From Investigating a Case of Cellulitis to Exploring Nosocomial Infection Control of ST1 Legionella pneumophila Using Genomic Approaches

Author:

Michel Charlotte12ORCID,Echahidi Fedoua1ORCID,Place Sammy3ORCID,Filippin Lorenzo3,Colombie Vincent3ORCID,Yin Nicolas2ORCID,Martiny Delphine24,Vandenberg Olivier56,Piérard Denis1ORCID,Hallin Marie67ORCID

Affiliation:

1. Department of Microbiology, Universitair Ziekenhuis Brussel (UZ Brussel), Vrije Universiteit Brussel (VUB), Laarbeeklaan 101, 1090 Brussels, Belgium

2. Department of Microbiology, Laboratoire Hospitalier Universitaire de Bruxelles (LHUB-ULB), Rue Haute 322, 1000 Brussels, Belgium

3. Department of Internal Medicine and Infectious Diseases, EpiCURA Hospital, 7301 Hornu, Belgium

4. Faculty of Medicine and Pharmacy, Mons University, Chemin du Champ de Mars 37, 7000 Mons, Belgium

5. Innovation and Business Development Unit, Laboratoire Hospitalier Universitaire de Bruxelles (LHUB-ULB), Rue Haute 322, 1000 Brussels, Belgium

6. Centre for Environmental Health and Occupational Health, School of Public Health, Université Libre de Bruxelles (ULB), Avenue Roosevelt 50, 1050 Brussels, Belgium

7. European Plotkin Institute for Vaccinology (EPIV), Université Libre de Bruxelles (ULB), Avenue Roosevelt 50, 1050 Brussels, Belgium

Abstract

Legionella pneumophila can cause a large panel of symptoms besides the classic pneumonia presentation. Here we present a case of fatal nosocomial cellulitis in an immunocompromised patient followed, a year later, by a second case of Legionnaires’ disease in the same ward. While the first case was easily assumed as nosocomial based on the date of symptom onset, the second case required clear typing results to be assigned either as nosocomial and related to the same environmental source as the first case, or community acquired. To untangle this specific question, we applied core-genome multilocus typing (MLST), whole-genome single nucleotide polymorphism and whole-genome MLST methods to a collection of 36 Belgian and 41 international sequence-type 1 (ST1) isolates using both thresholds recommended in the literature and tailored threshold based on local epidemiological data. Based on the thresholds applied to cluster isolates together, the three methods gave different results and no firm conclusion about the nosocomial setting of the second case could been drawn. Our data highlight that despite promising results in the study of outbreaks and for large-scale epidemiological investigations, next-generation sequencing typing methods applied to ST1 outbreak investigation still need standardization regarding both wet-lab protocols and bioinformatics. A deeper evaluation of the L. pneumophila evolutionary clock is also required to increase our understanding of genomic differences between isolates sampled during a clinical infection and in the environment.

Funder

Belgian Ministry of Social Affairs

Publisher

MDPI AG

Reference38 articles.

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2. Relapsing Legionella pneumophila cellulitis: A case report and review of the literature;Han;J. Infect. Chemother.,2010

3. Cutaneous Legionella infections in allogeneic hematopoietic cell transplantation recipients;Vaidya;Dermatol. Online J.,2020

4. A real-time PCR for specific detection of the Legionella pneumophila serogroup 1 ST1 complex;Ginevra;Clin. Microbiol. Infect.,2020

5. Echahidi, F.M.C. (2024, April 16). Activity Report from 2011 to 2022 Reference Centre for Legionella pneumophila UZ Brussel—LHUB-ULB [Internet]. National Reference Centre for Legionella pneumophila, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Department of Microbiology and Infection Control, Brussels. Available online: https://www.sciensano.be/sites/default/files/legionella_2011-2022_nrc_rapport_english_final.pdf.

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