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Mayaro virus detection by integrating sample preparation with isothermal amplification in portable devices.
Alipanah, Morteza; Manzanas, Carlos; Hai, Xin; Lednicky, John A; Paniz-Mondolfi, Alberto; Morris, J Glenn; Fan, Z Hugh.
Affiliation
  • Alipanah M; Interdisciplinary Microsystems Group, Department of Mechanical and Aerospace Engineering, University of Florida, P.O. Box 116250, Gainesville, FL, 32611, USA.
  • Manzanas C; Interdisciplinary Microsystems Group, Department of Mechanical and Aerospace Engineering, University of Florida, P.O. Box 116250, Gainesville, FL, 32611, USA.
  • Hai X; Interdisciplinary Microsystems Group, Department of Mechanical and Aerospace Engineering, University of Florida, P.O. Box 116250, Gainesville, FL, 32611, USA.
  • Lednicky JA; Emerging Pathogens Institute, University of Florida, P.O. Box 100009, Gainesville, FL, 32610, USA. jlednicky@phhp.ufl.edu.
  • Paniz-Mondolfi A; Department of Environmental and Global Health, University of Florida, PO Box 100188, Gainesville, FL, 32610, USA. jlednicky@phhp.ufl.edu.
  • Morris JG; Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, 1425 Madison Ave, New York, NY, 10029, USA.
  • Fan ZH; Emerging Pathogens Institute, University of Florida, P.O. Box 100009, Gainesville, FL, 32610, USA.
Anal Bioanal Chem ; 415(23): 5605-5617, 2023 Sep.
Article in En | MEDLINE | ID: mdl-37470813
Mayaro virus (MAYV) is an emerging mosquito-borne alphavirus that causes clinical symptoms similar to those caused by Chikungunya virus (CHIKV), Dengue virus (DENV), and Zika virus (ZIKV). To differentiate MAYV from these viruses diagnostically, we have developed a portable device that integrates sample preparation with real-time, reverse-transcription, loop-mediated isothermal amplification (rRT-LAMP). First, we designed a rRT-LAMP assay targeting MAYV's non-structural protein (NS1) gene and determined the limit of detection of at least 10 viral genome equivalents per reaction. The assay was specific for MAYV, without cross-reactions with CHIKV, DENV, or ZIKV. The rRT-LAMP assay was integrated with a sample preparation device (SPD) wherein virus lysis and RNA enrichment/purification were carried out on the spot, without requiring pipetting, while subsequent real-time amplification device (RAD) enables virus detection at the point of care (POC). The functions of our platform were demonstrated using purified MAYV RNA or blood samples containing viable viruses. We have used the devices for detection of MAYV in as short as 13 min, with limit of detection to as low as 10 GEs/reaction.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chikungunya virus / Zika Virus / Zika Virus Infection Type of study: Diagnostic_studies Limits: Animals / Humans Language: En Journal: Anal Bioanal Chem Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chikungunya virus / Zika Virus / Zika Virus Infection Type of study: Diagnostic_studies Limits: Animals / Humans Language: En Journal: Anal Bioanal Chem Year: 2023 Type: Article Affiliation country: United States