Bacterial meningitis continues to be an important cause of mortality and morbidity. A major contributing factor to such mortality and morbidity is our incomplete knowledge on the pathogenesis of this disease. E. coli is the most common Gram-negative bacillary organism causing meningitis, but the pathogenesis of E. coli meningitis remains incompletely understood. Several lines of evidence from human cases and experimental animal models of E. coli meningitis indicate that E. coli penetration into the brain follows a high level of bacteremia and cerebral capillaries are the portal of entry into the brain. Since E. coli penetration into the brain occurred in the cerebral microvasculature, we developed the blood-brain barrier model with human brain microvascular endothelial cells (HBMEC) to study E. coli penetration of the blood-brain barrier. Our HBMEC monolayer, upon cultivation on collagen-coated Transwells, exhibits spatial organization of tight and adherens junction proteins as well as a polarized monolayer, a unique property of the blood-brain barrier endothelial cells. We have shown for the first time that meningitis-causing E. coli strains exhibit the ability to invade the HBMEC monolayer in vitro and that the ability of HBMEC invasion is correlated with E. coli penetration into the brain in vivo. The mechanisms involved in E. coli penetration of the blood-brain barrier, however, remain incompletely understood. Our preliminary studies revealed a novel mechanism exploited by meningitis-causing E. coli for invasion of the blood-brain barrier, and also suggest that such mechanism is likely to contribute to another meningitis-causing pathogen for penetration of the blood-brain barrier. Determination and characterization of such new mechanism will, therefore, provide a paradigm-shifting strategy for elucidating the pathogenesis of bacterial meningitis.

Public Health Relevance

Bacterial meningitis is of considerable public health interest, and it is important to develop a new strategy for its prevention and therapy. This project aims to elucidate the novel mechanism involved in the pathogenesis of bacterial meningitis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AI113273-02
Application #
9243956
Study Section
Special Emphasis Panel (ZRG1-IDM-B (80)S)
Program Officer
Ernst, Nancy Lewis
Project Start
2016-03-15
Project End
2018-02-28
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
2
Fiscal Year
2017
Total Cost
$202,500
Indirect Cost
$77,500
Name
Johns Hopkins University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Zhao, Wei-Dong; Liu, Dong-Xin; Wei, Jia-Yi et al. (2018) Caspr1 is a host receptor for meningitis-causing Escherichia coli. Nat Commun 9:2296
Wang, Xiangru; Maruvada, Ravi; Morris, Andrew J et al. (2016) Sphingosine 1-Phosphate Activation of EGFR As a Novel Target for Meningitic Escherichia coli Penetration of the Blood-Brain Barrier. PLoS Pathog 12:e1005926
Kim, Kwang Sik (2016) Human Meningitis-Associated Escherichia coli. EcoSal Plus 7: