Publications by authors named "Nora Madani"

Article Synopsis
  • - Tularemia in Europe is caused by the bacterium Francisella tularensis subsp. holarctica, primarily affecting wildlife and humans, with classification based on specific genetic markers (canSNPs).
  • - Four main genetic clades (B.4, B.6, B.12, B.16) have been identified, with clade B.6 being common in Western Europe and B.12 in Eastern and Central Europe.
  • - Researchers developed a molecular typing method using high-resolution melting (HRM) primers to analyze 109 canSNPs, aiming to enhance the tracking and understanding of this bacterium’s presence in Western Europe.
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In France, tularemia is caused by subsp. and is a sporadic disease affecting mainly wildlife animals and humans. species presents low genetic diversity that remains poorly described in France, as only a few genomes of isolates from the country are available so far.

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Studies that examine social influences on child eating/weight status, including parental feeding, are particularly lacking among Arab populations. Due to variations in societal norms and perceptions of what embodies a healthy weight status, feeding practices may vary among cultures; Unique patterns of feeding behaviors may exist among parents of Saudi descent. This study aimed to collect and analyze qualitative data in order to detect themes and characterize feeding behaviors among mothers of preschoolers in Saudi Arabia.

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Here, we report the complete genome sequences of three strains of subsp. (11-789-5S, 11-935-13S, and 11-930-9S), isolated from brown hares and a tick during a tularemia outbreak in France, where tularemia is endemic.

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Tularemia, caused by Francisella tularensis, is endemic in France. The surveillance of this disease in wildlife is operated by the SAGIR Network and by the National Reference Laboratory for Tularemia. Wild animals found dead or dying collected by the SAGIR network are necropsied and when tularemia is suspected culture and/or PCR are performed to confirm the diagnosis.

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Background: Bacillus anthracis, the highly dangerous zoonotic bacterial pathogen species is currently composed of three genetic groups, called A, B and C. Group A is represented worldwide whereas group B is present essentially in Western Europe and Southern Africa. Only three strains from group C have been reported.

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Background: Bacillus anthracis is known to have low genetic variability. In spite of this lack of diversity, multiple-locus variable-number tandem repeat (VNTR) analysis (MLVA) and single nucleotide polymorphisms (SNPs) including the canonical SNPs assay (canSNP) have proved to be highly effective to differentiate strains. Five different MLVA schemes based on a collection of 31 VNTR loci (MLVA8, MLVA15, MLVA20, MLVA25 and MLVA31) with increased resolving power have been described.

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Francisella tularensis, the causative agent of tularemia, is commonly transmitted by ticks. To ensure accurate F. tularensis reporting rates in epidemiological surveys, specific discrimination between F.

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Single nucleotide polymorphisms (SNPs) are important diagnostic markers for the detection and differentiation of Bacillus anthracis. High-Resolution Melting (HRM) and Melting Temperature (Tm)-shift methods are two approaches that enable SNP detection without the need for expensive labeled probes. We evaluated the potential diagnostic capability of those methods to discriminate B.

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