Meningitis Caused by Escherichia coli Producing TEM-52 Extended-Spectrum β-Lactamase within an Extensive Outbreak in a Neonatal Ward: Epidemiological Investigation and Characterization of the Strain

Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We report here an extensive outbreak in a neonatal ward with a case of meningitis caused by an ESBL-producing Escherichia coli strain. Between 24 March and 2...

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Published inJournal of Clinical Microbiology Vol. 48; no. 7; pp. 2459 - 2463
Main Authors Moissenet, Didier, Salauze, Béatrice, Clermont, Olivier, Bingen, Edouard, Arlet, Guillaume, Denamur, Erick, Mérens, Audrey, Mitanchez, Delphine, Vu-Thien, Hoang
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LanguageEnglish
Published Washington, DC American Society for Microbiology 01.07.2010
American Society for Microbiology (ASM)
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Abstract Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We report here an extensive outbreak in a neonatal ward with a case of meningitis caused by an ESBL-producing Escherichia coli strain. Between 24 March and 29 April 2009, among the 59 neonates present in the ward, 26 neonates with ESBL-producing E. coli rectal colonization were detected (44%). One of the colonized neonates developed meningitis with a favorable outcome after treatment combining imipenem, gentamicin, and ciprofloxacin. Despite strict intensification of hygiene and isolation procedures for more than 1 month, ward closure to new admissions was necessary to control the outbreak. Randomly amplified polymorphic DNA and pulsed-field gel electrophoresis analysis performed on 31 isolates recovered from 26 neonates and two mother's milk samples showed a clonal strain. ESBL PCR assays indicated that the strain harbored a TEM-52 ESBL encoded by an IncI1 replicon. Phylogenetic analysis by multilocus sequence typing showed that the strain belonged to rare phylogenetic group C, which is closely related to group B1 but appears as group A by the triplex PCR phylogrouping method. The strain harbored the virulence genes fuyA, aer, and iroN and was virulent in a mouse model of septicemia. This work indicates the high potential of colonization, transmission, and virulence of some ESBL-producing E. coli clones.
AbstractList Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum beta -lactamases (ESBL) in neonatal wards can be difficult to control. We report here an extensive outbreak in a neonatal ward with a case of meningitis caused by an ESBL-producing Escherichia coli strain. Between 24 March and 29 April 2009, among the 59 neonates present in the ward, 26 neonates with ESBL-producing E. coli rectal colonization were detected (44%). One of the colonized neonates developed meningitis with a favorable outcome after treatment combining imipenem, gentamicin, and ciprofloxacin. Despite strict intensification of hygiene and isolation procedures for more than 1 month, ward closure to new admissions was necessary to control the outbreak. Randomly amplified polymorphic DNA and pulsed-field gel electrophoresis analysis performed on 31 isolates recovered from 26 neonates and two mother's milk samples showed a clonal strain. ESBL PCR assays indicated that the strain harbored a TEM-52 ESBL encoded by an IncI1 replicon. Phylogenetic analysis by multilocus sequence typing showed that the strain belonged to rare phylogenetic group C, which is closely related to group B1 but appears as group A by the triplex PCR phylogrouping method. The strain harbored the virulence genes fuyA, aer, and iroN and was virulent in a mouse model of septicemia. This work indicates the high potential of colonization, transmission, and virulence of some ESBL-producing E. coli clones.
ABSTRACT Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We report here an extensive outbreak in a neonatal ward with a case of meningitis caused by an ESBL-producing Escherichia coli strain. Between 24 March and 29 April 2009, among the 59 neonates present in the ward, 26 neonates with ESBL-producing E . coli rectal colonization were detected (44%). One of the colonized neonates developed meningitis with a favorable outcome after treatment combining imipenem, gentamicin, and ciprofloxacin. Despite strict intensification of hygiene and isolation procedures for more than 1 month, ward closure to new admissions was necessary to control the outbreak. Randomly amplified polymorphic DNA and pulsed-field gel electrophoresis analysis performed on 31 isolates recovered from 26 neonates and two mother's milk samples showed a clonal strain. ESBL PCR assays indicated that the strain harbored a TEM-52 ESBL encoded by an IncI1 replicon. Phylogenetic analysis by multilocus sequence typing showed that the strain belonged to rare phylogenetic group C, which is closely related to group B1 but appears as group A by the triplex PCR phylogrouping method. The strain harbored the virulence genes fuyA , aer , and iroN and was virulent in a mouse model of septicemia. This work indicates the high potential of colonization, transmission, and virulence of some ESBL-producing E . coli clones.
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Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We report here an extensive outbreak in a neonatal ward with a case of meningitis caused by an ESBL-producing Escherichia coli strain. Between 24 March and 29 April 2009, among the 59 neonates present in the ward, 26 neonates with ESBL-producing E. coli rectal colonization were detected (44%). One of the colonized neonates developed meningitis with a favorable outcome after treatment combining imipenem, gentamicin, and ciprofloxacin. Despite strict intensification of hygiene and isolation procedures for more than 1 month, ward closure to new admissions was necessary to control the outbreak. Randomly amplified polymorphic DNA and pulsed-field gel electrophoresis analysis performed on 31 isolates recovered from 26 neonates and two mother's milk samples showed a clonal strain. ESBL PCR assays indicated that the strain harbored a TEM-52 ESBL encoded by an IncI1 replicon. Phylogenetic analysis by multilocus sequence typing showed that the strain belonged to rare phylogenetic group C, which is closely related to group B1 but appears as group A by the triplex PCR phylogrouping method. The strain harbored the virulence genes fuyA, aer, and iroN and was virulent in a mouse model of septicemia. This work indicates the high potential of colonization, transmission, and virulence of some ESBL-producing E. coli clones.
Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We report here an extensive outbreak in a neonatal ward with a case of meningitis caused by an ESBL-producing Escherichia coli strain. Between 24 March and 29 April 2009, among the 59 neonates present in the ward, 26 neonates with ESBL-producing E . coli rectal colonization were detected (44%). One of the colonized neonates developed meningitis with a favorable outcome after treatment combining imipenem, gentamicin, and ciprofloxacin. Despite strict intensification of hygiene and isolation procedures for more than 1 month, ward closure to new admissions was necessary to control the outbreak. Randomly amplified polymorphic DNA and pulsed-field gel electrophoresis analysis performed on 31 isolates recovered from 26 neonates and two mother's milk samples showed a clonal strain. ESBL PCR assays indicated that the strain harbored a TEM-52 ESBL encoded by an IncI1 replicon. Phylogenetic analysis by multilocus sequence typing showed that the strain belonged to rare phylogenetic group C, which is closely related to group B1 but appears as group A by the triplex PCR phylogrouping method. The strain harbored the virulence genes fuyA , aer , and iroN and was virulent in a mouse model of septicemia. This work indicates the high potential of colonization, transmission, and virulence of some ESBL-producing E . coli clones.
Author Mérens, Audrey
Denamur, Erick
Arlet, Guillaume
Clermont, Olivier
Mitanchez, Delphine
Bingen, Edouard
Salauze, Béatrice
Vu-Thien, Hoang
Moissenet, Didier
AuthorAffiliation Service de Microbiologie, Hôpital Armand Trousseau, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Saint Antoine, Université Pierre et Marie Curie-Paris 6, Paris, France, 1 INSERM U722 and Université Denis Diderot-Paris 7, Site Xavier Bichat, Paris, France, 2 Service de Microbiologie, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Laboratoire d'Etudes de Génétique Bactérienne dans les Infections de l'Enfant (EA3105), Université Denis Diderot-Paris 7, Paris, France, 3 Service de Microbiologie, Hôpital Tenon, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Saint Antoine, Université Pierre et Marie Curie-Paris 6, Paris, France, 4 Laboratoire de Biologie, Hôpital d'Instruction des Armées Bégin, St. Mandé, France, 5 Service de Néonatologie, Hôpital Armand Trousseau, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Saint Antoine, Université Pierre et Marie Curie-Paris 6, Paris, France 6
AuthorAffiliation_xml – name: Service de Microbiologie, Hôpital Armand Trousseau, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Saint Antoine, Université Pierre et Marie Curie-Paris 6, Paris, France, 1 INSERM U722 and Université Denis Diderot-Paris 7, Site Xavier Bichat, Paris, France, 2 Service de Microbiologie, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Laboratoire d'Etudes de Génétique Bactérienne dans les Infections de l'Enfant (EA3105), Université Denis Diderot-Paris 7, Paris, France, 3 Service de Microbiologie, Hôpital Tenon, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Saint Antoine, Université Pierre et Marie Curie-Paris 6, Paris, France, 4 Laboratoire de Biologie, Hôpital d'Instruction des Armées Bégin, St. Mandé, France, 5 Service de Néonatologie, Hôpital Armand Trousseau, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Saint Antoine, Université Pierre et Marie Curie-Paris 6, Paris, France 6
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Snippet Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We report here...
Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum beta-lactamases (ESBL) in neonatal wards can be difficult to control. We report...
ABSTRACT Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We...
Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum beta -lactamases (ESBL) in neonatal wards can be difficult to control. We report...
Outbreaks caused by Enterobacteriaceae isolates producing extended-spectrum β-lactamases (ESBL) in neonatal wards can be difficult to control. We report here...
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SubjectTerms Bacteriology
beta-Lactamases - genetics
beta-Lactamases - metabolism
Biological and medical sciences
Disease Outbreaks
Electrophoresis, Gel, Pulsed-Field
Enterobacteriaceae
Epidemiology
Escherichia coli
Escherichia coli - drug effects
Escherichia coli - genetics
Escherichia coli - isolation & purification
Escherichia coli - pathogenicity
Fundamental and applied biological sciences. Psychology
Hospital Units
Humans
Infant, Newborn
Meningitis, Escherichia coli - epidemiology
Meningitis, Escherichia coli - microbiology
Microbial Sensitivity Tests
Microbiology
Miscellaneous
Polymerase Chain Reaction
Title Meningitis Caused by Escherichia coli Producing TEM-52 Extended-Spectrum β-Lactamase within an Extensive Outbreak in a Neonatal Ward: Epidemiological Investigation and Characterization of the Strain
URI http://jcm.asm.org/content/48/7/2459.abstract
https://www.ncbi.nlm.nih.gov/pubmed/20519482
https://search.proquest.com/docview/733500739
https://search.proquest.com/docview/754868653
https://pubmed.ncbi.nlm.nih.gov/PMC2897521
Volume 48
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