The basis of Influenza A virus strain-dependent reassortment potential
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 1R01AI179873-01
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Key facts
Disease
UnspecifiedStart & end year
20242029Known Financial Commitments (USD)
$416,635Funder
National Institutes of Health (NIH)Principal Investigator
ASSISTANT PROFESSOR Samuel DiazResearch Location
United States of AmericaLead Research Institution
UNIVERSITY OF CALIFORNIA AT DAVISResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Pathogen morphology, shedding & natural history
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
Abstract DESCRIPTION: Influenza viruses can exchange genome segments and generate new viruses when they infect the same cell, a process called reassortment. These new viruses can worsen seasonal flu epidemics or spark global pandemics. We recently found that patterns of reassortment show strong strain-dependence, and do not necessarily track similarity between coinfecting strains or their subtype (H1N1 or H3N2). The specific factors underlying this strain dependence remain unclear. The role of protein incompatibilities in restricting segment exchange was thought to be associated with different subtypes. However, experimental tests of the role of subtype in promoting or restricting reassortment remain very limited, and the specific protein incompatibilities (antigenic versus polymerase complex) that are most important in shaping reassortment remain unknown. Using our high-throughput tools, we propose to uncover the basis of strain dependent reassortment potential. First, we will quantify reassortment patterns within and between co-circulating human influenza strains of both subtypes and measure differences in entry and coinfection. Second, we will use mutants to test the effect of antigenic versus polymerase complex segments in driving reassortment potential. Finally, we will examine whether post-reassortment mutations can compensate fitness in strains arising from between-subtype reassortment and their fitness in different host cell types. Collectively these aims will provide basic insight into the factors affecting strain dependence in reassortment potential and provide actionable data to refocus surveillance and pandemic preparedness efforts.