Comparative basolateral amygdala connectomics reveals dissociable single-neuron projection patterns to frontal cortex in macaques and mice.

Basolateral amygdala (BLA) is a key hub for affect in the brain, and dysfunction within this area contributes to a host of psychiatric disorders. BLA is extensively and reciprocally interconnected with frontal cortex, and some aspects of its function are evolutionarily conserved across rodents, anthropoid primates, and humans. Neuron density in BLA is substantially lower in primates compared to murine rodents, and frontal cortex (FC) is dramatically expanded in primates, particularly the more anterior granular and dysgranular areas.

Comparative basolateral amygdala connectomics reveals dissociable single-neuron projection patterns to frontal cortex in macaques and mice.

The basolateral amygdala (BLA) projects to the frontal cortex (FC) in both rodents and primates, but the comparative organization of single-neuron BLA-FC projections is unknown. Using a barcoded connectomic approach, we found that BLA neurons are more likely to project to multiple distinct parts of FC in mice than in macaques. Further, while single BLA neuron projections to nucleus accumbens are similarly organized in mice and macaques, BLA-FC connections differ.

Understanding low COVID-19 booster uptake among US adults.

Background: Vaccinations against SARS-CoV-2 have consistently been shown to reduce the risk of severe COVID-19 disease. However, uptake of boosters has stalled in the United States at less than 20% of the eligible population. The objective of this study was to assess the reasons for not having obtained a bivalent booster within an existing COVID-19 cohort.