scholarly journals Real-Time PCR-Based Pathotyping of Newcastle Disease Virus by Use of TaqMan Minor Groove Binder Probes

2009 ◽  
Vol 47 (7) ◽  
pp. 2114-2123 ◽  
Author(s):  
T. Farkas ◽  
E. Szekely ◽  
S. Belak ◽  
I. Kiss
2012 ◽  
Vol 157 (5) ◽  
pp. 833-844 ◽  
Author(s):  
Alia Yacoub ◽  
Mikael Leijon ◽  
Michael J. McMenamy ◽  
Karin Ullman ◽  
John McKillen ◽  
...  

2005 ◽  
Vol 150 (12) ◽  
pp. 2429-2438 ◽  
Author(s):  
H. M. Pham ◽  
S. Konnai ◽  
T. Usui ◽  
K. S. Chang ◽  
S. Murata ◽  
...  

Parasitology ◽  
2003 ◽  
Vol 127 (5) ◽  
pp. 489-496 ◽  
Author(s):  
G. VON SAMSON-HIMMELSTJERNA ◽  
S. BUSCHBAUM ◽  
N. WIRTHERLE ◽  
M. PAPE ◽  
T. SCHNIEDER

TaqMan minor groove binder probes were evaluated as to their suitability for the real-time allelic discrimination of the β-tubulin codon 200 TTC/TAC single nucleotide polymorphism in cyathostomin species. Amplification of titrated cloned full-length β-tubulin cDNA revealed that the TaqMan minor groove binder PCR is capable of specifically detecting as few as 10 copies. Testing of DNA from single adult and larval stages of several different species of cyathostomin allowed reproducible genotyping of individual worms. Using the real-time PCR approach, the throughput of samples was considerably increased compared with conventional post-PCR readout procedure. Only 7·8% homozygous TAC L3 were found among 102 L3 which were genotyped from phenotypically BZ-resistant small strongyle populations. The percentages of the homozygous TTC and heterozygous TTC/TAC were 41·3% and 50·9%, respectively. This resulted in a total TAC-allele percentage of only 33·3%. These findings correspond to data obtained by genotyping of an experimentally selected BZ-resistant cyathostomin population. It is concluded that the β-tubulin codon 200 polymorphism is not the sole mechanism involved in the process of BZ resistance in cyathostomins.


2013 ◽  
Vol 60 (3) ◽  
Author(s):  
Dawid Nidzworski ◽  
Edyta Wasilewska ◽  
Krzysztof Smietanka ◽  
Bogusław Szewczyk ◽  
Zenon Minta

Newcastle disease virus (NDV), member of the Paramyxoviridae family and avian influenza virus (AIV), member of the Orthomyxoviridae family, are two main avian pathogens causing serious economic problems in poultry health. Both are enveloped, single-stranded, negative-sense RNA viruses and cause similar symptoms, ranging from sub-clinical infections to severe diseases, including decrease in egg production, acute respiratory syndrome, and high mortality. Similar symptoms hinder the differentiation of infection with the two viruses by standard veterinary procedures like clinical examination or necropsy. To overcome this problem, we have developed a new duplex real-time PCR assay for the detection and differentiation of these two viruses. Eighteen NDV strains, fourteen AIV strains, and twelve other (negative control) strains viruses were isolated from allantoic fluids of specific pathogen-free (SPF), embryonated eggs. Four-weeks-old SPF chickens were co-infected with both viruses (NDV - LaSota and AIV - H7N1). Swabs from cloaca and trachea were collected and examined. The results obtained in this study show that by using duplex real-time PCR, it was possible to detect and distinguish both viruses within less than three hours and with high sensitivity, even in case a bird was co-infected. Additionally, the results show the applicability of the real-time PCR assay in laboratory practice for the identification and differentiation of Newcastle disease and influenza A viruses in birds.


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