Literature DB >> 33366504

Complete mitochondrial genome of the important bio-control fungus Purpureocillium lilacinum (Ophiocordycipitaceae, Hypocreales) and its phylogenetic analysis.

Jianping Li1, Guodong Zhang2,3,4, Hong Yu2,3, Luodong Huang5, Wenbo Zeng6, Yuanbing Wang2,3,4.   

Abstract

Purpureocillium lilacinum is widely used as commercialized bio-control agents for controlling plant parasitic nematodes, as well as other insects and plant pathogens. In this study, the complete mitogenome of P. lilacinum was determined using the next-generation sequencing technology. The mitogenome is a circular molecule of 23,495 bp containing 15 protein-coding genes (PCGs), 2 rRNA (rnl and rns) genes and 22 tRNA genes. The overall base composition is 35.5% A, 36.0% T, 12.9% C and 15.6% G, with a CG content of 28.5%. Phylogenetic analysis inferred from 14 concatenated PCGs of 47 taxa shows that P. lilacinum is clustered with the genus Tolypocladium of Ophiocordycipitaceae and forms a separate clade with strong statistical support. This study contributes to our understanding about sytematics and evolutionary biology of cordycipitoid fungi.
© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Mitochondrial genome; Purpureocillium lilacinum; phylogenetic analysis

Year:  2019        PMID: 33366504      PMCID: PMC7748819          DOI: 10.1080/23802359.2019.1699466

Source DB:  PubMed          Journal:  Mitochondrial DNA B Resour        ISSN: 2380-2359            Impact factor:   0.658


Plant parasitic nematodes cause great economic losses in total amount to $157 billion annually around the world (Abad et al. 2008). Purpureocillium lilacinum, previously named as Paecilomyces lilacinus, belongs to the family Ophiocordycipitaceae (Hypocreales) that is one of the most widely used as bio-control agents to control plant nematodes. It is commonly isolated from soil, plant roots, nematodes and insects, and is also an opportunistic pathogen of immunodeficient humans and other vertebrates (Luangsa-ard et al. 2011; Xie et al. 2016; de Sequeira et al. 2017). Its whole genome and comparative genomic analyses, as well as phylogenetic relationships with other related pathogens have been widely investigated (Luangsa-ard et al. 2011; Prasad et al. 2015; Wang et al. 2016). However, little is known about its mitogenome. This study aims to report the complete mitogenome of P. lilacinum and reveal its phylogenetic position in the order Hypocreales. Purpureocillium lilacinum, parasitic on the adults of Coleoptera, was collected from Wenshan city of Yunnan in southwestern China (23°35'40”N, 103°50'49”E, alt. 1521 m). Among the collections, the strain WS1608 isolated from the synnema of P. lilacinum associated with an adult of Coleoptera was deposited at Wenshan Biological Resources Development and Research Center, Wenshan University, China. Mycelia cultured on PDA at 25 °C for 15 days under dark conditions were prepared to extract total genomic DNA using DNeasy Plant Genomic DNA purification Mini Kit (QIAGEN). The whole-genome sequencing was conducted by Novogene Co., Ltd. (Beijing, China) on the Illumina sequencing platform (HiSeq-PE150). The high-throughput sequencing data were assembled using the software SPAdes v. 3.11.0 (Bankevich et al. 2012). The mitochondrial genome was annotated using MFannot tool and ARWEN web server, combined with artificial correction technology. The Organellar Genome DRAW tool was used to drew the mitogenomic circular map (Lohse et al. 2007). The annotated mitogenome of P. lilacinum WS1608 was submitted to GenBank under accession No. MN 635609. Its annotated mitogenome is a closed loop and represents a typical mitogenome of Hypocreales fungi. The total length of this mitogenome is 23,495 bp containing 15 protein-coding genes (PCGs), 2 rRNA (rnl and rns) genes and 22 tRNA genes. The overall base composition is as follows: 35.5% A, 36.0% T, 12.9% C and 15.6% G, with a CG content of 28.5%. To determine the phylogenetic position of P. lilacinum, mitogenomic sequences of 47 taxa were downloaded from NCBI. The concatenated 14 PCGs from 47 mitogenomes were aligned using MUSCLE (Edgar 2004). Phylogenetic analysis was performed using the Bayesian inference (BI) method with the software MrBayes v.3.1.2 (Ronquist and Huelsenbeck 2003). The BI analysis was run on MrBayes v.3.1.2 for 5 million generations using the GTR + G + I model. Our phylogenetic topological structure is consistent with the previous study that was inferred from both BI and maximum likelihood (ML) analyses based on 27 taxa of the order Hypocreales (Figure 1) (Li et al. 2019). Purpureocillium lilacinum is clustered with the genus Tolypocladium of Ophiocordycipitaceae and forms a separate clade with strong statistical support by the posterior probabilities (BI-PP = 100%).
Figure 1.

Phylogenetic analysis of 47 taxa in Sordariomycetes based on 14 concatenated mitochondrial protein-coding genes (PCGs). The 14 PCGs include subunits of the respiratory chain complexes (cob, cox1, cox2, cox3), ATPase subunits (atp6, atp8, atp9), NADH: quinone reductase subunits (nad1, nad2, nad3, nad4, nad4L, nad5, nad6). The phylogenetic tree is built by Bayesian inference (BI) and posterior probabilities are shown above internodes.

Phylogenetic analysis of 47 taxa in Sordariomycetes based on 14 concatenated mitochondrial protein-coding genes (PCGs). The 14 PCGs include subunits of the respiratory chain complexes (cob, cox1, cox2, cox3), ATPase subunits (atp6, atp8, atp9), NADH: quinone reductase subunits (nad1, nad2, nad3, nad4, nad4L, nad5, nad6). The phylogenetic tree is built by Bayesian inference (BI) and posterior probabilities are shown above internodes.
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1.  Purpureocillium, a new genus for the medically important Paecilomyces lilacinus.

Authors:  Jennifer Luangsa-Ard; Jos Houbraken; Tineke van Doorn; Seung-Beom Hong; Andrew M Borman; Nigel L Hywel-Jones; Robert A Samson
Journal:  FEMS Microbiol Lett       Date:  2011-06-23       Impact factor: 2.742

2.  MrBayes 3: Bayesian phylogenetic inference under mixed models.

Authors:  Fredrik Ronquist; John P Huelsenbeck
Journal:  Bioinformatics       Date:  2003-08-12       Impact factor: 6.937

3.  MUSCLE: multiple sequence alignment with high accuracy and high throughput.

Authors:  Robert C Edgar
Journal:  Nucleic Acids Res       Date:  2004-03-19       Impact factor: 16.971

4.  SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing.

Authors:  Anton Bankevich; Sergey Nurk; Dmitry Antipov; Alexey A Gurevich; Mikhail Dvorkin; Alexander S Kulikov; Valery M Lesin; Sergey I Nikolenko; Son Pham; Andrey D Prjibelski; Alexey V Pyshkin; Alexander V Sirotkin; Nikolay Vyahhi; Glenn Tesler; Max A Alekseyev; Pavel A Pevzner
Journal:  J Comput Biol       Date:  2012-04-16       Impact factor: 1.479

5.  OrganellarGenomeDRAW (OGDRAW): a tool for the easy generation of high-quality custom graphical maps of plastid and mitochondrial genomes.

Authors:  Marc Lohse; Oliver Drechsel; Ralph Bock
Journal:  Curr Genet       Date:  2007-10-24       Impact factor: 3.886

6.  Genome sequence of the metazoan plant-parasitic nematode Meloidogyne incognita.

Authors:  Pierre Abad; Jérôme Gouzy; Jean-Marc Aury; Philippe Castagnone-Sereno; Etienne G J Danchin; Emeline Deleury; Laetitia Perfus-Barbeoch; Véronique Anthouard; François Artiguenave; Vivian C Blok; Marie-Cécile Caillaud; Pedro M Coutinho; Corinne Dasilva; Francesca De Luca; Florence Deau; Magali Esquibet; Timothé Flutre; Jared V Goldstone; Noureddine Hamamouch; Tarek Hewezi; Olivier Jaillon; Claire Jubin; Paola Leonetti; Marc Magliano; Tom R Maier; Gabriel V Markov; Paul McVeigh; Graziano Pesole; Julie Poulain; Marc Robinson-Rechavi; Erika Sallet; Béatrice Ségurens; Delphine Steinbach; Tom Tytgat; Edgardo Ugarte; Cyril van Ghelder; Pasqua Veronico; Thomas J Baum; Mark Blaxter; Teresa Bleve-Zacheo; Eric L Davis; Jonathan J Ewbank; Bruno Favery; Eric Grenier; Bernard Henrissat; John T Jones; Vincent Laudet; Aaron G Maule; Hadi Quesneville; Marie-Noëlle Rosso; Thomas Schiex; Geert Smant; Jean Weissenbach; Patrick Wincker
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8.  Genome and Transcriptome Sequences Reveal the Specific Parasitism of the Nematophagous Purpureocillium lilacinum 36-1.

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9.  Experimental Hyalohyphomycosis by Purpureocillium lilacinum: Outcome of the Infection in C57BL/6 Murine Models.

Authors:  Danielly C M de Sequeira; Rodrigo C Menezes; Manoel M E Oliveira; Paulo R Z Antas; Paula M De Luca; Joseli de Oliveira-Ferreira; Cintia de Moraes Borba
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