Microbial viruses can control host abundances via density-dependent lytic predator-prey dynamics. Less clear is how temperate viruses, which coexist and replicate with their host, influence microbial communities. Here we show that virus-like particles are relatively less abundant at high host densities. This suggests suppressed lysis where established models predict lytic dynamics are favoured. Meta-analysis of published viral and microbial densities showed that this trend was widespread in diverse ecosystems ranging from soil to freshwater to human lungs. Experimental manipulations showed viral densities more consistent with temperate than lytic life cycles at increasing microbial abundance. An analysis of 24 coral reef viromes showed a relative increase in the abundance of hallmark genes encoded by temperate viruses with increased microbial abundance. Based on these four lines of evidence, we propose the Piggyback-the-Winner model wherein temperate dynamics become increasingly important in ecosystems with high microbial densities; thus 'more microbes, fewer viruses'.
2014-2017 was an unprecedented period of successive record-breaking hot years, which coincided with the most severe, widespread, and longest-lasting globalscale coral bleaching event ever recorded. The 2014-2017 global-scale coral bleaching event (GCBE) resulted in very high coral mortality on many reefs, rapid deterioration of reef structures, and far-reaching environmental impacts. Through the papers in this special issue of Coral Reefs entitled The 2014-2017 Global Coral Bleaching Event: Drivers, Impacts, and Lessons Learned, as well as papers published elsewhere, we have a good analysis of the 2014-2017 GCBE and its impacts. These studies have provided key insights into how climate change-driven marine heatwaves are destroying coral reef ecosystems: (a) The 2014-2017 GCBE is unique in the satellite record in its spatial scale, duration, intensity, and repetition of bleaching. (b) The impacts have been the most severe ever seen at many reefs. (c) Timing of observations matters and needs to be considered during the analysis of impacts. (d) On both global and local scales, the intensity of heat stress and impacts varied. (e) We continue to see important differences among and within coral taxa, with key roles played by algal symbionts and the microbiome. (f) Heat stress and bleaching both play a role in subsequent disease, which plays a key role in mortality. (g) Impacts ripple far beyond corals, with significant changes to the fish and invertebrate community that may last decades. (h) The structure of both individual coral's skeletons and entire reefs has been eroded much more quickly than previously realized. (i) The 2014-2017 GCBE provided little support for the proposed ''lifeboat'' hypothesis, whereby deep or mesophotic reefs serve as a means of coral reef salvation. (j) While marine protected areas (MPAs) provide protection from local stressors, they not only do not protect reefs from global-scale stressors, but also here is also little evidence they provide significant resilience. Keywords Coral bleaching Á Heat stress Á Coral Reef Watch Á CoralTemp Á Marine heatwave Á Symbionts Á Microbiome Á Coral disease Á El Niño Á ENSO
Background Predation pressure and herbivory exert cascading effects on coral reef health and stability. However, the extent of these cascading effects can vary considerably across space and time. This variability is likely a result of the complex interactions between coral reefs’ biotic and abiotic dimensions. A major biological component that has been poorly integrated into the reefs' trophic studies is the microbial community, despite its role in coral death and bleaching susceptibility. Viruses that infect bacteria can control microbial densities and may positively affect coral health by controlling microbialization. We hypothesize that viral predation of bacteria has analogous effects to the top-down pressure of macroorganisms on the trophic structure and reef health. Results Here, we investigated the relationships between live coral cover and viruses, bacteria, benthic algae, fish biomass, and water chemistry in 110 reefs spanning inhabited and uninhabited islands and atolls across the Pacific Ocean. Statistical learning showed that the abundance of turf algae, viruses, and bacteria, in that order, were the variables best predicting the variance in coral cover. While fish biomass was not a strong predictor of coral cover, the relationship between fish and corals became apparent when analyzed in the context of viral predation: high coral cover (> 50%) occurred on reefs with a combination of high predator fish biomass (sum of sharks and piscivores > 200 g m−2) and high virus-to-bacteria ratios (> 10), an indicator of viral predation pressure. However, these relationships were non-linear, with reefs at the higher and lower ends of the coral cover continuum displaying a narrow combination of abiotic and biotic variables, while reefs at intermediate coral cover showed a wider range of parameter combinations. Conclusions The results presented here support the hypothesis that viral predation of bacteria is associated with high coral cover and, thus, coral health and stability. We propose that combined predation pressures from fishes and viruses control energy fluxes, inhibiting the detrimental accumulation of ecosystem energy in the microbial food web.
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