Introduction to Mycology
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Chlamydospore Agar M113 Chlamydospore Agar Is Used for Differentiating Candida Albicans from Other Species of Candida on the Basis of Chlamydospore Formation
HiMedia Laboratories Technical Data Chlamydospore Agar M113 Chlamydospore Agar is used for differentiating Candida albicans from other species of Candida on the basis of chlamydospore formation. Composition** Ingredients Gms / Litre Ammonium sulphate 1.000 Monopotassium phosphate 1.000 Biotin 0.000005 Trypan blue 0.100 Purified polysaccharide 20.000 Agar 15.000 Final pH ( at 25°C) 5.1±0.2 **Formula adjusted, standardized to suit performance parameters Directions Suspend 37.1 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Mix well and pour into sterile Petri plates. Principle And Interpretation Candida albicans is a diploid sexual fungus (a form of yeast), and the causitive agent of opportunistic oral and vaginal infections in humans (1). C. albicans is a commensal of skin, gastrointestinal and genitourinary tract. However, under certain conditions overgrowth of this results into oesopharyngeal candidiasis, vulvovaginal candidiasis and candidemia. Chlamydospores formation is the most differential characteristic of C. albicans (1). Chlamydospore Agar was specially designed for the differentiation of C. albicans from other species on the basis of chlamydospores formation. It is prepared according to the formula of Nickerson and Mankowshi (2). Ammonium sulphate acts as sources of ions that simulate metabolism. Monopotassium phosphate provides buffering to the medium. Biotin provides the necessary vitamins required for metabolism. Purified polysaccharide acts as a source of carbon. Trypan blue is a vital dye absorbed selectively by the chlamydospores and imparts blue colour to chlamydospores, whereas the filaments are colourless. Test for chlamydospores: Scratch cut mark like X onto the agar surface with inoculum using sterile needle. -
Fungal Infections from Human and Animal Contact
Journal of Patient-Centered Research and Reviews Volume 4 Issue 2 Article 4 4-25-2017 Fungal Infections From Human and Animal Contact Dennis J. Baumgardner Follow this and additional works at: https://aurora.org/jpcrr Part of the Bacterial Infections and Mycoses Commons, Infectious Disease Commons, and the Skin and Connective Tissue Diseases Commons Recommended Citation Baumgardner DJ. Fungal infections from human and animal contact. J Patient Cent Res Rev. 2017;4:78-89. doi: 10.17294/2330-0698.1418 Published quarterly by Midwest-based health system Advocate Aurora Health and indexed in PubMed Central, the Journal of Patient-Centered Research and Reviews (JPCRR) is an open access, peer-reviewed medical journal focused on disseminating scholarly works devoted to improving patient-centered care practices, health outcomes, and the patient experience. REVIEW Fungal Infections From Human and Animal Contact Dennis J. Baumgardner, MD Aurora University of Wisconsin Medical Group, Aurora Health Care, Milwaukee, WI; Department of Family Medicine and Community Health, University of Wisconsin School of Medicine and Public Health, Madison, WI; Center for Urban Population Health, Milwaukee, WI Abstract Fungal infections in humans resulting from human or animal contact are relatively uncommon, but they include a significant proportion of dermatophyte infections. Some of the most commonly encountered diseases of the integument are dermatomycoses. Human or animal contact may be the source of all types of tinea infections, occasional candidal infections, and some other types of superficial or deep fungal infections. This narrative review focuses on the epidemiology, clinical features, diagnosis and treatment of anthropophilic dermatophyte infections primarily found in North America. -
NEWSLETTER 2017•Issue 2
NEWSLETTER 2017•Issue 2 page 2 Deep dermatophytosis page 4 Deep dermatophytosis: A case report page 5 Fereydounia khargensis: A new and uncommon opportunistic yeast from Malaysia page 6 Itraconazole: A quick guide for clinicians Visit us at AFWGonline.com and sign up for updates Editors’ welcome Dr Mitzi M Chua Dr Ariya Chindamporn Adult Infectious Disease Specialist Associate Professor Associate Professor Department of Microbiology Department of Microbiology & Parasitology Faculty of Medicine Cebu Institute of Medicine Chulalongkorn University Cebu City, Philippines Bangkok, Thailand This year we celebrate the 8th year of AFWG: 8 years of pursuing excellence in medical mycology throughout the region; 8 years of sharing expertise and encouraging like-minded professionals to join us in our mission. We are happy to once again share some educational articles from our experts and keep you updated on our activities through this issue. Deep dermatophytosis may be a rare skin infection, but late diagnosis or ineffective treatment may lead to mortality in some cases. This issue of the AFWG newsletter focuses on this fungal infection that usually occurs in immunosuppressed individuals. Dr Pei-Lun Sun takes us through the basics of deep dermatophytosis, presenting data from published studies, and emphasizes the importance of treating superficial tinea infections before starting immunosuppressive treatment. Dr Ruojun Wang and Professor Ruoyu Li share a case of deep dermatophytosis caused by Trichophyton rubrum. In this issue, we also feature a new fungus, Fereydounia khargensis, first discovered in 2014. Ms Ratna Mohd Tap and Dr Fairuz Amran present 2 cases of F. khargensis and show how PCR sequencing is crucial to correct identification of this uncommon yeast. -
Chapter 13: Ecosystem Mycology: Saprotrophs, and Mutualisms Between Plants and Fungi
21st Century Guidebook to Fungi, Second Edition of the online version, by David Moore, Geoffrey D. Robson and Anthony P. J. Trinci [URL: http://www.davidmoore.org.uk/21st_Century_Guidebook_to_Fungi_PLATINUM/] Chapter 13: Ecosystem mycology: saprotrophs, and mutualisms between plants and fungi 13.1 Ecosystem mycology 13.2 Fungi as recyclers and saprotrophs 13.3 Make the earth move 13.4 Fungal toxins: food contamination and deterioration 13.5 Decay of structural timber in dwellings 13.6 Using fungi to remediate toxic and recalcitrant wastes 13.7 Release of chlorohydrocarbons to the atmosphere by wood decay fungi 13.8 Introduction to mycorrhizas 13.9 Types of mycorrhiza 13.10 Arbuscular (AM) endomycorrhizas 13.11 Ericoid endomycorrhizas 13.12 Arbutoid endomycorrhizas 13.13 Monotropoid endomycorrhizas 13.14 Orchidaceous endomycorrhizas 13.15 Ectomycorrhizas 13.16 Ectendomycorrhizas 13.17 The effects of mycorrhizas and their commercial applications, and the impact of environmental and climate changes 13.18 Introduction to lichens 13.19 Introduction to endophytes 13.20 Epiphytes 13.21 Chapter 13 References and further reading Chapter 13: Ecosystem mycology: saprotrophs, and mutualisms between plants and fungi In this Chapter on ecosystem mycology we cover fungi as saprotrophs, and the mutualisms between plants and fungi, concentrating on fungi as recyclers that can make the earth move. Fungi also cause food contamination and deterioration through their formation of toxins, although some of these, like statins and strobilurins, are exploited commercially for our own practical purposes. The ability of fungi to degrade wood makes them responsible for the decay of structural timber in dwellings, but on the other hand enables them to be used to remediate toxic and recalcitrant wastes. -
Basidiomycete Mycelia in Forest Soils: Dimensions, Dynamics and Roles in Nutrient Distribution
Mycol. Res. 109 (1): 7–20 (January 2005). f The British Mycological Society 7 DOI: 10.1017/S0953756204001753 Printed in the United Kingdom. Review Basidiomycete mycelia in forest soils: dimensions, dynamics and roles in nutrient distribution John W. G. CAIRNEY Centre for Horticulture and Plant Sciences, University of Western Sydney, Parramatta Campus, Locked Bag 1797, Penrith South DC, NSW 1797, Australia. E-mail: [email protected] Received 15 July 2004; accepted 3 October 2004. Basidiomycete mycelia are ubiquitous in forest soils where they fulfil a range of key ecological functions. Population studies, based largely on basidiome collections, indicate that mycelia of many ectomycorrhizal and saprotrophic basidiomycetes can spread vegetatively for considerable distances through soil, but the extent to which these become physically or physiologically fragmented is unclear. This review considers aspects of the distribution, dynamics and translocatory activities of individual basidiomycete mycelia in forest soil, highlighting current gaps in our understanding and possible ways to address these. INTRODUCTION in soil have been constrained by a lack of suitable techniques for discrimination between them, but some On the basis of basidiome collections, it is evident that progress is now being made. A useful method for esti- forest soils in a broad range of habitats house diverse mating ECM mycelial biomass in forest soils has, for communities of basidiomycetes (e.g. Schmit, Murphy example, recently been developed (Wallander et al. & Mueller 1999, de la Luz Fierros, Navarrete-Heredia 2001). This involves burying mesh bags containing & Guzma´n-Davalos 2000, Ferris, Peace & Newton sand in forest plots and comparing mycelial biomass in 2000, Packham et al. -
Hypha and Its Characteristics
Clinical Microbiology: Open Access Commentary Hypha and its Characteristics Giusina Caggiano* Department of Biomedical Sciences, University of Bari, Bari, Italy DESCRIPTION growing tip, dividing the hypha into individual cells. Hyphae can branch by the bifurcation of a growing tip or by the emergence A fungus or actinobacterium's hypha is a long, branching of a new tip from an existing hypha. The behaviour of hypha can filamentous structure. Hyphae are the primary mode of be described as follows: environmental stimuli, such as the vegetative growth and are referred to collectively as a mycelium. application of an electric field, can control the direction of A hypha is made up of one or more cells that are surrounded by hyphal growth. Hyphae can detect reproductive units from afar a tubular cell wall. Most fungi divide their hyphae into cells via and grow towards them. To penetrate a permeable surface, internal cross-walls known as "septa". Septa are typically hyphae can weave through it. Hyphae can be modified in a perforated by pores large enough to allow ribosomes, variety of ways to perform specific functions. Some parasitic mitochondria, and occasionally nuclei to pass between cells. In fungi develop haustoria that aid in absorption within host cells. contrast to plants and oomycetes, which have cellulosic cell walls, Arbuscules of mutualistic mycorrhizal fungi perform a similar the major structural polymer in fungal cell walls is typically function in nutrient exchange and are therefore important in chitin. Some fungi have aseptate hyphae, which mean that their assisting plant nutrient and water absorption. In lichens, hyphae hyphae are not divided by septa. -
FUNGI Why Care?
FUNGI Fungal Classification, Structure, and Replication -Commonly present in nature as saprophytes, -transiently colonising or etiological agenses. -Frequently present in biological samples. -They role in pathogenesis can be difficult to determine. Why Care? • Fungi are a cause of nosocomial infections. • Fungal infections are a major problem in immune suppressed people. • Fungal infections are often mistaken for bacterial infections, with fatal consequences. Most fungi live harmlessly in the environment, but some species can cause disease in the human host. Patients with weakened immune function admitted to hospital are at high risk of developing serious, invasive fungal infections. Systemic fungal infections are a major problem among critically ill patients in acute care settings and are responsible for an increasing proportion of healthcare- associated infections THE IMPORTANCE OF FUNGI • saprobes • symbionts • commensals • parasites The fungi represent a ubiquitous and diverse group of organisms, the main purpose of which is to degrade organic matter. All fungi lead a heterotrophic existence as saprobes (organisms that live on dead or decaying matter), symbionts (organisms that live together and in which the association is of mutual advantage), commensals (organisms living in a close relationship in which one benefits from the relationship and the other neither benefits nor is harmed), or as parasites (organisms that live on or within a host from which they derive benefits without making any useful contribution in return; in the case of pathogens, the relationship is harmful to the host). Fungi have emerged in the past two decades as major causes of human disease, especially among those individuals who are immunocompromised or hospitalized with serious underlying diseases. -
What Are Fungi?
Medical Mycology (BIOL 4849) Summer 2007 Dr. Cooper What are Fungi? Fungi in the Tree of Life • Living organisms on earth first arose about 3.5 billion years ago – Prokaryotic – Anaerobic • Oldest fossils of fungi are about 460 million years old • Coincides with the rapid expansion of multi-cellular organisms • Major multicellular eukaryotes are divided into Kingdoms – Animals – Plants – Fungi • Each of these three kingdoms differ in their basic cellular structure and mode of nutrition (defined by Whittaker, 1969) – Plants - photosynthetic, cellulosic cell walls – Animals - digestive systems, wall-less cells – Fungi - absorptive nutrition, chitinous walls • The estimates for the expansion of multicellular organisms are based upon phylogenetic analyses of Carl Woese – Examined ribosomal RNA (rRNA) • Present in prokaryotes and eukaryotes • Relatively stable, but changes occur over time; thereby acting as a chronometer – Distinguished three separate groups (Domains) of living organisms • Domains - rRNA sequence differences correlate with differences in cellular structure and physiology – Bacteria - “true bacteria” – Archaea - “ancient prokaryotes” – Eucarya - eukaryotes • Taxonomic grouping of “Kingdom” lies beneath that of “Domain” • Though the fossil evidence suggests fungi were present on earth about 450 million years ago, aquatic fungi (Phylum Chytridiomycota) most likely were present about a million years before this time Page 1 of 15 Copyright © 2007 Chester R. Cooper, Jr. Medical Mycology (BIOL 4849) Lecture 1, Summer 2007 • About -
Chapter 5 Conidiophore Initiation and Conidiogenesis 5.1
102 Chapter 5 Conidiophore initiation and conidiogenesis 5.1 INTRODUCTION In this chapter are described the processes of conidiophore initiation and conidiogenesis in some Australian cercosporoid fungi. The involvement of wall layers of the conidiophore mother cell in conidiophore initiation is examined, and the events involved in conidiogenesis are then considered in terms of the following successive developmental steps proposed by Minter et al. (1982). (a) Conidiophore initiation. Ultrastructural studies showed that the production of conidiophores from stroma cells in Cercospora beticola can be enteroblastic or holoblastic (Pons et al., 1985). In enteroblastic initiation, the outer, opaque layer of the conidiophore wall was continuous with the middle wall layer of the stroma cell. The outer layer of the generative cell either stopped abruptly or else merged imperceptibly with the wall of the conidiophore. The latter type of conidiophore initiation resembled that from vegetative hyphae in Pleiochaeta setosa (Kirchn.) Hughes (Harvey, 1974). (b) Conidium ontogeny, described as 'the ways in which conidial cell walls are produced' (Minter et al., 1982). The accepted view that conidium initiation is holoblastic in the cercosporoid fungi (Ellis, 1971) was supported by the results of Pons et al. (1985). (c) Conidium delimitation, described as 'the ways in which delimiting septa are produced' (Minter et al., 1982). Every conidium is delimited by a septum prior to abscission, but the exact structure of the septum, the stage of development at which it is formed (relative to the stage of expansion of the conidium) and the timing of the plugging of the septal pore by Woronin bodies (which interrupt its cytoplasmic connection with the conidiogenous cell) can vary. -
Use of Propolis for Topical Treatment of Dermatophytosis in Dog
Open Journal of Veterinary Medicine, 2014, 4, 239-245 Published Online October 2014 in SciRes. http://www.scirp.org/journal/ojvm http://dx.doi.org/10.4236/ojvm.2014.410028 Use of Propolis for Topical Treatment of Dermatophytosis in Dog Tonatiuh Alejandro Cruz Sánchez1, Perla Alejandra Estrada García1, Cristian Ismael López Zamora1, Marcela Autran Martínez2, Víctor Pérez Valencia2, Amparo Londoño Orozco1 1Facultad de Estudios Superiores Cuautitlán, Universidad Nacional Autónoma de México, Cuautitlán Izcalli, México 2Belén Veterinary Hospital, Tultitlan, México Email: [email protected] Received 12 July 2014; revised 10 August 2014; accepted 16 September 2014 Copyright © 2014 by authors and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/ Abstract Here we present three clinical cases of canine dermatophytosis resolved with topical propolis treatment that involved alopecia and well-demarcated erythematous lesions. These cases were positively identified by direct observation of samples from the affected zones with 10% KOH. Each sample was cultured, leading to the isolation of Microsporum gypseum in one case and Microspo- rum canis in the other two cases. The animals’ subsequent treatment included bathing using a commercial soap with propolis every seven days for 3 to 8 weeks, as well as the use of a propolis- containing ointment elaborated in our laboratory, which was applied to the lesions once a day for three weeks. From the second week of treatment, all cultures were negative. At the end of treat- ment, all cases displayed full recovery of the injuries and hair growth in these areas. -
1 Differential Morphological Changes in Response to Environmental Stimuli in A
bioRxiv preprint doi: https://doi.org/10.1101/372078; this version posted July 19, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Differential morphological changes in response to environmental stimuli in a 2 fungal plant pathogen 3 4 Carolina Sardinha Franciscoa, Xin Maa, Maria Manuela Zwyssiga, Bruce A. McDonalda, 5 Javier Palma-Guerreroa 6 7 aPlant Pathology Group, Institute of Integrative Biology, ETH Zürich, 8092 Zürich, 8 Switzerland 9 10 Running Title: Pleomorphism in Zymoseptoria tritici 11 12 #Address correspondence to Javier Palma-Guerrero, [email protected] 13 1 bioRxiv preprint doi: https://doi.org/10.1101/372078; this version posted July 19, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 14 ABSTRACT 15 During their life cycles, pathogens have to adapt to many biotic and abiotic 16 environmental constraints to maximize their overall fitness. Morphological transitions are 17 one of the least understood of the many strategies employed by fungal plant pathogens 18 to adapt to constantly changing environments. We characterized the responses of the 19 wheat pathogen Zymoseptoria tritici to a series of environmental stimuli using 20 microscopy, transcriptomic analyses, and survival assays to explore the effects of 21 changing environments on morphology and adaptation. We found that all tested stimuli 22 induced morphological changes, with distinct responses observed among four different 23 strains. The transcription analyses indicated a co-regulation of morphogenesis and 24 virulence factors in Z. -
Acquired Immunodeficiency Syndrome (AIDS), 1-23 Aspergillosis In, 16-18
Index Acquired immunodeficiency syndrome enzyme activities and, 336-339 (AIDS), 1-23 fatty acid synthesis and, 334-336 aspergillosis in, 16-18 ergosterol synthesis inhibition by, candidiasis in, 6-11 316-320 coccidioidomycosis in, 15--16 membrane and cell functions and 14 cryptococcosis in, 11-15 alpha-methylsterol effects, 326- histoplasmosis in, 15--16 329 host resistance in, 6 membrane lipid interactions of, 339- immunofluorescent staining for tissue 341 section in, 4-5 selective toxicity of, 325--326 Malassezia furfur in, 21 Antigen nocardiosis in, 18-20 of Aspergillus fumigatus, 198-199 pathologic diagnosis in, 3-4 advancing line immunoelectrophoresis Actinomyces, monoclonal antibodies in, for, 176 196 of Blastomyces dermatitidis, 199 Adriamycin, 133 of Candida albicans, 199-200 Adrucil, 133 of Coccidioides immitis, 200 Aerosporin, 114 of Cryptococcus neoformans, 200--201 Alkeran, 133 crossed immunoelectrophoresis for, Amantadine HCI, 140 174-175 Amikacin sulfate, 107 crossed-tandon immunoelectrophoresis Amikin,107 for, 176-178 Aminoglycoside, 106f, 107 of dermatophyte, 201 Aminosalicylic acid, 123-124 of Histoplasma capsulatum, 201-202 Amphotericin B, 127 methods for determining chemical na- Ancobon, 127-128 ture of, 180 Antifungal agents, systemic, 126f, 127- monitoring isolation of, 176-181 129 rocket immunoelectrophoresis for, 176 Antifungal azole derivatives, 313-351 of Sporothrix schenckii, 202 cytochrome P-450 interation with, of zygomycetes, 202 320--323 Antineoplastic agents, 131-135, 132f,134t ergosterol depletion effects