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Biology subjects

Anderson, C. B.

Publications and source records attributed to Anderson, C. B..

3 recordsLinked to original sources

Local tree cover predicts mosquito species richness and disease vector presence in a tropical countryside landscape

ContextLand use change and deforestation drive both biodiversity loss and zoonotic disease transmission in tropical countrysides. For mosquito communities that can include disease vectors, forest loss has been linked to reduced biodiversity and increased vector presence. The spatial scales at which land use and tree cover shape mosquito communities present a knowledge gap relevant to both biodiversity and public health. ObjectivesWe investigated the responses of mosquito species richness and Aedes albopictus disease vector presence to land use and to tree cover surrounding survey sites at different spatial scales. We also investigated species compositional turnover across land uses and along environmental gradients. MethodsWe paired a field survey of mosquito communities in agricultural, residential, and forested lands in rural southern Costa Rica with remotely sensed tree cover data. We compared mosquito richness and vector presence responses to tree cover measured across scales from 30m to 1000m, and across land uses. We analyzed compositional turnover between land uses and along environmental gradients of tree cover, temperature, elevation, and geographic distance. ResultsTree cover was both positively correlated with mosquito species richness and negatively correlated with the presence of the common invasive dengue vector Ae. albopictus at small spatial scales of 90 - 250m. Land use predicted community composition and Ae. albopictus presence. ConclusionsThe results suggest that local tree cover preservation and expansion can support mosquito species richness and reduce disease vector presence. The identified spatial range at which tree cover shapes mosquito communities can inform the development of land management practices to protect both ecosystem and public health.

ecology↗

Single-Cell RNAseq Analysis Reveals Robust Anti-PD-1-Mediated Increase of Immune Infiltrate in Metastatic Castration-Sensitive Prostate Cancer

Compared to other malignancies, the tumor microenvironment (TME) of primary and castration-resistant prostate cancer (CRPC) is relatively devoid of immune infiltrates. While androgen deprivation therapy (ADT) induces a complex immune infiltrate in localized prostate cancer, both in animal models and humans, the TME composition of metastatic, castration-sensitive prostate cancer (mCSPC) is relatively unknown and the effects of ADT and other treatments are poorly characterized in this context. To address this challenge, we analyzed metastatic sites from patients enrolled on a phase 2 clinical trial (NCT03951831), in which men were treated with standard-of-care chemo-hormonal therapy with anti-PD-1 immunotherapy, at the single cell level. Longitudinal protein activity-based analysis of TME subpopulations identified immune subpopulations conserved across multiple metastatic sites, their dynamic, treatment-mediated evolution, and associated clinical response features. Our study revealed a therapy-resistant, transcriptionally distinct tumor subpopulation, which comprises an increasing number of cells in treatment-refractory patients, and identified several druggable targets in both tumor and immune cells as candidates to advance treatment and improve outcomes for patients with mCSPC.

cancer biology↗

GAD65Cre drives reporter expression in multiple taste cell types

In taste buds, Type I cells represent the majority of cells (50-60%) and primarily have a glial-like function in taste buds. However, recent studies suggest that they have additional sensory and signaling functions including amiloride-sensitive salt transduction, oxytocin modulation of taste, and substance P mediated GABA release. Nonetheless, the overall function of Type I cells in transduction and signaling remains unclear, primarily because of the lack of a reliable reporter for this cell type. GAD65 expression is specific to Type I taste cells and GAD65 has been used as a Cre driver to study Type I cells in salt taste transduction. To test the specificity of transgene-driven expression, we crossed GAD65Cre mice with floxed tdTomato and Channelrhodopsin (ChR2) lines and examined the progeny with immunochemistry, chorda tympani recording, and calcium imaging. We report that while many tdTomato+ taste cells express NTPDase2, a specific marker of Type I cells, we see expression of tdTomato in both Gustducin and SNAP25 positive taste cells. We also see ChR2 in cells just outside the fungiform taste buds. Chorda tympani recordings in the GAD65Cre/ChR2 mice show large responses to blue light, larger than any response to standard taste stimuli. Further, several isolated tdTomato positive taste cells responded to KCl depolarization with increases in intracellular calcium, indicating the presence of voltage-gated calcium channels. Taken together, these data suggest that GAD65Cre mice drive expression in multiple taste cell types and thus cannot be considered a reliable reporter of Type I cell function.

neuroscience↗