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A Signaling Protease Required for Melanization in Drosophila Affects Resistance and Tolerance of Infections

236

Citations

30

References

2008

Year

TLDR

Organisms defend against infections through resistance and tolerance, yet most studies examine only one, leaving the interplay between these traits poorly understood. The study proposes nine possible pairwise combinations of resistance and tolerance changes to explore their interactions. A CG3066 mutation in Drosophila melanization triggers diverse, pathogen‑dependent shifts in both resistance and tolerance, demonstrating that melanization modulates these defenses in complex ways.

Abstract

Organisms evolve two routes to surviving infections—they can resist pathogen growth (resistance) and they can endure the pathogenesis of infection (tolerance). The sum of these two properties together defines the defensive capabilities of the host. Typically, studies of animal defenses focus on either understanding resistance or, to a lesser extent, tolerance mechanisms, thus providing little understanding of the relationship between these two mechanisms. We suggest there are nine possible pairwise permutations of these traits, assuming they can increase, decrease, or remain unchanged in an independent manner. Here we show that by making a single mutation in the gene encoding a protease, CG3066, active in the melanization cascade in Drosophila melanogaster, we observe the full spectrum of changes; these mutant flies show increases and decreases in their resistance and tolerance properties when challenged with a variety of pathogens. This result implicates melanization in fighting microbial infections and shows that an immune response can affect both resistance and tolerance to infections in microbe-dependent ways. The fly is often described as having an unsophisticated and stereotypical immune response where single mutations cause simple binary changes in immunity. We report a level of complexity in the fly's immune response that has strong ecological implications. We suggest that immune responses are highly tuned by evolution, since selection for defenses that alter resistance against one pathogen may change both resistance and tolerance to other pathogens.

References

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