Photosynthesis |
Input of organic compounds to the holobiont |
Verbruggen and Tribollet, 2011; Burriesci et al., 2012; Davy et al., 2012; Tremblay et al., 2012
|
Nitrogen fixation |
Input of fixed nitrogen to the holobiont |
Olson et al., 2009; Lema et al., 2012; Santos et al., 2014; Bednarz et al., 2015; Cardini et al., 2015
|
Fixed nitrogen and carbon cycling and regulation |
Control of organic compound distribution |
Kimes et al., 2010 |
Production of dimethylsulfoniopropionate (DMSP) |
Bacterial populations control on the coral surface |
Barott and Rohwer, 2012 |
Degradation of dimethylsulfoniopropionate (DMSP) |
Increase carbon and sulfur availability; production of sulfur-based antimicrobial compounds such as tropodithietic acid (TDA) |
Kirkwood et al., 2010; Raina et al., 2016
|
Production of mediated signals to larval settlement facilitation |
Contribute to larval settlement modulation or regulation |
Webster et al., 2004; Heyward and Negri, 2010; Ritson-Williams et al., 2010; Shikuma et al., 2014
|
Production of antibiotics and competition with pathogens |
Biological control of pathogens |
Ritchie, 2006; Gochfeld and Aeby, 2008; Kirkwood et al., 2010; Alagely et al., 2011; Kvennefors et al., 2012
|
Production of quorum sensing (QS) signal molecules, such as N-acylhomoserine lactones (AHLs) |
Allow microbial interactions within the holobiont; can act on bacterial colonization control, bioluminescence, pathogenesis control and extracellular enzyme production |
Henke and Bassler, 2004; Ng and Bassler, 2009; Tait et al., 2010; Sharp and Ritchie, 2012; Certner and Vollmer, 2015; Meyer et al., 2015
|
Mechanisms influencing the protection of skeletogenic cells |
Enhance the survival of skeletogenic cell types |
Domart-Coulon et al., 2004 |
Production of mycosporine-like amino acids (MAA) |
Protection of coral tissue against ultraviolet radiation |
Dunlap and Shick, 1998 |