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Ahlers, J.

Publications and source records attributed to Ahlers, J..

2 recordsLinked to original sources

Signals in flux: Investigating the seasonal turnover of the diel vertical migration-inducing kairomone 5α-cyprinol sulfate

5-cyprinol sulfate (CPS) is a chemical signal released by cyprinid fish that plays a crucial role in predator-prey interactions by inducing diel vertical migration (DVM) in Daphnia, a key process driving freshwater ecosystem dynamics. While CPS-mediated DVM has long been considered a stable and predictable response to predator abundance, this study challenges previous assumptions by demonstrating that CPS undergoes rapid turnover in aquatic systems. We show that CPS exudation is tightly linked to fish feeding intensity, independent of fish size, while microbial degradation emerges as the dominant removal process, with degradation rates reaching up to 85.7% per day in lake water. Seasonal field data from a mesotrophic lake reveal that CPS concentrations range from 40 to 900 ng/L over a season, peaking in late summer, putatively indicating increased fish feeding and shifts in prey availability. Using an integrated approach combining laboratory feeding trials, field sampling, and predictive modeling, we present a temperature-dependent framework that captures the interplay between CPS exudation and degradation. Our findings highlight a fundamental reconsideration of CPS as an environmental cue: rather than reflecting predator abundance, CPS concentrations primarily track predator feeding activity, dynamically modulating the strength of DVM and its cascading effects on freshwater food webs. This study provides the first in-situ quantification of CPS turnover, offering new insights into the temporal variability of chemical signaling and its ecosystem-wide consequences in fluctuating aquatic environments.

ecology↗

Microbiome and Metabolome driven differentiation of TGF-β producing Tregs leads to Senescence and HIV latency

Current therapeutic interventions to eradicate latent HIV ("reservoir") and restore immune function in ART-treated HIV infection have yet to show efficacy. To explore mechanisms of HIV persistence, we apply an integrated systems biology approach and identify a distinct group of individuals with poor CD4 T-cell reconstitution (Immunologic non-responders, "INRs") and high frequencies of cells with inducible HIV. Contrary to the prevailing notion that immune activation drives HIV persistence and immune dysfunction, peripheral blood leukocytes from these subjects have enhanced expression of a network of genes regulated by cellular senescence driving transcription factors (TFs) FOXO3, SMAD2 and IRF3. In these subjects, increased frequencies of regulatory T cells and expression of the TGF-{beta} signaling cascade are complimented by the downregulation of cell cycle, metabolic and pro-inflammatory pathways. Lactobacillaceae family and metabolites (members of the butyrate family - i.e. -ketobutyrate) were correlated with Treg frequencies in "Senescent-INRs" ex vivo, triggered the differentiation of TGF-{beta} producing Tregs and promoted HIV latency establishment in vitro. These cascades, downstream of PD-1/TGF-{beta}, prevent memory T cell differentiation and are associated with an increase in frequencies of cells with inducible HIV ex vivo. Our findings identify cellular senescence responses that can be targeted by PD-1 or TGF-{beta} specific interventions that have shown safety and efficacy in cancer, and may prove to be crucial for HIV eradication.

immunology↗