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Grant: Doctoral Research Award: Canada Graduate Scholarships

University of British Columbia

$105,000.00

Characterizing interactions between Parkinson's disease-associated Akkermansia muciniphila and the host immune response: how immune-evading Akkermansia may contribute to a prodromal disease state.

FY 2021-22

Summary
Parkinson's disease (PD) is the second most common neurodegenerative disorder in the world, causing motor dysfunction that worsens over time. Gut changes are experienced by nearly all PD patients, and can predate diagnosis by several decades. The types of bacteria present in the gut are different between PD patients and neurotypical people, meaning that bacteria may play an important role in PD development. Akkermansia muciniphila is a bacterium that is usually associated with reduced inflammation, but is enriched in the guts of PD patients and can increase gut inflammation in specific contexts. Akkermansia strongly influences the immune system, which may help to mitigate bacterial infections and in turn reduce PD risk. There are many strains (types) of Akkermansia; while most research has focused on one strain, evidence suggests that different strains have different effects on the human host. I propose to characterize the genetic and functional differences between Akkermansia strains that have been isolated from PD patients and neurotypical people, and determine whether PD-derived strains are associated with worse inflammation during intestinal infection. I will first compare the genomes of eight newly-isolated Akkermansia strains with 39 publicly-available strains in order to determine whether PD strains form a distinct group. I will then characterize their growth and their interaction with host immune system. Select strains of interest will be transferred into mice, who will then be infected with an intestinal pathogen. Infection severity will be monitored, and specific biochemical tests will be used to explore corresponding immune mechanisms. Finally, I will try to promote anti-inflammatory immune mechanisms in these mice using nutritional supplements. Understanding whether PD-derived Akkermansia differs from other strains will help determine the significance of gut bacteria in PD and contribute to the development of effective Akkermansia probiotic therapies.
Program
Doctoral Research Award: Canada Graduate Scholarships
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
459033
Name
Metcalfe-Roach Avril
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Characterizing interactions between Parkinson's disease-associated Akkermansia muciniphila and the host immune response: how immune-evading Akkermansia may contribute to a prodromal disease state.
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Research Award: Canada Graduate Scholarships
Keyworddelim
Aging; Akkermansia Muciniphila; Gut-Brain Axis; Immunity; Infection; Microbiome; Parkinson'S Disease
Abstract
Parkinson's disease (PD) is the second most common neurodegenerative disorder in the world, causing motor dysfunction that worsens over time. Gut changes are experienced by nearly all PD patients, and can predate diagnosis by several decades. The types of bacteria present in the gut are different between PD patients and neurotypical people, meaning that bacteria may play an important role in PD development. Akkermansia muciniphila is a bacterium that is usually associated with reduced inflammation, but is enriched in the guts of PD patients and can increase gut inflammation in specific contexts. Akkermansia strongly influences the immune system, which may help to mitigate bacterial infections and in turn reduce PD risk. There are many strains (types) of Akkermansia; while most research has focused on one strain, evidence suggests that different strains have different effects on the human host. I propose to characterize the genetic and functional differences between Akkermansia strains that have been isolated from PD patients and neurotypical people, and determine whether PD-derived strains are associated with worse inflammation during intestinal infection. I will first compare the genomes of eight newly-isolated Akkermansia strains with 39 publicly-available strains in order to determine whether PD strains form a distinct group. I will then characterize their growth and their interaction with host immune system. Select strains of interest will be transferred into mice, who will then be infected with an intestinal pathogen. Infection severity will be monitored, and specific biochemical tests will be used to explore corresponding immune mechanisms. Finally, I will try to promote anti-inflammatory immune mechanisms in these mice using nutritional supplements. Understanding whether PD-derived Akkermansia differs from other strains will help determine the significance of gut bacteria in PD and contribute to the development of effective Akkermansia probiotic therapies.
Competitiondate
202111
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Metcalfe-Roach, Avril
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~