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Details

Autor(en) / Beteiligte
Titel
Methicillin resistance alters the biofilm phenotype and attenuates virulence in Staphylococcus aureus device-associated infections
Ist Teil von
  • PLoS pathogens, 2012-04, Vol.8 (4), p.e1002626
Ort / Verlag
United States: Public Library of Science
Erscheinungsjahr
2012
Link zum Volltext
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • Clinical isolates of Staphylococcus aureus can express biofilm phenotypes promoted by the major cell wall autolysin and the fibronectin-binding proteins or the icaADBC-encoded polysaccharide intercellular adhesin/poly-N-acetylglucosamine (PIA/PNAG). Biofilm production in methicillin-susceptible S. aureus (MSSA) strains is typically dependent on PIA/PNAG whereas methicillin-resistant isolates express an Atl/FnBP-mediated biofilm phenotype suggesting a relationship between susceptibility to β-lactam antibiotics and biofilm. By introducing the methicillin resistance gene mecA into the PNAG-producing laboratory strain 8325-4 we generated a heterogeneously resistant (HeR) strain, from which a homogeneous, high-level resistant (HoR) derivative was isolated following exposure to oxacillin. The HoR phenotype was associated with a R₆₀₂H substitution in the DHHA1 domain of GdpP, a recently identified c-di-AMP phosphodiesterase with roles in resistance/tolerance to β-lactam antibiotics and cell envelope stress. Transcription of icaADBC and PNAG production were impaired in the 8325-4 HoR derivative, which instead produced a proteinaceous biofilm that was significantly inhibited by antibodies against the mecA-encoded penicillin binding protein 2a (PBP2a). Conversely excision of the SCCmec element in the MRSA strain BH1CC resulted in oxacillin susceptibility and reduced biofilm production, both of which were complemented by mecA alone. Transcriptional activity of the accessory gene regulator locus was also repressed in the 8325-4 HoR strain, which in turn was accompanied by reduced protease production and significantly reduced virulence in a mouse model of device infection. Thus, homogeneous methicillin resistance has the potential to affect agr- and icaADBC-mediated phenotypes, including altered biofilm expression and virulence, which together are consistent with the adaptation of healthcare-associated MRSA strains to the antibiotic-rich hospital environment in which they are frequently responsible for device-related infections in immuno-compromised patients.
Sprache
Englisch
Identifikatoren
ISSN: 1553-7374, 1553-7366
eISSN: 1553-7374
DOI: 10.1371/journal.ppat.1002626
Titel-ID: cdi_plos_journals_1289108450
Format
Schlagworte
Acetylglucosamine - genetics, Acetylglucosamine - metabolism, Adaptations, Adhesins, Adhesins, Bacterial - genetics, Adhesins, Bacterial - metabolism, Animal models, Animals, Anti-Bacterial Agents - pharmacology, Antibiotic resistance, Antibodies, Autolysins, Bacteriology, beta -Lactam antibiotics, Biofilms, Biofilms - growth & development, Biology, Cell envelopes, Clinical isolates, Colonization, Data processing, Drug resistance, Drug resistance in microorganisms, Enzymes, Equipment Contamination, Fibronectin-binding protein, Gene Expression Regulation, Bacterial - drug effects, Gene Expression Regulation, Bacterial - physiology, Genetic aspects, Health aspects, Hospitals, Humans, Immunocompromised hosts, Immunological tolerance, Infection, Male, MecA protein, Medical equipment, Medical research, Methicillin, Methicillin Resistance - drug effects, Methicillin Resistance - physiology, Methicillin-Resistant Staphylococcus aureus - genetics, Methicillin-Resistant Staphylococcus aureus - metabolism, Methicillin-Resistant Staphylococcus aureus - pathogenicity, Mice, Microbial mats, Microbiology, N-Acetylmuramoyl-L-alanine Amidase - genetics, N-Acetylmuramoyl-L-alanine Amidase - metabolism, Oxacillin, Oxacillin - pharmacology, Penicillin, Penicillin-Binding Proteins - genetics, Penicillin-Binding Proteins - metabolism, Phenotype, phosphodiesterase, Physiological aspects, Polysaccharides, Polysaccharides, Bacterial - genetics, Polysaccharides, Bacterial - metabolism, Proteinase, Staphylococcus aureus, Staphylococcus infections, Stress, Toxins, Transcription, Virulence, Virulence (Microbiology)

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