Pathogenicity Classification of Fungi Status December 2014 (CGM/141218-03)
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
42 Genome Scale Model Reconstruction of the Methylotrophic
GENOME SCALE MODEL RECONSTRUCTION OF THE METHYLOTROPHIC YEAST OGATAEA POLYMORPHA Simone Schmitz, RWTH Aachen University, Germany [email protected] Ulf W. Liebal, RWTH Aachen University, Germany Aarthi Ravikrishnan, Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences; Institute of Technology Madras, India Constantin V.L. Schedel, RWTH Aachen University, Germany Lars M. Blank, RWTH Aachen University, Germany Birgitta E. Ebert, RWTH Aachen University, Germany Key words: Ogataea (Hansenula) polymorpha, metabolic model, phenotype microarray experiments, methylotrophic yeast Ogataea polymorpha is a thermotolerant, methylotrophic yeast with significant industrial applications. It is a promising host to generate platform chemicals from methanol, derived e.g. from carbon capture and utilization streams. Full development of the organism into a production strain requires additional strain design, supported by metabolic modeling on the basis of a genome-scale metabolic model. However, to date, no genome-scale metabolic model is available for O. polymorpha. To overcome this limitation, we used a published reconstruction of the closely related yeast Pichia pastoris as reference and corrected reactions based on KEGG annotations. Additionally, we conducted phenotype microarray experiments to test O. polymorpha’s metabolic capabilities to grown on or respire 192 different carbon sources. Over three-quarter of the substrate usage was correctly reproduced by the model. However, O. polymorpha failed to metabolize eight substrates and gained 38 new substrates compared to the P. pastoris reference model. To enable the usage of these compounds, metabolic pathways were inferred from literature and database searches and potential enzymes and genes assigned by conducting BLAST searches. To facilitate strain engineering and identify beneficial mutants, gene-protein-reaction relationships need to be included in the model. -
Developments in Fungal Taxonomy
CLINICAL MICROBIOLOGY REVIEWS, July 1999, p. 454–500 Vol. 12, No. 3 0893-8512/99/$04.00ϩ0 Copyright © 1999, American Society for Microbiology. All Rights Reserved. Developments in Fungal Taxonomy JOSEP GUARRO,* JOSEPA GENE´, AND ALBERTO M. STCHIGEL Unitat de Microbiologia, Departament de Cie`ncies Me`diques Ba`siques, Facultat de Medicina i Cie`ncies de la Salut, Universitat Rovira i Virgili, 43201 Reus, Spain INTRODUCTION .......................................................................................................................................................454 THE CONCEPT OF SPECIES IN FUNGI .............................................................................................................455 PHYLOGENY AND EVOLUTION...........................................................................................................................455 NOMENCLATURE.....................................................................................................................................................456 CURRENT MYCOLOGICAL TYPING METHODS..............................................................................................457 Morphology..............................................................................................................................................................457 Downloaded from Molecular Techniques ............................................................................................................................................459 Other Techniques....................................................................................................................................................460 -
Monograph on Dematiaceous Fungi
Monograph On Dematiaceous fungi A guide for description of dematiaceous fungi fungi of medical importance, diseases caused by them, diagnosis and treatment By Mohamed Refai and Heidy Abo El-Yazid Department of Microbiology, Faculty of Veterinary Medicine, Cairo University 2014 1 Preface The first time I saw cultures of dematiaceous fungi was in the laboratory of Prof. Seeliger in Bonn, 1962, when I attended a practical course on moulds for one week. Then I handled myself several cultures of black fungi, as contaminants in Mycology Laboratory of Prof. Rieth, 1963-1964, in Hamburg. When I visited Prof. DE Varies in Baarn, 1963. I was fascinated by the tremendous number of moulds in the Centraalbureau voor Schimmelcultures, Baarn, Netherlands. On the other hand, I was proud, that El-Sheikh Mahgoub, a Colleague from Sundan, wrote an internationally well-known book on mycetoma. I have never seen cases of dematiaceous fungal infections in Egypt, therefore, I was very happy, when I saw the collection of mycetoma cases reported in Egypt by the eminent Egyptian Mycologist, Prof. Dr Mohamed Taha, Zagazig University. To all these prominent mycologists I dedicate this monograph. Prof. Dr. Mohamed Refai, 1.5.2014 Heinz Seeliger Heinz Rieth Gerard de Vries, El-Sheikh Mahgoub Mohamed Taha 2 Contents 1. Introduction 4 2. 30. The genus Rhinocladiella 83 2. Description of dematiaceous 6 2. 31. The genus Scedosporium 86 fungi 2. 1. The genus Alternaria 6 2. 32. The genus Scytalidium 89 2.2. The genus Aurobasidium 11 2.33. The genus Stachybotrys 91 2.3. The genus Bipolaris 16 2. -
Clasificación Del Clado De Ogataea, Un Punto De Vista Integral
INSTITUTO POLITÉCNICO NACIONAL ESCUELA NACIONAL DE CIENCIAS BIOLÓGICAS Clasificación del clado de Ogataea, un punto de vista integral. PROYECTO DE INVESTIGACIÓN (TESIS) QUE PARA OBTENER EL TÍTULO DE QUÍMICO BACTERIÓLOGO PARASITÓLOGO PRESENTA: ERIKA BERENICE MARTÍNEZ RUIZ MÉXICO, DF. 2013 El presente trabajo se realizó en el Laboratorio de Micología Médica del Departamento de Microbiología de la Escuela Nacional de Ciencias Biológicas, del IPN. Se llevó a cabo bajo la dirección de la Dra. Aída Verónica Rodríguez Tovar y el Dr. Néstor Octavio Pérez Ramírez. Se contó con la colaboración de la Dra. Paulina Estrada de los Santos del Laboratorio de Microbiología Industrial del Departamento de Microbiología de la ENCB, del IPN. AGRADECIMIENTOS Gracias al Instituto Politécnico Nacional, porque al ser una de las Instituciones de más alto Reconocimiento a Nivel Nacional y figurar entre las mejores a nivel Internacional, me brindó un lugar en su matrícula, una preparación académica de excelencia y una nueva sangre que con orgullo portaré día con día porque “Soy Politécnico por convicción y no por circunstancia”. Gracias a la Escuela Nacional de Ciencias Biológicas, que más que una escuela se volvió un segundo hogar en estos últimos 5 años para mí, porque me dio las armas para estar a la altura de los mejores, porque con orgullo intentaré seguir dejando en alto el nombre de mi escuela. Además de brindarnos el apoyo en equipos, instalaciones y materiales para llevar a cabo este proyecto. Dra. Aída y Dr. Néstor, mis asesores, ¡gracias! porque confiaron en mí en un momento de incertidumbre, porque me apoyaron, me escucharon, me impulsaron a seguir adelante y me transmitieron una parte de sus amplios conocimientos. -
1 §4-71A-24 LIST of NONRESTRICTED MICROORGANISMS October 25, 2001 SCIENTIFIC NAME FUNGI Absidia Coerulea Absidia Corymbifera Ab
§4-71A-24 LIST OF NONRESTRICTED MICROORGANISMS October 25, 2001 SCIENTIFIC NAME FUNGI Absidia coerulea Absidia corymbifera Absidia ramosa Absidia spinosa Acremonium falciforme Acremonium kiliense Acremonium recifei Acremonium vitis Agaricus bitorquis Agaricus bisporus Agaricus campestris Agaricus sp. (Portabello mushroom) Alternaria alternata Alternaria geophilia Apiotrichum humicola Arthrobotrys - all species in genus Aspergillus candidus Aspergillus clavatus Aspergillus cremeus Aspergillus flavipipes Aspergillus flavus Aspergillus fumigatus Aspergillus glaucus Aspergillus nidulans Aspergillus niger Aspergillus ochraceus Aspergillus restrictus Aspergillus terreus Aspergillus ustus Aspergillus versicolor Aspergillus wentii Asteromyces cruciatus Aureobasidium pullulans Auricularia polytricha Bipolaris hawaiiensis Blastomyces dermatitidis Blastoschizomyces capitatus Boletus californicus Boletus granulatus Boletus luteus 1 Nonrestricted Microorganisms §4-71A-24 SCIENTIFIC NAME Boletus variegatus Byssochlamys fulva Candida albicans Candida famata Candida geochares Candida glabrata Candida humicola Candida kefyr Candida krusei Candida lipolytica Candida lusitaniae Candida parapsilosis Candida pseudotropicalis Candida quilliermondii Candida rugosa Candida stellatoidea Candida tropicalis Candida zeylanoides Candelabrella - all species in genus Chaetomium globosum Chrysosporium keratinophilum Chrysosporium liquorum Chrysosporium pruinosum Cladosporium bantianum Cladosporium carrionii Cladosporium trichoides Collybia velutipes Cryptococcus albidus -
Chromoblastomycosis Patricia Chang1, Elba Arana2, Roberto Arenas3
2XU'HUPDWRORJ\2QOLQH Case Report Chromoblastomycosis Patricia Chang1, Elba Arana2, Roberto Arenas3 1Department of Dermatology, Hospital General de Enfermedades IGSS and Hospital Ángeles, Guatemala, 2Elective student, Hospital General de Enfermedades IGSS and Hospital Ángeles, Guatemala, 3Mycology section, “Dr. Manuel Gea González” Hospital, Mexico City, Mexico Corresponding author: Dr. Patricia Chang, E-mail: [email protected] ABSTRACT Chromoblastomycosis is a subcutaneous, chronic, granulomatous mycosis that occurs more frequently in tropical and subtropical countries. We report a case of chromoblastomycosis of the earlobe due to Fonsecaea sp in a male patient of 34 years old, due to its uncommon localization. Key words: Chromoblastomycosis; Fonsecaea pedrosoi; Fonsecaea compacta; Cladosporium carrionii; Fumagoid cells INTRODUCTION plate, hematic crusts and one retroauricular nodule with slightly warty appearance (Figs. 1 and 2). The rest of the The chromoblastomycosis is a sub cutaneous mycosis physical exam was within normal limits. in tropical and subtropical areas considered as an American disease, the main agents are Fonsecaea The patient says that his disease started 3 years ago pedrosoi, in endemic areas of tropical and subtropical with a small asymptomatic “pimple” in his right ear environments; Fonsecaea compacta, Cladosporium that slowly increased its size until he decided to consult. carrionii. The diagnosis of the disease is through the In the last 6 months he had an occasional itch and presence of fumagoids cells. was prescribed different antibiotics and non-specific creams. He does not remember bruising the area. In our environment, chromoblastomycosis is the third most common subcutaneous mycosis. It predominates Three clinical diagnosis were made based on the in the lower limbs in warty form and F pedrosoi is the clinical data: chromoblastomycosis; leishmaniasis; most frequent etiological agent. -
Orthologous Promoters from Related Methylotrophic Yeasts Surpass
Vogl et al. AMB Expr (2020) 10:38 https://doi.org/10.1186/s13568-020-00972-1 ORIGINAL ARTICLE Open Access Orthologous promoters from related methylotrophic yeasts surpass expression of endogenous promoters of Pichia pastoris Thomas Vogl1,2 , Jasmin Elgin Fischer1†, Patrick Hyden1†, Richard Wasmayer1†, Lukas Sturmberger1 and Anton Glieder1* Abstract Methylotrophic yeasts such as Komagataella phafi (syn. Pichia pastoris, Pp), Hansenula polymorpha (Hp), Candida boidinii (Cb) and Pichia methanolica (Pm) are widely used protein production platforms. Typically, strong, tightly regulated promoters of genes coding for their methanol utilization (MUT) pathways are used to drive heterologous gene expression. Despite highly similar open reading frames in the MUT pathways of the four yeasts, the regulation of the respective promoters varies strongly between species. While most endogenous Pp MUT promoters remain tightly repressed after depletion of a repressing carbon, Hp, Cb and Pm MUT promoters are derepressed to up to 70% of methanol induced levels, enabling methanol free production processes in their respective host background. Here, we have tested a series of orthologous promoters from Hp, Cb and Pm in Pp. Unexpectedly, when induced with metha- nol, the promoter of the HpMOX gene reached very similar expression levels as the strong methanol, inducible, and most frequently used promoter of the Pp alcohol oxidase 1 gene (PPpAOX1). The HpFMD promoter even surpassed PPpAOX1 up to three-fold, when induced with methanol, and reached under methanol-free/derepressed conditions similar expression as the methanol induced PPpAOX1. These results demonstrate that orthologous promoters from related yeast species can give access to otherwise unobtainable regulatory profles and may even considerably surpass endogenous promoters in P. -
Ep 3323422 A1
(19) TZZ¥¥ ¥ _T (11) EP 3 323 422 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 23.05.2018 Bulletin 2018/21 A61K 38/00 (2006.01) C07K 7/08 (2006.01) (21) Application number: 16306539.4 (22) Date of filing: 22.11.2016 (84) Designated Contracting States: (72) Inventors: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB • MARBAN, Céline GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO 68000 COLMAR (FR) PL PT RO RS SE SI SK SM TR • METZ-BOUTIGUE, Marie-Hélène Designated Extension States: 67000 STRASBOURG (FR) BA ME • LAVALLE, Philippe Designated Validation States: 67370 WINTZENHEIM KOCHERSBERG (FR) MA MD • SCHAAF, Pierre 67120 MOLSHEIM (FR) (71) Applicants: • HAIKEL, Youssef • Université de Strasbourg 67000 STRASBOURG (FR) 67000 Strasbourg (FR) • Institut National de la Santé et de la Recherche (74) Representative: Cabinet Becker et Associés Médicale 25, rue Louis le Grand 75013 Paris (FR) 75002 Paris (FR) (54) NEW D-CONFIGURED CATESLYTIN PEPTIDE (57) The present invention relates to a cateslytin pep- no acids residues of said cateslytin are D-configured. The tide having an amino acid sequence consisting or con- invention also relates to the use of said cateslytin peptide sisting essentially in the sequence of SEQ ID NO: 1, as a drug, especially in the treatment of an infection in a wherein at least 80%, preferably at least 90%, of the ami- patient in needs thereof. EP 3 323 422 A1 Printed by Jouve, 75001 PARIS (FR) EP 3 323 422 A1 Description Field of the Invention 5 [0001] The present invention relates to the field of medicine, in particular of infections. -
Utilization of the Internal Transcribed Spacer Regions As Molecular Targets
Medical Mycology 2002, 40, 87±109 Accepted 9July 2001 Review article Utilizationof the internaltranscribed spacer regions as molecular targets to detect andidentify human fungal pathogens P.C.IWEN*, S.H.HINRICHS* & M.E.RUPP Downloaded from https://academic.oup.com/mmy/article/40/1/87/961355 by guest on 29 September 2021 y *Department ofPathology and Microbiology,University ofNebraska MedicalCenter, Omaha, Nebraska, USA; Internal Medicine, y University ofNebraska MedicalCenter, Omaha, Nebraska, USA Advancesin molecular technology show greatpotential for the rapiddetection and identication of fungifor medical,scienti c andcommercial purposes. Numerous targetswithin the fungalgenome have been evaluated, with much of the current work usingsequence areas within the ribosomalDNA (rDNA) gene complex. This sectionof the genomeincludes the 18S,5 8Sand28S genes which codefor ribosomal ¢ RNA(rRNA) andwhich havea relativelyconserved nucleotide sequence among fungi.It alsoincludes the variableDNA sequence areas of the interveninginternal transcribedspacer (ITS) regionscalled ITS1 and ITS2. Although not translatedinto proteins,the ITScoding regions have a criticalrole in the developmentof functional rRNA,with sequencevariations among species showing promiseas signature regionsfor molecularassays. This review of the current literaturewas conducted to evaluateclinical approaches for usingthe fungalITS regions as molecular targets. Multipleapplications using the fungalITS sequences are summarized here including those for cultureidenti cation, phylogenetic -
Hansenula Polymorpha
Inversion of the Chromosomal Region between Two Mating Type Loci Switches the Mating Type in Hansenula polymorpha Hiromi Maekawa*, Yoshinobu Kaneko Yeast Genetic Resources Laboratory, Graduate School of Engineering, Osaka University, Osaka, Japan Abstract Yeast mating type is determined by the genotype at the mating type locus (MAT). In homothallic (self-fertile) Saccharomycotina such as Saccharomyces cerevisiae and Kluveromyces lactis, high-efficiency switching between a and a mating types enables mating. Two silent mating type cassettes, in addition to an active MAT locus, are essential components of the mating type switching mechanism. In this study, we investigated the structure and functions of mating type genes in H. polymorpha (also designated as Ogataea polymorpha). The H. polymorpha genome was found to harbor two MAT loci, MAT1 and MAT2, that are ,18 kb apart on the same chromosome. MAT1-encoded a1 specifies a cell identity, whereas none of the mating type genes were required for a identity and mating. MAT1-encoded a2 and MAT2-encoded a1 were, however, essential for meiosis. When present in the location next to SLA2 and SUI1 genes, MAT1 or MAT2 was transcriptionally active, while the other was repressed. An inversion of the MAT intervening region was induced by nutrient limitation, resulting in the swapping of the chromosomal locations of two MAT loci, and hence switching of mating type identity. Inversion-deficient mutants exhibited severe defects only in mating with each other, suggesting that this inversion is the mechanism of mating type switching and homothallism. This chromosomal inversion-based mechanism represents a novel form of mating type switching that requires only two MAT loci. -
Chromoblastomycosis
Chromoblastomycosis Also known as … Chromomycosis, Cladosporiosis, Verrucous dermatitis, Fonseca’s disease, Pedroso’s disease What is Chromoblastomycosis? Chromoblastomycosis is a long-term or chronic fungal infection of the skin and tissue underneath the superficial layer of the skin (called the subcutaneous tissue). It is more common in rural, tropical and subtropical areas of the world; it tends to present more severely in those with a suppressed or compromised immune system. What causes Chromoblastomycosis? The fungi that cause chromoblastomycosis tend to be found on wood/bark and in the soil. These tend to enter the skin through a penetrating injury (a splinter, nail, or similar mechanism) especially in farmers, miners & rural area workers There are six fungi that are responsible for the vast majority of cases: Fonsecaea pedrosoi, Fonsecaea compacta, Fonsecaea monophora, Phialophora verrucosa, Cladophialophora carrionii (formerly Cladosporium carrionii), and Rhinocladiella aquaspersa. What does Chromoblastomycosis look like? Chromoblastomycosis is characterised by slow growing, scaly, cauliflower-like (verrucous) lumps. Lesions may clear at the centre forming a ring-like area with a raised border. Surrounding smaller lesions (Satellites) may develop around the site from scratching. The lesions can appear anywhere on the body, but the most affected areas are the feet, legs & arms. What other problems can occur with chromoblastomycosis? The lesions may become secondarily infected with bacteria. The appearance of the lesions associated with chromoblastomycosis can be quite distressing. Very rarely, the long-term or chronic lesions develop a type of skin cancer within, called squamous cell carcinomas (SCCs). How is chromoblastomycosis diagnosed? The diagnosis is usually made after taking a sample from the lesions for fungal scraping, a skin biopsy or tissue culture. -
Polyketides, Toxins and Pigments in Penicillium Marneffei
Toxins 2015, 7, 4421-4436; doi:10.3390/toxins7114421 OPEN ACCESS toxins ISSN 2072-6651 www.mdpi.com/journal/toxins Review Polyketides, Toxins and Pigments in Penicillium marneffei Emily W. T. Tam 1, Chi-Ching Tsang 1, Susanna K. P. Lau 1,2,3,4,* and Patrick C. Y. Woo 1,2,3,4,* 1 Department of Microbiology, The University of Hong Kong, Pokfulam, Hong Kong; E-Mails: [email protected] (E.W.T.T.); [email protected] (C.-C.T.) 2 State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Pokfulam, Hong Kong 3 Research Centre of Infection and Immunology, The University of Hong Kong, Pokfulam, Hong Kong 4 Carol Yu Centre for Infection, The University of Hong Kong, Pokfulam, Hong Kong * Authors to whom correspondence should be addressed; E-Mails: [email protected] (S.K.P.L.); [email protected] (P.C.Y.W.); Tel.: +852-2255-4892 (S.K.P.L. & P.C.Y.W.); Fax: +852-2855-1241 (S.K.P.L. & P.C.Y.W.). Academic Editor: Jiujiang Yu Received: 18 September 2015 / Accepted: 22 October 2015 / Published: 30 October 2015 Abstract: Penicillium marneffei (synonym: Talaromyces marneffei) is the most important pathogenic thermally dimorphic fungus in China and Southeastern Asia. The HIV/AIDS pandemic, particularly in China and other Southeast Asian countries, has led to the emergence of P. marneffei infection as an important AIDS-defining condition. Recently, we published the genome sequence of P. marneffei. In the P. marneffei genome, 23 polyketide synthase genes and two polyketide synthase-non-ribosomal peptide synthase hybrid genes were identified.