کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3406852 1223604 2011 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Multiplex RT-PCR detection and microarray typing of vesicular disease viruses
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ویروس شناسی
پیش نمایش صفحه اول مقاله
Multiplex RT-PCR detection and microarray typing of vesicular disease viruses
چکیده انگلیسی

A vesicular disease multiplex reverse transcription (RT)-PCR with an accompanying microarray assay was developed for simultaneous detection and typing of foot-and-mouth disease virus (FMDV) and vesicular stomatitis virus (VSV), and for the detection of swine vesicular disease virus (SVDV) and vesicular exanthema of swine virus (VESV). The multiplex RT-PCR successfully detected viral RNA from a collection of 49 strains of vesicular viruses, including multiple strains from all seven serotypes of FMDV and both serotypes of VSV. The multiplex RT-PCR was also able to produce amplified products from the RNA genome of all four viruses simultaneously in mixed samples. An indirect (post-PCR labelling) amplicon labelling method and a direct (concurrent labelling with PCR) amplicon labelling method were compared for the purpose of microarray detection and typing. Accurate detection and typing was achieved with all strains tested in the microarray assay which utilized 163 virus- and serotype-specific probes. It was observed that microarray increased detection for some samples compared to using multiplex RT-PCR alone. This was most likely due to signal amplification resulting from fluorescent labelling. The limit of detection of the microarray assay was as low as 4.6 TCID50/mL for FMDV. No amplification products or microarray reactivity was observed with non-target livestock pathogens tested or with samples collected from healthy cattle, sheep and pigs. All FMDV and VSV serotypes were detected as early as 2 days post-inoculation from oral swabs obtained from cattle infected experimentally.


► We developed a multiplex RT-PCR and microarray for detection/typing of 4 vesicular disease virus.
► 49 strains of vesicular viruses from all serotypes were accurately detected and typed.
► The multiplex RT-PCR amplified products from the genome of all four viruses in mixed samples.
► All FMDV and VSV serotypes were detected at 2 dpi from samples from cattle infected experimentally.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Virological Methods - Volume 175, Issue 2, August 2011, Pages 236–245
نویسندگان
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