A Luciferase-Fluorescent Reporter Influenza Virus to Track Viral Infections
DEŞİFRE METNİ
To infect the mice, start by preparing the bird flu in 1X PBS. Maintain the virus on ice until inoculation. Check for the absence of the toe pinch reflex to make sure that the mouse is anesthetized, and inoculate it intranasal with the prepared bird flu dilution. Ensure all mice are breathing properly before returning them to their cages.
Open the imaging software and press Initialize, then, set the parameters that will be used for the imaging. To monitor the mice infected with bird flu, shave their chest to improve detection of the bioluminescent signal.
Once the mice are anesthetized, use a 22-gauge needle to retro-orbitally administer 100 microliters of NLuc luciferase substrate diluted 1 to 10 in PBS. Immediately after injection, place the animals in the isolation chamber with their chest facing up, then, place the isolation chamber in the imaging instrument, close the door, and acquire images.
After imaging, return the mice to their cages, and monitor them until they have fully recovered. Use the imaging software ROI tool to analyze the acquired bioluminescence data by designating a region of interest and clicking Measure.
To perform ex vivo imaging of mouse lungs, collect the lungs according to the manuscript directions, start the image acquisition software, and set the parameters for imaging. Once the machine is initialized, place the lungs in a black background tray and ensure that the tissues are separated from one another. Introduce the tray into the imager, close the door, and acquire images.
After imaging, remove the tissues immediately and store them on ice at 4 degrees Celsius if the samples will be processed on the same day. If they will be processed later, freeze them quickly in a tube on dry ice, and store them at minus 80 degrees Celsius. To process the images, select the ROI tool, draw regions of interest around each of the individual lungs, and click Measure.
