Physiological and Dual Transcriptional Analysis of Microalga <i>Graesiella emersonii–Amoeboaphelidium protococcarum</i> Pathosystem Uncovers Conserved Defense Response and Robust Pathogenicity
The underlying mechanisms of microalgal host–pathogen interactions remain largely unknown. In this study, we applied physiological and simultaneous dual transcriptomic analysis to characterize the microalga <i>Graesiella emersonii–</i><i>Amoeboaphelidium protococcarum</i> int...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2021-11-01
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| Series: | International Journal of Molecular Sciences |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1422-0067/22/23/12847 |
| Summary: | The underlying mechanisms of microalgal host–pathogen interactions remain largely unknown. In this study, we applied physiological and simultaneous dual transcriptomic analysis to characterize the microalga <i>Graesiella emersonii–</i><i>Amoeboaphelidium protococcarum</i> interaction. Three infection stages were determined according to infection rate and physiological features. Dual RNA-seq results showed that the genes expression of <i>G. emersonii</i> and <i>A. protococcarum</i> were strongly dynamically regulated during the infection. For microalgal hosts, similar to plant defense response, the expression of defense genes involved in the pattern recognition receptors, large heat shock proteins, and reactive oxygen scavenging enzymes (glutathione, ferritin, and catalase) were significantly upregulated during infection. However, some genes encoding resistance proteins (R proteins) with a leucine-rich repeat domain exhibited no significant changes during infection. For endoparasite <i>A. protococcarum</i>, genes for carbohydrate-active enzymes, pathogen–host interactions, and putative effectors were significantly upregulated during infection. Furthermore, the genes in cluster II were significantly enriched in pathways associated with the modulation of vacuole transport, including endocytosis, phagosome, ubiquitin-mediated proteolysis, and SNARE interactions in vesicular transport pathways. These results suggest that <i>G. emersonii</i> has a conserved defense system against pathogen and that endoparasite <i>A. protococcarum</i> possesses a robust pathogenicity to infect the host. Our study characterizes the first transcriptomic profile of microalgae–endoparasite interaction, providing a new promising basis for complete understanding of the algal host defense strategies and parasite pathogenicity. |
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| ISSN: | 1661-6596 1422-0067 |