Dermatite fúngica associada à Rhodotorula glutinis em cão - Canis familiaris ): relato de caso / Fungal dermatitis associated to Rhodotorula glutinis in dog (Canis familiaris): case report

O fungo Rhodotorula sp. era considerado como não patogênico, mas, com o aumento de casos de humanos imunossuprimidos nas últimas duas décadas, as espécies R. mucilaginosa, R. glutinis e R. minuta se tornaram agentes potencialmente patogênicos. Poucos relatos clínicos veterinários associados à Rhodotorula spp. foram descritos, e o objetivo deste trabalho foi descrever um caso de dermatite fúngica causada por R. glutinis em cão imunossuprimido devido à leishmaniose visceral e osteossarcoma, na cidade de Cuiabá-Mato Grosso. Um cão, macho, 11 anos, sem raça definida, foi trazido ao Hospital Veterinário apresentando lesões de pele com diagnóstico de dermatofitose e foi prescrito tratamento tópico à base de óleo de melaleuca, sem melhora após um mês de tratamento. O animal retornou ao Hospital Veterinário com hemorragia na região lesionada da cauda, e foi realizada biópsia para exames microbiológico e histopatológico. Nas análises microbiológica e histopatológica, foi isolada uma levedura e detectada a presença de estrutura semelhante a leveduras na coloração de prata, respectivamente. A levedura isolada foi identificada como R. glutinis por meio do sequenciamento do DNA. Um novo tratamento foi instituído, sem melhora do quadro clínico. O animal foi diagnosticado também com leishmaniose e osteossarcoma, provavelmente ocasionando a immunossupressão, e seu quadro evoluiu a óbito.(AU)

The fungi Rhodotorula sp was considered nonpathogenic, but with the increase of immunosuppressed humans in the last two decades, the species R. mucilaginosa, R. glutinis and R. minuta became potentially pathogenic agents. There have been few veterinary clinical reports associated with Rhodotorula spp. and this work aims to describe the first case of fungal dermatitis caused by R. glutinis in immunosuppressed dog due to visceral leishmaniasis and osteosarcoma in the city of Cuiabá-Mato Grosso. An 11-year-old male mongrel dog was examined to the Veterinary Hospital with skin lesions and the diagnosis was dermatophytosis and the treatment was implemented with topical tea tree oil for one month, but the treatment failed. The animal returned to the Veterinary Hospital with bleeding in the injured area of the tail and biopsy was performed for microbiological and histopathology evaluation. In the microbiological and histopathological analysis, yeast was isolated and yeast-like structures in silver staining were observed, respectively. The isolated yeast was identified as R. glutinis by DNA sequencing. A new treatment was implemented without clinical improvement. The animal was diagnosed with leishmaniasis and osteosarcoma, which probably caused immunosuppression, and its clinical conditions evolved to death.(AU)

Isolation and molecular characterization of symbiotic fungus from Acromyrmex ambiguus and Acromyrmex heyeri ants of Rio Grande do Sul State, Brazil / Isolamento e caracterização molecular do fungo simbionte de formigas-cortadeiras (Acromyrmex heyeri e Acromyrmex ambiguus) do Rio Grande do Sul, Brasil

Leaf-cutting ants of the genera Atta and Acromyrmex determine serious agricultural problems and live on symbiosis with Leucoagaricus gongylophorus. The aim of this study is to identify morphological and molecularly, as well as to verify the genotypic variability of the symbiotic fungus cultivated by A. heyeri and A. ambiguus from three different regions of the state of Rio Grande do Sul, Brazil. Fungus gardens were collected and fragments of mycelia were grown in selective medium. Total DNA was extracted and amplification of the ITS region was performed by PCR using universal primers. After DNA sequencing, the chromatograms were assembled and phylogenetic analyzes were performed by the Neighbor-Joining method. A total of six isolates of L. gongylophorus were obtained and their identities were confirmed by molecular analyses. Phylogenetic analysis of the ITS region showed a tree with two distinct groups regarding the fungus isolates from A. heiyeri and A. ambiguous. In this study, it was verified that A. heyeri and A. ambiguous, cultivate the same fungus. Additionally, the molecular marker used in this study showed variations in L. gongylophorus, evidencing two distinct branches in the phylogenetic tree, according to the ant species that cultivate L. gongylophorus. However, other studies involving the inclusion of a great number of isolates of L. gongylophorus, as well as the use of other molecular markers to validate the possible variations in the phylogenetic relationship of this symbiotic fungus are required.

Formigas-cortadeiras dos gêneros Atta e Acromyrmex causam elevados prejuízos à agricultura e são dependentes obrigatórias da simbiose com Leucoagaricus gongylophorus. O objetivo deste estudo foi identificar morfologicamente e molecularmente, bem como verificar a variabilidade genotípica do fungo simbionte,cultivado por Acromyrmex heyeri e Acromyrmex ambiguus em três regiões do RS, Brasil. Jardins de fungo foram coletados do interior de formigueiros e fragmentos de micélio foram cultivados em meio de cultura seletivo. O DNA total foi extraído e a amplificação da região ITS foi realizada por PCR, utilizando primers universais. Após sequenciamento, os cromatogramas foram montados e as análises filogenéticas foram realizadas pelo método de Neighbor-Joining. Dos jardins de fungo, obtiveram-se seis isolados de L. gongylophorus, confirmados por análise molecular. A análise filogenética da região ITS mostrou uma árvore com dois grupos distintosem relação aos isolados do fungo oriundos de ninhos de A. heyeri e A. ambiguus. Neste estudo, evidenciou-se que as espécies de formigas A. heyeri e A. ambiguus cultivam o mesmo fungo. Entretanto, o marcador molecular estudado evidenciou variações de L. gongylophorus que permitiram formar duas ramificações diferentes na árvore filogenética relacionada à espécie de formiga que o cultiva. Todavia, para validar as possíveis variações nas relações filogenéticas deste fungo simbionte, é necessária a inclusão de um maior número de isolados de L. gongylophorus, bem como o emprego de outros marcadores moleculares.

Microscopia de epifluorescência para a determinção de biomassa micelial em substrato de cultivo sólido particulado / Microscopía e epifluorescencia para la deteminación de biomasa micelial en sustrato de cultivo sólido particulado / Epifluorscence mmicroscopy for the deterination of mycelial biomass in particulated solid substrate cultivatoon

A determinação de biomassa micelial fúngica crescida em substratos de cultivo sólido particulado (SCSP) é ainda um desafio devido à dificuldade de separação do micélio e o substrato. O objetivo deste trabalho foi avaliar a técnica de microscopia de epifluorescência para determinação da biomassa micelial de Pleurotus ostreatus em SCSP. Para determinação da exatidão da metodologia P. ostreatus foi crescido em meio líquido de extrato de malte e; a biomassa micelial foi separada por centrifugação, liofilizada e moída. Concentrações conhecidas do pó do micélio foram misturadas ao SCSP, composto de bagaço de cana de açúcar e fibra de soja, previamente autoclavado. Em seguida, a biomassa micelial foi determinada por microscopia de epifluorescência. Para promover a variação da biomassa micelial a ser determinada por microscopia de epifluorescência, SCSP adicionado de diferentes concentrações de ferro foram utilizados para o crescimento do fungo. Concluiu-se que a técnica apresenta baixa precisão e exatidão, o que implica na necessidade de maiores estudos para aplicação desta técnica para a determinação de biomassa micelial crescida em SCSP.

Determination of fungal mycelial biomass grown on solid substrate cultivation (SSC) is still a challenge due to the difficulty in separating mycelium and substrate. The objective of this study was to evaluate the epifluorescence microscopy to determine the mycelial biomass of Pleurotus ostreatus grown in SSC. P. ostreatus was grown in malt extract liquid medium and mycelial biomass was separated by centrifugation. It was then lyophilized and milled. Mycelial powder was added at known concentrations to SSC composed of sugarcane bagasse and soy fiber, previously autoclaved. Mycelial biomass was determined by epifluorescence microscopy. In order to promote mycelial biomass variation for the determination by epifluorescence microscopy, SSC added at different iron concentrations was used for fungus growth. It was concluded that the technique has low precision and accuracy, which implies the need for further studies in order to apply this technique for the determination of mycelial biomass grown in SSC.

Four Unrecorded Wood Decay Fungi from Seoul in Korea

During the investigation of Korean indigenous fungi from Seoul, three genera-Fuscoporia, Porostereum, and Trametopsis, and four species-Fuscoporia senex, Phlebia acerina, Porostereum spadiceum, and Trametopsis cervina were found. Their morphological characteristics were examined and their identification was confirmed by molecular analysis based on internal transcribed spacer (ITS) and nuclear large subunit ribosomal DNA region sequences. These fungi are new to Korea and registered here with descriptions.

Microscopia de epifluorescência para a determinação de biomassa micelial em substrato de cultivo sólido particulado / Epifluorescense microscopy for the determination of mycelial biomass in particulated solid substrate cultivation / Microscopia de pifluorescencia para la determinación de biomasa micelial en sustrato de cultivo solido particulado

A determinação de biomassa micelial fúngica crescida em substratos de cultivo sólido particulado (SCSP) é ainda um desafio devido à dificuldade de separação do micélio e o substrato. O objetivo deste trabalho foi avaliar a técnica de microscopia de epifluorescência para determinação da biomassa micelial de Pleurotus ostreatus em SCSP. Para determinação da exatidão da metodologia P. ostreatus foi crescido em meio líquido de extrato de malte e; a biomassa micelial foi separada por centrifugação, liofilizada e moída. Concentrações conhecidas do pó do micélio foram misturadas ao SCSP, composto de bagaço de cana de açúcar e fibra de soja, previamente autoclavado. Em seguida, a biomassa micelial foi determinada por microscopia de epifluorescência. Para promover a variação da biomassa micelial a ser determinada por microscopia de epifluorescência, SCSP adicionado de diferentes concentrações de ferro foram utilizados para o crescimento do fungo. Concluiu- -se que a técnica apresenta baixa precisão e exatidão, o que implica na necessidade de maiores estudos para aplicação desta técnica para a determinação de biomassa micelial crescida em SCSP.

Determination of fungal mycelial biomass grown on solid substrate cultivation (SSC) is still a challenge due to the difficulty in separating mycelium and substrate. The objective of this study was to evaluate the epifluorescence microscopy to determine the mycelial biomass of Pleurotus ostreatus grown in SSC. P. ostreatus was grown in malt extract liquid medium and mycelial biomass was separated by centrifugation. It was then lyophilized and milled. Mycelial powder was added at known concentrations to SSC composed of sugarcane bagasse and soy fiber, previously autoclaved. Mycelial biomass was determined by epifluorescence microscopy. In order to promote mycelial biomass variation for the determination by epifluorescence microscopy, SSC added at different iron concentrations was used for fungus growth. It was concluded that the technique has low precision and accuracy, which implies the need for further studies in order to apply this technique for the determination of mycelial biomass grown in SSC.

La determinación de biomasa micelial fúngica crecida en sustratos de cultivo sólido particulado (SCSP) es todavía un reto debido a la dificultad de separación del micelio y el sustrato. El objetivo de este estudio fue evaluar la técnica de microscopía de epifluorescencia para determinación de la biomasa micelial de Pleurotus ostreatus en SCSP. Para determinación de exactitud de la metodología P. ostreatus se cultivó en medio líquido de extracto de malta y; la biomasa micelial separada por centrifugación, liofilizada y molida. Concentraciones conocidas del polvo del micelio fueron mezcladas al SCSP, compuesto de bagazo de caña de azúcar y fibra de soya, previamente tratado en autoclave. A continuación, la biomasa micelial a ser determinada por microscopía de epifluorescencia. Para promover la variación de la biomasa micelial a ser determinada por microscopía de epifluorescencia, SCSP añadida con diferentes concentraciones de hierro fueron utilizados para el crecimiento del hongo. Se concluye que la técnica presenta baja precisión y exactitud, lo que implica en la necesidad de realizar más estudios para aplicación de esta técnica para la determinación de biomasa micelial crecida en SCSP.

Antioxidant activity of Agaricus brasiliensis basidiocarps on different maturation phases

Different maturation phases of basidiocarp could affect the bioactivity and concentration of some active substances. A. brasiliensis Wasser et al.(A. blazei Murrill) has shown antitumor activity that could be related to the antioxidant activity. However there is no information of the best basidiocarp maturation phase for extracting antioxidant substances in order to determine the moment of harvesting in mushroom cultivation. The objective of this work was to evaluate the antioxidant activity of A. brasiliensis strains on different basidiocarp maturation phases. The best condition for extraction of A. brasiliensis antioxidants is with methanol as solvent at 60 ºC for 60 min. Strains with closed basidiocarp have higher antioxidant activity than with opened basidiocarp. Antioxidant activity varies in each strain. It was concluded that A. brasiliensis is a natural source of antioxidant compounds. Also there is higher antioxidant activity in closed than opened caps and consequently higher functional activity. It reinforces the synergic action among different A. brasiliensis compounds as a functional food and the importance of further investigation for isolation and characterization of antioxidant substances of A. brasiliensis. It also determines the best harvest period in order to obtain the highest antioxidant activity from basidiocarp.

Case report of Schizophyllum commune sinusitis in an immunocompetent patient / Informe de un caso de sinusitis por Schizophyllum commune en enfermo inmuno-competente

Schizophyllum commune is a basidiomycete fungus with broad distribution in nature; however, it is a rare cause of infectious disease. We report the isolation of this mould in a 46 year-old immunocompetent patient with chronic sinusitis previously treated with multiple antibiotics and topical nasal steroids. Material obtained via a left maxillary sinus antrostomy showed septate hyaline hyphae with clamp connections on direct examination with KOH and histopathological studies. Further growth on Sabouraud agar produced a white mould that, based on its microscopic and macroscopic characteristics, was identified as S. commune. Despite its low frequency, this fungus should be considered a possible pathogen, particularly in samples obtained from paranasal sinuses.

Schizophyllum commune es un hongo basidiomiceto con una amplia distribución en la naturaleza, que con poca frecuencia causa enfermedad infecciosa. Se informa el aislamiento de este moho, en un paciente inmuno-competente de 46 años con sinusitis crónica tratada previamente con múltiples antibióticos y esteroides tópicos nasales. Por una antrostomía maxilar izquierda se obtuvo una muestra que en el examen directo con KOH y tinciones histopatológicas, mostró hifas septadas hialinas con conexiones en asa. En agar Sabouraud creció un moho blanco que por sus características macroscópicas y microscópicas se identificó como S. commune. El paciente fue tratado con itraconazol y después de cuatro meses hubo resolución de las manifestaciones clínicas. A pesar de su baja frecuencia, este hongo se debe considerar como posible patógeno, en especial en muestras de senos paranasales.

Cloning and functional characterization of the gene encoding the transcription factor Acel in the basidiomycete Phanerochaete chrysosporium

In this report we describe the isolation and characterization of a gene encoding the transcription factor Acel (Activation protein of cup 1 Expression) in the white rot fungus Phanerochaete chrysosporium. Pc-acel encodes a predicted protein of 633 amino acids containing the copper-fist DNA binding domain typically found in fungal transcription factors such as Acel, Macl and Haal from Saccharomyces cerevisiae. The Pc-acel gene is localized in Scaffold 5, between coordinates 220841 and 222983. A S. cerevisiae acel null mutant strain unable to grow in high-copper medium was fully complemented by transformation with the cDNA of Pc-acel. Moreover, Northern blot hybridization studies indicated that Pc-acel cDNA restores copper inducibility of the yeast cup 1 gene, which encodes the metal-binding protein metallothionein implicated in copper resistance. To our knowledge, this is first report describing an Acel transcription factor in basidiomycetes.

Chemical constituents of basidiomycete Hydnum repandum / 中草药

Objective To study the chemical constituents of the fruiting bodies of Hydnum repandum.Methods Separation and purification were performed on silica gel, Sephadex LH-20 and ODS CC. Their sturctures were established by 2D-NMR (1H-1HCOSY, HMQC, HMBC, and NOESY), MS, HR-MS spectra, and ORD data. Results Eleven compounds were obtained and identified as sarcodonin A ( Ⅰ ),scabronine B (Ⅱ), 3β-hydroxy-5α, 8α-epidioxyergosta-6, 22-dien (Ⅲ), (22E, 24R)-ergosta-7, 22-diene3β, 5α, 6β- triol (Ⅳ), (22E, 24R)-ergosta-7, 22-diene-3β-ol (Ⅴ), benzoic acid (Ⅵ), 4-hydroxylbenzaldehyde (Ⅶ), 4-monopropanoylbenzenediol (Ⅷ), ethyl-β-D-glucopyranoside (Ⅸ), thioacetic anhydride ( Ⅹ ), (2S, 2'R, 3S, 4R)-2-(2-hydroxyoctadecanoylamino) docosane-1, 3, 4-triol (Ⅺ). Conclusion All of the compounds are isolated from this fungus for the first time.

Transformation of the Edible Basidiomycete, Pleurotus ostreatus to Phleomycin Resistance

For transformation of Pleurotus ostreatus, two novel vectors, pPhKM1 and pPhKM2, were constructed, using the regulatory sequences of the P. sajor-caju beta-tubulin gene (TUB1) and the ble gene encoding phleomycin binding protein. pPhKM1 contains ble fused to the TUB1 promoter and the Schizophyllum commune GPD terminator. pPhKM2 contains ble fused to the promoter and terminator regions of P. sajor-caju TUB1. To confirm phleomycin-resistance activity, each vector was cotransformed with pTRura3-2 into the P. ostreatus homokaryotic ura - strain. The transforming DNA was stably integrated into the genomic DNA. Subsequently, phleomycin resistance was conferred on wild-type dikaryotic P. ostreatus by transformation with pPhKM1 or pPhKM2. This transformation system generated stable phleomycin-resistant transformants.