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Grant: Discovery Launch Supplement

The University of Western Ontario

$12,500.00

Understanding cell envelope modification pathways to facilitate development of improved control strategies for bacterial foodborne pathogens

FY 2024-25

Summary
Most antimicrobials that kill or inhibit growth of bacterial pathogens target the cell envelope (i.e. exterior of the bacterial cell). Cell envelope composition and structure, as well as the expression of cell envelope genes, are severely affected by environmental conditions. Given the unique environment of foods (e.g. pH, temperature, salt content) and food-related settings (e.g. use of sanitizers), it is imperative to understand how these conditions affect the structure and regulation of expression of cell envelope components, since this will in turn affect the successful implementation of antimicrobial strategies against foodborne pathogens. The human and animal pathogen Listeria monocytogenes (Lm) contaminates foods and poses a major threat as it can grow at refrigerated temperatures to potentially infectious levels for susceptible individuals. In elderly, immunocompromised, and pregnant individuals infection with Lm, or listeriosis, has a 20-30% mortality rate. Lm contamination of foods is particularly problematic for ready-to-eat (RTE) food products, which aren't cooked before consumption. Detection of Lm in high-risk RTE food products leads to product recalls which pose significant economic hardships to our food industry. Our previous research using Lm isolates from food recalls and outbreaks showed that the environment (e.g. temperature and pH), as well as Lm serotype, affect resistance to the bacteriocin nisin and to an anti-Lm phage cocktail in both a fresh-style cheese model and in cold-smoked salmon. Understanding the molecular strategies employed by Lm to counteract cell envelope-acting treatments in relevant food matrices would improve our use of antimicrobial strategies in foods and decrease potential outbreaks and recalls. The short-term goals of my research program are to: Aim1. Characterize expression of key Lm cell envelope constituents under food-relevant environmental conditions. Aim2. Identify genes essential for Lm growth in food-related matrices. The long-term vision of my program is to use this information to improve current and develop new strategies for foodborne pathogen control. Novelty and Significance: There is a current lack of understanding of how the food-specific environment affects the cell envelope composition of the important, deadly, and costly foodborne pathogen Lm. Given how cell envelope composition in turn affects the efficiency of antimicrobial strategies, it is imperative to fill this knowledge gap and harness our enhanced understanding for the discovery of novel, and improvement of current, control strategies for foodborne pathogens. My research to date has focused on understanding cell envelope stress response in different microbes, using an arsenal of microbiological, molecular, and biochemical techniques, therefore, my group has the unique and novel opportunity to translate and apply these approaches to better understand the survival strategies employed by Lm in RTE foods.
Program
Discovery Launch Supplement
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
DGECR-2024-00212
Name nom
Guariglia Oropeza, Veronica
Department département
Microbiology and Immunology
Organization id
36
Institution établissement
The University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2024
Competition year année de concours
2024
Award amount
12500
Program id
DGECR
Program name en
Discovery Launch Supplement
Program name fr
Supplément Tremplin vers la découverte
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5201
Research subject group en
Microbiology
Research subject group fr
Microbiologie
Research subject en
Bacteriology
Research subject fr
Bactériologie
Field of research list names en
Not available
Field of research list names fr
Non disponible
Socioeconomic objective list names en
Not available
Socioeconomic objective list names fr
Non disponible
Application title
Understanding cell envelope modification pathways to facilitate development of improved control strategies for bacterial foodborne pathogens
Keywords
listeria monocytogenes; cell wall stress response; gene regulation; food safety; transcriptomics; foodborne pathogens
Application summary
Most antimicrobials that kill or inhibit growth of bacterial pathogens target the cell envelope (i.e. exterior of the bacterial cell). Cell envelope composition and structure, as well as the expression of cell envelope genes, are severely affected by environmental conditions. Given the unique environment of foods (e.g. pH, temperature, salt content) and food-related settings (e.g. use of sanitizers), it is imperative to understand how these conditions affect the structure and regulation of expression of cell envelope components, since this will in turn affect the successful implementation of antimicrobial strategies against foodborne pathogens. The human and animal pathogen Listeria monocytogenes (Lm) contaminates foods and poses a major threat as it can grow at refrigerated temperatures to potentially infectious levels for susceptible individuals. In elderly, immunocompromised, and pregnant individuals infection with Lm, or listeriosis, has a 20-30% mortality rate. Lm contamination of foods is particularly problematic for ready-to-eat (RTE) food products, which aren't cooked before consumption. Detection of Lm in high-risk RTE food products leads to product recalls which pose significant economic hardships to our food industry. Our previous research using Lm isolates from food recalls and outbreaks showed that the environment (e.g. temperature and pH), as well as Lm serotype, affect resistance to the bacteriocin nisin and to an anti-Lm phage cocktail in both a fresh-style cheese model and in cold-smoked salmon. Understanding the molecular strategies employed by Lm to counteract cell envelope-acting treatments in relevant food matrices would improve our use of antimicrobial strategies in foods and decrease potential outbreaks and recalls. The short-term goals of my research program are to: Aim1. Characterize expression of key Lm cell envelope constituents under food-relevant environmental conditions. Aim2. Identify genes essential for Lm growth in food-related matrices. The long-term vision of my program is to use this information to improve current and develop new strategies for foodborne pathogen control. Novelty and Significance: There is a current lack of understanding of how the food-specific environment affects the cell envelope composition of the important, deadly, and costly foodborne pathogen Lm. Given how cell envelope composition in turn affects the efficiency of antimicrobial strategies, it is imperative to fill this knowledge gap and harness our enhanced understanding for the discovery of novel, and improvement of current, control strategies for foodborne pathogens. My research to date has focused on understanding cell envelope stress response in different microbes, using an arsenal of microbiological, molecular, and biochemical techniques, therefore, my group has the unique and novel opportunity to translate and apply these approaches to better understand the survival strategies employed by Lm in RTE foods.
The University of Western Ontario - $12,500 Grant (20… | Canada Spends