Niokhor Dione
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Niokhor Dione has a total of 3 co-authors. Here are the top co-authors by number of shared publications:
- Kodjovi Dodji Mlaga
The Microbiome and Mucosal Defence Research Unit, Institut de Recherche Clinique de Montréal, Montreal, QC H2W 1R7, Canada
2 shared publications - Kossi Kabo
Dakar Institut Pasteur de Dakar
2 shared publications - Tchadjobo Tchacondo
Laboratoire des Sciences Biomédicales, Alimentaires et de la Santé Environnementale, École Supérieure des Techniques Biologiques et Alimentaires, Université de Lomé, Lomé 01 BP 1515, Togo
2 shared publications
Latest Publications
- Open Access
- 26 November 2025
- Published by MDPI AG in Microorganisms
- Vol. 13 (12) , 2694
First Isolation and Genomic Characterization of Escherichia ruysiae in Togo from a Five-Year-Old Patient with Gastroenteritis and Bloody Diarrhea
Escherichia ruysiae is a recently characterized species within the Escherichia genus, often misclassified as E. coli due to limitations in existing operating procedures and diagnostic databases. In this study, we report the first isolation and genomic characterization of E. ruysiae in Togo, from a five-year-old female patient who was hospitalized with gastroenteritis and bloody diarrhea and subsequently died after eight days. Biochemical tests and MALDI-TOF initially identified the microorganism as E. coli, but phylogenomic and Average Nucleotide Identity (ANI) analysis confirmed it to be E. ruysiae, Clade IV with enteroaggregative associated genes. Whole genome sequencing of the strain FK53-34 enables the identification of resistance genes, including blaEC-15, eptA, and pmrF. The virulence profile of the strain included, but was not limited to aap, aatABC, and senB genes, which may support its pathogenicity and virulence. Multilocus sequence typing (MLST) did not match any known sequence type, which is obvious for a newly characterized microorganism. This study highlights the critical need for enhanced diagnostic tools and surveillance systems to identify emerging pathogens, including Escherichia ruysiae.
- 26 November 2025
- Published by MDPI AG in Microorganisms
- Vol. 13 (12) , 2694
Open AccessFirst Isolation and Genomic Characterization of Escherichia ruysiae in Togo from a Five-Year-Old Patient with Gastroenteritis and Bloody Diarrhea
Escherichia ruysiae is a recently characterized species within the Escherichia genus, often misclassified as E. coli due to limitations in existing operating procedures and diagnostic databases. In this study, we report the first isolation and genomic characterization of E. ruysiae in Togo, from a five-year-old female patient who was hospitalized with gastroenteritis and bloody diarrhea and subsequently died after eight days. Biochemical tests and MALDI-TOF initially identified the microorganism as E. coli, but phylogenomic and Average Nucleotide Identity (ANI) analysis confirmed it to be E. ruysiae, Clade IV with enteroaggregative associated genes. Whole genome sequencing of the strain FK53-34 enables the identification of resistance genes, including blaEC-15, eptA, and pmrF. The virulence profile of the strain included, but was not limited to aap, aatABC, and senB genes, which may support its pathogenicity and virulence. Multilocus sequence typing (MLST) did not match any known sequence type, which is obvious for a newly characterized microorganism. This study highlights the critical need for enhanced diagnostic tools and surveillance systems to identify emerging pathogens, including Escherichia ruysiae.
- Open Access
- 30 July 2025
- Published by MDPI AG in Preprints.org
First Genomic Characterization of Escherichia ruysiae Isolated from a Five-Year-Old Patient with Gastroenteritis and Bloody Diarrhea in Togo
Escherichia ruysiae is a recently characterized species within the Escherichia genus, often misclassified as E. coli due to limitations in existing operating procedure and diagnostic databases. In this study, we report the first isolation and genomic characterization of E. ruysiae in Togo, from a five-year-old female patient who was hospitalized with gastro-enteritis and bloody diarrhea and subsequently died after eight days. Biochemical tests and MALDI-TOF initially identified the microorganism as E. coli, but phylogenomic and Average Nucleotide Identity (ANI) analysis confirmed it to be E. ruysiae, Clade IV with enteroaggregative associated genes. Whole genome sequencing of the strain FK53-34 enables the identification of resistance genes including blaPBP, blaampH, acrA, emrF, baeS et tolC and various aminoglycoside-modifying enzymes, blaEC-15, eptA and pmrF. The virulence profile of the strain included but not limited to, aap, aatABC, senB, prmF genes which support its pathogenicity and virulence. Multilocus sequence typing (MLST) did not match any known sequence type, which is obvious for a newly characterized mi-croorganism. This study highlights the critical need for enhanced diagnostic tools and surveillance systems to identify emerging pathogens, including Escherichia ruysiae
- 30 July 2025
- Published by MDPI AG in Preprints.org
Open AccessFirst Genomic Characterization of Escherichia ruysiae Isolated from a Five-Year-Old Patient with Gastroenteritis and Bloody Diarrhea in Togo
Escherichia ruysiae is a recently characterized species within the Escherichia genus, often misclassified as E. coli due to limitations in existing operating procedure and diagnostic databases. In this study, we report the first isolation and genomic characterization of E. ruysiae in Togo, from a five-year-old female patient who was hospitalized with gastro-enteritis and bloody diarrhea and subsequently died after eight days. Biochemical tests and MALDI-TOF initially identified the microorganism as E. coli, but phylogenomic and Average Nucleotide Identity (ANI) analysis confirmed it to be E. ruysiae, Clade IV with enteroaggregative associated genes. Whole genome sequencing of the strain FK53-34 enables the identification of resistance genes including blaPBP, blaampH, acrA, emrF, baeS et tolC and various aminoglycoside-modifying enzymes, blaEC-15, eptA and pmrF. The virulence profile of the strain included but not limited to, aap, aatABC, senB, prmF genes which support its pathogenicity and virulence. Multilocus sequence typing (MLST) did not match any known sequence type, which is obvious for a newly characterized mi-croorganism. This study highlights the critical need for enhanced diagnostic tools and surveillance systems to identify emerging pathogens, including Escherichia ruysiae