Global transcriptomic response of the AI-3 isomers 3,5-DPO and 3,6-DPO in Salmonella Typhimurium
Bacterial intercellular signaling mediated by small molecules, also called autoinducers (AIs), enables synchronized behavior in response to environmental conditions, and in many bacterial pathogens, intercellular signaling controls virulence gene expression. However, in the intestinal pathogen Salmo...
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creator | Lallement, Claire Goldring, William P. D. Jelsbak, Lotte |
description | Bacterial intercellular signaling mediated by small molecules, also called autoinducers (AIs), enables synchronized behavior in response to environmental conditions, and in many bacterial pathogens, intercellular signaling controls virulence gene expression. However, in the intestinal pathogen
Salmonella enterica
subsp.
enterica
serovar Typhimurium (
S
. Typhimurium), although three signals, named AI-1, AI-2 and AI-3, have been described, their roles in virulence remain elusive. AI-3 is the 3,6- isomer of a previously described
Vibrio cholerae
signaling molecule; 3,5-dimethylpyrazin-2-ol (3,5-DPO). To elucidate the role of AI-3/DPO in
S
. Typhimurium, we have mapped the global transcriptomic responses to 3,5- and 3,6-DPO isomers in
S
. Typhimurium. Our studies showed that DPO affects expression of almost 8% of all genes. Specifically, expression of several genes involved in gut-colonization respond to DPO. Interestingly, most of the affected genes are similarly regulated by 3,5-DPO and 3,6-DPO, respectively, indicating that the two isomers have overlapping roles in
S
. Typhimurium. |
doi_str_mv | 10.1007/s00203-023-03450-x |
format | Article |
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Salmonella enterica
subsp.
enterica
serovar Typhimurium (
S
. Typhimurium), although three signals, named AI-1, AI-2 and AI-3, have been described, their roles in virulence remain elusive. AI-3 is the 3,6- isomer of a previously described
Vibrio cholerae
signaling molecule; 3,5-dimethylpyrazin-2-ol (3,5-DPO). To elucidate the role of AI-3/DPO in
S
. Typhimurium, we have mapped the global transcriptomic responses to 3,5- and 3,6-DPO isomers in
S
. Typhimurium. Our studies showed that DPO affects expression of almost 8% of all genes. Specifically, expression of several genes involved in gut-colonization respond to DPO. Interestingly, most of the affected genes are similarly regulated by 3,5-DPO and 3,6-DPO, respectively, indicating that the two isomers have overlapping roles in
S
. Typhimurium.</description><identifier>ISSN: 0302-8933</identifier><identifier>EISSN: 1432-072X</identifier><identifier>DOI: 10.1007/s00203-023-03450-x</identifier><identifier>PMID: 36929450</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Archives & records ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biochemistry ; Biofilms ; Biomedical and Life Sciences ; Biotechnology ; Brief Report ; Cell Biology ; E coli ; Ecology ; Environmental conditions ; Gene expression ; Gene Expression Profiling ; Gene Expression Regulation, Bacterial ; Genes ; Isomers ; Kinases ; Lactones - metabolism ; Life Sciences ; Microbial Ecology ; Microbiology ; Motility ; Pathogens ; Physiology ; Roles ; Salmonella ; Salmonella typhimurium - genetics ; Salmonella typhimurium - metabolism ; Signaling ; Transcriptome ; Transcriptomics ; Vibrio cholerae - genetics ; Virulence</subject><ispartof>Archives of microbiology, 2023-04, Vol.205 (4), p.117-117, Article 117</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023</rights><rights>2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-92a2b9974800da068f174ab25706eded19f9dcfc3580e03b8974ce3c4be6f12f3</cites><orcidid>0000-0002-3139-4570 ; 0000-0002-6642-7424 ; 0000-0002-8760-7491</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00203-023-03450-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00203-023-03450-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36929450$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lallement, Claire</creatorcontrib><creatorcontrib>Goldring, William P. D.</creatorcontrib><creatorcontrib>Jelsbak, Lotte</creatorcontrib><title>Global transcriptomic response of the AI-3 isomers 3,5-DPO and 3,6-DPO in Salmonella Typhimurium</title><title>Archives of microbiology</title><addtitle>Arch Microbiol</addtitle><addtitle>Arch Microbiol</addtitle><description>Bacterial intercellular signaling mediated by small molecules, also called autoinducers (AIs), enables synchronized behavior in response to environmental conditions, and in many bacterial pathogens, intercellular signaling controls virulence gene expression. However, in the intestinal pathogen
Salmonella enterica
subsp.
enterica
serovar Typhimurium (
S
. Typhimurium), although three signals, named AI-1, AI-2 and AI-3, have been described, their roles in virulence remain elusive. AI-3 is the 3,6- isomer of a previously described
Vibrio cholerae
signaling molecule; 3,5-dimethylpyrazin-2-ol (3,5-DPO). To elucidate the role of AI-3/DPO in
S
. Typhimurium, we have mapped the global transcriptomic responses to 3,5- and 3,6-DPO isomers in
S
. Typhimurium. Our studies showed that DPO affects expression of almost 8% of all genes. Specifically, expression of several genes involved in gut-colonization respond to DPO. Interestingly, most of the affected genes are similarly regulated by 3,5-DPO and 3,6-DPO, respectively, indicating that the two isomers have overlapping roles in
S
. Typhimurium.</description><subject>Archives & records</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biochemistry</subject><subject>Biofilms</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Brief Report</subject><subject>Cell Biology</subject><subject>E coli</subject><subject>Ecology</subject><subject>Environmental conditions</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genes</subject><subject>Isomers</subject><subject>Kinases</subject><subject>Lactones - metabolism</subject><subject>Life Sciences</subject><subject>Microbial Ecology</subject><subject>Microbiology</subject><subject>Motility</subject><subject>Pathogens</subject><subject>Physiology</subject><subject>Roles</subject><subject>Salmonella</subject><subject>Salmonella typhimurium - genetics</subject><subject>Salmonella typhimurium - metabolism</subject><subject>Signaling</subject><subject>Transcriptome</subject><subject>Transcriptomics</subject><subject>Vibrio cholerae - genetics</subject><subject>Virulence</subject><issn>0302-8933</issn><issn>1432-072X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kE1LxDAQhoMoun78AQ8S8OLB6CTT7cdx8RsWVnAFbzFNU7fSNjVpQf-9WXdV8OBhmIE87zuTl5BDDmccIDn3AAKQgQiF0RjY-wYZ8QgFg0Q8bZIRIAiWZog7ZNf7VwAu0jTdJjsYZyILihF5vqltrmraO9V67aqut02lqTO-s6031Ja0Xxg6uWNIK28b4zzF0zG7vJ9R1RZhjr_mqqUPqm5sa-pa0flHt6iawVVDs0-2SlV7c7Due-Tx-mp-ccums5u7i8mUaRRxzzKhRJ5lSZQCFAritORJpHIxTiA2hSl4VmaFLjWOUzCAeRpQbVBHuYlLLkrcIycr387Zt8H4XjaV18trWmMHL0USvg5CQBTQ4z_oqx1cG65bUknEEZMlJVaUdtZ7Z0rZuapR7kNykMv85Sp_GfKXX_nL9yA6WlsPeWOKH8l34AHAFeDDU_ti3O_uf2w_AZRIjnM</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Lallement, Claire</creator><creator>Goldring, William P. 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D.</au><au>Jelsbak, Lotte</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global transcriptomic response of the AI-3 isomers 3,5-DPO and 3,6-DPO in Salmonella Typhimurium</atitle><jtitle>Archives of microbiology</jtitle><stitle>Arch Microbiol</stitle><addtitle>Arch Microbiol</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>205</volume><issue>4</issue><spage>117</spage><epage>117</epage><pages>117-117</pages><artnum>117</artnum><issn>0302-8933</issn><eissn>1432-072X</eissn><abstract>Bacterial intercellular signaling mediated by small molecules, also called autoinducers (AIs), enables synchronized behavior in response to environmental conditions, and in many bacterial pathogens, intercellular signaling controls virulence gene expression. However, in the intestinal pathogen
Salmonella enterica
subsp.
enterica
serovar Typhimurium (
S
. Typhimurium), although three signals, named AI-1, AI-2 and AI-3, have been described, their roles in virulence remain elusive. AI-3 is the 3,6- isomer of a previously described
Vibrio cholerae
signaling molecule; 3,5-dimethylpyrazin-2-ol (3,5-DPO). To elucidate the role of AI-3/DPO in
S
. Typhimurium, we have mapped the global transcriptomic responses to 3,5- and 3,6-DPO isomers in
S
. Typhimurium. Our studies showed that DPO affects expression of almost 8% of all genes. Specifically, expression of several genes involved in gut-colonization respond to DPO. Interestingly, most of the affected genes are similarly regulated by 3,5-DPO and 3,6-DPO, respectively, indicating that the two isomers have overlapping roles in
S
. Typhimurium.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36929450</pmid><doi>10.1007/s00203-023-03450-x</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-3139-4570</orcidid><orcidid>https://orcid.org/0000-0002-6642-7424</orcidid><orcidid>https://orcid.org/0000-0002-8760-7491</orcidid></addata></record> |
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subjects | Archives & records Bacterial Proteins - genetics Bacterial Proteins - metabolism Biochemistry Biofilms Biomedical and Life Sciences Biotechnology Brief Report Cell Biology E coli Ecology Environmental conditions Gene expression Gene Expression Profiling Gene Expression Regulation, Bacterial Genes Isomers Kinases Lactones - metabolism Life Sciences Microbial Ecology Microbiology Motility Pathogens Physiology Roles Salmonella Salmonella typhimurium - genetics Salmonella typhimurium - metabolism Signaling Transcriptome Transcriptomics Vibrio cholerae - genetics Virulence |
title | Global transcriptomic response of the AI-3 isomers 3,5-DPO and 3,6-DPO in Salmonella Typhimurium |
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