DAF-16 and SMK-1 Contribute to Innate Immunity During Adulthood in Caenorhabditis elegans

Aging is accompanied by a progressive decline in immune function termed immunosenescence. Deficient surveillance coupled with the impaired function of immune cells compromises host defense in older animals. The dynamic activity of regulatory modules that control immunity appears to underlie age-dependent modifications to the immune system. In the roundworm Caenorhabditis elegans levels of p38 MAP kinase diminish over time, reducing the expression of immune effectors that clear bacterial pathogens. Along with the pathway, innate immunity in C. elegans is regulated by the insulin signaling pathway. Here we asked whether , a Forkhead box (FOXO) transcription factor whose activity is inhibited by insulin signaling, plays a role in host defense later in life. While in younger C. elegans is inactive unless stimulated by environmental insults, we found that even in the absence of acute stress the transcriptional activity of increases in an age-dependent manner. Beginning in the reproductive phase of adulthood, upregulates a subset of its transcriptional targets, including genes required to kill ingested microbes. Accordingly, has little to no role in larval immunity, but functions specifically during adulthood to confer resistance to bacterial pathogens. We found that DAF-16-mediated immunity in adults requires , a regulatory subunit of the PP4 protein phosphatase complex. Our data suggest that as the function of one branch of the innate immune system of C. elegans () declines over time, DAF-16-mediated immunity ramps up to become the predominant means of protecting adults from infection, thus reconfiguring immunity later in life.