In vitro effect of Chrysosporium indicum and Chrysosporium keratinophylum on Toxocara canis eggs / Efecto in vitro de Chrysosporium indicum y Chrysosporium keratinophylum sobre huevos de Toxocara canis

The degree of antagonism exercised by fungi on geohelminth development varies according to the morphological alterations caused by different fungal species. Saprophytic fungi may exert ovicidal or ovistatic effects. The aim of this study was to apply scanning electron microscopy (SEM) to observe the action of two soil saprophytic species of Chrysosporium (C. indicum and C. keratinophylum) on Toxocara canis eggs. The fungal strains to be tested were incubated for 28 days at 28 °C in 2% water agar with a suspension of unembryonated T. canis eggs. A suspension of T. canis eggs in 2% water agar was used as control group. The assay was done in triplicate for each fungus and the control group. SEM observations were performed on the 4th, 7th, 14th, 21st, and 28th day after inoculation. The effect of the fungi on eggs was evaluated in accordance with the alterations observed on the surface and the changes in the normal characteristics of the eggs. Hyphae around the eggs, appresoria penetrating the shell and changes in the typical egg membrane were observed in this assay. Type 3 effect (alterations that occur both in the embryo and the shell, and hyphal penetration of the eggs) was the prevalent effect. SEM allowed us to observe clearly the morphological alterations in T. canis eggs due to the effect of C. indicum and C. keratinophylum. Both saprophytic species of Chrysosporium alter the egg structure and alterations increase as exposure increases.

El grado de antagonismo ejercido por los hongos sobre el desarrollo de los geohelmintos depende de la especie fúngica y las alteraciones morfológicas que causan. Los hongos saprofitos pueden tener efecto ovicida u ovistático sobre los huevos. El objetivo fue aplicar la microscopía electrónica de barrido (MEB) para observar la acción de 2 especies de Chrysosporium (C. indicum y C. keratinophylum) saprofitas de suelos, sobre huevos de Toxocara canis.Las especies a ensayar se sembraron en agar agua al 2% con una suspensión de huevos no embri-onados de T. canis y se incubaron 28 días a 28 °C. Como grupo control se utilizó una suspensión de huevos de T. canis en agar agua al 2%. El ensayo se realizó por triplicado para cada hongo y el grupo control. Las observaciones con MEB se realizaron a los 4, 7, 14, 21 y 28 días de incubación. La acción de los hongos se evaluó según las alteraciones en la superficie y los cambios en las características normales de los huevos. En este ensayo se observaron: hifas rodeando los huevos, appresorios penetrando la cubierta y cambios en la membrana característica del huevo, prevaleciendo el efecto tipo 3 (alteraciones que se producen tanto en el embrión como en la cubierta y penetración de hifas al interior de los huevos). La aplicación de la MEB permitió observar claramente que las 2 especies de Chrysosporium saprofitas de suelos, afectan el normal desarrollo de los huevos de T. canis, alteran su estructura y las alteraciones aumentan con el tiempo de exposición.

The Dynamic Genome and Transcriptome of the Human Fungal Pathogen Blastomyces and Close Relative Emmonsia.

Three closely related thermally dimorphic pathogens are causal agents of major fungal diseases affecting humans in the Americas: blastomycosis, histoplasmosis and paracoccidioidomycosis. Here we report the genome sequence and analysis of four strains of the etiological agent of blastomycosis, Blastomyces, and two species of the related genus Emmonsia, typically pathogens of small mammals. Compared to related species, Blastomyces genomes are highly expanded, with long, often sharply demarcated tracts of low GC-content sequence. These GC-poor isochore-like regions are enriched for gypsy elements, are variable in total size between isolates, and are least expanded in the avirulent B. dermatitidis strain ER-3 as compared with the virulent B. gilchristii strain SLH14081. The lack of similar regions in related species suggests these isochore-like regions originated recently in the ancestor of the Blastomyces lineage. While gene content is highly conserved between Blastomyces and related fungi, we identified changes in copy number of genes potentially involved in host interaction, including proteases and characterized antigens. In addition, we studied gene expression changes of B. dermatitidis during the interaction of the infectious yeast form with macrophages and in a mouse model. Both experiments highlight a strong antioxidant defense response in Blastomyces, and upregulation of dioxygenases in vivo suggests that dioxide produced by antioxidants may be further utilized for amino acid metabolism. We identify a number of functional categories upregulated exclusively in vivo, such as secreted proteins, zinc acquisition proteins, and cysteine and tryptophan metabolism, which may include critical virulence factors missed before in in vitro studies. Across the dimorphic fungi, loss of certain zinc acquisition genes and differences in amino acid metabolism suggest unique adaptations of Blastomyces to its host environment. These results reveal the dynamics of genome evolution and of factors contributing to virulence in Blastomyces.

Disseminated infection caused by Emmonsia pasteuriana in a renal transplant recipient.

Emmonsia pasteuriana is a thermally dimorphic fungus identified in very few human cases. Here, we report a case of a 43-year-old male renal transplant patient from China presenting with multiple painful skin eruptions on his head, nose and left thigh, later accompanied by respiratory failure. Histopathology of the biopsy collected from the left thigh upper ulcer and occipital nodule both demonstrated chronic inflammation with granuloma formation and yeast-like elements. Emmonsia pasteuriana was cultured from two biopsy specimens and their identity was confirmed by sequencing of the rDNA internal transcribed spacer. The patient in intensive care showed marked clinical improvement with antifungal treatment.

First detection of adiaspiromycosis in the lungs of a deer.

Adiaspiromycosis is a pulmonary infection caused by the soil fungi, Emmonsia crescens and E. parva. It primarily affects small mammals and can range from an asymptomatic condition to fatal disseminated disease. We detected a granuloma containing fungal spherules, which were morphologically consistent with the adiaspores of E. crescens in the lungs of a female Hokkaido sika deer. This is the first reported case of adiaspiromycosis involving a cervid in the world.

Adiaspiromicose pulmonar humana / Human pulmonary adiaspiromycosis

A adiaspiromicose é uma doença fúngica sistêmica que acomete usualmente roedores e raramente atinge o homem. É causada pelo fungo Emmonsia crescens e ocorre após a inalação da forma contagiante (conídios). Embora estas formas não se multipliquem nem se disseminem no organismo humano, induzem uma reação inflamatória crônica granulomatosa de padrão miliar que pode levar a falência respiratória e morte. Apresentamos aqui um caso de adiaspiromicose pulmonar humana em paciente imunocompetente que exibia infiltrado intersticial pulmonar difuso ao exame de imagem e fora diagnosticado mediante biópsia pulmonar.

Adiaspiromycosis is a systemic fungal disease that usually affects rodents and rarely infects humans. It is caused by the fungus Emmonsia crescens and occurs after inhalation of its contagious form (conidia). Although these forms neither multiply nor spread in the human body, they cause a chronic granulomatous inflammatory reaction of miliary pattern, which may lead to respiratory failure and death. In this study we present a case of human pulmonary adiaspiromycosis in an immunocompetent patient that showed a diffuse pulmonary interstitial infiltrate diagnosed by pulmonary biopsy.

Emmonsia crescens infection in a British water vole (Arvicola terrestris).

Emmonsia crescens, a dimorphic fungus of the order Onygenales, is primarily a pathogen of lower animals and rarely humans. Inhaled conidia of E. crescens fail to germinate in the lungs, and instead simply enlarge in lung tissue to become giant adiaspores. We present here the case of fatal Emmonsia crescens infection in a wild-caught British water vole (Arvicola terrestris). Histopathological examination of the animal, which died in captivity, revealed a multifocally extensive granulomatous reaction containing oval adiaspores scattered irregularly throughout the lungs. Mycological examination of fungus cultured from lung tissue and PCR amplification and sequencing of rDNA gene fragments of the cultured organism confirmed the diagnosis of massive infection by E. crescens.

Pathogenicity of the Chrysosporium anamorph of Nannizziopsis vriesii for veiled chameleons (Chamaeleo calyptratus).

Veiled chameleons (Chamaeleo calyptratus) were experimentally challenged with the fungus Chrysosporium anamorph of Nannizziopsis vriesii (CANV). Chameleons were exposed to conidia in their captive environment, or were inoculated by direct application of a conidial suspension inoculum on intact and on abraded skin. The CANV induced lesions in all experimental groups and was recovered from infected animals, fulfilling Koch's postulates and confirming that it may act as a primary fungal pathogen in this species of reptile. A breach in cutaneous integrity, as simulated by mild scarification, increased the risk of infection but was not required for the CANV to express pathogenicity. Initial hyphae proliferation occurred in the outer epidermal stratum corneum, with subsequent invasion of the deeper epidermal strata and dermis. A spectrum of lesions was observed ranging from liquefactive necrosis of the epidermis to granulomatous inflammation in the dermis. CANV dermatomycosis appears to be contagious and can readily spread within a reptile collection, either directly through contact with infective arthroconidia or indirectly via fomites. Dense tufts of arthroconidiating hyphae were demonstrated histologically on the skin surface of many animals that developed dermatomycosis, and these arthroconidia may act as infective propagules involved in the transfer of disease between reptiles.

Pulmonary adiaspiromycosis: report of two cases / Adiaspiromicose pulmonar: relato de dois casos

Relatam-se casos de adiaspiromicose pulmonar em homens brancos de 29 e 54 anos, lavradores, com sintomas "gripais" e achados radiológicos sugestivos de doença granulomatosa intersticial. Biópsias transbrônquicas e transtoracoscópicas foram realizadas. A funçäo pulmonar foi avaliada por espirometria. Um paciente usou cetoconazol. Enfatizam-se possibilidades de confusäo diagnóstica na adiaspiromicose pulmonar

Yeast tissue phase of Emmonsia pasteuriana inoculated in golden hamster by intratesticular way.

The scope of our study was to present an experimental model reproducing the dimorphic yeast-like population (as for Histoplasma capsulatum, Blastomyces dermatitidis) similar to that observed in the cutaneous biopsy of an Italian woman who had never traveled abroad, being intravenous drug user and HIV positive for 10 years, finally infected with the new dimorphic fungus Emmonsia pasteuriana. Experimental inoculation was unsuccessful by intraperitoneal (i.p.) and intravenous (i.v.) ways in a mouse and in a guinea-pig model inoculated by cutaneous or subcutaneous routes, reason for that we chose the golden hamster, highly sensitive to dimorphic fungi as agents of systemic mycoses as histoplasmosis, blastomycosis, sporotrichosis, penicilliosis marneffei, paracoccidioidomycosis when the inoculation was done by intraperitoneal route. We inoculated young golden hamsters by i.p. and intratesticular ways. Only by this last route we reproduced an orchiepididymitis with necrosis, haemorrhages and a polymorphic yeast-like population similar to the polymorphism observed in the cutaneous biopsy of the patient. The intratesticular affinity of E. pasteuriana provided an interesting model for this infection.

Disseminated infection due to Chrysosporium zonatum in a patient with chronic granulomatous disease and review of non-Aspergillus fungal infections in patients with this disease.

We report the first case of Chrysosporium zonatum infection in a 15-year-old male with chronic granulomatous disease who developed a lobar pneumonia and tibia osteomyelitis while on prophylaxis with gamma interferon. The fungus was isolated from sputum and affected bone, and hyphae were observed in the bone by histopathology. Therapy with amphotericin B eradicated the osteomyelitis and pneumonia, but pneumonia recurred in association with pericarditis and pleuritis during therapy with itraconazole. These manifestations subsided, and no recurrences occurred with liposomal amphotericin B therapy. Infections caused by Chrysosporium species are very rare, and C. zonatum has not previously been reported to cause mycosis in humans. This species, the anamorph of the heterothallic ascomycete Uncinocarpus orissi (family Onygenaceae), is distinguished by its thermotolerance, by colonies which darken from yellowish white to buff, and by club-shaped terminal aleurioconidia borne at the ends of short, typically curved stalks. The case isolate produced fertile ascomata in mating tests with representative isolates. The median (range) MICs for our isolate as well as those for two other human isolates and a nonhuman isolate determined by the National Committee for Clinical Laboratory Standards method adapted for moulds were 128 microg/ml (>128 microg/ml) for flucytosine, and 48 microg/ml (32 to >128 microg/ml) for fluconazole.

Los alergenos del ambiente tabacalero / Allergens of tobacco environment

Se halló 16 a 60 esporos fúngicos/litro aire y de 100 a 100.000 esporos de actinomicetos termófilos/g polvo del piso en los secaderos de tabaco. Los hongos eran Alternaria sp (21 por ciento), Aspergillus sp (15 por ciento), Asp. fumigatus (7 por ciento), Asp. glaucus (5,5 por ciento), Asp. nidulans (13,3 por ciento), Chaetomiun sp (2,3 por ciento), Chrysosporium spp (5,5 por ciento), Cladosporium sp (3,1 por ciento), Curvularia sp (0,8 por ciento), Dactylaria sp (3,1 por ciento), Nogrospora sp (5,5 por ciento), Penicillium spp (11,7 por ciento), Talaromyces sp (2,3 por ciento) y no identificado (3,9 por ciento). Los Thermoactinomyces eran Tha. thalpophilus (66,6 por ciento), Tha. sacchari (6,7 por ciento), Tha. vulgaris (6,7 por ciento) y otros Tha. spp (20 por ciento). También el humo de cigarrillos contenía esporos viables de Thermoactinomyces. El 7 ñ 3,3 por ciento de los trabajadores tenían anticuerpos anti-Tha. thalpophilus demostrados por doble inmunodifusión

Adiaspiromicose pulmonar granulomatosa disseminada / Disseminated granulomatous pulmonary adiaspiromycosis

Os autores apresentam 4 casos de adiaspiromicose humana pulmonar difusa, diagnóstica in vivo. A apresentaçäo é justificada pela raridade de casos relatados a doença é um achado de necrópsia na forma de uma lesäo granulomatosa única - granuloma pulmonar adiaspiromicótico. A inalaçäo maciça leva à forma difusa - adiaspiromicose pulmonar granulomatosa disseminada -, que se apresenta como infiltrado intersticial (nodular ou retículo-nodular), difuso ou localizado, podendo determinar insuficiência respiratória. É questionável a disseminaçäo endógena

Pathogenicity of some Chrysosporium species isolated in France.

In order to appreciate the pathogenicity of several geophilic Chrysosporium species (including Anixiopsis stercoraria, Chrysosporium keratinophilum, C. tropicum, C. pannorum, C. state Arthroderma curreyi, C. state of A. multifidum, and C. state of A. tuberculatum), the authors have realized two series of experimental infestations. Inoculation of these fungi on the back of guinea pigs produced rare erythematous scaling lesions which spontaneously disappeared 3-5 weeks later. No real hair invasion was observed. In white mice, eight weeks after intraperitoneal inoculation, granulomas with necrotic center were observed in the peritoneal tissue with C. keratinophilum, C. tropicum, C. state of A. curreyi and C. state A. tuberculatum. Conidia were often intact in necrotic centers and retrocultures were positive. With C. state of A. curreyi, spherical spores associated with rare budding cells were noted. The pathogenic role of these keratinophilic fungi is uncertain. However, their ability to remain viable for several weeks in skin and peritoneal tissue indicates that they could become pathogen in certain circumstances.

Avirulence and decreased virulence in mutants of Emmonsia crescens, a causative agent of adiaspiromycosis.

Three mutants of Emmonsia crescens with altered morphology and pathogenicity for mice are described. The mutant M-1 is avirulent and does not form adiaspores of normal morphology on agar medium at 37 degree C. The mutants M-2 and M-12 have a considerably decreased virulence. The pathogenicity of E. crescens depends on the ability to differentiate adiaspores of perfect morphology. The loss of virulence and the decrease of virulence of mutants seem to be caused by the pleiotrophic effect of mutation of the genetic base, which regulates the differentiation of adiaspores. The conidia of the wild strain of E. crescens killed by UV-irradiation do not induce the formation of granulomas with adiaspores after i.p. inoculation into mice.

Mutants of Emmonsia crescens--their pathogenicity and size of adiaspores in vivo.

The pathogenicity of seven morphological mutants of Emmonsia crescens was tested by means of intraperitoneal inoculation in mice. All mutants caused adiaspiromycosis. Adiaspores were isolated from granulomas after 2 months and their diameters were determined. Adiaspores from granulomas caused by five mutants (M-5, M-6, M-8, M-9 and M-16) were significantly smaller than adiaspores from granulomas caused by the wild strain, from which the mutants were derived. Two mutants (M-6 and M-9) produced adiaspores of the smallest diameter (130.5 and 119.9 mum) with the lowest variance of values, differing thus most from the original wild strain with adiaspores of 230.4 mum in diameter. A positive correlation was found between the size of the adiaspore in vivo and growth rate of the mycelial stage of Emmonsia crescens in vitro. The mutation characterized by the decreased growth rate of the mycelial stage is phenotypically manifested in the adiasporic stage of the life cycle of Emmonsia crescens, i.e. by the smaller average size of adiaspores in granulomas.