ArticleEukaryotic cell2014
Genomic insights into processes driving the infection of Alexandrium tamarense by the Parasitoid Amoebophrya sp.
Article in Eukaryotic cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 20 citations in OpenAlex.
- RNA-Binding Proteins in Dinoflagellates.International journal of molecular sciences · 2026Review
- High-Throughput Sequencing of Environmental DNA as a Tool for Monitoring Eukaryotic Communities and Potential Pathogens in a Coastal Upwelling Ecosystem.Frontiers in veterinary science · 2021Article
- Temporal Variability and Ecological Interactions of Parasitic Marine Syndiniales in Coastal Protist Communities.mSphere · 2020Article
- An aerobic eukaryotic parasite with functional mitochondria that likely lacks a mitochondrial genome.Science advances · 2019Article
- Article
- Comparative Time-Scale Gene Expression Analysis Highlights the Infection Processes of TwoFrontiers in microbiology · 2018Article
- Article
- Insights into the loss factors of phytoplankton blooms: The role of cell mortality in the decline of two inshoreLimnology and oceanography · 2017Article
- Probing the evolution, ecology and physiology of marine protists using transcriptomics.Nature reviews. Microbiology · 2017Review
- Trait changes induced by species interactions in two phenotypically distinct strains of a marine dinoflagellate.The ISME journal · 2016Article
Corrections and comments
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Authors and funding
5 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The regulatory circuits during infection of dinoflagellates by their parasites are largely unknown on the molecular level. Here we provide molecular insights into these infection dynamics. Alexandrium tamarense is one of the most prominent harmful algal bloom dinoflagellates. Its pathogen, the dinoflagellate parasitoid Amoebophrya sp., has been observed to infect and control the blooms of this species. We generated a data set of transcripts from three time points (0, 6, and 96 h) during the infection of this parasite-host system. Assembly of all transcript data from the parasitoid (>900,000 reads/313 Mbp with 454/Roche next-generation sequencing [NGS]) yielded 14,455 contigs, to which we mapped the raw transcript reads of each time point of the infection cycle. We show that particular surface lectins are expressed at the beginning of the infection cycle which likely mediate the attachment to the host cell. In a later phase, signal transduction-related genes together with transmembrane transport and cytoskeleton proteins point to a high integration of processes involved in host recognition, adhesion, and invasion. At the final maturation stage, cell division- and proliferation-related genes were highly expressed, reflecting the fast cell growth and nuclear division of the parasitoid. Our molecular insights into dinoflagellate parasitoid interactions point to general mechanisms also known from other eukaryotic parasites, especially from the Alveolata. These similarities indicate the presence of fundamental processes of parasitoid infection that have remained stable throughout evolution within different phyla.
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