Thursday, November 21, 2024
11/21/2024
PROJECT SUMMARY Hematophagous arthropods transmit numerous viruses, many of which are serious human pathogens. To combat the growing public health impact of arthropod-transmitted viruses, many metagenomics studies have been performed to characterize the arthropod virome. The importance of proactive virus discovery cannot be understated because it allows risk assessments to be performed and viral diagnostic assays and control strategies to be developed before virus spillover occurs. Most metagenomics studies designed to identify novel arthropod- associated viruses have focused on mosquitoes, with other hematophagous arthropods being largely neglected. Another limitation of many previous studies is that virus isolation was not attempted, with newly discovered viruses known only from sequence data, which has impeded their phenotypic and serological characterization. The overall goal of this grant application is to define the virosphere of understudied hematophagous arthropods and to identify and characterize novel viruses capable of vertebrate cell replication. Two specific aims have been designed to achieve this goal. In specific aim 1, a diverse range blood-feeding arthropods (ticks, midges, sandflies, blackflies, and fleas) will be assayed for novel and previously recognized viruses by unbiased high-throughput sequencing (UHTS). These experiments will be performed using homogenates already in our possession and prepared from >37,000 arthropods from North America. Total RNA will be directly extracted from every homogenate and viral sequences will be identified using UHTS and an established bioinformatics pipeline, allowing the virosphere of the arthropods to be defined. Additionally, the codon and dinucleotide frequencies of every novel virus will be determined to provide insight into their host ranges and to identify those most likely to replicate in vertebrate cells. In this regard, vertebrates and invertebrates preferentially have certain codon and dinucleotide usage biases and the preferences of RNA viruses often mimic those of their hosts. In specific aim 2, an aliquot of each homogenate will be inoculated onto human and nonhuman primate cells then two blind passages will be performed. Total RNA will be extracted from all final culture passages and analyzed by UHTS and bioinformatics in order to specifically identify vertebrate-infecting viruses. If an isolate is not recovered but the homogenate is predicted to contain a vertebrate-infecting virus, as determined in the codon and dinucleotide frequency analysis, virus isolation will be attempted using additional vertebrate cell lines. The in vitro replication kinetics and yields of every novel virus capable of vertebrate cell replication will be determined. The studies proposed in this grant application provide the groundwork for future in vivo experiments, where viruses capable of vertebrate cell replication will be further characterized. Experimental infections will be performed with vertebrate animals and arthropods to assess viral virulence and to identify competent vector species, respectively. Future experiments will also be performed to determine the incidence and seroprevalence of select viruses in human and vertebrate animal populations.
HHS’ Tracking Accountability in Government Grants System (TAGGS) website provides access to detailed descriptions of grants, loans, aggregated direct payments and other types of financial assistance awarded by the HHS Operating Divisions (OPDIVs) and the Office of the Secretary Staff Divisions (STAFFDIVs).
