Gangliogenesis and Embryonic Development in Biomphalaria glabrata

Biomphalaria glabrata is an intermediate host for a parasitic species, Schistosoma mansoni, which can infect humans causing schistosomiasis. The majority of research conducted on these snails focuses on host-parasite relationships. Thus, very little is known regarding their nervous system, especially during embryonic and juvenile development. This project aims to investigate the transition from the embryonic nervous system consisting of a network of neurons to a developed ganglionic nervous system consisting of a separation between clusters of nerve cell bodies, or ganglia, and connectives. To investigate when this process, known as gangliogenesis, occurs, immunofluorescence is used to visualize the serotonergic nervous system at various ages, thus, providing a better understanding of the timeline in which this process occurs. This study, additionally, aims to discern changes in gene expression throughout embryonic and early juvenile development by identifying differential gene expression patterns through RNA sequencing. Though we will be doing the transcriptome analysis with whole embryos and juveniles rather than just the isolated nervous system, we hypothesize that we will still be able to identify transcripts associated with the nervous system and its development. This process will also allow for the identification of candidate genes putatively involved in gangliogenesis in B. glabrata

Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen.

ABSTRACT: Identifying the genetic determinants of pain is a scientific imperative given the magnitude of the global health burden that pain causes. Here, we report a genetic screen for nociception, performed under the auspices of the International Mouse Phenotyping Consortium. A biased set of 110 single-gene knockout mouse strains was screened for 1 or more nociception and hypersensitivity assays, including chemical nociception (formalin) and mechanical and thermal nociception (von Frey filaments and Hargreaves tests, respectively), with or without an inflammatory agent (complete Freund\u27s adjuvant). We identified 13 single-gene knockout strains with altered nocifensive behavior in 1 or more assays. All these novel mouse models are openly available to the scientific community to study gene function. Two of the 13 genes (Gria1 and Htr3a) have been previously reported with nociception-related phenotypes in genetically engineered mouse strains and represent useful benchmarking standards. One of the 13 genes (Cnrip1) is known from human studies to play a role in pain modulation and the knockout mouse reported herein can be used to explore this function further. The remaining 10 genes (Abhd13, Alg6, BC048562, Cgnl1, Cp, Mmp16, Oxa1l, Tecpr2, Trim14, and Trim2) reveal novel pathways involved in nociception and may provide new knowledge to better understand genetic mechanisms of inflammatory pain and to serve as models for therapeutic target validation and drug development