Your browser doesn't support javascript.
loading
Identification of Human Junctional Adhesion Molecule 1 as a Functional Receptor for the Hom-1 Calicivirus on Human Cells.
Sosnovtsev, Stanislav V; Sandoval-Jaime, Carlos; Parra, Gabriel I; Tin, Christine M; Jones, Ronald W; Soden, Jo; Barnes, Donna; Freeth, Jim; Smith, Alvin W; Green, Kim Y.
Afiliação
  • Sosnovtsev SV; Caliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA ss216m@nih.gov.
  • Sandoval-Jaime C; Caliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
  • Parra GI; Caliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
  • Tin CM; Caliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
  • Jones RW; Caliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
  • Soden J; Retrogenix Ltd., Whaley Bridge, High Peak, United Kingdom.
  • Barnes D; Retrogenix Ltd., Whaley Bridge, High Peak, United Kingdom.
  • Freeth J; Retrogenix Ltd., Whaley Bridge, High Peak, United Kingdom.
  • Smith AW; Laboratory for Calicivirus Studies, Oregon State University, Corvallis, Oregon, USA.
  • Green KY; Caliciviruses Section, Laboratory of Infectious Diseases, NIAID, NIH, Bethesda, Maryland, USA.
mBio ; 8(1)2017 02 14.
Article em En | MEDLINE | ID: mdl-28196955
ABSTRACT
The Hom-1 vesivirus was reported in 1998 following the inadvertent transmission of the animal calicivirus San Miguel sea lion virus to a human host in a laboratory. We characterized the Hom-1 strain and investigated the mechanism by which human cells could be infected. An expression library of 3,559 human plasma membrane proteins was screened for reactivity with Hom-1 virus-like particles, and a single interacting protein, human junctional adhesion molecule 1 (hJAM1), was identified. Transient expression of hJAM1 conferred susceptibility to Hom-1 infection on nonpermissive Chinese hamster ovary (CHO) cells. Virus infection was markedly inhibited when CHO cells stably expressing hJAM were pretreated with anti-hJAM1 monoclonal antibodies. Cell lines of human origin were tested for growth of Hom-1, and efficient replication was observed in HepG2, HuH7, and SK-CO15 cells. The three cell lines (of hepatic or intestinal origin) were confirmed to express hJAM1 on their surface, and clustered regularly interspaced short palindromic repeats/Cas9-mediated knockout of the hJAM1 gene in each line abolished Hom-1 propagation. Taken together, our data indicate that entry of the Hom-1 vesivirus into these permissive human cell lines is mediated by the plasma membrane protein hJAM1 as a functional receptor.IMPORTANCE Vesiviruses, such as San Miguel sea lion virus and feline calicivirus, are typically associated with infection in animal hosts. Following the accidental infection of a laboratory worker with San Miguel sea lion virus, a related virus was isolated in cell culture and named Hom-1. In this study, we found that Hom-1 could be propagated in a number of human cell lines, making it the first calicivirus to replicate efficiently in cultured human cells. Screening of a library of human cell surface membrane proteins showed that the virus could utilize human junctional adhesion molecule 1 as a receptor to enter cells and initiate replication. The Hom-1 virus presents a new system for the study of calicivirus biology and species specificity.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Virais / Replicação Viral / Moléculas de Adesão Celular / Receptores de Superfície Celular / Vesivirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Revista: MBio Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Virais / Replicação Viral / Moléculas de Adesão Celular / Receptores de Superfície Celular / Vesivirus Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Revista: MBio Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos
...