c Streptococcus agalactiae (group B streptococcus [GBS]) colonizes the rectovaginal tract in 20% to 30% of women and during pregnancy can be transmitted to the newborn, causing severe invasive disease. Current routine screening and antibiotic prophylaxis have fallen short of complete prevention of GBS transmission, and GBS remains a leading cause of neonatal infection. We have investigated the ability of Streptococcus salivarius, a predominant member of the native human oral microbiota, to control GBS colonization. Comparison of the antibacterial activities of multiple S. salivarius strains by use of a deferred-antagonism test showed that S. salivarius strain K12 exhibited the broadest spectrum of activity against GBS. K12 effectively inhibited all GBS strains tested, including disease-implicated isolates from newborns and colonizing isolates from the vaginal tract of pregnant women. Inhibition was dependent on the presence of megaplasmid pSsal-K12, which encodes the bacteriocins salivaricin A and salivaricin B; however, in coculture experiments, GBS growth was impeded by K12 independently of the megaplasmid. We also demonstrated that K12 adheres to and invades human vaginal epithelial cells at levels comparable to GBS. Inhibitory activity of K12 was examined in vivo using a mouse model of GBS vaginal colonization. Mice colonized with GBS were treated vaginally with K12. K12 administration significantly reduced GBS vaginal colonization in comparison to nontreated controls, and this effect was partially dependent on the K12 megaplasmid. Our results suggest that K12 may have potential as a preventative therapy to control GBS vaginal colonization and thereby prevent its transmission to the neonate during pregnancy.
S treptococcus agalactiae (group B streptococcus [GBS]) is aGram-positive organism that is currently the leading infectious agent responsible for neonatal morbidity and mortality in the United States (1). The primary risk factor for newborn disease is maternal GBS colonization within the gastrointestinal or vaginal tract (1). GBS colonization of the vaginal tract during pregnancy may be constant, intermittent, or transient in nature among individual women (2). In lieu of an effective vaccine, the current recommendations from the Centers for Disease Control and Prevention include late-gestational screening and intrapartum antibiotic prophylaxis (IAP) for GBS-positive mothers, which has resulted in reduced early-onset GBS disease and infant colonization (1). However, IAP with ampicillin for GBS-positive mothers has been determined an independent risk factor for ampicillin-resistant Escherichia coli early-onset sepsis (3) and has recently been shown to reduce beneficial Bifidobacterium spp. in week-old newborn intestinal flora (4). There are likely to be other unrecognized negative effects of antibiotic exposure on long-term gut health, which prompts development of alternative prophylactic strategies. Several studies have proposed the use of probiotic strains to control GBS and have observed inhibitory acti...