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Waqas Nawaz
11-ARID-975
DVM 5th

Routes:
1234-

Chorioallontoic Membrane (CAM)
Allontoic Cavity
Amniotic Cavity
Yolk Sac
Routes for inocculation of virus in an emryonated egg
Materials:



Eggs: 9-day old or 10-day old embryonated eggs.
Candle the eggs and mark the inoculation sites.

Eggs should be placed in an egg rack with the inoculation site uppermost.






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Egg shell punch.
Cotton wool.
A 70 percent alcohol solution in water.
Syringe 1 mL.
Needles preferably 25 gauge, 16 mm.
Stationery tape (also called cello or sticky tape) or melted wax to seal the
inoculation site.
Inoculum. This must be free of microbial contamination.
Discard tray.
Biohazard Box

Inoculum: A substance (a virus or toxin or immune serum) that is introduced into the body to
produce or increase immunity to a particular disease.

Procedure:
 Swab the end of the eggs to be inoculated with 70% ethanol. Allow the
alcohol to evaporate.
 Place used cotton wool in discard tray.
 Candle the egg with high intensity LED torch and mark “X” over the
embryo’s eye.
 Draw a line on the shell marking the air space.
 With a sterile egg shell puncher or carborundum disc pierce a hole in the end
of the egg at the marked inoculation site.
 Attach a needle to 1 ml syringe.
 Draw 0.1ml of inoculums (Viral suspension) into 1 ml syringe.
 Place the needle through the hole in the eggshell keep the needle and syringe
vertical. The needle will need to penetrate approximately 16 mm into the egg
to reach specific site of inoculation.
 Inject 0.1 ml of inoculums into the egg.
 Withdraw the needle from the egg.
 Seal the hole in the shell with stationery tape or melted wax.
 Discard the used needles and syringes in a biohazard box.
 Place the inoculated eggs into a second incubator. Check the temperature
and humidity of incubator.
 In the case of amniotic inoculation, when the needle reaches the embryo a
thrust will strike the embryo and the embryo will move away from the
needle. Then inject the virus suspension.

Expected Results:
 The virus suspension are succesfully inoculated into the eggs. The growth of
the virus can be detected by visible pocks in the egg.
 Death of embryo may also occure.

Advantages:










Widely used method for the isolation of virus and growth.
Ideal substrate for the viral growth and replication.
Isolation and cultivation of many avian and few mammalian viruses.
Cost effective and maintenance is much easier.
Less labor is needed.
The embryonated eggs are readily available.
Sterile and wide range of tissues and fluids
They are free from contaminating bacteria and many latent viruses.
Specific and non specific factors of defense are not involved in embryonated
eggs.
 Widely used method to grow virus for some vaccine production.

Disadvantages:
 The site of inoculation for varies with different virus. That is, each virus
have different sites for their growth and replication.
Major problem with cell cultures:
 The process requires trained technicians with experience in working on a full
time basis.
 State health laboratories and hospital laboratories do not isolate and identify
viruses in clinical work.
 Tissue or serum for analysis is sent to central laboratories to identify virus.

WAQAS NAWAZ
11-ARID-975
DVM 5th Semester

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Routes for inocculation of virus in an emryonated egg

  • 1. Waqas Nawaz 11-ARID-975 DVM 5th Routes: 1234- Chorioallontoic Membrane (CAM) Allontoic Cavity Amniotic Cavity Yolk Sac
  • 3. Materials:   Eggs: 9-day old or 10-day old embryonated eggs. Candle the eggs and mark the inoculation sites. Eggs should be placed in an egg rack with the inoculation site uppermost.          Egg shell punch. Cotton wool. A 70 percent alcohol solution in water. Syringe 1 mL. Needles preferably 25 gauge, 16 mm. Stationery tape (also called cello or sticky tape) or melted wax to seal the inoculation site. Inoculum. This must be free of microbial contamination. Discard tray. Biohazard Box Inoculum: A substance (a virus or toxin or immune serum) that is introduced into the body to produce or increase immunity to a particular disease. Procedure:  Swab the end of the eggs to be inoculated with 70% ethanol. Allow the alcohol to evaporate.  Place used cotton wool in discard tray.  Candle the egg with high intensity LED torch and mark “X” over the embryo’s eye.  Draw a line on the shell marking the air space.  With a sterile egg shell puncher or carborundum disc pierce a hole in the end of the egg at the marked inoculation site.  Attach a needle to 1 ml syringe.  Draw 0.1ml of inoculums (Viral suspension) into 1 ml syringe.  Place the needle through the hole in the eggshell keep the needle and syringe vertical. The needle will need to penetrate approximately 16 mm into the egg to reach specific site of inoculation.  Inject 0.1 ml of inoculums into the egg.  Withdraw the needle from the egg.  Seal the hole in the shell with stationery tape or melted wax.  Discard the used needles and syringes in a biohazard box.
  • 4.  Place the inoculated eggs into a second incubator. Check the temperature and humidity of incubator.  In the case of amniotic inoculation, when the needle reaches the embryo a thrust will strike the embryo and the embryo will move away from the needle. Then inject the virus suspension. Expected Results:  The virus suspension are succesfully inoculated into the eggs. The growth of the virus can be detected by visible pocks in the egg.  Death of embryo may also occure. Advantages:          Widely used method for the isolation of virus and growth. Ideal substrate for the viral growth and replication. Isolation and cultivation of many avian and few mammalian viruses. Cost effective and maintenance is much easier. Less labor is needed. The embryonated eggs are readily available. Sterile and wide range of tissues and fluids They are free from contaminating bacteria and many latent viruses. Specific and non specific factors of defense are not involved in embryonated eggs.  Widely used method to grow virus for some vaccine production. Disadvantages:  The site of inoculation for varies with different virus. That is, each virus have different sites for their growth and replication. Major problem with cell cultures:  The process requires trained technicians with experience in working on a full time basis.  State health laboratories and hospital laboratories do not isolate and identify viruses in clinical work.  Tissue or serum for analysis is sent to central laboratories to identify virus. WAQAS NAWAZ 11-ARID-975 DVM 5th Semester