Dengue virus (DENV), a mosquito-transmitted RNA virus, can cause human hemorrhagic fever, shock and even death, in severe cases. DENV has also been documented as a blood transfusion-transmitted virus. AABB's Transfusion-Transmitted Diseases Committee has recently identified DENV as a high-priority emerging infectious agent with potential risk of transfusion transmission in the United States. Currently, there is no blood screening measure conducted for DENV. Detection methods for DENV in most clinical and research laboratories are nucleic acid amplification assays and enzyme-linked immunosorbent assays (ELISAs). The cost for nucleic acid amplification is high and ELISAs are time-consuming. Therefore, developing an inexpensive, fast, and sensitive test for detection of DENV is crucial to reduce the risk of transfusion-mediated infection and improve timely surveillance. Driven by this need, in this project, we will develop a gold nanoparticle-based, rapid, sensitive and cost-effective label-free Surface Enhanced Raman Spectroscopy (SERS) assay for selective DENV detection in blood. We expect this SERS assay will reduce the reagent cost to 1/10th the cost of nucleic acid amplification assay and detection limit can be below 10 viruses /ml. Furthermore, the SERS assay can be developed into an automated screening assay, which is suitable in blood screen facilities.

Public Health Relevance

Dengue virus can cause dengue hemorrhagic fever, which is the most important mosquito-transmitted viral infection of humans, poses threats to the general human population, including recipients of blood transfusions. In this project, we will develop a gold nanoparticle-based, rapid, sensitive and cost-effective assay for Dengue virus detection in blood.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15AI113706-01
Application #
8773448
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Cassetti, Cristina
Project Start
2014-07-01
Project End
2017-06-30
Budget Start
2014-07-01
Budget End
2017-06-30
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Southern Mississippi
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
City
Hattiesburg
State
MS
Country
United States
Zip Code
39406
Paul, Amber M; Acharya, Dhiraj; Neupane, Biswas et al. (2018) Congenital Zika Virus Infection in Immunocompetent Mice Causes Postnatal Growth Impediment and Neurobehavioral Deficits. Front Microbiol 9:2028
Acharya, Dhiraj; Bastola, Pradip; Le, Linda et al. (2016) An ultrasensitive electrogenerated chemiluminescence-based immunoassay for specific detection of Zika virus. Sci Rep 6:32227
Paul, Amber M; Acharya, Dhiraj; Le, Linda et al. (2016) TLR8 Couples SOCS-1 and Restrains TLR7-Mediated Antiviral Immunity, Exacerbating West Nile Virus Infection in Mice. J Immunol 197:4425-4435
Acharya, Dhiraj; Bai, Fengwei (2016) An Overview of Current Approaches Toward the Treatment and Prevention of West Nile Virus Infection. Methods Mol Biol 1435:249-91
Jones, Stacy; Sinha, Sudarson Sekhar; Pramanik, Avijit et al. (2016) Three-dimensional (3D) plasmonic hot spots for label-free sensing and effective photothermal killing of multiple drug resistant superbugs. Nanoscale 8:18301-18308
Paul, Amber M; Fan, Zhen; Sinha, Sudarson S et al. (2015) Bio-Conjugated Gold Nanoparticle Based SERS Probe for Ultrasensitive Identification of Mosquito-Borne Viruses Using Raman Fingerprinting. J Phys Chem C Nanomater Interfaces 119:23669-23775