Coral bleaching is the disruption of the symbiosis between the coral host and its endosymbiotic algae. The prevalence and severity of the disease have been correlated with high seawater temperature. During the last decade, the major hypothesis to explain coral bleaching is that high water temperatures cause irreversible damage to the symbiotic algae resulting in loss of pigment and/or algae from the holobiont. Here, we discuss the evidence for an alternative but not mutually exclusive concept, the microbial hypothesis of coral bleaching.
Coral reefs develop through the massive and long-term build-up of calcareous skeleta of scleractinian corals. These corals are modular cnidarians that secrete a CaCO3 exoskeleton on and in which other organisms may grow. Scleractinian corals are made up of one or more polyps composed of an external protective body layer (ectoderm), an inner gastrodermal layer that carries out most of the coral's digestive and reproductive functions and between them an acellular mesoglea (Figure 1). The ectodermal layer that is apposed to the substrata produces CaCO3 as a support for the coral tissue layers. In colonial forms, there is a tissue and gastrovascular confluence between polyps so that nutrients and signaling can be transferred between different parts of the colony. Corals are conduits to numerous microorganisms, including the intracellular zooxanthellae, other protists such as thraustochytrids, prokaryotes (bacteria and archaea) and viruses (Rohwer et al., 2002; Wegley et al., 2004; Kramarsky-Winter et al., 2006; Davy and Patten, 2007; Rosenberg et al., 2007; Harel et al., 2008; Marhaver et al., 2008). Many of these organisms may be considered symbionts and play an important role in coral health.
Bleaching is defined as the disruption of the symbiosis between the coral host and its endosymbiotic zooxanthellae (of the genus Symbiodinium). This can be the result of the loss of the algal symbiont and/or of the algal pigments. The coral tissues then become transparent making the underlying white calcium carbonate skeleton visible. Other signs of bleaching include thinning of host tissue, reduction in mucus and often inhibition of sexual reproduction. If bleaching is not reversed, corals will die.
Various studies carried out during the last few years have led to the view that coral bleaching is a disease that is affected by biotic and environmental factors. A disease is defined as a process resulting in tissue damage or alteration of physiological function, producing visible symptoms (Stedman, 2005). Accordingly, coral bleaching is clearly a disease and should be referred to as such. Bleaching has been shown to be induced by a variety of factors, including high temperature and irradiance (reviewed in Jokiel, 2004), low salinity (Goreau, 1964), sediments (Peters, 1984), exposure to cyanide (Cervino et al., 2003), decreased seawater temperature (Muscatine et al., 1991) and bacterial infection (Kushmaro et al., 1996, 1997; Ben-Haim and Rosenberg, 2002). All of these stressors caused bleaching both in the laboratory and in the sea (Brown, 1997).
During the last two decades, there have been reports of bleaching being caused by a variety of microbial pathogens. The assertion that these biotic agents were indeed the causative agent of this disease was demonstrated by applying Koch's postulates. Unfortunately, despite the growing evidence for the role of bacteria in coral bleaching and other diseases, there are still some authors who discount the direct effect that microorganisms play in the disease processes (for example, Ainsworth et al., 2008).
The discovery of bacterial bleaching of corals
Extensive bleaching of the coral Oculina patagonica in the eastern Mediterranean Sea occurs every summer (Kushmaro et al., 1996). Kushmaro et al. (1996, 1997) reported that the bleaching of O. patagonica was the result of an infection by Vibrio shiloi (Figure 2). The demonstration that V. shiloi was the causative agent of the disease was established by rigorously satisfying all of Koch's postulates, including the fact that bleached coral in the sea contained the bacterium (Kushmaro et al., 1996, 1997), whereas it was absent from healthy corals (see Figure 3a). Furthermore, Kushmaro et al. (1998) showed that the infection and subsequent bleaching occurred only at temperatures above 25 °C. Thus, for bleaching to occur, both elevated temperature and the causative agent must be present.
Steps in the infections of O. patagonica by V. shiloi
The specific steps in the infection of O. patagonica by V. shiloi have been studied extensively (Rosenberg and Falkovitz, 2004). The bacteria are chemotactic to the coral mucus, adhere to a β-galactoside-containing receptor on the coral surface, penetrate into the epidermal layer (Figure 3) and multiply intracellularly, reaching 108–109 cells per cm3. The intracellular V. shiloi produces an extracellular peptide toxin (PYPVYPPPVVP) that inhibits algal photosynthesis. Another important factor for the virulence of V. shiloi is the expression of superoxide dismutase. Adhesion, production of the toxin and expression of superoxide dismutase are all temperature-dependent reactions, occurring at summer (25–30 °C) but not at winter (16–20 °C) temperatures. Thus, V. shiloi cannot infect, multiply or survive in the coral during the winter. Sussman et al. (2003) demonstrated that the marine fireworm Hermodice carunculata is a winter reservoir and spring–summer vector for V. shiloi.
Effect of ultraviolet radiation on bleaching of O. patagonica
One of the stress factors reported to induce bleaching on coral reefs is high solar radiation (Lesser et al., 1990). Gleason and Wellington (1993) concluded that it was the high ultraviolet radiation that affected the corals inducing bleaching in Montastrea annularis. The generality of this conclusion was challenged when it was shown that colonies of O. patagonica in shallow water (0–80 cm) tidal pools (high ultraviolet radiation) showed negligible bleaching, even though summer temperatures there in shallow water were 2–4 °C warmer than in the open water (Fine et al., 2002). In this study, fragments transplanted from 4 m depth to shallow reef flats (>30 cm depth) in May showed no bleaching, whereas fragments transplanted from the shallow reef to 4 m depth underwent extensive bleaching. Moreover, when O. patagonica was incubated with V. shiloi in aquaria exposed to bright sunlight, the bacteria were rapidly killed and no bleaching occurred. However, when the corals were protected from ultraviolet light with a Pexiglass filter, V. shiloi multiplied and bleaching was induced. Thus in the case of bacterial bleaching of O. patagonica, ultraviolet radiation actually inhibits bleaching occurring in very shallow water (<80 cm depth) by killing the pathogen (Fine et al., 2002).
Bacterial bleaching of Pocillopora damicornis by Vibrio coralliilyticus
The coral O. patagonica is a temperate Mediterranean coral not found on coral reefs, so it was important to test whether bacterial pathogens could also cause bleaching of reef corals. A new species Vibrio coralliilyticus was initially isolated from a bleached coral, Pocillopora damicornis, present on the Zanzibar coral reef (Ben-Haim and Rosenberg, 2002; Ben-Haim et al., 2003). When bleaching of P. damicornis was observed on the Eilat coral reef, V. coralliilyticus was isolated from five different bleached coral colonies. It was absent from healthy corals. Using the different V. coralliilyticus strains, it was demonstrated that this Vibrio species is an etiological agent, bleaching P. damicornis in the Indian Ocean and Red Sea.
The infection of P. damicornis by V. coralliilyticus shows strong temperature dependence (Ben-Haim et al., 2003). Below 22 °C no signs of infection occurred. From 24 to 26 °C, the infection resulted in bleaching, whereas from 27 to 29 °C the infection caused rapid tissue lysis. Earlier, Jokiel and Coles (1990) reported that corals undergo tissue lysis following bleaching when the temperature is elevated. In the case of V. coralliilyticus infection, the tissue lysis was shown to be the result of the synthesis of a potent metalloproteinase by the pathogen at temperatures above 26 °C.
Association of Vibrio spp. with bleached corals in the Caribbean and Great Barrier Reef
Ritchie et al. (1994) enumerated the culturable heterotrophic bacteria of bleached and healthy Montastrea annularis coral colonies in the Caribbean. Vibrio spp. were never isolated from healthy corals but represented 30% of isolates from bleached corals. A similar shift in the bacterial community occurred on Agaricia sp. during the 1995–1996 and 1998–1999 bleaching events on reefs of San Salvador Island, Bahamas (McGrath and Smith, 1999). Prior to bleaching, Vibrio comprised ca. 20%, whereas during bleaching they rose to 40% and at the height of bleaching they represented over 60% of the culturable bacteria. When the corals recovered, the Vibrio population decreased to 20%. Clearly, these pioneering experiments could not distinguish between the Vibrio being the cause or result of the disease.
Bourne et al. (2008) carried out a comprehensive study of changes in the microbial composition of the coral Acropora millepora over 2.5 years, which included a severe bleaching event on the Great Barrier Reef (January–February 2002). The data obtained by culture-independent techniques led to several important conclusions: (i) as corals bleached, the microbial community shifted, revealing a correlation between increasing temperature and the appearance of Vibrio-affiliated sequences; (ii) this shift commenced prior to visual signs of bleaching and (iii) the coral microbial associations shifted again after the bleaching event, returning to a profile similar to the fingerprints obtained prior to bleaching. The authors suggest that microbial shifts can act as an indicator of stress prior to the appearance of visual signs of bleaching. They speculate further that the temperature-induced change in the microbial community prior to bleaching could result in a decrease in antibiotics secreted by symbiotic microorganisms, thereby causing the coral to become more susceptible to bacterial infection. This is in agreement with Ritchie (2006) who demonstrated that bacterial-produced antibiotics in coral mucus can regulate the coral microbial community.
Yellow blotch disease
Another disease that involves the disruption of the symbiosis between the coral animal and the endosymbiotic zooxanthellae is the yellow blotch disease that has been described on the major Caribbean reef-building coral Montastrea spp. (Cervino et al., 2004a). During the early stages of the disease, a pale yellow blotch develops on the coral tissue, which eventually expands as the disease progresses. This paleness represents a decrease in chlorophyll concentration and a lack of symbiotic zooxanthellae. Four Vibrio spp., isolated from diseased corals, when inoculated onto healthy corals, either individually or as a consortium, caused disease signs similar to those of yellow blotch disease. Virulence of the Vibrio spp. increased with increasing temperature (Cervino et al., 2004b). The authors conclude that the disease targets the zooxanthellae rather than the coral tissue.
Changes in microbial communities and disease signs in O. patagonica and the development of resistance of O. patagonica to V. shiloi
We have been studying the V. shiloi/O. patagonica model system of coral bleaching in the sea and in the laboratory for over 10 years. Sometime between 2002 and 2004, we found that the corals became resistant to the pathogen. The evidence for the development of resistance is based on the following (Reshef et al., 2006):
From 1995 to 2002, the pathogen V. shiloi was readily isolated from 46/50 bleached and bleaching corals collected from the wild; from 2004 to the present, we have been unable to isolate V. shiloi from bleached or bleaching corals.
From 1995 to 2002, all laboratory strains of V. shiloi caused bleaching in controlled aquaria experiments; from 2004 to the present, none of the same strains bleached O. patagonica in the lab.
From 1995 to 2002, V. shiloi adhered to the corals, penetrated into the ectoderm and multiplied intracellularly to 108–109 cells per cm3; now, V. shiloi adheres, penetrates the ectoderm and is rapidly killed.
Before the corals became resistant, the isolation and infection were so reproducible that for several years we used the system to demonstrate Koch's postulates in the teaching laboratory. Not only can we now not isolate V. shiloi from bleached corals but also molecular techniques fail to recover the 16S rRNA gene from ca. 1000 clones that were sequenced (Koren and Rosenberg, 2006).
Recently, Ainsworth et al. (2008) confirmed that V. shiloi is not currently present in bleached O. patagonica, using fluorescence in situ hybridization technology. However, the authors draw certain conclusions that are not justified by their data. To begin with, they claim the only microorganisms in close association with coral tissue were in the coral skeleton, an unusual conclusion considering the amount of mucus produced by the coral, and the abundant amount of coral-associated microbial sequences revealed by Koren and Rosenberg (2006) from colonies collected from the same sites. It is possible that due to the limitations of the fluorescence in situ hybridization techniques employed, these authors did not observe the presence of microorganisms in the coral mucus and gastrodermal cavity. Second, the fact that they were unable to observe any intracellular bacteria does not lead to the conclusion that bacteria are not the primary cause of bleaching. Many pathogens, especially those that produce toxins, do not grow intracellularly. Bacteria that are present in the coral mucus or in the gastrodermal cavity could induce bleaching by this path. Third, they claim that the bleaching occurring in O. patagonica in the absence of V. shiloi occurs in the same manner as described earlier. However, this is not the case, the disease signs have changed significantly. Bleaching of O. patagonica begins in the spring when the temperature reaches ca. 25 °C (well below the 29 °C summer temperatures during the previous periods of bleaching in corals). In addition, the geographic distribution of bleached corals has changed and spread north along the coast (YL, unpublished results). But most convincing is the fact that in the past, the bleached corals did not develop gonads with ova and sperm (Fine et al., 2002), whereas now they do (R Armoza, personal communication). These differences may be the result of the absence of the pathogen or of a change in the virulence factor, or of the development of an immune response, such as the release of host cytokines (for example, Mastroeni and Sheppard, 2004), or some combination thereof, though this warrants further study. Indeed, current research efforts are concentrating on understanding the differences in symptoms, causality and possibly novel causative agents.
The microbial hypothesis of coral bleaching and future research
Current understanding of disease etiology is that disease is the result of multiple cues, including environmental ones, that influence the causative agent (for example, to become virulent) and the host's susceptibility (Figure 4). There is no reason why coral diseases should not be investigated by applying the same principles.
Therefore, given that different abiotic and biotic factors can induce bleaching, the fundamental question remains: what is the etiology of patchy bleaching and of mass bleaching that occurs periodically on coral reefs around the world? For this question, there are at least two different viewpoints. Most coral biologists take the position that high temperature and light act directly on the symbiotic algae to inhibit photosynthesis and produce reactive oxygen species, leading to bleaching (Jones et al., 1998). According to this hypothesis, microorganisms play no role in the bleaching process and that changes in the microbial community of bleached corals are a result, not a cause, of the process. The second viewpoint, taken by certain coral microbiologists (including the authors of this review) is that high temperature acts on the coral microorganisms as well as on the coral host causing a change in the microbial community that in some cases contributes directly or indirectly to bleaching, that is, the microbial hypothesis of coral bleaching.
The microbial hypothesis of coral bleaching emerges from research spanning the last 10 years that has demonstrated that the coral holobiont is a complex and dynamic symbiosis involving the coral host, its endosymbiotic zooxanthellae and a large number and variety of accompanying microorganisms. In a healthy coral, the metabolic activities of each organism interact with the others to contribute to the growth, reproduction and disease resistance of the holobiont. For example, the coral animal captures prey, feeds on it and then the products of digestion may also provide nutrients for its associated microorganisms. The coral may also feed directly on its associated microorganisms (Kushmaro and Kramarsky-Winter, 2004). The algae perform photosynthesis that yields fixed carbon and oxygen that are major components needed for animal and bacterial respiration. When stressed, the symbiosis is broken down and the symbionts may be digested (Titlyanov et al., 1996). Precisely how bacteria contribute to the holobiont is an area of current research. It has clearly been shown that some coral bacteria can fix nitrogen, others degrade complex polysaccharides and others produce antibiotics that may help prevent infection by pathogens. We postulate that coral bleaching results from a disruption of the equilibrium between the different components of the coral holobiont, resulting in a decrease in the endosymbiotic zooxanthellae.
Let us now consider how high light/temperature can affect the coral microbial community in a manner that leads to bleaching. As mentioned above, microbiological studies using both culturing and molecular techniques have demonstrated that increases in water temperature leads to a large decrease in some of the abundant coral bacteria and an increase in other bacterial species. Furthermore, the change in the bacterial community appears to occur prior to measurable bleaching (Bourne et al., 2008). As it has been shown in man and other animal studies that the resident microbial community contributes to resistance to bacterial infection (for example, Silva et al., 2004), it is reasonable to assume that altering the coral microbiota can result in changes in resistance to infection. This is supported by the finding that during bleaching, corals lose their antibacterial properties (Ritchie, 2006).
The microbial pathogen(s) that cause the bleaching could come from sea water, through a vector, or from the resistant coral microbial community itself. In the latter case, we predict that the increased temperature would result in a much higher concentration of the pathogen and that virulent genes would be expressed. One possible virulence factor is a diffusible toxin, such as the toxin of V. shiloi that targets the algae rather than the coral tissue.
The microbial hypothesis of coral bleaching is testable. For example, do microorganisms which increase in number when the temperature is raised produce toxins that inhibit photosynthesis of the algae? Are such microbial toxins found in corals at the early stages of the bleaching event? In this regard, it would be interesting to test whether the Vibrio spp. that increased during the mass bleaching event on the Great Barrier Reef (Bourne et al., 2008) synthesize toxins at the elevated temperatures.
It is important to keep in mind that certain pathogens have the capacity to cause disease only in a host under special conditions that favor the microbe. In the case of coral bleaching, increased seawater temperature can ‘cause’, in principle, bleaching by either inducing the microbe to be more virulent or the host to be more susceptible. Therefore, we would like to emphasize that the concept that bleaching is the result of high temperature acting on the zooxanthellae or on the bacterial community of the coal holobiont are neither mutually exclusive nor inclusive. It could be that both mechanisms act synergistically. It is also possible that other mechanisms are involved, such as temperature-induced virulence of certain viruses. Clearly, further multidisciplinary research including a combination of coral microbiology together with coral host physiology is required to clarify the coral bleaching disease process.
Ainsworth TD, Fine M, Roff G, Hoegh-Guldberg O . (2008). Bacteria are not the primary cause of bleaching in the Mediterranean coral Oculina patagonica. ISME J 2: 67–73.
Ben-Haim Y, Rosenberg E . (2002). A novel Vibrio sp. pathogen of the coral Pocillopora damicornis. Mar Biol 141: 47–55.
Ben-Haim Y, Zicherman-Keren M, Rosenberg E . (2003). Temperature-regulated bleaching and lysis of the coral Pocillopora damicornis by the novel pathogen Vibrio coralliilyticus. Appl Envir Microbiol 69: 4236–4242.
Bourne D, Iida Y, Uthicke S, Smith-Keune C . (2008). Changes in coral-associated microbial communities during a bleaching event. ISME J 2: 350–363.
Brown BE . (1997). Coral bleaching: causes and consequences. Coral Reefs 16: S129–S138.
Cervino JM, Hayes RL, Goreau TJ, Smith GW . (2004a). Zooxanthellae regulation of yellow blotch/band and other coral diseases contrasted with temperature related bleaching: in situ destruction vs expulsion. Symbiosis 37: 63–85.
Cervino JM, Hayes RL, Honovich M, Goreau TJ, Jones S, Rubec PJ . (2003). Changes in zooxanthellae density, morphology and mitotic index in hermatypic corals and anemones exposed to cyanide. Mar Pollut Bull 46: 573–586.
Cervino JM, Hayes RL, Polson SW, Polson SC, Goreau TJ, Martinez RJ et al. (2004b). Relationship of Vibrio species infection and elevated temperatures to yellow blotch/band disease in Caribbean corals. Appl Environ Microbiol 70: 6855–6864.
Davy JE, Patten NL . (2007). Morphological diversity of virus-like particles within the surface microlayer of scleractinian corals. Aquat Microb Ecol 47: 37–44.
Fine M, Banin E, Israely T, Rosenberg E, Loya Y . (2002). Ultraviolet (UV) radiation prevents bacterial bleaching of the Mediterranean coral Oculina patagonica. Mar Ecol Progr Ser 226: 249–254.
Galloway SB, Work TM, Bochsler VS, Harley RA, Kramarsky-Winter E, McLaughlin SM et al. (2007). Coral Disease and Health Workshop: Coral Histopathology II. NOAA Technical Memorandum NOS NCCOS 56 and NOAA Technical Memorandum CRCP 4. National Oceanic and Atmospheric Administration, Silver Spring, MD. pp 10–11.
Gleason DF, Wellington GM . (1993). Ultraviolet radiation and coral bleaching. Nature 365: 836–838.
Goreau TF . (1964). Mass expulsion of zooxanthellae from Jamaican reef communities after Hurricane Flora. Science 145: 383–386.
Harel M, Ben-Dov E, Rasoulouniriana D, Siboni N, Kramarsky-Winter E, Loya Y et al. (2008). A newThraustochytrid, strain Fng1, isolated from the surface mucus of the hermatypic coral Fungia granulosa. FEMS Microbiol Ecol 64: 378–387.
Jokiel PL . (2004). Temperature stress and coral bleaching. In: Rosenberg E, Loya Y (eds). Coral Health and Disease. Springer-Verlag: New York. pp 401–425.
Jokiel PL, Coles SL . (1990). Response of Hawaiian and other Indo-Pacific reef corals to elevated temperature. Coral Reefs 8: 155–162.
Jones RJ, Hoegh-Guldberg O, Larkum AWD, Schreiber U . (1998). Temperature-induced bleaching of corals begins with impairment of the CO2 fixation mechanism in zooxanthellae. Plant Cell Environ 21: 1219–1230.
Koren O, Rosenberg E . (2006). Bacteria associated with mucus and tissues of the coral Oculina patagonica in summer and winter. Appl Environ Microbiol 72: 5254–5259.
Kramarsky-Winter E, Harel M, Siboni N, Ben Dov E, Brickner I, Loya Y et al. (2006). Identification of a protist–coral association and its possible ecological role. Mar Ecol Progr Ser 317: 67–73.
Kushmaro A, Kramarsky-Winter E . (2004). Bacteria as a source of coral nutrition. In: Rosenberg E, Loya Y (eds). Coral Health and Disease. Springer-Verlag: New York. pp 231–241.
Kushmaro A, Loya Y, Fine M, Rosenberg E . (1996). Bacterial infection and coral bleaching. Nature 380: 396.
Kushmaro A, Rosenberg E, Fine M, Ben-Haim Y, Loya Y . (1998). Effect of temperature on bleaching of the coral Oculina patagonica by Vibrio shiloi AK-1. Mar Ecol Prog Ser 171: 131–137.
Kushmaro A, Rosenberg E, Fine M, Loya Y . (1997). Bleaching of the coral Oculina patagonica by Vibrio AK-1. Mar Ecol Prog Ser 147: 159–165.
Lesser MP, Stochaj WR, Tapley DW, Shick JM . (1990). Bleaching in coral reef anthozoans: effects of irradiance, ultraviolet radiation, and temperature on the activities of protective enzymes against active oxygen. Coral Reefs 8: 225–232.
Marhaver KL, Rohwer F, Edwards R . (2008). Viral communities associated with healthy and bleaching corals. Environ Microbiol 10: 2277–2286.
Mastroeni P, Sheppard M . (2004). Salmonella infections in the mouse model:host resistance factors and in vivo dynamics of bacterial spread and distribution in the tissue. Microbes Infect 6: 398–405.
McGrath TA, Smith GW . (1999). Community shifts in the surface mucopolysaccharide layer microbiota of Agaricia sp. during the 1995/6 and 1998/9 bleaching events on patch reefs of San Salvador Island, Bahamas. In: Cortès JN, Fonseca AG (eds). Proceedings of the 29th Meeting of the Association of Marine Laboratories of the Caribbean, 2000. Cumana, Venezuela. CIMAR, Universidad de Costa Rica: San Jose, Costa Rica.
Muscatine L, Grossman D, Doino J . (1991). Release of symbiotic algae by tropical sea-anemones and corals after cold shock. Mar Ecol Prog Ser 77: 233–243.
Peters E . (1984). A survey of cellular reactions to environmental stress and disease in Caribbean scleractinian corals. Helgol Meeresunters 37: 113–137.
Reshef L, Koren O, Loya Y, Zilber-Rosenberg I, Rosenberg E . (2006). The coral probiotic hypothesis. Environ Microbiol 8: 2068–2073.
Ritchie KB . (2006). Regulation of microbial populations by coral surface mucus and mucus-associated bacteria. Mar Ecol Prog Ser 322: 1–14.
Ritchie KB, Dennis JH, McGrath T, Smith GW . (1994) In: Kass LB (ed). Proceedings of the 5th Symposium of the National History of the Bahamas, vol. 5 Bahamian Field Station: San Salvador, Bahamas. pp 75–80.
Rohwer F, Seguritan V, Azam F, Knowlton N . (2002). Diversity and distribution of coral-associated bacteria. Mar Ecol Prog Ser 243: 1–10.
Rosenberg E, Falkovitz L . (2004). The Vibrio shiloi/Oculina patagonica model system of coral bleaching. Ann Rev Microbiol 58: 143–159.
Rosenberg E, Koren O, Reshef L, Efrony R, Zilber-Rosenberg I . (2007). The role of microorganisms in coral health, disease and evolution. Nat Rev Microbiol 5: 355–362.
Silva AM, Barbosa FHF, Duarte R, Vieira LQ, Arantes RME, Nicoli JR . (2004). Effect of Bifidobacterium longum ingestion on experimental salmonellosis in mice. J Appl Microbiol 97: 29–37.
Stedman TL . (2005). Stedmans’ Medical Dictionary, 27th edn. Lippencott Williams and Wilkins: Philadelphia, PA, USA.
Sussman M, Loya Y, Fine M, Rosenberg E . (2003). The marine fireworm Hermodice carunculata is a winter reservior and spring-summer vector for the coral-bleaching pathogen Vibrio shiloi. Environ Microbiol 5: 250–255.
Titlyanov EA, Titlyanova TV, Leletkin VA, Tsukahara J, van Woesik R, Yamazato K . (1996). Degradation of zooxanthellae and regulation of their density in hermatypic corals. Mar Ecol Progr Ser 139: 167–178.
Wegley L, Yu Y, Breitbart M, Casas V, Kline DI, Rohwer F . (2004). Coral-associated archaea. Mar Ecol Prog Ser 273: 89–96.
This study was supported by ISF Grants 511/02-1 and 1169/07. We thank Nachshon Siboni for his help with the graphics and Amikam Shoob for his help with the photography. We thank Ove Hoegh-Guldberg and Tracy Ainsworth from the Centre for Marine Studies, University of Queensland, for inspiring us to write this article.
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Rosenberg, E., Kushmaro, A., Kramarsky-Winter, E. et al. The role of microorganisms in coral bleaching. ISME J 3, 139–146 (2009). https://doi.org/10.1038/ismej.2008.104
- coral bleaching
- coral disease
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