Clinical Features and Genomic Epidemiology of Bloodstream Infections due to Enterococcal Species Other Than Enterococcus faecalis or E. faecium in Patients With Cancer

Author:

Axell-House Dierdre B123,Ashley Patrycja A1,Egge Stephanie L12,Tran Truc T2,Pedroza Claudia4,Zhang Meng4,Dinh An Q25,Simar Shelby R5,Sahasrabhojane Pranoti V6,Miller William R123,Shelburne Samuel A6ORCID,Hanson Blake M5ORCID,Arias Cesar A123

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Houston Methodist Hospital , Houston, Texas , USA

2. Center for Infectious Diseases, Houston Methodist Research Institute , Houston, Texas , USA

3. Department of Medicine, Weill Cornell Medical College , New York City, New York , USA

4. Center for Clinical Research and Evidence-Based Medicine, University of Texas Health Science Center at Houston , Houston, Texas , USA

5. Center for Infectious Diseases, School of Public Health, University of Texas Health Science Center at Houston , Houston, Texas , USA

6. Department of Infectious Diseases, Infection Control, and Employee Health, The University of Texas MD Anderson Cancer Center , Houston, Texas , USA

Abstract

Abstract Background Non–Enterococcus faecium, non–E. faecalis (NFF) enterococci are a heterogeneous group of clinically pathogenic enterococci that include species with intrinsic low-level vancomycin resistance. Patients with cancer are at increased risk for bacteremia with NFF enterococci, but their clinical and molecular epidemiology have not been extensively described. Methods We conducted a retrospective review of all patients (n = 70) with NFF bacteremia from 2016 to 2022 at a major cancer center. The main outcomes assessed were 30-day mortality, microbiological failure (positive blood cultures for ≥4 days), and recurrence of bacteremia (positive blood culture <14 days after clearance). Whole-genome sequencing was performed on all available NFF (n = 65). Results Patients with hematological malignancies made up 56% of the cohort (77% had leukemia). The majority of solid malignancies (87%) were gastrointestinal in origin. The majority of infections (83%) originated from an intra-abdominal source. The most common NFF species were E. gallinarum (50%) and E. casseliflavus (30%). Most (61%) patients received combination therapy. Bacteremia recurred in 4.3% of patients, there was a 30-day mortality of 23%, and 4.3% had microbiological failure. E. gallinarum and E. casseliflavus isolates were genetically diverse with no spatiotemporal clustering to suggest a single strain. Frequencies of ampicillin resistance (4.3%) and daptomycin resistance (1.9%) were low. Patients with hematologic malignancy had infections with NFF enterococci that harbored more resistance genes than patients with solid malignancy (P = .005). Conclusions NFF bacteremia is caused by a heterogeneous population of isolates and is associated with significant mortality. Hematological malignancy is an important risk factor for infection with NFF resistant to multiple antibiotics.

Funder

NIH

NIAID

Houston Methodist Clinical Scholars

W.R.M.

Publisher

Oxford University Press (OUP)

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