Grant: Master's Award: Canada Graduate Research Scholarships - Master's program
University of Victoria (British Columbia)
$27,000.00
Prior Influenza A Virus Infection as a Catalyst for Fatal Staphylococcus aureus Bacteremia
EF 2025-26
Résumé
The Staphylococcus aureus bacterium and influenza A virus are two pathogens many of us have encountered at least once. S. aureus can cause many different infections, including skin, lung, and bloodstream infections. Its infection of the bloodstream, called S. aureus bacteremia (SAB), is a major cause for concern due to its estimated case fatality rate of 15-50%. Influenza A virus (IAV) is mainly known for causing mild infections of the respiratory tract during the annual flu season, but the virus can cause occasional pandemics with more severe consequences.
Interestingly, these two pathogens are known to work together, since IAV can help S. aureus infect the lungs, which worsens disease symptoms. However, we do not know if IAV infection can increase the risk of S. aureus infection in areas other than the lungs. To investigate this, we analysed data from human SAB cases and found that, concerningly, if a person had an IAV infection before contracting SAB, their risk of death increased by up to 8%.
To investigate how prior IAV infection increases the risk of dying from SAB, we will infect mice with both pathogens. This will allow us to measure how both the virus and bacteria grow, understand how the immune system responds to the infections, and see how the organs are impacted. By infecting mice first with IAV, letting them recover, and then infecting with S. aureus, we can see how having a prior virus infection changes the outcome of a later bacterial infection.
This research will address a major gap in our understanding of how these two infections might affect one another. This can help us develop better treatments which will improve patient outcomes.
Programme
Master's Award: Canada Graduate Research Scholarships - Master's program
Bénéficiaire
Emplacement
British Columbia, Canada
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
573088
Name
Nickel Karen E
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Prcname2
Special Cases - Awards Programs
Projecttitle
Prior Influenza A Virus Infection as a Catalyst for Fatal Staphylococcus aureus Bacteremia
Programtype2
Studentship Programs
Orgnameinp2
University of Victoria (British Columbia)
Cihramount2
$27,000
Cihrequipment2
$0
Programname2
Master's Award: Canada Graduate Research Scholarships - Master's program
Keyworddelim
Bacteremia; Co-Infection; Immune Response; Infection; Influenza A Virus Infection; Mouse Models; Patient-Driven Data; S. Aureus; S. Aureus Infection; Sepsis
Abstract
The Staphylococcus aureus bacterium and influenza A virus are two pathogens many of us have encountered at least once. S. aureus can cause many different infections, including skin, lung, and bloodstream infections. Its infection of the bloodstream, called S. aureus bacteremia (SAB), is a major cause for concern due to its estimated case fatality rate of 15-50%. Influenza A virus (IAV) is mainly known for causing mild infections of the respiratory tract during the annual flu season, but the virus can cause occasional pandemics with more severe consequences.
Interestingly, these two pathogens are known to work together, since IAV can help S. aureus infect the lungs, which worsens disease symptoms. However, we do not know if IAV infection can increase the risk of S. aureus infection in areas other than the lungs. To investigate this, we analysed data from human SAB cases and found that, concerningly, if a person had an IAV infection before contracting SAB, their risk of death increased by up to 8%.
To investigate how prior IAV infection increases the risk of dying from SAB, we will infect mice with both pathogens. This will allow us to measure how both the virus and bacteria grow, understand how the immune system responds to the infections, and see how the organs are impacted. By infecting mice first with IAV, letting them recover, and then infecting with S. aureus, we can see how having a prior virus infection changes the outcome of a later bacterial infection.
This research will address a major gap in our understanding of how these two infections might affect one another. This can help us develop better treatments which will improve patient outcomes.
Competitiondate
202512
Approvedterm2
1 yr 0 mth
Pinamesdelim
Nickel, Karen E
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $27,000~ $0~