the species level. The 12 isolates phenotypically characterised as Sporothrix spp. obtained conclusive results using molecular identification, and were characterised as S. brasiliensis, as well as the isolate phenotypically characterised as S. schenckii (Table II).
After computing the association between the clinical variables and the morpho-physiological characteristics of the isolates with a discordant phenotype, which were characterised as Sporothrix spp. and the isolate characterised as S. schenckii, there was no significant association with any of the variables tested (Table III).
Even the p-value did not show statistical significance in the tests performed, the distribution between groups L1, L2 and L3 in the isolates with discordant phenotype was not proportional when compared to the distribution of lesions of the general feline population of the study.
We also computed the association between these variables and the thermotolerance results and the presence or absence of melanin for each isolate, where it was possible to observe a correlation between thermotolerance and respiratory signs and general condition of the animals (Table IV). There was no correlation with the presence or absence of visible amounts of melanin, as macroscopically visualised, with any of the variables tested (p > 0.05).
In the phylogenetic analysis (Fig. 2), it was possible to visualise the presence of 14 isolates (29.8%) characterised as S. brasiliensis, with a small intraspecific variation, that is, there was a variation when compared to the type strain of S. brasiliensis.
When we compare both groups with or without intraspecific variations and the clinical and epidemiological variations of the cats, it was not possible to observe any correlation (Table V).
When we observed the distribution of isolates with discordant and concordant phenotype and isolates with and without intraspecific variation, by the municipalities of Rio de Janeiro state, it was possible to observe that isolates characterised phenotypically as S. brasiliensis and with intraspecific variation are not present in the municipalities of Duque de Caxias and São João de Meriti. Isolates characterised as Sporothrix spp. and with intraspecific variation were not found only in São João de Meriti (Fig. 1).
In Fig. 3 it is possible to observe the 13 animals that showed a discordant phenotype through molecular characterisation and the 14 animals that within the molecular characterisation showed intraspecific variations, together with the clinical and epidemiological characteristics of each animal. When we described the data of the 14 strains that showed intraspecific variations, 10 were from cats that showed respiratory signs, seven from those showing mucosal lesions, eight from cats with unfavorable outcomes and all of them produced melanin. In the 13 strains that showed phenotypes classified as Sporothrix spp. and S. schenckii, six of these animals had mucosal lesions, seven with the presence of respiratory signs, 10 with unfavorable outcomes and all 13 isolates had visible pigmentation.
In the 47 animals, 17 cats obtained clinical cure, of these, 11 were treated with itraconazole and six with ketoconazole. Unfavorable outcome occurred in 30 cats, of these, 14 were treated with itraconazole and 16 with ketoconazole. Comparing the treatment time to favorable outcome in groups by Kaplan-Meier method, with and without intraspecific genetic variation, no significant difference was observed (Log rank p-value = 0.55).
In the 13 strains that showed discordant phenotypes, only three had a cure as the clinical outcome, and the median time of treatment until cure was 31 weeks. The remaining 14 animals, without discordant phenotype and which also had a cure as the outcome, obtained a median time of treatment of 23 weeks. Thus, comparing the treatment time to favorable outcome with the phenotype, the group with discordant phenotype had a longer time to reach a favorable outcome when compared to the group without discordant phenotype (p-value = 0.041), and it is possible to observe in the Fig. 4.

DISCUSSION
The main focus of the present study was the phenotypic and molecular characterisation at the species level of 47 isolates of Sporothrix spp. from cats treated at INI/ Fiocruz, Rio de Janeiro, Brazil, from 2010 to 2011. Polyphasic taxonomy was performed to identify the isolates. The clinical and epidemiological characteristics of the feline population from which the isolates were obtained were included in the study and analysed together with the results of the characterisation of the fungal species.
After the description of the species of the genus Sporothrix, the identification of clinical isolates has been performed worldwide, especially in regions where a large number of sporotrichosis cases occur (Marimon et al. 2008, Oliveira et al. 2011a, Almeida-Paes et al. 2014, Liu et al. 2014, Rodrigues et al. 2016b). However, the number of isolates characterised from animals is still *: isolates with discordant phenotype to molecular characterisation; **: isolates without discordant phenotype to molecular characterisation; ***: p < 0.05.   low in relation to isolates obtained from humans (Oliveira et al. 2011b, Rodrigues et al. 2013b), mainly to the fact that zoonotic sporotrichosis is not cosmopolitan as classical sporotrichosis. In addition, the association between clinical/epidemiological data of the cats with sporotrichosis and S. brasiliensis has not been performed so far. Cases of feline sporotrichosis have been documented in Malaysia, and studies conducted the characterisation of these isolates. However, the clinical and epidemiological characteristics of the cats have been poorly explored (Kano et al. 2015, Han et al. 2017. The description of the clinical profile of the feline population affected by sporotrichosis in Brazil and in other countries is similar (Davies & Troy 1996), even though the epidemic occurring in Rio de Janeiro has particularities such as zoonotic transmission. In our study, it was uncastrated males, without any defined breed, and with unrestricted access to the street that were the most frequently affected by sporotrichosis, corroborating with the findings of other authors who carried out studies in Brazil, in the same region of the epidemic and in other places (Schubach et al. 2004, Pereira et al. 2010, Madrid et al. 2012, Gremião et al. 2015. The animals from which the isolates were obtained came from the state of Rio de Janeiro, the vast majority from the municipality of Rio de Janeiro (74.5%), followed by Nova Iguaçu (14.9%), São João de Meriti (6.4%), and Duque de Caxias (4.2%). It was reported (Silva et al. 2012) that the human cases of sporotrichosis in the metropolitan region of Rio de Janeiro were located in greater concentrations in the city of Rio de Janeiro, followed by neighboring municipalities, such as Duque de Caxias, São João de Meriti, Nova Iguaçu, Nilópolis, Belford Roxo and Mesquita. The fact that there are more cases, both human and animal, in Rio de Janeiro is problaby due to the fact that Fiocruz is based in the same municipality. These findings corroborate the epidemiological data found in our study, since the animals included were mostly from the municipality of Rio de Janeiro and the municipalities of the Baixada Fluminense region, with the areas where there were human and animal overlapping cases.
Nodules and skin ulcers were the most commonly observed lesions in the cats evaluated, corroborating the findings of other authors (Davies & Troy 1996, Schubach et al. 2004, Madrid et al. 2010, Pereira et al. 2010). However, the distribution of skin lesions observed in our study corroborated findings from the two largest studies on feline sporotrichosis performed to date (Schubach et al. 2004, Pereira et al. 2010, with a higher frequency of L3 group followed by L1 and L2 groups. The extracutaneous signs were similar to those previously described (Pereira et al. 2010), with sneezing, rhinorrhea and lymphadenomegaly the most frequent ones. The presence of respiratory signs was associated with therapeutic failure and the death of the animals (Pereira et al. 2010). The difficulty in treating cats with sporotrichosis when there is nasal involvement, indicating that the severity and extent of the lesions in this region may make it difficult to cure, has been demonstrated previously (Gremião et al. 2015).
The cats studied here were submitted to systemic oral azole therapy and the occurrence of unfavorable outcomes was striking. The treatment of feline sporotrichosis with azole is complicated in some cases, with clinical cure rates varying in studies conducted in Rio de Janeiro (Schubach et al. 2004, Pereira et al. 2010, Gremião et al. 2015, and this may be related to the etiological agent predominantly associated with the epizotic disease in the region, S. brasiliensis, which is the most virulent of the pathogenic species of genus Sporothrix (Arrillaga-Moncrieff et al. 2009, Almeida-Paes et al. 2015, in murine model studies. However in Rio de Janeiro epidemics, Almeida-Paes et al. (2014) reported that human sporotrichosis caused by S. schenckii requires extended treatment times and high doses of itraconazole when compared to cases of sporotrichosis caused by S. brasiliensis. This may suggest that Sporothrix virulence may be associated with the initial severity of the cases.
The characterisation of the isolates of Sporothrix spp. from cats is fundamental in regions where zoonotic transmission occurs, because these animals are the main source of infection of this fungus for humans in most cases (Oliveira et al. 2011a, Gremião et al. 2017. However, up to now, characterisation at the species level proposed by Marimon et al. (2007) is not performed as routine in most diagnostic laboratories because it re-quires specialised training for personnel, adequate laboratory structure and these techniques are time-consuming.
Despite the importance of knowing which pathogenic species of the genus Sporothrix are circulating in Brazil, especially in the regions where the largest number of feline sporotrichosis occur, few studies on isolates obtained from cats have been carried out to identify species circulating in the state of Rio de Janeiro, the main area of zoonotic transmission by the genus Sporothrix. Since the beginning of the sporotrichosis epidemic in Rio de Janeiro in 1998, 15 feline isolates from this region (Rodrigues et al. 2013b) were characterised by means of molecular analysis, however, this was limited to the identification the species, without taking into account the clinical and epidemiological characteristics of the feline population as described in the present study.
S. brasiliensis has been described as an emerging species, highly pathogenic for humans and animals, but with a regional geographic distribution associated with Brazil (Marimon et al. 2007, Arrillaga-Moncrieff et al. 2009, Oliveira et al. 2011a, Rodrigues et al. 2013b. This was the only species found in our study, corroborating with the single study with isolates from the epizootic region of feline sporotrichosis in Rio de Janeiro (Rodrigues et al. 2013b). In the southeastern region of Brazil, authors have described the prevalence of S. brasiliensis in cats affected by sporotrichosis, and reported cases in all the states of Rio de Janeiro (Rodrigues et al. 2013b), São Paulo (Rodrigues et al. 2013b), Minas Gerais (Rodrigues et al. 2013b) and Espírito Santo (Oliveira et al. 2013), corroborating our results. We believe that these findings are basically due to the proximity of the states of São Paulo, Minas Gerais and Espírito Santo to the epizootic region of Rio de Janeiro and the possibility of cats migrating from the endemic area to these adjacent regions with their owners. Outside the Southeast region, in the state of Rio Grande do Sul, there has also been a description of S. brasiliensis circulating among animals (Oliveira et al. 2011b, Sanchotene et al. 2015. In six isolates characterised by molecular techniques as S. brasiliensis, the pigmentation of the colony was not observed macroscopically, but they developed globular and dematiaceous conidia, as described in previous studies (Oliveira et al. 2011a). In one isolate, although macroscopically was observed pigmentation, microscopically there was only production of hyaline conidia. The major explanation for this variation are the different culture media recommended for macroscopic and microscopic evaluation of Sporothrix spp.
In 12 isolates (25.5%) it was not possible to reach a taxonomic classification at the species level only by means of phenotypic characteristics, other authors also failed to reach a taxonomic classification (Oliveira et al. 2011a(Oliveira et al. , 2013. In 11 of these isolates, only sucrose was assimilated in the carbohydrate assimilation test, this being suggestive of the species S. pallida or S. globosa, but these are not classified as S. pallida because of the presence of dematiaceous conidia and neither as S. globosa because these isolates are thermotolerant at 37ºC, which do not occur with S. globosa isolates, that are unable to grown at this temperature (Marimon et al. 2007). In one isolate, sucrose and raffinose was not assimilated in the carbohydrate assimilation test, which is suggestive of S. brasiliensis, but there was no development of dematiaceous conidia. Therefore, it was not possible to identify the species of these 12 isolates by this method. One isolate was phenotypically identified as S. schenckii, but did not showed triangular conidia, which was also observed in a previous study (Oliveira et al. 2011a). According to Marimon et al. (2007), the triangular conidia could be a peculiar feature of the strains characterised as S. schenckii. Since this isolate was further characterised as S. brasiliensis, the absence of triangular conidia corroborates the study of Marimon et al. (2007). Due to this diversity of results in the phenotypic tests, we strongly suggest that the identification of species of the genus Sporothrix using only morphological and physiological tests should be used with precaution.
All isolates of this study showed growth at 37ºC, and they were classified into those having low and high thermotolerance. These isolates showed association with respiratory signs and general health condition, probably due to the fact that strains with higher thermotolerance have greater ease of dissemination (Almeida-Paes et al. 2015), generating more severe conditions and respiratory signs in the cats.
All isolates included in this study were identified as S. brasiliensis by the T3B PCR fingerprinting technique. Thus, we detected 13 isolates with differences between their phenotypic and molecular identification, corroborating reports from other authors studying Sporothrix isolates from humans in the same region (Oliveira et al. 2011a, Almeida-Paes et al. 2014) and in different regions (Rodrigues et al. 2013a). Despite the inconclusive phenotypic results in 12 isolates, the characterisation was performed using the molecular T3B PCR fingerprinting technique, through which we successfully identified the species S. brasiliensis in all of these cases. In another case it was categorised phenotypically as S. schenckii, however, in the molecular technique it was characterised as S. brasiliensis. Additionally, this technique proved to be simple and fast, as previously demonstrated by our group . These results suggest that the characterisation of pathogenic species of the genus Sporothrix should be based on the association of phenotypic and molecular techniques that allow one to differentiate between the species.
There was a small degree of intraspecific variation among our isolates classified as S. brasiliensis, as has also been found in other study with human isolates . However, no association was found between these findings and the clinical and epidemiological data from the felines, suggesting that more studies should be carried out with a larger number of isolates and more techniques, in order to study possible relationships between the genotypes and phenotypes of Sporothrix spp. and the clinical characteristics of the animals naturally infected by these fungi.
The 13 isolates phenotypically characterised that had discordant results compared to molecular results, when associated with treatment time to favorable outcome showed a significant result, demonstrating that these animals had a longer time to reach the cure, when compared to the group that did not had discordant phenotype. Although the p-value was not statistically significant, the distribution between the L1, L2 and L3 groups in the isolates that showed phenotype discordant from the molecular identification, it was not proportional to the distribution of lesions in the general feline population in the study. The major inconsistency in the phenotypic tests was the assimilation of unexpected carbohydrates, which can reflect an adaptation to survive under unpredicted nutritional conditions. We suggest therefore, that isolates that show a discordant phenotype may be more virulent, requiring more investigations on virulence so that such a comparison can be made.
We conclude that S. brasiliensis is the etiological agent associated with feline sporotrichosis in the metropolitan region of Rio de Janeiro, Brazil. For now, we recommend the use of molecular techniques for the effective identification of feline isolates, due to the lack of agreement between phenotypic and genotypic methods. Although the number of isolates of Sporothrix from cats with sporotrichosis included in this study is the largest so far in Brazil, it was still not representative due to the large number of cats presenting this mycosis in this country, with the sample number being a limiting factor for some of the analyses performed. In order for the correlation between the species found and the clinical and epidemiological data on the cats might be performed more reliably and so that an investigation into other species circulating in the region might be carried out, we suggest performing a multi-center study that includes a larger quantity of clinical isolates of Sporothrix in different areas of high occurrence of the disease.