Broad, long-term objectives: The research objectives stated herein, and in future studies that would build upon these findings, seek to reveal general scientific principles in the mechanisms that drive 'spillover' and adaption of zoonotic RNA viruses. Significance: RNA viruses contribute to more than half of all human infectious diseases that have originated as zoonoses. Wildlife studies to form a complete understanding of RNA viral- host interactions, especially those that directly test the impact of ecological pressures onviral spread during contact and the first adaptive steps of the virus during spillover can provide important insights. Specifically, the study of the emergence and adaption of hantaviruses can provide critical data for: (1) models for prediction of RNA viral emergence and mitigation; (2) identification of viral and host targets for therapeutic intervention; and (3) a basic understandin of the selective pressures that modulate viral-host interactions and viral genetic variation.
Specific aims : We propose field and laboratory studies using South American hantaviruses as a model system to test specific selective pressures to reveal evolutionary mechanisms of RNA virus adaption in reservoir (HR) and spillover host (HS) host systems. The three Aims proposed will: (1) define viral emergence within host reservoirs and sympatric rodent species during extrinsic (environmental) pressure; (2) reveal the relationship of extrinsic (environment & ecological) pressures on preexisting intrahost genetic variation in wild rodent populations; and, (3) define viral fitness, virulence, and genotype during adaptation to new host species in vitro. Research design and methods: The proposed field site for Aim 1 lies in eastern Paraguay, where two hantaviruses co-circulate, and where elevated seroprevalence levels of hantaviruses are associated with anthropogenic alteration of land use. We propose to assess effects of: (1) increased food resources and (2) reduced predation on virus prevalence (Aim 1) and intra- and interhost genetic variation in rodents within native and disturbed forest areas (Aim 2).
In Aim 3, we focus on the fitness and virulence of these viruses and the genetic changes that lead to adaptation. Using primary endothelial cell culture-based approaches, we will define the impact of intrinsic (host) selective pressures occurring when a new host species, HS, interacts with virus as it replicates, adapts to a new host host.

Public Health Relevance

Greater than half of all human infectious diseases begin through the cross-species transmission of RNA viruses from wildlife to humans. Hantaviruses provide an exceptional model system for the study of RNA virus spillover as significant source of outbreaks; zoonotic infections and human disease. This study examines genetic determinants which facilitate spread in its rodent reservoir and its adaptation in vitro to new rodents; which wll in turn provide understanding and prediction of human-environmental interactions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI103053-04
Application #
9248840
Study Section
Virology - B Study Section (VIRB)
Program Officer
Challberg, Mark D
Project Start
2014-04-01
Project End
2018-03-31
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
4
Fiscal Year
2017
Total Cost
$367,746
Indirect Cost
$91,313
Name
University of Tennessee Knoxville
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
003387891
City
Knoxville
State
TN
Country
United States
Zip Code
37996