Baïdy Dièye
Research Subjects
Baïdy Dièye has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
- Adja Bousso Gueye
Pôle de Microbiologie, Institut Pasteur de Dakar, 36 avenue Pasteur, Dakar BP 220, Senegal
1 shared publication - Aissatou Ahmet Niang
Laboratoire de Bactériologie-Virologie, Faculté de Médecine, de Pharmacie et d’Odontologie-Stomatologie, Université Cheikh Anta Diop, Dakar BP 5005, Senegal
1 shared publication - Amadou Diop
Laboratoire de Bactériologie-Virologie, Centre Hospitalier National d’Enfants Albert Royer, Dakar BP 25755, Senegal
1 shared publication - Arfang Diamanka
Département de Biologie Végétale, Faculté des Sciences et Techniques, Université Cheikh Anta Diop, Dakar BP 5005, Senegal
1 shared publication - Cheikh Fall
Pôle de Microbiologie, Institut Pasteur de Dakar, 36 avenue Pasteur, Dakar BP 220, Senegal
1 shared publication - El Hadji Aly Niang
Pôle de Microbiologie, Institut Pasteur de Dakar, 36 avenue Pasteur, Dakar BP 220, Senegal
1 shared publication
Latest Publications
- Open Access
- 21 February 2026
- Published by MDPI AG in Microorganisms
- Vol. 14 (2) , 506
Genomic Characterization of Salmonella Isolates Causing Infections in Children with Sickle Cell Disease in Dakar, Senegal
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.
- 21 February 2026
- Published by MDPI AG in Microorganisms
- Vol. 14 (2) , 506
Open AccessGenomic Characterization of Salmonella Isolates Causing Infections in Children with Sickle Cell Disease in Dakar, Senegal
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.