Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “MICROSPORUM”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 91 records · Page 5Linked to original sources

Metabolism of sulfur-containing amino acids in the dermatophyte Microsporum gypseum. I. Neutral amino acids.

The dermatophyte Microsporum gypseum was cultivated on a glucose-arginine medium to which on out of six sulfur-containing amino acids was added (L-cystine, L-djenkolic acid, DL-lanthionine DL-homocystine, L-methionine, or L-methionine-sulfone at a concentration of 5 mM with respect to sulfur content). The addition of these substances did not stimulate the growth and some amino acids (djenkolic acid and particularly methionine and methionine-sulfone) were inhibitory. All tested compounds were utilized during the growth not only as sulfur source but as a source of carbon and nitrogen as well. In four substrates excess sulfur was excreted after oxidation into the medium in the form of sulfate. Small amounts of sulfite were also observed. It usually reacted with remaining disulfides in the medium forming S-sulfo compounds (R-S.SO3H). Cystine and djenkolic acid were oxidized rapidly and completely. In contrast, lanthionine and particularly homocystine were oxidized slowly and only after a longer adaptation. To some extent lanthionine was already oxidized extracellularly in the medium. With methionine and its sulfone, excess sulfur was not removed by oxidation but by demethiolation to methane thiol and further volatile products.

Alanine↗

Metabolism of sulfur-containing amino acids in the dermatophyte Microsporum gypseum. II. Acidic amino acid derivatives.

The dermatophyte Microsporum gypseum was cultivated on a glucose-arginine medium supplemented with five strongly acidic derivatives of cysteine (L-cysteine sulfinic acid, L-cysteic acid, L-serine-O-sulfate and taurine at a concentration of 5 mmol/l, and L-S-sulfocysteine at a concentration of 2.5 mmol/l). The addition of these substances did not stimulate the growth as compared with the control containing 0.5 mmol/l cystine. Cysteine sulfinic acid and cysteic acid showed rather inhibitory effects. A strong inhibition of the growth was caused by the presence of serine sulfate. During the growth, all substances investigated were gradually consumed and utilized not only as a source of sulfur but of nitrogen and carbon as well. Cysteine sulfinic acid and S-sulfocysteine were utilized most rapidly. Cysteic acid was also rapidly utilized but after a certain adaptation. Taurine was utilized slowly and serine sulfate very slowly. Excess sulfur contained in the substances used was excreted into the medium in the form of sulfate. Sulfate excretion was most rapid with cysteine sulfinic acid and slowest with taurine. With cysteine sulfinic acid, S-sulfocysteine and cysteic acid, small amounts of sulfite were found in the medium. The results obtained are in accordance with the presumption that cysteine sulfinic acid (but not cysteic acid and taurine) is an intermediate of cysteine catabolism in dermatophytes.

Amino Acids, Sulfur↗

Utilization of various concentrations of free cystine by the fungus Microsporum gypseum.

The dermatophyte Microsporum gypseum was cultivated on two liquid media enriched with 50 to 1000 micrograms/ml free L-cystine. The presence of cystine in concentrations above 250 micrograms/ml (gelatin medium) or 500 micrograms/ml (glucose-glutamate medium) inhibited the growth. In all variants, however, cystine was utilized from the very beginning of growth and exhausted completely until stationary phase. The rate of cystine metabolization grew with its concentration to 500 micrograms/ml but decreased again with 1000 micrograms/ml. The excess sulfur was oxidized and excreted back into the medium mainly as inorganic sulfate. Moreover, sulfite was also produced which immediately reacted with the residual cystine in the medium giving rise to S-sulfocysteine. Sulfite excretion was higher in the initial phases of growth and on the medium with poorer growth (gelatin medium). The sulfate-to-sulfite ratio was different on the two media used but was little influenced by cystine concentration. The excretion of strongly acidic compounds (sulfate, sulfite, and S-sulfocysteine) reduced the usual alkalinization of the medium in the course of growth.

Culture Media↗

Purification of diacylglycerol kinase from Microsporum gypseum and its phosphorylation by the catalytic subunit of protein kinase A.

Diacylglycerol (DG) kinase (EC 2.7.1.107) was purified to homogeneity from the soluble extract of Microsporum gypseum, a dermatophyte. Purified enzyme showed a final specific activity of 2172 pmol/min/mg protein and its apparent molecular weight on SDS-PAGE was found to be 93 kDa. The activity of purified enzyme was inhibited in a dose-dependent manner in the presence of DG-kinase inhibitor (D5919, Sigma). DG-kinase activity was found to be stimulated in the presence of phosphatidylcholine, phosphatidylethanolamine, and cardiolipin while the activity was alleviated in the presence of phosphatidic acid and arachidonic acid. Kinase activity was partially inhibited when assayed after prior treatment with alkaline phosphatase. Treatment of DG-kinase with the catalytic subunit of protein kinase A (PKA)-stimulated DG-kinase activity in a dose-dependent manner. Incubation of DG-kinase with the catalytic subunit of PKA led to the phosphorylation of DG-kinase as revealed by autoradiography. The phosphorylated band disappeared completely in the presence of specific PKA inhibitor. Increased activity of DG-kinase on incubation with the catalytic subunit of PKA was possibly due to the phosphorylation of the former by the latter. Whether this in vitro phosphorylation and activation of DG-kinase occurs under physiological conditions remains to be elucidated.

Adenosine Triphosphate↗

Tinea corporis caused by Microsporum canis: report of a nosocomial outbreak.

In an unusual nosocomial outbreak, 13 staff and 11 patients in an acute and chronic health care facility were infected with the zoophilic dermatophyte, Microsporum canis. The dermatophyte was apparently introduced into the facility by a single infected patient. Likely modes of subsequent disease transmission include person-to-person contact, handling of contaminated laundry, and use of a shared razor. Infection control measures for managing such outbreaks are discussed.

Adult↗

Morphological and biochemical variability of Microsporum canis strains.

Seventy-two strains of Microsporum canis, of different origins, were examined from a morphological point of view and tested in relation to their hydrolytic activity on tyrosine, xanthine, casein, gelatin, their ureasic activity and their capacity to assimilate different nitrogenous substances. The morphological aspects, that vary within the M. canis isolates, were constant in the strains isolated from rabbits. A strain with particular features was isolated many times from the dogs and cats coming from the same breeder. In one case of pseudomycetoma, different isolates suggested the co-existence in animals of two different strains, one present on fur, the other responsible for deep lesions.

Animals↗

Detection of circulating antibodies to purified keratinolytic proteinase in sera from guinea pigs infected with Microsporum canis by enzyme-linked immunosorbent assay.

A keratinolytic proteinase (KPase) which is regarded as an important factor in the pathogenesis of dermatophytosis was isolated and purified from Microsporum (M.) canis culture filtrates. Enzyme-linked immunosorbent assay (ELISA) was used to determine the occurrence of circulating antibodies to this enzyme in sera samples from guinea pigs with superficial fungal infections caused by M. canis. Of sera samples from guinea pigs infected with M. canis, 75% were reactive within 10 weeks, however, those ELISA values were relatively low compared with those from guinea pigs immunized with KPase. The presence of circulating antibodies was first detected 2 weeks post inoculation with M. canis, corresponding to the period when the lesions were most severe. The titers of the ELISA antibodies reached a peak at 4 weeks; at that time the lesions had disappeared completely.

Animals↗

Studies on the macroconidia of Microsporum canis. Characteristics of in vitro amino acid incorporating system.

The characteristics of an in vitro polyuridylic acid dependent amino acid incorporating system prepared from germinating macroconidia of Microsporum canis are described. The incorporation of 14C-phenylalanine into polyphenylalanine is dependent on S-30 extract, adenosine triphosphate, magnesium ions and polyuridylic acid. Incorporation is slightly enhanced by yeast transfer ribonucleic acid and pyruvate kinase. The system is highly sensitive to ribonuclease, puromycin and miconazole (an antifungal agent), moderately sensitive to sodium fluoride and much less sensitive to phenethylalcohol, cycloheximide, chloramphenicol and deoxyribonuclease. Cell-free extract from ungerminated conidia has less capacity to synthesize the protein and during germination a marked increase in the protein synthetic activity is observed. The results from experiments wherein ribosomes and S-100 fraction from germinated and ungerminated spores are unterchanged, revealed that the defect in the extract from the ungerminated spore is in the ribosomes.

Cell-Free System↗

Fungus invasion of human hair tissue in tinea capitis caused by Microsporum canis: light and electron microscopic study.

Previously, we reported a morphological change of Trichophyton violaceum in hair tissue in black dot ringworm. To investigate the morphology of Microsporum canis in human hais tissue, three cases of tinea capitis by M. canis were examined by both light and electron microscopy. The fungal elements, which were located deeplyin the keratogenous zone, showed nonseptate hyphae in the outer part of the hair cortex. With the upward development of hair tissues, some hyphae invaded the keratinized inner root sheath and were there transformed into arthrospores, which then occupied the large volume of the inner root sheath; each spore was surrounded by an electron-lucent halo. In some affected hair follicles, at the follicular isthmus level, a microabscess composed of polymorphonuclear leukocytes was often formed in the outer root sheath adjacent to the arthrospores in the keratinized inner root sheath. On the other hand, the remaining hyphae in the cortex became degenerated. Fungi did not invade the hair-germinative cells. There is a distinct relationship between the morphological change of fungi and the differentiation of hair cells in tinea capitis by M. canis as well as in that by T. violaceum, although the direction of invasion and pathological roles of fungal elements within hair tissue are significantly different between the two species of fungi.

Child, Preschool↗

Extensive dermatophytoses caused by Trichophyton mentagrophytes and Microsporum canis in a patient with AIDS.

Retrospective studies have shown the occurrence of episodes of deep or superficial fungal infections in 58 to 81% of HIV/AIDS patients as a result of impairment of cell immunity. We describe a case of disseminated cutaneous dermatophytoses caused by Trichophyton mentagrophytes and Microsporum canis in a patients with AIDS. Diagnostic and therapeutic problems in relation to this unusual presentation are emphasized as well as the importance of an early mycologic diagnosis to prescribe antifungal therapy.

AIDS-Related Opportunistic Infections↗

Studies in the differentiation between Microsporum ferrugineum Ota and Trichophyton soudanense Joyeux.

A study, conducted with 20 isolates of Microsporum ferrugineum and 12 isolates of Trichophyton soudanense, revealed that some of the discrepancies in the literature regarding their characteristics and differentiation were due to methodology, strain variation and the use of an insufficient number of isolates. We found all isolates of T. soudanense to be urease negative and gelatinase positive (usually by the first week); to produce brown to black colonies on Lowenstein-Jensen medium; to rapidly decompose casein and more slowly tyrosine; to grow well or better at 37 degrees C as compared to room temperature; to produce reflexive branching on cornmeal Tween agar and abundant microconidia on casero medium and to exhibit no sexual reaction with either mating type of arthroderma simii. All but one isolate demonstrated restricted growth on lactose agar and only three isolates perforated hair. In contrast, we found 18 of 20 isolates of M. ferrugineum to be urease positive in urea broth (most isolates were negative on urea agar); all produced light-colored colonies on Lowenstein-Jensen medium; spreading colonies on lactose agar and failed to perforate hair in vitro or to produce reflexive branching. Most isolates manifested poorer to no growth at 37 degrees C compared to room temperature and all but one failed to decompose casein and tyrosine. A few strains produced macroconidia and/or microconidia on casero medium and some reacted sexually with A. simii (a) (-) mating type. Gelatin hydrolysis was variable.(ABSTRACT TRUNCATED AT 250 WORDS)

Culture Media↗

Scanning electron microscopy on Microsporum audouini complex.

Several strains of Microsporum audouini, M. langeroni and M. rivalieri were observed by light and scanning electron microscopies. The macroaleuriospore shape and ornamentation were illustrated and compared for the 3 species as the pectinate hyphae for M. langeroni and M. rivalieri and the chlamydospores and particular hyphae for M. audouini and M. langeroni. The 3 species are morphologically very close but they are distinguishable from each other on the basis of morphology, geographic distribution and pathogenicity.

Dermatomycoses↗

Disturbances in toxicological experiments caused by Microsporum canis.

Cutaneous lesions which can lead to false positive results have been observed in several rabbits used for the determination of the cutaneous irritation capacity of a product (ITA, PII). The responsible agent was Microsporum canis. A preventive treatment by an antifungal agent did not modify toxicological experimental results.

Animals↗

Electron microscopy of Microsporum cookei after 'in vitro' treatment with protoanemonin: a combined SEM and TEM study.

The ranunculaceous derivative protoanemonin (PrA) was studied as an antifungal agent on the dermatophyte Microsporum cookei. The ultrastructural changes that PrA brought about in this fungus were observed with both the transmission and scanning electron microscopes. The main anomalies noted were abnormally shaped hyphae and within the cytoplasm, multimembranous bodies which were irregular in shape and size, and tubules of 25 and 60 nm in diameters. Mitochondria, nuclei and vacuoles were also variously affected by PrA. Although multifarious, the observed cellular alterations in M. cookei can be considered the result of a PrA interaction with cytoplasmic microtubules. Since these cell structures contain a great number of ASH groups, our previous hypothesis, that sulphydryl groups are the primary targets of this molecule, appears to be supported.

Antifungal Agents↗

Microscopic observation of human hairs infected with Microsporum ferrugineum.

Human hairs infected with Microsporum ferrugineum were examined by light and scanning electron microscopy to obtain information on the parasitic form. The fungus invaded the hair filaments and developed hyphae between the hair cuticles and cortex. Spheroids of arthroconidia were frequently observed to invade the hair follicle. A mosaic sheath of massive spheroids was observed around the hair filaments. The smooth-walled arthroconidia with chitinous surfaces were single, spherical or subspherical particles of 2.0-2.5 X 2.5-3.5 microns, and 2-celled, gourd-shaped (constricted at the septum) particles of 2.5-3.0 X 5.0-7.0 microns.

Child↗

Atypical cases of Microsporum canis infection in the adult.

Eleven adult patients (7 males, 4 females) were found to be infected with Microsporum canis. There was involvement of the scalp in three patients: in one male and one female there were kerion-like lesions and in one male the lesions resembled seborrheic dermatitis. There were three cases of tinea barbae, males aged 28, 65 and 82 years, in the first resembling an infected single lesion of granuloma annulare, the second with a kerion-like lesion and the third with an abscess-like tumor. There were five patients with lesions in glabrous areas: one male with a lesion of the palm resembling erythema multiforme and one with an infection of the auricular lobe resembling a seborrheic dermatitis or otitis externa; of three females with tinea faciei one had a lesion simulating granuloma faciale, one simulating lymphocytic infiltration and one simulating discoid lupus erythematosus. A cat was the source of infection in three cases; in the remainder it could not be determined with certainty. It is of note that a continuous increase in infection with M. canis has been observed in Israel during the past five years.

Adult↗

Optimization of protoplast formation, regeneration, and viability in Microsporum gypseum.

Factors affecting high yields, regeneration frequencies, and viability of protoplasts from clonal cultures of Microsporum gypseum were investigated. Maximum yields of protoplasts were obtained after 6 hrs digestion of 2-4 days old mycelium with Novozyme 234 using CaCl2 (0.4 M) as an osmotic stabilizer and glycine + HCl (pH 4.5) as the buffer system. Mercaptoethanol + dithiothreitol (0.01 M) proved to be the best pretreatment of mycelium prior to digestion with enzyme. A regeneration frequency of 94.4% was obtained using the top agar method with complete medium (pH 6.5) containing 0.5% agar and 0.4 M CaCl2 as an osmoticum. Colonies from regenerated protoplasts on medium containing CaCl2 were pigmented and completely powdery with high sporulation. Protoplast viability was studied in osmotic stabilizer supplemented with glucose or glutamine. After 24 hrs, glucose (2%) and glutamine (2%) enhanced protoplast viability by 22% and 23%, respectively. Protein synthesis, as measured by 3H-lysine uptake, matched the viability profile determined by fluorescence microscopy.

Buffers↗

The septal ontogeny, germination and electron microscopy of Microsporum gypseum macroaleurioconidia.

Microsporum gypseum strains obtained from human and animal cases of dermatophytosis were used to study the septal ontogeny, the germination, and the electron microscopy of the macroaleurioconidia, which are produced so abundantly by this organism. It was found that the number of septa in a macroaleurioconidium depends upon the stage of development, and that their order of formation remains relatively constant. The macroaleurioconidial cell wall proved to be impressive on electron microscopy. The use of a wetting agent (Tween 80) and negative pressure proved necessary for adequate fixation. Poor penetration of the fixing agent is attributable to the electron-dense encrustations over the entire surface of the macroaleurioconidium.

Animals↗