Maione Domenico, Margarit Immaculada, Rinaudo Cira D, Masignani Vega, Mora Marirosa, Scarselli Maria, Tettelin Hervé, Brettoni Cecilia, Iacobini Emilia T, Rosini Roberto, D'Agostino Nunzio, Miorin Lisa, Buccato Scilla, Mariani Massimo, Galli Giuliano, Nogarotto Renzo, Nardi-Dei Vincenzo, Vegni Filipo, Fraser Claire, Mancuso Giuseppe, Teti Giuseppe, Madoff Lawrence C, Paoletti Lawrence C, Rappuoli Rino, Kasper Dennis L, Telford John L, Grandi Guido
Chiron srl, Via Fiorentina 1, 53100 Siena, Italy.
Science. 2005 Jul 1;309(5731):148-50. doi: 10.1126/science.1109869.
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.
B族链球菌(GBS)是一种多血清型细菌病原体,是新生儿危及生命感染的主要原因。为了开发一种具有广泛保护作用的疫苗,我们分析了8株GBS分离株的基因组序列,并克隆和测试了312种表面蛋白作为疫苗。四种蛋白在小鼠中引发了保护作用,它们的组合对一大组菌株,包括所有流行血清型,都具有高度保护作用。保护作用还与细菌表面抗原的可及性以及调理吞噬抗体的诱导相关。本文所述的多基因组分析和筛选是识别针对高度可变病原体的潜在疫苗候选物的有力策略。