Eduardo Alvarez-Duarte

Dr. Eduardo Alvarez-Duarte

Universidad de Chile, Santiago, Región Metropolitana, Chile
orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 June 2018 in Persoonia - Molecular Phylogeny and Evolution of Fungi
Verified
Journal Article
Open access
PCP.W. Crous
P.W. Crous
MWM.J. Wingfield
M.J. Wingfield
TBTreena Burgess
Treena Burgess
GHG.E.ST.J. Hardy
G.E.ST.J. Hardy
JGJ. Gené
J. Gené
JGJ.Z. Groenewald
J.Z. Groenewald
Novel species of fungi described in this study include those from various countries as follows:Australia,Chaetopsina eucalyptionEucalyptusleaf litter,Colletotrichum cobbittiensefromCordyline stricta×C. australishybrid,Cyanodermella banksiaeonBanksia ericifoliasubsp.macrantha, Discosia macrozamiaeonMacrozamia miquelii, Elsinoë banksiigenaonBanksia marginata, Elsinoë elaeocarpionElaeocarpussp.,Elsinoë leucopogonisonLeucopogonsp.,Helminthosporium livistonaeonLivistona australis,Idriellomyces eucalypti(incl.Idriellomycesgen. nov.) onEucalyptus obliqua,Lareunionomyces eucalyptionEucalyptussp.,Myrotheciomyces corymbiae(incl.Myrotheciomycesgen. nov.,Myrotheciomycetaceaefam. nov.),Neolauriomyces eucalypti(incl.Neolauriomycesgen. nov.,Neolauriomycetaceaefam. nov.) onEucalyptussp.,Nullicamyces eucalypti(incl.Nullicamycesgen. nov.) onEucalyptusleaf litter,Oidiodendron eucalyptionEucalyptus maidenii,Paracladophialophora cyperacearum(incl.Paracladophialophoraceaefam. nov.) andPericonia cyperacearumon leaves ofCyperaceae,Porodiplodia livistonae(incl.Porodiplodiagen. nov.,Porodiplodiaceaefam. nov.) onLivistona australis,Sporidesmium melaleucae(incl.Sporidesmialesord. nov.) onMelaleucasp.,Teratosphaeria sieberionEucalyptus sieberi,Thecaphora australiensisin capsules of a variant ofOxalis exilis.Brazil,Aspergillus serratalhadensisfrom soil,Diaporthe pseudoinconspicuafromPoincianella pyramidalis,Fomitiporella pertenuison dead wood,Geastrum magnosporumon soil,Marquesius aquaticus(incl.Marquesiusgen. nov.) from submerged decaying twig and leaves of unidentified plant,Mastigosporella pigmentatafrom leaves ofQualea parviflorae,Mucor souzaefrom soil,Mycocalia aquaphilaon decaying wood from tidal detritus,Preussia citrullinaas endophyte from leaves ofCitrullus lanatus,Queiroziella brasiliensis(incl.Queiroziellagen. nov.) as epiphytic yeast on leaves ofPortea leptantha,Quixadomyces cearensis(incl.Quixadomycesgen. nov.) on decaying bark,Xylophallus clavatuson rotten wood.Canada,Didymella carionCarum carviandCoriandrum sativum.Chile,Araucasphaeria foliorum(incl.Araucasphaeriagen. nov.) onAraucaria araucana,Aspergillus tumidusfrom soil,Lomentospora valparaisensisfrom soil.Colombia,Corynespora pseudocassiicolaonByrsonimasp.,Eucalyptostroma eucalyptorumonEucalyptus pellita,Neometulocladosporiella eucalypti(incl.Neometulocladosporiellagen. nov.) onEucalyptus grandis×urophylla,Tracylla eucalypti(incl.Tracyllaceaefam. nov.,Tracyllalalesord. nov.) onEucalyptus urophylla.Cyprus,Gyromitra anthracobia(incl.Gyromitrasubg.Pseudoverpa) on burned soil.Czech Republic,Lecanicillium restrictumfrom the surface of the wooden barrel,Lecanicillium testudineumfromscales ofTrachemys scripta elegans.Ecuador,Entoloma yanacolorandSaproamanita quitensison soil.France,Lentithecium carbonneanumfrom submerged decorticatedPopulusbranch.Hungary,Pleuromyces hungaricus(incl.Pleuromycesgen. nov.) from a largeFagus sylvaticalog.Iran,Zymoseptoria crescentaonAegilops triuncialis.Malaysia,Ochroconis musicolaonMusasp.Mexico,Cladosporium michoacanensefrom soil.New Zealand, Acrodontium metrosiderionMetrosideros excelsa, Polynema podocarpionPodocarpus totara, Pseudoarthrographis phlogis(incl.Pseudoarthrographisgen. nov.) onPhlox subulata.Nigeria,Coprinopsis afrocinereaon soil.Pakistan,Russula mansehraensison soil underPinus roxburghii.Russia,Baorangia alexandrion soil in deciduous forests withQuercus mongolica.South Africa,Didymocyrtis brachylaenaeonBrachylaena discolor.Spain,Alfaria dactylisfrom fruit ofPhoenix dactylifera, Dothiora infuscansfrom a blackened wall,Exophiala nidicolafrom the nest of an unidentified bird,Matsushimaea monilioidesfrom soil,Terfezia morenoion soil.United Arab Emirates,Tirmania honrubiaeon soil.USA,Arxotrichum wyomingense(incl.Arxotrichumgen. nov.) from soil,Hongkongmyces snookiorumfrom submerged detritus from a fresh water fen,Leratiomyces tesquorumfrom soil,Talaromyces tabacinusonleaves ofNicotiana tabacum.Vietnam,Afroboletus vietnamensison soil in an evergreen tropical forest,Colletotrichum condaoensefromIpomoea pes-caprae.Morphological and culture characteristics along with DNA barcodes are provided.

31 December 2020 in Persoonia - Molecular Phylogeny and Evolution of Fungi
Verified
Journal Article
Open access
PCP.W. Crous
P.W. Crous
Don CowanDon Cowan
Don Cowan
GMG. Maggs-Kölling
G. Maggs-Kölling
NYNeriman Yilmaz
Neriman Yilmaz
ELE. Larsson
E. Larsson
JGJ.Z. Groenewald
J.Z. Groenewald
Novel species of fungi described in this study include those from various countries as follows: Australia, Austroboletus asper on soil, Cylindromonium alloxyli on leaves of Alloxylon pinnatum, Davidhawksworthia quintiniae on leaves of Quintinia sieberi, Exophiala prostantherae on leaves of Prostanthera sp., Lactifluus lactiglaucus on soil, Linteromyces quintiniae (incl. Linteromyces gen. nov.) on leaves of Quintinia sieberi, Lophotrichus medusoides from stem tissue of Citrus garrawayi, Mycena pulchra on soil, Neocalonectria tristaniopsidis (incl. Neocalonectria gen. nov.)and Xyladictyochaeta tristaniopsidis on leaves of Tristaniopsis collina, Parasarocladium tasmanniae on leaves of Tasmannia insipida, Phytophthora aquae-cooljarloo from pond water, Serendipita whamiae as endophyte from roots of Eriochilus cucullatus, Veloboletus limbatus (incl. Veloboletus gen. nov.)onsoil. Austria, Cortinarius glaucoelotus onsoil. Bulgaria, Suhomyces rilaensis from the gut of Bolitophagus interruptus found on a Polyporus sp. Canada, Cantharellus betularum among leaf litter of Betula, Penicillium saanichii from house dust. Chile, Circinella lampensis on soil, Exophiala embothrii from rhizosphere of Embothrium coccineum. China, Colletotrichum cycadis on leaves of Cycas revoluta. Croatia, Phialocephala melitaea on fallen branch of Pinus halepensis. Czech Republic, Geoglossum jirinae on soil, Pyrenochaetopsis rajhradensis from dead wood of Buxus sempervirens. Dominican Republic, Amanita domingensis on litter of deciduous wood, Melanoleuca dominicana on forest litter. France, Crinipellis nigrolamellata (Martinique) on leaves of Pisonia fragrans, Talaromyces pulveris from bore dust of Xestobium rufovillosum infesting floorboards. French Guiana, Hypoxylon hepaticolor on dead corticated branch. Great Britain, Inocybe ionolepis on soil. India, Cortinarius indopurpurascens among leaf litter of Quercus leucotrichophora. Iran, Pseudopyricularia javanii on infected leaves of Cyperus sp., Xenomonodictys iranica (incl. Xenomonodictys gen. nov.) on wood of Fagus orientalis. Italy, Penicillium vallebormidaense from compost. Namibia, Alternaria mirabibensis on plant litter, Curvularia moringae and Moringomyces phantasmae (incl. Moringomyces gen. nov.) on leaves and flowers of Moringa ovalifolia, Gobabebomyces vachelliae (incl. Gobabebomyces gen. nov.) on leaves of Vachellia erioloba, Preussia procaviae on dung of Procavia capensis. Pakistan, Russula shawarensis from soil on forest floor. Russia, Cyberlindnera dauci from Daucus carota. South Africa, Acremonium behniae on leaves of Behnia reticulata, Dothiora aloidendri and Hantamomyces aloidendri (incl. Hantamomyces gen. nov.) on leaves of Aloidendron dichotomum, Endoconidioma euphorbiae on leaves of Euphorbia mauritanica , Eucasphaeria proteae on leaves of Protea neriifolia , Exophiala mali from inner fruit tissue of Malus sp., Graminopassalora geissorhizae on leaves of Geissorhiza splendidissima, Neocamarosporium leipoldtiae on leaves of Leipoldtia schultzii, Neocladosporium osteospermi on leaf spots of Osteospermum moniliferum, Neometulocladosporiella seifertii on leaves of Combretum caffrum, Paramyrothecium pituitipietianum on stems of Grielum humifusum, Phytopythium paucipapillatum from roots of Vitis sp., Stemphylium carpobroti and Verrucocladosporium carpobroti on leaves of Carpobrotus quadrifolius, Suttonomyces cephalophylli on leaves of Cephalophyllum pilansii. Sweden, Coprinopsis rubra on cow dung, Elaphomyces nemoreus fromdeciduouswoodlands. Spain, Polyscytalum pini-canariensis on needles of Pinus canariensis, Pseudosubramaniomyces septatus from stream sediment, Tuber lusitanicum on soil under Quercus suber. Thailand, Tolypocladium flavonigrum on Elaphomyces sp. USA, Chaetothyrina spondiadis on fruits of Spondias mombin, Gymnascella minnisii from bat guano, Juncomyces patwiniorum on culms of Juncus effusus, Moelleriella puertoricoensis on scale insect, Neodothiora populina (incl. Neodothiora gen. nov.) on stem cankers of Populus tremuloides, Pseudogymnoascus palmeri fromcavesediment. Vietnam, Cyphellophora vietnamensis on leaf litter, Tylopilus subotsuensis on soil in montane evergreen broadleaf forest. Morphological and culture characteristics are supported by DNA barcodes.

1 June 2009 in Journal of Clinical Microbiology
Verified
Journal Article
Open access
Eduardo Alvarez-DuarteEduardo Alvarez-Duarte
Eduardo Alvarez-Duarte
DSD. A. Sutton
D. A. Sutton
JCJ. Cano
J. Cano
AFA. W. Fothergill
A. W. Fothergill
Alberto StchigelAlberto Stchigel
Alberto Stchigel
JGJosep Guarro
Josep Guarro
Several members of the order Mucorales (subphylum Mucoromycotina ) are important agents of severe human infections. The identification of these fungi by using standard mycologic methods is often difficult and time consuming. Frequently, the etiological agent in clinical cases is reported either as a Mucor sp., which is not the most frequent genus of zygomycetes, or only as a member of the Mucorales . For this reason, the actual spectrum of species of zygomycetes and their incidences in the clinical setting is not well known. The goals of this study were to compare the results of the molecular identification of an important set of clinical isolates, received in a mycological reference center from different regions of the United States, with those obtained by using the traditional morphological methods and to determine the spectrum of species involved. We tested 190 isolates morphologically identified as zygomycetes by using sequencing of the internal transcribed spacer (ITS) region of the ribosomal DNA. Molecular identification revealed that Rhizopus oryzae represented approximately half (44.7%) of these isolates. The remainder was identified as Rhizopus microsporus (22.1%), Mucor circinelloides (9.5%), Mycocladus corymbifer (formerly Absidia corymbifera ) (5.3%), Rhizomucor pusillus (3.7%), Cunninghamella bertholletiae (3.2%), Mucor indicus (2.6%), Cunninghamella echinulata (1%), and Apophysomyces elegans (0.5%). The most common anatomic sites for clinically significant zygomycetes, as determined by isolates sent to the Fungus Testing Laboratory for identification and/or susceptibility testing and included in this study, were the sinuses, lungs, and various cutaneous locations, at 25.8%, 26.8%, and 28%, respectively. These sites represented approximately 80% of the isolates evaluated. A high level of correlation (92.6%) between morphological and molecular identifications was found.

1 December 2015 in Materials Science and Engineering: C
Verified
Journal Article
Closed access
CFCarmen Fonseca
Carmen Fonseca
AOAlmudena Ochoa
Almudena Ochoa
MUMaria Teresa Ulloa
Maria Teresa Ulloa
Eduardo Alvarez-DuarteEduardo Alvarez-Duarte
Eduardo Alvarez-Duarte
DCDaniel Canales
Daniel Canales
PZPaula Zapata
Paula Zapata

1 April 2010 in Revista Iberoamericana de Micologia
Verified
Journal Article
Closed access
Eduardo Alvarez-DuarteEduardo Alvarez-Duarte
Eduardo Alvarez-Duarte
Alberto StchigelAlberto Stchigel
Alberto Stchigel
Jose F. Cano-LiraJose F. Cano-Lira
Jose F. Cano-Lira
DSDeanna A. Sutton
Deanna A. Sutton
AFAnnette W. Fothergill
Annette W. Fothergill
JGJosep Guarro
Josep Guarro

1 January 2011 in Medical Mycology
Verified
Journal Article
Closed access
Eduardo Alvarez-DuarteEduardo Alvarez-Duarte
Eduardo Alvarez-Duarte
Jose F. Cano-LiraJose F. Cano-Lira
Jose F. Cano-Lira
Alberto StchigelAlberto Stchigel
Alberto Stchigel
DSDeanna A. Sutton
Deanna A. Sutton
AFAnnette W. Fothergill
Annette W. Fothergill
JGJosep Guarro
Josep Guarro
Two new species in the order Mucorales, Mucor velutinosus and Mucor ellipsoideus, isolated from human clinical specimens in the USA, are described and illustrated. The former species is similar to Mucor ramosissimus, from which it can be differentiated by its ability to grow at 37°C and produce verrucose sporangiospores. Mucor ellipsoideus is also able to grow and sporulate at 37°C like M. indicus, the nearest phylogenetic species in this study, however, the former has narrow ellipsoidal sporangiospores in contrast to the subglobose to ellipsoidal sporangiospores of M. indicus. Analysis of the sequences of the ITS and the D1-D2 regions of the rRNA genes confirmed the novelty of these species. The in vitro antifungal susceptibility of the new species showed that amphotericin B was active against all isolates and posaconazole and itraconazole showed low activity.