Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 1 July 2005:
Vol. 309. no. 5731, pp. 148 - 150
DOI: 10.1126/science.1109869

Reports

Identification of a Universal Group B Streptococcus Vaccine by Multiple Genome Screen

Domenico Maione,1* Immaculada Margarit,1* Cira D. Rinaudo,1 Vega Masignani,1 Marirosa Mora,1 Maria Scarselli,1 Hervé Tettelin,2 Cecilia Brettoni,1 Emilia T. Iacobini,1 Roberto Rosini,1 Nunzio D'Agostino,1 Lisa Miorin,1 Scilla Buccato,1 Massimo Mariani,1 Giuliano Galli,1 Renzo Nogarotto,1 Vincenzo Nardi Dei,1 Filipo Vegni,1 Claire Fraser,2 Giuseppe Mancuso,3 Giuseppe Teti,3 Lawrence C. Madoff,4 Lawrence C. Paoletti,4 Rino Rappuoli,1 Dennis L. Kasper,4 John L. Telford,1 Guido Grandi1{dagger}

Group B Streptococcus (GBS) is a multiserotype bacterial pathogen representing a major cause of life-threatening infections in newborns. To develop a broadly protective vaccine, we analyzed the genome sequences of eight GBS isolates and cloned and tested 312 surface proteins as vaccines. Four proteins elicited protection in mice, and their combination proved highly protective against a large panel of strains, including all circulating serotypes. Protection also correlated with antigen accessibility on the bacterial surface and with the induction of opsonophagocytic antibodies. Multigenome analysis and screening described here represent a powerful strategy for identifying potential vaccine candidates against highly variable pathogens.

1 Chiron srl, Via Fiorentina 1, 53100 Siena, Italy.
2 Institute for Genome Research, 9712 Medical Center Drive, Rockville, MD 20850, USA.
3 Department of Pathology and Experimental Microbiology, University of Messina Medical School, 98125 Messina, Italy.
4 Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02125, USA.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: guido_grandi{at}chiron.com

Read the Full Text






ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)