http://orcid.org/0000-0001-9503-6126
Figures
Abstract
The Japanese chestnut (Castanea crenata) carries resistance to Phytophthora cinnamomi, the destructive and widespread oomycete causing ink disease. The European chestnut (Castanea sativa), carrying little to no disease resistance, is currently threatened by the presence of the oomycete pathogen in forests, orchards and nurseries. Determining the genetic basis of P. cinnamomi resistance, for further selection of molecular markers and candidate genes, is a prominent issue for implementation of marker assisted selection in the breeding programs for resistance. In this study, the first interspecific genetic linkage map of C. sativa x C. crenata allowed the detection of QTLs for P. cinnamomi resistance. The genetic map was constructed using two independent, control-cross mapping populations. Chestnut populations were genotyped using 452 microsatellite and single nucleotide polymorphism molecular markers derived from the available chestnut transcriptomes. The consensus genetic map spans 498,9 cM and contains 217 markers mapped with an average interval of 2.3 cM. For QTL analyses, the progression rate of P. cinnamomi lesions in excised shoots inoculated was used as the phenotypic metric. Using non-parametric and composite interval mapping approaches, two QTLs were identified for ink disease resistance, distributed in two linkage groups: E and K. The presence of QTLs located in linkage group E regarding P. cinnamomi resistance is consistent with a previous preliminary study developed in American x Chinese chestnut populations, suggesting the presence of common P. cinnamomi defense mechanisms across species. Results presented here extend the genomic resources of Castanea genus providing potential tools to assist the ongoing and future chestnut breeding programs.
Citation: Santos C, Nelson CD, Zhebentyayeva T, Machado H, Gomes-Laranjo J, Costa RL (2017) First interspecific genetic linkage map for Castanea sativa x Castanea crenata revealed QTLs for resistance to Phytophthora cinnamomi. PLoS ONE 12(9): e0184381. https://doi.org/10.1371/journal.pone.0184381
Editor: Yong Pyo Lim, Chungnam National University, REPUBLIC OF KOREA
Received: June 19, 2017; Accepted: August 22, 2017; Published: September 7, 2017
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: Authors acknowledge the funding provided by Centro de Estudos Florestais (CEF), which is a research unit funded by Fundação para a Ciência e Tecnologia I.P. (FCT), Portugal (UID/AGR/00239/2013). We acknowledge Fundação para a Ciência e Tecnologia through the project PTDC/AGR-CFL/101707/2008 and the PhD grant SFRH/BD/85140/2012 and also Programa ProDer, Medida 4.1 Refª 45967 “Developing processes and Technologies aiming the production of ink disease resistant. chestnut rootstocks, compatible with national varieties certified with molecular markers” and Programa ProDer, Medida 4.1 Refª 53593 “Innovation in the production chain of chestnut: competitiveness and sustainability”. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Chestnuts (Castanea spp., Fagaceae family) are found around the world in the temperate zone, where they are highly valued by different cultures for the nutritious nuts, valuable timber and landscaping purposes. European chestnut (Castanea sativa Mill.) produces the highest quality and most appreciated nuts, being a major economic income for the European mountainous producing regions and most of that income is being threatened by chestnut depopulation. The emergence of heavily damaging diseases, namely ink disease and chestnut blight, caused by Phytophthora cinnamomi and Cryphonectria parasitica, respectively are responsible for the decline of the European production from 430,000 Tons to 140,000 Tons in the past 50 years.
P. cinnamomi is one among the most destructive pathogens associated with the decline of forestry, ornamental and fruit species [1,2]. When introduced to an environment, this pathogen has had enormous impacts on natural systems, and has been shown to reduce the native biodiversity in Europe, the USA, Australia, New Zealand and Africa. In Portugal, ink disease has become widespread, since P. cinnamomi was first recorded in 1838. In North America, prior to the decimation of the American chestnut (C. dentata Borkhausen) by chestnut blight, ink disease was partially responsible for its decline in the southeastern part of its range [3]. Although C. sativa and C. dentata are susceptible to ink disease and chestnut blight, the Japanese and Chinese chestnuts (C. crenata Sieb. & Zucc. and C. mollissima Blume, respectively) show resistance to both diseases [4]. Taking notice of this fact, The American Chestnut Foundation (TACF) have pursued a backcross breeding program, using C. mollissima as donor parents of resistance, to introgress resistance to C. parasitica into American chestnut. Nevertheless, ink disease is currently recognized in the USA as a serious threat to the American chestnut restoration program [5]. Consequently, breeding for resistance to P. cinnamomi was recently initiated in USA [6].
In Portugal, a chestnut breeding program was initiated in 2006 aiming to introgress the resistance from C. crenata into C. sativa, by crossing both species. Hybrid progenies, segregating for P. cinnamomi resistance, have been obtained and extensively studied in order to understand the chestnut resistance mechanisms to ink disease. Accurate phenotyping methodologies were developed to score diverse metrics of resistance of each progeny aiming to identify marker:trait associations [7]. Moreover, a group of hybrid genotypes selected as the most resistant to P. cinnamomi, are being propagated as improved genetic materials for new rootstocks release to the market in the near future.
Despite the economic and ecological importance of woody plants, mapping of QTLs for important phenotypic traits have been rather limited on these species when compared with major crops or model plants. For chestnut, extensive genomic resources have been developed mainly for C. mollissima and C. dentata [8–10]. Nevertheless, the availability of genetic maps and QTLs’ identification is limited for other Castanea species. Kubisiak et al. (1997) [9] published the first genetic map based on a F2 population of an interspecific cross of C. dentata and C. mollissima, where three QTLs for blight resistance were proposed. In 2005, Sisco et al. [10], presented an updated version of the genetic map adding 304 markers. Recently, a new genetic map of C. mollissima was created using 1393 new markers constituting the reference map in which the physical map was anchored [8,11]. So far, only one genetic map was released for C. sativa, based on a F1 full-sib population of 96 trees, which was used for mapping QTLs for adaptive traits [12,13]. In the present study, the first C. sativa x C. crenata genetic map was constructed using markers developed from C. mollissima, C. dentata, C. sativa and C. crenata transcriptomes. Additionally, QTLs for P. cinnamomi resistance were detected and mapped for the first time in C. sativa x C. crenata, which is a major breakthrough on a tree which the genome has not yet been sequenced. These new genomic resources should be useful mainly in Europe and in the USA, aiming at improving resistance to ink disease or even for another woody species threatened by P. cinnamomi such as cork oak, Quercus suber.
Materials and methods
C. sativa x C. crenata mapping populations
Genetic map construction and QTL mapping were carried out using two full-sib families of C. sativa (female) x C. crenata (male), obtained from controlled pollination. Genotypic data were collected for 52 progenies from C. sativa (cultivar Aveleira) x C. crenata2 cross (SxC) and 81 progenies from C. sativa (cultivar Bária) x C. crenata1 cross (BxC) (Table 1).
The crosses were performed at the germplasm bank of Universidade de Trás-os-Montes e Alto Douro, Vila Real, Portugal (47°17010″N, 7°44043″W), located at 423 m above sea level on a slope facing southwest stand.
Phenotyping resistance to P. cinnamomi
Resistance to P. cinnamomi was previously measured in Santos et al., (2015) [7]. Progression rate of P. cinnamomi lesions in inoculated excised shoots was chosen as phenotypic metric as it provided the most differentiation among progenies: from 0.15 cm/day for the most resistant genotype to 1.13 cm/day for the most susceptible one. To obtain these data, excised shoots (the majority with a length of 15 cm) were collected from 45 SxC progenies, in spring and autumn, and were inoculated with an hypervirulent strain of P. cinnamomi (IMI 340340). The mean number of excised shoots inoculated per genotype was 7.94 in spring and 7.60 in autumn [7].
The external lesion length was measured at five time points after inoculation (5, 7, 9, 12 and 14 days after inoculation) and the lesion progression rates (cm/day) were calculated for each individual, across both seasons [7].
Phenotype experiments were performed in a controlled chamber with temperatures ranging between 18 and 22°C, photoperiod 16 h light/8 h dark and 65% relative humidity.
Molecular markers source and genotyping
A total of 2972 transcriptome-derived molecular markers developed from four chestnut species (C. dentata, C. mollissima, C. crenata and C. sativa) (419 simple sequence repeats-SSRs and 2553 single nucleotide polymorphism-SNPs) were screened in the parental genotypes (C. sativa and C. crenata). From those, 452 markers (180 SSRs and 272 SNPs) were selected for genotyping the progenies, since they presented polymorphism (at least between two parents from one cross) and a unique amplification product (in case of SSRs) (Table 1). A total of 155 SSRs developed from C. mollissima (named by CmSInumber), plus 25 developed from C. sativa and C. crenata (named by CsPTnumber and CcPTnumber, respectively) were used [11,14]. SNP markers were developed from C. mollissima CCall_Unigene_V2 assembly data and from C. dentata AC454_Unigene_V3 contig data (http://www.hardwoodgenomics.org/); they were called as CCallv2contig number_SNP position and AC454v3contig number_SNP position, respectively. In this study, in order to simplify the nomenclature, they were named as CC_contig_number SNP position and AC_contig_number SNP position, respectively. From those SNPs developed from C. mollissima, 1536 were used for chestnut reference genetic map and were denominated as CmSNP00001-CmSNP01536 [11]. This nomenclature was kept common for SNPs used in this study and in the C. mollissima reference genetic map. When available, linkage group (LG) information from the reference map (linkage groups A to L) was placed in front of marker name.
For SSR detection, a M13-specific sequence was added to the 5’ end of each forward primer [15] fluorescent dye (6-FAM, NED, PET or VIC) was added to the 5’ end of each forward primer. Loci were amplified individually in 12.5 μl reaction containing: 20 ng of template DNA, 0.16 μM of 5’-dye-labeled M13 primer, 0.04 μM of 5′-tailed forward primer, 0.16 μM of reverse PIG-tailed primer, 66 μM of dNTPs, 2 mM of MgCl2, 2 μl 5x GoTaq Flexi Buffer (Promega) and 1.0 U of GoTaq® Flexi DNA Polymerase (Promega). Amplifications were undertaken in a Biometra® T1 Thermocycler using the following profile: 94°C for 2 min; 94°C for 30 s, 60°C (annealing temperature for primer forward and reverse) for 45 s, 72°C for 45 s during 30 cycles; 94°C for 30 s, 53°C (annealing temperature for 5’-dye-labeled M13 primer) for 45 s, 72°C for 45 s during 8 cycles; 72°C for 10 min; indefinite hold at 4°C. Completed reactions were loaded onto an ABI PRISM 310 Genetic Analyzer (Applied Biosystems, Foster City, CA, USA) and run according to the manufacturer’s protocol. Allele sizes were determined using the ROX500 internal size standard and the global southern algorithm implemented by ABI PRISM GeneMapper software version 4.0 (Applied Biosystems).
GoldenGate BeadArray platform and GenomeStudio software were employed for SNP detection, clustering, genotype calling and confidence scores assignment. However, data for all SNPs were inspected manually and edited if necessary [16].
For various logistical reasons only for 26 individuals from the SxC cross were available for SNP genotyping
Total genomic DNA was extracted from 100 mg of fresh leaves using the DNeasy™ Plant Mini Kit (Qiagen, Germany) according to the manufacturer’s instructions.
Linkage map construction
Marker segregation analyses and linkage map construction were performed using JoinMap v.3.0 software (van Ooijen 2001). Maps were first constructed separately for both mapping families: SxC and BxC, using CP population model. Linkage Groups (LGs) were determined as a logarithm of the odds (LOD score) with a minimum threshold of 4.0. Linkage maps were calculated using the Kosambi mapping function [17] and applying default mapping parameters: all linkage recombination estimates smaller than 0.4 and a LOD larger than 1.0. Syntenic groups among the three maps were identified and combined through the JoinMap “Combine Groups for Map Integration” function. Map orientation was assigned by comparison with C. mollissima reference map [11]. Linkage groups were drawn using MapChart 2.0 software [18].
QTL mapping
QTL analyses were performed using MapQTL 5.0 software (Van Ooijen 2004). Utilizing the consensus genetic map created here, QTLs for P. cinnamomi resistance were detected using SxC population.
Marker significance level was estimated using the Kruskal-Wallis analysis (K-W, non-parametric test); and the interval mapping method was used to detect the presence of a putative QTL [19]. Multiple QTL model (MQM) computation was also applied, using cofactors significantly associated to the trait (P < 0.02), that were estimated by applying a backward elimination procedure (“Automatic cofactor Selection” MapQTL function). The significant LOD threshold (P < 0.05) was estimated from 1000 permutations of the phenotypic trait, for each LG. QTLs were declared when LOD scores (MQM) exceeded the minimum significance threshold for each LG and the associated markers showed K-W test with significance levels above 0.005.
The R2 value, representing the percentage of the phenotypic variance explained by the marker genotype at the QTL, was taken from the peak QTL position as estimated by MapQTL software.
Each significant QTL was characterized by the peak marker and the other associated markers within the QTL region, the percentage of phenotypic variation explained (R2), LOD score and K-W test. QTL representations were drawn using MapChart 2.0 software [18].
As the molecular markers were developed from transcriptome sequences, putative resistance genes within the QTL intervals genes were identified through BLASTn query against the NCBI database.
Results
The consensus genetic map consists of 217 markers (112 SNPs and 105 SSRs) mapped to 12 LGs, in accordance to chestnut karyotype (n = 12) (Fig 1). According to the genetic reference map [11], all molecular markers developed from C. mollissima (CmSInumber and CmSNPnumber) were correctly mapped on each LG; however, not all marker positions are in the same order. Moreover, 25 additional markers (14 SNPs and 11 SSRs) were also grouped to four extra LGs, that were assigned as LG_D1, LG_E1, LG_H1 and LG_J1, according to the genetic reference map (S1 Fig). These groups are included here because they will likely be merged into the consensus map when more progenies/markers are added to this data set. About 34.3% of markers mapped for C. sativa x C. crenata were also mapped on the consensus C. mollissima reference map (Fig 1 and S1 Fig, in blue).
Marker positions on LGs were assigned to reference map LGs [11], by using the common markers mapped on both genetic maps (in blue).
The interspecific genetic map spans a total genetic distance of 498.9 cM (67,3% of genetic distance in the C. mollissima reference map) with an average interval of 2.3 cM between markers. The genetic length of the linkage groups ranged in size from 16.3 (LG_D) to 92.1 cM (LG_A), with an average of 41.6 cM. From all markers mapped, six (2.7%) of them exhibited poor goodness-of-fit (X2 values > 5.0). On the other hand, high segregation distortion was observed for the most of the unmapped markers.
QTL analyses for resistance to P. cinnamomi was performed for the SxC population where both genotypic and phenotypic data were available. Two QTLs, revealing loci with significant effects (KW test, P<0.005) and LOD scores above the estimated threshold, were identified in two LGs: LG_E and LG_K and therefore the QTL intervals were named Pc_E, and Pc_K, respectively (Table 2 and Fig 2). The percentage of the phenotypic variance explained by Pc_E, and Pc_K varied from about 9 to 13%, respectively (Table 2). These QTL intervals were localized to regions about 8 cM and 1 cM in genetic length, respectively. Nine molecular markers (SNPs) in total were associated with the detected QTLs (Table 2 and Fig 2). The strongest QTL marker (based on LOD scores and K-W test) was identified in Pc_E showing the highest significance levels in K-W test (α = 0.005 to 0.001).
QTLs are represented by black boxes. Asterisks represents the significance levels obtained by Kruskal-Wallis test: ** = 0.05, **** = 0.005 and ***** = 0.001.
Regarding all markers mapped on the QTLs identified, they were developed from transcripts potentially involved in diverse cellular processes. Genes underlying Pc_E QTL may be involved in resistance response via NDR1/HIN1-like protein 3 [20], hormone signaling, transport of phospholipids, regulation of gene expression through protein PAF1 homolog and/or Zinc-finger PHD-type (Table 2). On the other hand, the markers associated to Pc_K QTL were developed from a EST containing a Myb/SANT domain (involved in regulation of gene expression by alteration of chromatin structure [21]), a cellulose synthase, a ribosomal protein and/or genes with uncharacterized functions to date (Table 2).
Discussion
Two QTLs associated with resistance to P. cinnamomi were identified for the first time in a C. sativa x C. crenata mapping population, providing an improved understanding about the genetic architecture of pathogen resistance in tree species and especially Castanea spp. QTLs were genetically mapped on a new chestnut interspecific linkage map constructed with functional EST-molecular markers, located in transcribed regions (transcriptome-derived). The majority of the markers genotyped are shared with those used for C. mollissima reference map construction [11], which enabled the confirmation of each LG grouped, increasing the robustness of the presented map. All markers with known position on the reference map were mapped on the same LG presented, providing evidence of strong conservation across Castanea species. Furthermore, about 34.3% of markers mapped for C. sativa x C. crenata were also mapped on the consensus C. mollissima reference map. The observation that not all marker positions are in the same order as in the C. mollissima reference map, may be explained by the presence of more subtle differences between the species, however cytogenetic studies are needed to confirm this supposition.
Combining two full-sib populations from unrelated parents for genetic mapping constitutes a strategy to increase genetic diversity, since native alleles from different species are sampled. The reported genetic map contains 217 molecular markers mapped in 12 LGs, achieving a coverage of 498.9 cM with a marker density of 1 marker / 2.3 cM, on average. In Quercus robur and Q. petraea genetic maps, a similar average of marker density was obtained: 1 marker / 2.9 and 2.7 cM, respectively [22,23]. In chestnut, Casasoli et al. (2001) [12] achieved a C. sativa genetic map covering 720 cM, and an average of marker density of about 1 marker / 9 cM. A higher density map was expected in this study, since from the 2972 molecular markers available, 452 were polymorphic between two parents in one cross and used for genotyping. The polymorphism rate obtained for C. sativa x C. crenata populations (about 15.2%) was higher than polymorphism rate obtained for C. mollissima population used for constructing the reference map (about 12.6%) [11]. This indicates that the markers developed from C. mollissima and C. dentata transcriptomes have a high transferability to the samples of C. sativa and C. crenata, mainly for SSRs. Nevertheless, about 44% of the polymorphic markers were not joined to the obtained LGs and therefore were excluded for map construction. Several issues could explain the number of unmapped markers: 1) low number of individuals per population (74 SxC and 81 BxC); 2) missing values, mainly for SNP data, since only 26 individuals were genotyped; but also for SSR data (34% of the 180 SSR markers were excluded from analysis for presenting more than 25% of missing values); 3) marker distortion and 4) absence of segregating markers in some genomic regions, obviating significant linkages between markers with more distant positions. The last hypothesis, could also explain the observation of four extra LGs relative to the expected number (2n = 24, n = 12) (S1 Fig). Concerning the distorted segregation, it appears to be common in interspecific crosses between woody plants. In this study, unmapped markers showed high distortion, probably because of zygotic compatibility issues, which could explain their exclusion from the consensus map. On the other hand, only 2.7% of the mapped markers showed distortion, which is a lower rate when compared with other studies of inter- or intra-specific crosses in Castanea and another woody species [9,24–26]. Accordingly, in the C. sativa genetic map, 10% of the markers showed distortion, however the molecular markers used in that study were RAPD, ISSR and isoenzymes. Indeed, the consensus genetic map constructed for Quercus spp. with EST-SSRs showed only 0.9 to 6.8% of distorted markers, depending on the populations [23].
P. cinnamomi susceptibility was previously evaluated for each SxC progeny, using diverse and accurate methodologies [7]. Due to the recalcitrance of the species, which imposes limitations for in vitro establishment and stem cuttings propagation, to produce clonal individuals from each progeny, only 16 SxC progenies were able to be phenotyped, using the standard root inoculation test in biological replicates of each genotype. In the present study, lesion progression rate determined in excised shoots inoculated with the pathogen, was used as phenotypic metric for QTL analyses, because: i) we could have several stems from all progenies; ii) lesion progression rates followed a continuous variation, from 0.15 to 1.13 cm/day, depending on the genotype, enabling the analysis of the trait in a quantitative manner and iii) the results from excised shoot inoculation method were strongly and negatively correlated (-0.85, P<0.001) with the days of survival in root inoculation assays, performed for the subset of SxC progeny [7].
Significant QTLs were detected in two LGs of the consensus map: LG_E and LG_K. The P. cinnamomi resistance QTL mapped on LG_E was the strongest in our C. sativa x C. crenata population. Accordingly, P. cinnamomi resistance QTL on LG_E were previously reported in a pilot study using two chestnut backcross families (C. mollissima x C. dentata hybrid) [6], suggesting a potential important role of those genomic regions in P. cinnamomi resistance. Moreover, new QTL analyses were performed for recent backcross families obtained in 2014 by TACF, revealing QTLs for P. cinnamomi resistance again on LG_E and also in LG_K (Tatyana Zhebentyayeva, personal communication). Hence, QTL results obtained for American x Chinese chestnut crosses and European x Japanese chestnut crosses show consistency, indicating that those parents might share resistant haplotypes, located on LG_E and LG_K. These findings suggest common resistance mechanisms to different diseases caused by fungal or fungal-like pathogens across Castanea genus as have been recently suggested by Staton et al. (2015) [27].
The QTLs reported in this study, should provide an extensive list of candidate genes for P. cinnamomi resistance, since the QTL intervals extend to as much as 8 cM. In the future, several resistance candidate genes will be identified in the QTL intervals from chestnut genome (in preparation). Nevertheless, some putative genes underlying the QTLs presented were identified, providing some clues about resistance genes involved in P. cinnamomi response. Presence of putative resistance proteins, cellulose synthase, regulation of gene expression and hormone signaling may be involved in P. cinnamomi resistance, as it has been suggested by previous studies of tree-Phytophthora interactions [28–31]. The strongest evidence that the QTLs identified here underlie resistance candidate genes, corresponds to the mapping of markers associated to resistance proteins (NDR1/HIN1-Like protein 3) [20] and to the mapping of AC_32934_470 and AC_36335_960 markers on LG_E and LG_K, respectively. These SNPs were developed from genes containing Zinc finger and MYB/SANT domains associated to regulation of gene expression under stress responses [32–34]. Therefore, they may be candidates for downstream studies and applications. In this context, the expression level of transcripts belonging to MYB/SANT and Zinc Finger families have been quantified for three progenies and parents of the breeding program [31]. This recent study showed that Myb4 gene (containing a MYB/SANT domain) may be involved in the chestnut resistance mechanism in C. crenata and in hybrid resistant genotypes, by regulating salicylic acid signaling or lignin synthesis in order to avoid pathogen progression [31]. The function of the putative resistance genes underlying the QTLs identified will be confirmed in further research using transcriptomics, proteomics and functional analysis.
Understanding the basic genetic structure of ink disease resistance will increase the accuracy of genomic selection for disease resistance. Since QTL effects vary across environmental and genetic backgrounds, additional populations will be genotyped and phenotyped to validate the QTLs here proposed. Additionally, in the near future, C. sativa x C. crenata populations will also be genotyped using a Genotyping-by-Sequencing (GBS) platform, which will increase the map density and consequently the resolution of QTL mapping. The future availability of the chestnut genome sequence will allow the identification of all genetic elements within each P. cinnamomi resistance QTL.
In summary, the genetic linkage map and QTLs here presented constitute the first effort developed in an interspecific cross between C. sativa and C. crenata to map genomic regions associated with P. cinnamomi resistance and also extend the chestnut genomic resources available. This constitutes a foundation for marker-assisted selection to be applied in the ongoing and future chestnut breeding programs worldwide.
Supporting information
S1 Fig. Four extra LGs obtained for C. sativa x C. crenata interspecific cross.
Marker positions on LGs were assigned to reference map LGs [11], by using the common markers mapped on both genetic maps (in blue).
https://doi.org/10.1371/journal.pone.0184381.s001
(TIF)
Acknowledgments
We acknowledge Lourdes Santos (INIAV) for germination of progeny seeds. Authors acknowledge the funding provided by Centro de Estudos Florestais (CEF), which is a research unit funded by Fundação para a Ciência e Tecnologia I.P. (FCT), Portugal (UID/AGR/00239/2013). We acknowledge Fundação para a Ciência e Tecnologia through the project PTDC/AGR-CFL/101707/2008 and the PhD grant SFRH/BD/85140/2012 and also Programa ProDer, Medida 4.1 Refª 45967 “Developing processes and Technologies aiming the production of ink disease resistant.chestnut rootstocks, compatible with national varieties certified with molecular markers” and Programa ProDer, Medida 4.1 Refª 53593 “Innovation in the production chain of chestnut: competitiveness and sustainability”.
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