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Pathogenic Differences between Nipah Virus Bangladesh and Malaysia Strains in Primates: Implications for Antibody Therapy.
Mire, Chad E; Satterfield, Benjamin A; Geisbert, Joan B; Agans, Krystle N; Borisevich, Viktoriya; Yan, Lianying; Chan, Yee-Peng; Cross, Robert W; Fenton, Karla A; Broder, Christopher C; Geisbert, Thomas W.
Afiliação
  • Mire CE; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
  • Satterfield BA; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Geisbert JB; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
  • Agans KN; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Borisevich V; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
  • Yan L; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Chan YP; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
  • Cross RW; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Fenton KA; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
  • Broder CC; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Geisbert TW; Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Sci Rep ; 6: 30916, 2016 08 03.
Article em En | MEDLINE | ID: mdl-27484128
Nipah virus (NiV) is a paramyxovirus that causes severe disease in humans and animals. There are two distinct strains of NiV, Malaysia (NiVM) and Bangladesh (NiVB). Differences in transmission patterns and mortality rates suggest that NiVB may be more pathogenic than NiVM. To investigate pathogenic differences between strains, 4 African green monkeys (AGM) were exposed to NiVM and 4 AGMs were exposed to NiVB. While NiVB was uniformly lethal, only 50% of NiVM-infected animals succumbed to infection. Histopathology of lungs and spleens from NiVB-infected AGMs was significantly more severe than NiVM-infected animals. Importantly, a second study utilizing 11 AGMs showed that the therapeutic window for human monoclonal antibody m102.4, previously shown to rescue AGMs from NiVM infection, was much shorter in NiVB-infected AGMs. Together, these data show that NiVB is more pathogenic in AGMs under identical experimental conditions and suggests that postexposure treatments may need to be NiV strain specific for optimal efficacy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus Nipah / Infecções por Henipavirus Limite: Animals País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus Nipah / Infecções por Henipavirus Limite: Animals País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos