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W tym Artykule

  • Podsumowanie
  • Streszczenie
  • Wprowadzenie
  • Protokół
  • Wyniki
  • Dyskusje
  • Ujawnienia
  • Podziękowania
  • Materiały
  • Odniesienia
  • Przedruki i uprawnienia

Podsumowanie

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.

Streszczenie

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. 

Wprowadzenie

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 ....

Protokół

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

  1. Design 2-5 gRNAs for each target gene as some gRNAs work better than others. gRNAs that target a gene of interest can be either manu....

Wyniki

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.......

Dyskusje

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.......

Ujawnienia

RH works for the Insect Transformation Facility, which provides services in insect genetic modification.

Podziękowania

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 ....

Materiały

NameCompanyCatalog NumberComments
Artificial Membrane FeederHemotekSP5W1-3Company location: Blackburn, UK
ATPInvitrogen18330019Company location: Carlsbad, CA, USA
Borosilicate glass mirocapillary tubes, 1 mm outer diameterWorld Precision Instruments1B100-6Company Location: Sarasota, FL, USA
BV10 Needle BevelerSutter InstrumentsBV-10-BCompany Location: Nobato, CA, USA
Whatman Circular filter paper (12.5 cm)Sigma AldrichWHA1001125Company Location: St. Louis, MO, USA
Conical tube (50 mL)Thermo Fisher Scientific339652Company Location: Waltham, MA, USA
Fisherbrand course filter paper with fast flow rateThermo Fisher Scientific09-800Company Location: Waltham, MA, USA
Cover glass (24 x 40 mm)Thermo Fisher Scientific50-311-20Company Location: Waltham, MA, USA
Dental damHenry Schein Inc1010171Company Location: Melville, NY USA
Scotch double-sided tapeThermo Fisher ScientificNC0879005Company Location: Waltham, MA, USA
FemtoJet 4i microinjectorEppendorf5252000021Company Location: Hamburg, Germany
Glass vial (2 dram)Thermo Fisher Scientific033401CCompany Location: Waltham, MA, USA
Halocarbon oilSigma AldrichH8898-50MLCompany Location: St. Louis, MO, USA
P-2000 Laser Needle PullerSutter InstrumentsP-2000/GCompany Location: Nobato, CA, USA
ParafilmThermo Fisher Scientific50-998-944Company Location: Waltham, MA, USA
PC-100 Weighted Needle PullerNarishigePC-100This is compatabile with the earlier PC-10 model, which has been discontinued. Company Location: Amityville, NY, USA
Phire Direct PCR KitThermo Fisher ScientificF140WHCompany Location: Waltham, MA, USA
Kodak Photo-Flo (1%)Thermo Fisher Scientific50-268-05Company Location: Waltham, MA, USA
Quartz glass mirocapillary tubes, 1 mm outer diameterCapillary Tube Supplies LimitedQGCT 1.0Company Location: Cornwall, UK
Guide-it™ sgRNA Screening KitTakara, Bio USA632639This kit allows you to determine if gRNAs cut DNA sequences in vitro. Company Location: Mountain View, CA, USA
SigmacoteSigma AldrichSL2-100MLCompany Location: St. Louis, MO, USA
Small petri dishes (35X10 mm)Thermo Fisher Scientific50-190-0273Company Location: Waltham, MA, USA
Sodium citrate chicken bloodLampire biologicals7201406Company Location: Everett, PA, USA
Fisherbrand Square petri dish (10 cm x 10 cm)Thermo Fisher ScientificFB0875711ACompany Location: Waltham, MA, USA
TegadermHenry Schein Inc.7771180Company Location: Melville, NY USA
Tropical fish foodTetraminN/A
Whatman filter paperThermo Fisher Scientific09-927-826Company Location: Waltham, MA, USA
Whatman filter paper, 4.25 cmSigma Aldrich1001-042Company Location: St. Louis, MO, USA

Odniesienia

  1. Hamer, G. L., et al. Culex pipiens (Diptera: Culicidae): a bridge vector of West Nile virus to humans. Journal of Medical Entomology. 45 (1), 125-128 (2008).
  2. Bailey, C. L., et al. Isolat....

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CRISPR Cas9Mosquito EmbryoMicro injectionCulex MosquitoesWest Nile FeverSt Louis EncephalitisFilarial NematodesCanine HeartwormElephantiasisGenome EditingMosquito SurvivalNull Mutations

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