Research' Project 1 focuses on significant endemic viral pathogens from humans and viruses from animal hosts that have strong zoonotic potential. High-throughput whole-genome next-generation sequencing (NGS), combined with bioinformatics algorithms, will be used to sequence and analyze the genomes from more than 10,000 strains representing seven viral species. This will characterize the genetic diversity over a range of virus families, including many NIAID priority pathogens, to understand critical evolutionary mechanisms central to viral evolution, pathogenesis, transmission, and/or antiviral resistance. Specifically we aim to: 1) compare and contrast the genetic diversity and evolutionary dynamics of viruses circulating within and/or between humans and animal reservoirs, 2) elucidate viral-host-microbiome determinants that influence viral pathogenesis, and 3) perform deep sequencing to understand intra-host viral diversity, transmission dynamics, and antiviral resistance. Collectively, this project will use multiple genomics approaches (e.g., genomic sequencing, metagenomics, and transcriptomics) to provide the scientific community with genomic data sets of broad use from important viral families. These data will be analyzed using phylogenetics and other bioinformatics algorithms to show the spatial and temporal evolution of these pathogens. Finally, the data generated will identify, track, and predict antigenic drift/shift, recombination, escape from natural or vaccine-induced host immune responses, antiviral resistance, inter- and intra-species transmission, and the response of a host's commensal microbiota to viral infection. The information generated from these studies will help us to produce superior vaccines and antivirals, and the data sets will prove critical for rapid responses to the emergence of novel pathogens (i.e., pandemic preparedness) that arise naturally or as a result of bioterrorism.

Public Health Relevance

Viruses are global pathogens that cause significant disease in humans. Frequent transmission of animal viruses to human hosts and human-to-human transmission result in outbreaks, epidemics, or pandemics. Therefore, Project 1 will target significant and emerging viral pathogens from human and animal hosts for genome sequencing in an effort to sequence virus species that could significantly impact public health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI110819-04
Application #
9241322
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2017-04-01
Budget End
2018-03-31
Support Year
4
Fiscal Year
2017
Total Cost
Indirect Cost
Name
J. Craig Venter Institute, Inc.
Department
Type
DUNS #
076364392
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Rajagopala, Seesandra V; Singh, Harinder; Patel, Mira C et al. (2018) Cotton rat lung transcriptome reveals host immune response to Respiratory Syncytial Virus infection. Sci Rep 8:11318
Shrivastava, Susmita; Puri, Vinita; Dilley, Kari A et al. (2018) Whole genome sequencing, variant analysis, phylogenetics, and deep sequencing of Zika virus strains. Sci Rep 8:15843
Peirano, Gisele; Matsumura, Yasufumi; Adams, Mark D et al. (2018) Genomic Epidemiology of Global Carbapenemase-Producing Enterobacter spp., 2008-2014. Emerg Infect Dis 24:1010-1019
Inman, Jason M; Sutton, Granger G; Beck, Erin et al. (2018) Large-Scale Comparative Analysis of Microbial Pan-genomes using PanOCT. Bioinformatics :
Clarke, Thomas H; Brinkac, Lauren M; Sutton, Granger et al. (2018) GGRaSP: a R-package for selecting representative genomes using Gaussian mixture models. Bioinformatics 34:3032-3034
Holden, Victoria I; Wright, Meredith S; Houle, Sébastien et al. (2018) Iron Acquisition and Siderophore Release by Carbapenem-Resistant Sequence Type 258 Klebsiella pneumoniae. mSphere 3:
Becka, Scott A; Zeiser, Elise T; Marshall, Steven H et al. (2018) Sequence heterogeneity of the PenA carbapenemase in clinical isolates of Burkholderia multivorans. Diagn Microbiol Infect Dis 92:253-258
Chan, Agnes P; Choi, Yongwook; Brinkac, Lauren M et al. (2018) Multidrug resistant pathogens respond differently to the presence of co-pathogen, commensal, probiotic and host cells. Sci Rep 8:8656
Oldfield, Lauren M; Fedorova, Nadia; Puri, Vinita et al. (2018) Sequences of Zika Virus Genomes from a Pediatric Cohort in Nicaragua. Genome Announc 6:
Marino, Nicole D; Panas, Michael W; Franco, Magdalena et al. (2018) Identification of a novel protein complex essential for effector translocation across the parasitophorous vacuole membrane of Toxoplasma gondii. PLoS Pathog 14:e1006828

Showing the most recent 10 out of 72 publications