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      What helminth genomes have taught us about parasite evolution

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          SUMMARY

          The genomes of more than 20 helminths have now been sequenced. Here we perform a meta-analysis of all sequenced genomes of nematodes and Platyhelminthes, and attempt to address the question of what are the defining characteristics of helminth genomes. We find that parasitic worms lack systems for surface antigenic variation, instead maintaining infections using their surfaces as the first line of defence against the host immune system, with several expanded gene families of genes associated with the surface and tegument. Parasite excretory/secretory products evolve rapidly, and proteases even more so, with each parasite exhibiting unique modifications of its protease repertoire. Endoparasitic flatworms show striking losses of metabolic capabilities, not matched by nematodes. All helminths do however exhibit an overall reduction in auxiliary metabolism (biogenesis of co-factors and vitamins). Overall, the prevailing pattern is that there are few commonalities between the genomes of independently evolved parasitic worms, with each parasite having undergone specific adaptations for their particular niche.

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          Most cited references38

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          Gene Ontology: tool for the unification of biology

          Genomic sequencing has made it clear that a large fraction of the genes specifying the core biological functions are shared by all eukaryotes. Knowledge of the biological role of such shared proteins in one organism can often be transferred to other organisms. The goal of the Gene Ontology Consortium is to produce a dynamic, controlled vocabulary that can be applied to all eukaryotes even as knowledge of gene and protein roles in cells is accumulating and changing. To this end, three independent ontologies accessible on the World-Wide Web (http://www.geneontology.org) are being constructed: biological process, molecular function and cellular component.
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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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              The Schistosoma japonicum genome reveals features of host-parasite interplay.

              (2009)
              Schistosoma japonicum is a parasitic flatworm that causes human schistosomiasis, which is a significant cause of morbidity in China and the Philippines. Here we present a draft genomic sequence for the worm. The genome provides a global insight into the molecular architecture and host interaction of this complex metazoan pathogen, revealing that it can exploit host nutrients, neuroendocrine hormones and signalling pathways for growth, development and maturation. Having a complex nervous system and a well-developed sensory system, S. japonicum can accept stimulation of the corresponding ligands as a physiological response to different environments, such as fresh water or the tissues of its intermediate and mammalian hosts. Numerous proteases, including cercarial elastase, are implicated in mammalian skin penetration and haemoglobin degradation. The genomic information will serve as a valuable platform to facilitate development of new interventions for schistosomiasis control.
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                Author and article information

                Journal
                Parasitology
                Parasitology
                PAR
                Parasitology
                Cambridge University Press (Cambridge, UK )
                0031-1820
                1469-8161
                February 2015
                08 December 2014
                : 142
                : Suppl 1 , The Evolution of Parasite Genomes and the Origins of Parasitism
                : S85-S97
                Affiliations
                [1]Parasite Genomics, Wellcome Trust Sanger Institute , Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK
                Author notes
                [* ]Corresponding author: Parasite Genomics, Wellcome Trust Sanger Institute , Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK. E-mail: mz3@ 123456sanger.ac.uk
                Article
                S0031182014001449 00144
                10.1017/S0031182014001449
                4413821
                25482650
                a7d7fc0c-657e-4779-8c20-a2a527704dd1
                © Cambridge University Press 2014

                This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence ( http://creativecommons.org/licenses/by/3.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 04 June 2014
                : 11 August 2014
                : 14 August 2014
                Page count
                Figures: 2, Tables: 1, References: 72, Pages: 13
                Categories
                Research Article

                Parasitology
                parasite genomics,phylogeny,comparative transcriptomics,evolution of parasitism,cestoda,trematoda,nematoda

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