AR TICLE a Phylogenetically-Based Nomenclature for Cordycipitaceae
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Verticillium Wilt of Canola CP
INDUSTRY BIOSECURITY PLAN FOR THE GRAINS INDUSTRY Threat Specific Contingency Plan Verticillium wilt of canola Verticillium longisporum Prepared by Kurt Lindbeck and Plant Health Australia June 2011 PLANT HEALTH AUSTRALIA | Contingency Plan – Verticillium wilt of canola (Verticillium longisporum) Disclaimer The scientific and technical content of this document is current to the date published and all efforts were made to obtain relevant and published information. New information will be included as it becomes available, or when the document is reviewed. The material contained in this publication is produced for general information only. It is not intended as professional advice on any particular matter. No person should act or fail to act on the basis of any material contained in this publication without first obtaining specific, independent professional advice. Plant Health Australia and all persons acting for Plant Health Australia in preparing this publication, expressly disclaim all and any liability to any persons in respect of anything done by any such person in reliance, whether in whole or in part, on this publication. The views expressed in this publication are not necessarily those of Plant Health Australia. Further information For further information regarding this contingency plan, contact Plant Health Australia through the details below. Address: Level 1, 1 Phipps Close DEAKIN ACT 2600 Phone: +61 2 6215 7700 Fax: +61 2 6260 4321 Email: [email protected] Website: www.planthealthaustralia.com.au | PAGE 2 PLANT HEALTH AUSTRALIA | Contingency Plan – Verticillium wilt of canola (Verticillium longisporum) 1 Purpose and background of this contingency plan ................................................................. 5 2 Australian Grains Industry .......................................................................................................... 5 3 Eradication or containment decision matrix ............................................................................ -
Unravelling the Diversity Behind the Ophiocordyceps Unilateralis (Ophiocordycipitaceae) Complex: Three New Species of Zombie-Ant Fungi from the Brazilian Amazon
Phytotaxa 220 (3): 224–238 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.220.3.2 Unravelling the diversity behind the Ophiocordyceps unilateralis (Ophiocordycipitaceae) complex: Three new species of zombie-ant fungi from the Brazilian Amazon JOÃO P. M. ARAÚJO1*, HARRY C. EVANS2, DAVID M. GEISER3, WILLIAM P. MACKAY4 & DAVID P. HUGHES1, 5* 1 Department of Biology, Penn State University, University Park, Pennsylvania, United States of America. 2 CAB International, E-UK, Egham, Surrey, United Kingdom 3 Department of Plant Pathology, Penn State University, University Park, Pennsylvania, United States of America. 4 Department of Biological Sciences, University of Texas at El Paso, 500 West University Avenue, El Paso, Texas, United States of America. 5 Department of Entomology, Penn State University, University Park, Pennsylvania, United States of America. * email: [email protected]; [email protected] Abstract In tropical forests, one of the most commonly encountered relationships between parasites and insects is that between the fungus Ophiocordyceps (Ophiocordycipitaceae, Hypocreales, Ascomycota) and ants, especially within the tribe Campono- tini. Here, we describe three newly discovered host-specific species, Ophiocordyceps camponoti-atricipis, O. camponoti- bispinosi and O. camponoti-indiani, on Camponotus ants from the central Amazonian region of Brazil, which can readily be separated using morphological traits, in particular the shape and behavior of the ascospores. DNA sequence data support inclusion of these species within the Ophiocordyceps unilateralis complex. Introduction In tropical forests, social insects (ants, bees, termites and wasps) are the most abundant land-dwelling arthropods. -
The Holomorph of Parasarcopodium (Stachybotryaceae), Introducing P
Phytotaxa 266 (4): 250–260 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2016 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.266.4.2 The holomorph of Parasarcopodium (Stachybotryaceae), introducing P. pandanicola sp. nov. on Pandanus sp. SAOWALUCK TIBPROMMA1,2,3,4,5, SARANYAPHAT BOONMEE2, NALIN N. WIJAYAWARDENE2,3,5, SAJEEWA S.N. MAHARACHCHIKUMBURA6, ERIC H. C. McKENZIE7, ALI H. BAHKALI8, E.B. GARETH JONES8, KEVIN D. HYDE1,2,3,4,5,8 & ITTHAYAKORN PROMPUTTHA9,* 1Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kun- ming 650201, Yunnan, People’s Republic of China 2Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 4World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, P. R. China 5Mushroom Research Foundation, 128 M.3 Ban Pa Deng T. Pa Pae, A. Mae Taeng, Chiang Mai 50150, Thailand 6Department of Crop Sciences, College of Agricultural and Marine Sciences Sultan Qaboos University, P.O. Box 34, AlKhoud 123, Oman 7Manaaki Whenua Landcare Research, Private Bag 92170, Auckland, New Zealand 8Botany and Microbiology Department, College of Science, King Saud University, Riyadh, KSA 11442, Saudi Arabia 9Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, 50200, Thailand *Corresponding author: e-mail: [email protected] Abstract Collections of microfungi on Pandanus species (Pandanaceae) in Krabi, Thailand resulted in the discovery of a new species in the genus Parasarcopodium, producing both its sexual and asexual morphs. -
University of California Santa Cruz Responding to An
UNIVERSITY OF CALIFORNIA SANTA CRUZ RESPONDING TO AN EMERGENT PLANT PEST-PATHOGEN COMPLEX ACROSS SOCIAL-ECOLOGICAL SCALES A dissertation submitted in partial satisfaction of the requirements for the degree of DOCTOR OF PHILOSOPHY in ENVIRONMENTAL STUDIES with an emphasis in ECOLOGY AND EVOLUTIONARY BIOLOGY by Shannon Colleen Lynch December 2020 The Dissertation of Shannon Colleen Lynch is approved: Professor Gregory S. Gilbert, chair Professor Stacy M. Philpott Professor Andrew Szasz Professor Ingrid M. Parker Quentin Williams Acting Vice Provost and Dean of Graduate Studies Copyright © by Shannon Colleen Lynch 2020 TABLE OF CONTENTS List of Tables iv List of Figures vii Abstract x Dedication xiii Acknowledgements xiv Chapter 1 – Introduction 1 References 10 Chapter 2 – Host Evolutionary Relationships Explain 12 Tree Mortality Caused by a Generalist Pest– Pathogen Complex References 38 Chapter 3 – Microbiome Variation Across a 66 Phylogeographic Range of Tree Hosts Affected by an Emergent Pest–Pathogen Complex References 110 Chapter 4 – On Collaborative Governance: Building Consensus on 180 Priorities to Manage Invasive Species Through Collective Action References 243 iii LIST OF TABLES Chapter 2 Table I Insect vectors and corresponding fungal pathogens causing 47 Fusarium dieback on tree hosts in California, Israel, and South Africa. Table II Phylogenetic signal for each host type measured by D statistic. 48 Table SI Native range and infested distribution of tree and shrub FD- 49 ISHB host species. Chapter 3 Table I Study site attributes. 124 Table II Mean and median richness of microbiota in wood samples 128 collected from FD-ISHB host trees. Table III Fungal endophyte-Fusarium in vitro interaction outcomes. -
The Interspecific Fungal Hybrid Verticillium Longisporum Displays Sub-Genome-Specific
bioRxiv preprint doi: https://doi.org/10.1101/341636; this version posted February 22, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 The interspecific fungal hybrid Verticillium longisporum displays sub-genome-specific 2 gene expression 3 4 Jasper R.L. Depotterabc, Fabian van Beverena¶, Luis Rodriguez-Morenoae¶, H. Martin 5 Kramera¶, Edgar A. Chavarro Carreroa¶, Gabriel L. Fiorina, Grardy C.M. van den Berga, 6 Thomas A. Woodb&, Bart P.H.J. Thommaac&*, Michael F. Seidlad&* 7 8 aLaboratory of Phytopathology, Wageningen University & Research, Wageningen, The 9 Netherlands 10 bDepartment of Crops and Agronomy, National Institute of Agricultural Botany, Cambridge, 11 United Kingdom 12 cUniversity of Cologne, Institute for Plant Sciences, Cluster of Excellence on Plant Sciences 13 (CEPLAS), Cologne, Germany 14 dTheoretical Biology & Bioinformatics, Utrecht University, Utrecht, the Netherlands 15 eDepartamento de Biología Celular, Genética y Fisiología, Universidad de Málaga, Málaga, 16 Spain 17 18 *Corresponding authors 19 E-mail: [email protected] (BPHJT) 20 E-mail: [email protected] (MFS) 21 22 ¶These authors contributed equally to this work 23 &These authors contributed equally to this work 1 bioRxiv preprint doi: https://doi.org/10.1101/341636; this version posted February 22, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. -
Predicting Disease Occurrence of Cabbage Verticillium Wilt in Monoculture Using Species Distribution Modeling
Predicting disease occurrence of cabbage Verticillium wilt in monoculture using species distribution modeling Kentaro Ikeda1 and Takeshi Osawa2 1 Department of Agriculture, Gunma Prefectural Office, Isesaki, Gunma, Japan 2 Graduate School of Urban Environmental Sciences, Tokyo Metropolitan University, Hachioji, Tokyo, Japan ABSTRACT Background: Although integrated pest management (IPM) is essential for conservation agriculture, this method can be inadequate for severely infected fields. The ability to predict the potential occurrence of severe infestation of soil-borne disease would enable farmers to adopt suitable methods for high-risk areas, such as soil disinfestation, and apply other options for lower risk areas. Recently, researchers have used species distribution modeling (SDM) to predict the occurrence of target plant and animal species based on various environmental variables. In this study, we applied this technique to predict and map the occurrence probability of a soil-borne disease, Verticillium wilt, using cabbage as a case study. Methods: A disease survey assessing the distribution of Verticillium wilt in cabbage fields in Tsumagoi village (central Honshu, Japan) was conducted two or three times annually from 1997 to 2013. Road density, elevation and topographic wetness index (TWI) were selected as explanatory variables for disease occurrence potential. A model of occurrence probability of Verticillium wilt was constructed using the MaxEnt software for SDM analysis. As the disease survey was mainly conducted in an agricultural area, the area was weighted as “Bias Grid” and area except for the agricultural area was set as background. Results: Grids with disease occurrence showed a high degree of coincidence with Submitted 16 March 2020 those with a high probability occurrence. -
Kb Lineage- Specific Genomic Region Tames Virulence in Pathogenic
Received: 19 February 2021 | Accepted: 30 March 2021 DOI: 10.1111/mpp.13071 ORIGINAL ARTICLE A 20- kb lineage- specific genomic region tames virulence in pathogenic amphidiploid Verticillium longisporum Rebekka Harting1 | Jessica Starke1 | Harald Kusch1 | Stefanie Pöggeler2 | Isabel Maurus1 | Rabea Schlüter3 | Manuel Landesfeind4 | Ingo Bulla5 | Minou Nowrousian6 | Ronnie de Jonge7,8 | Gertrud Stahlhut2 | Katharina J. Hoff5,9 | Kathrin P. Aßhauer4 | Andrea Thürmer10 | Mario Stanke5,9 | Rolf Daniel10 | Burkhard Morgenstern4 | Bart P. H. J. Thomma 8 | James W. Kronstad11 | Susanna A. Braus- Stromeyer1 | Gerhard H. Braus 1 1Department of Molecular Microbiology and Genetics, Institute of Microbiology and Genetics and Göttingen Center for Molecular Biosciences, University of Göttingen, Göttingen, Germany 2Department of Genetics of Eukaryotic Microorganisms, Institute of Microbiology and Genetics and Göttingen Center for Molecular Biosciences, University of Göttingen, Göttingen, Germany 3Imaging Center of the Department of Biology, University of Greifswald, Greifswald, Germany 4Department of Bioinformatics, Institute of Microbiology and Genetics and Göttingen Center for Molecular Biosciences, University of Göttingen, Göttingen, Germany 5Institute for Mathematics and Computer Science, University of Greifswald, Greifswald, Germany 6Department of Molecular and Cellular Botany, Ruhr- Universität Bochum, Bochum, Germany 7Plant– Microbe Interactions, Department of Biology, Science4Life, Utrecht University, Utrecht, Netherlands 8Laboratory of Phytopathology, -
Multigene Phylogeny and Morphology Reveal a New Species, Ophiocordyceps Vespulae, from Jilin Province, China
Phytotaxa 478 (1): 033–048 ISSN 1179-3155 (print edition) https://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2021 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.478.1.2 Multigene phylogeny and morphology reveal a new species, Ophiocordyceps vespulae, from Jilin Province, China FENG-YAO LONG1, 2, 6, LI-WU QIN3, 7, YUAN-PIN XIAO2, 4, 8, KEVIN D. HYDE4, 9, SHAO-XIAN WANG3, 10* & TING-CHI WEN1, 2, 5, 11* 1 School of Pharmacy, Guizhou University, Guiyang 550025, Guizhou, China. 2 The Engineering Research Center of Southwest Bio-Pharmaceutical Resources, Ministry of Education, Guizhou University, Guiyang 550025, Guizhou, China. 3 Changbai Mountain Academy of Sciences, Jilin Provincial Joint Key Laboratory of Changbai Mountains Biocoenosis & Biodiversity, Erdaobaihe 133613, Jilin, China. 4 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100 Thailand. 5Mushroom Research Institute,Guizhou University,Guiyang,550025,China 6 [email protected]; https://orcid.org/0000-0002-5818-694X 7 [email protected]; https://orcid.org/0000-0002-5586-2885 8 [email protected]; https://orcid.org/0000-0003-1730-3545 9 [email protected]; https://orcid.org/0000-0002-2191-0762 10 [email protected]; https://orcid.org/0000-0002-0921-1790 11 [email protected]; https://orcid.org/0000-0003-1744-5869 *Corresponding author Abstract Ophiocordyceps is entomopathogenic and is the best studied genus in Ophiocordycipitaceae. Members of Ophiocordyceps and ants form sophisticated interactions. However, taxonomy and evolutionary relationships of this group of pathogens remain unclear. During a survey in Changbai Mountains, Jiling Province, China, a new entomogenous species, Ophiocordyceps vespulae sp. -
Effects of the Fungus Isaria Fumosorosea
This article was downloaded by: [University of Florida] On: 11 June 2013, At: 06:27 Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Biocontrol Science and Technology Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/cbst20 Effects of the fungus Isaria fumosorosea (Hypocreales: Cordycipitaceae) on reduced feeding and mortality of the Asian citrus psyllid, Diaphorina citri (Hemiptera: Psyllidae) Pasco B. Avery a , Vitalis W. Wekesa b c , Wayne B. Hunter b , David G. Hall b , Cindy L. McKenzie b , Lance S. Osborne c , Charles A. Powell a & Michael E. Rogers d a University of Florida, Institute of Food and Agricultural Sciences, Indian River Research and Education Center, 2199 South Rock Road, Fort Pierce, FL, 34945, USA b USDA, ARS, U.S. Horticultural Research Laboratory, Subtropical Insect Research Unit, 2001 South Rock Road, Ft. Pierce, FL, 34945, USA c University of Florida, Institute of Food and Agricultural Sciences, Mid-Florida Research and Education Center, Department of Entomology and Nematology, 2725 Binion Road, Apopka, FL, 32703, USA d University of Florida, Institute of Food and Agricultural Sciences, Citrus Research and Education Center, 700 Experiment Station Road, Lake Alfred, FL, 33850, USA Published online: 25 Aug 2011. To cite this article: Pasco B. Avery , Vitalis W. Wekesa , Wayne B. Hunter , David G. Hall , Cindy L. McKenzie , -
Comprehensive Analysis of Verticillium Nonalfalfae in Silico Secretome
bioRxiv preprint doi: https://doi.org/10.1101/237255; this version posted December 21, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Comprehensive analysis of Verticillium nonalfalfae in silico secretome uncovers putative effector proteins expressed during hop invasion 1 Kristina Marton1, Marko Flajšman1, Sebastjan Radišek2, Katarina Košmelj1, Jernej Jakše1, 2 Branka Javornik1, Sabina Berne1* 3 1Department of Agronomy, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia 4 2Slovenian Institute of Hop Research and Brewing, Žalec, Slovenia 5 * Correspondence: 6 Sabina Berne 7 [email protected] 8 Abstract 9 Background: The vascular plant pathogen Verticillium nonalfalfae causes Verticillium wilt in several 10 important crops. VnaSSP4.2 was recently discovered as a V. nonalfalfae virulence effector protein in 11 the xylem sap of infected hop. Here, we expanded our search for candidate secreted effector proteins 12 (CSEPs) in the V. nonalfalfae predicted secretome using a bioinformatic pipeline built on V. 13 nonalfalfae genome data, RNA-Seq and proteomic studies of the interaction with hop. 14 Results: The secretome, rich in carbohydrate active enzymes, proteases, redox proteins and proteins 15 involved in secondary metabolism, cellular processing and signaling, includes 263 CSEPs. Several 16 homologs of known fungal effectors (LysM, NLPs, Hce2, Cerato-platanins, Cyanovirin-N lectins, 17 hydrophobins and CFEM domain containing proteins) and avirulence determinants in the PHI 18 database (Avr-Pita1 and MgSM1) were found. The majority of CSEPs were non-annotated and were bioRxiv preprint doi: https://doi.org/10.1101/237255; this version posted December 21, 2017. -
Identification of Culture-Negative Fungi in Blood and Respiratory Samples
IDENTIFICATION OF CULTURE-NEGATIVE FUNGI IN BLOOD AND RESPIRATORY SAMPLES Farida P. Sidiq A Dissertation Submitted to the Graduate College of Bowling Green State University in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY May 2014 Committee: Scott O. Rogers, Advisor W. Robert Midden Graduate Faculty Representative George Bullerjahn Raymond Larsen Vipaporn Phuntumart © 2014 Farida P. Sidiq All Rights Reserved iii ABSTRACT Scott O. Rogers, Advisor Fungi were identified as early as the 1800’s as potential human pathogens, and have since been shown as being capable of causing disease in both immunocompetent and immunocompromised people. Clinical diagnosis of fungal infections has largely relied upon traditional microbiological culture techniques and examination of positive cultures and histopathological specimens utilizing microscopy. The first has been shown to be highly insensitive and prone to result in frequent false negatives. This is complicated by atypical phenotypes and organisms that are morphologically indistinguishable in tissues. Delays in diagnosis of fungal infections and inaccurate identification of infectious organisms contribute to increased morbidity and mortality in immunocompromised patients who exhibit increased vulnerability to opportunistic infection by normally nonpathogenic fungi. In this study we have retrospectively examined one-hundred culture negative whole blood samples and one-hundred culture negative respiratory samples obtained from the clinical microbiology lab at the University of Michigan Hospital in Ann Arbor, MI. Samples were obtained from randomized, heterogeneous patient populations collected between 2005 and 2006. Specimens were tested utilizing cetyltrimethylammonium bromide (CTAB) DNA extraction and polymerase chain reaction amplification of internal transcribed spacer (ITS) regions of ribosomal DNA utilizing panfungal ITS primers. -
The Genus Simplicillium
A peer-reviewed open-access journal MycoKeys 60: 69–92 (2019) The genus Simplicillium 69 doi: 10.3897/mycokeys.60.38040 RESEARCH ARTICLE MycoKeys http://mycokeys.pensoft.net Launched to accelerate biodiversity research The genus Simplicillium De-Ping Wei1,2,3,4, Dhanushka N. Wanasinghe3,5, Kevin D. Hyde2,4, Peter E. Mortimer3, Jianchu Xu3,5, Yuan-Pin Xiao2,6,7, Chitrabhanu S. Bhunjun2,7, Chaiwat To-anun1 1 Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand 2 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand3 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, China 4 Mushroom Research Foundation, 128 M.3 Ban Pa Deng T. Pa Pae, A. Mae Taeng, Chiang Mai 50150, Thailand5 World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, China 6 Engineering Research Center of Southwest Bio- Pharmaceutical Resources, Ministry of Education, Guizhou University, Guiyang, Guizhou Province, 550025, China 7 School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand Corresponding author: Peter E. Mortimer ([email protected]) Academic editor: Cecile Gueidan | Received 6 July2019 | Accepted 9 September 2019 | Published 19 November 2019 Citation: Wei D-P, Wanasinghe DN, Hyde KD, Mortimer PE, Xu J-C, Xiao Y-P, Bhunjun CS, To-anun C (2019) The genus Simplicillium. MycoKeys 60: 69–92. https://doi.org/10.3897/mycokeys.60.38040 Abstract Simplicillium species have a wide host range and an extensive distribution. Some species are associated with rusts, as well as other plant pathogenic fungi and play an important role in biological control.