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. 2008 Apr;116(4):441-7.
doi: 10.1289/ehp.10966.

Sunscreens cause coral bleaching by promoting viral infections

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Sunscreens cause coral bleaching by promoting viral infections

Roberto Danovaro et al. Environ Health Perspect. 2008 Apr.

Abstract

Background: Coral bleaching (i.e., the release of coral symbiotic zooxanthellae) has negative impacts on biodiversity and functioning of reef ecosystems and their production of goods and services. This increasing world-wide phenomenon is associated with temperature anomalies, high irradiance, pollution, and bacterial diseases. Recently, it has been demonstrated that personal care products, including sunscreens, have an impact on aquatic organisms similar to that of other contaminants.

Objectives: Our goal was to evaluate the potential impact of sunscreen ingredients on hard corals and their symbiotic algae.

Methods: In situ and laboratory experiments were conducted in several tropical regions (the Atlantic, Indian, and Pacific Oceans, and the Red Sea) by supplementing coral branches with aliquots of sunscreens and common ultraviolet filters contained in sunscreen formula. Zooxanthellae were checked for viral infection by epifluorescence and transmission electron microscopy analyses.

Results: Sunscreens cause the rapid and complete bleaching of hard corals, even at extremely low concentrations. The effect of sunscreens is due to organic ultraviolet filters, which are able to induce the lytic viral cycle in symbiotic zooxanthellae with latent infections.

Conclusions: We conclude that sunscreens, by promoting viral infection, potentially play an important role in coral bleaching in areas prone to high levels of recreational use by humans.

Keywords: UV filters; bleaching; corals; sunscreens; viruses.

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Figures

Figure 1
Figure 1
Impact of sunscreen addition on nubbins of Acropora. Untreated (brown) and treated (bleached) nubbins of (A) Acropora cervicornis (Caribbean Sea, Mexico); (B) Acropora divaricata (Celebes Sea, Indonesia); (C) Acropora sp. (Red Sea, Egypt); and (D) Acropora intermedia (Andaman Sea, Thailand). Images were taken within 62 hr of the start of sunscreen incubations. Scale bar = 2 cm.
Figure 2
Figure 2
Effect of 100-μL sunscreens on Acropora divaricata nubbins after 24-hr incubation at various temperatures. (A) control; (B) nubbins incubated at 28°C; and (C) nubbins incubated at 30°C. Scale bar = 1 cm.
Figure 3
Figure 3
Zooxanthellae release from hard corals in control and sunscreen addition samples. (A) TEM images of healthy zooxanthellae (intact cell structure and membrane) in control untreated Acropora nubbin, and (B) zooxanthellae damaged by sunscreen treatment: cells appear swollen and vacuolated, without chloroplasts and double the size of the controls; the thylakoids are unpacked and dispersed inside the cells, and cell-membrane integrity is lost (arrowhead). (C) Autofluorescence images showing healthy (red) zooxanthellae in control sample and (B) some healthy (H) and damaged and partially damaged (T, transparent and pale) zooxanthellae released after sunscreen treatment. Scale bars = 2 μm (A, B) and 5 μm (C, D).
Figure 4
Figure 4
Epifluorescence microscopy analysis of the level of damage in zooxanthellae released after sun-screen (SS) addition.
Figure 5
Figure 5
Viral enrichment factors of ambient seawater (as the ratios of viral density in treated and control samples) after the addition of sunscreen, nutrient, and mitomycin C. (A) Viral enrichment factor of ambient seawater within 24 hr after sunscreen and organic nutrients addition. (B) Viral enrichment factor of ambient seawater within 12 hr after sunscreen and mitomycin C addition. Organic nutrients (lipids, proteins, and carbohydrates) were added at concentrations equivalent to those contained in sunscreens according to Danovaro and Corinaldesi (2003). Values are ± SE.
Figure 6
Figure 6
TEM images of viruslike particles (VLPs) associated with zooxanthellae released from nubbins after sunscreen treatment. (A, B) VLPs attached to zooxanthellae membranes. (C) Viruses attached to outer part of zooxanthellae with visible tail penetrating cell membrane. Scale bars = 100 nm (A, B); 200 nm (C). Arrowheads indicate sections magnified in insets.

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