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CHROMagar COL-APSE: a selective bacterial culture medium for the isolation and differentiation of colistin-resistant Gram-negative pathogens.

Identifieur interne : 000056 ( PubMed/Corpus ); précédent : 000055; suivant : 000057

CHROMagar COL-APSE: a selective bacterial culture medium for the isolation and differentiation of colistin-resistant Gram-negative pathogens.

Auteurs : Muhd Haziq F. Abdul Momin ; David C. Bean ; Rene S. Hendriksen ; Marisa Haenni ; Lynette M. Phee ; David W. Wareham

Source :

RBID : pubmed:28984232

Abstract

A selective chromogenic culture medium for the laboratory isolation and differentiation of colistin resistant Acinetobacter, Pseudomonas, Stenotrophomonas and Enterobacteriaceae spp. (CHROMagar COL-APSE) was developed, evaluated and compared to an existing selective bacterial culture medium (SuperPolymyxin).

DOI: 10.1099/jmm.0.000602
PubMed: 28984232

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pubmed:28984232

Le document en format XML

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<title xml:lang="en">CHROMagar COL-APSE: a selective bacterial culture medium for the isolation and differentiation of colistin-resistant Gram-negative pathogens.</title>
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<name sortKey="Abdul Momin, Muhd Haziq F" sort="Abdul Momin, Muhd Haziq F" uniqKey="Abdul Momin M" first="Muhd Haziq F" last="Abdul Momin">Muhd Haziq F. Abdul Momin</name>
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<nlm:affiliation>1​Antimicrobial Research Group, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.</nlm:affiliation>
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<name sortKey="Bean, David C" sort="Bean, David C" uniqKey="Bean D" first="David C" last="Bean">David C. Bean</name>
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<nlm:affiliation>2​School of Applied and Biomedical Sciences, Federation University Australia, Ballarat, Australia.</nlm:affiliation>
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<name sortKey="Hendriksen, Rene S" sort="Hendriksen, Rene S" uniqKey="Hendriksen R" first="Rene S" last="Hendriksen">Rene S. Hendriksen</name>
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<nlm:affiliation>3​Technical University of Denmark, National Food Institute, WHO Collaborating Centre for Antimicrobial Resistance in Foodborne Pathogens and Genomics, European Union Reference Laboratory for Antimicrobial Resistance (EURL-AMR), Kgs Lyngby, Denmark DK-2800, Denmark.</nlm:affiliation>
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<name sortKey="Haenni, Marisa" sort="Haenni, Marisa" uniqKey="Haenni M" first="Marisa" last="Haenni">Marisa Haenni</name>
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<nlm:affiliation>4​Unité Antibiorésistance et Virulence Bactériennes, Université Lyon-ANSES Site de Lyon, Lyon, France.</nlm:affiliation>
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<name sortKey="Phee, Lynette M" sort="Phee, Lynette M" uniqKey="Phee L" first="Lynette M" last="Phee">Lynette M. Phee</name>
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<nlm:affiliation>1​Antimicrobial Research Group, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.</nlm:affiliation>
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<nlm:affiliation>1​Antimicrobial Research Group, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.</nlm:affiliation>
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<name sortKey="Bean, David C" sort="Bean, David C" uniqKey="Bean D" first="David C" last="Bean">David C. Bean</name>
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<name sortKey="Hendriksen, Rene S" sort="Hendriksen, Rene S" uniqKey="Hendriksen R" first="Rene S" last="Hendriksen">Rene S. Hendriksen</name>
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<nlm:affiliation>3​Technical University of Denmark, National Food Institute, WHO Collaborating Centre for Antimicrobial Resistance in Foodborne Pathogens and Genomics, European Union Reference Laboratory for Antimicrobial Resistance (EURL-AMR), Kgs Lyngby, Denmark DK-2800, Denmark.</nlm:affiliation>
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<name sortKey="Haenni, Marisa" sort="Haenni, Marisa" uniqKey="Haenni M" first="Marisa" last="Haenni">Marisa Haenni</name>
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<nlm:affiliation>4​Unité Antibiorésistance et Virulence Bactériennes, Université Lyon-ANSES Site de Lyon, Lyon, France.</nlm:affiliation>
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<name sortKey="Phee, Lynette M" sort="Phee, Lynette M" uniqKey="Phee L" first="Lynette M" last="Phee">Lynette M. Phee</name>
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<nlm:affiliation>1​Antimicrobial Research Group, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.</nlm:affiliation>
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<name sortKey="Wareham, David W" sort="Wareham, David W" uniqKey="Wareham D" first="David W" last="Wareham">David W. Wareham</name>
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<title level="j">Journal of medical microbiology</title>
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<div type="abstract" xml:lang="en">A selective chromogenic culture medium for the laboratory isolation and differentiation of colistin resistant Acinetobacter, Pseudomonas, Stenotrophomonas and Enterobacteriaceae spp. (CHROMagar COL-APSE) was developed, evaluated and compared to an existing selective bacterial culture medium (SuperPolymyxin).</div>
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<Month>10</Month>
<Day>06</Day>
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<Year>2017</Year>
<Month>11</Month>
<Day>06</Day>
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<Volume>66</Volume>
<Issue>11</Issue>
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<Year>2017</Year>
<Month>Nov</Month>
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<Title>Journal of medical microbiology</Title>
<ISOAbbreviation>J. Med. Microbiol.</ISOAbbreviation>
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<ArticleTitle>CHROMagar COL-APSE: a selective bacterial culture medium for the isolation and differentiation of colistin-resistant Gram-negative pathogens.</ArticleTitle>
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<AbstractText Label="PURPOSE" NlmCategory="OBJECTIVE">A selective chromogenic culture medium for the laboratory isolation and differentiation of colistin resistant Acinetobacter, Pseudomonas, Stenotrophomonas and Enterobacteriaceae spp. (CHROMagar COL-APSE) was developed, evaluated and compared to an existing selective bacterial culture medium (SuperPolymyxin).</AbstractText>
<AbstractText Label="METHODOLOGY" NlmCategory="METHODS">The medium was challenged with 84 isolates, including polymyxin B (POL B)-susceptible and -resistant type strains and colistin (COL)-resistant organisms recovered from human and animal samples. Susceptibility to COL and POL B was determined by agar dilution and broth microtitre dilution. The lower limit for the detection of COL-resistant organisms was also calculated for both CHROMagar COL-APSE and SuperPolymyxin media. The ability to isolate and correctly differentiate COL-resistant organisms within mixed cultures was also assessed and compared using both media.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Using CHROMagar COL-APSE, Gram-negative pathogens (n=71) with intrinsic (n=8) or acquired COL (n=63) resistance were recovered with 100 % specificity down to the lower limit of detection of 10(1) colony-forming units (c.f.u.). The growth on SuperPolymyxin was similar, but notably weaker for COL-resistant non-fermentative bacteria (Acinetobacter, Pseudomonas and Stenotrophomonas). CHROMagar COL-APSE was also more sensitive in supporting the growth of Enterobacteriaceae with COL resistance associated with the carriage of mcr-1.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">CHROMagar COL-APSE is a sensitive and specific medium for the growth of COL-resistant bacterial pathogens. Due to the low limit of detection (10(1) c.f.u.), it may be useful as a primary isolation medium in the surveillance and recovery of COL-resistant bacteria from complex human, veterinary and environmental samples, especially those with plasmid-mediated MCR-1 or novel mechanisms of polymyxin resistance.</AbstractText>
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<Affiliation>5​Division of Infection, Barts Health NHS Trust, London, UK.</Affiliation>
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