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Method Article

Establishing Bacterial Infection in Drosophila Larvae

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March 31st, 2026

In This Article

Abstract

Source: Hiroyasu, A., D et. al., Extraction of Hemocytes from Drosophila melanogaster Larvae for Microbial Infection and Analysis. J. Vis. Exp. (2018)

This video demonstrates the procedure for establishing a bacterial infection in Drosophila larvae by placing them into a bacterial droplet and pricking them with a tungsten needle. The larvae are then incubated on a grooved, nutrient-rich agar plate to study host-pathogen interactions.

Protocol

1. In vivo infection

  1. Warm the Drosophila fruit juice agar plate at room temperature for 15 min.
    1. Add 30 g of agar to 700 mL of water and autoclave it for 40 min.
    2. Dissolve 0.5 g of methyl paraben in 10 mL of absolute ethanol.
    3. Add the methyl paraben solution to 300 mL of fruit juice concentrate.
    4. Quickly mix the juice concentrate into the autoclaved agar solution and dispense 5 mL into 10 × 35 mm Petri dishes.
    5. After the plates have cooled for 15 min, store them at 4 °C.
  2. Prepare 3rd instar larvae.
  3. Place the yeast paste on an agar plate. Make a fine cut in the agar plate where larvae can migrate to avoid drying (Figure 1A). Assemble a 0.001 mm pointed tungsten needle with holding forceps using paraffin film (Figure 1B, C).
  4. Pipette 50 µL of high-titer mCherry expressing-Coxiella burnetii (5.95×109 GE/mL) onto the paraffin film under the stereo microscope and place the larvae into the pool of bacteria.
  5. Place the larvae in the pool of bacteria, prick them with a tungsten needle (Figure 3D), and transfer them onto an agar plate (Figure 1E).
  6. Transfer the remaining pathogen medium onto the agar plate and seal the plate with paraffin film.
  7. Keep the larvae on the plate in moist air until the desired time post-infection (Figure 1F). In this experiment, C. burnetii-infected larvae are on the plate for 24 h.

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Results

In vivo infection setup; petri dish, needle, larval examples; bioassay experimental process.

Figure 1: In vivo infection. A) Drosophila fruit juice agar plates and yeast paste...

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Stereo microscopeAmscopeSM-1BSZ-L6W 
ForcepsVWR82027-402 
Coxiella burnetii - mCherryDr. Heinzen, R.  
Drosophila fruit juice platesCold Spring Harbor Protocols http://cshprotocols.cshlp.org/content/2007/9/pdb.rec11113.full
AgarFisher BioreagentsBP1423-500 
Methyl parabenAmresco0572-500G 
Absolute ethanolFisher BioreagentsBP2818-500 
Welch's 100% Grape juice frozen concentrate, 340 mLAmazonB0025UJVGM 
Petri dishes, 10 x 35 mmFisher Scientific08-757-100A 
Yeast, Bakers Dried ActiveMP Biomedicals210140001Add 2 parts of water to 1 part of yeast (v/v)
Tungsten needleFine Science Tools10130-20 
Holding forcepsVWRHS8313 
Listeria monocytogenesATCCstrain: 10403SListeria monocytogenes strain 10403S (Bishop and Hinrichs, 1987) was grown in Difco Brain-heart infusion (BHI) broth (BD Biosciences) containing 50 µg/ml streptomycin at 30 °C.

Tags

Tungsten NeedleHemolymph EntryGrooved Agar PlateHemocyte PhagocytosisHost Pathogen InteractionMicrobial InfectionSteriomicroscopeParaffin Film