<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Berger-Bächi B</dc:creator>
  <dc:date>2002</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The introduction and increasing use of antibiotics for antibacterial therapy has initiated a rapid development and expansion of antibiotic resistance in microorganisms, particularly in human pathogens. Additionally, a shift to an increase in number and severity of Gram-positive infections has been observed the last decades. Common to these pathogens is their tendency to accumulate multiple resistances under antibiotic pressure and selection. Methicillin-resistant Staphylococcus aureus (MRSA), that have acquired multiresistance to all classes of antibiotics, have become a serious nosocomial problem. Recently, the emergence of the first MRSA with reduced vancomycin susceptibility evoked the specter of a totally resistant S. aureus. Problems with multiresistance expand also to penicillin-resistant Streptococcus pneumoniae that are partially or totally resistant to multiple antibiotics, and to vancomycin-resistant Enterococcus ssp., completely resistant to all commonly used antibiotics. The rapid development of resistance is due to mutational events and/or gene transfer and acquisition of resistance determinants, allowing strains to survive antibiotic treatment.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/243749</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1078/1438-4221-00185</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/12139425</dc:relation>
  <dc:source>International journal of medical microbiology : IJMM. - 2002</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Anti-Bacterial Agents</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Community-Acquired Infections</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Drug Resistance, Multiple, Bacterial</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Glycopeptides</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Gram-Positive Bacteria</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Gram-Positive Bacterial Infections</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Methicillin Resistance</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Peptides</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Selection, Genetic</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Vancomycin Resistance</dc:subject>
  <dc:title xmlns:ns12="xml" ns12:lang="en">Resistance mechanisms of gram-positive bacteria.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
