%0 Journal Article %1 livermore_multiple_2002 %A Livermore, David M %D 2002 %J Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America %K Agents, Bacterial, Cell Drug Family, Frequency, Gene Humans, Integrins, Membrane Microbial Multigene Multiple, Mutation, Permeability, Pseudomonas Resistance, Sensitivity Tests, aeruginosa {Anti-Bacterial} %N 5 %P 634--40 %R 11823954 %T Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa: our worst nightmare? %U http://www.ncbi.nlm.nih.gov/pubmed/11823954 %V 34 %X Pseudomonas aeruginosa carries multiresistance plasmids less often than does Klebsiella pneumoniae, develops mutational resistance to cephalosporins less readily than Enterobacter species, and has less inherent resistance than Stenotrophomonas maltophilia. What nevertheless makes P. aeruginosa uniquely problematic is a combination of the following: the species' inherent resistance to many drug classes; its ability to acquire resistance, via mutations, to all relevant treatments; its high and increasing rates of resistance locally; and its frequent role in serious infections. A few isolates of P. aeruginosa are resistant to all reliable antibiotics, and this problem seems likely to grow with the emergence of integrins that carry gene cassettes encoding both carbapenemases and amikacin acetyltransferases.

@article{livermore_multiple_2002, abstract = {Pseudomonas aeruginosa carries multiresistance plasmids less often than does Klebsiella pneumoniae, develops mutational resistance to cephalosporins less readily than Enterobacter species, and has less inherent resistance than Stenotrophomonas maltophilia. What nevertheless makes P. aeruginosa uniquely problematic is a combination of the following: the species' inherent resistance to many drug classes; its ability to acquire resistance, via mutations, to all relevant treatments; its high and increasing rates of resistance locally; and its frequent role in serious infections. A few isolates of P. aeruginosa are resistant to all reliable antibiotics, and this problem seems likely to grow with the emergence of integrins that carry gene cassettes encoding both carbapenemases and amikacin acetyltransferases.}, added-at = {2011-03-11T10:05:34.000+0100}, author = {Livermore, David M}, biburl = {https://www.bibsonomy.org/bibtex/2376d8c6c7e0f913737fd48416737800a/jelias}, doi = {11823954}, interhash = {bc6c116394138822a63299a3ebf7b490}, intrahash = {376d8c6c7e0f913737fd48416737800a}, issn = {1537-6591}, journal = {Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America}, keywords = {Agents, Bacterial, Cell Drug Family, Frequency, Gene Humans, Integrins, Membrane Microbial Multigene Multiple, Mutation, Permeability, Pseudomonas Resistance, Sensitivity Tests, aeruginosa {Anti-Bacterial}}, month = mar, note = {{PMID:} 11823954}, number = 5, pages = {634--40}, shorttitle = {Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa}, timestamp = {2011-03-11T10:06:41.000+0100}, title = {Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa: our worst nightmare?}, url = {http://www.ncbi.nlm.nih.gov/pubmed/11823954}, volume = 34, year = 2002 }