The cultivated potato, Solanum tuberosum, is affected by a variety of diseases with late blight, caused by Phytophthora infestans, being the most severe. Wild potato species have proven to be a continuing source of resistance, sometimes of an extreme type, to this disease. The present study constructs the first late blight linkage map of a member of series Piurana, S. paucissectum, a tuber-bearing relative of potato, using probes for conserved sequences from potato and tomato. Eight probes mapped to unexpected linkage groups, but syntenic differences with prior maps of potato were not supported by any blocks of rearranged chromosome segments. All 12 linkage groups were resolved and significant associations with late blight resistance were found on chromosomes 10, 11 and 12. A major quantitative trait locus (QTL) on chromosome 11 accounts for more than 25% of the phenotypic variance measured in a field trial. Crossing of S. paucissectum with cultivated potato resulted in very few seeds indicating partial reproductive barriers. Differential reactions of accessions of this potential donor species with simple and complex isolates of P. infestans suggest that it carries major resistance genes that are not those previously described from the Mexican species, S. demissum. However, the additivity of the QTL effects argues for the quantitative nature of resistance in this cross.

We analyzed the cytoplasmic diversity of CIP potato breeding germplasm. Cytoplasm types were assigned to 978 genotypes consisting of 265 foreign accessions used as input germplasm, 642 breeding lines developed by CIP, and 71 varieties released from CIP material. We found T (45 %), D (38 %), and W (11 %) to be the most frequent cytoplasm types in CIP breeding germplasm. Comparing the initial input germplasm to CIP breeding lines, the frequency of T-type cytoplasm decreased from 64 to 38 %, while those of D-and W-type cytoplasms increased from 26 to 41 % and from 6 to 14 %, respectively. We conclude that the CIP breeding program, as many others worldwide, has experienced a genetic bottleneck in terms of cytoplasmic diversity due to the unintended and continuous use of cytoplasmic-based male-sterile maternal lineages derived from Solanum demissum and S. stoloniferum in parental line and variety development. Nonetheless, the finding of male-fertile T-type breeding lines must have alleviated the problem to a certain extent, thus enabling CIP breeding progress.

Major gene inheritance of resistance to Potato leafroll virus (PLRV) was demonstrated in a parthenogenic population derived from the highly resistant tetraploid andigena landrace, LOP-868. This major gene or chromosome region seems to control a single mechanism for resistance to infection and virus accumulation in this source. About 149 dihaploid lines segregated in a ratio of 107 resistant to 32 susceptible, fitting the expected ratio for inheritance of a duplex gene under random chromatid segregation. A tetraploid AFLP map was constructed using as reference the ultra high density (UHD) map. All AFLP markers associated with PLRV resistance mapped to the same linkage group. Map position was confirmed by analysis of previously-mapped SSR markers. Rl (adg) is located on the upper arm of chromosome V, at 1 cM from its most closely linked AFLP marker, E35M48.192. This marker will be used to develop allele-specific primers or a pair of flanking PCR-based markers for their use in marker assisted selection.

The challenges of breeding autotetraploid potato (Solanum tuberosum) have motivated the development of alternative breeding strategies. A common approach is to obtain uniparental dihaploids from a tetraploid of interest through pollination with S. tuberosum Andigenum Group (formerly S. phureja) cultivars. The mechanism underlying haploid formation of these crosses is unclear, and questions regarding the frequency of paternal DNA transmission remain. Previous reports have described aneuploid and euploid progeny that, in some cases, displayed genetic markers from the haploid inducer (HI). Here, we surveyed a population of 167 presumed dihaploids for large-scale structural variation that would underlie chromosomal addition from the HI, and for small-scale introgression of genetic markers. In 19 progeny, we detected 10 of the 12 possible trisomies and, in all cases, demonstrated the noninducer parent origin of the additional chromosome. Deep sequencing indicated that occasional, short-tract signals appearing to be of HI origin were better explained as technical artifacts. Leveraging recurring copy number variation patterns, we documented subchromosomal dosage variation indicating segregation of polymorphic maternal haplotypes. Collectively, 52% of the assayed chromosomal loci were classified as dosage variable. Our findings help elucidate the genomic consequences of potato haploid induction and suggest that most potato dihaploids will be free of residual pollinator DNA.

In potato breeding and selection, storability should be regarded as equally important as yield, disease resistance, and quality. A study documenting the dormancy period, sprouting behavior, and weight loss of 17 International Potato Center potato elite and advanced clones was carried out in Tashkent, Uzbekistan, under cellar and cold store conditions, during 2008 and 2009. Ninety tubers of each of 17 clones were allocated to experimental units of 30 tubers each placed in trays and randomized in three replications following a random complete block design. Therefore, there were three replications of 30 seed tubers each per entry. The dormancy period ranged from 77 to 115 days and from 100 to 186 days under cellar and cold storage, respectively. There was a relatively high positive correlation (0.69) for dormancy period between storage systems, indicating that clones demonstrating longer and shorter dormancy periods under one system will also behave similarly under the other system. A negative correlation (−0.53 and −0.88) was found between dormancy period and length of the longest sprout in cellar and cold store, respectively, meaning that clones with shorter dormancy often showed a greater length of their longest sprout. The weight loss percentage per tuber was similar in both storage systems, from 5.0% to 8.0% in the cellar and from 5.0% to 9.8% in the cold store, although for different storage periods (an average of 110 and 166 days under cellar and cold storage conditions, respectively). The study indicated that under cellar conditions, clones with a longer dormancy period and slower rate of sprout growth have less weight loss during storage and therefore better keeping quality.