@article{e6eadd2250424662972f4c7b72d7f148,
title = "Virus-induced spore formation as a defense mechanism in marine diatoms",
abstract = "Algal viruses are important contributors to carbon cycling, recycling nutrients and organic material through host lysis. Although viral infection has been described as a primary mechanism of phytoplankton mortality, little is known about host defense responses. We show that viral infection of the bloom-forming, planktonic diatom Chaetoceros socialis induces the mass formation of resting spores, a heavily silicified life cycle stage associated with carbon export due to rapid sinking. Although viral RNA was detected within spores, mature virions were not observed. {\textquoteleft}Infected{\textquoteright} spores were capable of germinating, but did not propagate or transmit infectious viruses. These results demonstrate that diatom spore formation is an effective defense strategy against viral-mediated mortality. They provide a possible mechanistic link between viral infection, bloom termination, and mass carbon export events and highlight an unappreciated role of viruses in regulating diatom life cycle transitions and ecological success.",
keywords = "Chaetoceros socialis, diatoms, life cycle, resting spores, single-stranded RNA virus",
author = "Angela Pelusi and {De Luca}, Pasquale and Francesco Manfellotto and Kimberlee Thamatrakoln and Bidle, {Kay D.} and Marina Montresor",
note = "Funding Information: AP has been supported by a PhD fellowship from Stazione Zoologica Anton Dohrn (SZN) and by a fellowship of the project ABBaCo (Restauro Ambientale e Balneabilit{\`a} del SIN Bagnoli-Coroglio), funded by the Italian Ministry for Education, University and Research (grant no. C62F16000170001). This work was partly supported by awards from the Gordon and Betty Moore Foundation (Investigator Award no. 3789) and US National Science Foundation (OCE-1537951) to KDB. The authors thank Dr. Yuji Tomaru (National Research Institute of Fisheries and Environment of Inland Sea, Fisheries Research Agency) for providing the C. socialis L-4 host and CsfrRNAV, the Electron Microscopy Unit (SZN) for assistance in TEM preparations, the Molecular Biology and Sequencing Unit (SZN) for sequencing, and Carmen Minucci for technical support. Funding Information: AP has been supported by a PhD fellowship from Stazione Zoologica Anton Dohrn (SZN) and by a fellowship of the project ABBaCo (Restauro Ambientale e Balneabilit{\`a} del SIN Bagnoli‐Coroglio), funded by the Italian Ministry for Education, University and Research (grant no. C62F16000170001). This work was partly supported by awards from the Gordon and Betty Moore Foundation (Investigator Award no. 3789) and US National Science Foundation (OCE‐1537951) to KDB. The authors thank Dr. Yuji Tomaru (National Research Institute of Fisheries and Environment of Inland Sea, Fisheries Research Agency) for providing the L‐4 host and CsfrRNAV, the Electron Microscopy Unit (SZN) for assistance in TEM preparations, the Molecular Biology and Sequencing Unit (SZN) for sequencing, and Carmen Minucci for technical support. C. socialis Publisher Copyright: {\textcopyright} 2020 The Authors. New Phytologist {\textcopyright} 2020 New Phytologist Foundation",
year = "2021",
month = feb,
doi = "10.1111/nph.16951",
language = "English (US)",
volume = "229",
pages = "2251--2259",
journal = "New Phytologist",
issn = "0028-646X",
publisher = "Wiley-Blackwell",
number = "4",
}