{"title":"Detection of environmental DNA of the Japanese orange fly, Bactrocera tsuneonis (Diptera: Tephritidae), from immature mandarin orange fruits","authors":"Hajime Ono, Shohei Ota, Shinya Kanno, Yuta Nomura, Minoru Narahara, Yoshio Okazaki","doi":"10.1007/s13355-024-00890-9","DOIUrl":null,"url":null,"abstract":"<div><p>Early detection of insect pest outbreaks is critical for effective pest control. However, this is challenging, especially for pest species such as the Japanese orange fly, <i>Bactrocera tsuneonis</i> (Miyake) (Diptera: Tephritidae), whose larvae grow inside fruits. <i>B</i>. <i>tsuneonis</i> is a univoltine citrus pest, with females laying their eggs directly into the fruits during summer, and larvae develop inside the fruits until pupation in early winter. To monitor <i>B</i>. <i>tsuneonis</i> outbreaks, we developed and validated methods for the detection of environmental DNA (eDNA) in immature fruits collected during summer using quantitative real-time PCR. eDNA samples were prepared from individual fruits with oviposition pinholes left by gravid females during ovipositor probing and oviposition. By immersing the fruits in distilled water for 1 h to extract eDNA, <i>B</i>. <i>tsuneonis</i> eDNA was detected in 20% of the fruits. In addition, <i>B</i>. <i>tsuneonis</i> eDNA was detected in a fruit without oviposition pinholes, albeit at a low rate, suggesting that residual eDNA on fruit surfaces during mating and searching for oviposition sites can be detected. While there remains a possibility of cross-contamination between infected and uninfected fruits due to the lack of negative controls during eDNA extraction, we conducted preliminary field examination in several orchards where <i>B</i>. <i>tsuneonis</i> was either visually observed or not. <i>B</i>. <i>tsuneonis</i> eDNA was detected even at a location where adults were not observed visually, but were captured using plastic-tub traps, indicating a low population density. Thus, our method has practical applicability in various areas, regardless of <i>B</i>. <i>tsuneonis</i> population density.</p></div>","PeriodicalId":8551,"journal":{"name":"Applied Entomology and Zoology","volume":"60 1","pages":"45 - 51"},"PeriodicalIF":1.3000,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Entomology and Zoology","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s13355-024-00890-9","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Early detection of insect pest outbreaks is critical for effective pest control. However, this is challenging, especially for pest species such as the Japanese orange fly, Bactrocera tsuneonis (Miyake) (Diptera: Tephritidae), whose larvae grow inside fruits. B. tsuneonis is a univoltine citrus pest, with females laying their eggs directly into the fruits during summer, and larvae develop inside the fruits until pupation in early winter. To monitor B. tsuneonis outbreaks, we developed and validated methods for the detection of environmental DNA (eDNA) in immature fruits collected during summer using quantitative real-time PCR. eDNA samples were prepared from individual fruits with oviposition pinholes left by gravid females during ovipositor probing and oviposition. By immersing the fruits in distilled water for 1 h to extract eDNA, B. tsuneonis eDNA was detected in 20% of the fruits. In addition, B. tsuneonis eDNA was detected in a fruit without oviposition pinholes, albeit at a low rate, suggesting that residual eDNA on fruit surfaces during mating and searching for oviposition sites can be detected. While there remains a possibility of cross-contamination between infected and uninfected fruits due to the lack of negative controls during eDNA extraction, we conducted preliminary field examination in several orchards where B. tsuneonis was either visually observed or not. B. tsuneonis eDNA was detected even at a location where adults were not observed visually, but were captured using plastic-tub traps, indicating a low population density. Thus, our method has practical applicability in various areas, regardless of B. tsuneonis population density.
期刊介绍:
Applied Entomology and Zoology publishes articles concerned with applied entomology, applied zoology, agricultural chemicals and pest control in English. Contributions of a basic and fundamental nature may be accepted at the discretion of the Editor. Manuscripts of original research papers, technical notes and reviews are accepted for consideration. No manuscript that has been published elsewhere will be accepted for publication.