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<i>Streptococcus canis</i> is a common colonizing bacterium of the urogenital tract of cats and dogs that can also cause invasive disease in these animal populations and in humans. Although the virulence mechanisms of <i>S. canis</i> are not well-characterized, an M-like protein, SCM, has recently identified been as a potential virulence factor. SCM is a surface-associated protein that binds to host plasminogen and IgGs suggesting its possible importance in host-pathogen interactions. In this study, we developed in vitro and ex vivo blood component models and murine models of <i>S. canis</i> vaginal colonization, systemic infection, and dermal infection to compare the virulence potential of the zoonotic <i>S. canis</i> vaginal isolate G361 and its isogenic SCM-deficient mutant (G361∆<i>scm</i>). We found that while <i>S. canis</i> establishes vaginal colonization and causes invasive disease in vivo, the contribution of the SCM protein to virulence phenotypes in these models is modest. We conclude that SCM is dispensable for invasive disease in murine models and for resistance to human blood components ex vivo, but may contribute to mucosal persistence, highlighting a potential contribution to the recently appreciated genetic diversity of SCM across strains and hosts.