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The mutual interplay between calcification and coccolithovirus infection
Authors:Christopher T Johns  Austin R Grubb  Jozef I Nissimov  Frank Natale  Viki Knapp  Alwin Mui  Helen F Fredricks  Benjamin A S Van Mooy  Kay D Bidle
Institution:1. Department of Marine and Coastal Sciences, Rutgers University, New Brunswick, NJ, 08901 USA;2. Department of Marine and Coastal Sciences, Rutgers University, New Brunswick, NJ, 08901 USA

University of South Carolina, Honors College, Columbia, SC, 29208 USA;3. Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA, 02543 USA

Abstract:Two prominent characteristics of marine coccolithophores are their secretion of coccoliths and their susceptibility to infection by coccolithoviruses (EhVs), both of which display variation among cells in culture and in natural populations. We examined the impact of calcification on infection by challenging a variety of Emiliania huxleyi strains at different calcification states with EhVs of different virulence. Reduced cellular calcification was associated with increased infection and EhV production, even though calcified cells and associated coccoliths had significantly higher adsorption coefficients than non-calcified (naked) cells. Sialic acid glycosphingolipids, molecules thought to mediate EhV infection, were generally more abundant in calcified cells and enriched in purified, sorted coccoliths, suggesting a biochemical link between calcification and adsorption rates. In turn, viable EhVs impacted cellular calcification absent of lysis by inducing dramatic shifts in optical side scatter signals and a massive release of detached coccoliths in a subpopulation of cells, which could be triggered by resuspension of healthy, calcified host cells in an EhV-free, ‘induced media’. Our findings show that calcification is a key component of the E. huxleyi-EhV arms race and an aspect that is critical both to the modelling of these host–virus interactions in the ocean and interpreting their impact on the global carbon cycle.
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