| Literature DB >> 25368410 |
Emrah Altindis1, Roberta Cozzi1, Benedetta Di Palo1, Francesca Necchi1, Ravi P Mishra1, Maria Rita Fontana1, Marco Soriani1, Fabio Bagnoli1, Domenico Maione1, Guido Grandi2, Sabrina Liberatori1.
Abstract
New generation vaccines are in demand to include only the key antigens sufficient to confer protective immunity among the plethora of pathogen molecules. In the last decade, large-scale genomics-based technologies have emerged. Among them, the Reverse Vaccinology approach was successfully applied to the development of an innovative vaccine against Neisseria meningitidis serogroup B, now available on the market with the commercial name BEXSERO® (Novartis Vaccines). The limiting step of such approaches is the number of antigens to be tested in in vivo models. Several laboratories have been trying to refine the original approach in order to get to the identification of the relevant antigens straight from the genome. Here we report a new bioinformatics tool that moves a first step in this direction. The tool has been developed by identifying structural/functional features recurring in known bacterial protective antigens, the so called "Protectome space," and using such "protective signatures" for protective antigen discovery. In particular, we applied this new approach to Staphylococcus aureus and Group B Streptococcus and we show that not only already known protective antigens were re-discovered, but also two new protective antigens were identified.Entities:
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Year: 2014 PMID: 25368410 PMCID: PMC4350036 DOI: 10.1074/mcp.M114.039362
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911