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The identification of novel immunogenic antigens as potential Shigella vaccine components.
de Alwis, Ruklanthi; Liang, Li; Taghavian, Omid; Werner, Emma; The, Hao Chung; Thu, Trang Nguyen Hoang; Duong, Vu Thuy; Davies, D Huw; Felgner, Philip L; Baker, Stephen.
Afiliación
  • de Alwis R; Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
  • Liang L; Viral Research and Experimental Medicine Centre, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
  • Taghavian O; Vaccine Research & Development Center, School of Medicine, University of California Irvine, Irvine, CA, USA.
  • Werner E; Vaccine Research & Development Center, School of Medicine, University of California Irvine, Irvine, CA, USA.
  • The HC; Laboratory of Molecular Biology, Cambridge Biomedical Campus, Cambridge, UK.
  • Thu TNH; The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Duong VT; The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Davies DH; The Hospital for Tropical Diseases, Wellcome Trust Major Overseas Programme, Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
  • Felgner PL; Vaccine Research & Development Center, School of Medicine, University of California Irvine, Irvine, CA, USA.
  • Baker S; Vaccine Research & Development Center, School of Medicine, University of California Irvine, Irvine, CA, USA.
Genome Med ; 13(1): 8, 2021 01 15.
Article en En | MEDLINE | ID: mdl-33451348
BACKGROUND: Shigella is a major diarrheal pathogen for which there is presently no vaccine. Whole genome sequencing provides the ability to predict and derive novel antigens for use as vaccines. Here, we aimed to identify novel immunogenic Shigella antigens that could serve as Shigella vaccine candidates, either alone, or when conjugated to Shigella O-antigen. METHODS: Using a reverse vaccinology approach, where genomic analysis informed the Shigella immunome via an antigen microarray, we aimed to identify novel immunogenic Shigella antigens. A core genome analysis of Shigella species, pathogenic and non-pathogenic Escherichia coli, led to the selection of 234 predicted immunogenic Shigella antigens. These antigens were expressed and probed with acute and convalescent serum from microbiologically confirmed Shigella infections. RESULTS: Several Shigella antigens displayed IgG and IgA seroconversion, with no difference in sero-reactivity across by sex or age. IgG sero-reactivity to key Shigella antigens was observed at birth, indicating transplacental antibody transfer. Six antigens (FepA, EmrK, FhuA, MdtA, NlpB, and CjrA) were identified in in vivo testing as capable of producing binding IgG and complement-mediated bactericidal antibody. CONCLUSIONS: These findings provide six novel immunogenic Shigella proteins that could serve as candidate vaccine antigens, species-specific carrier proteins, or targeted adjuvants.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunas contra la Shigella / Antígenos Bacterianos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Genome Med Año: 2021 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunas contra la Shigella / Antígenos Bacterianos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Genome Med Año: 2021 Tipo del documento: Article País de afiliación: Singapur