Aug 17, 2020

Public workspaceChicken immunization with Keyhole limpet hemocynin (KLH)-gp120 fragment (254-274) conjugate raises anti-KLH antibodies in egg yolks.

  • 1University of the West Indies St. Augustine
  • University of the West Indies
  • angel.vaillant@sta.uwi.edu
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Protocol CitationAngel A Justiz-Vaillant 2020. Chicken immunization with Keyhole limpet hemocynin (KLH)-gp120 fragment (254-274) conjugate raises anti-KLH antibodies in egg yolks.. protocols.io https://dx.doi.org/10.17504/protocols.io.bjvtkn6n
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: August 17, 2020
Last Modified: August 17, 2020
Protocol Integer ID: 40595
Abstract
Chicken immunization with peptides is inefective if only just the peptides are being inoculated. However, to make the immune response effective the fragment 254-274 of HIV-1 was conjugated with a carrier protein (KLH) that produced a critical immune response, assessed by ELISA, Immunoblot analysis and dot blot [1-4]. The Polson method (1990) can be used effectively to separate the IgY antibody from the egg yolk of immunized chickens [5].

References

1. Schade R, Pfister C, Italatsch R, Henklien P (1991) Polyclonal antibodies from chicken egg yolk-an alternative to the production of mammalian IgG type antibodies in rabbits. ATLA 19: 403-419.

2. Justiz Vaillant AA, Akpaka PE, Smikle M, McFarlane-Anderson N (2012) In vitro Inhibition of Staphylococcus aureus Isolates by Anti-Anti-Idiotypic Antibodies to Staphylococcal Protein (SpA). J Vaccines Vaccin 3: 127-131.

3. Collins AM, Roberton DM, Hosking CS, Flannery GR (1991) Oral immunization with xenogeneic antibodies stimulates the production of systemic and mucosal anti-idiotypic antibodies. Immunology 73: 388-393.

4. Ho DD, Kaplan JC, Rackauskas IE, Gurney ME (1988) Second conserved domain of gp120 is important for HIV infectivity and antibody neutralization. Science 239: 1021-1023.

5. Polson A (1990) Isolation of IgY from the yolks of eggs by a chloroform polyethylene glycol procedure. Immunol Invest 19: 253-258.
Materials
MATERIALS
Reagent5 x 2ml No-Waste™ Freund's Incomplete Adjuvant (FIA)G-BiosciencesCatalog #786-099
Reagent2ml No-Waste™ Freund's Complete Adjuvant (FCA)G-BiosciencesCatalog #786-709
ReagentFragment 254-274 of Gp120 of HIV (peptide)
Two healthy layer chickens (brown Leghorn), aged approximately 6 months, are injected intramuscularly at multiple sites on the breast with the peptide-keyhole limpet hemocyanin (KLH) conjugate.
The chickens are immunized on day 0, with 0.2 µmol/ml of the fragment 254-274 of HIV gp120-conjugated to KLH (immunogen) in 0.5 ml complete Freund’s adjuvant (Sigma-Aldrich Co, St. Louis Missouri).
On days 15, 60, and 90 chickens are immunized with 0.2 µmol/ml of the immunogen in 0.5 ml incomplete Freund’s adjuvant (Sigma-Aldrich Co, St. Louis Missouri).
The eggs are collected post-immunization.The immunoglobulin Y is separated using the Polson method (1990).
The 96 well microtitre plate is coated overnight at 4°C with 1 µg/µl per well of a mixture of Keyhole limpet hemocynin (KLH) in carbonate-bicarbonate buffer pH 9.6.
Then plate is treated with bovine serum albumin solution and washed 4X with PBS-Tween.
50 µl of water soluble fraction from eggs is added and incubated for 1h at room temperature and the microplate is rewashed 4X with PBS-Tween.
Then 50 µl of rabbit anti-chicken IgY-peroxidase conjugate diluted 1:30,000 in PBS-non-fat milk is added to each well and incubated for 1h at RT. The plate is washed 4X with PBS-Tween.
50 µl of 4 mg/ml o-phenylenediamine solution (OPD) is added and the plate is incubated 15 minutes at RT in the dark.
The reaction is stopped with 50 µl of 3M H2SO4 solution.
The plate is visually assessed for the development of colour and read in a microplate reader at 492 nm.
A cut-off point should be calculated as the mean of the optical density of negative controls x 2 SD. The higher the OD value the higher will be the quantities of anti-KLH in hens.