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HIV-1 interaction with an O-glycan-specific bacterial lectin enhances virus infectivity and resistance to neutralizing antibodies.
Heindel, Daniel W; Figueroa Acosta, Dania M; Goff, Marisa; Yengo, Clauvis Kunkeng; Jan, Muzafar; Liu, Xiaomei; Wang, Xiao-Hong; Petrova, Mariya I; Zhang, Mo; Sagar, Manish; Barnette, Phillip; Pandey, Shilpi; Hessell, Ann J; Chan, Kun-Wei; Kong, Xiang-Peng; Chen, Benjamin K; Mahal, Lara K; Bensing, Barbara A; Hioe, Catarina E.
Afiliação
  • Heindel DW; Divison of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Figueroa Acosta DM; Divison of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Goff M; Divison of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Yengo CK; Divison of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Jan M; Divison of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Liu X; Divison of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Wang XH; VA New York Harbor Healthcare System-Manhattan, New York, NY, USA.
  • Petrova MI; Department of Bioscience Engineering, University of Antwerp, Antwerp, Belgium.
  • Zhang M; Department of Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Sagar M; Department of Medicine, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Barnette P; Department of Virology, Immunology and Microbiology, Boston University Chobanian & Avedisian School of Medicine, Boston, MA, USA.
  • Pandey S; Division of Pathobiology and Immunology, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, OR, USA.
  • Hessell AJ; Division of Pathobiology and Immunology, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, OR, USA.
  • Chan KW; Division of Pathobiology and Immunology, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, OR, USA.
  • Kong XP; Department of Biochemistry and Molecular Pharmacology New York University Grossman School of Medicine, New York, NY, USA.
  • Chen BK; Department of Biochemistry and Molecular Pharmacology New York University Grossman School of Medicine, New York, NY, USA.
  • Mahal LK; Divison of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Bensing BA; Department of Chemistry, University of Alberta, Edmonton, AB, Canada.
  • Hioe CE; Department of Medicine, San Francisco Veterans Affairs Medical Center and University of California, San Francisco, CA, USA.
iScience ; 27(8): 110390, 2024 Aug 16.
Article em En | MEDLINE | ID: mdl-39108723
ABSTRACT
Bacteria dysbiosis and its accompanying inflammation or compromised mucosal integrity is associated with an increased risk of HIV-1 transmission. However, HIV-1 may also bind bacteria or bacterial products to impact infectivity and transmissibility. This study evaluated HIV-1 interactions with bacteria through glycan-binding lectins. The Streptococcal Siglec-like lectin SLBR-N, a part of the fimbriae shrouding the bacteria surface that recognizes α2,3 sialyated O-linked glycans, was noted for its ability to enhance HIV-1 infectivity in the context of cell-free infection and cell-to-cell transfer. Enhancing effects were recapitulated with O-glycan-binding plant lectins, signifying the importance of O-glycans. N-glycan-binding bacterial lectins FimH and Msl had no effect. SLBR-N was demonstrated to capture and transfer infectious HIV-1 virions, bind to O-glycans on HIV-1 Env, and increase HIV-1 resistance to neutralizing antibodies targeting different regions of Env. This study highlights the potential contribution of O-glycan-binding lectins from commensal bacteria at the mucosa in promoting HIV-1 infection.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos