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Establishment of an immunofluorescence assay to detect IgM antibodies to Nipah virus using HeLa cells expressing recombinant nucleoprotein.
Kaku, Yoshihiro; Park, Eun-Sil; Noguchi, Akira; Inoue, Satoshi; Lunt, Ross; Malbas, Fedelino F; Demetria, Catalino; Neoh, Hui-Min; Jamal, Rahman; Morikawa, Shigeru.
Afiliação
  • Kaku Y; Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo, 162-8640, Japan. Electronic address: ykaku@niid.go.jp.
  • Park ES; Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo, 162-8640, Japan.
  • Noguchi A; Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo, 162-8640, Japan.
  • Inoue S; Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo, 162-8640, Japan.
  • Lunt R; Australian Animal Health Laboratory, 5 Portarlington Road, East Geelong, Vic, 3220, Australia.
  • Malbas FF; Research Institute for Tropical Medicine, 9002 Research Dr, Alabang, Muntinlupa, 1781, Metro Manila, Philippines.
  • Demetria C; Research Institute for Tropical Medicine, 9002 Research Dr, Alabang, Muntinlupa, 1781, Metro Manila, Philippines.
  • Neoh HM; UKM Medical Molecular Biology Institute (UMBI), Pusat Perubatan UKM, Jalan Yaacob Latiff, Bandar Tun Razak, Universiti Kebangsaan Malaysia, 56000, Cheras, Kuala Lumpur, Malaysia.
  • Jamal R; UKM Medical Molecular Biology Institute (UMBI), Pusat Perubatan UKM, Jalan Yaacob Latiff, Bandar Tun Razak, Universiti Kebangsaan Malaysia, 56000, Cheras, Kuala Lumpur, Malaysia.
  • Morikawa S; Department of Veterinary Science, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Tokyo, 162-8640, Japan.
J Virol Methods ; 269: 83-87, 2019 07.
Article em En | MEDLINE | ID: mdl-30954461
ABSTRACT
A novel indirect fluorescent antibody test (IFAT) for detection of IgM against Nipah virus (NiV) was developed using HeLa 229 cells expressing recombinant NiV nucleocapsid protein (NiV-N). The NiV IFAT was evaluated using three panels of sera a) experimentally produced sera from NiV-N-immunized/pre-immunized macaques, b) post-infection human sera associated with a Nipah disease outbreak in the Philippines in 2014, and c) human sera from a non-exposed Malaysian population. Immunized macaque sera showed a characteristic granular staining pattern of the NiV-N expressed antigen in HeLa 229 cells, which was readily distinguished from negative-binding results of the pre-immunized macaque sera. The IgM antibody titers in sequential serum samples (n = 7) obtained from three Nipah patients correlated well with previously published results using conventional IgM capture ELISA and SNT serology. The 90 human serum samples from unexposed persons were unreactive by IFAT. The IFAT utilizing NiV-N-expressing HeLa 229 cells to detect IgM antibody in an early stage of NiV infection is an effective approach, which could be utilized readily in local laboratories to complement other capabilities in NiV-affected countries.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoglobulina M / Técnica Indireta de Fluorescência para Anticorpo / Proteínas do Capsídeo / Infecções por Henipavirus / Anticorpos Antivirais Tipo de estudo: Diagnostic_studies / Evaluation_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Imunoglobulina M / Técnica Indireta de Fluorescência para Anticorpo / Proteínas do Capsídeo / Infecções por Henipavirus / Anticorpos Antivirais Tipo de estudo: Diagnostic_studies / Evaluation_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article