| Literature DB >> 25332378 |
Lisa Marie Schlecht1,2, Brian M Peters3,1, Bastiaan P Krom4, Jeffrey A Freiberg3,1, Gertrud M Hänsch5, Scott G Filler6, Mary Ann Jabra-Rizk7,8, Mark E Shirtliff7,1.
Abstract
Candida albicans and Staphylococcus aureus are often co-isolated in cases of biofilm-associated infections. C. albicans can cause systemic disease through morphological switch from the rounded yeast to the invasive hyphal form. Alternatively, systemic S. aureus infections arise from seeding through breaks in host epithelial layers although many patients have no documented portal of entry. We describe a novel strategy by which S. aureus is able to invade host tissue and disseminate via adherence to the invasive hyphal elements of Candida albicans. In vitro and ex vivo findings demonstrate a specific binding of the staphylococci to the candida hyphal elements. The C. albicans cell wall adhesin Als3p binds to multiple staphylococcal adhesins. Furthermore, Als3p is required for C. albicans to transport S. aureus into the tissue and cause a disseminated infection in an oral co-colonization model. These findings suggest that C. albicans can facilitate the invasion of S. aureus across mucosal barriers, leading to systemic infection in co-colonized patients.Entities:
Mesh:
Year: 2014 PMID: 25332378 PMCID: PMC4274785 DOI: 10.1099/mic.0.083485-0
Source DB: PubMed Journal: Microbiology ISSN: 1350-0872 Impact factor: 2.777