A collection of 142 accessions of 23 Malus species, derived hybrids and cul
tivar accessions from the USDA-ARS Plant Genetic Resources Unit's core coll
ection, which represents an extensive range of Malus species, was screened
with a set of previously described SSR (simple sequence repeat) markers. Th
e markers were used to determine genetic identities, estimate genetic diver
sity, identify genetic relationships among the accessions, and determine th
e utility of SSR primers developed from Malus x domestica for making geneti
c assessments across the whole Malus genus. All eight primer pairs amplifie
d multiple fragments when used in polymerase chain reactions with DNA from
these accessions. High levels of variation were detected with a mean of 26.
4 alleles per locus and a mean direct count heterozygosity across all eight
loci equal to 0.623. The eight primer pairs used in this study unambiguous
ly differentiated all but five pairs of accessions in this collection of 14
2 accessions of 23 Malus species, derived hybrids and cultivars. These SSR
data were not useful in identifying genetic relationships among this divers
e collection of accessions, with the majority of the accessions not cluster
ing in ways concordant with taxonomic information and/or geographic origin.
The resulting phenogram resolved only two meaningful clusters, for the tax
onomically isolated Section Chloromeles and for M. fusca accessions, reflec
ting genetic relationships arising from geographic origin. The detection of
identical accessions in the collection, which were previously considered t
o be unique, highlights the critical need to further bolster collections of
certain Malus species.