The establishment of species-specific primers for the molecular identification of ten stored-product psocids based on ITS2 rDNA

被引:14
|
作者
Zhao, Zi-Hua [1 ]
Cui, Bing-Yi [1 ]
Li, Zhi-Hong [1 ]
Jiang, Fan [1 ,5 ]
Yang, Qian-Qian [1 ,6 ]
Kucerova, Zuzana [2 ]
Stejskal, Vaclav [2 ]
Opit, George [3 ]
Cao, Yang [4 ]
Li, Fu-Jun [4 ]
机构
[1] China Agr Univ, Dept Entomol, Coll Plant Protect, Beijing 100193, Peoples R China
[2] Res Inst Crop Prod, Drnovska 507, CR-16106 Prague 6, Czech Republic
[3] Oklahoma State Univ, Dept Entomol & Plant Pathol, Noble Res Ctr 127, Stillwater, OK 74078 USA
[4] Acad State Adm Grain, Beijing 100037, Peoples R China
[5] Chinese Acad Inspect & Quarantine, Inst Plant Quarantine Res, Beijing 100176, Peoples R China
[6] China Jiliang Univ, Coll Life Sci, Hangzhou 310018, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
对外科技合作项目(国际科技项目); 北京市自然科学基金;
关键词
INTERNAL TRANSCRIBED SPACERS; PSOCOPTERA LIPOSCELIDIDAE; DNA BARCODES; REGION; DISPERSAL;
D O I
10.1038/srep21022
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Psocids are important stored product pests found worldwide that can be spread through grain trade. Most stored-product psocids, including eggs, nymphs, and adults, are very small (similar to 1 mm) and difficult to identify morphologically. Here, we collected 10 economically important stored-product Liposcelis spp. psocids (L. bostrychophila, L. entomophila, L. decolor, L. paeta, L. brunnea, L. corrodens, L. mendax, L. rufa, L. pearmani, and L. tricolor) from 35 geographical locations in 5 countries (China, Czech Republic, Denmark, Germany, and the United States). The ITS2 rDNA gene was extracted and sequenced. The interspecific genetic distance of the stored-product psocids was significantly higher than the intraspecific genetic distance according to the barcoding gap analysis. Ten pairs of species-specific primers based on the ITS2 rDNA were developed for psocid identification. The sensitivity estimation indicated that the species-specific primers could correctly amplify the target ITS2 gene and successfully identify psocids at 1.0 ng/mL. Additionally, these species-specific primers could quantify specificity and identify 10 stored-product psocids; this approach could also be used to accurately identify other stored-product psocids. This work provides a practical approach for the precise examination of 10 stored-product psocid species and also contributes to the development of an identification method using ITS2 rDNA.
引用
收藏
页数:8
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