TY - JOUR
T1 - Bacteria induce an amoeboid phase in coccolithophores that persists after bloom collapse
AU - Zweifel, Sophie T.
AU - Henshaw, Richard J.
AU - Müller, Oliver
AU - Keegstra, Johannes M.
AU - Charlton, Samuel G.V.
AU - Pioli, Roberto
AU - Martínez-Pérez, Clara
AU - Alcolombri, Uria
AU - Clerc, Estelle
AU - Stocker, Roman
N1 - Publisher Copyright:
Copyright © 2025 The Authors, some rights reserved.
PY - 2025/8/29
Y1 - 2025/8/29
N2 - Coccolithophores, including bloom-forming species, Gephyrocapsa huxleyi (formerly Emiliania huxleyi), contribute ~1 to 10% of phytoplankton biomass and are critical for oceanic biogeochemical cycles. G. huxleyi is a model system for investigating algal-bacterial-viral interactions and responses to environmental changes and follows a biphasic lifecycle with motile haploid and nonmotile diploid phases. Here, we report a third, “amoeboid” phase: Light and electron microscopy revealed haploid cells rapidly transitioning to an elongated amoeboid cell with reduced motility. Metamorphosis was triggered by exposure to bacteria isolated from G. huxleyi mesocosm blooms, but not by classical phytoplankton stressors including viral infection. The amoeboid phase persisted beyond the collapse of the haploid population and was only observed in the bloom-forming coccolithophore species G. huxleyi and Gephyrocapsa oceanica under conditions reminiscent of late-stage algal blooms. These findings highlight a previously uncharacterized life phase in this ubiquitous phytoplankton and suggest a bacteria-resilient morphotype following algal bloom collapse.
AB - Coccolithophores, including bloom-forming species, Gephyrocapsa huxleyi (formerly Emiliania huxleyi), contribute ~1 to 10% of phytoplankton biomass and are critical for oceanic biogeochemical cycles. G. huxleyi is a model system for investigating algal-bacterial-viral interactions and responses to environmental changes and follows a biphasic lifecycle with motile haploid and nonmotile diploid phases. Here, we report a third, “amoeboid” phase: Light and electron microscopy revealed haploid cells rapidly transitioning to an elongated amoeboid cell with reduced motility. Metamorphosis was triggered by exposure to bacteria isolated from G. huxleyi mesocosm blooms, but not by classical phytoplankton stressors including viral infection. The amoeboid phase persisted beyond the collapse of the haploid population and was only observed in the bloom-forming coccolithophore species G. huxleyi and Gephyrocapsa oceanica under conditions reminiscent of late-stage algal blooms. These findings highlight a previously uncharacterized life phase in this ubiquitous phytoplankton and suggest a bacteria-resilient morphotype following algal bloom collapse.
UR - https://www.scopus.com/pages/publications/105014935517
U2 - 10.1126/sciadv.adw7280
DO - 10.1126/sciadv.adw7280
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C2 - 40864715
AN - SCOPUS:105014935517
SN - 2375-2548
VL - 11
JO - Science advances
JF - Science advances
IS - 35
M1 - eadw7280
ER -