Ankyrin-repeat proteins from sponge symbionts modulate amoebal phagocytosis

Bacteria-eukaryote symbiosis occurs in all stages of evolution, from simple amoebae to mammals, and from facultative to obligate associations. Sponges are ancient metazoans that form intimate symbiotic interactions with complex communities of bacteria. The basic nutritional requirements of the sponge are in part satisfied by the phagocytosis of bacterial food particles from the surrounding water. How bacterial symbionts, which are permanently associated with the sponge, survive in the presence of phagocytic cells is largely unknown. Here, we present the discovery of a genomic fragment from an uncultured gamma-proteobacterial sponge symbiont that encodes for four proteins, whose closest known relatives are found in a sponge genome. Through recombinant approaches, we show that these four eukaryotic-like, ankyrin-repeat proteins (ARP) when expressed in Eschericha coli can modulate phagocytosis of amoebal cells and lead to accumulation of bacteria in the phagosome. Mechanistically, two ARPs appear to interfere with phagosome development in a similar way to reduced vacuole acidification, by blocking the fusion of the early phagosome with the lysosome and its digestive enzymes. Our results show that ARP from sponge symbionts can function to interfere with phagocytosis, and we postulate that this might be one mechanism by which symbionts can escape digestion in a sponge host. © 2013 John Wiley & Sons Ltd

Microbial indicators as a diagnostic tool for assessing water quality and climate stress in coral reef ecosystems

Microorganisms play a fundamental role in the functioning and stability of coral reef ecosystems. However, environmental disturbances can trigger alterations to the natural microbial community composition and their functional traits with potentially detrimental consequences for host organisms, such as corals, sponges and algae and concomitant implications for the entire coral reef ecosystem. Coral reefs are increasingly affected by localized impacts such as declining water quality and global pressures derived from human-induced climate change, which severely alters the natural conditions on reefs and can push dominating benthic life forms towards the limit of their resistance and resilience. Microorganisms can respond very rapidly to these altered environmental conditions so defining their natural variability over spatial and temporal gradients is critical for early and accurate identification of environmental disturbances. The rapid response of microbes to environmental change is likely to confer significant advantages over traditional reef monitoring methods, which are based on visual signs of health deterioration in benthic coral reef macroorganisms. This review discusses the potential of microbes as early warning indicators for environmental stress and coral reef health and proposes priorities for future research