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Systemic Staphylococcus aureus infection mediated by Candida albicans hyphal invasion of mucosal tissue

Identifieur interne : 000C80 ( Main/Exploration ); précédent : 000C79; suivant : 000C81

Systemic Staphylococcus aureus infection mediated by Candida albicans hyphal invasion of mucosal tissue

Auteurs : Lisa Marie Schlecht [Allemagne, États-Unis] ; Brian M. Peters [États-Unis] ; Bastiaan P. Krom [Pays-Bas] ; Jeffrey A. Freiberg [États-Unis] ; Gertrud M. H Nsch [Allemagne] ; Scott G. Filler [États-Unis] ; Mary Ann Jabra-Rizk [États-Unis] ; Mark E. Shirtliff [États-Unis]

Source :

RBID : PMC:4274785

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.


Url:
DOI: 10.1099/mic.0.083485-0
PubMed: 25332378
PubMed Central: 4274785


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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infection mediated by
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hyphal invasion of mucosal tissue</title>
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infection mediated by
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hyphal invasion of mucosal tissue</title>
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<wicri:regionArea>Division of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, 1124 W. Carson St., Torrance, CA 90502</wicri:regionArea>
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<region type="state">Californie</region>
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<name sortKey="Jabra Rizk, Mary Ann" sort="Jabra Rizk, Mary Ann" uniqKey="Jabra Rizk M" first="Mary Ann" last="Jabra-Rizk">Mary Ann Jabra-Rizk</name>
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<p>
<italic>Candida albicans</italic>
and
<italic>Staphylococcus aureus</italic>
are often co-isolated in cases of biofilm-associated infections.
<italic>C. albicans</italic>
can cause systemic disease through morphological switch from the rounded yeast to the invasive hyphal form. Alternatively, systemic
<italic>S. aureus</italic>
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
<italic>S. aureus</italic>
is able to invade host tissue and disseminate via adherence to the invasive hyphal elements of
<italic>Candida albicans. In vitro</italic>
and
<italic>ex vivo</italic>
findings demonstrate a specific binding of the staphylococci to the candida hyphal elements. The
<italic>C. albicans</italic>
cell wall adhesin Als3p binds to multiple staphylococcal adhesins. Furthermore, Als3p is required for
<italic>C. albicans</italic>
to transport
<italic>S. aureus</italic>
into the tissue and cause a disseminated infection in an oral co-colonization model. These findings suggest that
<italic>C. albicans</italic>
can facilitate the invasion of
<italic>S. aureus</italic>
across mucosal barriers, leading to systemic infection in co-colonized patients.</p>
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</affiliations>
</record>

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HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000C80 | SxmlIndent | more

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