TECHNICAL SHEET
Ref.CDVP009
192 tests/kit
ILT
Poultry
ILT
ILT is an enzyme immunoassay(EIA) for the detection of specific IgG
antibodies against Infectious Laryngotracheitis(ILT) virus antigens in
poultry sera of vaccinated or convalescent animals of the disease.
General Information
Infectious Laryngotracheitis is a disease caused by Infectious
Laryngotracheitis (ILT)virus, belonging to the Herpesviridae family.
It is a very common disease in countries with industrial poultry
farming, and causes important losses.
The disease may manifest in an acute or mild form. depending on the
virus strain virulence. Symptoms usually appear 6-15 days after infection.
In acute infections mortality rates are very high.
Mild infections usually don’t cause significant mortality rates, but
they favor tremendously the category of circulating secondary agents, such
as Haemophilus sp., Mycoplasma sp., Pasteurella sp., etc.
The animals which survive infections, can expel virus during more than 1
year after infection, and they can cause recurrent infections in new lots
of poultry which are bought in the exploitation.
Another important aspect of this virus is its latency in poultry, that
can sharpen by any stress factor ; meaning a grave risk of virus spreading
from complementary poultry lots to industrial poultry lots.
One must seriously take this factor into account for disease epidemiology
control.
Principle of the test
The Cypress Diagnostic ILT test is based on the principle of an enzyme
Immunoassay (EIA). The assay system utilizes an inactivated specific
antigen. This specific antigen is coated on the microtiter well.
First, the test sample or controls are allowed to react with the solid
phase specific antigen. If there are specific antibodies, they will bound
to the antigen. After 1 hour incubation at 37°C, the wells are washed
with the washing solution to remove unbound material.
In a second step, an Anti-Chicken IgG/HRPO conjugate is added to the wells
resulting in the specific antibody against infectious Laryngotracheitis
virus being sandwiched between the solid phase antigen and enzyme
conjugate antibody. After 1 hour incubation at 37°C, the wells are washed
with the washing solution to remove unbound material.
A substrate/chromogen solution is added and incubated 15 minutes ,
resulting in the development of a blue color in the wells where a complex
Antigen/ Anti-ILT virus antibody/Anti-Chicken IgG-HRPO conjugate was
formed previously.
The color development is stopped with the addition of the stop reaction
solution and the color turns yellow. The yellow color is measured
spectrophotometrically at 450 nm.
The concentration of poultry specific IgG antibody against Infectious
Larygotracheitis(ILT) virus is proportional to the color intensity of the
test sample.
Rev.09.95
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