Optimizing methods to detect colonization with fluoroquinolone-resistant viridans group streptococci prior to hematopoietic cell transplantation

ABSTRACT Patients undergoing hematopoietic cell transplantation (HCT) who receive fluoroquinolone prophylaxis are at high risk for bacteremia due to fluoroquinolone-resistant viridans group streptococci (FQ-R VGS), particularly Streptococcus mitis . Detecting colonization with FQ-R VGS may identify neutropenic patients at risk for streptococcal bacteremia during FQ prophylaxis, but the optimal specimen screening site and microbiologic screening method are unknown. We therefore simultaneously collected buccal, oropharyngeal, and perianal swabs from patients upon admission for HCT, and performed selective culture with both direct plating and broth enrichment. FQ-R VGS were detected in 62 (90%) of 69 participants. Direct plating resulted in a positive percent agreement (PPA) of 79% (95% confidence interval [CI]: 67%–88%) for detecting FQ-R VGS from buccal swabs, and a PPA of 86% (95% CI: 74%–93%) from oropharyngeal swabs compared to detection by any specimen or method. Broth enrichment yielded a PPA of 97% (95% CI: 89%–100%) for both buccal and oropharyngeal swabs. Perianal swabs had low PPA. For detecting FQ-R S. mitis group, the direct plating PPA was 74% (95% CI: 60%–85%) for buccal and 72% (95% CI: 58%–84%) for oropharyngeal swabs, while the broth enrichment PPA was 82% (95% CI: 69%–91%) and 58% (95% CI: 43%–72%), respectively. Combining direct plating and broth enrichment of buccal swabs had a PPA of 96% (95% CI: 86%–100%) for detecting FQ-R S. mitis group. Buccal swabs are a reliable specimen to detect FQ-R VGS colonization when using broth enrichment, and combining direct plating and broth enrichment may optimize detection of FQ-R S. mitis group. IMPORTANCE Viridans group streptococci (VGS) are important causes of bloodstream infections in patients with cancer undergoing hematopoietic cell transplantation. These infections frequently occur despite using prophylactic fluoroquinolone antibiotics, suggesting that some patients are colonized with fluoroquinolone-resistant VGS (FQ-R VGS). A test that reliably detects carriage of FQ-R VGS might help identify patients at highest risk of streptococcal infection, but the optimal methods to detect FQ-R VGS colonization were previously unknown. In this study, we compared different body sites and culture methods for detecting colonization with FQ-R VGS. We found that buccal (cheek) swabs reliably detected these resistant bacteria, including members of the Streptococcus mitis group, and adding a broth enrichment step further improved detection from buccal samples. These findings support buccal sampling with broth enrichment as a practical approach for detecting colonization with FQ-R VGS and establish a foundation for future studies to define the clinical significance of FQ-R VGS colonization.

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Journal
Journal of Clinical Microbiology
Published
2026-08-21
DOI
https://doi.org/10.1128/jcm.00687-26
Primary Topic
Neutropenia and Cancer Infections
Type
article
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article

Optimizing methods to detect colonization with fluoroquinolone-resistant viridans group streptococci prior to hematopoietic cell transplantation

Michael J. Satlin, Supram Hosuru Subramanya, Casey L. Cazer, Barry N. Kreiswirth et al.
Journal of Clinical Microbiology
Neutropenia and Cancer Infections
article

Optimizing methods to detect colonization with fluoroquinolone-resistant viridans group streptococci prior to hematopoietic cell transplantation

Michael J. Satlin, Supram Hosuru Subramanya, Casey L. Cazer, Barry N. Kreiswirth, Rosemary Soave, Laura B. Goodman, Jamie Marino, Lee Gottesdiener, Juliet Barker, Tsiporah Shore, Markus Plate, Lars F. Westblade, John R. Lee
article en

Abstract

ABSTRACT Patients undergoing hematopoietic cell transplantation (HCT) who receive fluoroquinolone prophylaxis are at high risk for bacteremia due to fluoroquinolone-resistant viridans group streptococci (FQ-R VGS), particularly Streptococcus mitis . Detecting colonization with FQ-R VGS may identify neutropenic patients at risk for streptococcal bacteremia during FQ prophylaxis, but the optimal specimen screening site and microbiologic screening method are unknown. We therefore simultaneously collected buccal, oropharyngeal, and perianal swabs from patients upon admission for HCT, and performed selective culture with both direct plating and broth enrichment. FQ-R VGS were detected in 62 (90%) of 69 participants. Direct plating resulted in a positive percent agreement (PPA) of 79% (95% confidence interval [CI]: 67%–88%) for detecting FQ-R VGS from buccal swabs, and a PPA of 86% (95% CI: 74%–93%) from oropharyngeal swabs compared to detection by any specimen or method. Broth enrichment yielded a PPA of 97% (95% CI: 89%–100%) for both buccal and oropharyngeal swabs. Perianal swabs had low PPA. For detecting FQ-R S. mitis group, the direct plating PPA was 74% (95% CI: 60%–85%) for buccal and 72% (95% CI: 58%–84%) for oropharyngeal swabs, while the broth enrichment PPA was 82% (95% CI: 69%–91%) and 58% (95% CI: 43%–72%), respectively. Combining direct plating and broth enrichment of buccal swabs had a PPA of 96% (95% CI: 86%–100%) for detecting FQ-R S. mitis group. Buccal swabs are a reliable specimen to detect FQ-R VGS colonization when using broth enrichment, and combining direct plating and broth enrichment may optimize detection of FQ-R S. mitis group. IMPORTANCE Viridans group streptococci (VGS) are important causes of bloodstream infections in patients with cancer undergoing hematopoietic cell transplantation. These infections frequently occur despite using prophylactic fluoroquinolone antibiotics, suggesting that some patients are colonized with fluoroquinolone-resistant VGS (FQ-R VGS). A test that reliably detects carriage of FQ-R VGS might help identify patients at highest risk of streptococcal infection, but the optimal methods to detect FQ-R VGS colonization were previously unknown. In this study, we compared different body sites and culture methods for detecting colonization with FQ-R VGS. We found that buccal (cheek) swabs reliably detected these resistant bacteria, including members of the Streptococcus mitis group, and adding a broth enrichment step further improved detection from buccal samples. These findings support buccal sampling with broth enrichment as a practical approach for detecting colonization with FQ-R VGS and establish a foundation for future studies to define the clinical significance of FQ-R VGS colonization.

Journal of Clinical Microbiology
Cornell University (US), Hackensack Meridian Health (US), New York State College of Veterinary Medicine (US), Center for Discovery (US), Weill Cornell Medicine (US), University of Pennsylvania (US)
National Institute of Allergy and Infectious Diseases, National Center for Advancing Translational Sciences
Openalex Percentile: Top 13%
Neutropenia and Cancer Infections
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