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      The Transcriptomes of Xiphinema index and Longidorus elongatus Suggest Independent Acquisition of Some Plant Parasitism Genes by Horizontal Gene Transfer in Early-Branching Nematodes

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          Abstract

          Nematodes have evolved the ability to parasitize plants on at least four independent occasions, with plant parasites present in Clades 1, 2, 10 and 12 of the phylum. In the case of Clades 10 and 12, horizontal gene transfer of plant cell wall degrading enzymes from bacteria and fungi has been implicated in the evolution of plant parasitism. We have used ribonucleic acid sequencing (RNAseq) to generate reference transcriptomes for two economically important nematode species, Xiphinema index and Longidorus elongatus, representative of two genera within the early-branching Clade 2 of the phylum Nematoda. We used a transcriptome-wide analysis to identify putative horizontal gene transfer events. This represents the first in-depth transcriptome analysis from any plant-parasitic nematode of this clade. For each species, we assembled ~30 million Illumina reads into a reference transcriptome. We identified 62 and 104 transcripts, from X. index and L. elongatus, respectively, that were putatively acquired via horizontal gene transfer. By cross-referencing horizontal gene transfer prediction with a phylum-wide analysis of Pfam domains, we identified Clade 2-specific events. Of these, a GH12 cellulase from X. index was analysed phylogenetically and biochemically, revealing a likely bacterial origin and canonical enzymatic function. Horizontal gene transfer was previously shown to be a phenomenon that has contributed to the evolution of plant parasitism among nematodes. Our findings underline the importance and the extensiveness of this phenomenon in the evolution of plant-parasitic life styles in this speciose and widespread animal phylum.

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          Genome sequence of the nematode C. elegans: a platform for investigating biology.

          (1999)
          The 97-megabase genomic sequence of the nematode Caenorhabditis elegans reveals over 19,000 genes. More than 40 percent of the predicted protein products find significant matches in other organisms. There is a variety of repeated sequences, both local and dispersed. The distinctive distribution of some repeats and highly conserved genes provides evidence for a regional organization of the chromosomes.
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            Top 10 plant-parasitic nematodes in molecular plant pathology.

            The aim of this review was to undertake a survey of researchers working with plant-parasitic nematodes in order to determine a 'top 10' list of these pathogens based on scientific and economic importance. Any such list will not be definitive as economic importance will vary depending on the region of the world in which a researcher is based. However, care was taken to include researchers from as many parts of the world as possible when carrying out the survey. The top 10 list emerging from the survey is composed of: (1) root-knot nematodes (Meloidogyne spp.); (2) cyst nematodes (Heterodera and Globodera spp.); (3) root lesion nematodes (Pratylenchus spp.); (4) the burrowing nematode Radopholus similis; (5) Ditylenchus dipsaci; (6) the pine wilt nematode Bursaphelenchus xylophilus; (7) the reniform nematode Rotylenchulus reniformis; (8) Xiphinema index (the only virus vector nematode to make the list); (9) Nacobbus aberrans; and (10) Aphelenchoides besseyi. The biology of each nematode (or nematode group) is reviewed briefly. © 2013 BSPP AND JOHN WILEY & SONS LTD.
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              Massive horizontal gene transfer in bdelloid rotifers.

              Horizontal gene transfer in metazoans has been documented in only a few species and is usually associated with endosymbiosis or parasitism. By contrast, in bdelloid rotifers we found many genes that appear to have originated in bacteria, fungi, and plants, concentrated in telomeric regions along with diverse mobile genetic elements. Bdelloid proximal gene-rich regions, however, appeared to lack foreign genes, thereby resembling those of model metazoan organisms. Some of the foreign genes were defective, whereas others were intact and transcribed; some of the latter contained functional spliceosomal introns. One such gene, apparently of bacterial origin, was overexpressed in Escherichia coli and yielded an active enzyme. The capture and functional assimilation of exogenous genes may represent an important force in bdelloid evolution.
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                Author and article information

                Journal
                Genes (Basel)
                Genes (Basel)
                genes
                Genes
                MDPI
                2073-4425
                23 October 2017
                October 2017
                : 8
                : 10
                : 287
                Affiliations
                [1 ]INRA, Université Côte d’Azur, CNRS, ISA, 06903, Sophia Antipolis Cedex, France; etienne.danchin@ 123456sophia.inra.fr (E.G.J.D.); laetitia.zurletto@ 123456sophia.inra.fr (L.P.-B.); Corinne.Rancurel@ 123456sophia.inra.fr (C.R.); martine.darocha@ 123456sophia.inra.fr (M.D.R.); Daniel.Esmenjaud@ 123456sophia.inra.fr (D.E.)
                [2 ]Cell and Molecular Sciences Group, Dundee Effector Consortium, James Hutton Institute, Invergowrie, Dundee DD2 5DA, UK; Peter.Thorpe@ 123456hutton.ac.uk (P.T.); simon.bajew@ 123456crg.eu (S.B.); guzeyeva@ 123456mail.ru (E.S.G.); John.Jones@ 123456hutton.ac.uk (J.T.J.)
                [3 ]Ecological Sciences Group, IPM@Hutton, James Hutton Institute, Invergowrie, Dundee DD2 5DA, UK; Roy.Neilson@ 123456hutton.ac.uk
                [4 ]Centre of Parasitology of the A.N. Severtsov Institute of Ecology and Evolution, Russian Academy of Sciences, Leninskii Prospect 33, Moscow 119071, Russia
                [5 ]Commissariat à l’Energie Atomique (CEA), Institut de Génomique (IG), Genoscope, 92057, Evry, France; dasilva@ 123456genoscope.cns.fr (C.D.S.); jguy@ 123456genoscope.cns.fr (J.G.); klabadie@ 123456genoscope.cns.fr (K.L.)
                [6 ]Laboratory of Nematology, Department of Plant Sciences, Wageningen University, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands; Hans.Helder@ 123456wur.nl
                [7 ]School of Biology, University of St Andrews, North Haugh, St Andrews KY16 9TZ, UK
                [8 ]Biological Chemistry, John Innes Centre, Norwich Research Park, Norwich NR4 7UH, UK
                [9 ]School of Life Sciences, University of Dundee, Dundee, DD1 5EH, UK
                Author notes
                [* ]Correspondence: s.evesvandenakker@ 123456dundee.ac.uk ; Tel.: +44-(0)-1382-568-926
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-8833-9679
                Article
                genes-08-00287
                10.3390/genes8100287
                5664137
                29065523
                6d3b6206-0889-48ee-9ee9-0459e4ac72cb
                © 2017 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 September 2017
                : 18 October 2017
                Categories
                Article

                glycoside hydrolase,horizontal gene transfer,nematodes,plant parasitism

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