low-pH medium in vitro or the environment within a macrophage decreases the transcriptional levels of fimA, fimZ and lrp in Salmonella enterica serovar Typhimurium
Many Salmonella Typhimurium isolates produce type 1 fimbriae and exhibit fimbrial phase variation in vitro. Static broth culture favours the production of fimbriae, while solid agar medium inhibits the generation of these appendages. Little information is available regarding whether S. Typhimurium c...
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creator | Wang, Ke-Chuan Hsu, Yuan-Hsun Huang, Yi-Ning Chen, Ter-Hsin Lin, Jiunn-Horng Hsuan, Shih-Ling Chien, Maw-Sheng Lee, Wei-Cheng Yeh, Kuang-Sheng |
description | Many Salmonella Typhimurium isolates produce type 1 fimbriae and exhibit fimbrial phase variation in vitro. Static broth culture favours the production of fimbriae, while solid agar medium inhibits the generation of these appendages. Little information is available regarding whether S. Typhimurium continues to produce type 1 fimbriae during in vivo growth. We used a type 1 fimbrial phase-variable strain S. Typhimurium LB5010 and its derivatives to infect RAW 264.7 macrophages. Following entry into macrophages, S. Typhimurium LB5010 gradually decreased the transcript levels of fimbrial subunit gene fimA, positive regulatory gene fimZ, and global regulatory gene lrp. A similar decrease in transcript levels was detected by RT-PCR when the pH of static broth medium was shifted from pH 7 to a more acidic pH 4. A fimA-deleted strain continued to multiply within macrophages as did the parental strain. An lrp deletion strain was unimpaired for in vitro growth at pH 7 or pH 4, while a strain harboring an lrp-containing plasmid exhibited impaired in vitro growth at pH 4. We propose that acidic medium, which resembles one aspect of the intracellular environment in a macrophage, inhibits type 1 fimbrial production by down-regulation of the expression of lrp, fimZ and fimA. |
doi_str_mv | 10.1007/s12038-013-9347-2 |
format | Article |
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Static broth culture favours the production of fimbriae, while solid agar medium inhibits the generation of these appendages. Little information is available regarding whether S. Typhimurium continues to produce type 1 fimbriae during in vivo growth. We used a type 1 fimbrial phase-variable strain S. Typhimurium LB5010 and its derivatives to infect RAW 264.7 macrophages. Following entry into macrophages, S. Typhimurium LB5010 gradually decreased the transcript levels of fimbrial subunit gene fimA, positive regulatory gene fimZ, and global regulatory gene lrp. A similar decrease in transcript levels was detected by RT-PCR when the pH of static broth medium was shifted from pH 7 to a more acidic pH 4. A fimA-deleted strain continued to multiply within macrophages as did the parental strain. An lrp deletion strain was unimpaired for in vitro growth at pH 7 or pH 4, while a strain harboring an lrp-containing plasmid exhibited impaired in vitro growth at pH 4. We propose that acidic medium, which resembles one aspect of the intracellular environment in a macrophage, inhibits type 1 fimbrial production by down-regulation of the expression of lrp, fimZ and fimA.</description><identifier>ISSN: 0250-5991</identifier><identifier>EISSN: 0973-7138</identifier><identifier>DOI: 10.1007/s12038-013-9347-2</identifier><identifier>PMID: 23938383</identifier><language>eng</language><publisher>India: Springer-Verlag</publisher><subject>agar ; Antigens, Bacterial - genetics ; appendages ; Bacterial Proteins - genetics ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Cell culture ; Down-Regulation ; fimbriae ; Fimbriae Proteins - genetics ; Gene Expression Regulation, Bacterial ; Hydrogen-Ion Concentration ; Life Sciences ; macrophages ; Macrophages - metabolism ; Microbiology ; Plant Sciences ; plasmids ; Protein Binding ; regulator genes ; reverse transcriptase polymerase chain reaction ; Salmonella ; Salmonella enterica ; Salmonella enterica subsp. enterica serovar Typhimurium ; Salmonella typhimurium ; Salmonella typhimurium - genetics ; Salmonella typhimurium - growth & development ; Salmonella typhimurium - pathogenicity ; Temperature effects ; transcription (genetics) ; Transcription Factors - genetics ; Transcription, Genetic ; Zoology</subject><ispartof>Journal of biosciences, 2013-09, Vol.38 (3), p.499-507</ispartof><rights>Indian Academy of Sciences 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-54458863112e24098399c11d4e00cbac24f7a4e8e1136b5078ee2e3171a3e4903</citedby><cites>FETCH-LOGICAL-c429t-54458863112e24098399c11d4e00cbac24f7a4e8e1136b5078ee2e3171a3e4903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12038-013-9347-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12038-013-9347-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23938383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Ke-Chuan</creatorcontrib><creatorcontrib>Hsu, Yuan-Hsun</creatorcontrib><creatorcontrib>Huang, Yi-Ning</creatorcontrib><creatorcontrib>Chen, Ter-Hsin</creatorcontrib><creatorcontrib>Lin, Jiunn-Horng</creatorcontrib><creatorcontrib>Hsuan, Shih-Ling</creatorcontrib><creatorcontrib>Chien, Maw-Sheng</creatorcontrib><creatorcontrib>Lee, Wei-Cheng</creatorcontrib><creatorcontrib>Yeh, Kuang-Sheng</creatorcontrib><title>low-pH medium in vitro or the environment within a macrophage decreases the transcriptional levels of fimA, fimZ and lrp in Salmonella enterica serovar Typhimurium</title><title>Journal of biosciences</title><addtitle>J Biosci</addtitle><addtitle>J Biosci</addtitle><description>Many Salmonella Typhimurium isolates produce type 1 fimbriae and exhibit fimbrial phase variation in vitro. Static broth culture favours the production of fimbriae, while solid agar medium inhibits the generation of these appendages. Little information is available regarding whether S. Typhimurium continues to produce type 1 fimbriae during in vivo growth. We used a type 1 fimbrial phase-variable strain S. Typhimurium LB5010 and its derivatives to infect RAW 264.7 macrophages. Following entry into macrophages, S. Typhimurium LB5010 gradually decreased the transcript levels of fimbrial subunit gene fimA, positive regulatory gene fimZ, and global regulatory gene lrp. A similar decrease in transcript levels was detected by RT-PCR when the pH of static broth medium was shifted from pH 7 to a more acidic pH 4. A fimA-deleted strain continued to multiply within macrophages as did the parental strain. An lrp deletion strain was unimpaired for in vitro growth at pH 7 or pH 4, while a strain harboring an lrp-containing plasmid exhibited impaired in vitro growth at pH 4. We propose that acidic medium, which resembles one aspect of the intracellular environment in a macrophage, inhibits type 1 fimbrial production by down-regulation of the expression of lrp, fimZ and fimA.</description><subject>agar</subject><subject>Antigens, Bacterial - genetics</subject><subject>appendages</subject><subject>Bacterial Proteins - genetics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Cell culture</subject><subject>Down-Regulation</subject><subject>fimbriae</subject><subject>Fimbriae Proteins - genetics</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Hydrogen-Ion Concentration</subject><subject>Life Sciences</subject><subject>macrophages</subject><subject>Macrophages - metabolism</subject><subject>Microbiology</subject><subject>Plant Sciences</subject><subject>plasmids</subject><subject>Protein Binding</subject><subject>regulator genes</subject><subject>reverse transcriptase polymerase chain reaction</subject><subject>Salmonella</subject><subject>Salmonella enterica</subject><subject>Salmonella enterica subsp. enterica serovar Typhimurium</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - genetics</subject><subject>Salmonella typhimurium - growth & development</subject><subject>Salmonella typhimurium - pathogenicity</subject><subject>Temperature effects</subject><subject>transcription (genetics)</subject><subject>Transcription Factors - genetics</subject><subject>Transcription, Genetic</subject><subject>Zoology</subject><issn>0250-5991</issn><issn>0973-7138</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNks1u1DAQgCMEoqXwAFzAEhcOBDy2k9jHqgKKVIlD2wsXy5ud7LpK7DBOturz8KI4TUGIA0KWbEv-5kfzuSheAn8PnDcfEggudclBlkaqphSPimNuGlk2IPXjfBcVLytj4Kh4ltIN52CU5E-LIyGN1HkdFz_6eFuO52zArZ8H5gM7-Ikii8SmPTIMB08xDBgmduunfX53bHAtxXHvdsi22BK6hOmensiF1JIfJx-D61mPB-wTix3r_HD6btm_MRe2rKdxKXXp-iEG7HuXC01IvnUsIcWDI3Z1N-79MFPu6nnxpHN9whcP50lx_enj1dl5efH185ez04uyVcJMZaVUpXUtAQQKxY2WxrQAW4WctxvXCtU1TqFGAFlvKt5oRIESGnASleHypHi75h0pfp8xTXbwqV3aCxjnZEFJI2RVif9BBa-zCmMy-uYv9CbOlMdzT9XKgAadKVipPNqUCDs7kh8c3VngdpFtV9k2y7aLbCtyzKuHzPMm-_sd8ctuBsQKpPwUdkh_lP5H1tdrUOeidTvyyV5fCg4qf5-6VrWSPwGyYb5c</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Wang, Ke-Chuan</creator><creator>Hsu, Yuan-Hsun</creator><creator>Huang, Yi-Ning</creator><creator>Chen, Ter-Hsin</creator><creator>Lin, Jiunn-Horng</creator><creator>Hsuan, Shih-Ling</creator><creator>Chien, Maw-Sheng</creator><creator>Lee, Wei-Cheng</creator><creator>Yeh, Kuang-Sheng</creator><general>Springer-Verlag</general><general>Springer India</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H99</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L.F</scope><scope>L.G</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20130901</creationdate><title>low-pH medium in vitro or the environment within a macrophage decreases the transcriptional levels of fimA, fimZ and lrp in Salmonella enterica serovar Typhimurium</title><author>Wang, Ke-Chuan ; Hsu, Yuan-Hsun ; Huang, Yi-Ning ; Chen, Ter-Hsin ; Lin, Jiunn-Horng ; Hsuan, Shih-Ling ; Chien, Maw-Sheng ; Lee, Wei-Cheng ; Yeh, Kuang-Sheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-54458863112e24098399c11d4e00cbac24f7a4e8e1136b5078ee2e3171a3e4903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>agar</topic><topic>Antigens, Bacterial - genetics</topic><topic>appendages</topic><topic>Bacterial Proteins - genetics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Cell culture</topic><topic>Down-Regulation</topic><topic>fimbriae</topic><topic>Fimbriae Proteins - genetics</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Hydrogen-Ion Concentration</topic><topic>Life Sciences</topic><topic>macrophages</topic><topic>Macrophages - metabolism</topic><topic>Microbiology</topic><topic>Plant Sciences</topic><topic>plasmids</topic><topic>Protein Binding</topic><topic>regulator genes</topic><topic>reverse transcriptase polymerase chain reaction</topic><topic>Salmonella</topic><topic>Salmonella enterica</topic><topic>Salmonella enterica subsp. enterica serovar Typhimurium</topic><topic>Salmonella typhimurium</topic><topic>Salmonella typhimurium - genetics</topic><topic>Salmonella typhimurium - growth & development</topic><topic>Salmonella typhimurium - pathogenicity</topic><topic>Temperature effects</topic><topic>transcription (genetics)</topic><topic>Transcription Factors - genetics</topic><topic>Transcription, Genetic</topic><topic>Zoology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Ke-Chuan</creatorcontrib><creatorcontrib>Hsu, Yuan-Hsun</creatorcontrib><creatorcontrib>Huang, Yi-Ning</creatorcontrib><creatorcontrib>Chen, Ter-Hsin</creatorcontrib><creatorcontrib>Lin, Jiunn-Horng</creatorcontrib><creatorcontrib>Hsuan, Shih-Ling</creatorcontrib><creatorcontrib>Chien, Maw-Sheng</creatorcontrib><creatorcontrib>Lee, Wei-Cheng</creatorcontrib><creatorcontrib>Yeh, Kuang-Sheng</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biosciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Ke-Chuan</au><au>Hsu, Yuan-Hsun</au><au>Huang, Yi-Ning</au><au>Chen, Ter-Hsin</au><au>Lin, Jiunn-Horng</au><au>Hsuan, Shih-Ling</au><au>Chien, Maw-Sheng</au><au>Lee, Wei-Cheng</au><au>Yeh, Kuang-Sheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>low-pH medium in vitro or the environment within a macrophage decreases the transcriptional levels of fimA, fimZ and lrp in Salmonella enterica serovar Typhimurium</atitle><jtitle>Journal of biosciences</jtitle><stitle>J Biosci</stitle><addtitle>J Biosci</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>38</volume><issue>3</issue><spage>499</spage><epage>507</epage><pages>499-507</pages><issn>0250-5991</issn><eissn>0973-7138</eissn><abstract>Many Salmonella Typhimurium isolates produce type 1 fimbriae and exhibit fimbrial phase variation in vitro. Static broth culture favours the production of fimbriae, while solid agar medium inhibits the generation of these appendages. Little information is available regarding whether S. Typhimurium continues to produce type 1 fimbriae during in vivo growth. We used a type 1 fimbrial phase-variable strain S. Typhimurium LB5010 and its derivatives to infect RAW 264.7 macrophages. Following entry into macrophages, S. Typhimurium LB5010 gradually decreased the transcript levels of fimbrial subunit gene fimA, positive regulatory gene fimZ, and global regulatory gene lrp. A similar decrease in transcript levels was detected by RT-PCR when the pH of static broth medium was shifted from pH 7 to a more acidic pH 4. A fimA-deleted strain continued to multiply within macrophages as did the parental strain. An lrp deletion strain was unimpaired for in vitro growth at pH 7 or pH 4, while a strain harboring an lrp-containing plasmid exhibited impaired in vitro growth at pH 4. We propose that acidic medium, which resembles one aspect of the intracellular environment in a macrophage, inhibits type 1 fimbrial production by down-regulation of the expression of lrp, fimZ and fimA.</abstract><cop>India</cop><pub>Springer-Verlag</pub><pmid>23938383</pmid><doi>10.1007/s12038-013-9347-2</doi><tpages>9</tpages></addata></record> |
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subjects | agar Antigens, Bacterial - genetics appendages Bacterial Proteins - genetics Biomedical and Life Sciences Biomedicine Cell Biology Cell culture Down-Regulation fimbriae Fimbriae Proteins - genetics Gene Expression Regulation, Bacterial Hydrogen-Ion Concentration Life Sciences macrophages Macrophages - metabolism Microbiology Plant Sciences plasmids Protein Binding regulator genes reverse transcriptase polymerase chain reaction Salmonella Salmonella enterica Salmonella enterica subsp. enterica serovar Typhimurium Salmonella typhimurium Salmonella typhimurium - genetics Salmonella typhimurium - growth & development Salmonella typhimurium - pathogenicity Temperature effects transcription (genetics) Transcription Factors - genetics Transcription, Genetic Zoology |
title | low-pH medium in vitro or the environment within a macrophage decreases the transcriptional levels of fimA, fimZ and lrp in Salmonella enterica serovar Typhimurium |
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