{"title":"尿路致病性大肠杆菌感染过程中膜基因的时间调控。","authors":"William R Schwan, Hua Ding","doi":"10.1155/2017/8694356","DOIUrl":null,"url":null,"abstract":"<p><p>Uropathogenic <i>Escherichia coli</i> (UPEC) adhere to cells in the human urinary tract via type 1 pili that undergo phase variation where a 314-bp <i>fimS</i> DNA element flips between Phase-ON and Phase-OFF orientations through two site-specific recombinases, FimB and FimE. Three <i>fim-lux</i> operon transcriptional fusions were created and moved into the clinical UPEC isolate NU149 to determine their temporal regulation in UPEC growing in the urinary tract. Within murine urinary tracts, the UPEC strains demonstrated elevated transcription of <i>fimA</i> and <i>fimB</i> early in the infection, but lower transcription by the fifth day in murine kidneys. In contrast, <i>fimE</i> transcription was much lower than either <i>fimA</i> or <i>fimB</i> early, increased markedly at 24 h after inoculation, and then dropped five days after inoculation. Positioning of <i>fimS</i> was primarily in the Phase-ON position over the time span in UPEC infected bladders, whereas in UPEC infected murine kidneys the Phase-OFF orientation was favored by the fifth day after inoculation. Hemagglutination titers with guinea pig erythrocytes remained constant in UPEC growing in infected murine bladders but fell substantially in UPEC infected kidneys over time. Our results show temporal <i>in vivo</i> regulation of <i>fim</i> gene expression in different environmental niches when UPEC infects the murine urinary tract.</p>","PeriodicalId":16788,"journal":{"name":"Journal of Pathogens","volume":"2017 ","pages":"8694356"},"PeriodicalIF":1.1000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2017/8694356","citationCount":"11","resultStr":"{\"title\":\"Temporal Regulation of <i>fim</i> Genes in Uropathogenic <i>Escherichia coli</i> during Infection of the Murine Urinary Tract.\",\"authors\":\"William R Schwan, Hua Ding\",\"doi\":\"10.1155/2017/8694356\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Uropathogenic <i>Escherichia coli</i> (UPEC) adhere to cells in the human urinary tract via type 1 pili that undergo phase variation where a 314-bp <i>fimS</i> DNA element flips between Phase-ON and Phase-OFF orientations through two site-specific recombinases, FimB and FimE. Three <i>fim-lux</i> operon transcriptional fusions were created and moved into the clinical UPEC isolate NU149 to determine their temporal regulation in UPEC growing in the urinary tract. Within murine urinary tracts, the UPEC strains demonstrated elevated transcription of <i>fimA</i> and <i>fimB</i> early in the infection, but lower transcription by the fifth day in murine kidneys. In contrast, <i>fimE</i> transcription was much lower than either <i>fimA</i> or <i>fimB</i> early, increased markedly at 24 h after inoculation, and then dropped five days after inoculation. Positioning of <i>fimS</i> was primarily in the Phase-ON position over the time span in UPEC infected bladders, whereas in UPEC infected murine kidneys the Phase-OFF orientation was favored by the fifth day after inoculation. Hemagglutination titers with guinea pig erythrocytes remained constant in UPEC growing in infected murine bladders but fell substantially in UPEC infected kidneys over time. Our results show temporal <i>in vivo</i> regulation of <i>fim</i> gene expression in different environmental niches when UPEC infects the murine urinary tract.</p>\",\"PeriodicalId\":16788,\"journal\":{\"name\":\"Journal of Pathogens\",\"volume\":\"2017 \",\"pages\":\"8694356\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1155/2017/8694356\",\"citationCount\":\"11\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pathogens\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2017/8694356\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2017/12/27 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pathogens","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2017/8694356","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2017/12/27 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Temporal Regulation of fim Genes in Uropathogenic Escherichia coli during Infection of the Murine Urinary Tract.
Uropathogenic Escherichia coli (UPEC) adhere to cells in the human urinary tract via type 1 pili that undergo phase variation where a 314-bp fimS DNA element flips between Phase-ON and Phase-OFF orientations through two site-specific recombinases, FimB and FimE. Three fim-lux operon transcriptional fusions were created and moved into the clinical UPEC isolate NU149 to determine their temporal regulation in UPEC growing in the urinary tract. Within murine urinary tracts, the UPEC strains demonstrated elevated transcription of fimA and fimB early in the infection, but lower transcription by the fifth day in murine kidneys. In contrast, fimE transcription was much lower than either fimA or fimB early, increased markedly at 24 h after inoculation, and then dropped five days after inoculation. Positioning of fimS was primarily in the Phase-ON position over the time span in UPEC infected bladders, whereas in UPEC infected murine kidneys the Phase-OFF orientation was favored by the fifth day after inoculation. Hemagglutination titers with guinea pig erythrocytes remained constant in UPEC growing in infected murine bladders but fell substantially in UPEC infected kidneys over time. Our results show temporal in vivo regulation of fim gene expression in different environmental niches when UPEC infects the murine urinary tract.