Improvement and use of CRISPR/Cas9 to engineer a sperm-marking strain for the invasive fruit pest Drosophila suzukii

被引:28
作者
Ahmed, Hassan M. M. [1 ,2 ]
Hildebrand, Luisa [1 ]
Wimmer, Ernst A. [1 ]
机构
[1] Georg August Univ Gottingen, Dept Dev Biol, Johann Friedrich Blumenbach Inst Zool & Anthropol, Gottingen Ctr Mol Biosci, D-37077 Gottingen, Germany
[2] Univ Khartoum, Fac Agr, Dept Crop Protect, POB 32, Khartoum 13314, Khartoum North, Sudan
关键词
Cherry vinegar fly; Insect transgenesis; Molecular entomology; Pest management; Spotted Wing Drosophila; SPOTTED-WING DROSOPHILA; MATSUMURA DIPTERA DROSOPHILIDAE; SEXING SYSTEM; PROMOTER; GENE; MUTAGENESIS; EXPRESSION; ENDONUCLEASE; EFFICIENCY; GERMLINE;
D O I
10.1186/s12896-019-0588-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The invasive fruit pest Drosophila suzukii was reported for the first time in Europe and the USA in 2008 and has spread since then. The adoption of type II clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) as a tool for genome manipulation provides new ways to develop novel biotechnologically-based pest control approaches. Stage or tissue-specifically expressed genes are of particular importance in the field of insect biotechnology. The enhancer/promoter of the spermatogenesis-specific beta-2-tubulin (beta 2t) gene was used to drive the expression of fluorescent proteins or effector molecules in testes of agricultural pests and disease vectors for sexing, monitoring, and reproductive biology studies. Here, we demonstrate an improvement to CRISPR/Cas-based genome editing in D. suzukii and establish a sperm-marking system. Results: To improve genome editing, we isolated and tested the D. suzukii endogenous promoters of the small nuclear RNA gene U6 to drive the expression of a guide RNA and the Ds heat shock protein 70 promoter to express Cas9. For comparison, we used recombinant Cas9 protein and in vitro transcribed gRNA as a preformed ribonucleoprotein. We demonstrate the homology-dependent repair (HDR)-based genome editing efficiency by applying a previously established transgenic line that expresses DsRed ubiquitously as a target platform. In addition, we isolated the Ds_beta 2t gene and used its promoter to drive the expression of a red fluorescence protein in the sperm. A transgenic sperm-marking strain was then established by the improved HDR-based genome editing. Conclusion: The deployment of the endogenous promoters of the D. suzukii U6 and hsp70 genes to drive the expression of gRNA and Cas9, respectively, enabled the effective application of helper plasmid co-injections instead of preformed ribonucleoproteins used in previous reports for HDR-based genome editing. The sperm-marking system should help to monitor the success of pest control campaigns in the context of the Sterile Insect Technique and provides a tool for basic research in reproductive biology of this invasive pest. Furthermore, the promoter of the beta 2t gene can be used in developing novel transgenic pest control approaches and the CRISPR/Cas9 system as an additional tool for the modification of previously established transgenes.
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页数:14
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