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. 2022 Sep 20;66(9):e0068822.
doi: 10.1128/aac.00688-22. Epub 2022 Sep 6.

Multidrug-Resistant Gram-Negative Bacteria in Burn Patients

Affiliations

Multidrug-Resistant Gram-Negative Bacteria in Burn Patients

Laura Ruegsegger et al. Antimicrob Agents Chemother. .

Abstract

Patients with burn injuries are at high risk for infectious complications, and infections are the most common cause of death after the first 72 h of hospitalization. Hospital-acquired infections caused by multidrug resistant (MDR) Gram-negative bacteria (GNB) in this population are concerning. Here, we evaluated carriage with MDR GNB in patients in a large tertiary-care burn intensive care unit. Twenty-nine patients in the burn unit were screened for intestinal carriage. Samples were cultured on selective media. Median time from admission to the burn unit to first sample collection was 9 days (IQR 5 - 17 days). In 21 (72%) patients, MDR GNB were recovered; the most common bacterial species isolated was Pseudomonas aeruginosa, which was found in 11/29 (38%) of patients. Two of these patients later developed bloodstream infections with P. aeruginosa. Transmission of KPC-31-producing ST22 Citrobacter freundii was detected. Samples from two patients grew genetically similar C. freundii isolates that were resistant to ceftazidime-avibactam. On analysis of whole-genome sequencing, blaKPC-31 was part of a Tn4401b transposon that was present on two different plasmids in each C. freundii isolate. Plasmid curing experiments showed that removal of both copies of blaKPC-31 was required to restore susceptibility to ceftazidime-avibactam. In summary, MDR GNB colonization is common in burn patients and patient-to-patient transmission of highly resistant GNB occurs. These results emphasize the ongoing need for infection prevention and antimicrobial stewardship efforts in this highly vulnerable population.

Keywords: Citrobacter; Pseudomonas aeruginosa; burn; carbapenemase; ceftazidime-avibactam; hospital infections; plasmid-mediated resistance.

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Conflict of interest statement

The authors declare a conflict of interest. R.A.B.: Grant/Research Support: Achaogen, Allecra, Entasis, Merck, Roche, Shionogi, Wockhardt. D.v.D. is a consultant for Actavis, Tetraphase, Sanofi-Pasteur, MedImmune, Astellas, Merck, Allergan, T2Biosystems, Roche, Achaogen, Neumedicine, Shionogi, Pfizer, Entasis, QPex, Wellspring, Karius, Union, Melinta, and Utility. All remaining authors have nothing to disclose.

Figures

FIG 1
FIG 1
The plasmid structures of the two blaKPC-31 harboring plasmids, p59174-43.6 (left) and p59174-80.5 (right). Colored arrows indicate open reading frames, with purple, orange, green, red, and blue arrows representing replication genes, mobile elements, plasmid transfer genes, the antimicrobial and heavy metal resistance gene, and plasmid backbone genes, respectively. The bottom panel shows the Tn4401 insertion in the IS5 in p59174-80.5.

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