Biology subjects

Sultanova, Z.

Publications and source records attributed to Sultanova, Z..

3 recordsLinked to original sources

bioRxiv2025

Age-dependent gut microbiota dynamics and their association with male fitness traits in Drosophila melanogaster

Growing evidence suggests that the gut microbiota plays a key role in shaping life history in a wide range of species, including well-studied model organisms like Drosophila melanogaster. Although recent studies have explored the relationship between gut microbiota and female life history, the link between gut microbiota and male life history remains understudied. In this study, we explored the role of gut microbiota in shaping male life history traits by correlating variation in life history traits across genetically homogeneous isolines with their naturally occurring gut microbiota. Using 22 isolines from the Drosophila melanogaster Genetic Reference Panel (DGRP), we measured lifespan, early/late-life reproduction, and early/late-life physiological performance. We characterized the gut microbiota composition in young (5 days old) and old (26 days old) flies using 16S rDNA sequencing. We observed significant variation in male life history traits across isolines, as well as age-related changes in gut microbiota composition. Using machine learning, we showed that gut microbiota composition could predict the age of the organisms with high accuracy. Associations between gut microbiota and life history traits were notable, particularly involving the Acetobacter genus. In early life, the abundance of Acetobacter ascendens was associated with functional aging, while Acetobacter indonesiensis was linked to reproductive senescence. In late life, higher abundances of A. ascendens and Acetobacter pasteurianus were negatively associated with lifespan. These findings highlight the potential role of gut microbiota, especially the Acetobacter genus, in male fitness and aging.

microbiology↗

bioRxiv2023

Early-adulthood intermittent fasting and reduced insulin/IGF-1 signalling additively increase lifespan and slow down reproductive ageing

The developmental theory of ageing proposes that age-specific decline in the force of natural selection results in suboptimal levels of gene expression in adulthood, leading to functional senescence. This theory explicitly predicts that optimising gene expression in adulthood can ameliorate functional senescence and improve fitness. Reduced insulin/IGF-1 signalling (rIIS) extends the reproductive lifespan of Caenorhabditis elegans at the cost of reduced reproduction. Here, we show that adulthood-only rIIS improves late-life reproduction without any detrimental effects on other life-history traits in both benign and stressful conditions. Remarkably, we show that rIIS additively extends late-life reproduction and lifespan when animals are exposed to a fluctuating food environment - intermittent fasting (IF) - resulting in reduced food intake in early adulthood. Full factorial genome-wide RNA-Seq across the life course demonstrated that IF and rIIS modulate the age-specific expression of pro-longevity genes. IF, rIIS and combined IF + rIIS treatment downregulated genes involved in peptide metabolism in early life and differentially regulated immunity genes in later life. Importantly, combined IF + rIIS treatment uniquely regulated a large cluster of genes in mid-life that are associated with immune response. These results suggest that optimising gene expression in adulthood can decelerate reproductive ageing and increase fitness.

molecular biology↗

bioRxiv2020

Genetic sex determination and sex-specific lifespan in tetrapods - evidence of a toxic Y effect

Sex-specific lifespans are ubiquitous across the tree of life and exhibit broad taxonomic patterns that remain a puzzle, such as males living longer than females in birds and vice versa in mammals. The prevailing "unguarded-X" hypothesis (UXh) explains this by differential expression of recessive mutations in the X/Z chromosome of the heterogametic sex (e.g., females in birds and males in mammals), but has only received indirect support to date. An alternative hypothesis is that the accumulation of deleterious mutations and repetitive elements on the Y/W chromosome might lower the survival of the heterogametic sex ("toxic Y" hypothesis). Here, we report lower survival of the heterogametic relative to the homogametic sex across 138 species of birds, mammals, reptiles and amphibians, as expected if sex chromosomes shape sex-specific lifespans. We then analysed bird and mammal karyotypes and found that the relative sizes of the X and Z chromosomes are not associated with sex-specific lifespans, contrary to UXh predictions. In contrast, we found that Y size correlates negatively with male survival in mammals, where toxic Y effects are expected to be particularly strong. This suggests that small Y chromosomes benefit male lifespans. Our results confirm the role of sex chromosomes in explaining sex differences in lifespan, but indicate that, at least in mammals, this is better explained by "toxic Y" rather than UXh effects.

evolutionary biology↗