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Genomic reconstruction and directed interventions in a multidrug-resistant Shigellosis outbreak in Seattle, WA, USA: a genomic surveillance study - 25/05/23

Doi : 10.1016/S1473-3099(22)00879-9 
Giannoula S Tansarli, MD a, †, Dustin R Long, MD d, †, Adam Waalkes, BS a, Lori A Bourassa, PhD a, Stephen J Libby, PhD a, Kelsi Penewit, BS a, Jared Almazan, BS a, Jason Matsumoto, BS e, Chloe Bryson-Cahn, MD c, f, Krista Rietberg, MPH f, BreeAnna M Dell, PhD g, Noël V Hatley, MPH g, Stephen J Salipante, MD a, Ferric C Fang, ProfMD a, b, e, ⁎
a Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA, USA 
b Department of Microbiology, University of Washington School of Medicine, Seattle, WA, USA 
c Division of Allergy and Infectious Diseases, Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA 
d Division of Critical Care Medicine, Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, USA 
e Clinical Microbiology Laboratory, Harborview Medical Center, Seattle, WA, USA 
f Infection Prevention and Control, Harborview Medical Center, Seattle, WA, USA 
g Public Health—Seattle & King County, Communicable Diseases, Epidemiology, and Immunizations, Seattle, WA, USA 

* Correspondence to: Prof Ferric C Fang, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA 98195-7110, USA Department of Laboratory Medicine and Pathology University of Washington School of Medicine Seattle WA 98195-7110 USA

Summary

Background

Shigella spp have been associated with community-wide outbreaks in urban settings. We analysed a sustained shigellosis outbreak in Seattle, WA, USA, to understand its origins and mechanisms of antimicrobial resistance, define ongoing transmission patterns, and optimise strategies for treatment and infection control.

Methods

We did a retrospective study of all Shigella isolates identified from stool samples at the clinical laboratories at Harborview Medical Center and University of Washington Medical Center (Seattle, WA, USA) from May 1, 2017, to Feb 28, 2022. We characterised isolates by species identification, phenotypic susceptibility testing, and whole-genome sequencing. Demographic characteristics and clinical outcomes of the patients were retrospectively examined.

Findings

171 cases of shigellosis were included. 78 (46%) patients were men who have sex with men (MSM), and 88 (52%) were people experiencing homelessness (PEH). Although 84 (51%) isolates were multidrug resistant, 100 (70%) of 143 patients with data on antimicrobial therapy received appropriate empirical therapy. Phylogenomic analysis identified sequential outbreaks of multiple distinct lineages of Shigella flexneri and Shigella sonnei. Discrete clonal lineages (ten in S flexneri and nine in S sonnei) and resistance traits were responsible for infection in different at-risk populations (ie, MSM, PEH), enabling development of effective guidelines for empirical treatment. The most prevalent lineage in Seattle was probably introduced to Washington State via international travel, with subsequent domestic transmission between at-risk groups.

Interpretation

An outbreak in Seattle was driven by parallel emergence of multidrug-resistant strains involving international transmission networks and domestic transmission between at-risk populations. Genomic analysis elucidated not only outbreak origin, but directed optimal approaches to testing, treatment, and public health response. Rapid diagnostics combined with detailed knowledge of local epidemiology can enable high rates of appropriate empirical therapy even in multidrug-resistant infection.

Funding

None.

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Vol 23 - N° 6

P. 740-750 - juin 2023 Regresar al número
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