Introduction

Phytophthora infestans, causing late blight in potato, is one of the most devastating pathogens and threatens food production worldwide. The use of resistant varieties is considered to be the most sustainable approach for the management of late blight. Today, commercial potato crops are mainly protected by the use of disease-free seeds and frequent fungicide application (Fry 2007; Struik and Wiersema 1999). However, considerable financial and environmental costs are incurred for fungicides and their application (Vleeshouwers et al. 2011). Production of disease-free seeds causes considerable additional costs for the refined infrastructure and regular operation of the facilities. Furthermore, the capacity of the pathogen to develop resistance to modern fungicides (Goodwin et al. 1996; Grünwald et al. 2001) necessitates the development of durably resistant varieties. Therefore, breeders have been extremely interested in creating resistant cultivars ever since the first late blight epidemic in Europe in the 1840s that caused the Irish potato famine. Breeding activities at the beginning of the twentieth century have mainly focused on dominant resistance genes, as the complete resistance they conferred was easy to follow and promised a fast and effective way to protect the crop against late blight. Dominant resistance genes were initially identified in the Mexican species Solanum demissum and introgressed by crossing and backcrossing into cultivated potato. Eleven potato resistance (R) gene differentials from S. demissum have been identified (Black et al. 1953; Malcolmson and Black 1966). The S. demissum R genes from MaR1, -R2, -R3, -R4 and -R10 have been introgressed into potato cultivars. However, their durability proved to be a problem due to the rapid appearance of compatible races of the pathogen after market introduction (Wastie 1991). In recent years, other wild species of the genus Solanum are also being considered as possible sources of resistance in addition to S. demissum. Introgression of these genes into cultivars sometimes requires interspecific bridge crosses (Hermsen and Ramanna 1973). This approach resulted in the introgression of Rpi-blb2 from S. bulbocastanum into the cultivars Toluca (NL 2006) and Bionica (NL 2008) (Haverkort et al. 2009).

In the last two decades, the chromosomal positions of many R genes from S. demissum have been determined. Eight R genes have been mapped; R1 on chromosome V (Leonards-Schippers et al. 1992), R2 on chromosome IV (Li et al. 1998), R3a and R3b (Huang et al. 2004), R6 and R7 (El-Kharbotly et al. 1996) R10 and R11 (Bradshaw et al. 2006) on chromosome XI. R5, R8 and R9 have been suggested to be allelic variants of R3, located on chromosome XI (Huang 2005). Furthermore, four R genes from S. demissum have been cloned, R1 (Ballvora et al. 2002), R2 (Lokossou et al.2009), R3a (Huang et al. 2005) and R3b (Li et al. 2011). In the Mexican species S. bulbocastanum, three R genes were identified and cloned, the alleles RB (Helgeson et al. 1998; Naess et al. 2000; Song et al. 2003) and Rpi-blb1 (van der Vossen et al. 2003) on chromosome VIII, Rpi-blb2 on chromosome VI (van der Vossen et al. 2005) and Rpi-blb3 on chromosome IV (Park et al. 2005). In the wild species S. pinnatisectum a dominant R gene, Rpi1, was mapped by Kuhl et al. (2001) to chromosome VII. On chromosome IX genes from S. mochiquense (Rpi-moc1; Smilde et al. 2005), S. phureja (Rpi-phu1; Sliwka et al. 2006), S. venturii (Rpi-vnt1; Foster et al. 2009; Pel et al. 2009), S. dulcamara (Rpi-dlc1; Golas et al. 2010) and S. caripense (Trognitz and Trognitz 2004; Nakitandwe et al. 2007) were mapped. In S. berthaultii three genes, Rpi-ber (Rauscher et al. 2006), Rpi-ber1 and Rpi-ber2 (Park et al. 2009), were mapped to the long arm of chromosome X. Besides these resistance genes, there are additional sources of resistance from a wide range of species, which have not been located in the genome yet. S. microdontum, S. paucissectum and S. stoloniferum are considered as important resistance sources (Sandbrink et al. 2000; Villamon et al. 2005; Wang et al. 2008).

Despite the rapid breakdown of R1, R2, R3, R4 and R10 in the past, S. demissum is still considered a valuable source for both race-specific and race-non-specific resistance (Niederhauser and Mills 1953; Colon et al. 1995 ). Differentials MaR8 and MaR9 were shown to be durably resistant to several P. infestans isolates (Haynes et al. 2002), however, R8 and R9 have never been used in breeding (Huang 2005). Haynes et al. (2002) evaluated 22 potato clones including seven late blight differentials for late blight resistance in seven US locations in 1997. The authors found that the area under disease progress curve (AUDPC) of MaR8 was very low. Evaluation of the reaction of potato differentials to over 5,000 P. infestans isolates, collected in various parts of the world, showed that the resistances of differentials MaR5, MaR8 and MaR9 were most durable (Swiezynski et al. 2000). Also, P. infestans isolates derived from clonal lineage US8, the most common and aggressive genotype of P. infestans present in the US (Fry and Goodwin 1997) overcame all known R gene differentials except MaR8 and MaR9, both in detached leaf assay and in field trials (Bisognin et al. 2002).

The apparent durability of the R gene in MaR8 led us to study the molecular basis of the resistance in this plant. Here, we describe the use of dedicated molecular marker techniques [NBS- and cluster directed profiling (CDP)] and genetic analysis of the resistance to P. infestans isolate IPO-C (race 1, 2, 3, 4, 5, 6, 7, 10, 11) in MaR8, and provide evidence that this resistance is located on the distal end of the long arm of chromosome IX.

Materials and methods

Plant material and mapping population

MaR8, corresponding to 2424a(5) and PI 303149 (Black et al. 1953; Malcolmson and Black 1966), and cultivar concurrent were maintained and multiplied in the laboratory of plant breeding in vitro. MaR8, as resistant female parent, and the susceptible cultivar Concurrent were crossed to generate an F1 mapping population in the summer of 2008 (population code 3020). Seeds were sown under sterile conditions and 100 plants were maintained in in vitro culture.

Phytophthora infestans isolates and disease testing

Phytophthora infestans isolate IPO-C (race 1, 2, 3, 4, 5, 6, 7, 10, 11) was kindly provided by Prof. Francine Govers (Laboratory of Phytopathology, Wageningen University). IPO-C was used in detached leaf assays as described by Vleeshouwers et al. (1999) but also to inoculate field trials. In 2009 and 2010, respectively, four and two in vitro plants per genotype from population 3020 were planted in the beginning of June. Spreader rows and the border rows consisted of the susceptible potato cultivars Bintje and Nicola, which served to support a local late blight epidemic. In the beginning of July, the trial fields were inoculated. For the inoculum production, a large number of detached leaves of potato cultivar Bintje were inoculated with isolate IPO-C. After 6 days, spores were washed off to prepare a spore suspension in large containers. Zoospore release was induced by incubating the containers at 10°C. After the release of the zoospores, the inoculum was adjusted to a concentration of 5 × 104 zoospores/ml. At nightfall, the zoospore suspension was sprayed on the potato field using a tractor using a spraying arm. After 2 weeks severe late blight symptoms were observed in susceptible plants and a clear segregation of resistance and susceptibility was observed in F1 population 3020. Scoring was performed in a qualitative way (resistant or susceptible).

DNA isolation and marker analysis

Genomic DNA was isolated as described by Fulton et al. (1995). Young leaf tissue was collected for DNA isolation according to the CTAB protocol with the Retsch machine (RETSCH Inc., Hannover, Germany). Primers used for marker analysis are listed in Table 1. PCR reactions were performed using DreamTaq™ polymerase (Fermentas) in a standard PCR program (start: 94°C for 30 s; amplification: 35 cycles of 94°C for 30 s, 55°C for 30 s; 72°C for 1 min; termination: 72°C for 2 min).

Table 1 Markers used for mapping of R8 in the F1 population MaR8 × Concurrent
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NBS profiling was performed as described by Van der Linden et al. (2004), with minor modifications. The restriction enzyme digestion of genomic DNA and the ligation of adapters were made in one incubation step. Restriction enzymes MseI, HaeIII and RsaI were used for restriction ligation reactions and NBS primers NBS1, NBS2, NBS3, NBS5a6 and NBS9 in combination with the adaptor primer were used for the successive PCR reactions. Primers with corresponding names and sequences have been described previously (Van der Linden et al. 2004; Wang et al. 2008; Mantovani et al.2006; Brugmans et al. 2008). Totally, 15 primer enzyme combinations were used for NBS profiling. For R gene CDP, R2 and Tm-2 2 primers (R2LF1, R2LF2, R2LF3, R2LF4, R2LR2, R2LR3, R2LR4, Tm1F, Tm1R, Tm3F, Tm3R, Tm6F, Tm15F, Tm15R, Tm19F, Tm19R, Mcq19F, Mcq21R and Mcq23F) were used as described by Verzaux (2010). HotStarTaq™ polymerase (QIAGEN) was used in the first PCR and DreamTaq™ polymerase (Fermentas) in a second PCR. For designing Hero-CDP-primers, Hero-like sequences available from NCBI (http://www.ncbi.nlm.nih.gov/) and S. phureja DM1-3 516R44 (CIP801092) whole genome assembly scaffoldsv3 available from the Potato Genome Sequencing Consortium (PGSC; http://www.potatogenome.net/index.php/Data; http://potatogenomics.plantbiology.msu.edu/) were collected and aligned. Primers were designed on cluster specific conserved domains encoding CC and LRR. A total of six Hero-CDP degenerate primers were designed and one produced a marker that was linked to R8 (Table 1). For Sw5-CDP seven specific primers described by Dianese et al. (2010) were used. Like in NBS profiling, the CDP primers were used in combination with a labeled adaptor primer (fluorescent dye IRD700) to enable visualization on a denaturing polyacrylamide gel using a NEN® IR2 DNA analyser (LI-COR® Biosciences, Lincoln, NE, USA). NBS profiling was carried out first on a set of 10 resistant and 10 susceptible F1 plants, including the parents. If in this first round polymorphic bands between the parents and co-segregation of these bands with resistance in the F1 plants were found, a second round of NBS profiling was carried out on genomic DNA of the remaining F1 progeny. If multiple markers are found with one primer/enzyme combination, numbers behind the dash are consecutive numbers ordered from low to high molecular weight produced by the same primer enzyme combination. For example, marker CDPTm21-1 and CDPTm21-2 were produced using primer/enzyme combination Tm15R/MseI.

In order to screen for cleaved amplified polymorphic sequences (CAPS), PCR was done using primers listed in Table S1a and successively the PCR products were digested using the restriction enzymes listed in Table S1b. 5 μl of PCR product were added to a 15 μl restriction enzyme digestion according to the manufacturers’ instructions.

Isolation and sequence analysis of NBS fragments

Fragments were excised as described in the Odyssey® manual for band extraction (Westburg, The Netherlands) and re-amplified with the specific profiling primer and the adapter primer. PCR products were checked on agarose gels and purified with QIAquick PCR purification spin columns (QIAGEN Benelux, The Netherlands). Fragments were cloned into the pGEM-T Easy vector (Promega, USA) prior to sequencing with M13 primers. Sequencing was carried out with the BigDye Terminator kit and an ABI 3700 automated sequencer from Applied Biosystems (USA). Blast analysis of the sequences was performed using the websites from NCBI, PGCS and SGN (http://blast.ncbi.nlm.nih.gov/Blast.cgi; http://potatogenomics.plantbiology.msu.edu/index.php?p=blast; http://solgenomics.net). ClustalX (Jeanmougin et al. 1998) was used to align sequences.

Map construction

Co-segregating, simplex-inherited NBS and CDP markers from the tetraploid female parent (MaR8) were scored as dominant markers (Wu et al. 1992). The marker order was determined by TetraploidMap (Hackett and Luo 2003; http://www.bioss.ac.uk/knowledge/tetraploidmap/). The map distance was calculated based on the frequency of the recombination between markers.

Publicly available potato and tomato genetic maps from the SH × RH population (Van Os et al. 2006), SGN (http://sgn.cornell.edu/cview/map.pl?map_id = 9&show_offsets = 1&show_ruler = 1) and GABI (http://www.gabipd.org/database/) databases were included for comparison of marker positions and synteny.

Results

Segregation of resistance in the mapping population

F1 progeny and the parental clones MaR8 and cv Concurrent were screened for resistance against P. infestans isolate IPO-C. The detached leaf assay with leaves from greenhouse grown plants turned out not to be suitable for the F1 population. In contrast to the mother plant MaR8, the F1 plants showed no clear resistance. Initial screens indicated some variation in resistance, however, these findings were not reproducible for most of the individuals. In contrast, highly reproducible results were obtained in two field trials performed in Wageningen, The Netherlands, in the summer of 2009 and 2010. MaR8 plants remained devoid of late blight symptoms, while cv Concurrent was completely infected within 2 weeks after inoculation. Among 100 F1 genotypes screened, 52 were resistant, 46 were susceptible and 2 showed intermediate phenotypes. This demonstrates that the resistance in MaR8 is inherited as a dominant simplex allele (χ 2 = 0.54, P > 0.05) at a single locus. The corresponding gene is referred to as R8 hereafter.

Identification of R8 flanking markers

In order to identify markers linked to R8, we used NBS profiling since this technique can also give an indication about the R gene family of the targeted gene. Initially, NBS profiling experiments were carried out using combinations of the NBS5a6 primer and three enzymes (HaeIII, RsaI and MseI) on both parents and 10 resistant and 10 susceptible F1 individuals from the mapping population. Marker, NBS5a6H was linked to the resistance phenotype and was found at a frequency of one recombinant in twenty F1 plants. Subsequently, an additional set of NBS primers (NBS1, NBS2, NBS3 and NBS9) was used which resulted in the identification of an additional marker, NBS1M showing linkage to the resistance but without recombinants in twenty F1 plants. The NBS5a6H and NBS1M markers were tested on the complete F1 progeny. 22 additional recombinants were found between NBS5a6H and R8, and three recombinants were identified between NBS1M and R8. These recombinants were not overlapping resulting in 26 recombinants between NBS1M and NBS5a6. This showed that the two NBS profiling markers flank the R8 gene (Fig. 1).

Fig. 1
figure 1

Positions of NBS profiling markers and R gene homologs on chromosome 9. Markers in large font indicate the NBS profiling markers that were linked to R8. Potato genome sequences, the tomato genome sequences and the marker sequence database from the SGN were searched using the NBS5a6H and NBS1M by BLAST analysis. The bars on the left indicate S. phureja scaffolds (PGSC v3). In the middle are the tomato EXPEN 2000 genetic map and the tomato SL2.40 Ch9 physical map (SGN). On the right positions of tomato genome sequences with homology to R genes are shown. Horizontal and diagonal lines indicate corresponding marker positions in the different maps

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Localization of R8 flanking markers in the genome

The NBS5a6H (361 bp) and NBS1M (301 bp) fragments were cut out of the gel and sequenced (genbank accession numbers: JF317286 and JF317287 respectively). In potato scaffold PGSC0003DMS000000483, a 93% identity match was found for the NBS5a6H sequence. PGSC0003DMS000000483 could be located to chromosome IX using genetic and physical maps of tomato (Fig. 1). NBS1M showed 97% identity to potato scaffold PGSC0003DMS000001347. This scaffold could be linked to the telomeric region at the long arm of chromosome IX using markers C2_At1g09815 and C2_At3g24160 (Fig. 1). The proposed inversions between potato and tomato on chromosome IX (Tanksley et al. 1992) did not affect the positioning of the R8 flanking markers.

For marker NBS1M, there was no similarity to sequences with known function. The sequence of marker NBS5a6H, however, showed 90% identity to the tomato Hero gene (Ernst et al. 2002), which is located on chromosome IV. Apparently, Hero-like genes are not only present on chromosome IV but are located in other genomic regions as well (Fig. 1).

Localisation of R8 on chromosome IX

In order to verify that R8 and its flanking markers were on chromosome IX, more closely linked markers near the R8 gene were required. Therefore, R gene CDP was performed. Two R gene clusters known to locate on chromosome IV (R2 and Hero), and two clusters known to locate on chromosome IX (Tm-2 2 and Sw5) were targeted for R gene-CDP. Using R2-CDP no bands linked to the resistance were found among 24 primer/enzyme combinations (data not shown). Three linked markers, CDPTm21-1 (240 bp), CDPTm21-2 (345 bp) and CDPTm22 (120 bp), were identified using Tm-2 2 primers out of 36 primer/enzyme combinations. CDPTm21-1 and CDPTm21-2 were identified using the same primer enzyme combination (Tm15R/MseI). All Tm-2 2-CDP markers are at 2 cM distance (proximal) from R8 (Fig. 2). Two markers, CDPSw54 (277 bp) and CDPSw55 (165 bp), were identified using Sw-5-CDP. Both markers were located at 1 cM to the opposite side (distal) of the R8 gene as CDPTm21-1, CDPTm21-2 and CDPTm22 (Fig. 2). Interestingly, one fully co-segregating marker, CDPHero3 (500 bp; Fig. 3), was found using Hero-CDP out of 18 primer/enzyme combinations (Fig. 2). All CDP markers were excised from the gel and subjected to sequence analysis. CDPTm21-1 and CDPTm22 indeed showed similarity to Tm-2 2. CDPSw54 and CDPSw55 were confirmed to be similar to Sw-5, a S. lycopersicon tospovirus resistance gene (Brommonschenkel and Tanksley 1997; Spassova et al. 2001). Unfortunately, the sequences of CDPTm21-2 and CDP3, remained unresolved due to technical reasons. The relative positions of the Tm-2 2 and Sw-5 homologous markers in the R8 map are in agreement with relative positions of Rpi-moc1, which is homologous to Tm-2 2 (Foster et al. 2009) and Sw-5, as inferred from publically available genetic maps of chromosome IX (Fig. 2). In addition, the draft sequence of the complete tomato chromosome IX shows that Tm-2 2 and Sw-5 like sequences are located close to each other near the telomere (Fig. 1).

Fig. 2
figure 2

Comparison of different genetic maps of chromosome IX. From left to right the potato SHxRH map (Van Os et al. 2006), the R8 map produced in this study and the combined Solanaceae pathogen resistance map as extracted from the GABI website (May 20th, 2011). Only the long arms of chromosome IX are shown. The dotted arrows indicate relative positions of studied markers shared between the different maps

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Fig. 3
figure 3

Morphology of marker CDPHero3. Part of a LI-COR gel containing co-segregating marker CDPHero3 which was obtained with Hero4064F1/HaeIII primer/enzyme combination. Pr, Ps, R, S, and M indicate the resistant parent, susceptible parent, resistant and susceptible F1 genotypes, and molecular weight marker, respectively. The arrow on the left points at the CDPHero3 band, the right arrow points at molecular weight marker

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To further confirm the map position of R8 and the newly identified profiling markers on chromosome IX, known markers (GP101, S2g3, TG591A, GP41, CT220, T0521, S1d11, S1d5-a, T1065, TG328, TG424, and St_At3g23400) from the SGN and GABI databases on the long arm of chromosome IX were selected and tested for linked polymorphisms after digestion with 24 selected restriction enzymes. Only TG328 did display an informative SCAR type polymorphism. A segregation of 87 presence to 12 absence genotypes was found which fits a 5:1 ratio (χ 2 = 0.23, >0.05), indicating that the TG328 marker allele is present in duplex in MaR8. TG328 located to SH9 BIN77 of the SHxRH map, was linked to Rpi-moc1 in the GABI map, and located 2 cM proximal relative to R8 (Fig. 2). Also three SSR markers (Stm1010, Stm1021, Stm0017) (Milbourne et al. 1998; Collins et al. 1999) were screened and one SSR marker, Stm1021, present in RH9 BIN65 of the SHxRH map located at 9 cM proximal to R8. Since no other useful polymorphisms could be found in known genetic markers in this region, we mined for potential polymorphic regions in the potato genome covering this region. Scaffold PGSC0003DMS000000184 which contained the flanking markers TG328, CDPTm21-1 and CDPTm22, was aligned to the tomato genome and several polymorphic regions were identified. PCR screens within these regions eventually identified an additional polymorphic marker (184-81), which located 1 cM proximal to R8 (Fig. 2).

Discussion

In this study, we report the genetic mapping of the R8 late blight resistance gene from the differential clone MaR8 to the distal end of chromosome IX. Previously, it was suggested that R8 was a R3 family member located on chromosome XI (Huang et al. 2005). This suggestion was generally accepted in literature. However, from this study it is now clear that this is not the case. Rather, R8 is located distal to Stm1021 and TG328, present in RH9 BIN65 and SH9 BIN77, respectively, of the SHxRH map (Fig. 2, Van Os et al. 2006), and proximal to Sw-5. Also Rpi-edn2, a gene from S. edinense conferring resistance to IPO-C (Verzaux 2010), was located distal (~15 cM) to Stm1021. Interestingly, Stm1021 was found to locate in between two known R gene clusters on chromosome IX, distal to the cluster containing Rpi-vnt1 (Foster et al. 2009; Pel et al. 2009) and proximal to the cluster containing Rpi-moc1 (Smilde et al. 2005), which is probably the same as Rpi-mcq1 (Foster et al. 2009). Both Rpi-vnt1 and Rpi-mcq1 were described to be homologous to Tm-2 2, a tomato gene conferring resistance to Tomato Mosaic Virus (Lanfermeijer et al. 2003). This gene is located near the centromere on the long arm of chromosome IX. We conclude that Tm-2 2 like sequences are dispersed over the long arm of chromosome IX and are concentrated in at least three different clusters. Besides the Rpi-vnt1, Rpi-mcq1, Rpi-edn2 and R8, the Rpi-phu1 gene also was mapped to the long arm of chromosome IX (Sliwka et al. 2006), although more proximal than R8, as inferred from map comparisons. The multitude of late blight resistance genes in this genomic region raises the question whether they could represent different alleles of the same gene or whether they are indeed different genes. Mining for R gene homologs in this region has revealed several potential R gene clusters, suggesting that each cluster could potentially harbor different late blight resistance genes. Primer enzyme combination Tm19F and MseI, used to produce CDPTm22, was previously shown to link to Rpi-edn2 at 6 cM distance (Verzaux 2010). CDPTm22, however, produced a marker band of a different size. Further research is required to show whether R8 and Rpi-edn2 are allelic variants or different genes. Although we show that Sw-5, Tm-2 2 or Hero sequences are present in this part of chromosome IX (Fig. 2), we cannot yet clarify to which family the R8 gene belongs.

In this study, we mapped eight profiling markers, of which six were R gene CDP markers. CDP is a refinement of the motif-directed profiling (MDP) marker technology (Van der Linden et al. 2004). However, it can easily be adapted to target other conserved gene families. For instance, it was adapted for Prx-Profiling (Peroxidase Profiling) in barley to map peroxidase genes and correlate them with QTL map positions for resistance (González et al. 2010). R genes from the same cluster usually have similarities in their sequences not shared with other R genes (McDowell and Simon 2006; Meyers et al. 2005). So it is possible to design specific primers for a particular R gene cluster. In this study, we have adapted the MDP technology to achieve marker saturation in an R gene cluster of interest, referred to as CDP. We show that comparative genomics tools can be used to predict chromosomal positions of the sequenced profiling markers. Besides the virtue of homology-based marker landing, an important pitfall is illustrated in this study. Highly similar sequences may sometimes be found in different clusters, as was shown for fragment NBS5a6H. For this fragment, high similarity was found with a sequence of tomato Hero gene that had previously been mapped to tomato chromosome IV (Ernst et al. 2002). The putative map position on chromosome IV for this marker, inferred from the high sequence similarity to Hero, was incorrect.

The availability of the sequence assembly of the entire chromosomes from tomato has allowed us to identify multiple gene clusters on the long arm of chromosome IX. These clusters have high levels of homology (>90% identity) to Sw-5 and Tm-2 2 respectively which are physically separated by millions of base pairs. This finding may provide indications as to how R gene clusters evolve. Several studies have indicated the role of unequal crossing over, resulting in local duplications leading to rapid evolution of R gene clusters (Leister 2004; Kuang et al. 2004; McDowell and Simon 2006). Duplication over long distances, as observed in this study, would suggest an excision and subsequent insertion mechanism. This could be associated with the excision and insertion of retrotransposons, which are present in many R gene clusters. An excision-insertion hypothesis for duplication is supported by the finding of a Hero-like gene on chromosome IX. This duplication cannot be a result from intra-chromosomal rearrangements such as unequal crossing over.

Finally, we would like to emphasize that differential clone MaR8 is durably resistant to many P. infestans isolates (Haynes et al. 2002), but it was not extensively used in breeding (Huang 2005). Localization of R8 is a first important step for introgression breeding and for molecular cloning of this gene. The combination of several of the R genes from S. demissum and other wild potatoes using cisgenic modification or pyramiding breeding strategies offer good ways to protect the plant against late blight (Jacobsen and Schouten 2007; Zhu et al. 2011). In this perspective, marker CDPHero3 and its closely flanking markers are suitable for tagging R8 introgressions in breeding material and to distinguish R8 from other R genes in stacking approaches. Furthermore, the identified markers will be instrumental for the map based cloning of the R8 gene.