Genomic Characterization of Salmonella Isolates Causing Infections in Children with Sickle Cell Disease in Dakar, Senegal
Authors:
- Amadou DiopADAmadou Diop
- Arfang DiamankaADArfang Diamanka
- Adja Bousso GuèyeAGAdja Bousso Guèye
- Baïdy DièyeBDBaïdy Dièye
- El Hadji Aly NiangENEl Hadji Aly Niang
- Ousmane SadioOSOusmane Sadio
- Mouhamadou Abdoulaye SonkoMSMouhamadou Abdoulaye Sonko
- Aïssatou Ahmet NiangANAïssatou Ahmet Niang
- Momar NdaoMNMomar Ndao
- Ken DewarKDKen Dewar
- Cheikh FallCFCheikh Fall
- François PaillierFPFrançois Paillier
Open Access
- 21 February 2026
- journal article
- research article
- Published by MDPI AG in Microorganisms
- Vol. 14 (2) , 506
Abstract
Salmonella is a major bacterial pathogen in low-income countries, where it circulates among humans, animals, and the environment. Children with sickle cell disease (SCD) are particularly vulnerable to severe Salmonella infections. This study aimed to characterize Salmonella isolates causing infections in Senegalese children with SCD. Using antimicrobial susceptibility testing, whole-genome sequencing, and bioinformatic analysis, we investigated antibiotic resistance, serovar diversity, and virulence factors on 23 isolates from SCD patients with diverse clinical infections. The isolates belonged to 12 serovars, with Enteritidis predominating (n = 7). Twenty-two isolates were fully susceptible to antibiotics, while one was multidrug-resistant. Eight isolates (Enteritidis and Typhimurium) carried a virulence plasmid harboring the spvRABCD gene cluster. Core Salmonella pathogenicity islands (SPIs-1 to -5, -11, and -13), as well as SPI-10 and SPI-23, were detected in all isolates, whereas other SPIs were variably present. These results show high serovar diversity and low antimicrobial resistance among Salmonella isolates in children with SCD in Dakar, Senegal. Our findings suggest that strains causing diarrhea in healthy individuals may also cause invasive disease in SCD patients, highlighting the need for dedicated surveillance in this vulnerable population.Keywords
Funding Information
- The World Academy of Sciences (22-291 RG/BIO/AF/AC_G FR 3240325161)
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