| Microsporum gypseum | |
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| Species: | Microsporum gypseum (E. Bodin) Guiart & Grigoraki (1928)
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Archorion Gypseum, Micropsorum Flavescens, Microsporum Scorteum, and Microsporum Xanthodes | |
Microsporum gypseum is a dermatophyte [1] comprising a complex of four species of fungi: Arthoderma incurvatum, Arthroderma gypsea, Arthroderma fulva and Arthoderma corniculata. A. incurvatum, A. gypsea, and A. fulva are considered the pathogenic species of the complex and are of the family Arthrodermataceae [2], while A. cornulata and is a saprophyte [3]. More recent studies suggest that M. gypseum comprises two teleomorphic species A. gypseum and A. Incruvatum [4] [1]. These all relate via they're imperfect anamorphic state because of their morphological similarities with one another [1]. The conidal states of A. gypsea and A. incurvata are believed to comprise M. gypseum, and the conidial states of A. fulva and A.corniculata are called M. fulvum and M. boullardii [5]. Because the anamorphic states of these fungi are so similar, they can only be identified by mating [1]. Two mating strains have been discovered, (+) and (-) [6]. The taxonomy is usually based on the conidia of the ana-phase of growth, while coverage is primarily comprised of the teleomorphic states [4]. The synonymy include Achorion gypseum, Microsporum glavescens, Microsporum scorteum, and Microsporum xanthodes, in increasing years [5] [1]. Historically there has additionally been nomenclature controversy between Microsporum and Microsporon [7].
History edit
The teleomorphic states of this species were originally the first to be discovered [3] by Arturo Nannizii for M. gypseum in 1927, but his contribution was largely ignored by the scientific community [6]. Until Christine Dawson and J.C. Gentles discovered anamorph Arthroderma uncurvatum, the teleomorph of Trichophyton ajelloi [6]. Shortly after this, D.M. Griffin rediscovered M. gypseum by Nanizzi, and another individual P.M. Stockdale also isolated the second teleomorph of the species naming it Nannizzia incurvatum [6]. Stockdale then comfirmed that Nannizzia incurvatum differed from the original isolate of M. gypseum isolated by Nannizzi and proposed that two teleomorphic states of M. gypseum exist for the anamorph, thereby naming the latter N. gypsea [6]. Various authors, such as Stockdale, M.F. Visset, and J.W. Rippon have agreed that the differences in structure of the anamorphic state of the complex of M. gypseum are inadequate for making distinctions between anamorphic states because of how similar they look [3]. It is now believed that very similar anamorphs, M. gypseum and M. fulvum, consist of three teleopmorphic states: N. gypsea, N. incurvatum, and N. fulva [6]. Shortly after, Arthroderma replaced Nannizzia [8], where Arthroderma is depicting the teleomorphic states, and Microsporum refers to the anamorphic states [6].
Morphology edit
The colonies of M. gypseum are described as cottony or powdery, they grow rapidly with a colour range of white to buff, with a reserve that can range from pink, to red, to yellow (cinnamon); they may occasionally have overtones of violet [7] [4] [1] [5] [8] [6]. The powdery substance on the colony is derived from the abundant amount of Macroconidia, while the edges of the colony are described as scalloped to ragged and can exhibit pleomorphism [1] [5] [6]. Macroconidia of M. gypseum have a substantial range that can occur as short pedicels, terminal, solitary, spindle shaped, large, thick walled, that are smooth or roughened,[7], borne directly on hyphae or on short branches[7]. They are often very large (40 to 150 by 8 to 15 μ), ellipsoid to fusiform, moderately thick, have verrucose and are septate (4-6 septa) [1] [4] [5]. The macroconidia also possess a rat-like tail at the edges of the conidia [5]. The asocarp of the fungus is globose in shape, is a pale buff nand 500-1250 μm in diameter, this excludes the appendages [4]. The Peridial hyphae are hyaline, pale buff, septate, and are branched with thinly but have densely verruculose walls [4]. Microconidia are drop shaped, clavate, (1.7-3.5 x 3.3-8.3 μm), unicellular, smooth-walled or can be slightly roughened and are created laterally on the hyphae [4] [8]. The abundance of microconidia is characteristic of the fungus [6]. The hyphae or appendages are of three kinds in the fungi, the first being straight, slender, smooth walled hyphae that can grow up to 250 μm long; they taper at 2.5-4.0 μm in diamater at the base but close to about 1.5-2 μm. The second are slender, smooth-walled, septate, spiral hyphae that are rarely branched, which have a base diameter of 2.5-3.5 μm that taper up to 1.5-2 μm in diameter. They are usually varibale in their coiled state, ranging from tightly to loosely coiled with numerous but variable amounts of turns. The third are thick-walled, verruculose, ellipsoid or fusiform macroconidia, that are 35-55 x 10-13.5 μm, with up to five septa [4]. The asci of the fungus are subglobose, thin-walled, evanescent, which are 5-7 μm in diameter and contain a total of eight ascospores [4]. The ascospores are smooth-walled, lenticular, 1.5-2 x 2.5-4 μm in diameter, and when in mass are yellow [4]. Additionally the Spiral hyphae seen on the ascocarp are also grown on mycelium [4]. The fungus does not have any specific nutritional requirements for growth [5]. The teleomorphic features of the microsporum on colonial and microscopic features are often done on Takashio's Medium [8]. However, distinguishing is best done by mating (+/-) or by genetics [8]. The species is heterothallic, and a such mating is controlled by a 1-locus, 2-allele compatibility system [5]. Comparatively A. Gypseum produces more spreading and a coarser granular colony; the Macroconidia also are wider and the surface colour is brighter and redder than A. incurvatum. A. Incurvatum is a pale buff and is finely granular, and occasionally has reddish to yellow reverse [1].
Ecology edit
The species is geophilic, is abundant in soil and can be isolated around the world; it is in world wide distribution [4] [1] [5]. However, it is rare in places such as the United States, United Kingdom, and Germany but common in South America [6]. It is defined to be either cosmopolitan or confined to a certain graphical regions [5]. The fungus can be found in soil of greenhouses and munition factories within these areas [9]. The species itself commonly infects humans whom are closely tied to these areas because of agricultural work [6] [10]. In these areas, soil moisture is indicative role in the presence of the M. Gypseum complex, areas with higher moisture tend to be preferred [11]. Correlations between infections and soil types indicate that most improved soils of the clayey or clayey-sandy type are preferred, particularly those fertilized with keratinous manure [10]. Additionally the fungus prefers soils with a pH of 7-7.5. Various soils in correlation with number of infections indicates that the fungus specifically prefers meadow chernozemic soil (74%), of which positive isolates occur [10].
The role of infection by the virus is influenced by the climate and geographical characteristics which favor the life of the dermatophyte as dictated by the average rainfall rate and average air temperatures [10]. There tends to be a greater number of infections in later seasons as emphasis is placed on age, sex, months of onset of infection, and marked localization of the fungus [10]. Adults, particularly males are typically infected, and of those infected usually involved in agricultural practices [10] [9] [6], such as greenhouses and plant nursery workers [9] [6]. School-age males are more prone then females because of contact in the soil [10]. Onset of infection usually occurs from August to November, when humans come into contact with soil more often [10] [9].
Epidemiology edit
The species is keratinophilic in nature, and is known for causing diseases on human skin [7]. The genus Microsporum contains a number of pathogens to both humans and animals [7]. The diseases it causes is classified as tinea or ringworm, with an adjective prescribing to the afflicted body part [9] [4]. Infection usually occurs as Tinea capitis with suppuration and kerion formation [9]. Pus formation can also occur from palpitated follicles [1]. The species is ectothrix in terms of hair infection and can infect more than one part of the scalp at a time [1] [6] [1]. The fungus produces hyphal growth at the scalp, and produces fronds (perforating organs) that invade the hair perpendicularly at the cortex near the edge of the cuticles [5]. This can cause hair to be easily removed and dislodged from the scalp [1]. Additionally, individuals with thick dark hair have a tendency to have a more severe inflammatory response [1]. Tinea Corporis, as well; this is characterized as an intense inflammatory response resembling a bacterial infection, thus surgical intervention is not needed because inflammation is due to the fungus alone [1] [1]. Also, Tinea Pedis, or athletes foot is common, while Tinea Unguium is rare [9]. Additionally Tinea manuum, of the thighs may occur as Nodular granulomatous perifolliculitis, has been noted with infection of the thighs [9] [6]. Favus (a severe form of Tinea Capitis) is rarely seen to be caused by this fungus [9] [6]. However the most common cause in humans seems to be Tinea Capitis and Tinea Corporis [4]. As such clinical manifestations are localized to localization of contact [5]. Transmission from animals to humans is supported; especially in those constrained to agricultural work [10] [12]. Handlers of laboratory animals, including guinea pigs, cats, and rabbits can also be at risk of contracting the fungi if the animals were predisposed to a certain area [9]. The fungus infects animals that associate themselves with soil on a repeated basis [4]. So as such animals like cattle are commonly affected but horses, rodents, monkeys and dogs have a tendency to acquire it [5] [1]. Entry of the fungus or contraction of one or more of these diseases is caused by deposition on human skin, and contact with soil is usually the primary cause of infection [9]. Quantitatively, animal or humans must acquire at least ten fungal spores on a keratin rich surface in order to become pathogenic [9]. Additionally of the mating types, the positive strain is more pathogenic then the negative strain [9]. Identification is usually classified on the appearance of the fungus on the host via a sample culture [4]. Both M. Gypseum and M. Fulvum have been commonly isolated from patients with human infections of the disease [5]. It is also possible for human to human interaction to occur because the disease itself does not disable a person's ability to come into contact with other people [5] [8].
The lesions are usually inflammatory, impetiginous, and sometimes bullous with rapid development and resolution; this is accompanied by scarring and permanent patches alopecia [5] [1]. Because inflammation resembles a ringworm-like structure, the greatest intensity of inflammation is at the advancing margin of the ring [5]. However Microsporum gypseum is categorized as a rare agent of infection, and usually only occurs in rural areas [12] [1]. The infections associated with hair can also be prone to fluorescence under a woods lamp [1]. Sometimes these clinical manifestations are not ringworm but appear as impetigo, scleroderma or psoriasis [13]. The fungus is also known to rarely cause Onychomycosis [12]. However, Onychomycosis is usually caused by another fungus Trichophyton rubrum [13]. Onychomycosis diagnosis is based on the criteria of Onsberg, a direct positive observation of growth of a pure culture of M. Ggpseum. [13].
Direct examination with KOH of skin, reveal mycelium and masses of arthroconidia in some chains; KOH examination of hair produces distinctive large macroconidia in chain or irregular masses of hair. Mycelium was also discovered to run parallel to its length [6]. Woods lamp tests on humans indicate the fungus by fluorescence [6].
Pathogenicity edit
The pathophysiological mechanisms associated with the fungi are due to either the presence of substances on the surface of the fungi, or substances released by the fungi [14]. These can include: surface adhesins, mannans, enzymes such as proteinases, peptisases, DNases, and lipases [14]. The extracellular proteases released assist the fungus in invading the host skin barrier (keratin rich) with the presence of keratinase (keratinolytic activity increases) [14]. They then use the proteases to enhance their survival by chemically or physically altering the environment to their benefit by digesting the host proteins, thus providing themselves with nutrition. These proteases are found in all stages of growth (lag to declining) but peak at the mid log phase. These proteases are determined to be secreted during the lag phase of growth as they are secreted without the presence of host related proteins. It is assumed that the regulation and secretion of these enzymes is in part due to other differently regulated enzymes [14]. Keratinolytic activity is also determined to be indicative of pathogenetic potential [14]. Excessive exogenous carbohydrates such as glucose have been found to play a recessive role in protease release, as the presence of glucose decreases the amount of keratin hydrolyzed [14]. The presence of hormones such as progesterone have also been seen to have an inhibitory effect on the growth of dermatophytes [5].
Treatment edit
Therapy regarding deep fungal infections should be provided with amphotericin B therapy [9]. Oral ketoconzazole with topical enilconazole has been found to help treat skin lesions [15]. Animal treatment is usually done with introconazole or ketoconzazole; most European countries use off label terbinafine in cats and dogs [15]. However the most common antifungal drug used for systemic use is griseofulvin because it’s often the cheapest; treatment is usually on a common dose regimen of 50 mg per kg every twelve to twenty four hours [15] [9]. Most of these administered drugs are variants of imidazoles. The treatment of Onychomycosis involves the administration of intraconazole with systematic griseofulvin in combination with topical enilconazole, sometimes a cicloperoxamine solution and systemic terbinafine is used [16]. The mistreatment of this fungal pathogen is due to the thought of bacterial infection and the administration of corticosteroids [13]. This causes a change in appearance of the lesion and can lead to a harder diagnosis. Mycological examination should form the basis of diagnosis before the administration of antibiotics or corticosteroids [13].
References edit
- ^ a b c d e f g h i j k l m n o p q r s t u Rippon, John Willard (1988). Medical mycology: the pathogenic fungi and the pathogenic actinomycetes (3rd ed.). Philadelphia, PA: Saunders. ISBN 0721624448.
- ^ Currah, R (1985). "Taxonomy of the Onygenales". Mycotaxon. 24: 1-216.
- ^ a b c Demange, C; Contet-Audonneau, N; Kombila, M; Miegeville, M; Berthonneau, M; De Vroey, C; Percebois, G (1992). "Microsporum gypseum complex in man and animals". Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology. 30 (4): 301–8. PMID 1432489.
- ^ a b c d e f g h i j k l m n o p Howard, edited by Dexter H. (2003). Pathogenic fungi in humans and animals (2nd ed. ed.). New York: Marcel Dekker. ISBN 0-2039-0910-0.
{{cite book}}:|edition=has extra text (help);|first1=has generic name (help) - ^ a b c d e f g h i j k l m n o p q r Kwon-Chung, K.J.; Bennett, John E. (1992). Medical mycology. Philadelphia: Lea & Febiger. ISBN 0-8121-1463-9.
- ^ a b c d e f g h i j k l m n o p q r s al.], Julius Kane ... [et (1997). Laboratory handbook of dermatophytes : a clinical guide and laboratory handbook of dermatophytes and other filamentous fungi from skin, hair, and nails. Belmont, CA: Star Pub. ISBN 0-89863-157-2.
- ^ a b c d e f Barron, George L. (1983). The genera of Hyphomycetes from soil (Reprint. ed.). Malabar, Fla.: Krieger. ISBN 0-8827-5004-6.
- ^ a b c d e f al.], editor in chief, James Versalovic ; editors, Karen C. Carroll ... [et (2011). Manual of clinical microbiology (e-book) (10th ed. ed.). Washington, D.C.: ASM Press. ISBN 9781555816728.
{{cite book}}:|edition=has extra text (help);|first1=has generic name (help)CS1 maint: multiple names: authors list (link) - ^ a b c d e f g h i j k l m n o DiSalvo, Edited by Arthur F. (1983). Occupational mycoses. Philadelphia, Pa.: Lea and Febiger. ISBN 0-8121-0885-X.
{{cite book}}:|first1=has generic name (help) - ^ a b c d e f g h i Chmel, L.; Buchvald, J. "Ecology and transmission of from soil to man". Medical Mycology. 8 (2): 149–156. doi:10.1080/00362177085190791.
- ^ Ranganathan; Balajee. "Microsporum gypseum complex in Madras, India". Mycoses. 43 (5): 177–180. doi:10.1046/j.1439-0507.2000.00557.x.
- ^ a b c Romano, C.; Asta, F.; Massai, L. "Tinea Incognito due to Microsporum gypseum in Three Children". Pediatric Dermatology. 17 (1): 41–44. doi:10.1046/j.1525-1470.2000.01709.x.
{{cite journal}}: line feed character in|pages=at position 4 (help) - ^ a b c d e Romano, C.; Massai, L.; Gallo, A.; Fimiani, M. "infection in the Siena area in 2005-2006". Mycoses. 52 (1): 67–71. doi:10.1111/j.1439-0507.2008.01543.x.
- ^ a b c d e f Singh, C. J. "Extracellular protease expression in Microsporum gypseum complex, its regulation and keratinolytic potential". Mycoses. 54 (4): e183–e188. doi:10.1111/j.1439-0507.2010.01871.x.
- ^ a b c Nardoni, S.; Mugnaini, L.; Papini, R.; Fiaschi, M.; Mancianti, F. "Canine and feline dermatophytosis due to Microsporum gypseum: A retrospective study of clinical data and therapy outcome with griseofulvin". Journal de Mycologie Médicale / Journal of Medical Mycology. 23 (3): 164–167. doi:10.1016/j.mycmed.2013.05.005.
- ^ Romano, C.; Ghilardi, A.; Fimiani, M. "Dystrophic onychomycosis due to Microsporum gypseum". Mycoses. 49 (4): 335–337. doi:10.1111/j.1439-0507.2006.01248.x.
External Links edit
Microsporum Gypseum in Index Fungorum
EthanBazos (talk) 22:57, 14 November 2014 (UTC)