Abstract

In addition to the implementation of standard methods of virological diagnostics used for the isolation of the Newcastle disease virus from suspect material, as well as for its identification, nowadays there is increasing use of molecular diagnostic methods, primarily reverse transcription polymerase chain reaction (RT-PCR) and the sequencing method. The objective of this work was to examine possibilities for the implementation of the above methods in the diagnosis of poultry infection caused by the Newcastle disease virus. The presence of hem agglutination antigens for the Newcastle disease virus was established in samples of allantoises liquid from 62 poultry embargoed eggs 72 h after inoculation, whose titers ranged from 1:16 to 1:2048, while the hem agglutination inhibition test (HI test) with the implementation of a referent immuno serum against the given cause provided the identification of isolated viruses in serum dilutions of 1:128 to 1:1024. The RT-PCR method and the PCR established that in eight examined samples one fragment each of viral RNA is formed in agars gel of a size of 254bp, which is characteristic for the Newcastle disease virus genome according to its nucleotide sequence. On the grounds of a comparative analysis of RNA sequences obtained from eight isolated NDV strains and the genome sequences of referent atypical poultry influenza viral strains using Mega 40 and BLAST programmers, it was established that the isolated strains of the Newcastle disease virus were highly virulent.

Highlights

  • Pored primene standardnih metoda virusolo{ke dijagnostike koje se koriste za izolovanje virusa Newcastle bolesti iz suspektnog materijala kao i za njegovu identifikaciju, danas su sve vi{e u upotrebi i molekularne metode dijagnostike i to pre svega lan~ana reakcija polimeraze (RT-PCR) i metoda sekvenciranja.

  • Za izvo|enje metode reverzne transkripcije RNK i lan~ane reakcije polimeraze kori{}eni su One Step RT-PCR kit (Applied Biosystems, SAD) i jedan par prajmera koji amplifikuju deo gena na molekulu RNK koji kodira sintezu fuzionog F proteina spolja{njeg omota~a virusa NDV i to: "forward" prajmer 5-CCTTGGTGAITCTATCCGIAG-3 i "reverse" prajmer 5-CTGCCACTGCTAGTTGIGATAATCC-3 (Seal i sar., 1995).

  • Za izvo|enje metode sekvenciranja izolovanih sojeva virusa Newcastle bolesti kori{}en je BigDye terminator kit v.

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Summary

Introduction

Pored primene standardnih metoda virusolo{ke dijagnostike koje se koriste za izolovanje virusa Newcastle bolesti iz suspektnog materijala kao i za njegovu identifikaciju, danas su sve vi{e u upotrebi i molekularne metode dijagnostike i to pre svega lan~ana reakcija polimeraze (RT-PCR) i metoda sekvenciranja. Za izvo|enje metode reverzne transkripcije RNK i lan~ane reakcije polimeraze kori{}eni su One Step RT-PCR kit (Applied Biosystems, SAD) i jedan par prajmera koji amplifikuju deo gena na molekulu RNK koji kodira sintezu fuzionog F proteina spolja{njeg omota~a virusa NDV i to: "forward" prajmer 5-CCTTGGTGAITCTATCCGIAG-3 i "reverse" prajmer 5-CTGCCACTGCTAGTTGIGATAATCC-3 (Seal i sar., 1995).

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