The Insight of Mycovirus from Trichoderma Spp
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Origin, Adaptation and Evolutionary Pathways of Fungal Viruses
Virus Genes 16:1, 119±131, 1998 # 1998 Kluwer Academic Publishers, Boston. Manufactured in The Netherlands. Origin, Adaptation and Evolutionary Pathways of Fungal Viruses SAID A. GHABRIAL Department of Plant Pathology, University of Kentucky, Lexington, KY, USA Abstract. Fungal viruses or mycoviruses are widespread in fungi and are believed to be of ancient origin. They have evolved in concert with their hosts and are usually associated with symptomless infections. Mycoviruses are transmitted intracellularly during cell division, sporogenesis and cell fusion, and they lack an extracellular phase to their life cycles. Their natural host ranges are limited to individuals within the same or closely related vegetative compatibility groups. Typically, fungal viruses are isometric particles 25±50 nm in diameter, and possess dsRNA genomes. The best characterized of these belong to the family Totiviridae whose members have simple undivided dsRNA genomes comprised of a coat protein (CP) gene and an RNA dependent RNA polymerase (RDRP) gene. A recently characterized totivirus infecting a ®lamentous fungus was found to be more closely related to protozoan totiviruses than to yeast totiviruses suggesting these viruses existed prior to the divergence of fungi and protozoa. Although the dsRNA viruses at large are polyphyletic, based on RDRP sequence comparisons, the totiviruses are monophyletic. The theory of a cellular self-replicating mRNA as the origin of totiviruses is attractive because of their apparent ancient origin, the close relationships among their RDRPs, genome simplicity and the ability to use host proteins ef®ciently. Mycoviruses with bipartite genomes ( partitiviruses), like the totiviruses, have simple genomes, but the CP and RDRP genes are on separate dsRNA segments. -
Residual Effects Caused by a Past Mycovirus Infection in Fusarium Circinatum
Article Residual Effects Caused by a Past Mycovirus Infection in Fusarium circinatum Cristina Zamora-Ballesteros 1,2,* , Brenda D. Wingfield 3 , Michael J. Wingfield 3, Jorge Martín-García 1,2 and Julio J. Diez 1,2 1 Sustainable Forest Management Research Institute, University of Valladolid—INIA, 34004 Palencia, Spain; [email protected] (J.M.-G.); [email protected] (J.J.D.) 2 Department of Vegetal Production and Forest Resources, University of Valladolid, 34004 Palencia, Spain 3 Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute, University of Pretoria, Pretoria 0002, South Africa; brenda.wingfi[email protected] (B.D.W.); Mike.Wingfi[email protected] (M.J.W.) * Correspondence: [email protected] Abstract: Mycoviruses are known to be difficult to cure in fungi but their spontaneous loss occurs commonly. The unexpected disappearance of mycoviruses can be explained by diverse reasons, from methodological procedures to biological events such as posttranscriptional silencing machinery. The long-term effects of a virus infection on the host organism have been well studied in the case of human viruses; however, the possible residual effect on a fungus after the degradation of a mycovirus is unknown. For that, this study analyses a possible residual effect on the transcriptome of the pathogenic fungus Fusarium circinatum after the loss of the mitovirus FcMV1. The mycovirus that previously infected the fungal isolate was not recovered after a 4-year storage period. Only 14 genes were determined as differentially expressed and were related to cell cycle regulation and amino acid metabolism. The results showed a slight acceleration in the metabolism of the host that had lost the mycovirus by the upregulation of the genes involved in essential functions for fungal development. -
Occurrence and Diversity of Mycobiota in Heavy Metal Contaminated Sediments of Mediterranean Coastal Lagoon El-Manzala, Egypt
Mycosphere 6 (2): 228–240(2015) ISSN 2077 7019 www.mycosphere.org Mycosphere Article Copyright © 2015 Online Edition Doi 10.5943/mycosphere/6/2/12 Occurrence and diversity of mycobiota in heavy metal contaminated sediments of Mediterranean coastal lagoon El-Manzala, Egypt Abdel-Azeem AM1, El-Morsy EM2, Nour El-Dein MM2, and Rashad HM3* 1 Laboratory of systematic Mycology, Botany Department, Faculty of Science, University of Suez Canal, Ismailia 41522, Egypt. 2 Department of Botany, Faculty of Science, Damietta University, New Damietta, Egypt. 3 Ashtoum El-Gamil protectorate, Egyptian Environmental Affair Agency, Port-Said, Egypt Abdel-Azeem AM, El-Morsy EM, Nour El-Dein MM, Rashad HM 2015 – Occurrence and diversity of mycobiota in heavy metal contaminated sediments of Mediterranean coastal lagoon El- Manzala, Egypt. Mycosphere 6(2), 228–240, Doi 10.5943/mycosphere/6/2/12 Abstract An investigation was conducted to assess the concentration of heavy metals in sediments in five selected locations along Manzala lagoon and correlate the effect of metal concentrations on benthic fungal population. Physiochemical analysis showed that pH values ranged between 7.93 and 8.1 while electric conductivity ranged between 5.64 and 12.76 dSm−1. The mean values of organic matter percentage ranged between 1.0 and 2.6%. The parent material of studied sediment samples is classified as fluviolacustrine type. Different concentrations of heavy metals (Zinc, lead, cadmium, iron, manganese and copper) recorded in soil samples reflect the degree of pollution in all studied sites. The concentrations of heavy metals are relatively high in all sites e.g. Zinc (6.4 to 17.3 μg/g), lead (0.6 to 7.2 μg/g), copper (1.1 to 2.1 μg/g), manganese (98.5 to 150.3 μg/g) and iron (560.8 to 694.1 μg/g) respectively. -
Soybean Thrips (Thysanoptera: Thripidae) Harbor Highly Diverse Populations of Arthropod, Fungal and Plant Viruses
viruses Article Soybean Thrips (Thysanoptera: Thripidae) Harbor Highly Diverse Populations of Arthropod, Fungal and Plant Viruses Thanuja Thekke-Veetil 1, Doris Lagos-Kutz 2 , Nancy K. McCoppin 2, Glen L. Hartman 2 , Hye-Kyoung Ju 3, Hyoun-Sub Lim 3 and Leslie. L. Domier 2,* 1 Department of Crop Sciences, University of Illinois, Urbana, IL 61801, USA; [email protected] 2 Soybean/Maize Germplasm, Pathology, and Genetics Research Unit, United States Department of Agriculture-Agricultural Research Service, Urbana, IL 61801, USA; [email protected] (D.L.-K.); [email protected] (N.K.M.); [email protected] (G.L.H.) 3 Department of Applied Biology, College of Agriculture and Life Sciences, Chungnam National University, Daejeon 300-010, Korea; [email protected] (H.-K.J.); [email protected] (H.-S.L.) * Correspondence: [email protected]; Tel.: +1-217-333-0510 Academic Editor: Eugene V. Ryabov and Robert L. Harrison Received: 5 November 2020; Accepted: 29 November 2020; Published: 1 December 2020 Abstract: Soybean thrips (Neohydatothrips variabilis) are one of the most efficient vectors of soybean vein necrosis virus, which can cause severe necrotic symptoms in sensitive soybean plants. To determine which other viruses are associated with soybean thrips, the metatranscriptome of soybean thrips, collected by the Midwest Suction Trap Network during 2018, was analyzed. Contigs assembled from the data revealed a remarkable diversity of virus-like sequences. Of the 181 virus-like sequences identified, 155 were novel and associated primarily with taxa of arthropod-infecting viruses, but sequences similar to plant and fungus-infecting viruses were also identified. -
Phylogeny and Nomenclature of the Genus Talaromyces and Taxa Accommodated in Penicillium Subgenus Biverticillium
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector available online at www.studiesinmycology.org StudieS in Mycology 70: 159–183. 2011. doi:10.3114/sim.2011.70.04 Phylogeny and nomenclature of the genus Talaromyces and taxa accommodated in Penicillium subgenus Biverticillium R.A. Samson1, N. Yilmaz1,6, J. Houbraken1,6, H. Spierenburg1, K.A. Seifert2, S.W. Peterson3, J. Varga4 and J.C. Frisvad5 1CBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands; 2Biodiversity (Mycology), Eastern Cereal and Oilseed Research Centre, Agriculture & Agri-Food Canada, 960 Carling Ave., Ottawa, Ontario, K1A 0C6, Canada, 3Bacterial Foodborne Pathogens and Mycology Research Unit, National Center for Agricultural Utilization Research, 1815 N. University Street, Peoria, IL 61604, U.S.A., 4Department of Microbiology, Faculty of Science and Informatics, University of Szeged, H-6726 Szeged, Közép fasor 52, Hungary, 5Department of Systems Biology, Building 221, Technical University of Denmark, DK-2800, Kgs. Lyngby, Denmark; 6Microbiology, Department of Biology, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands. *Correspondence: R.A. Samson, [email protected] Abstract: The taxonomic history of anamorphic species attributed to Penicillium subgenus Biverticillium is reviewed, along with evidence supporting their relationship with teleomorphic species classified inTalaromyces. To supplement previous conclusions based on ITS, SSU and/or LSU sequencing that Talaromyces and subgenus Biverticillium comprise a monophyletic group that is distinct from Penicillium at the generic level, the phylogenetic relationships of these two groups with other genera of Trichocomaceae was further studied by sequencing a part of the RPB1 (RNA polymerase II largest subunit) gene. -
Ancient Recombination Events and the Origins of Hepatitis E Virus Andrew G
Kelly et al. BMC Evolutionary Biology (2016) 16:210 DOI 10.1186/s12862-016-0785-y RESEARCH ARTICLE Open Access Ancient recombination events and the origins of hepatitis E virus Andrew G. Kelly, Natalie E. Netzler and Peter A. White* Abstract Background: Hepatitis E virus (HEV) is an enteric, single-stranded, positive sense RNA virus and a significant etiological agent of hepatitis, causing sporadic infections and outbreaks globally. Tracing the evolutionary ancestry of HEV has proved difficult since its identification in 1992, it has been reclassified several times, and confusion remains surrounding its origins and ancestry. Results: To reveal close protein relatives of the Hepeviridae family, similarity searching of the GenBank database was carried out using a complete Orthohepevirus A, HEV genotype I (GI) ORF1 protein sequence and individual proteins. The closest non-Hepeviridae homologues to the HEV ORF1 encoded polyprotein were found to be those from the lepidopteran-infecting Alphatetraviridae family members. A consistent relationship to this was found using a phylogenetic approach; the Hepeviridae RdRp clustered with those of the Alphatetraviridae and Benyviridae families. This puts the Hepeviridae ORF1 region within the “Alpha-like” super-group of viruses. In marked contrast, the HEV GI capsid was found to be most closely related to the chicken astrovirus capsid, with phylogenetic trees clustering the Hepeviridae capsid together with those from the Astroviridae family, and surprisingly within the “Picorna-like” supergroup. These results indicate an ancient recombination event has occurred at the junction of the non-structural and structure encoding regions, which led to the emergence of the entire Hepeviridae family. -
Metatranscriptomic Reconstruction Reveals RNA Viruses with the Potential to Shape Carbon Cycling in Soil
Metatranscriptomic reconstruction reveals RNA viruses with the potential to shape carbon cycling in soil Evan P. Starra, Erin E. Nucciob, Jennifer Pett-Ridgeb, Jillian F. Banfieldc,d,e,f,g,1, and Mary K. Firestoned,e,1 aDepartment of Plant and Microbial Biology, University of California, Berkeley, CA 94720; bPhysical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA 94550; cDepartment of Earth and Planetary Science, University of California, Berkeley, CA 94720; dEarth Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720; eDepartment of Environmental Science, Policy, and Management, University of California, Berkeley, CA 94720; fChan Zuckerberg Biohub, San Francisco, CA 94158; and gInnovative Genomics Institute, Berkeley, CA 94720 Contributed by Mary K. Firestone, October 25, 2019 (sent for review May 16, 2019; reviewed by Steven W. Wilhelm and Kurt E. Williamson) Viruses impact nearly all organisms on Earth, with ripples of influ- trophic levels (18). This phenomenon, termed “the viral shunt” (18, ence in agriculture, health, and biogeochemical processes. However, 19), is thought to sustain up to 55% of heterotrophic bacterial very little is known about RNA viruses in an environmental context, production in marine systems (20). However, some organic parti- and even less is known about their diversity and ecology in soil, 1 of cles released through viral lysis aggregate and sink to the deep the most complex microbial systems. Here, we assembled 48 indi- ocean, where they are sequestered from the atmosphere (21). Most vidual metatranscriptomes from 4 habitats within a planted soil studies investigating viral impactsoncarboncyclinghavefocused sampled over a 22-d time series: Rhizosphere alone, detritosphere on DNA phages, while the extent and contribution of RNA viruses alone, rhizosphere with added root detritus, and unamended soil (4 on carbon cycling remains unclear in most ecosystems. -
A Review Paper on Mycoviruses Aqleem Abbas* College of Plant Science and Technology, HZAU Wuhan, China
atholog P y & nt a M Abbas, J Plant Pathol Microbiol 2016, 7:12 l i P c f r o o b DOI: 10.4172/2157-7471.1000390 l i Journal of a o l n o r g u y o J ISSN: 2157-7471 Plant Pathology & Microbiology Review ArticleArticle Open Access A Review Paper on Mycoviruses Aqleem Abbas* College of Plant Science and Technology, HZAU Wuhan, China Abstract Mycoviruses are very significant viruses, which are found to be infecting fungi. These Mycoviruses require the living cells of their hosts for replicate like the plant and animal viruses. The genome of Mycoviruses mostly consist of double stranded RNA (dsRNA) and least of Mycoviruses genome consist of positive, single stranded RNA (-ssRNA). Moreover, DNA Mycoviruses have been reported recently. These viruses have been detected in almost all fungal phylum but still most of the Mycoviruses remain unknown. Mycoviruses are important in a sense that they mostly remain silent and rarely develop symptom in their hosts. Some Mycoviruses have been reported which are causing irregular growth, abnormal pigmentation and some are involved in changing their host sexual reproduction. For the management of Plant diseases, the importance of Mycoviruses arises because of their most significant effect that is they reduced virulence of their host. Technically the reduced virulence is called hypovirulence. This hypovirulence phenomena has increased importance of Mycoviruses because it has the potential to reduce the crop losses and forests caused by their hosts which are plant pathogenic fungi. In this review, I explore different aspects and importance of Mycoviruses. -
Phylogeny and Nomenclature of the Genus Talaromyces and Taxa Accommodated in Penicillium Subgenus Biverticillium
available online at www.studiesinmycology.org StudieS in Mycology 70: 159–183. 2011. doi:10.3114/sim.2011.70.04 Phylogeny and nomenclature of the genus Talaromyces and taxa accommodated in Penicillium subgenus Biverticillium R.A. Samson1, N. Yilmaz1,6, J. Houbraken1,6, H. Spierenburg1, K.A. Seifert2, S.W. Peterson3, J. Varga4 and J.C. Frisvad5 1CBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands; 2Biodiversity (Mycology), Eastern Cereal and Oilseed Research Centre, Agriculture & Agri-Food Canada, 960 Carling Ave., Ottawa, Ontario, K1A 0C6, Canada, 3Bacterial Foodborne Pathogens and Mycology Research Unit, National Center for Agricultural Utilization Research, 1815 N. University Street, Peoria, IL 61604, U.S.A., 4Department of Microbiology, Faculty of Science and Informatics, University of Szeged, H-6726 Szeged, Közép fasor 52, Hungary, 5Department of Systems Biology, Building 221, Technical University of Denmark, DK-2800, Kgs. Lyngby, Denmark; 6Microbiology, Department of Biology, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands. *Correspondence: R.A. Samson, [email protected] Abstract: The taxonomic history of anamorphic species attributed to Penicillium subgenus Biverticillium is reviewed, along with evidence supporting their relationship with teleomorphic species classified inTalaromyces. To supplement previous conclusions based on ITS, SSU and/or LSU sequencing that Talaromyces and subgenus Biverticillium comprise a monophyletic group that is distinct from Penicillium at the generic level, the phylogenetic relationships of these two groups with other genera of Trichocomaceae was further studied by sequencing a part of the RPB1 (RNA polymerase II largest subunit) gene. Talaromyces species and most species of Penicillium subgenus Biverticillium sensu Pitt reside in a monophyletic clade distant from species of other subgenera of Penicillium. -
Discovery of New Mycoviral Genomes Within Publicly Available Fungal Transcriptomic Datasets
bioRxiv preprint doi: https://doi.org/10.1101/510404; this version posted January 3, 2019. 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. Discovery of new mycoviral genomes within publicly available fungal transcriptomic datasets 1 1 1,2 1 Kerrigan B. Gilbert , Emily E. Holcomb , Robyn L. Allscheid , James C. Carrington * 1 Donald Danforth Plant Science Center, Saint Louis, Missouri, USA 2 Current address: National Corn Growers Association, Chesterfield, Missouri, USA * Address correspondence to James C. Carrington E-mail: [email protected] Short title: Virus discovery from RNA-seq data bioRxiv preprint doi: https://doi.org/10.1101/510404; this version posted January 3, 2019. 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. Abstract The distribution and diversity of RNA viruses in fungi is incompletely understood due to the often cryptic nature of mycoviral infections and the focused study of primarily pathogenic and/or economically important fungi. As most viruses that are known to infect fungi possess either single-stranded or double-stranded RNA genomes, transcriptomic data provides the opportunity to query for viruses in diverse fungal samples without any a priori knowledge of virus infection. Here we describe a systematic survey of all transcriptomic datasets from fungi belonging to the subphylum Pezizomycotina. -
Molecular Characterization of a Novel Mycovirus Isolated from Rhizoctonia Solani AG-1 IA 9-11
Molecular characterization of a novel mycovirus isolated from Rhizoctonia solani AG-1 IA 9-11 Yang Sun Yunnan Agricultural University Yan qiong Li Kunming University Wen han Dong Yunnan Agricultural University Ai li Sun Yunnan Agricultural University Ning wei Chen Yunnan Agricultural University Zi fang Zhao Yunnan Agricultural University Yong qing Li Zhaotong Plant Protection and Quarantine Station Gen hua Yang ( [email protected] ) Yunnan Agricultural University https://orcid.org/0000-0003-3322-1558 Cheng yun Li Yunnan Agricultural University Research Article Keywords: SMC, PRK, RT-like super family, RsRV-HN008, RdRp Posted Date: May 19th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-520549/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/9 Abstract The complete genome of the dsRNA virus isolated from Rhizoctonia solani AG-1 IA 9–11 (designated as Rhizoctonia solani dsRNA virus 11, RsRV11 ) were determined. The RsRV11 genome was 9,555 bp in length, contained three conserved domains, SMC, PRK and RT-like super family, and encoded two non- overlapping open reading frames (ORFs). ORF1 potentially coded for a 204.12 kDa predicted protein, which shared low but signicant amino acid sequence identities with the putative protein encoded by Rhizoctonia solani RNA virus HN008 (RsRV-HN008) ORF1. ORF2 potentially coded for a 132.41 kDa protein which contained the conserved motifs of the RNA-dependent RNA polymerase (RdRp). Phylogenetic analysis indicated that RsRV11 was clustered with RsRV-HN008 in a separate clade independent of other virus families. It implies that RsRV11, along with RsRV-HN008 possibly a new fungal virus taxa closed to the family Megabirnaviridae, and RsRV11 is a new member of mycoviruses. -
Plant Biomass-Acting Enzymes Produced by the Ascomycete Fungi Penicillium Subrubescens and Aspergillus Niger and Their Potential in Biotechnological Applications
Division of Microbiology and Biotechnology Department of Food and Environmental Sciences Faculty of Agriculture and Forestry University of Helsinki Plant biomass-acting enzymes produced by the ascomycete fungi Penicillium subrubescens and Aspergillus niger and their potential in biotechnological applications Sadegh Mansouri Doctoral Programme in Microbiology and Biotechnology ACADEMIC DISSERTATION To be presented, with the permission of the Faculty of Agriculture and Forestry of the University of Helsinki, for public examination in leture room B6, Latokartanonkaari 7, on October 27th 2017 at 12 o’clock noon. Helsinki 2017 Supervisors: Docent Kristiina S. Hildén Department of Food and Environmental Sciences University of Helsinki, Finland Docent Miia R. Mäkelä Department of Food and Environmental Sciences University of Helsinki, Finland Docent Pauliina Lankinen Department of Food and Environmental Sciences University of Helsinki, Finland Professor Annele Hatakka Department of Food and Environmental Sciences University of Helsinki, Finland Pre-examiners: Dr. Antti Nyyssölä VTT Technical Research Centre of Finland, Finland Dr. Kaisa Marjamaa VTT Technical Research Centre of Finland, Finland Opponent: Professor Martin Romantschuk Department of Environmental Sciences University of Helsinki, Finland Custos: Professor Maija Tenkanen Department of Food and Environmental Sciences University of Helsinki, Finland Dissertationes Schola Doctoralis Scientiae Circumiectalis, Alimentariae, Biologicae Cover: Penicillium subrubescens FBCC1632 on minimal medium amended with (upper row left to right) apple pectin, inulin, wheat bran, sugar beet pulp, (lower row left to right) citrus pulp, soybean hulls, cotton seed pulp or alfalfa meal (photos: Ronald de Vries). ISSN 2342-5423 (print) ISSN 2342-5431 (online) ISBN 978-951-51-3700-5 (paperback) ISBN 978-951-51-3701-2 (PDF) Unigrafia Helsinki 2017 Dedicated to my sweetheart wife and daughter Abstract Plant biomass contains complex polysaccharides that can be divided into structural and storage polysaccharides.