TY - JOUR
T1 - Validation of the specificity and sensitivity of species-specific primers that provide a reliable molecular diagnostic for Xiphinema diversicaudatum, X. index and X. vuittenezi
AU - Hübschen, Judith
AU - Kling, Lilo
AU - Ipach, Ulrike
AU - Zinkernagel, Volker
AU - Bosselut, Nathalie
AU - Esmenjaud, Daniel
AU - Brown, Derek J.F.
AU - Neilson, Roy
N1 - Funding Information:
We would like to thank Mrs. Brigitte Helmstätter for her help with the acquisition of the nematodes and useful comments and encouragement during the experiments, and S. Schütz, G. Bleyer and J.V. Herrmann for providing nematodes. Research at the Scottish Crop Research Institute is grant-aided by the Scottish Executive Environment and Rural Affairs Department. This work was supported by the Wiederaufbaukasse der rheinland-pfälzischen Weinbaugebiete (WAK).
PY - 2004/10
Y1 - 2004/10
N2 - Xiphinema diversicaudatum and X. index are vector nematode species of economic importance in viticulture regions as they can transmit Arabis Mosaic, Grapevine Fanleaf and Strawberry Latent Ringspot viruses to grapevine. Wang et al. (2003) designed species-specific diagnostic primers from ribosomal genes for both these vector species as well as a vector and a non-vector species X. italiae and X. vuittenezi, respectively. Our study aimed to confirm the specificity and determine the sensitivity and reliability of the primers for the two vector species, X. diversicaudatum and X. index when challenged with closely related longidorid species and general nematode communities typical of vineyard soil. With one exception, no PCR product was observed when the primers were tested against six Longidorus, one Paralongidorus and one Xiphinema non-target species. Occasionally (three out of eight replicate PCR reactions) a weak PCR product was noted when primers for X. index were tested with L. elongatus. Furthermore, when challenged with a range of non-target nematode species comprising the nematode community typical of viticulture soil, no PCR product was amplified. An experimental dilution series of extracted DNA rigorously demonstrated that DNA from an equivalent single specimen of the target virus-vector species, X. diversicaudatum and/or X. index, could be detected amongst 1000 equivalent non-target X. vuittenezi. Also, extracted DNA from an equivalent single target specimen was detected when added to DNA extracted from the overall soil nematode community. The primers were assessed further by using serial mixtures of actual nematodes rather than extracted DNA to simulate field soil. Using this method, a single target nematode could be detected amongst 200 non-target specimens. Given their specificity, sensitivity and reliability, it appears that these diagnostic primers will be of great benefit to phytosanitary/quarantine services related to the viticulture industry.
AB - Xiphinema diversicaudatum and X. index are vector nematode species of economic importance in viticulture regions as they can transmit Arabis Mosaic, Grapevine Fanleaf and Strawberry Latent Ringspot viruses to grapevine. Wang et al. (2003) designed species-specific diagnostic primers from ribosomal genes for both these vector species as well as a vector and a non-vector species X. italiae and X. vuittenezi, respectively. Our study aimed to confirm the specificity and determine the sensitivity and reliability of the primers for the two vector species, X. diversicaudatum and X. index when challenged with closely related longidorid species and general nematode communities typical of vineyard soil. With one exception, no PCR product was observed when the primers were tested against six Longidorus, one Paralongidorus and one Xiphinema non-target species. Occasionally (three out of eight replicate PCR reactions) a weak PCR product was noted when primers for X. index were tested with L. elongatus. Furthermore, when challenged with a range of non-target nematode species comprising the nematode community typical of viticulture soil, no PCR product was amplified. An experimental dilution series of extracted DNA rigorously demonstrated that DNA from an equivalent single specimen of the target virus-vector species, X. diversicaudatum and/or X. index, could be detected amongst 1000 equivalent non-target X. vuittenezi. Also, extracted DNA from an equivalent single target specimen was detected when added to DNA extracted from the overall soil nematode community. The primers were assessed further by using serial mixtures of actual nematodes rather than extracted DNA to simulate field soil. Using this method, a single target nematode could be detected amongst 200 non-target specimens. Given their specificity, sensitivity and reliability, it appears that these diagnostic primers will be of great benefit to phytosanitary/quarantine services related to the viticulture industry.
KW - Xiphinema
KW - diagnostics
KW - longidorids
KW - nematode
KW - virus vector
UR - http://www.scopus.com/inward/record.url?scp=4544247014&partnerID=8YFLogxK
U2 - 10.1007/s10658-004-0995-9
DO - 10.1007/s10658-004-0995-9
M3 - Article
AN - SCOPUS:4544247014
SN - 0929-1873
VL - 110
SP - 779
EP - 788
JO - European Journal of Plant Pathology
JF - European Journal of Plant Pathology
IS - 8
ER -