Drosophila melanogaster Larva Injection Protocol

Summary

Drosophila melanogaster adult flies have been extensively utilized as model organisms to investigate the molecular mechanisms underlying host antimicrobial innate immune responses and microbial infection strategies. To promote the D. melanogaster larva stage as an additional or alternative model system, a larval injection technique is described.

Abstract

The use of unconventional models to study innate immunity and pathogen virulence provides a valuable alternative to mammalian models, which can be costly and raise ethical issues. Unconventional models are notoriously cheap, easy to handle and culture, and do not take much space. They are genetically amenable and possess complete genome sequences, and their use presents no ethical considerations. The fruit fly Drosophila melanogaster, for instance, has provided great insights into a variety of behavior, development, metabolism, and immunity research. More specifically, D. melanogaster adult flies and larvae possess several innate defense reactions that are shared with vertebrate animals. The mechanisms regulating immune responses have been mostly revealed through genetic and molecular studies in the D. melanogaster model. Here a novel larval injection technique is provided, which will further promote investigations of innate immune processes in D. melanogaster larvae and explore the pathogenesis of a wide range of microbial infections.

Introduction

Drosophila melanogaster has been immensely utilized in biological and biomedical research for several decades, as the sophisticated array of genetic and molecular tools have steadily evolved for analysis of a wide range of studies^1,2,3,4. The evolutionarily conserved aspects of development, homeostasis and innate immunity in D. melanogaster have made it a valuable model organism for studying various human and insect diseases^5,6. Notably, the fundamental role of the D. melanogaster model for studying immunity has been largely exemplified in adult flies studies. However, D. melanogaster larvae studies have also contributed to the current knowledge and mainly explored cellular immune responses, specifically for wasp and nematode infections that occur through the insect cuticle^7,8,9,10. Drosophila melanogaster larvae possess three different types of blood cells, collectively called hemocytes: plasmatocytes, crystal cells, and lamellocytes^11,12,13. These cells can mount an array of immune responses when D. melanogaster larvae are infected with pathogens such as bacteria, fungi, viruses, and parasites^14,15,16. Cellular immune responses include direct engulfment (phagocytosis) of small molecules or bacteria, melanization, encapsulation of larger pathogens such as parasitoid eggs, and production of reactive oxygen species (ROS) and Nitric oxide synthases (NOS)^17,18,19.

In contrast, fewer studies have been published on the use of the D. melanogaster larval model to analyze humoral immune responses. This is mainly due to the application of feeding assays for oral infection of D. melanogaster larvae and several challenges associated with microinjecting larvae including the precise handling of larvae and proper use of the microneedle, especially during penetration^20,21. Thus, the limited knowledge of larval infection and technical difficulties (i.e., high mortality) have frequently made the D. melanogaster larval model difficult to use. A larval model will have the potential to identify novel molecular mechanisms that will provide further insights into host-pathogen interactions and the induction of specific host innate immune responses against pathogenic infections.

Here a simple and efficient protocol that can be used to inject D. melanogaster larvae with various pathogens, such as bacteria, is described in detail. In particular, D. melanogaster larvae are used for injections with the human pathogen Photorhabdus asymbiotica and the non-pathogenic bacteria Escherichia coli. This method can be used for the manipulation and analysis of D. melanogaster's immune responses to various microbial infections.

Protocol

1. Fly rearing

NOTE: The D. melanogaster life cycle is divided into four stages: embryo, larva, pupa, and adult. The generation time with optimal rearing conditions in the laboratory (~25 °C, 60% humidity, and sufficient food) is approximately 10 days from fertilized egg to eclosed adult.Females lay ~100 embryos per day, and embryogenesis lasts about 24 h²². The larvae undergo three developmental stages (instars; L1-L3) in ~4 days (L1 and L2: 24 h, and L3: 48 h). The first instar larvae begin to feed immediately on the surface of the medium. Second instar larvae burrow into the medium, whereas third instar larvae leave the medium and wander up the vial walls, looking for a place to pupariate for 24-48 h. The D. melanogaster line used for this protocol is Oregon R (FBsn0000276).

1. Add dry food containing a cornmeal-soy-based diet to a narrow polystyrene vial (25 mm x 95 mm) to aboue 1/5 to 2/5 volume. Then add 9 mL of water and allow the vial to sit for 1 min until the diet is completely hydrated.
2. Add about 10 granules of dry baker's yeast to the vial and place a mixture of at least 20 newly emerged male and female adult flies.
3. Incubate the vial at 25 °C on a 12:12-h light: dark photoperiodic cycle.
4. To ensure life cycle progression, check the fly vials daily and record the initial development stages.

2. Larvae selection for infection

1. Select larvae with a fine paintbrush (camel's hair is best) once they reach the wandering third instar stage on the day the infection will be carried out (Figure 1).
2. Wash the selected larvae with Ringer's solution (100 mM NaCl, 1.8 mM KCl, 2 mM CaCl₂, 1 mM MgCl₂, 5 mM HEPES pH 6.9) in a small Petri dish (60 mm x 15 mm) upon removal from their original vial²³.
3. Place the larvae on filter paper (150 mm diameter) that is slightly moistened with around 5 mL of Ringer's solution in a Petri dish (100 mm x 15 mm) (Figure 2A).
4. Add ~1 mL of Ringer's solution daily to the filter paper as needed to avoid dryness and larval desiccation.

3. Bacterial preparation

1. Culture P. asymbiotica bacteria on Luria Bertani (LB) agar media at 28 °C for 48 h.
2. Use a biosafety level 2 cabinet to transfer a single colony of P. asymbiotica to inoculate a liquid culture in 10 mL of LB media.
3. Incubate the P. asymbiotica liquid culture overnight at 28 °C in a rotary shaker set to 220 rpm.
4. Culture E. coli bacteria in a similar fashion, but carry out the initial growth on agar media and liquid culture incubation at 37 °C overnight.
5. Centrifuge each overnight bacterial culture for 3 min at 13,000 x g and 4 °C.
6. Discard the supernatant and wash the resulting bacterial pellets three times with 10 mL of sterile PBS.
7. Centrifuge the pellets again for 3 min at 13,000 x g and 4 °C.
8. Dilute each pellet with sterile PBS to adjust bacterial concentrations to the optical density (600 nm) of 0.25 for P. asymbiotica and 0.015 for E. coli, which correspond to 100-300 colony forming units per larva of each bacterial preparation, using a spectrophotometer.

4. Injector preparation

1. Prepare capillaries using 3.5″ glass capillary tubes and a micropipette puller. Set the instrument as follows: heat: 580; pull: 143; velocity: 25; delay: 1; pressure: 500.
2. Use straight serrated medium point forceps to open the glass capillary to the degree that will allow the delivery of the experimental treatments while causing minimal damage to the larvae (Figure 2B). To optimize this procedure while practicing injections, use Trypan Blue solution (dilute the stock 0.4% with PBS to 0.2%) to easily track leakage while injecting and the survival of the blue larvae.
3. Fill the capillary with mineral oil using a plastic, disposable 20 mL syringe with a hypodermic needle (22 G, 25 mm length).
4. Set up the nanoliter injector and eject the oil out of the capillary (Figure 2C).
5. Fill the capillary with the desired bacterial preparation for injection. Take the solution from a drop (~20 µL) that is placed on parafilm. In this protocol, 50.2 nL of two bacterial stocks were injected.

5. Larvae injection

1. Anesthetize D. melanogaster larvae using carbon dioxide for ~2 min prior to the procedure.
2. Gently transfer the anesthetized larvae to a filter paper moistened in Ringer's solution in preparation for injection under a stereomicroscope. The larvae will be lethargic or passive at this point.
3. To inject larvae, apply firm pressure on the dorsal side of the posterior end (the tracheal spiracles are apparent at the posterior end versus black mouthparts at the anterior end) using forceps (Figure 2D).
4. Insert the needle horizontally towards the posterior end of the larvae, near the cuticle. A successful injection will not result in a leakage of the injected solution from the larvae (Figure 3).
5. Remove the forceps that were used to apply pressure on the larvae's tail before withdrawing the needle. If not removed first, the forceps can force hemolymph and/or the intestine out of the larvae from the wound site.
6. Infect the appropriate number of larvae for the study being performed. In this particular protocol, 20 larvae for each experimental condition were injected.
7. Using forceps, gently transfer the injected larvae to a separate moist filter paper in a Petri dish (10 larvae per dish) or a food vial (depending on the purpose of the experiment) to allow for recovery.
8. Place the Petri dishes or food vials in an incubator at 25 °C. If larvae are kept in a Petri dish, add Ringer's solution as necessary to prevent desiccation.

6. Recording survival/mortality

1. Record the number of dead and live D. melanogaster larvae according to the set experimental time points. Live larvae will continue to develop into pupae and adults.
2. Use statistical programs, such as Prism, to enter the raw survival/mortality data, analyze them with the log-rank (Mantel-Cox) test, and represent the results in figures.

Results

When performed correctly, injections of D. melanogaster larvae show a bacterium-specific effect. The survival data were collected at several time points following infections of P. asymbiotica (strain ATCC43943), E. coli (strain K12), and PBS (Figure 4). Whereas D. melanogaster larvae are susceptible to P. asymbiotica, which compromises survival rapidly, larvae injected with E. coli or PBS controls exhibit prolonged survivals

Discussion

Drosophila melanogaster is among the most valuable, experimentally manipulated models used for investigations of innate immunity and pathogenesis of various microbial infections. This is due to its simple and fast life cycle, simple upkeep in a laboratory, well-established evolutionary genetics, and diverse genetic toolbox. Previous methods of D. melanogaster larvae injections, such as using a hybrid microfluidic device or a Narishige micromanipulator, require highly specialized equipment and can be cos...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Fly Food B (Bloomington Recipe)	LabExpress	7001-NV	Food B, in narrow vials, 100 vials/tray
100 x 15, Mono Petri Dishes Fully Stackable	VWR	25384-342	Diameter 100 x 15 mm
60 x 15, Mono Petri dishes Fully Stackable	VWR	25384-092	Diameter 60 x 15 mm
Glass capillaries	VWR	53440-186
Grade 1 qualitative filter paper standard grade, circle	VWR	28450-150	Diameter 150 mm
Lab culture Class II Type A2 Biosafety Safety Cabinet	ESCO	LA2-4A2-E
LB Agar	Fisher Scientific	BP1425-500	LB agar miller powder 500 g
LB Broth	Fisher Scientific	BP1426-500	LB broth miller powder 500 g
Mineral oil	Alfa Aesar, Thermo Fisher Scientific	31911-A1
NanoDrop 2000/2000c Spectrophotometer	Thermo Fisher Scientific	ND-2000C
Nanoject III Programmable Nanoliter Injector	Drummond	3-000-207
Narrow Drosophila Vials, Polystyrene	Genesee Scientific	32-109
Needles, hypodermic	VWR	89219-316	22 G, 25 mm
Next Generation Micropipette Puller	World Precision Instruments	SU-P1000
PBS	VWR	97062-732	Buffer PBS tablets biotech grade 200tab
Prism	GraphPad	Version 8
Syringes - plastic, disposable	VWR	76124-652	20 mL
Trypan Blue	Sigma-Aldrich	T8154