New Species-Specific Primers for Molecular Diagnosis of Bactrocera minax and Bactrocera tsuneonis (Diptera: Tephritidae) in China Based on DNA Barcodes

• Published in: Insects (Basel, Switzerland) Switzerland), 2019-12, Vol.10 (12), p.447
• Main Authors: Zheng, Linyu, Zhang, Yue, Yang, Wenzhao, Zeng, Yiying, Jiang, Fan, Qin, Yujia, Zhang, Jiafeng, Jiang, Zhaochun, Hu, Wenzhao, Guo, Dijin, Wan, Jia, Zhao, Zihua, Liu, Lijun, Li, Zhihong
• Format: Article
• Language: English
• Subjects: Bactrocera minax; Bactrocera tsuneonis; Cytochrome; Cytochrome-c oxidase; Cytochromes; Deoxyribonucleic acid; Diptera; DNA; DNA barcoding; Economic impact; Fruits; Gene sequencing; Identification; Identification methods; Insects; Laboratories; Methods; Morphology; New species; Nucleotide sequence; Oxidase; Physical characteristics; Polymerase chain reaction; Primers; Quarantine; Sibling species; Taxonomy; Tephritidae
• ISSN: 2075-4450; 2075-4450
• DOI: 10.3390/insects10120447

Tephritidae fruit flies (Diptera: Tephritidae) are regarded as important damage-causing species due to their ability to cause great economic losses in fruit and vegetable crops. and are two sibling species of the subgenus of that are distributed across a limited area of China, but have caused serious impacts. They share similar morphological characteristics. These characteristics can only be observed in the female adult individuals. The differences between them cannot be observed in preimaginal stages. Thus, it is difficult to distinguish them in preimaginal stages morphologically. In this study, we used molecular diagnostic methods based on cytochrome c oxidase subunit I and species-specific markers to identify these two species and improve upon the false-positive results of previous species-detection primers. DNA barcode sequences were obtained from 900 individuals of and 63 individuals of . Based on these 658 bp DNA barcode sequences of the cytochrome c oxidase subunit I gene, we successfully designed the species-specific primers for and . The size of the specific fragment was 422 bp and the size of the specific fragment was 456 bp. A series of PCR trials ensured the specificity of these two pairs of primers. Sensitivity assay results demonstrated that the detection limit for the DNA template concentration was 0.1~1 ng/μL for these two species. In this study, we established a more reliable, rapid, and low-cost molecular identification method for all life stages of and . Species-specific PCR can be applied in plant quarantine, monitoring and control of and .