This video demonstrates a technique to infect Drosophila by introducing a pathogenic bacteria directly into their body cavity. This method bypasses epithelial barriers and other passive defense mechanisms, allowing for the induction of systemic infection. Upon infection, the resulting immune response is assessed by monitoring fly mortality and performing downstream assays.
Protocol
1. Collect and Prepare Flies Rear D. melanogaster under the desired experimental conditions. Take care not to overcrowd the flies during rearing and make sure that larval densities are consistent across treatments since environmental conditions during the larval stage can profoundly affect immune defense phenotypes during the adult stage. Collect experimental flies 0 – 3 days after eclosion from the pupal case and transfer them onto fresh medium. House the collect…
Divulgazioni
The authors have nothing to disclose.
Materials
Incubator
Powers Scientific, Inc
DROS52SD
Paintbrush
CO2 Flypads
FlyStuff
59-114
CO2
Airgas
CD FG50
Drosophila rearing mix
6 oz Square Bottom Bottles, polypropylene
Genesee Scientific
32-130
Nosterile Extra Large Cotton Balls
Fisher brand
22-456-882
Microscope
Olympus Corporation
SZ51
Drosophila Vials polystyrene
VWR international
89092-720
Nosterile Large Cotton Balls
Fisher brand
22-456-883
2L flask
VWR international
89000-370
Petri Dishes with Clear Lids, Raised Ridge; 100 . x 15 mm;
VWR international
25384-302
LB Agar, Miller
Difco
244520
Inoculating Loop
VWR international
80094-488
Rainin Clasic Pipettes in various sizes
0.1 µl to 2 µl,
2 µl to 20 µl,
20 µl to 200 µl,
100 µl to 1000