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Related Concept Videos

Genomics02:02

Genomics

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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.
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Related Experiment Video

Updated: Jun 8, 2025

Characterization of a Pathogenic Escherichia coli Strain Derived from Oreochromis spp. Farms Using Whole-Genome Sequencing
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Characterization of a Pathogenic Escherichia coli Strain Derived from Oreochromis spp. Farms Using Whole-Genome Sequencing

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Genomic perspectives on foodborne illness.

David J Lipman1, Joshua L Cherry2,3, Errol Strain1

  • 1Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Regulatory Science, College Park, MD 20740.

Proceedings of the National Academy of Sciences of the United States of America
|November 5, 2024
PubMed
Summary

Whole-genome sequencing reveals that foodborne pathogen contamination episodes, like Salmonella, often persist for years and affect multiple states. Young children show higher susceptibility to these infections.

Keywords:
bacterial pathogensfood safetywhole genome sequencing

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Area of Science:

  • Foodborne illness
  • Microbial genomics
  • Public health surveillance

Background:

  • Whole-genome sequencing (WGS) is crucial for linking food poisoning cases to contamination sources.
  • Most foodborne illnesses are sporadic and not investigated due to limited genetic differentiation.

Purpose of the Study:

  • To analyze clusters of bacterial pathogen isolates (Salmonella, E. coli, Campylobacter, Listeria) with minimal genetic differences (SNPs).
  • To identify characteristics of the contamination episodes underlying these clusters.

Main Methods:

  • Examined clusters of whole-genome sequences from clinical isolates of four key bacterial pathogens.
  • Analyzed single-nucleotide polymorphism (SNP) differences to infer relationships and duration of contamination events.

Main Results:

  • Younger age groups exhibit increased susceptibility to Salmonella, E. coli, and Campylobacter infections.
  • A significant proportion of contamination episodes are long-lasting, with 50% of Salmonella clusters persisting for nearly three years.
  • Most cases across all four pathogens occurred in multi-state clusters, suggesting widespread commercial food contamination.

Conclusions:

  • WGS analysis of SNP clusters provides insights into foodborne contamination episode dynamics.
  • Findings highlight the prolonged nature of contamination events and the role of commercially distributed foods.
  • Age-related susceptibility patterns were observed, with nuances for specific Salmonella serovars.