Thursday, December 26, 2024
12/26/2024
ABSTRACT Streptococcus sanguinis is an abundant member of the oral microbiota and a promising oral probiotic since it has been associated with oral health in humans and shown to compete with oral pathogens. Conversely, S. sanguinis is also an important cause of bacterial endocarditis, a serious infection of the heart that affects >40,000 people in the U.S each year and has mortality rates exceeding 20%. Endocarditis is of critical concern to U.S dentists, who typically provide antibiotic prophylaxis to high-risk patients prior to invasive dental procedures. The underlying cause of the duality in S. sanguinis lifestyle as a health-associated commensal or a serious pathogen is poorly understood. Delineation of the S. sanguinis factors that are important for oral health versus endocarditis virulence would facilitate the development of efficacious and safe probiotics, and more targeted prophylactics against endocarditis during dental procedures. A significant barrier to progress in the field is the paucity of genetically-, epigenetically-, or phenotypically- characterized isolates. Numerous studies have employed a variety of poorly characterized strains, many of which are no longer classified as S. sanguinis, making it difficult to assess findings. Moreover, related Streptococcus species are notoriously genetically diverse, and additional epigenetic mechanisms have been demonstrated to drive phenotypic diversity and virulence even within clonal populations. Although the complete genome of SK36 has been published, its epigenetic profile (i.e. methylome) is unknown and, regardless, no single strain can capture the true capabilities of the species. This proposal will surmount these barriers by first using single-molecule real-time (SMRT) sequencing to generate complete genomes/epigenomes of 40 bona fide S. sanguinis strains, representing both oral and endocarditis isolates. This will reveal the core and accessory genomes related to oral and endocarditis environmental niches, in addition to the methylome of each isolate. The central hypothesis of this proposal is that the dual lifestyle of S. sanguinis is either A) facilitated by the presence or absence of specific genetic loci (i.e. virulence genes, islands, or plasmids) or B) epigenetically encoded and induced by transcriptomic alterations within permissive environmental niches. An in-vivo endocarditis model will be used to screen for infective endocarditis virulence and test whether targeted reengineered isogenic mutants are deficient for virulence, making them suitable candidates for development as oral probiotics. The immediate outcomes will be an S. sanguinis strain collection that is genetically-, epigenetically-, and phenotypically defined and which will be made available to the research community, and the ascertainment of whether S. sanguinis endocarditis virulence is genetically or epigenetically encoded. The long-term outcome will be the creation of strains engineered to have low endocarditis virulence. If virulence is controlled epigenetically in S. sanguinis as it is in some of its closest relatives, the loss of endocarditis virulence will be accompanied by an increase in oral competitiveness, making these strains ideal for oral probiotic development.
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