Comparative study of Taqman-based qPCR assay for the detection of Anisakis simplex and Pseudoterranova decipiens

সংরক্ষণ করুন:
গ্রন্থ-পঞ্জীর বিবরন
প্রকাশিত:PLoS One vol. 20, no. 4 (Apr 2025), p. e0320724
প্রধান লেখক: Kim, Mi-Gyeong
অন্যান্য লেখক: Min Ji Hong, Seo, Doo Won, Jung, Hyun Mi, Hyun-Ja Han, Kim, Seung Hwan, Joo, Insun
প্রকাশিত:
Public Library of Science
বিষয়গুলি:
অনলাইন ব্যবহার করুন:Citation/Abstract
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LEADER 00000nab a2200000uu 4500
001 3194938268
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022 |a 1932-6203 
024 7 |a 10.1371/journal.pone.0320724  |2 doi 
035 |a 3194938268 
045 2 |b d20250401  |b d20250430 
084 |a 174835  |2 nlm 
100 1 |a Kim, Mi-Gyeong 
245 1 |a Comparative study of Taqman-based qPCR assay for the detection of <i>Anisakis simplex</i> and <i>Pseudoterranova decipiens</i> 
260 |b Public Library of Science  |c Apr 2025 
513 |a Journal Article 
520 3 |a Anisakidosis is a foodborne parasitic infection caused by the consumption of raw or uncooked seafood that contains third stage larvae from the Anisakidae family. This infection has been observed across the globe, with a particularly high prevalence in South Korea and Japan. Consequently, there is a necessity to compare and analyze the optimal detection methods with a view to preventing Anisakis outbreaks. In this study, a species-specific Taqman-based qPCR method was developed for the detection of the internal transcribed spacer region and mtDNA genes of Anisakis simplex and Pseudoterranova decipiens. Parasite-specific primer/probe sets were selected based on the data from domestic and foreign detection methods. In addition, we have designed our own primer/probe sets based on the target region of each parasite. A comprehensive literature review and a self-creation process were undertaken to select thirteen detection method sets for A. simplex and P. decipiens. The sensitivity of these sets was then evaluated by comparing the Cq values from extracted DNA. The concentrations of six primer/probe sets detected through the screening process were then compared to optimize the test method. The resultant optimized method demonstrated a limit of detection of 0.0019 ng/µL for A. simplex and 0.0001 ng/µL for P. decipiens. The specificity test also confirmed that there was no cross-activity with the five parasite samples and the three types of anisakids plasmid DNA. This study would contribute development of a rapid detection method for anisakidosis, providing a foundation for proactive responses to food poisoning outbreaks. 
651 4 |a United States--US 
651 4 |a Japan 
653 |a Infections 
653 |a Plasmids 
653 |a Parasites 
653 |a Larvae 
653 |a Outbreaks 
653 |a Mitochondrial DNA 
653 |a Food poisoning 
653 |a Parasitic diseases 
653 |a Seafood 
653 |a Literature reviews 
653 |a Comparative studies 
653 |a Spacer region 
653 |a Food contamination 
653 |a Maximum likelihood method 
653 |a Optimization 
653 |a Deoxyribonucleic acid--DNA 
653 |a Design 
653 |a Crustaceans 
653 |a Marine mammals 
653 |a Fish 
653 |a Social 
653 |a Pseudoterranova decipiens 
653 |a Palustriella decipiens 
653 |a Anisakis simplex 
653 |a Environmental 
700 1 |a Min Ji Hong 
700 1 |a Seo, Doo Won 
700 1 |a Jung, Hyun Mi 
700 1 |a Hyun-Ja Han 
700 1 |a Kim, Seung Hwan 
700 1 |a Joo, Insun 
773 0 |t PLoS One  |g vol. 20, no. 4 (Apr 2025), p. e0320724 
786 0 |d ProQuest  |t Health & Medical Collection 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/3194938268/abstract/embedded/L8HZQI7Z43R0LA5T?source=fedsrch 
856 4 0 |3 Full Text  |u https://www.proquest.com/docview/3194938268/fulltext/embedded/L8HZQI7Z43R0LA5T?source=fedsrch 
856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/3194938268/fulltextPDF/embedded/L8HZQI7Z43R0LA5T?source=fedsrch