4.8 Article

Exposure to ultraviolet-B radiation increases the susceptibility of mosquitoes to infection with dengue virus

Journal

GLOBAL CHANGE BIOLOGY
Volume 29, Issue 19, Pages 5540-5551

Publisher

WILEY
DOI: 10.1111/gcb.16906

Keywords

Aedes aegypti; carryover effects; immune function; melanin; ultraviolet radiation; vector competence

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By 2100, it is predicted that greenhouse gases will reduce ozone and cloud cover over the tropics, leading to increased exposure of organisms to harmful UV-B radiation. UV-B radiation has damaging effects on DNA and plays a significant role in modulating immune function and disease susceptibility in humans and vertebrates. The impact of UV-B radiation on invertebrate immune function is largely unknown, but it has been found to impair insect immune response and make them more susceptible to infection with important pathogens.
By 2100, greenhouse gases are predicted to reduce ozone and cloud cover over the tropics causing increased exposure of organisms to harmful ultraviolet-B radiation (UVBR). UVBR damages DNA and is an important modulator of immune function and disease susceptibility in humans and other vertebrates. The effect of UVBR on invertebrate immune function is largely unknown, but UVBR together with ultraviolet-A radiation impairs an insect immune response that utilizes melanin, a pigment that also protects against UVBR-induced DNA damage. If UVBR weakens insect immunity, then it may make insect disease vectors more susceptible to infection with pathogens of socioeconomic and public health importance. In the tropics, where UVBR is predicted to increase, the mosquito-borne dengue virus (DENV), is prevalent and a growing threat to humans. We therefore examined the effect of UVBR on the mosquito Aedes aegypti, the primary vector for DENV, to better understand the potential implications of increased tropical UVBR for mosquito-borne disease risk. We found that exposure to a UVBR dose that caused significant larval mortality approximately doubled the probability that surviving females would become infected with DENV, despite this UVBR dose having no effect on the expression of an effector gene involved in antiviral immunity. We also found that females exposed to a lower UVBR dose were more likely to have low fecundity even though this UVBR dose had no effect on larval size or activity, pupal cuticular melanin content, or adult mass, metabolic rate, or flight capacity. We conclude that future increases in tropical UVBR associated with anthropogenic global change may have the benefit of reducing mosquito-borne disease risk for humans by reducing mosquito fitness, but this benefit may be eroded if it also makes mosquitoes more likely to be infected with deadly pathogens.

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