RESUMO

Phagocytic responses are critical for effective host defense against opportunistic fungal pathogens, such as Encephalitozoon cuniculi, an obligate intracellular fungus that causes emerging encephalitozoonosis in humans and other animals. Malassezia has immunomodulatory effects and can modulate the production of pro- and anti-inflammatory cytokines via keratinocytes and human monocytes. In this study, we evaluated the modulatory effects of heat-killed Malassezia pachydermatis suspension on macrophages challenged with Encephalitozoon cuniculi. Macrophages were treated with heat-killed M. pachydermatis suspension before being infected with spores of E. cuniculi. The cultures were stained with calcofluor, and the spores, internalized or not, were counted to determine their phagocytic capacity and index (PC and PI, respectively). Microbicidal and phagocytic activities were evaluated by transmission electron microscopy (TEM). The untreated macrophages had higher PC and PI and number of phagocytosed spores than treated macrophages. However, TEM revealed that treated macrophages had higher microbicidal activity because there were few spores in different degrees of degeneration and amorphous materials in the phagocytic vacuoles. Macrophages treated with heat-killed M. pachydermatis suspension had lower PC and PI and incipient presence of E. cuniculi in phagosomes. Treated macrophages had a mixed pattern of cytokine release with Th1, Th2, and Th17 profiles, with emphasis on interleukin (IL)-10, IL-4, IL-17, IL-6, and interferon (IFN)-γ secretion, and particularly high production of anti-inflammatory cytokines. Our results suggest that treatment with heat-killed M. pachydermatis suspension increases the release of cytokines and decreases the phagocytic activity of macrophages challenged with E. cuniculi.

Assuntos

RESUMO

Enterocytozoon bieneusi, also known as microsporidia, is an obligate, opportunistic, and neglected intracellular pathogen that causes diarrhea in humans. Although identified in the cat feces by epidemiological studies, no association with diarrhea has been demonstrated. We demonstrated a case of chronic enteritis by E. bieneusi in a 1-year-old male Maine Coon cat, neutered with diarrhea for nine months, by histopathological analysis of gastrointestinal biopsies and PCR of feces. The treatment with albendazole (10 days) followed by fenbendazole (5 days) proved to be effective and safe after diagnosis. This description highlights the need to investigate these pathogens in cases of diarrhea due to their importance in public health since they are zoonotic agents.

Assuntos

RESUMO

Phagocytic responses are critical for effective host defense against opportunistic fungal pathogens, such as Encephalitozoon cuniculi, an obligate intracellular fungus that causes emerging ncephalitozoonosis in humans and other animals. Malassezia has immunomodulatory effects and can modulate the production of pro- and anti-inflammatory cytokines via keratinocytes and human monocytes. In this study, we evaluated the modulatory effects of heat-killed Malassezia pachydermatis suspension on macrophages challenged with Encephalitozoon cuniculi. Macrophages were treated with heat-killed M. pachydermatis suspension before being infected with spores of E. cuniculi. The cultures were stained with calcofluor, and the spores, internal- ized or not, were counted to determine their phagocytic capacity and index (PC and PI, respectively). Micro-bicidal and phagocytic activities were evaluated by transmission electron microscopy (TEM). The untreated macrophages had higher PC and PI and number of phagocytosed spores than treated macrophages. However, TEM revealed that treated macrophages had higher microbicidal activity because there were few spores in different degrees of degeneration and amorphous materials in the phagocytic vacuoles. Macrophages treated with heat-killed M. pachydermatis suspension had lower PC and PI and incipient presence of E. cuniculi in phagosomes. Treated macrophages had a mixed pattern of cytokine release with Th1, Th2, and Th17 profiles, with emphasis on interleukin (IL)-10, IL-4, IL-17, IL-6, and interferon (IFN)-g secretion, and particularly high production of anti-inflammatory cytokines. Our results suggest that treatment with heat-killed M. pachyder-matis suspension increases the release of cytokines and decreases the phagocytic activity of macrophages challenged with E. cuniculi.

RESUMO

We investigated Malassezia spp. in external ear canal and haircoat of free-ranging golden-headed lion tamarins (Leontopithecus chrysomelas). A total of 199 animals were restrained, and 597 clinical samples were collected. After the amplification of the 26S ribosomal gene by polymerase chain reaction (PCR), the RFLP technique was performed. Two additional PCR protocols were performed in 10 randomly selected strains. Malassezia sp. was isolated in 38.2% (76/199) of the animals and 14.6% (87/597) of the samples; all strains were lipodependent. The 10 sequenced strains showed a high identity with Malassezia japonica, species described in man, but not in animals, so far.

Assuntos

RESUMO

Malassezia pachydermatis and Malassezia furfur are lipophilic yeasts of the cutaneous microbiome, although these organisms are occasionally responsible for serious invasive infections in neonates. Since phagocytosis is an important mechanism mediating the adaptive immune response, here we evaluated the phagocytosis capacity and production of nitric oxide and cytokine by macrophages after challenged with M. furfur CBS-1878 and M. pachydermatis CBS-1696. The phagocytic indexes was determined using RAW 264.7 cultivated or not with M. furfur or M. pachydermatis in the concentrations of 5:1 or 2:1 (yeasts:macrophages ratio) for 6 h, 24 h, and 48 h following the challenges. Evaluation of nitric oxide and pro- and anti-inflammatory cytokines (interleukin [IL]-2, IL-4, IL-6, IL-10, IL-17A, interferon (IFN)-γ and tumor necrosis factor [TNF]-α) by Griess method and flow cytometry, respectively, were performed in the different intervals by collecting the cell culture supernatant. Results showed a higher phagocytic index in the 5:1 ratio in 24 h for both species. Malassezia pachydermatis-infected macrophages had superior phagocytic indexes than M. furfur-infected macrophages. Phagocytosis evaluation at 48 h showed significant microorganisms proliferation and macrophages death, particularly in macrophages infected with M. pachydermatis, suggesting yeast evasion mechanism. Significant variations in the nitric oxide production were observed in macrophages infected with both species. Levels of TNF-α and IL-4 cytokines have increased in M. furfur and M. pachydermatis macrophage-infected cultures, respectively. The low microbicidal activity and the presence of pro- and anti-inflammatory cytokines reinforce the dichotomous character of the relation of these yeasts with the host, acting as a commensal in the cutaneous microbiome or causing infection.

RESUMO

Malassezia pachydermatis and Malassezia furfur are lipophilic yeasts of the cutaneous microbiome, although these organisms are occasionally responsible for serious invasive infections in neonates. Since phagocytosis is an important mechanism mediating the adaptive immune response, here we evaluated the phagocytosis capacity and production of nitric oxide and cytokine by macrophages after challenged with M. furfur CBS-1878 and M. pachydermatis CBS-1696. The phagocytic indexes was determined using RAW 264.7 cultivated or not with M. furfur or M. pachydermatis in the concentrations of 5:1 or 2:1 (yeasts:macrophages ratio) for 6 h, 24 h, and 48 h following the challenges. Evaluation of nitric oxide and pro- and anti-inflammatory cytokines (interleukin [IL]-2, IL-4, IL-6, IL-10, IL-17A, interferon (IFN)-gama and tumor necrosis factor [TNF]-a) by Griess method and flow cytometry, respectively, were performed in the different intervals by collecting the cell culture supernatant. Results showed a higher phagocytic index in the 5:1 ratio in 24 h for both species. Malassezia pachydermatis-infected macrophages had superior phagocytic indexes than M. furfur-infected macrophages. Phagocytosis evaluation at 48 h showed significant microorganisms proliferation and macrophages death, particularly in macrophages infected with M. pachydermatis, suggesting yeast evasion mechanism. Significant variations in the nitric oxide production were observed in macrophages infected with both species. Levels of TNF-a and IL-4 cytokines have increased in M. furfur and M. pachydermatis macrophage-infected cultures, respectively. The low microbicidal activity and the presence of pro- and anti-inflammatory cytokines reinforce the dichotomous character of the relation of these yeasts with the host, acting as a commensal in the cutaneous microbiome or causing infection.

RESUMO

We surveyed healthy captive cockatiels (Nymphicus hollandicus) for Escherichia coli and Salmonella spp. Cloacal swabs were collected from 94 cockatiels kept in commercial breeders, private residencies and pet shops in the cities of São Paulo/SP and Niterói/RJ (Brazil). Three strains of E. coli from each individual were tested for the presence of ExPEC-, APEC- and DEC-related genes. We evaluated the blaTEM, blaSHV, blaOXA, blaCMY, blaCTX-M, tetA, tetB, aadA, aphA, strAB, sul1, sul2, sul3, qnrA, qnrD, qnrB, qnrS, oqxAB, aac (6)'-Ib-cr, qepA resistance genes and markers for plasmid incompatibility groups. Salmonella spp. was not detected. E. coli was isolated in 10% of the animals (9/94). Four APEC genes (ironN, ompT, iss and hlyF) were detected in two strains (2/27-7%), and iss (1/27-4%) in one isolate. The highest resistance rates were observed with amoxicillin (22/27-82%), ampicillin (21/27-79%), streptomycin (18/27-67%), tetracycline (11/27-41%). Multiresistance was verified in 59% (16/27) of the isolates. We detected strAB, blaTEM, tetA, tetB, aadA, aphaA, sul1, sul2, sul3 resistance genes and plasmid Inc groups in 20 (74%) of the strains. E. coli isolated from these cockatiels are of epidemiological importance, since these pets could transmit pathogenic and multiresistant microorganisms to humans and other animals.

Assuntos

RESUMO

Abstract We surveyed healthy captive cockatiels (Nymphicus hollandicus) for Escherichia coli and Salmonella spp. Cloacal swabs were collected from 94 cockatiels kept in commercial breeders, private residencies and pet shops in the cities of São Paulo/SP and Niterói/RJ (Brazil). Three strains of E. coli from each individual were tested for the presence of ExPEC-, APEC- and DEC-related genes. We evaluated the blaTEM, blaSHV, blaOXA, blaCMY, blaCTX-M, tetA, tetB, aadA, aphA, strAB, sul1, sul2, sul3, qnrA, qnrD, qnrB, qnrS, oqxAB, aac (6)-Ib-cr, qepA resistance genes and markers for plasmid incompatibility groups. Salmonella spp. was not detected. E. coli was isolated in 10% of the animals (9/94). Four APEC genes (ironN, ompT, iss and hlyF) were detected in two strains (2/277%), and iss (1/274%) in one isolate. The highest resistance rates were observed with amoxicillin (22/2782%), ampicillin (21/2779%), streptomycin (18/2767%), tetracycline (11/2741%). Multiresistance was verified in 59% (16/27) of the isolates. We detected strAB, bla TEM, tetA, tetB, aadA, aphaA, sul1, sul2, sul3 resistance genes and plasmid Inc groups in 20 (74%) of the strains. E. coli isolated from these cockatiels are of epidemiological importance, since these pets could transmit pathogenic and multiresistant microorganisms to humans and other animals.

RESUMO

Abstract We surveyed healthy captive cockatiels (Nymphicus hollandicus) for Escherichia coli and Salmonella spp. Cloacal swabs were collected from 94 cockatiels kept in commercial breeders, private residencies and pet shops in the cities of São Paulo/SP and Niterói/RJ (Brazil). Three strains of E. coli from each individual were tested for the presence of ExPEC-, APEC- and DEC-related genes. We evaluated the blaTEM, blaSHV, blaOXA, blaCMY, blaCTX-M, tetA, tetB, aadA, aphA, strAB, sul1, sul2, sul3, qnrA, qnrD, qnrB, qnrS, oqxAB, aac (6)′-Ib-cr, qepA resistance genes and markers for plasmid incompatibility groups. Salmonella spp. was not detected. E. coli was isolated in 10% of the animals (9/94). Four APEC genes (ironN, ompT, iss and hlyF) were detected in two strains (2/27-7%), and iss (1/27-4%) in one isolate. The highest resistance rates were observed with amoxicillin (22/27-82%), ampicillin (21/27-79%), streptomycin (18/27-67%), tetracycline (11/27-41%). Multiresistance was verified in 59% (16/27) of the isolates. We detected strAB, bla TEM, tetA, tetB, aadA, aphaA, sul1, sul2, sul3 resistance genes and plasmid Inc groups in 20 (74%) of the strains. E. coli isolated from these cockatiels are of epidemiological importance, since these pets could transmit pathogenic and multiresistant microorganisms to humans and other animals.

Assuntos

RESUMO

We surveyed healthy captive cockatiels (Nymphicus hollandicus) for Escherichia coli and Salmonella spp. Cloacal swabs were collected from 94 cockatiels kept in commercial breeders, private residencies and pet shops in the cities of São Paulo/SP and Niterói/RJ (Brazil). Three strains of E. coli from each individual were tested for the presence of ExPEC-, APEC- and DEC-related genes. We evaluated the blaTEM, blaSHV, blaOXA, blaCMY, blaCTX-M, tetA, tetB, aadA, aphA, strAB, sul1, sul2, sul3, qnrA, qnrD, qnrB, qnrS, oqxAB, aac (6)′-Ib-cr, qepA resistance genes and markers for plasmid incompatibility groups. Salmonella spp. was not detected. E. coli was isolated in 10% of the animals (9/94). Four APEC genes (ironN, ompT, iss and hlyF) were detected in two strains (2/27–7%), and iss (1/27–4%) in one isolate. The highest resistance rates were observed with amoxicillin (22/27–82%), ampicillin (21/27–79%), streptomycin (18/27–67%), tetracycline (11/27–41%). Multiresistance was verified in 59% (16/27) of the isolates. We detected strAB, bla TEM, tetA, tetB, aadA, aphaA, sul1, sul2, sul3 resistance genes and plasmid Inc groups in 20 (74%) of the strains. E. coli isolated from these cockatiels are of epidemiological importance, since these pets could transmit pathogenic and multiresistant microorganisms to humans and other animals.(AU)

Assuntos

RESUMO

Los dermatofitos son hongos filamentosos queratinofílicos, que pueden actuar como agentes zoonóticos; no obstante, aún se debe determinar el papel que cumplen los animales salvajes en la transmisión de las dermatofitosis. El objetivo de este trabajo fue estudiar la presencia de dermatofitos en los pelos de animales de la fauna brasileña. Fueron analizados treinta y dos mamíferos salvajes sanos – de varios taxones - de los cuales 17 se hallaban en cautiverio y 15 en vida libre. Las muestras se obtuvieron por fricción con trozos de alfombras estériles que, una vez pasados por el pelo de los animales, fueron sembrados en agar Mycobiotic e incubados a 25 "C. Las colonias se identificaron de acuerdo a sus características macro y microscópicas. Se aislaron dermatofitos del 9,5% de los animales estudiados: Microsporum gypseum de un aguará guazú (Chrysocyon brachyurus), Microsporum cookie de un coatí (Nasua nasua) y Trichophyton ajelloi de un perro del monte (Speothos venaticus). En relación a la salud pública, estos animales representan uma posible fuente de infección para el hombre y otros animales.

Dermatophytes are keratinophilic fungi that can cause zoonosis. However, the role wild animals play in the transmission of these infections is yet to be determined. The aim of this study was to determine the presence of dermatophytes on the haircoat of Brazilian wild mammals. Thirty-two healthy wild mammals from several taxa were studied: 17 were captive and 15 were free-living individuals. Samples were obtained by rubbing the haircoat with sterile carpets. Samples were cultured on Mycobiotic agar, and the plates were incubated at 25 "C. Identification of the isolates was carried out on the basis of macro-and micromorphology. Dermatophytes were isolated from 9.5% of the animals: Microsporum gypseum from one maned wolf (Chrysocyon brachyurus), Microsporum cookie from one coati (Nasua nasua), and Trichophyton ajelloi from one bush dog (Speothos venaticus). These animals represent therefore sources of infection for both humans and other animals and are important for public health policies.

Dermatófitos são fungos filamentosos queratinofílicos e agentes de zoonoses; entretanto, o papel que os animais selvagens representam na transmissão das dermatofitoses ainda precisa ser determinado. O objetivo deste trabalho foi pesquisar dermatófitos no pelame de animais da fauna brasileira. Trinta e dois mamíferos selvagens sadios de vários táxons foram estudados, 17 de cativeiro e 15 de vida livre. As amostras foram obtidas por fricção de carpetes estéreis no pelame dos animais. As amostras foram semeadas em ágar Mycobiotic e incubadas a 25 "c, identificando-se as colônias por suas características macro e microscópicas. Isolaram-se dermatófitos de 9,5% dos animais pesquisados: Microsporum gypseum de um lobo-guará (Chrysocyon brachyurus), Microsporum cookie de um quati (Nasua nasua) e Trichophyton ajelloi de um cachorro-do-mato-vinagre (Speothos venaticus). Esses animais representam fontes de infecção para homens e outros animais, sendo importantes para a saúde pública.

Assuntos

RESUMO

ABSTRACT The objective of this study was to characterize genotypically Malassezia spp. isolated from the external ear canal of healthy horses. Fifty-five horses, 39 (70.9%) males and 16 (29.1%) females, from different breeds and adults were studied. External ear canals were cleaned and a sterile cotton swab was introduced to collect cerumen. A total of 110 samples were cultured into Dixon medium and were incubated at 32 °C for up to 15 days. Macro- and micromorphology and phenotypic identification were performed. DNA was extracted, strains were submitted to polymerase chain reaction technique, and the products obtained were submitted to Restriction Fragment Length Polymorphism using the restriction enzymes BstCI and HhaI. Strains were sent off to genetic sequencing of the regions 26S rDNA D1/D2 and ITS1-5.8S-ITS2 rDNA. Malassezia spp. were isolated from 33/55 (60%) animals and 52/110 (47%) ear canals. No growth on Sabouraud dextrose agar was observed, confirming the lipid dependence of all strains. Polymerase chain reaction-Restriction fragment length polymorphism permitted the molecular identification of Malassezia nana - 42/52 (81%) and Malassezia slooffiae - 10/52 (19%). Sequencing confirmed RFLP identification. It was surprising that M. nana represented over 80% of the strains and no Malassezia equina was isolated in this study, differing from what was expected.

Assuntos

RESUMO

The objective of this study was to characterize genotypically Malassezia spp. isolated from the external ear canal of healthy horses. Fifty-five horses, 39 (70.9%) males and 16 (29.1%) females, from different breeds and adults were studied. External ear canals were cleaned and a sterile cotton swab was introduced to collect cerumen. A total of 110 samples were cultured into Dixon medium and were incubated at 32 °C for up to 15 days. Macro- and micromorphology and phenotypic identification were performed. DNA was extracted, strains were submitted to polymerase chain reaction technique, and the products obtained were submitted to Restriction Fragment Length Polymorphism using the restriction enzymes BstCI and HhaI. Strains were sent off to genetic sequencing of the regions 26S rDNA D1/D2 and ITS1-5.8S-ITS2 rDNA. Malassezia spp. were isolated from 33/55 (60%) animals and 52/110 (47%) ear canals. No growth on Sabouraud dextrose agar was observed, confirming the lipid dependence of all strains. Polymerase chain reaction-Restriction fragment length polymorphism permitted the molecular identification of Malassezia nana - 42/52 (81%) and Malassezia slooffiae - 10/52 (19%). Sequencing confirmed RFLP identification. It was surprising that M. nana represented over 80% of the strains and no Malassezia equina was isolated in this study, differing from what was expected.(AU)

Assuntos

RESUMO

Many microorganisms are able to cause diseases in amphibians, and in the past few years one of the most reported has been Batrachochytrium dendrobatidis. This fungus was first reported in Brazil in 2005; following this, other reports were made in specimens deposited in museum collections, captive and free-living frogs. The aim of this study was to compare singleplex and nested-PCR techniques to detect B. dendrobatidis in free-living and apparently healthy adult frogs from the Brazilian Atlantic Forest. The sample collection area was a protected government park, with no general entrance permitted and no management of the animals there. Swabs were taken from the skin of 107 animals without macroscopic lesions and they were maintained in ethanol p.a. Fungal DNA was extracted and identification of B. dendrobatidis was performed using singleplex and nested-PCR techniques, employing specific primers sequences. B. dendrobatidis was detected in 61/107 (57%) and 18/107 (17%) animals, respectively by nested and singleplex-PCR. Nested-PCR was statistically more sensible than the conventional for the detection of B. dendrobatidis (Chi-square = 37.1; α = 1%) and the agreement between both techniques was considered just fair (Kappa = 0.27). The high prevalence obtained confirms that these fungi occur in free-living frogs from the Brazilian Atlantic Forest with no macroscopic lesions, characterizing the state of asymptomatic carrier. We concluded that the nested-PCR technique, due to its ease of execution and reproducibility, can be recommended as one of the alternatives in epidemiological surveys to detect B. dendrobatidis in healthy free-living frog populations.

Assuntos

RESUMO

Many microorganisms are able to cause diseases in amphibians, and in the past few years one of the most reported has been Batrachochytrium dendrobatidis. This fungus was first reported in Brazil in 2005; following this, other reports were made in specimens deposited in museum collections, captive and free-living frogs. The aim of this study was to compare singleplex and nested-PCR techniques to detect B. dendrobatidis in free-living and apparently healthy adult frogs from the Brazilian Atlantic Forest. The sample collection area was a protected government park, with no general entrance permitted and no management of the animals there. Swabs were taken from the skin of 107 animals without macroscopic lesions and they were maintained in ethanol p.a. Fungal DNA was extracted and identification of B. dendrobatidis was performed using singleplex and nested-PCR techniques, employing specific primers sequences. B. dendrobatidis was detected in 61/107 (57%) and 18/107 (17%) animals, respectively by nested and singleplex-PCR. Nested-PCR was statistically more sensible than the conventional for the detection of B. dendrobatidis (Chi-square = 37.1; α = 1%) and the agreement between both techniques was considered just fair (Kappa = 0.27). The high prevalence obtained confirms that these fungi occur in free-living frogs from the Brazilian Atlantic Forest with no macroscopic lesions, characterizing the state of asymptomatic carrier. We concluded that the nested-PCR technique, due to its ease of execution and reproducibility, can be recommended as one of the alternatives in epidemiological surveys to detect B. dendrobatidis in healthy free-living frog populations.(AU)

Assuntos

RESUMO

Many microorganisms are able to cause diseases in amphibians, and in the past few years one of the most reported has been Batrachochytrium dendrobatidis. This fungus was first reported in Brazil in 2005; following this, other reports were made in specimens deposited in museum collections, captive and free-living frogs. The aim of this study was to compare singleplex and nested-PCR techniques to detect B. dendrobatidis in free-living and apparently healthy adult frogs from the Brazilian Atlantic Forest. The sample collection area was a protected government park, with no general entrance permitted and no management of the animals there. Swabs were taken from the skin of 107 animals without macroscopic lesions and they were maintained in ethanol p.a. Fungal DNA was extracted and identification of B. dendrobatidis was performed using singleplex and nested-PCR techniques, employing specific primers sequences. B. dendrobatidis was detected in 61/107 (57%) and 18/107 (17%) animals, respectively by nested and singleplex-PCR. Nested-PCR was statistically more sensible than the conventional for the detection of B. dendrobatidis (Chi-square = 37.1; α = 1%) and the agreement between both techniques was considered just fair (Kappa = 0.27). The high prevalence obtained confirms that these fungi occur in free-living frogs from the Brazilian Atlantic Forest with no macroscopic lesions, characterizing the state of asymptomatic carrier. We concluded that the nested-PCR technique, due to its ease of execution and reproducibility, can be recommended as one of the alternatives in epidemiological surveys to detect B. dendrobatidis in healthy free-living frog populations.

Assuntos

RESUMO

Mamíferos marinhos em cativeiro são particularmente suscetíveis a infecções virais, bacterianas, fúngicas ou parasitárias que causam dermatite focal ou difusa, e que podem causar alopecias em pinípedes. Diversos tipos de lesões dermatológicas ocasionadas por fungos, incluindo lesão por Malassezia, já foram descritas nesses animais. Um lobo-marinho-subantártico (Arctocephalus tropicalis) mantido em cativeiro apresentou alopecia bilateral na região da nadadeira caudal e em região abaixo da nadadeira peitoral. Para diagnosticar a possível causa da alopecia foram realizados etograma (para avaliação do comportamento do animal), culturas bacteriana e micológica. Após confirmação da presença de Malassezia pachydermatis, foi estabelecido protocolo de tratamento, o qual se mostrou bastante eficaz para a resolução do quadro. O objetivo do presente trabalho é relatar um caso de alopecia em um lobo-marinho, abordando o diagnóstico e a terapêutica utilizados.

Marine mammals in captivity are particularly susceptible to viral, bacterial, fungal or parasitic infections that can cause focal or diffuse dermatitis, and may cause alopecia in pinnipeds. Various types of skin lesions caused by fungi have been described in these animals, including lesions due to Malassezia. A subantartic fur seal (Arctocephalus tropicalis) kept in captivity presented bilateral alopecia on the caudal flipper and on the region below the pectoral flipper. To diagnose the possible cause of alopecia, bacterial and mycological cultures were performed, as well as an ethogram to assess the behavior of the animal. After confirmation of the presence of Malassezia pachydermatis in the affected regions, a treatment protocol was established, which proved to be effective for the resolution of the clinical case. The objective of this study is to report a case of alopecia in a fur seal, addressing the diagnosis and treatment that were performed.

Los mamíferos marinos en cautiverio son particularmente susceptibles a infecciones virales, bacterianas, fúngicas o parasitarias que provocan una dermatitis focal o difusa, y pueden causar alopecia en los pinnípedos. Varios tipos de lesiones de piel causadas por hongos, incluyendo lesiones por Malassezia, han sido descriptas en estos animales. Un lobo marino subantártico (Arctocephalus tropicalis) mantenido en cautiverio presentó una alopecia bilateral en la región de la aleta caudal y de la región por debajo de la aleta pectoral. Para diagnosticar la posible causa de la alopecia se realizó un etograma (para evaluar el comportamiento del animal), y cultivos bacterianos y micológicos. Después de confirmada la presencia de Malassezia pachydermatis, se estableció un protocolo de tratamiento que resultó muy eficaz para la resolución del cuadro. El objetivo de este trabajo es presentar un caso de alopecia en un lobo marino, abordando el diagnóstico y la conducta terapéutica utilizada.

Assuntos

RESUMO

Mamíferos marinhos em cativeiro são particularmente suscetíveis a infecções virais, bacterianas, fúngicas ou parasitárias que causam dermatite focal ou difusa, e que podem causar alopecias em pinípedes. Diversos tipos de lesões dermatológicas ocasionadas por fungos, incluindo lesão por Malassezia, já foram descritas nesses animais. Um lobo-marinho-subantártico (Arctocephalus tropicalis) mantido em cativeiro apresentou alopecia bilateral na região da nadadeira caudal e em região abaixo da nadadeira peitoral. Para diagnosticar a possível causa da alopecia foram realizados etograma (para avaliação do comportamento do animal), culturas bacteriana e micológica. Após confirmação da presença de Malassezia pachydermatis, foi estabelecido protocolo de tratamento, o qual se mostrou bastante eficaz para a resolução do quadro. O objetivo do presente trabalho é relatar um caso de alopecia em um lobo-marinho, abordando o diagnóstico e a terapêutica utilizados.(AU)

Marine mammals in captivity are particularly susceptible to viral, bacterial, fungal or parasitic infections that can cause focal or diffuse dermatitis, and may cause alopecia in pinnipeds. Various types of skin lesions caused by fungi have been described in these animals, including lesions due to Malassezia. A subantartic fur seal (Arctocephalus tropicalis) kept in captivity presented bilateral alopecia on the caudal flipper and on the region below the pectoral flipper. To diagnose the possible cause of alopecia, bacterial and mycological cultures were performed, as well as an ethogram to assess the behavior of the animal. After confirmation of the presence of Malassezia pachydermatis in the affected regions, a treatment protocol was established, which proved to be effective for the resolution of the clinical case. The objective of this study is to report a case of alopecia in a fur seal, addressing the diagnosis and treatment that were performed.(AU)

Los mamíferos marinos en cautiverio son particularmente susceptibles a infecciones virales, bacterianas, fúngicas o parasitarias que provocan una dermatitis focal o difusa, y pueden causar alopecia en los pinnípedos. Varios tipos de lesiones de piel causadas por hongos, incluyendo lesiones por Malassezia, han sido descriptas en estos animales. Un lobo marino subantártico (Arctocephalus tropicalis) mantenido en cautiverio presentó una alopecia bilateral en la región de la aleta caudal y de la región por debajo de la aleta pectoral. Para diagnosticar la posible causa de la alopecia se realizó un etograma (para evaluar el comportamiento del animal), y cultivos bacterianos y micológicos. Después de confirmada la presencia de Malassezia pachydermatis, se estableció un protocolo de tratamiento que resultó muy eficaz para la resolución del cuadro. El objetivo de este trabajo es presentar un caso de alopecia en un lobo marino, abordando el diagnóstico y la conducta terapéutica utilizada.(AU)

Assuntos

RESUMO

Malassezia pachydermatis is associated with dermatomycoses and otomycosis in dogs and cats. This study compared the susceptibility of M. pachydermatis isolates from sick (G1) and healthy (G2) animals to azole and polyene antifungals using the M27-A3 protocol. Isolates from G1 animals were less sensitive to amphotericin B, nystatin, fluconazole, clotrimazole and miconazole.

RESUMO

Malassezia pachydermatisis associated with dermatomycoses and otomycosis in dogs and cats. This study compared the susceptibility of M. pachydermatis isolates from sick (G1) and healthy (G2) animals to azole and polyene antifungals using the M27-A3 protocol. Isolates from G1 animals were less sensitive to amphotericin B, nystatin, fluconazole, clotrimazole and miconazole.(AU)

Assuntos