Identification of new meningococcal serogroup B surface antigens through a systematic analysis of neisserial genomes

Rolando Pajon*, Daniel Yero, Olivia Niebla, Yanet Climent, Gretel Sardiñas, Darién García, Yasser Perera, Alejandro Llanes, Maité Delgado, Karem Cobas, Evelin Caballero, Stephen Taylor, Charlotte Brookes, Andrew Gorringe

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

The difficulty of inducing an effective immune response against the Neisseria meningitidis serogroup B capsular polysaccharide has lead to the search for vaccines for this serogroup based on outer membrane proteins. The availability of the first meningococcal genome (MC58 strain) allowed the expansion of high-throughput methods to explore the protein profile displayed by N. meningitidis. By combining a pan-genome analysis with an extensive experimental validation to identify new potential vaccine candidates, genes coding for antigens likely to be exposed on the surface of the meningococcus were selected after a multistep comparative analysis of entire Neisseria genomes. Eleven novel putative ORF annotations were reported for serogroup B strain MC58. Furthermore, a total of 20 new predicted potential pan-neisserial vaccine candidates were produced as recombinant proteins and evaluated using immunological assays. Potential vaccine candidate coding genes were PCR-amplified from a panel of representative strains and their variability analyzed using maximum likelihood approaches for detecting positive selection. Finally, five proteins all capable of inducing a functional antibody response vs N. meningitidis strain CU385 were identified as new attractive vaccine candidates: NMB0606 a potential YajC orthologue, NMB0928 the neisserial NlpB (BamC), NMB0873 a LolB orthologue, NMB1163 a protein belonging to a curli-like assembly machinery, and NMB0938 (a neisserial specific antigen) with evidence of positive selection appreciated for NMB0928. The new set of vaccine candidates and the novel proposed functions will open a new wave of research in the search for the elusive neisserial vaccine.

Original languageEnglish
Pages (from-to)532-541
Number of pages10
JournalVaccine
Volume28
Issue number2
DOIs
Publication statusPublished - 11 Dec 2009

Bibliographical note

Funding Information:
Research at the Health Protection Agency was funded by the UK Department of Health .

Keywords

  • BamC
  • Curli
  • Genomics
  • Neisseria meningitidis
  • Positive selection
  • Proteomics
  • Vaccine

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