24
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Transcriptomics and proteomics reveal two waves of translational repression during the maturation of malaria parasite sporozoites

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Plasmodium sporozoites are transmitted from infected mosquitoes to mammals, and must navigate the host skin and vasculature to infect the liver. This journey requires distinct proteomes. Here, we report the dynamic transcriptomes and proteomes of both oocyst sporozoites and salivary gland sporozoites in both rodent-infectious Plasmodium yoelii parasites and human-infectious Plasmodium falciparum parasites. The data robustly define mRNAs and proteins that are upregulated in oocyst sporozoites (UOS) or upregulated in infectious sporozoites (UIS) within the salivary glands, including many that are essential for sporozoite functions in the vector and host. Moreover, we find that malaria parasites use two overlapping, extensive, and independent programs of translational repression across sporozoite maturation to temporally regulate protein expression. Together with gene-specific validation experiments, these data indicate that two waves of translational repression are implemented and relieved at different times during sporozoite maturation, migration and infection, thus promoting their successful development and vector-to-host transition.

          Abstract

          Here, the authors report transcriptomes and proteomes of oocyst sporozoite and salivary gland sporozoite stages in rodent-infectious Plasmodium yoelii parasites and human infectious Plasmodium falciparum parasites and define two waves of translational repression during sporozoite maturation.

          Related collections

          Most cited references70

          • Record: found
          • Abstract: found
          • Article: not found

          Regulation of sexual development of Plasmodium by translational repression.

          G Mair (2006)
          Translational repression of messenger RNAs (mRNAs) plays an important role in sexual differentiation and gametogenesis in multicellular eukaryotes. Translational repression and mRNA turnover were shown to influence stage-specific gene expression in the protozoan Plasmodium. The DDX6-class RNA helicase, DOZI (development of zygote inhibited), is found in a complex with mRNA species in cytoplasmic bodies of female, blood-stage gametocytes. These translationally repressed complexes are normally stored for translation after fertilization. Genetic disruption of pbdozi inhibits the formation of the ribonucleoprotein complexes, and instead, at least 370 transcripts are diverted to a degradation pathway.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Seven-Year Efficacy of RTS,S/AS01 Malaria Vaccine among Young African Children.

            The candidate malaria vaccine RTS,S/AS01 is being evaluated in order to inform a decision regarding its inclusion in routine vaccination schedules.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              TRAP is necessary for gliding motility and infectivity of plasmodium sporozoites.

              Many protozoans of the phylum Apicomplexa are invasive parasites that exhibit a substrate-dependent gliding motility. Plasmodium (malaria) sporozoites, the stage of the parasite that invades the salivary glands of the mosquito vector and the liver of the vertebrate host, express a surface protein called thrombospondin-related anonymous protein (TRAP) that has homologs in other Apicomplexa. By gene targeting in a rodent Plasmodium, we demonstrate that TRAP is critical for sporozoite infection of the mosquito salivary glands and the rat liver, and is essential for sporozoite gliding motility in vitro. This suggests that in Plasmodium sporozoites, and likely in other Apicomplexa, gliding locomotion and cell invasion have a common molecular basis.
                Bookmark

                Author and article information

                Contributors
                Scott.Lindner@psu.edu
                stefan.kappe@seattlechildrens.org
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                31 October 2019
                31 October 2019
                2019
                : 10
                : 4964
                Affiliations
                [1 ]ISNI 0000 0001 2097 4281, GRID grid.29857.31, Department of Biochemistry and Molecular Biology, The Huck Center for Malaria Research, , Pennsylvania State University, ; W225 Millennium Science Complex, University Park, PA 16802 USA
                [2 ]ISNI 0000 0004 0463 2320, GRID grid.64212.33, Institute for Systems Biology, ; 401 Terry Avenue N., Seattle, WA 98109 USA
                [3 ]ISNI 0000 0001 2171 9311, GRID grid.21107.35, Department of Molecular Microbiology & Immunology, , Johns Hopkins Bloomberg School of Public Health, ; 615 N. Wolfe Street, Baltimore, MD 21205 USA
                [4 ]ISNI 0000 0000 9026 4165, GRID grid.240741.4, Center for Global Infectious Disease Research, Seattle Children’s Research Institute, ; 307 Westlake Avenue N. Suite 500, Seattle, WA 98109 USA
                [5 ]ISNI 0000000122986657, GRID grid.34477.33, Department of Global Health, , University of Washington, ; Seattle, WA USA
                [6 ]ISNI 0000000122986657, GRID grid.34477.33, Present Address: Department of Laboratory Medicine, , University of Washington, ; 1959 NE Pacific St., Seattle, WA 98195 USA
                Author information
                http://orcid.org/0000-0003-1799-3726
                http://orcid.org/0000-0002-6756-4471
                http://orcid.org/0000-0002-8226-4354
                http://orcid.org/0000-0002-4809-8831
                http://orcid.org/0000-0002-9820-3388
                http://orcid.org/0000-0001-8250-7822
                http://orcid.org/0000-0003-1500-2802
                http://orcid.org/0000-0003-2954-7547
                http://orcid.org/0000-0002-3216-9447
                http://orcid.org/0000-0003-1540-1731
                Article
                12936
                10.1038/s41467-019-12936-6
                6823429
                31673027
                cf4db48a-781b-4bbb-8d85-0f967e32b9a9
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 29 May 2019
                : 9 October 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/100000060, U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID);
                Award ID: 1K22AI101039
                Award ID: 1R01AI123341
                Award ID: R01AI132359
                Award Recipient :
                Funded by: U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
                Funded by: U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID)
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                parasite biology,proteomics,transcriptomics
                Uncategorized
                parasite biology, proteomics, transcriptomics

                Comments

                Comment on this article