کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3406927 1223610 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Multiplex RT-PCR for rapid detection and differentiation of class I and class II Newcastle disease viruses
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ویروس شناسی
پیش نمایش صفحه اول مقاله
Multiplex RT-PCR for rapid detection and differentiation of class I and class II Newcastle disease viruses
چکیده انگلیسی

A multiplex RT-PCR was developed for detection and differentiation of class I and class II strains of Newcastle disease virus (NDV). The method was shown to have high specificity and sensitivity. The results obtained from the multiplex RT-PCR for a total of 67 NDV field isolates obtained in 2009 were consistent with those obtained by nucleotide sequencing and phylogenetic analysis. A phylogenetic tree based on the partial sequences of the F gene revealed that the 67 field isolates of NDV could be divided into two classes. Twenty-seven NDV isolates were grouped into class I, and two genotypes were identified. Most of the class I isolates were determined to be of genotype 3, with the exception of isolate NDV09-034, which belonged to genotype 2. Forty class II NDV isolates were divided into three genotypes, namely genotype VII (27 isolates), genotype I (2 isolates) and genotype II (11 isolates). Isolates of genotypes I and II in class II were shown to be related to commercial vaccine strains used commonly in China. All isolates of genotype VII were predicted to be virulent, on the basis of the sequence motif at the cleavage site of the F gene. This genotype has become predominantly responsible for most outbreaks of ND in China in recent years. In conclusion, this multiplex RT-PCR provides a new assay for rapid detection and differentiation of both classes of NDV isolates.

Research highlights▶ Multiplex RT-PCR can differentiate class I and class II of NDVs. ▶ Molucular epidemiology of NDV isolates revealed that multiples genotypes were existed in China in 2009.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Virological Methods - Volume 171, Issue 1, January 2011, Pages 149–155
نویسندگان
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