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Establishing the Performance of Next-Generation Amplicon Sequencing for Detection of Giardia duodenalis in Ready-to-Eat Packaged Leafy Greens. | LitMetric

Establishing the Performance of Next-Generation Amplicon Sequencing for Detection of Giardia duodenalis in Ready-to-Eat Packaged Leafy Greens.

J Food Prot

Environmental Microbial and Food Safety Laboratory, Agricultural Research Service, U.S. Department of Agriculture, 20705 Beltsville, MD, USA. Electronic address:

Published: October 2024

AI Article Synopsis

  • Giardia duodenalis is a common intestinal parasite affecting humans and animals, with different genetic types that vary in their ability to infect different hosts.
  • This study developed a method using next-generation sequencing to detect mixed populations of G. duodenalis in fresh produce, specifically focusing on its presence in leafy greens like baby Romaine lettuce.
  • The results showed that the detection of G. duodenalis was effective with higher concentrations of cysts, demonstrating the potential of this new diagnostic approach for food safety and understanding foodborne illnesses.

Article Abstract

Giardia duodenalis is a globally distributed intestinal parasite that commonly infects both humans and animals. G. duodenalis is a species complex, which includes eight assemblages that vary both in genetic structure and host specificity. The prevalence of mixed-assemblage G. duodenalis cysts on food, an understudied infection route for G. duodenalis, remains unknown. In the present study, a method able to detect G. duodenalis mixed-assemblage infections using next-generation amplicon sequencing (NGS) of the beta-giardin gene was applied in combination with the US-FDA's BAM Chapter 19b protocol for the detection of G. duodenalis from fresh produce to ascertain the limit of detection of G. duodenalis on leafy greens. Ready-to-eat baby Romaine lettuce was inoculated with 5 (n = 5), 20 (n = 10), 100 (n = 10), 200 (n = 10), or 1,000 (n = 10) G. duodenalis cysts of the assemblage B strain H3. Detection of G. duodenalis was successful in 100% of the samples seeded with 1,000, 200, and 100 cysts, in 50% of the samples seeded with 20 cysts, and in none of the samples seeded with 5 cysts. We thus demonstrate robust detection of G. duodenalis on packaged leafy greens using the BAM Chapter 19B method coupled with assemblage-sensitive NGS. This protocol provides a new diagnostic tool useful for both prevalence studies and outbreak investigations involving fresh produce that may assist in better describing the role of G. duodenalis in foodborne illness and in protecting consumers from contaminated fresh produce.

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Source
http://dx.doi.org/10.1016/j.jfp.2024.100355DOI Listing

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