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CRISPR/Cas9 is increasingly used to characterize gene function in non-model organisms. This protocol describes how to generate knock-out lines of Culex pipiens, from preparing injection mixes, to obtaining and injecting mosquito embryos, as well as how to rear, cross, and screen injected mosquitoes and their progeny for desired mutations.
Culex mosquitoes are the major vectors of several diseases that negatively impact human and animal health including West Nile virus and diseases caused by filarial nematodes such as canine heartworm and elephantasis. Recently, CRISPR/Cas9 genome editing has been used to induce site-directed mutations by injecting a Cas9 protein that has been complexed with a guide RNA (gRNA) into freshly laid embryos of several insect species, including mosquitoes that belong to the genera Anopheles and Aedes. Manipulating and injecting Culex mosquitoes is slightly more difficult as these mosquitoes lay their eggs upright in rafts rather than individually like other species of mosquitoes. Here we describe how to design gRNAs, complex them with Cas9 protein, induce female mosquitoes of Culex pipiens to lay eggs, and how to prepare and inject newly laid embryos for microinjection with Cas9/gRNA. We also describe how to rear and screen injected mosquitoes for the desired mutation. The representative results demonstrate that this technique can be used to induce site-directed mutations in the genome of Culex mosquitoes and, with slight modifications, can be used to generate null-mutants in other mosquito species as well.
Culex mosquitoes are distributed throughout the temperate and tropical regions of the world and transmit several deadly viruses including West Nile virus1, St. Louis encephalitis2 as well as filarial nematodes that cause canine heartworm3 and elephantiasis4. Members of the Culex pipiens complex, which includes Cx. quinquefasciatus, Cx. pipiens pipiens and Cx. pipiens molestus, show striking variations in many aspects of their biology. For example, while Cx. quinquefasciatus and Cx. pipiens molestus are ....
In most research institutions, an approved Biosafety Protocol must be in place before transgenic insects are generated or maintained to ensure that genetically modified organisms will not escape or be removed from the laboratory facility. Additional government regulations might also apply. Before beginning a project of this nature, check all institutional policies and procedures to determine what documents and approvals are required.
1. Designing gRNAs and preparing injection mixes
Using the described protocol, we were able to successfully inject embryos of Cx. pipiens, and observed a high rate of survival among the injected embryos (~55%, Figure 1). Earlier trials had a lower percentage of survival, likely because the anterior of the egg follicle was attached to the medical dressing strip, preventing mosquito larvae from escaping from the chorion and successfully swimming into the water. Ensuring that the anterior end extends beyond the strip of medical dress.......
This protocol presents methods to introduce specific mutations into the genome of Culex mosquitoes and can be used to edit the genome of other mosquitoes as well. The protocol is significant in that it provides specific details of not only how to prepare the injection materials, but also a detailed video overview of how to induce mosquitoes to lay eggs, as well as how to prepare and inject those eggs. We also summarize of how to take advantage of the biology of female Cx. pipiens to lay eggs in individu.......
RH works for the Insect Transformation Facility, which provides services in insect genetic modification.
We thank Dr. David O’Brochta and all members of the Insect Genetic Technologies Coordination Research Network for the help and training that they provide to us and others on the implementation of genetic technologies. We especially thank Channa Aluvihare for optimizing the micromanipulation protocol to allow Culex embryos to be injected and hatch. We also thank Devante Simmons and Joseph Urso, undergraduate students working in the Meuti lab, for their assistance caring for and screening transgenic mosquitoes, and Zora Elmkami from the ITF for assistance rearing and prepping mosquitoes for injection. This work was supported by an Interdisciplinary Seeds ....
Name | Company | Catalog Number | Comments |
Artificial Membrane Feeder | Hemotek | SP5W1-3 | Company location: Blackburn, UK |
ATP | Invitrogen | 18330019 | Company location: Carlsbad, CA, USA |
Borosilicate glass mirocapillary tubes, 1 mm outer diameter | World Precision Instruments | 1B100-6 | Company Location: Sarasota, FL, USA |
BV10 Needle Beveler | Sutter Instruments | BV-10-B | Company Location: Nobato, CA, USA |
Whatman Circular filter paper (12.5 cm) | Sigma Aldrich | WHA1001125 | Company Location: St. Louis, MO, USA |
Conical tube (50 mL) | Thermo Fisher Scientific | 339652 | Company Location: Waltham, MA, USA |
Fisherbrand course filter paper with fast flow rate | Thermo Fisher Scientific | 09-800 | Company Location: Waltham, MA, USA |
Cover glass (24 x 40 mm) | Thermo Fisher Scientific | 50-311-20 | Company Location: Waltham, MA, USA |
Dental dam | Henry Schein Inc | 1010171 | Company Location: Melville, NY USA |
Scotch double-sided tape | Thermo Fisher Scientific | NC0879005 | Company Location: Waltham, MA, USA |
FemtoJet 4i microinjector | Eppendorf | 5252000021 | Company Location: Hamburg, Germany |
Glass vial (2 dram) | Thermo Fisher Scientific | 033401C | Company Location: Waltham, MA, USA |
Halocarbon oil | Sigma Aldrich | H8898-50ML | Company Location: St. Louis, MO, USA |
P-2000 Laser Needle Puller | Sutter Instruments | P-2000/G | Company Location: Nobato, CA, USA |
Parafilm | Thermo Fisher Scientific | 50-998-944 | Company Location: Waltham, MA, USA |
PC-100 Weighted Needle Puller | Narishige | PC-100 | This is compatabile with the earlier PC-10 model, which has been discontinued. Company Location: Amityville, NY, USA |
Phire Direct PCR Kit | Thermo Fisher Scientific | F140WH | Company Location: Waltham, MA, USA |
Kodak Photo-Flo (1%) | Thermo Fisher Scientific | 50-268-05 | Company Location: Waltham, MA, USA |
Quartz glass mirocapillary tubes, 1 mm outer diameter | Capillary Tube Supplies Limited | QGCT 1.0 | Company Location: Cornwall, UK |
Guide-it™ sgRNA Screening Kit | Takara, Bio USA | 632639 | This kit allows you to determine if gRNAs cut DNA sequences in vitro. Company Location: Mountain View, CA, USA |
Sigmacote | Sigma Aldrich | SL2-100ML | Company Location: St. Louis, MO, USA |
Small petri dishes (35X10 mm) | Thermo Fisher Scientific | 50-190-0273 | Company Location: Waltham, MA, USA |
Sodium citrate chicken blood | Lampire biologicals | 7201406 | Company Location: Everett, PA, USA |
Fisherbrand Square petri dish (10 cm x 10 cm) | Thermo Fisher Scientific | FB0875711A | Company Location: Waltham, MA, USA |
Tegaderm | Henry Schein Inc. | 7771180 | Company Location: Melville, NY USA |
Tropical fish food | Tetramin | N/A | |
Whatman filter paper | Thermo Fisher Scientific | 09-927-826 | Company Location: Waltham, MA, USA |
Whatman filter paper, 4.25 cm | Sigma Aldrich | 1001-042 | Company Location: St. Louis, MO, USA |
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