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A multiplex fluorescence microsphere immunoassay for increased understanding of Rift Valley fever immune responses in ruminants in Kenya.
Lindahl, Johanna F; Ragan, Izabela K; Rowland, R R; Wainaina, Martin; Mbotha, Deborah; Wilson, William.
Affiliation
  • Lindahl JF; International Livestock Research Institute, Nairobi, Kenya; Zoonosis Science Center, Uppsala University, Uppsala, Sweden; Swedish University of Agricultural Research, Uppsala, Sweden. Electronic address: J.Lindahl@cgiar.org.
  • Ragan IK; Department of Biomedical Sciences, Colorado State University, Fort Collins, CO, USA; Department of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA.
  • Rowland RR; Department of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, KS, USA.
  • Wainaina M; International Livestock Research Institute, Nairobi, Kenya.
  • Mbotha D; International Livestock Research Institute, Nairobi, Kenya; Institute for Parasitology and Tropical Veterinary Medicine, Freie Universitaet Berlin, Berlin, Germany.
  • Wilson W; Arthropod-Borne Animal Diseases Research Unit, USDA, ARS, Manhattan, KS, USA.
J Virol Methods ; 269: 70-76, 2019 07.
Article in En | MEDLINE | ID: mdl-30974177
ABSTRACT
Rift Valley fever virus (RVFV) is an important mosquito-borne pathogen with devastating impacts on agriculture and public health. With outbreaks being reported beyond the continent of Africa to the Middle East, there is great concern that RVFV will continue to spread to non-endemic areas such as the Americas and Europe. There is a need for safe and high throughput serological assays for rapid detection of RVFV during outbreaks and for surveillance. We evaluated a multiplexing fluorescence microsphere immunoassay (FMIA) for the detection of IgG and IgM antibodies in ruminant sera against the RVFV nucleocapsid Np, glycoprotein Gn, and non-structural protein NSs. Sheep and cattle sera from a region in Kenya with previous outbreaks were tested by FMIA and two commercially available competitive ELISAs (BDSL and IDvet). Our results revealed strong detection of RVFV antibodies against the Np, Gn and NSs antigen targets. Additionally, testing of samples with FMIA Np and Gn had 100% agreement with the IDvet ELISA. The targets developed in the FMIA assay provided a basis for a larger ruminant disease panel that can simultaneously screen several abortive and zoonotic pathogens.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rift Valley Fever / Immunoassay / Fluorescent Antibody Technique / High-Throughput Screening Assays / Antibodies, Viral Type of study: Diagnostic_studies / Evaluation_studies Limits: Animals Country/Region as subject: Africa Language: En Journal: J Virol Methods Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rift Valley Fever / Immunoassay / Fluorescent Antibody Technique / High-Throughput Screening Assays / Antibodies, Viral Type of study: Diagnostic_studies / Evaluation_studies Limits: Animals Country/Region as subject: Africa Language: En Journal: J Virol Methods Year: 2019 Document type: Article