Monoclonal Antibodies for Rift Valley Fever Virus Nucleocapsid: Application in IgG/IgM ELISA for Sero-Diagnosis.

IgG ELISA IgM capture ELISA Rift Valley fever virus monoclonal antibody nucleocapsid protein

Journal

Pathogens (Basel, Switzerland)
ISSN: 2076-0817
Titre abrégé: Pathogens
Pays: Switzerland
ID NLM: 101596317

Informations de publication

Date de publication:
13 Jul 2024
Historique:
received: 31 05 2024
revised: 07 07 2024
accepted: 11 07 2024
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 26 7 2024
Statut: epublish

Résumé

Rift Valley fever virus (RVFV) belonging to the Phenuiviridae family is responsible for a zoonotic disease called Rift Valley fever (RVF). Currently, RVFV has spread from Africa to Asia, and due to its ability to cause high mortality rates, it has significantly impacted human health and economic development in many societies. Highly specific and sensitive systems for sero-diagnosis of RVFV infection are needed for clinical use. BALB/c mice were immunized with recombinant RVFV nucleocapsid (rRVFV-N) protein and the spleen cells fused with SP2/0 myeloma cells to create hybridoma cell lines. The secreted monoclonal antibodies (MAbs) were purified and characterized. Enzyme-linked immunosorbent assay (ELISA) systems for the detection of IgG and IgM using the new MAbs were established and evaluated. Serum samples from 96 volunteers and 93 patients of suspected RVF from Kenya were tested compared with the ELISA systems based on inactivated viruses and the rabbit polyclonal antibody. Three monoclonal antibodies against rRVFV-N protein were established. The performance of the MAb-based sandwich IgG ELISA and the IgM capture ELISA perfectly matched the ELISA systems using the inactivated virus or the polyclonal antibody. Recombinant RVFV-N protein-specific MAbs were developed and they offer useful tools for RVFV studies. The MAb-based ELISA systems for detecting IgG and IgM offer safe and useful options for diagnosing RVFV infections in humans.

Identifiants

pubmed: 39057809
pii: pathogens13070582
doi: 10.3390/pathogens13070582
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : National Natural Science Foundation of China
ID : (2017) 81760605

Auteurs

Jiansheng Huang (J)

School of Medicine, Guizhou University, Guiyang 550002, China.

Ferdinard Adungo (F)

Kenya Medical Research Institute, Nairobi 54840-00200, Kenya.

Samson Limbaso Konongoi (SL)

Kenya Medical Research Institute, Nairobi 54840-00200, Kenya.

Shingo Inoue (S)

Department of Virology, Institute of Tropical Medicine, Nagasaki University, 1-12-4, Sakamoto, Nagasaki 852-8523, Japan.

Lin Zhan (L)

NHC Key Laboratory of Pulmonary Immunological Diseases, Guizhou Provincial People's Hospital, Guiyang 550002, China.
Guizhou Provincial People's Hospital, Guizhou University, Guiyang 550002, China.

Rosemary Sang (R)

Kenya Medical Research Institute, Nairobi 54840-00200, Kenya.

Salame Ashur (S)

Kenya Medical Research Institute, Nairobi 54840-00200, Kenya.

Allan Ole Kwallah (AO)

Kenya Medical Research Institute, Nairobi 54840-00200, Kenya.

Matilu Mwau (M)

Kenya Medical Research Institute, Nairobi 54840-00200, Kenya.

Kouichi Morita (K)

Department of Virology, Institute of Tropical Medicine, Nagasaki University, 1-12-4, Sakamoto, Nagasaki 852-8523, Japan.

Fuxun Yu (F)

NHC Key Laboratory of Pulmonary Immunological Diseases, Guizhou Provincial People's Hospital, Guiyang 550002, China.
Guizhou Provincial People's Hospital, Guizhou University, Guiyang 550002, China.

Classifications MeSH