Grant: Project Grant
University of British Columbia
$956,250.00
Peptidoglycan remodeling in Campylobacter jejuni: effects on shape and pathogenesis
EF 2021-22
Résumé
Campylobacter jejuni (Cj) is a leading cause of bacterial food poisoning in humans in the developed world. Yet, it lives harmlessly in the intestinal tract of birds, with up to 90% of commercial poultry products having live Cj on their surfaces. Furthermore, unlike most other prevalent pathogens, its specific pathogenic mechanisms have remained elusive.
Through genetic and computer-based screening, we have uncovered several new factors and means by which this pathogen is so successful in causing human disease, colonizing non-susceptible (commensal) hosts, and surviving in the environment outside of a host. One is its shape. Cj typically has a helical/corkscrew morphology, and this abets its ability to burrow into the intestinal mucosa of both susceptible (i.e., human) and commensal (i.e., poultry) hosts and to survive in inhospitable environments such as air and water. Changes to this shape alter Cj's ability to succeed in specific niches.
Our group has identified the first bacterial factors and biochemical characteristics important for maintaining Cj's helical cell morphology. All of these affect the peptidoglycan layer of the bacterial cell wall. We will use genetic, biochemical, and other approaches to further our understanding of how shape is determined and maintained in Cj, and the biological and pathogenic implications of Cj morphology. Given the importance of Cj shape to its success as a pathogen, this work should provide important insights into Cj biology, how and why Cj is such a prevalent cause of human disease, and clues to its eradication.
Programme
Project Grant
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
443799
Name
Gaynor Erin C
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Microbiology & Infectious Diseases
Projecttitle
Peptidoglycan remodeling in Campylobacter jejuni: effects on shape and pathogenesis
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$956,250
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Bacterial Morphology; Campylobacter Jejuni; Cell Division; Cytoskeletal Elements; Diarrheal Pathogen; Host-Pathogen Interactions; Pathogen Survival And Transmission; Pathogenesis; Peptidoglycan; Peptidoglycan Hydrolases
Abstract
Campylobacter jejuni (Cj) is a leading cause of bacterial food poisoning in humans in the developed world. Yet, it lives harmlessly in the intestinal tract of birds, with up to 90% of commercial poultry products having live Cj on their surfaces. Furthermore, unlike most other prevalent pathogens, its specific pathogenic mechanisms have remained elusive.
Through genetic and computer-based screening, we have uncovered several new factors and means by which this pathogen is so successful in causing human disease, colonizing non-susceptible (commensal) hosts, and surviving in the environment outside of a host. One is its shape. Cj typically has a helical/corkscrew morphology, and this abets its ability to burrow into the intestinal mucosa of both susceptible (i.e., human) and commensal (i.e., poultry) hosts and to survive in inhospitable environments such as air and water. Changes to this shape alter Cj's ability to succeed in specific niches.
Our group has identified the first bacterial factors and biochemical characteristics important for maintaining Cj's helical cell morphology. All of these affect the peptidoglycan layer of the bacterial cell wall. We will use genetic, biochemical, and other approaches to further our understanding of how shape is determined and maintained in Cj, and the biological and pathogenic implications of Cj morphology. Given the importance of Cj shape to its success as a pathogen, this work should provide important insights into Cj biology, how and why Cj is such a prevalent cause of human disease, and clues to its eradication.
Competitiondate
202104
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Gaynor, Erin C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $956,250~ $0~