<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>1(2)</volume><submitter>Iyoda S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Enterohemorrhagic Escherichia coli (EHEC) O157:H7 infection causes severe diseases such as bloody diarrhea and hemolytic uremic syndrome (HUS). Although EHEC O157:H7 strains have exhibited high genetic variability, their abilities to cause human diseases have not been fully examined.&lt;h4>Methods&lt;/h4>Clade typing and stx subtyping of EHEC O157:H7 strains, which were isolated in Japan during 1999-2011 from 269 HUS patients and 387 asymptomatic carriers (ACs) and showed distinct pulsed-field gel electrophoresis patterns, were performed to determine relationships between specific lineages and clinical presentation.&lt;h4>Results&lt;/h4>Clades 6 and 8 strains were more frequently found among the isolates from HUS cases than those from ACs (P = .00062 for clade 6, P &lt; .0001 for clade</pubmed_abstract><journal>Open forum infectious diseases</journal><pagination>ofu061</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4281788</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phylogenetic Clades 6 and 8 of Enterohemorrhagic Escherichia coli O157:H7 With Particular stx Subtypes are More Frequently Found in Isolates From Hemolytic Uremic Syndrome Patients Than From Asymptomatic Carriers.</pubmed_title><pmcid>PMC4281788</pmcid><pubmed_authors>Chiba K</pubmed_authors><pubmed_authors>Kubota T</pubmed_authors><pubmed_authors>Terajima J</pubmed_authors><pubmed_authors>Kikuchi K</pubmed_authors><pubmed_authors>Kobayashi H</pubmed_authors><pubmed_authors>Iguchi A</pubmed_authors><pubmed_authors>Kasahara H</pubmed_authors><pubmed_authors>Takashi K</pubmed_authors><pubmed_authors>Ueno H</pubmed_authors><pubmed_authors>Kimata K</pubmed_authors><pubmed_authors>Izumiya H</pubmed_authors><pubmed_authors>Asoshima N</pubmed_authors><pubmed_authors>Ogata K</pubmed_authors><pubmed_authors>Hiroi M</pubmed_authors><pubmed_authors>Tominaga K</pubmed_authors><pubmed_authors>Takamura M</pubmed_authors><pubmed_authors>Nakajima H</pubmed_authors><pubmed_authors>Kawano K</pubmed_authors><pubmed_authors>Nakamura H</pubmed_authors><pubmed_authors>Iwabuchi K</pubmed_authors><pubmed_authors>Morita-Ishihara T</pubmed_authors><pubmed_authors>Kurazono T</pubmed_authors><pubmed_authors>Sakamoto Y</pubmed_authors><pubmed_authors>Asano Y</pubmed_authors><pubmed_authors>Kojima Y</pubmed_authors><pubmed_authors>Hatakeyama T</pubmed_authors><pubmed_authors>Isobe J</pubmed_authors><pubmed_authors>Nishi K</pubmed_authors><pubmed_authors>Seto K</pubmed_authors><pubmed_authors>Hamada M</pubmed_authors><pubmed_authors>Ichihara S</pubmed_authors><pubmed_authors>Kitahashi T</pubmed_authors><pubmed_authors>Furukawa I</pubmed_authors><pubmed_authors>Horikawa K</pubmed_authors><pubmed_authors>Asai N</pubmed_authors><pubmed_authors>Satoh H</pubmed_authors><pubmed_authors>Konishi N</pubmed_authors><pubmed_authors>Tokoi Y</pubmed_authors><pubmed_authors>Ogura Y</pubmed_authors><pubmed_authors>Nagai Y</pubmed_authors><pubmed_authors>Kuroki T</pubmed_authors><pubmed_authors>Hirochi T</pubmed_authors><pubmed_authors>Ohnishi M</pubmed_authors><pubmed_authors>Saitoh E</pubmed_authors><pubmed_authors>Kudaka J</pubmed_authors><pubmed_authors>Kawanishi S</pubmed_authors><pubmed_authors>Kai A</pubmed_authors><pubmed_authors>Tanaka K</pubmed_authors><pubmed_authors>Yatsuyanagi J</pubmed_authors><pubmed_authors>Manning SD</pubmed_authors><pubmed_authors>Iyoda S</pubmed_authors><pubmed_authors>Naitoh H</pubmed_authors><pubmed_authors>Saitoh T</pubmed_authors><pubmed_authors>Harada S</pubmed_authors><pubmed_authors>Matsumoto Y</pubmed_authors><pubmed_authors>Migita Y</pubmed_authors><pubmed_authors>Kawase M</pubmed_authors><pubmed_authors>Shiraki Y</pubmed_authors><pubmed_authors>Kono T</pubmed_authors><pubmed_authors>Nakane K</pubmed_authors><pubmed_authors>Yabata J</pubmed_authors><pubmed_authors>Etoh Y</pubmed_authors><pubmed_authors>Arai R</pubmed_authors><pubmed_authors>Tanabe J</pubmed_authors><pubmed_authors>Honda M</pubmed_authors><pubmed_authors>Hara-Kudo Y</pubmed_authors><pubmed_authors>Obata H</pubmed_authors><pubmed_authors>Matsumoto K</pubmed_authors><pubmed_authors>Kameyama M</pubmed_authors><pubmed_authors>Matsumoto M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phylogenetic Clades 6 and 8 of Enterohemorrhagic Escherichia coli O157:H7 With Particular stx Subtypes are More Frequently Found in Isolates From Hemolytic Uremic Syndrome Patients Than From Asymptomatic Carriers.</name><description>&lt;h4>Background&lt;/h4>Enterohemorrhagic Escherichia coli (EHEC) O157:H7 infection causes severe diseases such as bloody diarrhea and hemolytic uremic syndrome (HUS). Although EHEC O157:H7 strains have exhibited high genetic variability, their abilities to cause human diseases have not been fully examined.&lt;h4>Methods&lt;/h4>Clade typing and stx subtyping of EHEC O157:H7 strains, which were isolated in Japan during 1999-2011 from 269 HUS patients and 387 asymptomatic carriers (ACs) and showed distinct pulsed-field gel electrophoresis patterns, were performed to determine relationships between specific lineages and clinical presentation.&lt;h4>Results&lt;/h4>Clades 6 and 8 strains were more frequently found among the isolates from HUS cases than those from ACs (P = .00062 for clade 6, P &lt; .0001 for clade</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Sep</publication><modification>2025-04-04T23:51:59.945Z</modification><creation>2019-06-06T13:41:11Z</creation></dates><accession>S-EPMC4281788</accession><cross_references><pubmed>25734131</pubmed><doi>10.1093/ofid/ofu061</doi></cross_references></HashMap>