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Multiple NDM-5-Expressing Escherichia Coli Isolates From an Immunocompromised Pediatric Host.
Flerlage, Tim; Brazelton de Cardenas, Jessica N; Garner, Cherilyn D; Hasan, Nur A; Karathia, Hiren; Qudeimat, Amr; Maron, Gabriela; Hayden, Randall.
Afiliação
  • Flerlage T; Division of Pediatric Critical Care Medicine, Department of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
  • Brazelton de Cardenas JN; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Garner CD; Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Hasan NA; Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Karathia H; CosmosID Incorporated, Rockville, Maryland, USA.
  • Qudeimat A; CosmosID Incorporated, Rockville, Maryland, USA.
  • Maron G; Department of Bone Marrow Transplant and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Hayden R; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Open Forum Infect Dis ; 7(2): ofaa018, 2020 Feb.
Article em En | MEDLINE | ID: mdl-32047833
ABSTRACT

BACKGROUND:

Genes conferring carbapenem resistance have disseminated worldwide among Gram-negative bacteria. Here we present longitudinal changes in clinically obtained Escherichia coli isolates from 1 immunocompromised pediatric patient. This report demonstrates potential for antibiotic resistance genes and plasmids to emerge over time in clinical isolates from patients receiving intensive anticancer chemotherapy and broad-spectrum antibiotics.

METHODS:

Thirty-three isolates obtained over 7 months from 1 patient were included. Clinical data were abstracted from the medical record. For each isolate, studies included phenotypic antibacterial resistance patterns, sequence typing, bacterial isolate sequencing, plasmid identification, and antibiotic resistance gene identification.

RESULTS:

Sites of isolation included blood, wound culture, and culture for surveillance purposes from the perianal area. Isolates were of 5 sequence types (STs). All were resistant to multiple classes of antibiotics; 23 (69.6%) were phenotypically resistant to all carbapenems. The blaNDM-5 gene was identified in 22 (67%) isolates, all of ST-167 and ST-940, and appeared to coincide with the presence of the IncFII and IncX3 plasmid.

CONCLUSIONS:

We present unique microbiologic data from 33 multidrug-resistant E. coli isolates obtained over the course of 7 months from an individual patient in the United States. Two E. coli sequence types causing invasive infection in the same patient and harboring the blaNDM-5 gene, encoded on the IncX3 plasmid and the IncFII plasmid, were identified. This study highlights the emergence of multidrug-resistant bacteria on antibiotic therapy and the necessity of adequate neutrophil number and function in the clearance of bacteremia.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Open Forum Infect Dis Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Open Forum Infect Dis Ano de publicação: 2020 Tipo de documento: Article