The authors thank Vanessa Meldener-Harrell for critical reading of the manuscript.

The use of mice as a source of blood for sand fly feeding was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health (NIH). The protocol was approved by the Animal Care and Use Committee of the NIAID, NIH (protocol number LPD 68E). Invertebrates are not covered under NIH guidelines.
1. Needle preparation (Figure 1)
<ol>
	<li>Pull needles and bevel as described in Meuti and Harrell19. Briefly, pull needles on a dual-stage glass micropipette puller, using borosilicate glass capillaries.</li>
	<li>Sharpen the needles by wet beveling on the micropipette beveller, using an extra fine stone.</li>
</ol>
2. Embryo collection and micromanipulation (Figure 2)
<ol>
	<li>Five days before the day of injection, blood feed sand fly females as performed routinely for colony maintenance. For details on sand fly colonies rearing procedures and required material, please refer to Lawyer et al.1 Maintain the insects in incubators at 70% humidity and 26 &#176;C, during their entire development.
	<ol>
		<li>One day post blood-feeding, capture blood-fed females by groups of 100-150 in plaster pots with a side port. Maintain the females by feeding them with sugar solution (30% sucrose &#8211; enough volume to soak a small cotton ball) which is usual for colony maintenance.</li>
	</ol>
	</li>
	<li>At day 2-3 post blood-feeding, do NOT moisten the plaster pots. Keeping the females on a dry substrate will prevent premature egg laying, since females prefer to lay eggs on a moist environment.</li>
	<li>On day 5 post blood-feeding, perform the embryo collection, micromanipulation, and microinjection. Introduce a moist filter paper into the egg-laying chamber. Freshly laid embryos do not have a fully developed chorion and appear white. Use black filter paper during the procedure to facilitate visualizing the white embryos.</li>
	<li>Transfer a small group of females from the plaster pot to the egg-laying chamber through the side ports by using a mouth aspirator. The presence of a moist substrate (the filter paper) induces females to oviposit.</li>
	<li>After 30-60 min, carefully retrieve the filter paper with newly laid embryos from the chamber. Keep the filter paper and embryos in a Petri dish for up to 3 hours. During this time, regularly assess the moisture level of the filter paper to ensure that it remains moist. During this time, repeat steps 2.4 to 2.6 with new groups of females and collect as many embryos as possible.</li>
	<li>Prepare microscope slides for the injection: manually collect the eggs one by one with a very fine paintbrush and carefully transfer them onto another piece of moist black filter paper placed on a microscope slide topped with a glass coverslip.
	<ol>
		<li>Add water to the filter paper, enough to keep the embryos moist but not causing them to float away from the coverslip or being sucked under the coverslip. Line up the embryos against the coverslip. The coverslip acts as a backstop preventing the eggs from rolling away during injection.</li>
	</ol>
	</li>
</ol>
3. Embryo Injections (Figure 3)
<ol>
	<li>Start injections 2.5 to 3 hours post start of egg collection. Perform injections at room temperature and ambient lab humidity.</li>
	<li>Make sure the aligned embryos have enough water so they are kept moist. 
	NOTE: It is critical that the embryos are kept moist during injections. If they are not moist during the injection process, injections become difficult because the needle has trouble piercing the embryo. The correct amount of water is the point at which the embryos have a meniscus of water around them, but the coverslip is not floating on top of the water causing the embryos to push under the coverslip. It is critical to monitor the amount of water around the embryos during injections. Add water as necessary to keep the embryos moist.</li>
	<li>Add water carefully by wetting a brush with water and transferring the water to the back end of the filter paper. Adding water in this fashion allows water to be added in a slow and controlled fashion so that just enough is added to keep the embryos moist. Too much water can cause the embryos to float out of alignment, making it difficult to inject the embryos.</li>
	<li>Back load injection mix into the microinjection needle. Add approximately 0.5 to 1 &#181;L of injection mix into the needle using a hand-drawn borosilicate needle filler, gel loading pipet tips can also be used. The injection mix is composed of one or several guide RNA (80 ng/&#181;L each) designed to target a specific locus mixed with commercial recombinant Cas9 protein (300 ng/&#181;L).</li>
	<li>Starting with the injection pressure at 30 psi, press the injection trigger to expel air out of the tip of the needle. This will force the injection mix to the tip of the needle allowing the injection mix to flow. At this point, slowly increase the hold/constant pressure until injection material starts to flow, then back off the hold/constant pressure so that it is just below the point of the injection mix flowing from the needle. The gated setting should deliver just enough injection material so that a small amount of material can be seen to enter the embryo. 
	NOTE: Injection of sand fly embryos under halocarbon oil similar to other protocols used for Drosophila and mosquitoes was initially tested, however the survival percentage for these injections was very low. Survival was improved by switching to injections on damp filter paper as described above.</li>
	<li>Insert the needle into the side of the embryo. Use the coverslip behind the embryo as a backstop which will aid the needle to pierce the embryo. Deliver a small amount of injection mix into the embryo before gently removing the needle.</li>
	<li>Immediately after removal of the needle, press the injector to remove any backfilled material from the needle tip. This will help to prevent the needle from clogging.</li>
	<li>Proceed to the next embryo. Between each injection, ensure that the filter paper is moist and the needle is not clogged.</li>
	<li>Once all embryos have been injected, count the number of injected embryos to keep a running tally.</li>
	<li>Remove the coverslip by adding water to the filter paper so the coverslip floats. At this point, use a probe (wood applicator stick with insect pin glued to the tip) to hold the filter paper in place while a finger is used to pull the coverslip away from the injected embryos.</li>
	<li>Blot away excess water from the filter paper once the coverslip has been removed.</li>
</ol>
4. Post-injection rearing (G0) (Figure 4)
<ol>
	<li>Transfer the filter paper with the embryos on top of several layers of moist filter paper placed in a Petri dish to maintain humidity. Keep the embryos here during the time needed to inject other embryos. Embryos can be held for a maximum of 3 hours like this. After injection they will slowly turn brown.</li>
	<li>Once all embryos have been injected, manually transfer them onto previously moistened small size plaster pots. Do not put too many embryos in each pot and maintain distance between them, to avoid possible fungal contamination between individuals. Cover the pots with a screen and store them as would typically be done for sand fly colony eggs, maintained in incubators at 70% humidity and 26 &#176;C, during their entire development.</li>
	<li>On day 1 post-injection, remove all the damaged and dead embryos with a paintbrush. Add 100 &#181;L of 0.5% propionic acid, drop by drop, onto the plaster pots containing the injected embryos to limit fungal contamination. The release of cytoplasm from embryos damaged during the injection process is particularly favorable to fungal growth.</li>
	<li>Check the plaster pots every day and remove any bad or dead embryos. If fungus is present, remove all infected embryos and add a few drops of 0.5% propionic acid.</li>
	<li>Larvae hatch between day 8 and 12 post-injection. Twice a day, transfer the newly emerged larvae onto new plaster pots, in groups of 5-10 maximum. Add a small amount of food and check the food 2-3 times a week.
	<ol>
		<li>Carefully monitor the quantity of larval food, as too much greatly increases the risk of fungal contamination. Sand fly larvae survive better in groups however they can be cannibalistic if there is not enough food.</li>
	</ol>
	</li>
	<li>When the larvae pupate, separate them by sex to maintain the females as virgins. If there are a lot of survivors, discard the males and keep only the females. 
	NOTE: Both males and females can carry and transmit mutations. However, as females have to be kept virgins before they are to be crossed, it is easier to use only the G0 injected females to avoid having to separate wt insects by sex. The G0 males can be kept as a backup if the number of adult survivors is low and will in this case be mated with sorted wt virgin females.</li>
</ol>
5. Selection and screening of mutant alleles (Figure 5)
<ol>
	<li>Mass-cross the G0 females with wt males in a cage. Blood-feed them altogether, as would be done for normal colony maintenance.</li>
	<li>One day post blood-feeding, transfer each G0 female with 2-3 wt males into individual plaster tubes using a mouth aspirator. Feed the flies with sugar on a small cotton ball changed every day and use a syringe of water to ensure the plaster moisture is suitable for egg-laying.</li>
	<li>After the G0 females have laid eggs (corresponding to G1), collect their bodies in individual, annotated Eppendorf tubes for later genotyping. Maintain the embryos as usually done for wt colonies.</li>
	<li>Extract the DNA from the G0 females by the method of choice.</li>
	<li>Screen the DNA for the presence of mutations, for example by designing a PCR assay using primers surrounding the region of expected CRISPR cuts.</li>
	<li>Keep only the G1 embryos laid by G0 females showing evidence of transformation. When these G1 embryos develop into pupae, separate them by sex and keep only the females. Cross the G1 females from the same G0 female to wt males, blood-feed them, then transfer in small groups of 2-3 females and 4-5 males into small size containers. 
	NOTE: All G1 individuals have a chance to carry a unique mutation, so if the number of surviving individuals is not too high then it is better to cross G1 females individually with wt males. The case of several females carrying a different mutation present in a same tube is rare but can occur. If such case is observed after genotyping, the G2 progeny females should then be mated individually to wt males. This mating scheme avoids the possibility of multiple mutations in the progeny.</li>
	<li>After egg-laying, collect the G1 female bodies and screen them for mutations. Keep only the tubes where at least one female showed evidence of mutation.</li>
	<li>For later generations make single pair in-crosses. After egg-laying, screen parents for presence of mutation. Repeat at each generation until both parents are homozygous for the same mutation. Once identified, they will be the founders of a homozygous mutant stock.</li>
</ol>

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We present here a recently developed embryo microinjection method for targeted mutagenesis by CRISPR/Cas9 in Phlebotomus papatasi sand flies. Embryo microinjection for insect genetic modification was developed in Drosophila in the mid-1980s21&#160;and is now routinely used in a wide variety of insects. Other methods for delivery of genetic modification materials have been developed for use in insects, such as ReMOT20,21<s...

Vector-borne diseases are a major public health threat in constant evolution. Hundreds of vector species spread across very distinct phylogenic families (e.g., mosquitoes, ticks, fleas) are responsible for the transmission of a huge number of microbial pathogens, resulting in more than 700,000 human deaths a year, according to the World Health Organization. Among vector insects, phlebotomine sand flies (Diptera, Psychodidae) constitute a vast group, with 80 proven vector species exhibiting distinct phenotypic traits and vectorial capacities found in different geographical regions. They are vectors for the protozoan parasites of the genus Leishmania, causing around 1.3 million new cases of Leishmaniases and between 20,000 and 30,000 deaths a year. Leishmaniases clinical outcomes are diverse, with symptoms ranging from self-limiting cutaneous lesions to visceral dissemination which is fatal in the absence of treatment.
Sand flies are strictly terrestrial insects. Their life cycle, relatively long compared to other Diptera, lasts up to three months, depending on different parameters such as temperature, humidity, and nutrition. It consists of one embryonic stage (6 to 11 days), four larval stages (lasting a total of 23 to 25 days) and one pupal stage (9 to 10 days) followed by metamorphosis and then adulthood. Sand flies require a humid and warm environment for rearing. Both males and females feed on sugars, obtained in the wild from flower nectars. Only females are blood-feeders, as they require proteins obtained from the blood meal for egg production1.
An important focus of research is to identify the nature of the vector/parasite interactions that lead to the development of transmissible infections. As with other vector insects, parameters intrinsic to sand flies have been shown to impact their vector competence, which is defined as their ability to carry and transmit pathogens to their hosts. For example, the expression of galectins by the Phlebotomus papatasi sand fly midgut cells, acting as receptors recognizing parasite surface components, can directly influence their vector competence for Leishmania major2,3. The insect immune response pathway, Immune Deficiency (IMD), is also crucial for the Phlebotomus papatasi sand fly vector competence for Leishmania major4. A critical role for vector insect immune response pathways in controlling their transmission of infectious pathogens has been similarly reported in Aedes aegypti mosquitos5,6,7, in the tsetse fly Glossina morsitans8, and in Anopheles gambiae mosquitoes9,10.
Studies of sand fly/Leishmania interactions have been limited by the lack of gene expression modification methods adapted for use in these insects. Only gene downregulation by small interfering RNA (siRNA) had been performed11,12,13,14 until recently. The technique, limited by the mortality associated with the microinjection of adult females, leads only to a partial loss of function, which cannot be transmitted from generation to generation.
CRISPR/Cas9 technology has revolutionized functional genomic research in non-model organisms such as sand flies. Modified from the adaptive immune system in prokaryotes for defense against bacteriophages15,16, the CRISPR Cas9 system has been rapidly adapted as a genome editing tool for superior eukaryotic organisms, including insects. The principle of CRISPR/Cas9 targeted genome-editing is based on the complementarity of a single guide RNA (sgRNA) to a specific genomic locus. The Cas9 nuclease binds to the sgRNA and creates a double-strand DNA (dsDNA) break in the genomic DNA where the sgRNA associates with its complementary sequence. The Cas9-sgRNA complex is guided to the target sequence by 17 to 20 complementary bases in the sgRNA to the chosen locus, the dsDNA break can then be repaired by two independent pathways: nonhomologous end joining (NHEJ) or homology-directed repair (HDR)17. NHEJ repair involves a simple closure of the break but frequently leads to small insertion/deletion events. DNA repair through HDR uses a donor DNA molecule sharing homology with the target DNA as a template for repair. Insects possess both machineries.
CRISPR/Cas9 technology can generate mutations in a chosen locus, through the NHEJ repair pathway; or for more complex genome editing strategies, such as knock-ins or expression reporters, through the HDR pathway with an appropriate donor template. In sand flies, null mutant alleles of the immune response factor Relish were generated through NHEJ-mediated CRISPR in Phlebotomus papatasi4. Sand fly embryos were also injected in another study with a CRISPR/Cas9 mix targeting the gene encoding Yellow. Still, no adults carrying the mutation were produced18. We describe here a detailed method of sand fly targeted mutagenesis by NHEJ-mediated CRISPR/Cas9, with a particular focus on the embryo microinjection, a critical step of the protocol.

<table><tbody><tr><td>Black Filter Paper 4.25CM PK100</td><td>VWR</td><td>28342-012</td><td>Cut into rectangles that are approximately 46 X 22mm. These are placed between the slide and the coverslip and act as a moist base layer for the embryos during injection.</td></tr><tr><td>Coverslips</td><td>Fisher Scientific</td><td>12-543A</td><td></td></tr><tr><td>Dissecting Microscope</td><td>Any brand</td><td></td><td>For aligning embryos</td></tr><tr><td>Glass slides</td><td>Fisher Scientific</td><td>12-550-A3</td><td>Base layer of the microinjection set up Figure 2A</td></tr><tr><td>Insect cage</td><td>custom made or several commercial options</td><td></td><td>polycarbonate cage for adults holding and mating Lawyer, Phillip, Mireille Killick-Kendrick, Tobin Rowland, Edgar Rowton, and Petr Volf. &amp;ldquo;Laboratory Colonization and Mass Rearing of Phlebotomine Sand Flies (Diptera, Psychodidae).&amp;rdquo; Parasite 24. Accessed August 6, 2020. https://doi.org/10.1051/parasite/2017041.</td></tr><tr><td>Larval food</td><td>custom made</td><td></td><td>a mix of rabbit chow and rabbit feces Lawyer, Phillip, Mireille Killick-Kendrick, Tobin Rowland, Edgar Rowton, and Petr Volf. &amp;ldquo;Laboratory Colonization and Mass Rearing of Phlebotomine Sand Flies (Diptera, Psychodidae).&amp;rdquo; Parasite 24. https://doi.org/10.1051/parasite/2017041.</td></tr><tr><td>Microcaps 100 ml</td><td>Drummond</td><td>1-000-1000</td><td>Used to back fill microinjection needles</td></tr><tr><td>Mouth aspirator</td><td>John W. Hock Company</td><td>Model 612</td><td>mouth aspirator with HEPA filter</td></tr><tr><td>Olympus SZX12</td><td>Olympus Life Sciences</td><td></td><td>Microinjection microscope</td></tr><tr><td>Ovipots</td><td>Nalge company</td><td></td><td>ovipots are made from 125-ml or 500-ml straigh-sided plolypropylene jars modified by drilling 2.5cm holes in the bottom and filled with 1cm of plaster of Paris. Lawyer, Phillip, Mireille Killick-Kendrick, Tobin Rowland, Edgar Rowton, and Petr Volf. &amp;ldquo;Laboratory Colonization and Mass Rearing of Phlebotomine Sand Flies (Diptera, Psychodidae).&amp;rdquo; Parasite 24. Accessed August 6, 2020. https://doi.org/10.1051/parasite/2017041.</td></tr><tr><td>Paint Brush 6-0</td><td>Any Art Supply Company</td><td>n/a</td><td>Used for aligning embryos</td></tr><tr><td>Propionic acid</td><td>Sigma-Aldrich</td><td>402907</td><td>antifungal agent</td></tr><tr><td>Standard Glass Capillaries</td><td>World Precision Instruments</td><td>1B100-3</td><td>Used for making microinjection needles</td></tr><tr><td>Trio-MPC100 Controller and MP845 Manipulator</td><td>Sutter Instruments</td><td></td><td>Microinjection Controller and Micromanipulator</td></tr></tbody></table>

sand fly (phlebotomus papatasi) embryo microinjection for crispr/cas9 mutagenesis

Sand flies are the natural vectors for Leishmania species, protozoan parasites producing a broad spectrum of symptoms ranging from cutaneous lesions to visceral pathology. Deciphering the nature of the vector/parasite interactions is of primary importance for better understanding of Leishmania transmission to their hosts. Among the parameters controlling the sand fly vector competence (i.e. their ability to carry and transmit pathogens), parameters intrinsic to these insects were shown to play a key role. Insect immune response, for example, impacts sand fly vector competence to Leishmania. The study of such parameters has been limited by the lack of methods of gene expression modification adapted for use in these non-model organisms. Gene downregulation by small interfering RNA (siRNA) is possible, but in addition to being technically challenging, the silencing leads to only a partial loss of function, which cannot be transmitted from generation to generation. Targeted mutagenesis by CRISPR/Cas9 technology was recently adapted to the Phlebotomus papatasi sand fly. This technique leads to the generation of transmissible mutations in a specifically chosen locus, allowing to study the genes of interest. The CRISPR/Cas9 system relies on the induction of targeted double-strand DNA breaks, later repaired by either Non-Homologous End Joining (NHEJ) or by Homology Driven Repair (HDR). NHEJ consists of a simple closure of the break and frequently leads to small insertion/deletion events. In contrast, HDR uses the presence of a donor DNA molecule sharing homology with the target DNA as a template for repair. Here, we present a sand fly embryo microinjection method for targeted mutagenesis by CRISPR/Cas9 using NHEJ, which is the only genome modification technique adapted to sand fly vectors to date.

The CRISPR/Cas9 microinjection protocol described here to generate sand fly mutants was established in a previous publication4. This approach produced highly efficient mutagenesis, as 11 out of 540 individuals survived the procedure, of which 9 were mutant. When designing guides for CRISPR/Cas9 mutation, a critical first step is to sequence the region around the area to be targeted. The template for sequencing should be from the strain that is going to be used as a source of embryos for injection....

Watch this Scientific Journal Video about Sand Fly Phlebotomus papatasi Embryo Microinjection for CRISPR/Cas9 Mutagenesis at JoVE.com

Sand Fly Phlebotomus papatasi Embryo Microinjection for CRISPR/Cas9 Mutagenesis

This protocol details the steps of CRISPR/Cas9 targeted mutagenesis in sand flies: embryo collection, injection, insect rearing, and identification as well as selection of mutations of interest.

Sand Fly (Phlebotomus papatasi) Embryo Microinjection for CRISPR/Cas9 Mutagenesis

Sand flies are the natural vectors for Leishmania species, protozoan parasites producing a broad spectrum of symptoms ranging from cutaneous lesions to ...

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Research

JoVE Journal

Genetics

7.1K Views.  National Institutes of Health. This protocol details the steps of CRISPR/Cas9 targeted mutagenesis in sand flies: embryo collection, injection, insect rearing, and identification as well as selection of mutations of interest.

Video: Sand Fly Phlebotomus papatasi Embryo Microinjection for CRISPR/Cas9 Mutagenesis

Delivery of Nucleic Acids through Embryo Microinjection in the Worldwide Agricultural Pest Insect, Ceratitis capitata

The Mediterranean fruit fly (medfly) Ceratitis capitata (Wiedemann) (Diptera: Tephritidae) is a pest species with extremely high agricultural relevance. This is due to its reproductive behavior: females damage the external surface of fruits and vegetables when they lay eggs and the hatched larvae feed on their pulp. Wild C. capitata populations are traditionally controlled through insecticide spraying and/or eco-friendly approaches, the most successful being the Sterile Insect Technique (SIT). The SIT relies on mass-rearing, radiation-based sterilization and field release of males that retain their capacity to mate but are not able to generate fertile progeny. The advent and the subsequent rapid development of biotechnological tools, together with the availability of the medfly genome sequence, has greatly boosted our understanding of the biology of this species. This favored the proliferation of new strategies for genome manipulation, which can be applied to population control.
In this context, embryo microinjection plays a dual role in expanding the toolbox for medfly control. The ability to interfere with the function of genes that regulate key biological processes, indeed, expands our understanding of the molecular machinery underlying medfly invasiveness. Furthermore, the ability to achieve germ-line transformation facilitates the production of multiple transgenic strains that can be tested for future field applications in novel SIT settings. Indeed, genetic manipulation can be used to confer desirable traits that can, for example, be used to monitor sterile male performance in the field, or that can result in early life-stage lethality. Here we describe a method to microinject nucleic acids into medfly embryos to achieve these two main goals.

Delivery of Nucleic Acids through Embryo Microinjection in the Worldwide Agricultural Pest Insect, Ceratitis capitata

The Mediterranean fruit fly (medfly) Ceratitis capitata (Diptera: Tephritidae) is a worldwide pest of agriculture. A deeper understanding of its biology is key to control medfly populations and thus reduce economic impact. Embryo microinjection is a fundamental tool allowing both germ-line transformation and reverse genetics studies in this species.

The Mediterranean fruit fly (medfly) Ceratitis capitata (Wiedemann) (Diptera: Tephritidae) is a pest species with extremely high agricultural relevance. ...

Embryo Microinjection and Transplantation Technique for Nasonia vitripennis Genome Manipulation

The jewel wasp Nasonia vitripennis has emerged as an effective model system for the study of processes including sex determination, haplo-diploid sex determination, venom synthesis, and host-symbiont interactions, among others. A major limitation of working with this organism is the lack of effective protocols to perform directed genome modifications. An important part of genome modification is delivery of editing reagents, including CRISPR/Cas9 molecules, into embryos through microinjection. While microinjection is well established in many model organisms, this technique is particularly challenging to perform in N. vitripennis primarily due to its small embryo size, and the fact that embryonic development occurs entirely within a parasitized blowfly pupa. The following procedure overcomes these significant challenges while demonstrating a streamlined, visual procedure for effectively removing wasp embryos from parasitized host pupae, microinjecting them, and carefully transplanting them back into the host for continuation and completion of development. This protocol will strongly enhance the capability of research groups to perform advanced genome modifications in this organism.

Embryo Microinjection and Transplantation Technique for Nasonia vitripennis Genome Manipulation

Microinjection of Nasonia vitripennis embryos is an essential method for generating heritable genome modifications. Described here is a detailed procedure for microinjection and transplantation of Nasonia vitripennis embryos, which will greatly facilitate future genome manipulation in this organism.

The jewel wasp Nasonia vitripennis has emerged as an effective model system for the study of processes including sex determination, haplo-diploid sex ...

Embryo Microinjection Techniques for Efficient Site-Specific Mutagenesis in Culex quinquefasciatus

Culex quinquefasciatus is a vector of a diverse range of vector-borne diseases such as avian malaria, West Nile virus (WNV), Japanese encephalitis, Eastern equine encephalitis, lymphatic filariasis, and Saint Louis encephalitis. Notably, avian malaria has played a major role in the extinction of numerous endemic island bird species, while WNV has become an important vector-borne disease in the United States. To gain further insight into C. quinquefasciatus biology and expand their genetic control toolbox, we need to develop more efficient and affordable methods for genome engineering in this species. However, some biological traits unique to Culex mosquitoes, particularly their egg rafts, have made it difficult to perform microinjection procedures required for genome engineering. To address these challenges, we have developed an optimized embryo microinjection protocol that focuses on mitigating the technical obstacles associated with the unique characteristics of Culex mosquitoes. These procedures demonstrate optimized methods for egg collection, egg raft separation and other handling procedures essential for successful microinjection in C. quinquefasciatus. When coupled with the CRISPR/Cas9 genome editing technology, these procedures allow us to achieve site-specific, efficient and heritable germline mutations, which are required to perform advanced genome engineering and develop genetic control technologies in this important, but currently understudied, disease vector.

Embryo Microinjection Techniques for Efficient Site-Specific Mutagenesis in Culex quinquefasciatus

This protocol describes microinjection procedures for Culex quinquefasciatus embryos that are optimized to work with CRISPR/Cas9 gene editing tools. This technique can efficiently generate site-specific, heritable, germline mutations that can be used for building genetic technologies in this understudied disease vector.

Culex quinquefasciatus is a vector of a diverse range of vector-borne diseases such as avian malaria, West Nile virus (WNV), Japanese encephalitis, ...

Embryo Injections for CRISPR-Mediated Mutagenesis in the Ant Harpegnathos saltator

The unique traits of eusocial insects, such as social behavior and reproductive division of labor, are controlled by their genetic system. To address how genes regulate social traits, we have developed mutant ants via delivery of CRISPR complex into young embryos during their syncytial stage. Here, we provide a protocol of CRISPR-mediated mutagenesis in Harpegnathos saltator, a ponerine ant species that displays striking phenotypic plasticity. H. saltator ants are readily reared in a laboratory setting. Embryos are collected for microinjection with Cas9 proteins and in vitro synthesized small guide RNAs (sgRNAs) using home-made quartz needles. Post-injection embryos are reared outside the colony. Following emergence of the first larva, all embryos and larvae are transported to a nest box with a few nursing workers for further development. This protocol is suitable for inducing mutagenesis for analysis of caste-specific physiology and social behavior in ants, but may also be applied to a broader spectrum of hymenopterans and other insects.

Embryo Injections for CRISPR-Mediated Mutagenesis in the Ant Harpegnathos saltator

Many characteristics of insect eusociality rely on within-colony communication and division of labor. Genetic manipulation of key regulatory genes in ant embryos via microinjection and CRISPR-mediated mutagenesis provides insights into the nature of altruistic behavior in eusocial insects.

The unique traits of eusocial insects, such as social behavior and reproductive division of labor, are controlled by their genetic system. To address how ...

phiC31 Integrase-Mediated Embryo Transgenesis in Drosophila

Embryo Microinjection for Transgenesis in Drosophila

Transgenesis in Drosophila is an essential approach to studying gene function at the organism level. Embryo microinjection is a crucial step for the construction of transgenic flies. Microinjection requires some types of equipment, including a microinjector, a micromanipulator, an inverted microscope, and a stereo microscope.&#160;Plasmids isolated with a plasmid miniprep kit are qualified for microinjection. Embryos at the pre-blastoderm or syncytial blastoderm stage, where nuclei share a common cytoplasm, are subjected to microinjection. A cell strainer eases the process of dechorionating embryos. The optimal time for dechorionation and desiccation of embryos needs to be determined experimentally. To increase the efficiency of embryo microinjection, needles prepared by a puller need to be beveled by a needle grinder. In the process of grinding needles, we utilize a foot air pump with a pressure gauge to avoid the capillary effect of the needle tip. We routinely inject 120-140 embryos for each plasmid and obtain at least one transgenic line for around 85% of plasmids. This article takes the phiC31 integrase-mediated transgenesis in Drosophila as an example and&#160;presents a detailed protocol for embryo microinjection for transgenesis in Drosophila.

Author Spotlight: Optimizing Embryo Microinjection for Transgenesis in Drosophila

This article takes the phiC31 integrase-mediated transgenesis in Drosophila as an example and presents an optimized protocol for embryo microinjection,&#160;a crucial step for creating transgenic flies.

Transgenesis in Drosophila is an essential approach to studying gene function at the organism level. Embryo microinjection is a crucial step for the ...

Genome Editing in the Yellow Fever Mosquito Aedes aegypti using CRISPR-Cas9

The emergence of the clustered, regularly interspersed, short palindromic repeats (CRISPR)-Cas9 technology has revolutionized the genetic engineering field and opened the doors for precise genome editing in multiple species, including non-model organisms. In the mosquito Aedes aegypti, loss-of-function mutations and DNA insertions have been accomplished with this technology. Here, we describe a detailed protocol for genome editing through embryonic microinjection in the mosquito A. aegypti using the CRISPR-Cas9 technology, focusing on both the generation of gene knockout and knockin lines. In this protocol, quartz needles are filled with a mixture of guide RNA, recombinant Cas9, and a plasmid containing a DNA cassette encoding a gene for a fluorescent marker, if gene knockin is desired. Embryos at the preblastoderm stage are lined up onto a strip of double-sided sticky tape placed onto a coverslip, which is subsequently mounted onto a glass slide. With the help of a microinjector, the needles are inserted gently into the posterior end of the embryos and a small volume of the CRISPR mixture is dispensed. When the embryos are hatched, the larvae are checked under the fluorescent scope, and the pupae are sex-sorted and separated in different cages. Once the adults emerge, these are reciprocally crossed with wild-type individuals, blood-fed, and placed for egg laying. Once these eggs are hatched, the fluorescent larvae collected represent individuals with stable insertion of the DNA cassette into their genome. These larvae are then grown to the adult stage, outcrossed to wild-type individuals, and then further assessed through molecular techniques to confirm that the exact sequence of the DNA cassette is present at the desired site of the mosquito genome. Homozygous lines can also be obtained by following the provided pipeline of crossing schema and molecular screening of the mutations.

Here, we describe a detailed protocol for genome editing through embryonic microinjection in the mosquito A. aegypti using the CRISPR-Cas9 technology.

The emergence of the clustered, regularly interspersed, short palindromic repeats (CRISPR)-Cas9 technology has revolutionized the genetic engineering ...

Embryo Microinjection and Knockout Mutant Identification of CRISPR/Cas9 Genome-Edited Helicoverpa Armigera (H&#252;bner)

The cotton bollworm, Helicoverpa armigera, is one of the most destructive pests in the world. A combination of molecular genetics, physiology, functional genomics, and behavioral studies has made H. armigera a model species in Lepidoptera Noctuidae. To study the in vivo functions of and interactions between different genes, clustered regularly interspaced short palindromic repeats (CRISPR)/ associated protein 9 (Cas9) genome editing technology is a convenient and effective method used for performing functional genomic studies. In this study, we provide a step-by-step systematic method to complete gene knockout in H. armigera using the CRISPR/Cas9 system. The design and synthesis of guide RNA (gRNA) are described in detail. Then, the subsequent steps consisting of gene-specific primer design for guide RNA (gRNA) creation, embryo collection, microinjection, insect rearing, and mutant detection are summarized. Finally, troubleshooting advice and notes are provided to improve the efficiency of gene editing. Our method will serve as a reference for the application of CRISPR/Cas9 genome editing in H. armigera as well as other Lepidopteran moths.

Embryo Microinjection and Knockout Mutant Identification of CRISPR/Cas9 Genome-Edited Helicoverpa Armigera H&#252;bner

Presented here is a protocol of Helicoverpa armigera (H&#252;bner) embryo microinjection and knockout mutant identification created by CRISPR/Cas9 genome editing. Mutant insects enable further research of gene function and interaction among different genes in vivo.

The cotton bollworm, Helicoverpa armigera, is one of the most destructive pests in the world. A combination of molecular genetics, physiology, functional ...

Behavior

Egg Microinjection and Efficient Mating for Genome Editing in the Firebrat Thermobia domestica

The firebrat Thermobia domestica is an ametabolous, wingless species that is suitable for studying the developmental mechanisms of insects that led to their successful evolutionary radiation on the earth. The application of genetic tools such as genome editing is the key to understanding genetic changes that are responsible for evolutionary transitions in an Evo-Devo approach. In this article, we describe our current protocol for generating and maintaining mutant strains of T. domestica. We report a dry injection method, as an alternative to the reported wet injection method, that allows us to obtain stably high survival rates in injected embryos. We also report an optimized environment setting to mate adults and obtain subsequent generations with high efficiency. Our method underlines the importance of taking each species&#8217; unique biology into account for the successful application of genome editing methods to non-traditional model organisms. We predict that these genome editing protocols will help in implementing T. domestica as a laboratory model and to further accelerate the development and application of useful genetic tools in this species.

Egg Microinjection and Efficient Mating for Genome Editing in the Firebrat Thermobia domestica

We provide a detailed protocol for rearing, microinjection of eggs and for efficient mating of the firebrat Thermobia domestica to generate and maintain mutant strains after genome editing.

The firebrat Thermobia domestica is an ametabolous, wingless species that is suitable for studying the developmental mechanisms of insects that led to ...

Developmental Biology

Microinjection of Corn Planthopper, Peregrinus maidis, Embryos for CRISPR/Cas9 Genome Editing

The corn planthopper, Peregrinus maidis, is&#160;a pest of maize and a vector of several maize viruses. Previously published methods describe the triggering of RNA interference (RNAi) in P. maidis through microinjection of double-stranded RNAs (dsRNAs) into nymphs and adults. Despite the power of RNAi, phenotypes generated via this technique are transient and lack long-term Mendelian inheritance. Therefore, the P. maidis toolbox needs to be expanded to include functional genomic tools that would enable the production of stable mutant strains, opening the door for researchers to bring new control methods to bear on this economically important pest. However, unlike the dsRNAs used for RNAi, the components used in CRISPR/Cas9-based genome editing and germline transformation do not easily cross cell membranes. As a result, plasmid DNAs, RNAs, and/or proteins must be microinjected into embryos before the embryo cellularizes, making the timing of injection a critical factor for success. To that end, an agarose-based egg-lay method was developed to allow embryos to be harvested from P. maidis females at relatively short intervals. Herein are provided detailed protocols for collecting and microinjecting precellular P. maidis embryos with CRISPR components (Cas9 nuclease that has been complexed with guide RNAs), and results of Cas9-based gene knockout of a P. maidis eye-color gene, white, are presented. Although these protocols describe CRISPR/Cas9-genome editing in P. maidis, they can also be used for producing transgenic P. maidis via germline transformation by simply changing the composition of the injection solution.

Microinjection of Corn Planthopper, Peregrinus maidis, Embryos for CRISPR/Cas9 Genome Editing

Herein are protocols for collecting and microinjecting precellular corn planthopper embryos for the purpose of modifying their genome via CRISPR/Cas9-based genome editing or for the addition of marked transposable elements through germline transformation.

The corn planthopper, Peregrinus maidis, is&#160;a pest of maize and a vector of several maize viruses. Previously published methods describe the ...

Bioengineering

Preparing and Injecting Embryos of Culex Mosquitoes to Generate Null Mutations using CRISPR/Cas9

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.&#160;

Preparing and Injecting Embryos of Culex Mosquitoes to Generate Null Mutations using CRISPR/Cas9

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 ...

Sand Fly (Phlebotomus papatasi) Embryo Microinjection for CRISPR/Cas9 Mutagenesis

Summary

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Chapters in this video

Delivery of Nucleic Acids through Embryo Microinjection in the Worldwide Agricultural Pest Insect, Ceratitis capitata

Embryo Microinjection and Transplantation Technique for Nasonia vitripennis Genome Manipulation

Embryo Microinjection Techniques for Efficient Site-Specific Mutagenesis in Culex quinquefasciatus

Embryo Injections for CRISPR-Mediated Mutagenesis in the Ant Harpegnathos saltator

Embryo Microinjection for Transgenesis in Drosophila

Genome Editing in the Yellow Fever Mosquito Aedes aegypti using CRISPR-Cas9

Embryo Microinjection and Knockout Mutant Identification of CRISPR/Cas9 Genome-Edited Helicoverpa Armigera (Hübner)

Egg Microinjection and Efficient Mating for Genome Editing in the Firebrat Thermobia domestica

Microinjection of Corn Planthopper, Peregrinus maidis, Embryos for CRISPR/Cas9 Genome Editing

Preparing and Injecting Embryos of Culex Mosquitoes to Generate Null Mutations using CRISPR/Cas9