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Environmental stresses, such as starvation and antibiotics, can cause stalling of bacterial ribosomes, which may alter gene expression through a transcription or translation attenuation mechanism. In <jats:styled-content style=\"fixed-case\"><jats:italic>P<\/jats:italic><\/jats:styled-content><jats:italic>seudomonas aeruginosa<\/jats:italic>, the expression of <jats:styled-content style=\"fixed-case\">MexXY<\/jats:styled-content> multidrug efflux system, which plays a significant role in resistance against aminoglycoside antibiotics, is controlled by a translation surveillance mechanism. Stalling of ribosome at the <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>5471 leader peptide (<jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>5471.1) m<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> leads to transcription of <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>5471, which subsequently up\u2010regulates the expression of <jats:styled-content style=\"fixed-case\">MexXY<\/jats:styled-content>. In this study, we found that mutation in a <jats:italic>suh<\/jats:italic><jats:styled-content style=\"fixed-case\"><jats:italic>B<\/jats:italic><\/jats:styled-content> gene leads to decreased susceptibility to aminoglycosides. Transcriptomic analysis revealed an up\u2010regulation of <jats:styled-content style=\"fixed-case\">MexXY<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>5471, which were demonstrated to be responsible for the decreased susceptibility of the <jats:italic>suh<\/jats:italic><jats:styled-content style=\"fixed-case\"><jats:italic>B<\/jats:italic><\/jats:styled-content> mutant. We further demonstrated that <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>5471.1 is essential for the up\u2010regulation of <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>5471 in the <jats:italic>suh<\/jats:italic><jats:styled-content style=\"fixed-case\"><jats:italic>B<\/jats:italic><\/jats:styled-content> mutant. Co\u2010immunoprecipitation assay revealed an interaction between <jats:styled-content style=\"fixed-case\">SuhB<\/jats:styled-content> and ribosome, suggesting a role of <jats:styled-content style=\"fixed-case\">SuhB<\/jats:styled-content> in translation. Indeed, higher amount of <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>5471.1 m<jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> was found to associate with ribosome isolated from the <jats:italic>suh<\/jats:italic><jats:styled-content style=\"fixed-case\"><jats:italic>B<\/jats:italic><\/jats:styled-content> mutant, indicating increased ribosome stalling. Therefore, this study identified <jats:styled-content style=\"fixed-case\">SuhB<\/jats:styled-content> as a novel ribosome associated protein that is involved in modulating ribosome activity.<\/jats:p>","DOI":"10.1111\/mmi.13126","type":"journal-article","created":{"date-parts":[[2015,7,14]],"date-time":"2015-07-14T20:39:56Z","timestamp":1436906396000},"page":"370-383","source":"Crossref","is-referenced-by-count":36,"title":["<scp>SuhB<\/scp> is a novel ribosome associated protein that regulates expression of <scp>MexXY<\/scp> by modulating ribosome stalling in <scp><i>P<\/i><\/scp><i>seudomonas aeruginosa<\/i>"],"prefix":"10.1111","volume":"98","author":[{"given":"Jing","family":"Shi","sequence":"first","affiliation":[{"name":"State Key Laboratory of Medicinal Chemical Biology Key Laboratory of Molecular Microbiology and Technology of the Ministry of Education Department of Microbiology College of Life Sciences Nankai University  Tianjin 300071 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