Hostname: page-component-8448b6f56d-sxzjt Total loading time: 0 Render date: 2024-04-24T11:31:34.863Z Has data issue: false hasContentIssue false

Observation of virus-like particles in thin sections of the bleaching scleractinian coral Acropora cytherea

Published online by Cambridge University Press:  05 July 2012

Yvan Bettarel*
Affiliation:
IRD, UMR 5119 ECOSYM, Université Montpellier 2, France
Nguyen Thanh Thuy
Affiliation:
National Institute of Hygiene and Epidemiology (NIHE), Laboratory of Electron Microscopy, Hanoi, Vietnam
Tran Quang Huy
Affiliation:
National Institute of Hygiene and Epidemiology (NIHE), Laboratory of Electron Microscopy, Hanoi, Vietnam
Phan Kim Hoang
Affiliation:
Vietnamese National Institute of Oceanography (VNIO), Nha Trang, Vietnam
Thierry Bouvier
Affiliation:
IRD, UMR 5119 ECOSYM, Université Montpellier 2, France
*
Correspondence should be addressed to: Y. Bettarel, IRD, UMR 5119 ECOSYM, Université Montpellier 2, France email: yvan.bettarel@ird.fr

Abstract

Virus-like particles were observed in thin sections of partially bleaching colonies of the scleractinian Acropora cytherea, collected in the Hon Mun Marine Protected Area (Vietnam). The most common particles were found in the cytoplasm of epidermal cells, exhibiting icosahedral symmetry and measuring 90–140 nm in diameter. Some had a tail-like structure resembling that of certain Hepadnaviridae such as the hepatitis B virus. Some others were tailless with a virion size. Overall, less than 10% of the cells showed obvious signs of infection. Images of virally-parasitized tissues of A. cytherea provide further evidence that corals are a target for viral infection. However, more research is required into their pathogenicity and involvement in bleaching events.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2012 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Bourne, D., Lida, Y., Uthicke, S. and Smith-Keune, C. (2008) Changes in coral-associated microbial communities during a bleaching event. The ISME Journal 2, 350363.CrossRefGoogle ScholarPubMed
Davy, S.K., Burchett, H.E., Dale, A.L., Davies, P., Davy, J.E., Muncke, C., Hoegh-Guldberg, O. and Wilson, W.H. (2006) Viruses: agents of coral disease? Diseases of Aquatic Organisms 69, 101110.CrossRefGoogle ScholarPubMed
Davy, J.E. and Patten, N.L. (2007) Morphological diversity of virus-like particles within the surface microlayer of scleractinian corals. Aquatic Microbial Ecology 47, 3744.CrossRefGoogle Scholar
Kaito, M., Ohba, H., Chiba, J., Kohara, M., Tanaka, H., Fujita, N., Gabazza, E.C., Watanabe, S., Konishi, M. and Adachi, Y. (2006) The ultrastructural morphology of native hepatitis B virus. Medical Molecular Morphology 39, 136145.CrossRefGoogle ScholarPubMed
Hoegh-Guldberg, O. (2010) Dangerous shifts in ocean ecosystem function? The ISME Journal 4, 10901092.CrossRefGoogle ScholarPubMed
Lohr, J., Munn, C.B. and Wilson, W.H. (2007) Characterization of a latent virus-like infection of symbiotic zooxanthellae. Applied and Environmental Microbiology 73, 29762981.CrossRefGoogle ScholarPubMed
Marhaver, K.L., Edwards, R.A. and Rohwer, F. (2008) Viral communities associated with healthy and bleaching corals. Environmental Microbiology 10, 22772286.CrossRefGoogle ScholarPubMed
Normile, D. (2010) Hard summer for corals kindles fears for survival of reefs. Science 329, 1001.CrossRefGoogle ScholarPubMed
Patten, N.L., Harrison, M.L. and Mitchell, G.J. (2008) Prevalence of virus-like particles within a staghorn scleractinian coral (Acropora muricata) from the Great Barrier Reef. Coral Reefs 27, 569580.CrossRefGoogle Scholar
Reed, K.C., Muller, E.M. and van Woesik, R. (2010) Coral immunology and resistance to disease. Diseases of Aquatic Organisms 90, 8592.CrossRefGoogle ScholarPubMed
Rosenberg, E., Koren, O., Reshe, L., Efrony, R. and Zilber-Rosenberg, I. (2007) The role of microorganisms in coral health, disease and evolution. Nature Reviews Microbiology 5, 355362.CrossRefGoogle ScholarPubMed
Rosenberg, E., Kushmaro, A., Kramarsky-Winter, E., Banin, E. and Yossi, L. (2009) The role of microorganisms in coral bleaching. The ISME Journal 3, 139146.CrossRefGoogle ScholarPubMed
Rohwer, F., Seguritan, V., Azam, F. and Knwolton, N. (2002) Diversity and distribution of coral-associated bacteria. Marine Ecology Progress Series 243, 110.CrossRefGoogle Scholar
Rohwer, F. and Thurber, R.V. (2009) Viruses manipulate the marine environment. Nature 459, 207212.CrossRefGoogle ScholarPubMed
Thurber, R.V., Willner-Hall, D., Rodriguez-Mueller, B., Desnues, C., Edwards, R.A., Angly, F., Dinsdale, E., Kelly, L. and Rohwer, F. (2009) Metagenomic analysis of stressed coral holobionts. Environmental Microbiology 11, 21482163.CrossRefGoogle Scholar
van Oppen, M.J.H., Leong, J.O., Gates, D.R. (2009) Coral–virus interactions: a double-edged sword? Symbiosis 47, 18.CrossRefGoogle Scholar
Wilkinson, C. (2008) Status of coral reefs of the world: 2008. Townsville, QL: Global Coral Reef Monitoring Network and Reef and Rainforest Research Centre, 296 pp.Google Scholar
Wilson, W.H. and Chapman, D.M. (2001) Observation of virus-like particles in thin sections of the plumose anemone, Metridium senile. Journal of the Marine Biological Association of the United Kingdom 81, 879880.CrossRefGoogle Scholar
Wilson, W.H., Francis, I., Ryan, K. and Davy, S.K. (2001) Temperature induction of viruses in symbiotic dinoflagellates. Aquatic Microbial Ecology 25, 99102.CrossRefGoogle Scholar
Wilson, W.H., Dale, A.L., Davy, J.E. and Davy, S.K. (2005) An enemy within? Observations of virus-like particles in reef corals. Coral Reefs 24, 145148.CrossRefGoogle Scholar