Biomarkers of aging in Drosophila

Low environmental temperature and dietary restriction (DR) extend lifespan in diverse organisms. In the fruit fly Drosophila, switching flies between temperatures alters the rate at which mortality subsequently increases with age but does not reverse mortality rate. In contrast, DR acts acutely to lower mortality risk; flies switched between control feeding and DR show a rapid reversal of mortality rate. Dietary restriction thus does not slow accumulation of aging‐related damage. Molecular species that track the effects of temperatures on mortality but are unaltered with switches in diet are therefore potential biomarkers of aging‐related damage. However, molecular species that switch upon instigation or withdrawal of DR are thus potential biomarkers of mechanisms underlying risk of mortality, but not of aging‐related damage. Using this approach, we assessed several commonly used biomarkers of aging‐related damage. Accumulation of fluorescent advanced glycation end products (AGEs) correlated strongly with mortality rate of flies at different temperatures but was independent of diet. Hence, fluorescent AGEs are biomarkers of aging‐related damage in flies. In contrast, five oxidized and glycated protein adducts accumulated with age, but were reversible with both temperature and diet, and are therefore not markers either of acute risk of dying or of aging‐related damage. Our approach provides a powerful method for identification of biomarkers of aging.     

Seasonal variation in the sex allocation of a neotropical solitary bee

We carried out a field study on the life history and sex allocationof the ground-nesting solitary bee Diadasina distincta (Hymenoptera: Anthophoridae).This species is multivoltine, undergoing five generations a yearbetween February and September. The numerical sex ratio of thisspecies was female biased overall (approximately 38% males)and showed a strong and consistent seasonal pattern. The numericalsex ratio was extremely female biased (approximately 20% males)from February until May, and then slightly male biased (approximately60% males) from June until September. Females were 3.26 timesthe size of males, and so the overall investment ratio was female biasedthroughout the year. The overall female bias and seasonal variationin sex allocation is unlikely to be explained by models thatinvoke overlapping generations or competition between brothersfor mates (local mate competition). We suggest that a possibleexplanation for the female bias in the early part of the seasonis local resource enhancement (LRE): nesting near larger numbersof sisters reduces parasitism. LRE is likely to decrease in importancein the later part of the season, when the biased numerical and investmentratios may be explained by models in which male and female offspringgain different fitness returns from resources invested.     

Murine model of colonization with fungal pathogen Candida auris to explore skin tropism,host risk factors and therapeutic strategies

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