Resistance to mecillinam produced by the co-operative action of mutations affecting lipopolysaccharide, spoT, and cya or crp genes of Salmonella typhimurium
Lipopolysaccharide (LPS), spoT, and cya or crp mutations individually do not affect the minimum inhibitory concentration of mecillinam on Salmonella typhimurium. However, when mutations of two of these types were combined in the same strain, high-level resistance appeared, and increased even further...
Gespeichert in:
Veröffentlicht in: | Molecular microbiology 1995-05, Vol.16 (3), p.587-595 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 595 |
---|---|
container_issue | 3 |
container_start_page | 587 |
container_title | Molecular microbiology |
container_volume | 16 |
creator | Anton, D N |
description | Lipopolysaccharide (LPS), spoT, and cya or crp mutations individually do not affect the minimum inhibitory concentration of mecillinam on Salmonella typhimurium. However, when mutations of two of these types were combined in the same strain, high-level resistance appeared, and increased even further when all three types of mutations were present. Most mutations affecting LPS (rfa, rfb, rfc) showed this behaviour, although to different degrees. The highest resistance to mecillinam was caused by galE and rfc mutations whereas almost no effect was noticed with rfaB or rfaK mutations. This phenomenon appears to be specific for mecillinam since none of several other antibiotics elicited it. Reduction of guanosine tetraphosphate (ppGpp) levels by introduction of a relA mutation did not significantly affect the MIC of mecillinam on strains carrying different combinations of spoT, galE, and cya or crp mutations. All the strains produced spherical cells in medium with a low concentration (0.05 microgram ml-1) of the antibiotic. These results suggest that the antibacterial action of mecillinam on S. typhimurium is somehow dependent on the interaction of LPS, cyclic AMP/cyclic AMP receptor protein (cAMP/CRP), and SpoT. The reported resistance to mecillinam of cya and crp mutants of Escherichia coli K-12 is probably due to the natural LPS defectiveness of this strain. |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_16816988</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16816988</sourcerecordid><originalsourceid>FETCH-LOGICAL-p847-9cad4083eafde4b080060188a4de4bb16ad225a9e9efa8e6010b5d21c332460e3</originalsourceid><addsrcrecordid>eNotUMtqwzAQ9KElTdN-QmFPPcUgW7YjH0voCwKFNofezFpaJyqSpVpywf_Sj21Mc9qdB8POXiRLVpcs5SL_vEquQ_hiLOOs4otksSmrMss2y-T3nYIOEXtJEB1YktoY3aMFPzg1SlLQThCPBNKlztOAUf8QoIza9eA6sGPEeQ-AXUcnuj-A0d55Z6aAUh5x0IrWELzbrwF7BXJCcAPIwcOBegpzygca63oyBiFO_qjtOOjR3iSXHZpAt-e5SvZPj_vtS7p7e37dPuxSL4pNWktUBROcsFNUtEwwVrFMCCxm2GYVqjwvsaaaOhR00lhbqjyTnOdFxYivkvv_2FPl75FCbKwOcj6mJzeGJqtEVtVCnIx3Z-PYWlKNH7TFYWrO3-R_Vn1z6w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16816988</pqid></control><display><type>article</type><title>Resistance to mecillinam produced by the co-operative action of mutations affecting lipopolysaccharide, spoT, and cya or crp genes of Salmonella typhimurium</title><source>Wiley-Blackwell Journals</source><source>MEDLINE</source><creator>Anton, D N</creator><creatorcontrib>Anton, D N</creatorcontrib><description>Lipopolysaccharide (LPS), spoT, and cya or crp mutations individually do not affect the minimum inhibitory concentration of mecillinam on Salmonella typhimurium. However, when mutations of two of these types were combined in the same strain, high-level resistance appeared, and increased even further when all three types of mutations were present. Most mutations affecting LPS (rfa, rfb, rfc) showed this behaviour, although to different degrees. The highest resistance to mecillinam was caused by galE and rfc mutations whereas almost no effect was noticed with rfaB or rfaK mutations. This phenomenon appears to be specific for mecillinam since none of several other antibiotics elicited it. Reduction of guanosine tetraphosphate (ppGpp) levels by introduction of a relA mutation did not significantly affect the MIC of mecillinam on strains carrying different combinations of spoT, galE, and cya or crp mutations. All the strains produced spherical cells in medium with a low concentration (0.05 microgram ml-1) of the antibiotic. These results suggest that the antibacterial action of mecillinam on S. typhimurium is somehow dependent on the interaction of LPS, cyclic AMP/cyclic AMP receptor protein (cAMP/CRP), and SpoT. The reported resistance to mecillinam of cya and crp mutants of Escherichia coli K-12 is probably due to the natural LPS defectiveness of this strain.</description><identifier>ISSN: 0950-382X</identifier><identifier>PMID: 7565117</identifier><language>eng</language><publisher>England</publisher><subject>Adenylyl Cyclases - genetics ; Adenylyl Cyclases - physiology ; Amdinocillin - pharmacology ; Anti-Bacterial Agents - classification ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; beta-Lactam Resistance - genetics ; Carbohydrate Epimerases - genetics ; Carbohydrate Epimerases - metabolism ; Carbohydrate Sequence ; Carrier Proteins ; Conjugation, Genetic ; Cyclic AMP Receptor Protein - genetics ; Cyclic AMP Receptor Protein - physiology ; Escherichia coli ; Guanosine Tetraphosphate - metabolism ; Hexosyltransferases - genetics ; Lipopolysaccharides - biosynthesis ; Lipopolysaccharides - chemistry ; Molecular Sequence Data ; Mutagenesis ; Pyrophosphatases - genetics ; Pyrophosphatases - physiology ; Salmonella typhimurium ; Salmonella typhimurium - drug effects ; Salmonella typhimurium - genetics ; Salmonella typhimurium - ultrastructure ; UDPglucose 4-Epimerase</subject><ispartof>Molecular microbiology, 1995-05, Vol.16 (3), p.587-595</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7565117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anton, D N</creatorcontrib><title>Resistance to mecillinam produced by the co-operative action of mutations affecting lipopolysaccharide, spoT, and cya or crp genes of Salmonella typhimurium</title><title>Molecular microbiology</title><addtitle>Mol Microbiol</addtitle><description>Lipopolysaccharide (LPS), spoT, and cya or crp mutations individually do not affect the minimum inhibitory concentration of mecillinam on Salmonella typhimurium. However, when mutations of two of these types were combined in the same strain, high-level resistance appeared, and increased even further when all three types of mutations were present. Most mutations affecting LPS (rfa, rfb, rfc) showed this behaviour, although to different degrees. The highest resistance to mecillinam was caused by galE and rfc mutations whereas almost no effect was noticed with rfaB or rfaK mutations. This phenomenon appears to be specific for mecillinam since none of several other antibiotics elicited it. Reduction of guanosine tetraphosphate (ppGpp) levels by introduction of a relA mutation did not significantly affect the MIC of mecillinam on strains carrying different combinations of spoT, galE, and cya or crp mutations. All the strains produced spherical cells in medium with a low concentration (0.05 microgram ml-1) of the antibiotic. These results suggest that the antibacterial action of mecillinam on S. typhimurium is somehow dependent on the interaction of LPS, cyclic AMP/cyclic AMP receptor protein (cAMP/CRP), and SpoT. The reported resistance to mecillinam of cya and crp mutants of Escherichia coli K-12 is probably due to the natural LPS defectiveness of this strain.</description><subject>Adenylyl Cyclases - genetics</subject><subject>Adenylyl Cyclases - physiology</subject><subject>Amdinocillin - pharmacology</subject><subject>Anti-Bacterial Agents - classification</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>beta-Lactam Resistance - genetics</subject><subject>Carbohydrate Epimerases - genetics</subject><subject>Carbohydrate Epimerases - metabolism</subject><subject>Carbohydrate Sequence</subject><subject>Carrier Proteins</subject><subject>Conjugation, Genetic</subject><subject>Cyclic AMP Receptor Protein - genetics</subject><subject>Cyclic AMP Receptor Protein - physiology</subject><subject>Escherichia coli</subject><subject>Guanosine Tetraphosphate - metabolism</subject><subject>Hexosyltransferases - genetics</subject><subject>Lipopolysaccharides - biosynthesis</subject><subject>Lipopolysaccharides - chemistry</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis</subject><subject>Pyrophosphatases - genetics</subject><subject>Pyrophosphatases - physiology</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - drug effects</subject><subject>Salmonella typhimurium - genetics</subject><subject>Salmonella typhimurium - ultrastructure</subject><subject>UDPglucose 4-Epimerase</subject><issn>0950-382X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotUMtqwzAQ9KElTdN-QmFPPcUgW7YjH0voCwKFNofezFpaJyqSpVpywf_Sj21Mc9qdB8POXiRLVpcs5SL_vEquQ_hiLOOs4otksSmrMss2y-T3nYIOEXtJEB1YktoY3aMFPzg1SlLQThCPBNKlztOAUf8QoIza9eA6sGPEeQ-AXUcnuj-A0d55Z6aAUh5x0IrWELzbrwF7BXJCcAPIwcOBegpzygca63oyBiFO_qjtOOjR3iSXHZpAt-e5SvZPj_vtS7p7e37dPuxSL4pNWktUBROcsFNUtEwwVrFMCCxm2GYVqjwvsaaaOhR00lhbqjyTnOdFxYivkvv_2FPl75FCbKwOcj6mJzeGJqtEVtVCnIx3Z-PYWlKNH7TFYWrO3-R_Vn1z6w</recordid><startdate>199505</startdate><enddate>199505</enddate><creator>Anton, D N</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>199505</creationdate><title>Resistance to mecillinam produced by the co-operative action of mutations affecting lipopolysaccharide, spoT, and cya or crp genes of Salmonella typhimurium</title><author>Anton, D N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p847-9cad4083eafde4b080060188a4de4bb16ad225a9e9efa8e6010b5d21c332460e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adenylyl Cyclases - genetics</topic><topic>Adenylyl Cyclases - physiology</topic><topic>Amdinocillin - pharmacology</topic><topic>Anti-Bacterial Agents - classification</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>beta-Lactam Resistance - genetics</topic><topic>Carbohydrate Epimerases - genetics</topic><topic>Carbohydrate Epimerases - metabolism</topic><topic>Carbohydrate Sequence</topic><topic>Carrier Proteins</topic><topic>Conjugation, Genetic</topic><topic>Cyclic AMP Receptor Protein - genetics</topic><topic>Cyclic AMP Receptor Protein - physiology</topic><topic>Escherichia coli</topic><topic>Guanosine Tetraphosphate - metabolism</topic><topic>Hexosyltransferases - genetics</topic><topic>Lipopolysaccharides - biosynthesis</topic><topic>Lipopolysaccharides - chemistry</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis</topic><topic>Pyrophosphatases - genetics</topic><topic>Pyrophosphatases - physiology</topic><topic>Salmonella typhimurium</topic><topic>Salmonella typhimurium - drug effects</topic><topic>Salmonella typhimurium - genetics</topic><topic>Salmonella typhimurium - ultrastructure</topic><topic>UDPglucose 4-Epimerase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anton, D N</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Molecular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anton, D N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Resistance to mecillinam produced by the co-operative action of mutations affecting lipopolysaccharide, spoT, and cya or crp genes of Salmonella typhimurium</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>1995-05</date><risdate>1995</risdate><volume>16</volume><issue>3</issue><spage>587</spage><epage>595</epage><pages>587-595</pages><issn>0950-382X</issn><abstract>Lipopolysaccharide (LPS), spoT, and cya or crp mutations individually do not affect the minimum inhibitory concentration of mecillinam on Salmonella typhimurium. However, when mutations of two of these types were combined in the same strain, high-level resistance appeared, and increased even further when all three types of mutations were present. Most mutations affecting LPS (rfa, rfb, rfc) showed this behaviour, although to different degrees. The highest resistance to mecillinam was caused by galE and rfc mutations whereas almost no effect was noticed with rfaB or rfaK mutations. This phenomenon appears to be specific for mecillinam since none of several other antibiotics elicited it. Reduction of guanosine tetraphosphate (ppGpp) levels by introduction of a relA mutation did not significantly affect the MIC of mecillinam on strains carrying different combinations of spoT, galE, and cya or crp mutations. All the strains produced spherical cells in medium with a low concentration (0.05 microgram ml-1) of the antibiotic. These results suggest that the antibacterial action of mecillinam on S. typhimurium is somehow dependent on the interaction of LPS, cyclic AMP/cyclic AMP receptor protein (cAMP/CRP), and SpoT. The reported resistance to mecillinam of cya and crp mutants of Escherichia coli K-12 is probably due to the natural LPS defectiveness of this strain.</abstract><cop>England</cop><pmid>7565117</pmid><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0950-382X |
ispartof | Molecular microbiology, 1995-05, Vol.16 (3), p.587-595 |
issn | 0950-382X |
language | eng |
recordid | cdi_proquest_miscellaneous_16816988 |
source | Wiley-Blackwell Journals; MEDLINE |
subjects | Adenylyl Cyclases - genetics Adenylyl Cyclases - physiology Amdinocillin - pharmacology Anti-Bacterial Agents - classification Bacterial Proteins - genetics Bacterial Proteins - metabolism beta-Lactam Resistance - genetics Carbohydrate Epimerases - genetics Carbohydrate Epimerases - metabolism Carbohydrate Sequence Carrier Proteins Conjugation, Genetic Cyclic AMP Receptor Protein - genetics Cyclic AMP Receptor Protein - physiology Escherichia coli Guanosine Tetraphosphate - metabolism Hexosyltransferases - genetics Lipopolysaccharides - biosynthesis Lipopolysaccharides - chemistry Molecular Sequence Data Mutagenesis Pyrophosphatases - genetics Pyrophosphatases - physiology Salmonella typhimurium Salmonella typhimurium - drug effects Salmonella typhimurium - genetics Salmonella typhimurium - ultrastructure UDPglucose 4-Epimerase |
title | Resistance to mecillinam produced by the co-operative action of mutations affecting lipopolysaccharide, spoT, and cya or crp genes of Salmonella typhimurium |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T08%3A32%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Resistance%20to%20mecillinam%20produced%20by%20the%20co-operative%20action%20of%20mutations%20affecting%20lipopolysaccharide,%20spoT,%20and%20cya%20or%20crp%20genes%20of%20Salmonella%20typhimurium&rft.jtitle=Molecular%20microbiology&rft.au=Anton,%20D%20N&rft.date=1995-05&rft.volume=16&rft.issue=3&rft.spage=587&rft.epage=595&rft.pages=587-595&rft.issn=0950-382X&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E16816988%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16816988&rft_id=info:pmid/7565117&rfr_iscdi=true |