Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assay

Abstract The fall armyworm [FAW, Spodoptera frugiperda (J E Smith)], a moth native to America, has spread throughout the world since it was first discovered in Africa in 2016. The FAW is a polyphagous migratory pest that can travel over long distances using seasonal winds or typhoons because of its...

Full description

Bibliographic Details
Main Authors: Angelina F. Osabutey, Bo Yoon Seo, A-Young Kim, Thu Anh Thi Ha, JinKyo Jung, Georg Goergen, Ebenezer Oduro Owusu, Gwan-Seok Lee, Young Ho Koh
Format: Article
Language:English
Published: Nature Portfolio 2022-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-04871-2
_version_ 1818954683785412608
author Angelina F. Osabutey
Bo Yoon Seo
A-Young Kim
Thu Anh Thi Ha
JinKyo Jung
Georg Goergen
Ebenezer Oduro Owusu
Gwan-Seok Lee
Young Ho Koh
author_facet Angelina F. Osabutey
Bo Yoon Seo
A-Young Kim
Thu Anh Thi Ha
JinKyo Jung
Georg Goergen
Ebenezer Oduro Owusu
Gwan-Seok Lee
Young Ho Koh
author_sort Angelina F. Osabutey
collection DOAJ
description Abstract The fall armyworm [FAW, Spodoptera frugiperda (J E Smith)], a moth native to America, has spread throughout the world since it was first discovered in Africa in 2016. The FAW is a polyphagous migratory pest that can travel over long distances using seasonal winds or typhoons because of its excellent flying ability, causing serious damage to many crops. For effective FAW control, accurate species identification is essential at the beginning of the invasion. In this study, the FAW-specific gene Sf00067 was discovered by performing bioinformatics to develop a fast and accurate tool for the species-specific diagnosis of this pest. An Sf00067 loop-mediated isothermal amplification (LAMP) assay was developed, and optimal conditions were established. The Sf00067 6 primer LAMP (Sf6p-LAMP) assay established in this study was able to diagnose various genotype-based strains of FAW captured in Korea and FAWs collected from Benin, Africa. Our FAW diagnostic protocol can be completed within 30 min, from the process of extracting genomic DNA from an egg or a 1st instar larva to species determination.
first_indexed 2024-12-20T10:26:04Z
format Article
id doaj.art-4482551dcb1948c9adee6af47b66b81a
institution Directory Open Access Journal
issn 2045-2322
language English
last_indexed 2024-12-20T10:26:04Z
publishDate 2022-01-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj.art-4482551dcb1948c9adee6af47b66b81a2022-12-21T19:43:49ZengNature PortfolioScientific Reports2045-23222022-01-0112111010.1038/s41598-022-04871-2Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assayAngelina F. Osabutey0Bo Yoon Seo1A-Young Kim2Thu Anh Thi Ha3JinKyo Jung4Georg Goergen5Ebenezer Oduro Owusu6Gwan-Seok Lee7Young Ho Koh8Department of Biomedical Gerontology, Hallym University Graduate SchoolCrop Protection Division, National Institute of Agricultural Science, Rural Development AdministrationDepartment of Biomedical Gerontology, Hallym University Graduate SchoolDepartment of Biomedical Gerontology, Hallym University Graduate SchoolCrop Cultivation and Environment Research Division, National Institute of Crop ScienceIITA Biological Control, Center for AfricaDepartment of Animal Biology and Conservation Science, University of GhanaCrop Protection Division, National Institute of Agricultural Science, Rural Development AdministrationDepartment of Biomedical Gerontology, Hallym University Graduate SchoolAbstract The fall armyworm [FAW, Spodoptera frugiperda (J E Smith)], a moth native to America, has spread throughout the world since it was first discovered in Africa in 2016. The FAW is a polyphagous migratory pest that can travel over long distances using seasonal winds or typhoons because of its excellent flying ability, causing serious damage to many crops. For effective FAW control, accurate species identification is essential at the beginning of the invasion. In this study, the FAW-specific gene Sf00067 was discovered by performing bioinformatics to develop a fast and accurate tool for the species-specific diagnosis of this pest. An Sf00067 loop-mediated isothermal amplification (LAMP) assay was developed, and optimal conditions were established. The Sf00067 6 primer LAMP (Sf6p-LAMP) assay established in this study was able to diagnose various genotype-based strains of FAW captured in Korea and FAWs collected from Benin, Africa. Our FAW diagnostic protocol can be completed within 30 min, from the process of extracting genomic DNA from an egg or a 1st instar larva to species determination.https://doi.org/10.1038/s41598-022-04871-2
spellingShingle Angelina F. Osabutey
Bo Yoon Seo
A-Young Kim
Thu Anh Thi Ha
JinKyo Jung
Georg Goergen
Ebenezer Oduro Owusu
Gwan-Seok Lee
Young Ho Koh
Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assay
Scientific Reports
title Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assay
title_full Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assay
title_fullStr Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assay
title_full_unstemmed Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assay
title_short Identification of a fall armyworm (Spodoptera frugiperda)-specific gene and development of a rapid and sensitive loop-mediated isothermal amplification assay
title_sort identification of a fall armyworm spodoptera frugiperda specific gene and development of a rapid and sensitive loop mediated isothermal amplification assay
url https://doi.org/10.1038/s41598-022-04871-2
work_keys_str_mv AT angelinafosabutey identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT boyoonseo identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT ayoungkim identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT thuanhthiha identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT jinkyojung identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT georggoergen identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT ebenezeroduroowusu identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT gwanseoklee identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay
AT younghokoh identificationofafallarmywormspodopterafrugiperdaspecificgeneanddevelopmentofarapidandsensitiveloopmediatedisothermalamplificationassay