The detection of recombinant, tuber necrosing isolates of Potato virus Y (PVYNTN) using a three-primer PCR based in the coat protein gene
Moravec, Tomáš; Čeřovská, Noemi; Boonham, N.
JOURNAL OF VIROLOGICAL METHODS 109 [1]: 63-68, 2003
Klíčová slova: Potato virus Y; Three primer PCR; Coat protein gene
Abstrakt: A simple and reliable procedure for reverse transcription-polymerase chain reaction (RT-PCR) detection and strain differentiation of Potato virus Y (PVY) was developed. Three primers were designed within the coat protein (CP) and nuclear inclusion protein b (NIb) region, exploiting a single base polymorphism identified as being present in all the recombinant PVYNTN isolates published. Samples infected with PVY produce a single band of 569 bp, while isolates belonging to PVYNTN strain give an additional band of 334 bp. The technique was tested on a collection of well-characterised isolates of PVY from a range of strains and was found to detect all of the isolates reported as belonging to the PVYNTN strain. All of the isolates detected possess a recombination event within the coat protein. Further sequence analysis revealed that all the recombinant PVYNTN isolates reported thus far would be detected using this assay, whilst isolates thought to be PVYNTN that do not possess the coat protein recombination event would not be detected.
DOI:
Autoři z ÚEB: Noemi Čeřovská, Tomáš Moravec
JOURNAL OF VIROLOGICAL METHODS 109 [1]: 63-68, 2003
Klíčová slova: Potato virus Y; Three primer PCR; Coat protein gene
Abstrakt: A simple and reliable procedure for reverse transcription-polymerase chain reaction (RT-PCR) detection and strain differentiation of Potato virus Y (PVY) was developed. Three primers were designed within the coat protein (CP) and nuclear inclusion protein b (NIb) region, exploiting a single base polymorphism identified as being present in all the recombinant PVYNTN isolates published. Samples infected with PVY produce a single band of 569 bp, while isolates belonging to PVYNTN strain give an additional band of 334 bp. The technique was tested on a collection of well-characterised isolates of PVY from a range of strains and was found to detect all of the isolates reported as belonging to the PVYNTN strain. All of the isolates detected possess a recombination event within the coat protein. Further sequence analysis revealed that all the recombinant PVYNTN isolates reported thus far would be detected using this assay, whilst isolates thought to be PVYNTN that do not possess the coat protein recombination event would not be detected.
DOI:
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