A global genomic analysis of Salmonella Concord reveals lineages with high antimicrobial resistance in Ethiopia
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Published:2023-06-14
Issue:1
Volume:14
Page:
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ISSN:2041-1723
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Container-title:Nature Communications
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language:en
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Short-container-title:Nat Commun
Author:
Cuypers Wim L.ORCID, Meysman PieterORCID, Weill François-XavierORCID, Hendriksen Rene S., Beyene Getenet, Wain John, Nair Satheesh, Chattaway Marie A.ORCID, Perez-Sepulveda Blanca M.ORCID, Ceyssens Pieter-Jan, de Block Tessa, Lee Winnie W. Y., Pardos de la Gandara MariaORCID, Kornschober Christian, Moran-Gilad Jacob, Veldman Kees T.ORCID, Cormican Martin, Torpdahl Mia, Fields Patricia I., Černý Tomáš, Hardy LiselotteORCID, Tack BiekeORCID, Mellor Kate C., Thomson NicholasORCID, Dougan Gordon, Deborggraeve Stijn, Jacobs JanORCID, Laukens KrisORCID, Van Puyvelde SandraORCID
Abstract
AbstractAntimicrobial resistant Salmonella enterica serovar Concord (S. Concord) is known to cause severe gastrointestinal and bloodstream infections in patients from Ethiopia and Ethiopian adoptees, and occasional records exist of S. Concord linked to other countries. The evolution and geographical distribution of S. Concord remained unclear. Here, we provide a genomic overview of the population structure and antimicrobial resistance (AMR) of S. Concord by analysing genomes from 284 historical and contemporary isolates obtained between 1944 and 2022 across the globe. We demonstrate that S. Concord is a polyphyletic serovar distributed among three Salmonella super-lineages. Super-lineage A is composed of eight S. Concord lineages, of which four are associated with multiple countries and low levels of AMR. Other lineages are restricted to Ethiopia and horizontally acquired resistance to most antimicrobials used for treating invasive Salmonella infections in low- and middle-income countries. By reconstructing complete genomes for 10 representative strains, we demonstrate the presence of AMR markers integrated in structurally diverse IncHI2 and IncA/C2 plasmids, and/or the chromosome. Molecular surveillance of pathogens such as S. Concord supports the understanding of AMR and the multi-sector response to the global AMR threat. This study provides a comprehensive baseline data set essential for future molecular surveillance.
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary
Reference92 articles.
1. Grimont PAD, W. F. X. Antigenic formulae of the Salmonella serovars, 9th ed. (World health organization collaborating center for reference and research on Salmonella, Insitut Pasteur, 2007). 2. Gal-Mor, O., Boyle, E. C. & Grassl, G. A. Same species, different diseases: how and why typhoidal and non-typhoidal Salmonella enterica serovars differ. Front. Microbiol. 5, 391 (2014). 3. Silva, C., Calva, E. & Maloy, S. One Health and food-borne disease: Salmonella transmission between humans, animals, and plants. Microbiol. Spectr. 2, OH-0020–OH-2013 (2014). 4. Liu, H., Whitehouse, C. A. & Li, B. Presence and persistence of salmonella in water: the impact on microbial quality of water and food safety. Front. Public Health 6, 159 (2018). 5. Hohmann, E. L. Nontyphoidal salmonellosis. Clin. Infect. Dis. 32, 263–269 (2001).
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