4.8 Article

Detection of Dengue Virus 2 with Single Infected Mosquito Resolution Using Yeast Affinity Bionanofragments and Plasmonic SERS Nanoboxes

Journal

ANALYTICAL CHEMISTRY
Volume 94, Issue 41, Pages 14177-14184

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c02012

Keywords

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Funding

  1. ARC DP [DP210103151, DP220100960]
  2. Commonwealth Scientific and Industrial Research Organization Fellowship
  3. National Health and Medical Research Council [APP1173669]
  4. Advance Queensland Industry Research Fellowship COVID19 [AQIRF104-2020-CV]
  5. Australian Government through the National Collaborative Research Infrastructure Strategy (NCRIS) program
  6. Therapeutic Innovation Australia (TIA)

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This study reports an innovative nanobased immunoassay platform for the early, specific, and ultrasensitive detection of DENV2 virus in infected mosquitoes. The platform uses nanomaterials and yeast affinity bionanofragments to enhance the sensitivity and specificity of detection, and employs electrohydrodynamically driven nanomixing to reduce nonspecific interactions. These nanotechnologies provide a significant innovation for preventing the transmission of DENV2.
Dengue disease is an emerging global threat triggered by dengue virus (DENV) transmission, primarily by the mosquito Aedes aegypti. The accurate surveillance and sensitive detection of DENV in mosquito populations are critical for the protection of human populations worldwide that are in the habitat of these mosquito species. There are four DENV serotypes with DENV2 reported to cause the most severe complications. There are limited ultrasensitive methods to early detect DENV2 mosquito infection and prevent human infection. Herein, we report an innovative nanobased immunoassay platform for early, specific, and ultrasensitive detection of DENV2-secreted nonstructural 1 (NS1) protein biomarker in single infected mosquitoes with the limit of detection of 500 fg of recombinant DENV2 NS1. The high sensitivity and DENV2 serotype specificity of the platform are the result of using nanomixing, plasmonic SERS nanoboxes, and yeast affinity bionanofragments displaying single-chain variable fragments (nanoyeast scFvs). Nanoyeast scFvs used for high affinity capture of DENV2 NS1 provided an innovative and cost-efficient alternative to monoclonal antibodies and differentiated DENV2 NS1 from other DENV serotypes and Zika virus NS1. The platform used electrohydrodynamically driven nanomixing to enhance NS1 capture by the nanoyeast scFvs while reducing nonspecific interactions. High sensitivity detection of captured DENV2 NS1 was achieved using NS1-specific surface-enhanced Raman scattering (SERS) nanotags. These nanotechnologies provide a significant innovation for early DENV2 detection in single infected mosquitoes, improving the accurate surveillance of mosquito habitats and preventing infection and severe disease arising from DENV2 transmission.

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