<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Zhang L</submitter><pubmed_abstract>Ionizing irradiation kills pathogens by destroying nucleic acids without protein structure destruction. However, how pathogens respond to irradiation stress has not yet been fully elucidated. Here, we observed that &lt;i>Pseudomonas aeruginosa&lt;/i> PAO1 could release nucleic acids into the extracellular environment under X-ray irradiation. Using scanning electron microscopy (SEM) and transmission electron microscopy (TEM), X-ray irradiation was observed to induce outer membrane vesicle (OMV) formation in &lt;i>P. aeruginosa&lt;/i> PAO1. The size distribution of the OMVs of the irradiated PAO1 was similar to that of the OMVs of the non-irradiated PAO1 according to nanoparticle tracking analysis (NTA). The pyocin-related proteins are involved in OMV production in &lt;i>P. aeruginosa&lt;/i> PAO1 under X-ray irradiation conditions, and that this is regulated by the key SOS gene &lt;i>recA&lt;/i>. The OMV production was significantly impaired in the irradiated PAO1 Δ&lt;i>lys&lt;/i> mutant, suggesting that Lys endolysin is associated with OMV production in &lt;i>P. aeruginosa&lt;/i> PAO1 upon irradiation stress. Meanwhile, no significant difference in OMV production was observed between PAO1 lacking the &lt;i>pqsR&lt;/i>, &lt;i>lasR&lt;/i>, or &lt;i>rhlR&lt;/i> genes and the parent strain, demonstrating that the irradiation-induced OMV biosynthesis of &lt;i>P. aeruginosa&lt;/i> was independent of the &lt;i>Pseudomonas&lt;/i> quinolone signal (PQS).</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>558233</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7770229</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Proteomic Analysis of Vesicle-Producing &lt;i>Pseudomonas aeruginosa&lt;/i> PAO1 Exposed to X-Ray Irradiation.</pubmed_title><pmcid>PMC7770229</pmcid><pubmed_authors>Zhao SQ</pubmed_authors><pubmed_authors>Jiang BG</pubmed_authors><pubmed_authors>Cheng XJ</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Ma CC</pubmed_authors><pubmed_authors>Liao XY</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Liu YB</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Li WF</pubmed_authors><pubmed_authors>Wang ZL</pubmed_authors><pubmed_authors>Xie YL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteomic Analysis of Vesicle-Producing &lt;i>Pseudomonas aeruginosa&lt;/i> PAO1 Exposed to X-Ray Irradiation.</name><description>Ionizing irradiation kills pathogens by destroying nucleic acids without protein structure destruction. However, how pathogens respond to irradiation stress has not yet been fully elucidated. Here, we observed that &lt;i>Pseudomonas aeruginosa&lt;/i> PAO1 could release nucleic acids into the extracellular environment under X-ray irradiation. Using scanning electron microscopy (SEM) and transmission electron microscopy (TEM), X-ray irradiation was observed to induce outer membrane vesicle (OMV) formation in &lt;i>P. aeruginosa&lt;/i> PAO1. The size distribution of the OMVs of the irradiated PAO1 was similar to that of the OMVs of the non-irradiated PAO1 according to nanoparticle tracking analysis (NTA). The pyocin-related proteins are involved in OMV production in &lt;i>P. aeruginosa&lt;/i> PAO1 under X-ray irradiation conditions, and that this is regulated by the key SOS gene &lt;i>recA&lt;/i>. The OMV production was significantly impaired in the irradiated PAO1 Δ&lt;i>lys&lt;/i> mutant, suggesting that Lys endolysin is associated with OMV production in &lt;i>P. aeruginosa&lt;/i> PAO1 upon irradiation stress. Meanwhile, no significant difference in OMV production was observed between PAO1 lacking the &lt;i>pqsR&lt;/i>, &lt;i>lasR&lt;/i>, or &lt;i>rhlR&lt;/i> genes and the parent strain, demonstrating that the irradiation-induced OMV biosynthesis of &lt;i>P. aeruginosa&lt;/i> was independent of the &lt;i>Pseudomonas&lt;/i> quinolone signal (PQS).</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2024-11-06T19:53:43.523Z</modification><creation>2021-02-20T17:24:34Z</creation></dates><accession>S-EPMC7770229</accession><cross_references><pubmed>33384665</pubmed><doi>10.3389/fmicb.2020.558233</doi></cross_references></HashMap>