Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samples

Abstract Shigella species, a group of intracellular foodborne pathogens, are the main causes of bacillary dysentery and shigellosis in humans worldwide. It is essential to determine the species of Shigella in outbreaks and food safety surveillance systems. The available immunological and molecular m...

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Published in:Scientific Reports
Main Authors: Babak Pakbin, Afshin Akhondzadeh Basti, Ali Khanjari, Wolfram Manuel Brück, Leila Azimi, Abdollah Karimi
Format: Article
Language:English
Published: Nature Portfolio 2022-01-01
Online Access:https://doi.org/10.1038/s41598-021-04484-1
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author Babak Pakbin
Afshin Akhondzadeh Basti
Ali Khanjari
Wolfram Manuel Brück
Leila Azimi
Abdollah Karimi
author_facet Babak Pakbin
Afshin Akhondzadeh Basti
Ali Khanjari
Wolfram Manuel Brück
Leila Azimi
Abdollah Karimi
author_sort Babak Pakbin
collection DOAJ
container_title Scientific Reports
description Abstract Shigella species, a group of intracellular foodborne pathogens, are the main causes of bacillary dysentery and shigellosis in humans worldwide. It is essential to determine the species of Shigella in outbreaks and food safety surveillance systems. The available immunological and molecular methods for identifying Shigella species are relatively complicated, expensive and time-consuming. High resolution melting (HRM) assay is a rapid, cost-effective, and easy to perform PCR-based method that has recently been used for the differentiation of bacterial species. In this study, we designed and developed a PCR-HRM assay targeting rrsA gene to distinguish four species of 49 Shigella isolates from clinical and food samples and evaluated the sensitivity and specificity of the assay. The assay demonstrated a good analytical sensitivity with 0.01–0.1 ng of input DNA template and an analytical specificity of 100% to differentiate the Shigella species. The PCR-HRM assay also was able to identify the species of all 49 Shigella isolates from clinical and food samples correctly. Consequently, this rapid and user-friendly method demonstrated good sensitivity and specificity to differentiate species of the Shigella isolates from naturally contaminated samples and has the potential to be implemented in public health and food safety surveillance systems.
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spelling doaj-art-e4b6cbc70866435cb7cb23bc0629c9ed2025-08-19T21:04:36ZengNature PortfolioScientific Reports2045-23222022-01-0112111310.1038/s41598-021-04484-1Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samplesBabak Pakbin0Afshin Akhondzadeh Basti1Ali Khanjari2Wolfram Manuel Brück3Leila Azimi4Abdollah Karimi5Institute for Life Technologies, University of Applied Sciences Western Switzerland Valais-WallisDepartment of Food Hygiene and Quality of Control, Faculty of Veterinary Medicine, University of TehranDepartment of Food Hygiene and Quality of Control, Faculty of Veterinary Medicine, University of TehranInstitute for Life Technologies, University of Applied Sciences Western Switzerland Valais-WallisPediatric Infections Research Center, Research Institute of Children’s Health, Shahid Beheshti University of Medical SciencesPediatric Infections Research Center, Research Institute of Children’s Health, Shahid Beheshti University of Medical SciencesAbstract Shigella species, a group of intracellular foodborne pathogens, are the main causes of bacillary dysentery and shigellosis in humans worldwide. It is essential to determine the species of Shigella in outbreaks and food safety surveillance systems. The available immunological and molecular methods for identifying Shigella species are relatively complicated, expensive and time-consuming. High resolution melting (HRM) assay is a rapid, cost-effective, and easy to perform PCR-based method that has recently been used for the differentiation of bacterial species. In this study, we designed and developed a PCR-HRM assay targeting rrsA gene to distinguish four species of 49 Shigella isolates from clinical and food samples and evaluated the sensitivity and specificity of the assay. The assay demonstrated a good analytical sensitivity with 0.01–0.1 ng of input DNA template and an analytical specificity of 100% to differentiate the Shigella species. The PCR-HRM assay also was able to identify the species of all 49 Shigella isolates from clinical and food samples correctly. Consequently, this rapid and user-friendly method demonstrated good sensitivity and specificity to differentiate species of the Shigella isolates from naturally contaminated samples and has the potential to be implemented in public health and food safety surveillance systems.https://doi.org/10.1038/s41598-021-04484-1
spellingShingle Babak Pakbin
Afshin Akhondzadeh Basti
Ali Khanjari
Wolfram Manuel Brück
Leila Azimi
Abdollah Karimi
Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samples
title Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samples
title_full Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samples
title_fullStr Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samples
title_full_unstemmed Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samples
title_short Development of high-resolution melting (HRM) assay to differentiate the species of Shigella isolates from stool and food samples
title_sort development of high resolution melting hrm assay to differentiate the species of shigella isolates from stool and food samples
url https://doi.org/10.1038/s41598-021-04484-1
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