Skip navigation
Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp011v53jx17s
Title: Identification of Bacterial Molecules in Interkingdom Signaling using a Novel High-throughput Screening Platform
Authors: Wang, David C.
Advisors: Bassler, Bonnie
Department: Molecular Biology
Class Year: 2014
Abstract: The coexistence of prokaryotes and eukaryotes in symbiotic and pathogenic relationships depends on the ability of both groups to detect and respond to one another’s secreted molecules. This process is known as interkingdom signaling, and was first used to describe eukaryotic detection of bacterial signaling molecules. However, few of these molecules have been identified, leaving the mechanisms of interkingdom interactions largely unclear. In a process called quorum sensing (QS), bacteria communicate within populations through the secretion and detection of molecules known as autoinducers (AIs). Caenorhabditis elegans, a well-characterized eukaryote with a sophisticated chemosensory system, detects and chemotax to a wide range of bacterial molecules, including bacterial AIs. C. elegans also chemotax to the pathogenic bacterium Vibrio cholerae and the primary V. cholerae AI CAI-1. In this study, we screen the V. cholerae genome to identify additional bacterial molecules that signal to C. elegans. Additionally, we demonstrate the development and use of a novel high-throughput screening platform that results in a 15-fold increase in mutant screening rate. In V. cholerae, we identified 34 candidate mutants that demonstrated altered ability to elicit C. elegans chemotaxis. 23 of the candidate genes are involved in QS, suggesting that bacterial QS may also regulate production and secretion of signals in interkingdom signaling. Additionally, we identified genes involved in toxin biosynthesis, secretion systems, and biofilm formation. These findings elucidate potential molecules and pathways through which bacteria communicate with eukaryotes, and provide insight on the mechanisms of interkingdom signaling and its roles in pathogenicity.
Extent: 73 pages
URI: http://arks.princeton.edu/ark:/88435/dsp011v53jx17s
Type of Material: Princeton University Senior Theses
Language: en_US
Appears in Collections:Molecular Biology, 1954-2016

Files in This Item:
File SizeFormat 
wang_david.pdf5.72 MBAdobe PDF    Request a copy


Items in Dataspace are protected by copyright, with all rights reserved, unless otherwise indicated.