Phenotypic and genotypic characterization of antimicrobial resistance in Escherichia coli O111 isolates
Objectives: The aim of this study was to generate baseline data on the prevalence and molecular basis of antimicrobial resistance in Escherichia coli O111 isolates. Methods: A total of 105 epidemiologically unrelated E. coli O111 isolates from humans and cattle (isolated between 1983 and 2003) were...
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description | Objectives: The aim of this study was to generate baseline data on the prevalence and molecular basis of antimicrobial resistance in Escherichia coli O111 isolates. Methods: A total of 105 epidemiologically unrelated E. coli O111 isolates from humans and cattle (isolated between 1983 and 2003) were tested for susceptibility to 17 antimicrobial agents by broth microdilution. Resistant isolates were screened by molecular methods for resistance genes, class 1 and 2 integrons and mutations in the quinolone-resistance determining regions. Results: Resistance was found in 76% of the isolates, with a prevalence of 72% for multiresistance. The most prevalent resistances were to streptomycin, sulfamethoxazole and tetracycline (72–68%), followed by spectinomycin, ampicillin and kanamycin/neomycin (39–25%). For each antimicrobial agent, the predominant resistance genes were ampicillin, blaTEM (94%); chloramphenicol, catA1 (100%); gentamicin, aac(3)-IV and aac(3)-II (50% each); kanamycin, aphA1 (100%); streptomycin, aadA1- like (66%); sulfamethoxazole, sul1 (59%); tetracycline, tet(A) (86%); and trimethoprim, dfrA1-like (83%). Class 1 integrons were found in 41% of the isolates. They carried aadA1, dfrA1-aadA1 and dfrA15-aadA1. A class 2 integron (dfrA1-sat1-aadA1) was found in one isolate. Only three isolates (3%) were resistant to nalidixic acid (reduced susceptibility to ciprofloxacin), with a single mutation in the gyrA gene. Conclusions: E. coli O111 strains exhibit a wide repertoire of genetic elements to sustain antimicrobial pressure. Two specific antimicrobial resistance pheno/genotypes, [STR-SPT]-SUL-TET/aadA1-sul1-tet(A) and STR-SUL-TET-AMP-[KAN-NEO]/strA/B-sul2-tet(A)-blaTEM-aphA1, are predominant. |
doi_str_mv | 10.1093/jac/dkl127 |
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C. ; Beutin, Lothar</creator><creatorcontrib>Guerra, Beatriz ; Junker, Ernst ; Schroeter, Andreas ; Helmuth, Reiner ; Guth, Beatriz E. C. ; Beutin, Lothar</creatorcontrib><description>Objectives: The aim of this study was to generate baseline data on the prevalence and molecular basis of antimicrobial resistance in Escherichia coli O111 isolates. Methods: A total of 105 epidemiologically unrelated E. coli O111 isolates from humans and cattle (isolated between 1983 and 2003) were tested for susceptibility to 17 antimicrobial agents by broth microdilution. Resistant isolates were screened by molecular methods for resistance genes, class 1 and 2 integrons and mutations in the quinolone-resistance determining regions. Results: Resistance was found in 76% of the isolates, with a prevalence of 72% for multiresistance. The most prevalent resistances were to streptomycin, sulfamethoxazole and tetracycline (72–68%), followed by spectinomycin, ampicillin and kanamycin/neomycin (39–25%). For each antimicrobial agent, the predominant resistance genes were ampicillin, blaTEM (94%); chloramphenicol, catA1 (100%); gentamicin, aac(3)-IV and aac(3)-II (50% each); kanamycin, aphA1 (100%); streptomycin, aadA1- like (66%); sulfamethoxazole, sul1 (59%); tetracycline, tet(A) (86%); and trimethoprim, dfrA1-like (83%). Class 1 integrons were found in 41% of the isolates. They carried aadA1, dfrA1-aadA1 and dfrA15-aadA1. A class 2 integron (dfrA1-sat1-aadA1) was found in one isolate. Only three isolates (3%) were resistant to nalidixic acid (reduced susceptibility to ciprofloxacin), with a single mutation in the gyrA gene. Conclusions: E. coli O111 strains exhibit a wide repertoire of genetic elements to sustain antimicrobial pressure. Two specific antimicrobial resistance pheno/genotypes, [STR-SPT]-SUL-TET/aadA1-sul1-tet(A) and STR-SUL-TET-AMP-[KAN-NEO]/strA/B-sul2-tet(A)-blaTEM-aphA1, are predominant.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkl127</identifier><identifier>PMID: 16603644</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Animals ; Anti-Bacterial Agents - pharmacology ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Biological and medical sciences ; Cattle ; Cattle Diseases - microbiology ; DNA, Bacterial - analysis ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; Drug Resistance, Bacterial - genetics ; Drug Resistance, Multiple, Bacterial - genetics ; Escherichia coli ; Escherichia coli - drug effects ; Escherichia coli - genetics ; Escherichia coli - isolation & purification ; Escherichia coli Infections - microbiology ; Escherichia coli Infections - veterinary ; Genes, Bacterial ; Humans ; Integrons ; Medical sciences ; Microbial Sensitivity Tests ; molecular epidemiology ; Pharmacology. Drug treatments ; Polymerase Chain Reaction ; resistance determinants ; resistance genes ; Sequence Analysis, DNA ; STEC</subject><ispartof>Journal of antimicrobial chemotherapy, 2006-06, Vol.57 (6), p.1210-1214</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Jun 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-4d953bd95af952c58ff2bba2fd19ea4edbbfce080be7cba6aa4e854ff35c6c8a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17863970$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16603644$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guerra, Beatriz</creatorcontrib><creatorcontrib>Junker, Ernst</creatorcontrib><creatorcontrib>Schroeter, Andreas</creatorcontrib><creatorcontrib>Helmuth, Reiner</creatorcontrib><creatorcontrib>Guth, Beatriz E. C.</creatorcontrib><creatorcontrib>Beutin, Lothar</creatorcontrib><title>Phenotypic and genotypic characterization of antimicrobial resistance in Escherichia coli O111 isolates</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Objectives: The aim of this study was to generate baseline data on the prevalence and molecular basis of antimicrobial resistance in Escherichia coli O111 isolates. Methods: A total of 105 epidemiologically unrelated E. coli O111 isolates from humans and cattle (isolated between 1983 and 2003) were tested for susceptibility to 17 antimicrobial agents by broth microdilution. Resistant isolates were screened by molecular methods for resistance genes, class 1 and 2 integrons and mutations in the quinolone-resistance determining regions. Results: Resistance was found in 76% of the isolates, with a prevalence of 72% for multiresistance. The most prevalent resistances were to streptomycin, sulfamethoxazole and tetracycline (72–68%), followed by spectinomycin, ampicillin and kanamycin/neomycin (39–25%). For each antimicrobial agent, the predominant resistance genes were ampicillin, blaTEM (94%); chloramphenicol, catA1 (100%); gentamicin, aac(3)-IV and aac(3)-II (50% each); kanamycin, aphA1 (100%); streptomycin, aadA1- like (66%); sulfamethoxazole, sul1 (59%); tetracycline, tet(A) (86%); and trimethoprim, dfrA1-like (83%). Class 1 integrons were found in 41% of the isolates. They carried aadA1, dfrA1-aadA1 and dfrA15-aadA1. A class 2 integron (dfrA1-sat1-aadA1) was found in one isolate. Only three isolates (3%) were resistant to nalidixic acid (reduced susceptibility to ciprofloxacin), with a single mutation in the gyrA gene. Conclusions: E. coli O111 strains exhibit a wide repertoire of genetic elements to sustain antimicrobial pressure. Two specific antimicrobial resistance pheno/genotypes, [STR-SPT]-SUL-TET/aadA1-sul1-tet(A) and STR-SUL-TET-AMP-[KAN-NEO]/strA/B-sul2-tet(A)-blaTEM-aphA1, are predominant.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Biological and medical sciences</subject><subject>Cattle</subject><subject>Cattle Diseases - microbiology</subject><subject>DNA, Bacterial - analysis</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>Drug Resistance, Bacterial - genetics</subject><subject>Drug Resistance, Multiple, Bacterial - genetics</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - isolation & purification</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Escherichia coli Infections - veterinary</subject><subject>Genes, Bacterial</subject><subject>Humans</subject><subject>Integrons</subject><subject>Medical sciences</subject><subject>Microbial Sensitivity Tests</subject><subject>molecular epidemiology</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymerase Chain Reaction</subject><subject>resistance determinants</subject><subject>resistance genes</subject><subject>Sequence Analysis, DNA</subject><subject>STEC</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c9rFDEUB_AgFrtWL_4BEoT2IIzN72SO0lZbWajgCuIlvMkk3WxnJ2syC61_vdFdWvDSS0JePjyS90XoDSUfKGn56QrcaX87UKafoRkVijSMtPQ5mhFOZKOF5IfoZSkrQoiSyrxAh1QpwpUQM3TzdenHNN1vosMw9vjm4eSWkMFNPsffMMU04hSqmOI6upy6CAPOvsQyweg8jiO-KG5ZsVtGwC4NEV9TSnEsaYDJl1foIMBQ_Ov9foS-f7pYnF028-vPV2cf542TgkyN6FvJu7pAaCVz0oTAug5Y6GnrQfi-64LzxJDOa9eBglozUoTApVPOAD9CJ7u-m5x-bX2Z7DoW54cBRp-2xSpDCGdCPwmpZpwZTSp89x9cpW0e6ycso1q1lBvzFNKKEVHR-x2qAywl-2A3Oa4h31tK7N8kbU3S7pKs-O2-47Zb-_6R7qOr4HgPoDgYQq5BxPLotFG8_ff-ZudqVv7u4R7yrVWaa2kvf_y06ouY08Xi3H7jfwDDmLeO</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>Guerra, Beatriz</creator><creator>Junker, Ernst</creator><creator>Schroeter, Andreas</creator><creator>Helmuth, Reiner</creator><creator>Guth, Beatriz E. C.</creator><creator>Beutin, Lothar</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20060601</creationdate><title>Phenotypic and genotypic characterization of antimicrobial resistance in Escherichia coli O111 isolates</title><author>Guerra, Beatriz ; Junker, Ernst ; Schroeter, Andreas ; Helmuth, Reiner ; Guth, Beatriz E. 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Antiparasitic agents</topic><topic>Biological and medical sciences</topic><topic>Cattle</topic><topic>Cattle Diseases - microbiology</topic><topic>DNA, Bacterial - analysis</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>Drug Resistance, Bacterial - genetics</topic><topic>Drug Resistance, Multiple, Bacterial - genetics</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - isolation & purification</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Escherichia coli Infections - veterinary</topic><topic>Genes, Bacterial</topic><topic>Humans</topic><topic>Integrons</topic><topic>Medical sciences</topic><topic>Microbial Sensitivity Tests</topic><topic>molecular epidemiology</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymerase Chain Reaction</topic><topic>resistance determinants</topic><topic>resistance genes</topic><topic>Sequence Analysis, DNA</topic><topic>STEC</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guerra, Beatriz</creatorcontrib><creatorcontrib>Junker, Ernst</creatorcontrib><creatorcontrib>Schroeter, Andreas</creatorcontrib><creatorcontrib>Helmuth, Reiner</creatorcontrib><creatorcontrib>Guth, Beatriz E. 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C.</au><au>Beutin, Lothar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenotypic and genotypic characterization of antimicrobial resistance in Escherichia coli O111 isolates</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>57</volume><issue>6</issue><spage>1210</spage><epage>1214</epage><pages>1210-1214</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>Objectives: The aim of this study was to generate baseline data on the prevalence and molecular basis of antimicrobial resistance in Escherichia coli O111 isolates. Methods: A total of 105 epidemiologically unrelated E. coli O111 isolates from humans and cattle (isolated between 1983 and 2003) were tested for susceptibility to 17 antimicrobial agents by broth microdilution. Resistant isolates were screened by molecular methods for resistance genes, class 1 and 2 integrons and mutations in the quinolone-resistance determining regions. Results: Resistance was found in 76% of the isolates, with a prevalence of 72% for multiresistance. The most prevalent resistances were to streptomycin, sulfamethoxazole and tetracycline (72–68%), followed by spectinomycin, ampicillin and kanamycin/neomycin (39–25%). For each antimicrobial agent, the predominant resistance genes were ampicillin, blaTEM (94%); chloramphenicol, catA1 (100%); gentamicin, aac(3)-IV and aac(3)-II (50% each); kanamycin, aphA1 (100%); streptomycin, aadA1- like (66%); sulfamethoxazole, sul1 (59%); tetracycline, tet(A) (86%); and trimethoprim, dfrA1-like (83%). Class 1 integrons were found in 41% of the isolates. They carried aadA1, dfrA1-aadA1 and dfrA15-aadA1. A class 2 integron (dfrA1-sat1-aadA1) was found in one isolate. Only three isolates (3%) were resistant to nalidixic acid (reduced susceptibility to ciprofloxacin), with a single mutation in the gyrA gene. Conclusions: E. coli O111 strains exhibit a wide repertoire of genetic elements to sustain antimicrobial pressure. Two specific antimicrobial resistance pheno/genotypes, [STR-SPT]-SUL-TET/aadA1-sul1-tet(A) and STR-SUL-TET-AMP-[KAN-NEO]/strA/B-sul2-tet(A)-blaTEM-aphA1, are predominant.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>16603644</pmid><doi>10.1093/jac/dkl127</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anti-Bacterial Agents - pharmacology Antibiotics. Antiinfectious agents. Antiparasitic agents Biological and medical sciences Cattle Cattle Diseases - microbiology DNA, Bacterial - analysis DNA, Bacterial - chemistry DNA, Bacterial - genetics Drug Resistance, Bacterial - genetics Drug Resistance, Multiple, Bacterial - genetics Escherichia coli Escherichia coli - drug effects Escherichia coli - genetics Escherichia coli - isolation & purification Escherichia coli Infections - microbiology Escherichia coli Infections - veterinary Genes, Bacterial Humans Integrons Medical sciences Microbial Sensitivity Tests molecular epidemiology Pharmacology. Drug treatments Polymerase Chain Reaction resistance determinants resistance genes Sequence Analysis, DNA STEC |
title | Phenotypic and genotypic characterization of antimicrobial resistance in Escherichia coli O111 isolates |
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