Live Attenuated Shigella dysenteriae Type 1 Vaccine Strains Overexpressing Shiga Toxin B Subunit

Abstract

ABSTRACTShigella dysenteriaeserotype 1 (S. dysenteriae1) is unique among theShigellaspecies and serotypes in the expression of Shiga toxin which contributes to more severe disease sequelae and the ability to cause explosive outbreaks and pandemics.S. dysenteriae1 shares characteristics with otherShigellaspecies, including the capability of causing clinical illness with a very low inoculum (10 to 100 CFU) and resistance to multiple antibiotics, underscoring the need for efficacious vaccines and therapeutics. Following the demonstration of the successful attenuating capacity of deletion mutations in theguaBAoperon inS. flexneri2a vaccine strains in clinical studies, we developed a series ofS. dysenteriae1 vaccine candidates containing the fundamental attenuating mutation inguaBA.All strains are devoid of Shiga toxin activity by specific deletion of the gene encoding the StxA subunit, which encodes enzymatic activity. The StxB subunit was overexpressed in several derivatives by either plasmid-based constructs or chromosomal manipulation to include a strong promoter. All strains are attenuated for growthin vitroin the HeLa cell assay and for plaque formation and were safe in the Serény test and immunogenic in the guinea pigs. Each strain induced robust serum and mucosal anti-S. dysenteriae1 lipopolysaccharide (LPS) responses and protected against wild-type challenge. Two strains engineered to overexpress StxB induced high titers of Shiga toxin neutralizing antibodies. These candidates demonstrate the potential for a live attenuated vaccine to protect against disease caused byS. dysenteriae1 and potentially to protect against the toxic effects of other Shiga toxin 1-expressing pathogens.