Project 2: Modeling the Pathogenic Processes of Shigella in the Human Colonoid Model Shigella is one of the most important diarrheal pathogens among children in developing countries. Recent data from the Global Enteric Multicenter Study (GEMS) identified Shigella as the most important pathogen in children in the two older age groups (encompassing children 12-59 months of age). Infections by this pathogen result in severe outcomes, increasing antibiotic resistance is limiting therapeutic options and there is no licensed vaccine for Shigella. The study of this enteric pathogen and advancement of new or improved vaccines and therapeutics has suffered from a lack of preclinical models that reflect relevant human disease pathophysiology. The human enteroid/colonoid ?mini-gut? model presents a technological leap in human GI system modeling that will allow identification of highly relevant host-pathogen interactions that are expected to lead to the discovery of novel points of intervention for therapeutic options and vaccine development. We propose to use this innovative system to answer questions about pathogenic processes that have not yet been sufficiently explored, including mechanisms of entry and invasion, apical and basolateral surface contributions, interactions with host cell factors including mucus, and the role of bacterial virulence factors including Pic. The development of the multi-cellular colonoids grown as a monolayers on Transwell filters yields direct access to both apical and basolateral surfaces which express physiologic mucus, facilitates the engraftment of immune cells such as macrophages and dendritic cells and allows quantification of neutrophil transmigration. This project will define optimal parameters for Shigella-colonoid infection studies that will allow identification of critical pathogenic mechanisms, and host cell responses. Furthermore, this system will be developed to serve as a preclinical model for evaluation of live attenuated Shigella vaccine candidates to accelerate advancement of urgently needed intervention strategies.

Public Health Relevance

Shigella is one of the most important diarrheal pathogens among children developing countries where it is among the top four pathogens contributing the highest disease burden and are associated with severe outcomes. The use of the enteroid/colonoid system, mimicking human GI physiology, will result in novel insights into disease mechanisms and identify new targets for urgently needed novel therapeutics and efficacious vaccines.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI125181-05
Application #
9982182
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
2021-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
5
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Maryland Baltimore
Department
Type
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Singh, Varsha; Yang, Jianbo; Yin, Jianyi et al. (2018) Cholera toxin inhibits SNX27-retromer-mediated delivery of cargo proteins to the plasma membrane. J Cell Sci 131:
Kumar, Pardeep; Kuhlmann, F Matthew; Chakraborty, Subhra et al. (2018) Enterotoxigenic Escherichia coli-blood group A interactions intensify diarrheal severity. J Clin Invest 128:3298-3311
Yin, Jianyi; Tse, Chung-Ming; Avula, Leela Rani et al. (2018) Molecular Basis and Differentiation-Associated Alterations of Anion Secretion in Human Duodenal Enteroid Monolayers. Cell Mol Gastroenterol Hepatol 5:591-609
Noel, Gaelle; Doucet, Michele; Nataro, James P et al. (2017) Enterotoxigenic Escherichia coli is phagocytosed by macrophages underlying villus-like intestinal epithelial cells: modeling ex vivo innate immune defenses of the human gut. Gut Microbes :0
Noel, Gaelle; Baetz, Nicholas W; Staab, Janet F et al. (2017) A primary human macrophage-enteroid co-culture model to investigate mucosal gut physiology and host-pathogen interactions. Sci Rep 7:45270