Scopus
YÖKSİS Eşleşti
Comparison of manual and automated nucleic acid extraction methods for detection of peste des petits ruminants virus RNA
Kafkas Universitesi Veteriner Fakultesi Dergisi · Mart 2015
YÖKSİS Kayıtları
Peste Des Petits Ruminants Virus RNA sının Tespitinde Manuel ve Otomatik Nükleik Asit Ekstraksiyon Yöntemlerinin Karşılaştırılması
Kafkas Universitesi Veteriner Fakultesi Dergisi · 2015 SCI-Expanded
PROFESÖR OĞUZHAN AVCI →
Comparison of Manual and Automated Nucleic Acid Extraction Methods for Detection of Peste Des Petits Ruminants Virus RNA
Kafkas Universitesi Veteriner Fakultesi Dergisi · 2015 SCI-Expanded
PROFESÖR OĞUZHAN AVCI →
Makale Bilgileri
DergiKafkas Universitesi Veteriner Fakultesi Dergisi
Yayın TarihiMart 2015
Cilt / Sayfa21 · 271-276
Scopus ID2-s2.0-84921808747
Özet
Peste des petits ruminants (PPR) is an economically important contagious disease of small ruminants. PCR-based techniques have been successfully used for rapid diagnosis of PPR. The method used for isolation of RNA from tissue samples is an important concern when using reverse transcription-PCR (RT-PCR) methods for the detection of PPR virus (PPRV). In this study, a commercial kit for manual preparation and an automated processing technique for RNA extraction were compared in terms of performance. Thirty-two small ruminants, each from different flocks, with PPR suspect submitted to laboratory were chosen to compare manual and automated extraction methods for the detection of PPRV. Vero cells were used for PPRV isolation. One-step RT-PCR was used for the detection of PPRV RNA. From the 32 submitted samples, CPE was observed in 11 samples. PPRV nucleic acid was detected in 11 of 32 samples that were manually extracted, while viral RNA was detected in 9 of 32 extracts prepared by the robot. Two samples that were negative with automated extraction were weakly positive in manual extraction. RNA quality and quantity were assessed using a spectrophotometer. According to the results, difference in quantity among two methods was statistically significant (P<0.0001, two-tailed paired t-test), and manual extraction method is suitable for detection of low amounts of PPRV RNA in clinical samples.
Yazarlar (3)
1
Murat Sevik
2
Oğuzhan Avci
ORCID: 0000-0001-9299-4695
3
Ömer Bariş Ince
Anahtar Kelimeler
Automated
Manual
Quality
Quantity
RNA purification
RT-PCR
Kurumlar
Agriculture and Rural Development Support Institution
Konya Turkey
Selçuk Üniversitesi
Selçuklu Turkey
Veterinary Control Institute
Meram Turkey