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Herrera Paredes, S.

Publications and source records attributed to Herrera Paredes, S..

3 recordsLinked to original sources

Rich mobilomes and a conserved adaptive core in bacteria from an intensifying Mexican soda lake

The haloalkaline maar lake at Rincon de Parangueo, in central Mexicos volcanic belt, is a doubly extreme habitat where high salinity and high alkalinity co-occur. Unlike the long-lived soda lakes that dominate the literature, it is a young system undergoing rapid desiccation, its salinity and pH intensifying over decades. Its microbes have been surveyed only by 16S amplicons, with no genome or mobilome reported from the site, and the wider soda-lake mobilome is known almost entirely from host-unlinked, short-read viromes. Using long-read sequencing, we recovered high-quality genomes for six isolates that dereplicate to three independent, bona fide haloalkaliphilic lineages spanning two distant families (Halomonadaceae, Bacillaceae). Each lineages closest relative is not its type strain but an isolate from another distant extreme habitat, including two other Mexican hypersaline systems. All three are aerobic, facultatively fermentative heterotrophs that meet high pH and salinity with the canonical toolkit -- multisubunit Mrp/Mnh Na+/H+ antiporters and a "salt-out" compatible-solute strategy -- whose distribution tracks phylogeny, with only complementary lineage-specific elaboration. In contrast, the isolates carry an unexpectedly rich and apparently active mobilome: a novel plasmid, multiple intact prophages, and multiple other mobile genetic elements alongside an above-average antiviral defense arsenal, including an 89-spacer CRISPR array. Horizontal transfer is thus likely active at Rincon de Parangueo but is not the vehicle of haloalkaliphily. Intensifying extremes like this one are tractable natural laboratories for dissecting how inherited toolkits and recent innovation shape microbial survival at the limits of life.

microbiology↗

Transcriptional responses to priority effects in nectar yeast

Priority effects, where the order and timing of species arrival influence the assembly of ecological communities, have been observed in a variety of taxa and habitats. However, the genetic and molecular basis of priority effects remains unclear in most cases, hindering the mechanistic understanding of priority effects. We sought to gain such understanding for the common nectar yeast Metschnikowia reukaufii, which engages in strong priority effects with other species of nectar yeast, including M. rancensis, another species commonly found in the nectar of our study plant, the hummingbird-pollinated Diplacus (Mimulus) aurantiacus. After inoculation into two contrasting types of synthetic nectar simulating early arrival of M. rancensis, we conducted whole-transcriptome sequencing of 108 genetically diverse strains of M. reukaufii. We found that several genes were differentially expressed in M. reukaufii strains when the nectar had been conditioned by growth of M. rancensis. Many of these genes were associated with amino acid metabolism, consistent with our previous finding that early-arriving species limit late-arriving species growth by reducing amino acid availability. Furthermore, investigation of expression quantitative trait loci (eQTLs) revealed that genes involved in amino acid transport and resistance to antifungal compounds were enriched in genetic variants, with differing effects on gene expression based on priority effects of M. rancensis. These results demonstrate that intraspecific variation in the ability of nectar yeasts to respond to nutrient limitation and direct fungal competition may underpin the molecular mechanisms of priority effects.

ecology↗

Myeloid deficiency of the intrinsic clock protein Bmal1 accelerates cognitive aging by disrupting microglial synaptic pruning

Aging is associated with loss of circadian immune responses and circadian gene transcription in peripheral macrophages. Microglia, the resident macrophages of the brain, also show diurnal rhythmicity in regulating local immune responses and synaptic remodeling. To investigate the interaction between aging and microglial circadian rhythmicity, we examined mice deficient in the core clock transcription factor, BMAL1. Aging Cd11bcre;Bmallox/lox mice demonstrated accelerated cognitive decline in association with suppressed hippocampal long-term potentiation and increases in immature dendritic spines. C1q deposition at synapses and synaptic engulfment were significantly decreased in aging Bmal1-deficient microglia, suggesting that BMAL1 plays a role in regulating synaptic pruning in aging. In addition to accelerated age-associated hippocampal deficits, Cd11bcre;Bmallox/lox mice also showed deficits in the sleep-wake cycle with increased wakefulness across light and dark phases. These results highlight an essential role of microglial BMAL1 in maintenance of synapse homeostasis in the aging brain. Significance StatementThis study demonstrates that myeloid deficiency of the circadian clock gene Bmal1 disrupts microglial synaptic pruning in the hippocampus, accelerates age-associated cognitive decline, and disrupts the sleep-wake cycle.

neuroscience↗