The Medical Research Council's Medical Mycology Committee (1943-1969). A chapter in the history of medical mycology in the United Kingdom.
Explore the source record for details and available documents.
SEARCH · Search PubMed
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.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
The effectiveness of Aspergillus differential medium (ADM) for the identification of Aspergillus strains was tested. The bright yellow-orange pigment was produced by 205 (88,7%) of 231 strains and resp. 97 (61,3%) of 158 strains, which during routine mycologic diagnostic as A.flavus and A.oryzae, respectively. Strains of the groups A.clavatus (76), A.glacus (100), A.fumigatus-(9), A.niger-(6), A.candidus-(3), A.wentii-(1), A.versicolor (23), A.nidulans (6), A.ustus (1) and A.terreus (1) gave negative results. Positive results were shown by 9 strains of the A.ochraceus group. It was shown that for the mycological examination of certain foods the ADM medium can make an important contribution to the identification of potential aflatoxin producers. However it is better not to use the ADM medium only alone but also together with other customary mycological nutrient media.
Sensitivity to ethylenediamine and to epoxy resin hardeners was found in three patients with long standing contact dermatitis. In one patient, a young man, the sensitivity was elicited by occupational contact with epoxy resin hardeners and subsequently sustained by use of Mycolog cream. In two patients, both elderly women, the condition was only due to use of Mycolog cream. These case histories and test results indicate that use of Mycolog cream can result in occupational disease viz. contact dermatitis from epoxy hardeners.
Mycolog contact allergy is due primarily to its ethylenediamine and fragrance components. In the evaluation of Mycolog-sensitive patients, the major constituents, including the perfume at 5% or 10% in petrolatum, should be tested.
Patients hospitalized in an intensive care unit must be considered to be exposed to a "high risk" in terms of candida infection. They often combine several of the factors favouring the development of "candida disease": generally deficient state, multiple antibiotics, iatrogenic or pathological immune depression. While certain patients who are admitted are already suffering from "candida infestation" (endogenous localization), the possibilities of exagenous infection are numerous. This study involved 63 patients spending at least one week in the department, from September 1977 to September 1978. Mycological (pharyngeal swab, urine culture, blood culture) and immunological (hemagglutination, immunoelectrophoresis, immunofluorescence) studies were carried out routinely on admission and then every week. Amongst the 63 patients studied, 12 were admitted with negative serology, which became positive during the first 10 days. 5 already had positive serology at the time of admission. From a mycological standpoint, the pharyngeal swab was frequently positive on admission (17 times out of 63). In 63 patients, the infection was acquired during the course of the hospital stay and, in this case, positive urine cultures were more regularly associated with a positive pharyngeal culture.
40 patients with haemoblastosis were examined clinically and by cultures for presence of yeast mycosis. Moreover, we analyzed specific antibodies with the help of cell agglutination, the passive haemagglutination and the precipitation using Candida antigen. 29 test persons were found having a yeast mycosis, 3 patients without clinical symptoms in pharynx showed presence of yeasts by culture, 8 test persons were clinically and mycologically negative. In cell agglutination we recorded titres of less than 1:20 to 1:5 160 and in haemagglutination titres of less than 1:20 to 1:5 160 and in haemagglutination such of less than 1:20 to 1:320. 5 patients showed positive precipitation reaction with antigen extracted of membranes of Candida albicans cells. We observed different titre motions with these patients: during illness the titre either rised or decreased clearly, or the patients were in a condition of humoral anergy against the Candida albicans antigen. It is hinted at the necessity to watch over susceptible patients mycologically.
OBJECTIVES: Evaluate the 2025 European Society of Clinical Microbiology and Infectious Diseases-European Fungal Infection Study Group webinar series to assess digital education as a scalable, equitable model for global professional development in medical mycology. METHODS: This observational study analyzed Zoom metadata across 17 webinars (January-December 2025). Metrics included registration, unique viewers, peak concurrent views, attendance rate, and duration. RESULTS: The series recorded 4631 registrations and 1372 unique participants. Median live attendance was 199 (interquartile range [IQR] 138-269), with a 39.3% attendance rate (IQR 33.7-47.5%) and peak concurrent viewership of 165 (IQR 106-229). Median session duration was 108 minutes. Webinars engaged a median of 60 countries (range 26-89) simultaneously, spanning 128 countries globally. Faculty comprised 67 unique experts from 23 countries with balanced gender representation (52.8% men, 47.2% women), of whom 16.4% (n = 11/67) were affiliated with institutions in low- and middle-income countries. CONCLUSION: Structured digital programs achieve wide global reach and sustained engagement. Strong participation in long-form sessions supports implementing Continuing Medical Education accreditation and unrestricted on-demand access to enhance global health equity.
Fungi are important and hyperdiverse organisms, yet chronically understudied. Most fungal clades have no reference genomes, impeding our understanding of their ecosystem functions and use as solutions in health and biotechnology. Also, opportunities for training in fungal biology and genomics are lacking, creating a bottleneck that hinders the recruitment and cultivation of a talented future mycological workforce. To address these issues, we developed Myco-Ed, an educational program offering training and scientific contributions through genome sequencing and analysis. Myco-Ed empowers students to pursue careers in fungal biology while improving fungal resources. Myco-Ed has been piloted at 12 institutions (15 classrooms) ranging from online e-Campuses to R1 universities, resulting in hundreds of fungal observations and many new high-quality reference genomes.
Mycological analyses were made on specimens obtained from the skin, oral rinse, urine, and feces of three subjects participating in a 56 day Skylab simulation test. Samples were taken over a 175 day period divided into three phases consisting of a prechamber, intrachamber, and postchamber period. A total of 69 species of filamentous fungi and 22 species of yeast and yeast-like fungi were recovered and identified. There was a marked decrease in the isolation incidence of both the filamentous and yeast and yeast-like fungi during the intrachamber period. This, taken with the fact that 71% of the filamentous species and 55% of the yeast and yeast-like species were isolated no more than twice, reflects the transitory nature of the relationship between the human body and most fungi. However, there was a relative increase in the potential pathogens Candida albicans and Candida parapsilosis during the intrachamber period. Over 50% of all fungi recovered were isolated from the nasal and oral cavities. There was no evidence of intercrew transfer of a particular species during the intrachamber period nor was there any evidence of microbial shock during the postchamber period.
A total of 41 calves which were naturally infected with Trichophyton verrucosum were treated with natamycin used as a total body spray. Ten other infected animals were not treated and considered as control animals. Clinical observation and mycological examination show partial improvement to complete recovery with simultaneous sterilisation of the infected skin areas. Five to six weeks after treatment, 88 per cent of the treated animals had recovered or showed a distinct improvement, 65 per cent had a negative culture. After 11 to 12 weeks these percentages were 95 and 91, respectively. All controls yielded a positive culture during the whole observation period. The method used for the detection of the presence of Trich verrucosum in skin scrapings and hairs permitted accurate diagnosis in as little as two to five days.
The taxonomical value of the specific distinction of C. albicans and C. stellatoidea was in mind, in the mycological study of: one homogenous group of 292 isolates of C. albicans and an other of 11 C. stellatoidae, of collection in majority. The growth in a liquid medium, the production: of chlamydospores, mycelium, pseudomycelium, germ-tubes, the fermentation and assimilation of carbohydrates, the tetrazolium-test, the actidione resistance and the maximal temperature for growth were the morpho-physiological characteristics studied. Were also reported some variations observed on two C. stellatoidea from which the type-strain of that species, cultured in two different laboratories.
Over a thirteen year period (1965 to 1977) a total of 4790 skin scrapings and hair samples of animals were examined mycologically. 887 strains of dermatophytes were isolated out of 885 of these samples (= 18,5%). Most frequently Trichophyton verrucosum was identified in samples from cattle, followed by Microsporum canis isolated from cats, dogs and zoo animals. T. mentagrophytes was mainly found on guinea pigs, chinchillas and dogs and T. equinum on horses. Although the total number of the samples examined within the last 8 years increased, the total of the dermatophytes isolated remained proportionately the same. The relative numbers of the various species of dermatophytes isolated did not change within the period of investigation.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.