Temporal Expression of Adhesion Factors and Activity of Global Regulators during Establishment ofStaphylococcus aureusNasal Colonization
Author(s) -
Marc Burian,
Maren Rautenberg,
Thomas P. Kohler,
Michaela Fritz,
Bernhard Krismer,
Clemens Unger,
W. H. Hoffmann,
Andreas Peschel,
Christiane Wolz,
Christiane Goerke
Publication year - 2010
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/651619
Subject(s) - colonization , staphylococcus aureus , microbiology and biotechnology , biology , virulence , gene expression , pathogen , staphylococcal infections , real time polymerase chain reaction , regulation of gene expression , gene , reverse transcription polymerase chain reaction , nose , human pathogen , bacteria , genetics , anatomy
The human pathogen Staphylococcus aureus successfully colonizes its primary reservoir, the nasal cavity, most likely by regulatory adaptation to the nose environment. Cotton rats represent an excellent model for the study of bacterial gene expression in the initial phases of colonization. To gain insight into the expression profile necessary for the establishment of colonization, we performed direct transcript analysis by quantitative real-time reverse-transcription polymerase chain reaction on cotton rat noses removed from euthanized animals on days 1, 4, or 10 after instillation of 2 human S. aureus nose isolates. Global virulence regulators (agr, sae) were not active in this early phase, but the essential 2-component regulatory system WalKR seems to play an important role. Accordingly, an elevated expression of walKR target genes (sak, sceD) could be detected. In agreement with previous studies that demonstrated the essential role played by wall teichoic acid (WTA) polymers in nasal colonization, we detected a strongly increased expression of WTA-biosynthetic genes. The expression profile switched to production of the adhesive proteins ClfB and IsdA at later stages of the colonization process. These data underscore the temporal differences in the roles of WTA and surface proteins in nasal colonization, and they provide the first evidence for a regulation of WTA biosynthesis in vivo.
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