Uncommon Fungi and Related Species
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10-ELS-OXF Kurtzman1610423 CH002 7..20
Part II Importance of Yeasts Kurtzman 978-0-444-52149-1 00002 Kurtzman 978-0-444-52149-1 00002 Chapter 2 c0002 Yeasts Pathogenic to Humans Chester R. Cooper, Jr. regularly encounter the organisms described below. In fact, many s0010 1. INTRODUCTION TO THE MEDICALLY medical mycologists spend entire careers without direct clinical expo- IMPORTANT YEASTS sure to many of these fungi. Rather, the purpose of this review is to enlighten the non-medical mycologist as to the diversity of yeast and p0010 Prior to global emergence of the human immunodeficiency virus mold species regularly associated with human and animal disease (HIV), which is the causative agent of acquired immunodeficiency that also, at least in part, present a unicellular mode of growth in vivo. syndrome (AIDS), approximately 200 fungal pathogens were recog- The following descriptions present a concise overview of the key p0025 nized from among the more than 100,000 then-known fungal spe- biological and clinical features of these fungi. Where appropriate, refer- cies (Kwon-Chung and Bennett 1992, Rippon 1988). About 50 of ences to recent reviews of particular disease agents and their patholo- these species were regularly associated with fungal disease (myco- gies are provided. For a global perspective of fungal diseases, including sis). Since then, there has been a concurrent dramatic increase in in-depth clinical discussions of specific pathologies, diagnoses, and both the number of known fungal species and the incidence of treatments, the reader is referred to several outstanding and recently mycoses that they cause. Moreover, the spectrum of pathogenic fungi published texts (Anaissie et al. -
Boards' Fodder
boards’ fodder Medical Mycology By Adriana Schmidt, MD, and Natalie M. Curcio, MD, MPH. (Updated July 2015*) SUPERFICIAL ORGANISM CLINICAL HISTO/KOH TREATMENT MYCOSES* Pityriasis Malessezia furfur Hypo- or hyper-pigmented Spaghetti & meatballs: Antifungal shampoos and/or versicolor macules short hyphae + yeast PO therapy Tinea nigra Hortaea werneckii (formerly Brown-black non-scaly Branching septate hyphae Topical imidazoles or palmaris Phaeoannellomyces werneckii) macules + budding yeast allylamines Black piedra Piedraia hortae Hard firm black Dark hyphae around concretions acrospores Cut hair off, PO terbinafine, White piedra Trichosporon ovoides or inkin Soft loose white Blastoconidia, imidazoles, or triazoles (formely beigelii) concretions arthroconidia Fluorescent small Microsporum Canis KOH: spores on outside spore ectothrix: M. audouinii of the hair shaft; “Cats And Dogs M. distortum Wood’s lamp --> yellow Sometimes Fight T. schoenleinii fluorescence & Growl” M. ferrugineum+/- gypseum Large spore Trichophyton spp. (T. tonsurans in North America; T. violaceum in KOH: spores within hair Topical antifungals; PO endothrix Europe, Asia, parts of Africa). shaft antifungals for T. manuum, Tinea corporis T. rubrum > T. mentag. Majocchi’s granuloma: T. rubrum capitis, unguium T. pedis Moccasin: T. rubrum, E. floccosum. Interdigital/vesicular: T. mentag T. unguium Distal lateral, proximal and proximal white subungual: T. rubrum. White superficial: T. mentag. HIV: T. rubrum SUBQ MYCOSES** ORGANISM TRANSMISSION CLINICAL HISTO/KOH TREATMENT -
Phylogeny of Chrysosporia Infecting Reptiles: Proposal of the New Family Nannizziopsiaceae and Five New Species
CORE Metadata, citation and similar papers at core.ac.uk Provided byPersoonia Diposit Digital 31, de Documents2013: 86–100 de la UAB www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158513X669698 Phylogeny of chrysosporia infecting reptiles: proposal of the new family Nannizziopsiaceae and five new species A.M. Stchigel1, D.A. Sutton2, J.F. Cano-Lira1, F.J. Cabañes3, L. Abarca3, K. Tintelnot4, B.L. Wickes5, D. García1, J. Guarro1 Key words Abstract We have performed a phenotypic and phylogenetic study of a set of fungi, mostly of veterinary origin, morphologically similar to the Chrysosporium asexual morph of Nannizziopsis vriesii (Onygenales, Eurotiomycetidae, animal infections Eurotiomycetes, Ascomycota). The analysis of sequences of the D1-D2 domains of the 28S rDNA, including rep- ascomycetes resentatives of the different families of the Onygenales, revealed that N. vriesii and relatives form a distinct lineage Chrysosporium within that order, which is proposed as the new family Nannizziopsiaceae. The members of this family show the mycoses particular characteristic of causing skin infections in reptiles and producing hyaline, thin- and smooth-walled, small, Nannizziopsiaceae mostly sessile 1-celled conidia and colonies with a pungent skunk-like odour. The phenotypic and multigene study Nannizziopsis results, based on ribosomal ITS region, actin and β-tubulin sequences, demonstrated that some of the fungi included Onygenales in this study were different from the known species of Nannizziopsis and Chrysosporium and are described here as reptiles new. They are N. chlamydospora, N. draconii, N. arthrosporioides, N. pluriseptata and Chrysosporium longisporum. Nannizziopsis chlamydospora is distinguished by producing chlamydospores and by its ability to grow at 5 °C. -
A New Duplex PCR-Assay for the Detection and Identification of Paracoccidioides Species
Journal of Fungi Article A New Duplex PCR-Assay for the Detection and Identification of Paracoccidioides Species Breno Gonçalves Pinheiro 1 , Ana Paula Pôssa 1,2, Paula Portella Della Terra 1,2 , Jamile Ambrósio de Carvalho 1, Giannina Ricci 3, Angela Satie Nishikaku 3 , Rosane Christine Hahn 4,5, Zoilo Pires de Camargo 1,2 and Anderson Messias Rodrigues 1,2,* 1 Laboratory of Emerging Fungal Pathogens, Department of Microbiology, Immunology, and Parasitology, Discipline of Cellular Biology, Federal University of São Paulo (UNIFESP), São Paulo 04023062, Brazil; [email protected] (B.G.P.); [email protected] (A.P.P.); [email protected] (P.P.D.T.); [email protected] (J.A.d.C.); [email protected] (Z.P.d.C.) 2 Department of Medicine, Discipline of infectious Diseases, Federal University of São Paulo (UNIFESP), São Paulo 04023062, Brazil 3 Centro de Diagnóstico e Pesquisa em Biologia Molecular Dr. Ivo Ricci, São Paulo 13561020, Brazil; [email protected] (G.R.); [email protected] (A.S.N.) 4 Laboratory of Mycology/Research, Faculty of Medicine, Federal University of Mato Grosso, Cuiabá 78060900, Brazil; [email protected] 5 Júlio Muller University Hospital, Federal University of Mato Grosso, Cuiabá 78048902, Brazil * Correspondence: [email protected]; Tel.: +55-1155764551 (ext. 1540) Abstract: Paracoccidioidomycosis (PCM) is a life-threatening systemic fungal infection caused Citation: Pinheiro, B.G.; Pôssa, A.P.; by members of the Paracoccidioides brasiliensis complex and P. lutzii. Routine diagnoses of PCM Della Terra, P.P.; de Carvalho, J.A.; down to the species level using classical mycological approaches are unspecific due to overlapping Ricci, G.; Nishikaku, A.S.; Hahn, R.C.; phenotypes. -
In Vitro and in Situ ACTIVATION of the COMPLEMENT SYSTEM by the FUNGUS Lacazia Loboi
Rev. Inst. Med. trop. S. Paulo 49(2):97-101, March-April, 2007 In vitro AND in situ ACTIVATION OF THE COMPLEMENT SYSTEM BY THE FUNGUS Lacazia loboi Fátima Regina VILANI-MORENO(1), Érika MOZER(2), Ana Márcia Guedes de SENE(2), Margarete de Oliveira FERASÇOLI(2), Tânia Cristina PEREIRA(2), Márcia Garcia MIRAS(2), Gláucia Heloísa de Paula SOUZA(3) & Andréa de Faria Fernandes BELONE(3) SUMMARY Since there are no studies evaluating the participation of the complement system (CS) in Jorge Lobo’s disease and its activity on the fungus Lacazia loboi, we carried out the present investigation. Fungal cells with a viability index of 48% were obtained from the footpads of BALB/c mice and incubated with a pool of inactivated serum from patients with the mycosis or with sterile saline for 30 min at 37 oC. Next, the tubes were incubated for 2 h with a pool of noninactivated AB+ serum, inactivated serum, serum diluted in EGTA-MgCl2, and serum diluted in EDTA. The viability of L. loboi was evaluated and the fungal suspension was cytocentrifuged. The slides were submitted to immunofluorescence staining using human anti-C3 antibody. The results revealed that 98% of the fungi activated the CS by the alternative pathway and no significant difference in L. loboi viability was observed after CS activation. In parallel, frozen histological sections from 11 patients were analyzed regarding the presence of C3 and IgG by immunofluorescence staining. C3 and IgG deposits were observed in the fungal wall of 100% and 91% of the lesions evaluated, respectively. The results suggest that the CS and immunoglobulins may contribute to the defense mechanisms of the host against L. -
Luciano Polonelli
Luciano Polonelli Department of Biomedical, Biotechnological and Translational Sciences, Unit of Microbiology and Virology, University of Parma, Parma, Italy Tel.: +39 0521 903429; Fax: +39 0521 993620; e-mail: [email protected] History of Medical Mycology File 2 (1895-1950) 1895 Giuseppe Marconi (1862-1940), born in Naples, Italy, Professor of Veterinary Pathology and Clinic in the Royal University of Pisa, Italy, isolated and cultivated for the first time Cryptococcus farciminosum, the agent of epizootic lymphangitis, in the form of sterile mycelium (1895). Piero Redaelli and Raffaele Ciferri transferred (1934) C. farciminosum to the genus Histoplasma, as H. farciminosum (Rivolta and Micellone 1883, Redaelli and Ciferri 1934), mainly because of its dimorphic nature that made it similar to the tissue form of H. capsulatum var. capsulatum Darling 1906. Robert J. Weeks, Arvind A. Padhye and Libero Ajello, at the Division of Mycotic Diseases, Center for Infectious Diseases, Centers for Disease Control (C.D.C.) Atlanta, Georgia, U.S.A. (1985), observed that this fungus generated macro- and microconidia resembling those of the capsulatum and duboisii varieties of H. capsulatum when incubated at room temperature, thus reducing the fungus to a varietal status as H. capsulatum var. farciminosum (Rivolta, 1873) Weeks, Padhye & Ajello, 1985. Raffaele Ciferri (1960) reduced Histoplasma duboisii (Vanbreuseghem, 1992) to varietal status as H. capsulatum var. duboisii (Vanbreuseghem, 1992), Ciferri, 1960 [Ajello, 1998; Marcone, 1895; Redaelli and Ciferri, 1934; Weeks et al., 1985]. 1 1896 The American surgeon Emmet Rixford (1865-1938), born in Bedford, Canada, first graduated in engineering and then Doctor in Medicine (1891), and Thomas C. -
The Taxonomic Status of Lacazia Loboi and Rhinosporidium Seeberi Has Been Finally Resolved with the Use of Molecular Tools Leonel Mendoza1, Libero Ajello2 & John W
Forum micológico Rev Iberoam Micol 2001; 18: 95-98 95 The taxonomic status of Lacazia loboi and Rhinosporidium seeberi has been finally resolved with the use of molecular tools Leonel Mendoza1, Libero Ajello2 & John W. Taylor3 1Medical Technology Program, Department of Microbiology, Michigan State University, East Lansing MI, 2School of Medicine, Emory University, Atlanta GA, and 3Department of Plant and Microbial Biology, University of California, Berkeley, CA, USA The etiologic agents of lobomycosis and rhinospo- fungal pathogen Paracoccidioides brasiliensis. More than ridiosis, Lacazia loboi and Rhinosporidium seeberi res- 70 years later, however, his hypothesis was still awaiting pectively, have long been confined in a taxonomic limbo. verification. Although their invasive cells in the tissues of infected To resolve this taxonomic standoff, a team of humans and other animals are abundant and readily detec- scientists from Sri Lanka, where R. seeberi infections are table histologically, they have been intractable to isolation common, and Brazil, where lobomycosis is endemic, and and culture. Thus, it has not been possible to objectively the USA was assembled to study R. seeberi’s and place them in any of the kingdoms in which all living enti- L. loboi’s phylogenetic links with other eukaryotic orga- ties are classified. In addition to their uncultivatable sta- nisms. The strategy was to collect fresh tissue samples tus, L. loboi and R. seeberi shared in common from cases of lobomycosis and rhinosporidiosis, isolate morphological features that resemble those of certain pat- genomic DNAs and then amplify their 18S small subunit hogenic fungi and protozoans: viz. essentially similar (SSU) rDNA by using standard primers and PCR techno- inflammatory host reactions, unresponsiveness to antifun- logy. -
Micologia Médica
Tópicos em Micologia Médica Jeferson Carvalhaes de Oliveira 4ª. Edição OLIVEIRA, Jeferson Carvalhaes de TÓPICOS em MICOLOGIA MÉDICA Rio de Janeiro 2014 Capa: Exame direto de tecido contrastado com nanquim. Criptococose, 400x Diagramação e ilustração da 1ª. Edição: Carla Vieira da Costa Revisão da 1ª. Edição: Maria Tereza Mateus Raush Apoio: Control-Lab FICHA CATALOGRÁFICA: ______________________________________________________________________________ OLIVEIRA, Jeferson Carvalhaes de. Tópicos em Micologia Médica / Jeferson Carvalhaes de Oliveira – Rio de Janeiro; 2014. 230 págs,; il. col. ISBN 85-900986-1-3 Inclui Bibliografia. 1. Tópicos em Micologia I. Título PREFÁCIO Muito honrado com o convite de nosso querido colega Prof. Jeferson Cavalhaes para que escrevesse algumas linhas sobre o Prof. Jaime de Azevedo Carneiro, um dos grandes expoentes da Micologia Médica, me chega- ram recordações dos contatos diários que mantínhamos na antiga Faculdade Nacional de Medicina, na Praia Vermelha. O nosso Prof. Jeferson Carvalhaes, hoje, doutorando do Instituto Oswaldo Cruz, era, então, na época, aluno monitor da disciplina de Parasitologia, quando escolheu, para sua atuação específica, o setor de Micologia che- fiado pelo Prof. Jaime Carneiro, homem com características humanas especiais, do qual se tornou discípulo e amigo. Jaime Carneiro culminou sua carreira universitária como Professor Titular na Universidade Federal Flumi- nense, ocupando também a chefia do laboratório de Micologia do Hospital Pedro Ernesto da UERJ. Notabili- zou-se, ainda, pela vasta colaboração científica em trabalhos referentes à patologia dos fungos. O Prof. Jaime Carneiro, por sua simplicidade, espírito crítico e expressiva atividade participativa, atraía com habilidade própria, peculiar aos homens da ciência, jovens alunos, educando pelo exemplo de dignidade e seriedade científica um grande número de estudantes que, após um período de aprendizado, passavam a ser discípulos em convivência familiar. -
Neglected Fungal Zoonoses: Hidden Threats to Man and Animals
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector REVIEW Neglected fungal zoonoses: hidden threats to man and animals S. Seyedmousavi1,2,3, J. Guillot4, A. Tolooe5, P. E. Verweij2 and G. S. de Hoog6,7,8,9,10 1) Department of Medical Microbiology and Infectious Diseases, Erasmus MC, Rotterdam, 2) Department of Medical Microbiology, Radboud University Medical Centre, Nijmegen, The Netherlands, 3) Invasive Fungi Research Center, Mazandaran University of Medical Sciences, Sari, Iran, 4) Department of Parasitology- Mycology, Dynamyic Research Group, EnvA, UPEC, UPE, École Nationale Vétérinaire d’Alfort, Maisons-Alfort, France, 5) Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran, 6) CBS-KNAW Fungal Biodiversity Centre, Utrecht, 7) Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands, 8) Peking University Health Science Center, Research Center for Medical Mycology, Beijing, 9) Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China and 10) King Abdullaziz University, Jeddah, Saudi Arabia Abstract Zoonotic fungi can be naturally transmitted between animals and humans, and in some cases cause significant public health problems. A number of mycoses associated with zoonotic transmission are among the group of the most common fungal diseases, worldwide. It is, however, notable that some fungal diseases with zoonotic potential have lacked adequate attention in international public health efforts, leading to insufficient attention on their preventive strategies. This review aims to highlight some mycoses whose zoonotic potential received less attention, including infections caused by Talaromyces (Penicillium) marneffei, Lacazia loboi, Emmonsia spp., Basidiobolus ranarum, Conidiobolus spp. -
Human Case of Lobomycosis Sameer Elsayed,*† Susan M
Human Case of Lobomycosis Sameer Elsayed,*† Susan M. Kuhn,† Duane Barber,*† Deirdre L. Church,*† Stewart Adams,‡ and Richard Kasper*† We describe a 42-year-old woman with histologically confirmed lobomycosis, a cutaneous fungal infection rarely reported outside of Latin America. Our case represents the first published report of imported human lobomycosis in Canada and the fifth in an industrialized country. Figure 1. Photomicrograph of keloidal skin lesion on patient’s right utaneous fungal infections are rarely reported outside upper arm. Cof Latin America. We document the first case of imported human lobomycosis in Canada. (1995 to 1996). During her time in South America, she lived mainly in rural camps and had extensive exposure to The Study freshwater, soil, and underground caves. Health problems In February 2001, a healthy, 42-year-old, female geolo- encountered during her travels included dengue fever, gist from Canada came to her dermatologist with a slowly amebic dysentery, and intestinal helminthiasis. Of note, growing, 1.5-cm diameter, dusky-red, nontender, plaque- she had never traveled to the African continent. like lesion surrounded by keloidal scar tissue on the poste- Her medical history was otherwise unremarkable. rior aspect of her right upper arm (Figure 1). It was located Family history was positive for hypothyroidism. She was a at the site of a scar from a previous excision attempt of a nonsmoker and a social alcohol drinker. She was on hor- similar lesion 2 years earlier. The original lesion was first mone replacement therapy but no other medications and noticed while the patient was visiting Southeast Asia in had no known allergies. -
Like Disease in Bottlenose Dolphin, Venezuela
may ulcerate and form large plaques. Lobomycosis-like Lobomycosis in Man disease, a syndrome pathoanatomically consistent with lobomycosis but for which a histologic diagnosis is lack- and Lobomycosis- ing, has been found in coastal bottlenose dolphins from Colombia, Ecuador, Peru, and Brazil, Guiana dolphins like Disease in Brazil (5,11), and Indo-Pacific bottlenose dolphins (T. in Bottlenose aduncus) in the tropical lagoon of Mayotte in the Indian Ocean (12). Dolphin, Venezuela L. loboi cells from lesions in bottlenose dolphins were smaller than those found in infected tissues in humans, Luis Bermudez, Marie-Françoise Van Bressem, which suggests that the organism may not be identical in Oscar Reyes-Jaimes, Alejandro J. Sayegh, the 2 hosts (13). Serologic data have indicated that dolphins and Alberto E. Paniz-Mondolfi and humans are infected with similar L. loboi strains (14). The possibility of humans acquiring lobomycosis from dol- We report 1 case of lobomycosis caused by Lacazia phins appears low; only 1 documented case of disease trans- loboi in a fisherman and 1 case of lobomycosis-like disease mission from a rescued dolphin to its attendant occurred in in a bottlenose dolphin (Tursiops truncatus) along the coast of Venezuela. These findings suggest that the marine en- the early 1970s (9). The ecology of lobomycosis in humans vironment is a likely habitat for L. loboi and a reservoir for and odontocetes seems to be unconnected. Infections oc- infection. cur mostly in persons inhabiting the Amazon Basin and in inshore and estuarine dolphins in North and South America (3–6). We report cases of lobomycosis in a fisherman and obomycosis (lacaziosis) is a chronic, granulomatous, lobomycosis-like disease in a bottlenose dolphin along the Lfungal infection of the skin and subcutaneous tissues coast of Venezuela. -
Genome Analysis Reveals Evolutionary Mechanisms of Adaptation In
www.nature.com/scientificreports OPEN Genome analysis reveals evolutionary mechanisms of adaptation in systemic dimorphic Received: 16 October 2017 Accepted: 1 March 2018 fungi Published: xx xx xxxx José F. Muñoz 1, Juan G. McEwen2,3, Oliver K. Clay3,4 & Christina A. Cuomo 1 Dimorphic fungal pathogens cause a signifcant human disease burden and unlike most fungal pathogens afect immunocompetent hosts. To examine the origin of virulence of these fungal pathogens, we compared genomes of classic systemic, opportunistic, and non-pathogenic species, including Emmonsia and two basal branching, non-pathogenic species in the Ajellomycetaceae, Helicocarpus griseus and Polytolypa hystricis. We found that gene families related to plant degradation, secondary metabolites synthesis, and amino acid and lipid metabolism are retained in H. griseus and P. hystricis. While genes involved in the virulence of dimorphic pathogenic fungi are conserved in saprophytes, changes in the copy number of proteases, kinases and transcription factors in systemic dimorphic relative to non-dimorphic species may have aided the evolution of specialized gene regulatory programs to rapidly adapt to higher temperatures and new nutritional environments. Notably, both of the basal branching, non-pathogenic species appear homothallic, with both mating type locus idiomorphs fused at a single locus, whereas all related pathogenic species are heterothallic. These diferences revealed that independent changes in nutrient acquisition capacity have occurred in the Onygenaceae and Ajellomycetaceae, and underlie how the dimorphic pathogens have adapted to the human host and decreased their capacity for growth in environmental niches. Among millions of ubiquitous fungal species that pose no threat to humans, a small number of species cause dev- astating diseases in immunocompetent individuals.