UNCOVERING MICROBIAL MODULATORS OF NEUROACTIVE MOLECULES AS NOVEL THERAPEUTICS.
Project Number:1DP5OD017924-01Contact PI / Project Leader:HSIAO, ELAINE
Title:UNCOVERING MICROBIAL MODULATORS OF NEUROACTIVE MOLECULES AS NOVEL THERAPEUTICS.
Awardee Organization:CALIFORNIA INSTITUTE OF TECHNOLOGY
Abstract Text:PROJECT SUMMARY/ABSTRACT Humans are colonized with diverse microbial communities, collectively called the commensal microbiota, that influence a wide array of biological processes. Recent studies demonstrate that in addition to their roles in nutrition, immunity and metabolism, the commensal microbiota also plays a fundamental role in the development and function of the nervous system, in addition to several complex host behaviors. The proposed research training program aims to uncover the mechanisms underlying the interaction between specific commensal microbes and the nervous system, and to elucidate the impact of these relationships on host physiology. Specifically, the proposed research will examine the role of commensal microbes on host serotonin (5-hydroxytrypatmine, 5-HT) metabolism, with aims to define the specific steps of the 5-HT pathway that are affected by commensal microbes, identify the particular microbial species and factors that affect host 5-HT, and apply these microbial 5-HT modulators toward ameliorating symptoms in models of 5-HT-related disease. Findings from these studies will advance our current understanding of how the commensal microbiota affects health and disease, and will further explore the innovative prospect of developing novel, microbe-based therapeutics, which can be readily modified for better function, regulatory control, targeting and delivery. The proposed studies on the interaction between the commensal microbiota and nervous system fills a novel area of multidisciplinary research that integrates not only neurobiology and microbiology, but also biochemistry (in the dissection of molecular alterations in the 5-HT pathway), chemical engineering (in the nanofabrication of microfluidic devices for high-throughput confinement, cultivation and functional screening of endogenous species of the microbiome) and molecular and behavioral neuroscience (in the investigation of pathologies seen in mouse models of serotonin-deficiency). My proposed training will span five years of independent research as a Senior Research Fellow at the California Institute of Technology. This title is typically reserved for individuals with previous post-doctoral experience and serves as a transitional stage toward advancing into a junior faculty position. Approximately one year after the award is conferred, I will recruit one full-time technician, with significant previous experience in laboratory research. I will also begin mentoring up to two biology or chemistry undergraduate students per year through Caltech's summer research program. Public Health Relevance Statement:PUBLIC HEALTH RELEVANCE: Consistent with the staggering finding that our bodies are comprised of over ten times more microbial cells than human eukaryotic cells, scientists are finding that the microbes that make up "us" play important roles in a variety of biological processes. The aim of my proposed research is to uncover how our commensal microbes communicate with the nervous system, and specifically, how particular microbial species alter host levels of serotonin and cause downstream changes in host physiology. Findings from these studies will advance our understanding of how the commensal microbiota impacts health and disease, and will inform the exciting prospect of developing microbe-based therapeutics for disorders of the nervous system. NIH Spending Category:Bioengineering; Biotechnology; Dental/Oral and Craniofacial Disease; NeurosciencesProject Terms:Adverse effects; Affect; Area; Award; base; Behavior; Behavioral; Biochemistry; Biological Process; Biology; Brain; California; cell type; Cells; Chemical Engineering; Chemistry; Colon; commensal microbes; Complex; Data Set; Development; Disease; Dissection; Enabling Factors; Enzymes; Eukaryotic Cell; Exhibits; experience; Faculty; Genomics; Goals; gut microbiota; Health; Human; Immunity; Individual; innovation; insight; Institutes; Interdisciplinary Study; Investigation; Laboratory Research; loss of function; Mediating; Mentors; Metabolism; metabolomics; Microbe; microbial; microbial community; Microbiology; microbiome; Microfluidic Microchips; Microfluidics; microorganism; Mining; Modeling; Modification; Molecular; mouse model; Mus; nanofabrication; nervous system disorder; Nervous System Physiology; Nervous system structure; Neurobiology; Neurologic; Neurosciences; Neurotransmitters; novel; novel therapeutics; nutrition; open source; Pathology; Pathway interactions; Peripheral Nervous System; Phenotype; Physiology; Play; Positioning Attribute; Postdoctoral Fellow; programs; Property; public health relevance; Recruitment Activity; relating to nervous system; Research; Research Training; restoration; Role; Scientist; screening; Serotonin; Serotonin Agents; Signal Transduction; Staging; Symptoms; targeted delivery; Technology; Testing; Therapeutic; Time; Training; Training Programs; transcriptomics; transmission process; undergraduate student
Title:UNCOVERING MICROBIAL MODULATORS OF NEUROACTIVE MOLECULES AS NOVEL THERAPEUTICS.
Awardee Organization:CALIFORNIA INSTITUTE OF TECHNOLOGY
Abstract Text:PROJECT SUMMARY/ABSTRACT Humans are colonized with diverse microbial communities, collectively called the commensal microbiota, that influence a wide array of biological processes. Recent studies demonstrate that in addition to their roles in nutrition, immunity and metabolism, the commensal microbiota also plays a fundamental role in the development and function of the nervous system, in addition to several complex host behaviors. The proposed research training program aims to uncover the mechanisms underlying the interaction between specific commensal microbes and the nervous system, and to elucidate the impact of these relationships on host physiology. Specifically, the proposed research will examine the role of commensal microbes on host serotonin (5-hydroxytrypatmine, 5-HT) metabolism, with aims to define the specific steps of the 5-HT pathway that are affected by commensal microbes, identify the particular microbial species and factors that affect host 5-HT, and apply these microbial 5-HT modulators toward ameliorating symptoms in models of 5-HT-related disease. Findings from these studies will advance our current understanding of how the commensal microbiota affects health and disease, and will further explore the innovative prospect of developing novel, microbe-based therapeutics, which can be readily modified for better function, regulatory control, targeting and delivery. The proposed studies on the interaction between the commensal microbiota and nervous system fills a novel area of multidisciplinary research that integrates not only neurobiology and microbiology, but also biochemistry (in the dissection of molecular alterations in the 5-HT pathway), chemical engineering (in the nanofabrication of microfluidic devices for high-throughput confinement, cultivation and functional screening of endogenous species of the microbiome) and molecular and behavioral neuroscience (in the investigation of pathologies seen in mouse models of serotonin-deficiency). My proposed training will span five years of independent research as a Senior Research Fellow at the California Institute of Technology. This title is typically reserved for individuals with previous post-doctoral experience and serves as a transitional stage toward advancing into a junior faculty position. Approximately one year after the award is conferred, I will recruit one full-time technician, with significant previous experience in laboratory research. I will also begin mentoring up to two biology or chemistry undergraduate students per year through Caltech's summer research program. Public Health Relevance Statement:PUBLIC HEALTH RELEVANCE: Consistent with the staggering finding that our bodies are comprised of over ten times more microbial cells than human eukaryotic cells, scientists are finding that the microbes that make up "us" play important roles in a variety of biological processes. The aim of my proposed research is to uncover how our commensal microbes communicate with the nervous system, and specifically, how particular microbial species alter host levels of serotonin and cause downstream changes in host physiology. Findings from these studies will advance our understanding of how the commensal microbiota impacts health and disease, and will inform the exciting prospect of developing microbe-based therapeutics for disorders of the nervous system. NIH Spending Category:Bioengineering; Biotechnology; Dental/Oral and Craniofacial Disease; NeurosciencesProject Terms:Adverse effects; Affect; Area; Award; base; Behavior; Behavioral; Biochemistry; Biological Process; Biology; Brain; California; cell type; Cells; Chemical Engineering; Chemistry; Colon; commensal microbes; Complex; Data Set; Development; Disease; Dissection; Enabling Factors; Enzymes; Eukaryotic Cell; Exhibits; experience; Faculty; Genomics; Goals; gut microbiota; Health; Human; Immunity; Individual; innovation; insight; Institutes; Interdisciplinary Study; Investigation; Laboratory Research; loss of function; Mediating; Mentors; Metabolism; metabolomics; Microbe; microbial; microbial community; Microbiology; microbiome; Microfluidic Microchips; Microfluidics; microorganism; Mining; Modeling; Modification; Molecular; mouse model; Mus; nanofabrication; nervous system disorder; Nervous System Physiology; Nervous system structure; Neurobiology; Neurologic; Neurosciences; Neurotransmitters; novel; novel therapeutics; nutrition; open source; Pathology; Pathway interactions; Peripheral Nervous System; Phenotype; Physiology; Play; Positioning Attribute; Postdoctoral Fellow; programs; Property; public health relevance; Recruitment Activity; relating to nervous system; Research; Research Training; restoration; Role; Scientist; screening; Serotonin; Serotonin Agents; Signal Transduction; Staging; Symptoms; targeted delivery; Technology; Testing; Therapeutic; Time; Training; Training Programs; transcriptomics; transmission process; undergraduate student