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      The salmon louse genome: Copepod features and parasitic adaptations.

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          Abstract

          Copepods encompass numerous ecological roles including parasites, detrivores and phytoplankton grazers. Nonetheless, copepod genome assemblies remain scarce. Lepeophtheirus salmonis is an economically and ecologically important ectoparasitic copepod found on salmonid fish. We present the 695.4 Mbp L. salmonis genome assembly containing ≈60% repetitive regions and 13,081 annotated protein-coding genes. The genome comprises 14 autosomes and a ZZ-ZW sex chromosome system. Assembly assessment identified 92.4% of the expected arthropod genes. Transcriptomics supported annotation and indicated a marked shift in gene expression after host attachment, including apparent downregulation of genes related to circadian rhythm coinciding with abandoning diurnal migration. The genome shows evolutionary signatures including loss of genes needed for peroxisome biogenesis, presence of numerous FNII domains, and an incomplete heme homeostasis pathway suggesting heme proteins to be obtained from the host. Despite repeated development of resistance against chemical treatments L. salmonis exhibits low numbers of many genes involved in detoxification.

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          Author and article information

          Journal
          Genomics
          Genomics
          Elsevier BV
          1089-8646
          0888-7543
          Aug 14 2021
          : 113
          : 6
          Affiliations
          [1 ] Institute of Marine Research, Postboks 1870 Nordnes, 5817 Bergen, Norway. Electronic address: rasmus@hi.no.
          [2 ] Institute of Marine Research, Postboks 1870 Nordnes, 5817 Bergen, Norway; Sea Lice Research Centre. Department of Biological Sciences, University of Bergen, Thormøhlens Gate 53, 5006 Bergen, Norway.
          [3 ] Sea Lice Research Centre. Department of Biological Sciences, University of Bergen, Thormøhlens Gate 53, 5006 Bergen, Norway.
          [4 ] Computational Biology Unit, Department of Informatics, University of Bergen, Thormøhlens Gate 55, 5008 Bergen, Norway.
          [5 ] Institute of Marine Research, Postboks 1870 Nordnes, 5817 Bergen, Norway.
          [6 ] EMBL-The European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, CB10 1SD, UK.
          [7 ] Sequencing Core Facility, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany.
          [8 ] Max Planck Genome Centre Cologne, Carl von Linné Weg 10, D-50829 Köln, Germany.
          [9 ] EMBL-The European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, CB10 1SD, UK; Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AE, UK.
          [10 ] Department of Biology, University of Victoria, Victoria, British Columbia V8W 3N5, Canada.
          [11 ] Centre for Integrative Genetics (CIGENE), Department of Animal and Aquacultural Sciences, Norwegian University of Life Sciences, Oluf Thesens vei 6, 1433 Ås, Norway.
          [12 ] Institute of Marine Research, Postboks 1870 Nordnes, 5817 Bergen, Norway; Sea Lice Research Centre. Department of Biological Sciences, University of Bergen, Thormøhlens Gate 53, 5006 Bergen, Norway. Electronic address: frank.nilsen@uib.no.
          Article
          S0888-7543(21)00309-8
          10.1016/j.ygeno.2021.08.002
          34403763
          41903447-397c-4ae9-b5c3-e0a231333b41
          History

          Peroxisome,Major vault,Genome assembly,FNII expansion,Arthropod,Comparative genomics,Repetitive DNA

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