Aim: Newcastle disease is still one of the major threats for poultry industry allover the world. Therefore, attempt was made in
this study to use the SYBR Green I real-time PCR with melting curves analysis as for detection and differentiation of NDV
strains in suspected infected birds.
Materials and Methods: Two sets of primers were used to amplify matrix and fusion genes in samples collected from
suspectly infected birds (chickens and pigeons). Melting curve analysis in conjunction with real time PCR was conducted for
identifying different pathotypes of the isolated NDVs. Clinical samples were propagated on specific pathogen free ECE and
tested for MDTand ICIP.
Results: The velogenic NDVs isolated from chickens and pigeons were distinguished with mean T 85.03±0.341 and m
83.78±0.237 respectively for M-gene amplification and for F-gene amplification the mean T were 84.04±0.037 and m
84.53±0.223. On the other hand the lentogenic NDV isolates including the vaccinal strains (HB1 and LaSota) have a higher
mean T (86.99±0.021 for M-gene amplification and 86.50±0.063 for F-gene amplification). The test showed no reaction with m
unrelated RNA samples. In addition, the results were in good agreement with both virus isolation and biological pathotyping
(MDT and ICIP). The assay offers an attractive alternative method for the diagnosis of NDV that can be easily applied in
laboratory diagnosis as a screening test for the detection and differentiation of NDVinfections.
Conclusion: As was shown by the successful rapid detection and pathotyping of 15 NDV strains in clinical samples
representing velogenic and lentogenic NDV strains, and the agreement with the results of virus isolation , biological
pathotyping and pathogenicity indices. The results of this report suggests that the described SybrGreen I real-time RT-PCR
assay in conjunction with Melting curve analysis used as a rapid, specific and simple diagnostic tools for detection and
pathotyping of different NDVs in clinically infected birds.