Genomic characterisation of multidrug-resistant Salmonella enterica serovar Kentucky ST198 isolates from various sources in Algeria, North Africa

<i>Salmonella enterica</i> serovar Kentucky (<i>S</i>. Kentucky) sequence type (ST) 198 has emerged as a globally disseminated multidrug-resistant (MDR) lineage posing significant public health challenges. The aim of this study was to characterise 125 <i>S</i>. Kentucky ST198 isolates collected from various sources in Algeria, including humans, animals, food and the environment, or obtained from humans in France (travellers returning from Algeria), between 2015 and 2022. Whole-genome sequencing was performed on 125 isolates to assess their genetic diversity and antimicrobial resistance (AMR) profiles. Phylogenetic analysis revealed that the Algerian <i>S</i>. Kentucky ST198 isolates were closely related to each other and belonged to the MDR lineage that emerged in Egypt before disseminating into Africa, the Middle East, Asia and Europe. These isolates also clustered closely with European and North African isolates carrying the <i>gyrA</i>_D87N mutation. We found that 90% of the isolates had MDR phenotypes, with resistance to critically important antibiotics, including ciprofloxacin, third-generation cephalosporins, azithromycin and chloramphenicol. Genomic analysis revealed that all the isolates had the three known non-synonymous resistance mutations in the quinolone-resistance-determining regions of DNA gyrase (g<i>yrA</i>) and DNA topoisomerase IV (<i>parC</i>). Multiple AMR genes were also identified, including <i>bla</i> <sub>CTX-M-15</sub>, <i>bla</i> <sub>CMY-2</sub>, <i>bla</i> <sub>CMY-4</sub>, <i>qnrB19</i>, <i>mph(A</i>), <i>cmlA1</i> and <i>floR</i>. The Algerian isolates also contained the main variant of SGI1, SGI1-K, with multiple rearrangements. Plasmid replicon analysis revealed that the most frequent plasmid types were IncI1 (13.6%), Col156 (8.8%) and Col(pVC) (8%). This study provides the first comprehensive genomic insight into <i>S</i>. Kentucky ST198 in Algeria, highlighting the urgent need for a reinforcement of AMR surveillance and control measures in the region. These findings enhance our overall understanding of the epidemiology and evolution of MDR <i>Salmonella</i> and highlight the importance of a One Health approach for combating the spread of resistant pathogens.

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Journal
Microbial Genomics
Published
2025-11-25
DOI
https://doi.org/10.1099/mgen.0.001581
Primary Topic
Salmonella and Campylobacter epidemiology
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article

Genomic characterisation of multidrug-resistant Salmonella enterica serovar Kentucky ST198 isolates from various sources in Algeria, North Africa

Faiza Mechouet, Soraya Sadat, Elisabeth Njamkepo, François‐Xavier Weill et al.
Microbial Genomics
Salmonella and Campylobacter epidemiology
article

Genomic characterisation of multidrug-resistant Salmonella enterica serovar Kentucky ST198 isolates from various sources in Algeria, North Africa

Faiza Mechouet, Soraya Sadat, Elisabeth Njamkepo, François‐Xavier Weill, Chafika Belkader, María Pardos de la Gándara, Sarah Sihem Zemam, Nabila Benamrouche, Amine Msela, Laëtitia Fabre, Rym Slimani, Abdehamid Deriet-Ammar, Dalila Torkya Boutabba
article en

Abstract

<i>Salmonella enterica</i> serovar Kentucky (<i>S</i>. Kentucky) sequence type (ST) 198 has emerged as a globally disseminated multidrug-resistant (MDR) lineage posing significant public health challenges. The aim of this study was to characterise 125 <i>S</i>. Kentucky ST198 isolates collected from various sources in Algeria, including humans, animals, food and the environment, or obtained from humans in France (travellers returning from Algeria), between 2015 and 2022. Whole-genome sequencing was performed on 125 isolates to assess their genetic diversity and antimicrobial resistance (AMR) profiles. Phylogenetic analysis revealed that the Algerian <i>S</i>. Kentucky ST198 isolates were closely related to each other and belonged to the MDR lineage that emerged in Egypt before disseminating into Africa, the Middle East, Asia and Europe. These isolates also clustered closely with European and North African isolates carrying the <i>gyrA</i>_D87N mutation. We found that 90% of the isolates had MDR phenotypes, with resistance to critically important antibiotics, including ciprofloxacin, third-generation cephalosporins, azithromycin and chloramphenicol. Genomic analysis revealed that all the isolates had the three known non-synonymous resistance mutations in the quinolone-resistance-determining regions of DNA gyrase (g<i>yrA</i>) and DNA topoisomerase IV (<i>parC</i>). Multiple AMR genes were also identified, including <i>bla</i> <sub>CTX-M-15</sub>, <i>bla</i> <sub>CMY-2</sub>, <i>bla</i> <sub>CMY-4</sub>, <i>qnrB19</i>, <i>mph(A</i>), <i>cmlA1</i> and <i>floR</i>. The Algerian isolates also contained the main variant of SGI1, SGI1-K, with multiple rearrangements. Plasmid replicon analysis revealed that the most frequent plasmid types were IncI1 (13.6%), Col156 (8.8%) and Col(pVC) (8%). This study provides the first comprehensive genomic insight into <i>S</i>. Kentucky ST198 in Algeria, highlighting the urgent need for a reinforcement of AMR surveillance and control measures in the region. These findings enhance our overall understanding of the epidemiology and evolution of MDR <i>Salmonella</i> and highlight the importance of a One Health approach for combating the spread of resistant pathogens.

Microbial GenomicsVol. 11(11)
Institut Pasteur (FR), Université Paris Cité (FR), Universidad de Zaragoza (ES), Centre Hospitalo-Universitaire Bab El Oued (DZ), Institut Pasteur d'Algérie (DZ), Mouloud Mammeri University of Tizi-Ouzou (DZ)
Openalex Percentile: Top 58%
Salmonella and Campylobacter epidemiology
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