Rt. Folkertsma et al., GENE POOL SIMILARITIES OF POTATO CYST-NEMATODE POPULATIONS ASSESSED BY AFLP ANALYSIS, Molecular plant-microbe interactions, 9(1), 1996, pp. 47-54
AFLP was used to characterize 24 potato cyst nematode populations. Thi
s novel DNA fingerprinting technique enabled the identification of 987
marker loci by screening only 12 primer combinations. Data on presenc
e or absence polymorphisms and data on the intensities of correspondin
g DNA fragments were collected. Separate analysis of both data sets re
vealed similar dendrograms for the nine G. rostochiensis populations i
ncluded in this study. Both dendrograms consisted of two groups contai
ning three and five related populations, respectively. One population
differed from either of these groups. Each group represented a differe
nt pathotype as defined by Kort et al. (J, Kort, H. Boss, H. J. Rumpen
horst, and A. R. Stone, Nematologica 23:333-339, 1977). Previously, a
similar arrangement was found after analysis of the genetic variation
using random amplified polymorphic DNA (RAPD) (R. T. Folkertsma, J. N.
A. M. Rouppe van der Voort, M. P. E. van Gent-Pelter, K. E. de Groot,
W. J. van den Bos, A. Schots, J. Bakker, and F. J. Gommers, Phytopath
ology 84:807-811, 1994). For the 15 G. pallida populations analyzed, c
omplex AFLP patterns were obtained and therefore only qualitative AFLP
data were used. Incongruities were observed between clustering on the
basis of AFLP data and classical pathotyping. This strongly confirms
earlier findings obtained with RAPDs, because the AFLP markers used in
this study outnumbered the population characteristics revealed by RAP
Ds by a factor of five. To arrive at a reliable pathotype designation
of potato cyst nematode populations molecular data and virulence chara
cteristics should be integrated. Possible causes for the difference in
distribution of polymorphisms among G. rostochiensis and G. pallida p
opulations are discussed.