作者: Umer Farooq , Q. M. Khan , T. Barrett
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摘要: Differential diagnosis of Rinderpest (RP) and Peste des petits ruminants (PPR) by host species clinical signs is not always exact; hence, laboratory confirmation necessary to establish the cause disease distinguish these two viruses, where small animals are source infection for large ruminants. In this study, reverse transcription polymerase chain reaction (RTPCR) was standardized against RP PPR. RNA viruses isolated using denaturing solution (Solution D) containing guanidium thiocynate, sarcosyl, sodium citrate s2 mercapto-ethanol. Regular PCR morbilli specific oligonuclotides based on sequences conserved region F P-gene. These P gene primers amplified 429bp 372bp, respectively both Nested performed differentiate PPR F-gene amplicons F3A/F4A F1A/F2A primers, respectively. set a product 235bp 309bp PPR, The results study indicated that RT-PCR can be successfully used detection differential