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Development of a Rapid Isothermal Amplification Assay for the Fall Armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae), Using Species-Specific Genomic Sequences
被引:0
|作者:
Park, Jeong Sun
[1
]
Lee, Keon Hee
[1
]
Kim, Min Jee
[2
]
Choi, Deuk-Soo
[3
]
Lee, Kyeong-Yeoll
[4
]
Edosa, Tariku Tesfaye
[5
]
Dinka, Teshale Daba
[5
]
Kwak, Woori
[6
]
Kim, Iksoo
[1
]
机构:
[1] Chonnam Natl Univ, Coll Agr & Life Sci, Dept Appl Biol, Gwangju 61186, South Korea
[2] Anim & Plant Quarantine Agcy, Honam Reg Off, Expt & Anal Div, Gunsan 54096, South Korea
[3] Quarantine Technol Inst Ins, Gimcheon 39660, South Korea
[4] Kyungpook Natl Univ, Coll Agr & Life Sci, Dept Appl Biosci, Daegu 41566, South Korea
[5] Ambo Agr Res Ctr, Ethiopian Inst Agr Res, POB 37, Ambo, Ethiopia
[6] Catholic Univ Korea, Dept Med & Biol Sci, Bucheon 14662, South Korea
来源:
关键词:
fall armyworm;
Spodoptera frugiperda;
loop-mediated isothermal amplification;
FAW-specific primers;
DNA;
PLANTS;
D O I:
10.3390/agronomy14010219
中图分类号:
S3 [农学(农艺学)];
学科分类号:
0901 ;
摘要:
The fall armyworm (FAW), Spodoptera frugiperda (Lepidoptera: Noctuidae), is native to tropical and subtropical regions of the Western Hemisphere, but is now regularly appearing in crop fields across South Korea, particularly in corn fields. Therefore, it is crucial to promptly and accurately identify the presence of FAW in crop fields to effectively eradicate it as a regulated quarantine species. We developed a loop-mediated isothermal amplification (LAMP) assay, which allows for rapid in-filed identification. To develop the LAMP assay, we selected FAW-specific genomic regions from the whole-genome sequences of one FAW and 13 other lepidopteran species and validated five primer sets that consistently produced positive reactions in ten FAW samples collected from eight different locations in four countries. The assay successfully identified FAW in a maximum of 45 min, starting from crude DNA extraction (similar to 15 min) to diagnosis (30 min) from the following samples, which were deposited outdoors for 30 days: a 1st-instar larva, an adult leg, an adult antenna, and 1/16 and 1/8 of an adult thorax. The five assays can be used selectively or in combination to cross-check and provide further confidence in the in-field diagnosis of FAW.
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