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Bacterial pathogens devise various mechanisms to withstand the activity of a wide range of antimicrobial compounds, among which the acquisition of carbapenemases is one of the most concerning. In\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>K<\/jats:italic>\n                    <\/jats:styled-content>\n                    <jats:italic>lebsiella pneumoniae<\/jats:italic>\n                    , the dissemination of the\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    carbapenemase is tightly connected to the global spread of certain clonal lineages. Although antibiotic resistance is a key driver for the global distribution of epidemic high\u2010risk clones, there seem to be other adaptive traits that may explain their success. Here, we exploited the power of deep transcriptome profiling (\n                    <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\n                    \u2010seq) to shed light on the transcriptomic landscape of 37 clinical\n                    <jats:styled-content style=\"fixed-case\">\n                      <jats:italic>K<\/jats:italic>\n                    <\/jats:styled-content>\n                    <jats:italic>. pneumoniae<\/jats:italic>\n                    isolates of diverse phylogenetic origins. We identified a large set of 3346 genes which was expressed in all isolates. While the core\u2010transcriptome profiles varied substantially between groups of different sequence types, they were more homogenous among isolates of the same sequence type. We furthermore linked the detailed information on differentially expressed genes with the clinically relevant phenotypes of biofilm formation and bacterial virulence. This allowed for the identification of a diminished expression of biofilm\u2010specific genes within the low biofilm producing\n                    <jats:styled-content style=\"fixed-case\">ST<\/jats:styled-content>\n                    258 isolates as a sequence type\u2010specific trait.\n                  <\/jats:p>","DOI":"10.1111\/1462-2920.13016","type":"journal-article","created":{"date-parts":[[2015,8,11]],"date-time":"2015-08-11T05:14:55Z","timestamp":1439270095000},"page":"4690-4710","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":27,"title":["Deep transcriptome profiling of clinical\n                    <scp>\n                      <i>K<\/i>\n                    <\/scp>\n                    <i>lebsiella pneumoniae<\/i>\n                    isolates reveals strain and sequence type\u2010specific 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