Generation of a Panel of Monoclonal Antibodies Against the Haemagglutinin-Neuraminidase Glycoprotein of Newcastle Disease Virus Strain Af2240
The Malaysian velogenic-viscerotropic Newcastle disease virus (NDV) strain AF2240 is responsible for high mortality and morbidity. Monoclonal antibodies (mAbs) have been known to be useful in the identification of NDV due to their binding specificity, their homogeneity and their ability to be pro...
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Main Author: | |
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Format: | Thesis |
Language: | English |
Published: |
2005
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Subjects: | |
Online Access: | http://psasir.upm.edu.my/id/eprint/5916/1/FBSB_2005_12%20IR.pdf |
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Summary: | The Malaysian velogenic-viscerotropic Newcastle disease virus (NDV) strain
AF2240 is responsible for high mortality and morbidity. Monoclonal antibodies
(mAbs) have been known to be useful in the identification of NDV due to their
binding specificity, their homogeneity and their ability to be produced in
unlimited quantities. It is, however, very difficult to obtain mAbs which are
specific to NDV commercially. Therefore, this project is to develop mAbs
against the local NDV strain AF2240. This velogenic-viscerotropic viral strain is
a reference strain that has often been used for vaccine development.
Hybridoma cells were created by fusing NDV-hyperimmunised Balblc
splenocytes with Sp210-Ag14 (Sp2) myeloma cells using polyethylene glycol
with the molecular weight of 1450 (PEG 1450). Positive clones were screened by
ELISA. High titre producing clones were selected from a series of limiting
dilutions. MAbs from stable hybridomas were further characterised by western
blot analysis, haemagglutination-inhibition test (HI) and haemolysis-inhibition
test (HLI).
Eight hybridoma cell lines producing mAbs against the haemagglutininneuraminidase
(HN) glycoprotein of NDV strain AF2240 were generated.
Isotyping showed that mAbs 1B9, 2D6 and 9D7 were IgG1, mAbs 1D5, 5A10
and 5F10 were IgG2a and mAbs 2G3 and 5E10 were IgG3. Kappa (K) light
chains were found in all mAbs. They can be divided into two groups: (1) mAbs
lD5, 5A10 and 5E10 which recognised conformational and linearised epitopes
and (2) mAbs 1B9, 2D6 and 9D7 which recognised only conformational
epitopes. All mAbs showed positive results in the HI test but not HLI test
conforming that they were specific to the HN protein and not the fusion (F)
protein. |
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