There has been a tremendous focus in bioinformatics on translation of data from the bench into information and knowledge for clinical decision-making. This includes analysis of human genetics for personalized medicine and treatment. However, there has been much less attention on translational bioinformatics for public health practice such as surveillance of emerging/re-emerging viruses. This involves data acquisition, integration, and analyses of viral genetics to infer origin, spread, and evolution suc as the emergence of new strains. The relevant scientific fields for this practice include certain aspects of molecular epidemiology and phylogeography. Recent attention has focused on viruses of zoonotic origin, which are defined as pathogens that are transmittable between animals and humans. In addition to seasonal influenza and West Nile virus, this classification of pathogens includes novel viruses such as Middle Eastern Respiratory Syndrome and influenza A H7N9. Despite the successes highlighted in the literature, there has been little utilization of bioinformatics resources and tools among state public health, agriculture, and wildlife agencies for zoonotic surveillance. Previously this type of resource has been restricted primarily to those in academia. While bioinformatics has been sparsely used for surveillance of zoonotic viruses, other applications such as Geospatial Information Systems (GIS) have been employed by state health agencies to analyze spatial patterns of infection. This includes software to produce disease maps using an array of data types such as clinical, geographical, or human mobility data for tasks such as, geocoding, clustering, or outbreak detection. In addition, advances in geospatial statistics have enabled health agencies to perform more powerful space-time analyses to infer spatiotemporal patterns. However, these GIS consider only traditional epidemiological data such as location and timing of reported cases and not the genetics of the virus that causes the disease. This prevents health agencies from understanding how changes in the genome of the virus and the associated environment in which it disseminates impacts disease risk. The long-term goal of this proposal is to enhance the identification of geospatial hotspots of zoonotic viruses by applying bioinformatics principles to access, integrate, and analyze viral genetics and spatiotemporal reportable disease data. This project will include approaches from bioinformatics, genetics, spatial statistics, GIS, and epidemiology. To do this, I will first measue the utilization of bioinformatics resources and tools as well as the current approaches and limitations identified by state agencies of public health, agriculture, and wildlife for detecting nd predicting hotspots (clusters) of zoonotic viruses (Aim 1). I will then use this feedback to develo a spatial decision support system for detecting and predicting zoonotic hotspots that applies bioinformatics principles to access, integrate, and analyze viral genetics, environmental, and spatiotemporal reportable disease data (Aim 2).
In Aim 3, I will then evaluate my system for cluster detection and prediction against a system that does not consider viral genetics and relies on traditional spatiotemporal data, and perform validation of the predictive capability. Additional evaluation of the user's satisfaction and system usability will be evaluated.

Public Health Relevance

I will develop and evaluate a spatial decision support system to support surveillance of zoonotic viruses in both human and animal populations. I will use approaches from bioinformatics and public health to integrate genetic sequence data from the virus with data from cases of reported infectious diseases and associated environmental data. A surveillance system that considers the genetics and environment of the virus along with public health data will assist public health officials in making informed decisions regarding risk of infectious diseases.

Agency
National Institute of Health (NIH)
Institute
National Library of Medicine (NLM)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31LM012176-02
Application #
9189635
Study Section
Biomedical Library and Informatics Review Committee (BLR)
Program Officer
Sim, Hua-Chuan
Project Start
2015-12-21
Project End
2018-12-20
Budget Start
2016-12-21
Budget End
2017-12-20
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Arizona State University-Tempe Campus
Department
Biomedical Engineering
Type
Sch Allied Health Professions
DUNS #
943360412
City
Tempe
State
AZ
Country
United States
Zip Code
85287