Phytophthora erythroseptica Pethyb. is a devastating fungal pathogen of potato (Solanum tuberosum). The pathogen causes a disease known as pink rot. Pink rot results in necrosis and decay of tubers; and is responsible for major losses pre and post harvest. Attributes of the disease are progressing toward epidemic proportions. To help prevent such dramatic outbreaks of the disease, understanding the factors associated with incidence will provide opportunities to control the pathogen. A link between pH and disease severity has been observed. We studied the effects of pH and Ca to determine their influence on disease development. Low pH and Ca deficiencies are often inter-related factors that can be causal of one another. The pH effect could be due to either H+ or Ca ions. To separate their interactive effects we tested each variable individually using hydroponics and nutrient solutions. We assessed disease severity by assigning an Infection Coefficient (IC) to each root and stolon samples. The IC values were determined by quantifying DNA and then creating a ratio of host to pathogen DNA within root tissue. The DNA was measured by quantitative RT PCR. Statistical analysis showed significance in greater pathogen presence at more acidic pH and lower levels of available Ca. Significant reductions in IC values were observed when pH was elevated above pH 7. There was a notable increase in colonizing pathogen DNA at pH 5. Ca was significant, and as levels of soluble Ca increased the degree of disease severity became smaller. The effect of Ca was found not to be dependent upon pH. These results suggest immediate and cost effective applied management strategies to reduce incidence and disease severity outbreaks. Amending the soil with lime to increase soil pH and Ca content is one such potential method.

Pathogen derived resistance (PDR) is a recent breakthrough where plant hosts can be made to be resistant to viral infections through transformation with conserved viral genes. Given the severity of Tospovirus diseases worldwide (particularly in tomato), PDR has the potential to garner large yield returns where pathogen populations have overcome the established resistance. Tomato breeding lines FLA7804, FLA8044, and the research line MP1 were used in transformation experiments with potions of the Tomato spotted wilt virus (TSWV) N-gene, and two other chimerical viral nucleocapsid gene constructs from, Impatiens necrotic spot virus (INSV), and Groundnut ringspot virus (GRSV). We conducted 19 independent transformations consisting of 300 to 700 14-day old whole cotyledons each for a total number of approximately 9,000 potentially transformed explants. Of those, approximately 6,300 explants failed to produce regenerants, 2,419 explants underwent abnormal development on elongation media, 187 failed to root, and 215 plants to be characterized genetically. Of the 215 plants, 9 were from FLA 7804, 96 from FLA 8044, and 110 from MP1. Both PCR and Southern blot hybridization analysis later confirmed that none of the 215 plants were transgenic. Opposite to tomato, we were able to transform Arabidopsis thaliana ecotype wassilewskija (Ws) via floral dip with the above listed constructs demonstrating that constructs were not deleterious within a plant once fully introgressed. Sixteen independent transformants in the T0 generation resulted from 19,000 germinated seed from three dipped plants resulting in a total transformation rate of 0.08%. Of the 1,000 T1 seed germinated on kanamycin media from each of the 16 putative Arabidopsis plants transformed with the construct containing elements of the N-gene from all three of the aforementioned tospoviruses, four populations exhibited simple Mendelian inheritance of the transgene. DNA walking analysis yielded amplification of the unknown region outside the nptII region of the insert for three of the four remaining transformants, which was subsequently sequenced and mapped to chromosomes 1, 3, and 4. There were 25 T1 individuals selected from each population and transferred to soil for DNA extraction and zygosity determination. Homozygous T2 seed was collected for future resistance studies.

The domesticated tomato Solanum lycopersicum (L.), formerly known as Lycopersicon esculentum is a genetically well-studied crop species with high-density linkage and molecular maps based on crosses done between cultivated tomato and its distant related wild species. Wild tomato species harbor a wealth of resistance to many pathogens that have been introgressed into domesticated tomato for genetic control of diseases and pests and for improvement of many agronomic traits. The wild tomato S. peruvianum (L.) is the source of the Sw-5 gene, characterized and mapped to chromosome 9 of the tomato genome and introgressed into elite tomato germplasm, providing resistance to the tospovirus Tomato spotted wilt virus (TSWV). TSWV has been reported to be a major problem for tomato growers in many parts of the world, which in some cases, has resulted in tomato fields having been abandoned for some time. Additionally, there are reports that new races of TSWV have evolved that overcome Sw-5. TSWV replicates in both, plant cells and in the alimentary canal cells of thrips and then transmitted to plants by this insect acting as a vector. Both, TSWV and thrips have co-evolved to infest and infect more than 1090 plants species in over 100 families, thrips becoming resistant to pesticides and easily escaping by hiding deep in plant parts. World trade has disseminated thrips all over the world and environmental pressures have forced TSWV to recombine its RNA to overcome new resistance.

[EN] The knowledge of the key genes which crucially affect the development and stress tolerance of plants is a very important task and indispensable for both, the basic and the applied research. The screening of populations of mutagenized plants permits the identification of mutants and, starting with their analysis, the identification of the genes responsible for a certain trait. Compared to alternative methods (e.g. chemical or physical mutagens) the insertional mutagenesis using T-DNA offers the additional advantage of labeling the altered gene with a piece of known sequence that will facilitate its identification and cloning. On the other hand, the tomato is one of the world¿s economically most important vegetables which over the last few years also gained the status of a model organism for certain traits. In order to identify the relevant genes involved in the response of plants to abiotic stresses and processes related to the vegetative and reproductive development, our laboratory performs in collaboration with Dr. Lozano¿s (University of Almería) and Dr- Bolarín¿s (CEBAS-Murcia) groups a project of insertional mutagenesis in tomato and related wild species, among them Solanum pennellii. The present PhD-thesis is embedded in this context and aims to create a collection of transgenic plants of S. pennellii, design new methods helpful for evaluating the tolerance to salt stress, the identification of traits related to water or salt stress and screen several lines of S. lycopersicum which were pre-selected for showing different aberrations that could be related to the tolerance to abiotic stresses. By tackling these tasks it was possible to obtain the following results. After obtaining more than two thousand diploid transgenic lines of S. pennellii, 887 of them were screened with the different systems developed for detecting mutant plants. Two of the methods designed were based on in vitro culture and one for the short-term evaluation in vivo. With the latter one a total of 68 tomato lines were screened and among them a mutant with alterations in its development which could be interesting for its relation to abiotic stress tolerance identified. In the collection of S. pennellii several plants showing phenotypes with different alterations were detected. Three of them received an advanced examination and it was possible to identify and clone the affected gene in one case. The detected mutants as much as the developed technologies are of great value for deepening the understanding of the processes related to abiotic stress tolerance in a crop with the outstanding importance of the tomato. / [ES] El conocimiento de los genes clave que afectan al desarrollo de las plantas y su tolerancia a estreses abióticos es un aspecto muy importante, tanto desde un punto de vista básico como aplicado. El escrutinio de poblaciones de plantas mutagenizadas permite la identificación de mutantes y, a partir de ellos, conocer los genes responsables de un carácter concreto. Cuando se compara con otras alternativas metodológicas (mutágenos químicos o físicos) la mutagénesis insercional con T-DNA aporta una ventaja adicional, ya que si el gen queda etiquetado por un fragmento de ADN de secuencia conocida su identificación y clonación es más sencilla. Por otro lado, el tomate es una de las especies con mayor importancia económica a nivel mundial que, en los últimos tiempos, se ha considerado también como especie modelo para el estudio de determinados caracteres. Para lograr la identificación de genes clave en la respuesta de las plantas a los estreses de tipo abiótico y en procesos del desarrollo tanto vegetativo como reproductivo, en nuestro laboratorio se está abordando, en colaboración con los grupos del Dr. Lozano (Universidad de Almería) y de la Dra. Bolarín (CEBAS - Murcia), un proyecto de mutagénesis insercional con tomate y especies silvestres relacionadas, entre ellas Solanum pennellii. La tesis doctoral presente se enmarca en este contexto y tiene como objetivos la creación de una colección de plantas transgénicas de S. pennellii, el diseño de nuevos métodos aptos para evaluar la tolerancia al estrés salino, la identificación de caracteres relacionados con el estrés hídrico o salino y el escrutinio de algunas líneas de S. lycopersicum pre-seleccionadas por mostrar diferentes alteraciones que puedan estar relacionadas con la tolerancia a estreses de tipo abiótico. Tras abordar estos objetivos se han obtenido los siguientes resultados. Tras obtener más de dos mil líneas transgénicas diploides de Solanum pennellii se han evaluado 887 líneas con los diferentes sistemas de identificación de mutantes diseñados. Dos de los métodos de evaluación diseñados se basaron en el cultivo in vitro y uno en un sistema de cultivo in vivo a corto plazo. Además, con esta última metodología se evaluaron 68 líneas de tomate entre las que se identificó un mutante de desarrollo de elevado interés por su relación con la tolerancia a estreses abióticos. Entre las líneas de Solanum pennellii analizadas se han identificado fenotipos con distintas alteraciones. En tres de estas líneas se llevó a cabo una evaluación más avanzada llegando a identificar y clonar el gen afectado en una de ellas. Tanto los mutantes identificados como las metodologías desarrolladas son de gran valor para seguir profundizando en los procesos relacionados con la tolerancia a estreses abióticos en una especie tan importante como el tomate. / [CA] El coneixement dels gens clau que afecten al desenvolupament de les plantes i la seua tolerància a estressos abiòtics és un aspecte molt important, des d'un punt de vista bàsic com a aplicat. L'escrutini de poblacions mutagenitzades de plantes permet la identificació de mutants i a partir d'ells conèixer els gens d'un caràcter concret. Quan es compara amb altres alternatives metodològiques (mutàgens físics o químics) la mutagènesi amb T-DNA aporta un avantatge addicional, ja que al tindre el gen un fragment etiquetat pel T-DNA de seqüència coneguda la seua identificació i clonació és més senzilla. D'altra banda, la tomaca és una de las espècies de major importància econòmica a nivell mundial que, en els últims temps, s'ha considerat també una espècie model per a l'estudi de determinats caràcters. Per a aconseguir la identificació de gens clau en la resposta de les plantes a estressos abiòtics i processos de desenvolupament tant vegetatiu com reproductiu, en el nostre laboratori s'està abordant amb col·laboració amb els grups del Dr. Lozano (Universitat d'Almeria) i la Dra. Bolarín (CEBAS-Murcia), un projecte de mutagènesi insercional amb tomaca i espècies silvestres relacionades, entre elles Solanum pennellii. La tesi doctoral s'emmarca en aquest context i té com a objectius la creació d'una col·lecció de plantes transgèniques de Solanum pennellii, el disseny de nous mètodes aptes per a avaluar la tolerància a l'estrès salí, la identificació de caràcters relacionats amb l'estrès hídric i salí, l'escrutini d'algunes línies de S. lycopersicum pre-seleccionades per mostrar diferents alteracions que puguen estar relacionades amb la tolerància a estressos de tipus abiòtic. En abordar estos objectius s'han obtingut els següents resultats. Després d'obtindre més de dos mil línies transgèniques diploides de Solanum pennellii s'han avaluat 821 línies amb els diferents sistemes d'identificació de mutants dissenyats. Dos dels mètodes d'avaluació dissenyats es basaren en el cultiu in vitro i un en un sistema de cultiu in vivo a curt termini. A més, amb aquesta última metodologia s'avaluaren 68 línies de tomaca entre les quals s'identificà un mutant de desenvolupament d'elevat interès per la seua relació amb la tolerància a estressos abiòtics. Entre les línies de Solanum pennellii analitzades s'han identificat fenotipus amb diferents alteracions. En tres d'estes línies es va dura a terme una avaluació més avançada arribant a identificar el gen afectat en una de les línies. Tant els mutants identificats com les metodologies desenvolupades són de gran valor per a seguir aprofundint en els processos relacionats amb la tolerància a estressos abiòtics en una espècie tan important como la tomaca. / Schleicher, P. (2017). Mutagenesis insercional en tomate y Solanum pennellii: Identificación de mutantes en inserción alterados en el desarrollo y la tolerancia a la salinidad [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/81860

Diploid potato populations between a primitive cultivated species, <I>Solanum phureja</I>, and a weedy species, <I>S. chacoense</I>, were used to examine the segregation of microsatellite markers and three traits in backcrosses. Two of the traits, anther culture competence and 2<I>n</I> pollen production, originated from <I>S. phureja</I> whereas the third, leptine production (a specific glycoalkaloid known to convey resistance to the Colorado potato beetle) originated from <I>S. chacoense</I>. Using CP2, a self-incompatible F₁ hybrid originating from a cross between <I>S. chacoense</I> clone 80-1 and <I>S. phureja</I> clone 1-3, three populations were developed: 1-3 x CP2 (PBCp), CP2 x 1-3 (PBCc), and CP2 x 80-1 (CBC). For the microsatellite study, four simple sequence repeat (SSR) primer pairs that amplified fragments within potato sequences found in the GenBank were used to look at segregation ratios in our backcross populations and to eliminate possible spurious genotypes bearing non-parental alleles in these populations. Seventeen spurious genotypes were discarded from PBCp; none was found in PBCc or CBC. Two SSR loci showed skewed segregation in PBCp (favoring transmissnion of the allele originally found in 80-1), PBCc showed normal segregation at all loci, and CBC showed distorted segregation at one locus (revealing a deficiency of homozygotes). In the study of anther culture, three components of ACR were investigated in a preliminary study: 1) embryos produced per anther (EPA), 2) embryo regeneration rate and 3) percentage of monoploids (2<I>n</I>=1<I>x</I>=12) among regenerants. CP2 was intermediate, 80-1 was low, and 1-3 was high for ACR. Only EPA was selected for further characterization in our populations. PBCp (78 genotypes) and CBC (57 genotypes), were characterized for anther culture response ACR/EPA in a series of studies. Nine high and ten low selections were identified in CBC, and ten high and ten low selections were identified in PBCp. EPA selections were used for bulk segregant analysis (BSA) using 214 RAPD primers. Two bands, one amplified by OPQ-10 and another by OPZ-4 were linked in coupling and in repulsion, respectively, to ACR in PBCp. One band amplified by OPW-14 primer was linked in coupling to ACR in CBC. One-way ANOVAs for data from remaining genotypes of the populations verified linkage of the markers to ACR/EPA. For 2n pollen production, a total of 77 PBCp genotypes was characterized; 80-1 produces low % 2<I>n</I> pollen, and 1-3 produces high % 2<I>n</I> pollen. Pollen samples were stained with propidium iodide and examined by flow cytometry. The frequency of 2n pollen varied continuously from 1.7 % to 40.6 % among the 41 genotypes that flowered sufficiently to allow three separate pollen collections. Variation due to the environment was observed where the frequency of 2n pollen appeared greater over a range of genotypes on single collection days. BSA could not be used due to limited population size and a low number of selections at the extremes of the distribution of phenotypes. The continuous variation for 2<I>n</I> pollen production suggests multigenic control of the trait. In the study of leptine content in reciprocal backcross populations, 87 genotypes within PBCp, and 42 genotypes within PBCc were characterized using gas chromatography of leaf samples. CP2 was intermediate, 1-3 had zero, and 80-1 was high for leptine content in the foliage. Leptines were present in low levels in 43 of 87 genotypes in PBCp, indicating simple genetic control. In PBCc, only 7 of 42 genotypes expressed leptines, generally at a higher level than in PBCp, indicating cytoplasmic inheritance. Ten high and ten nil selections within PBCp, and seven high and eight nil selections within PBCc were used for BSA using 214 RAPD primers. Three primers OPQ-2, OPT-16 and OPT-20 amplified bands segregating with high bulks in both populations. These markers were linked in coupling to leptine content in PBCp. Linkage was verified by ANOVAs for leptine content in the entire population. / Ph. D.

Genetic improvement of the potato through classical breeding has been limited by its tetraploid nature, the narrow genetic variability within cultivars, and interploidy barriers between tetraploid cultivars and diploid germplasm. Breeding at reduced ploidy levels has been proposed as a solution to these problems. Because of sterilities, somatic hybridization via protoplast fusion has been considered an alternative to sexual polyploidization for resynthesizing superior diploids from selected monoploids, and tetraploids from selected diploids and dihaploids. Successful application of somatic hybridization largely depends upon protoplast culturability and regenerability of a plant. The ability of callus formation and plant regeneration from protoplasts varies among plants. To understand the genetic basis for this variation, the mode of inheritance for protoplast culturability, defined as the ability to develop calli from cultured protoplasts, was studied in the diploid potato species, Solanum phureja. Based upon data from F₂ as well as from F₁ and backcross progenies, it was found that protoplast culturability in this potato species was controlled by two unlinked loci with dominant effect. In addition, there was quantitative variation for protoplast plating efficiency among culturable genotypes. Male sterility in cultivars of Solanum tuberosum ssp. tuberosum results from nuclear-cytoplasmic interactions. 'Donor-recipient' protoplast fusion and regeneration were conducted between a sterile S. tuberosum ssp. tuberosum cultivar, Russet Burbank, and fertile selections of S. tuberosum ssp. andigena which have a non-sensitive cytoplasm and were used as the cytoplasmic donor. Sixteen regenerated plants possessed nuclear background and chloroplast DNA of Russet Burbank. However, two of these regenerants had improved pollen stainability. The possible causes for the improvement of pollen stainability are discussed. In the last chapter, allelic polymorphism in a monoploid population derived from anther culture of a clone of S. phureja was assessed by isozyme electrophoresis. Fourteen monoploids and their anther donor were examined for six enzymes. No allozyme variation was detected in these plants. However, genetic variability among these monoploids was manifested by variations in some growth characters and general morphology. The limitation of enzymatic markers in detecting allelic polymorphism in these monoploids is discussed. / Ph. D.

Fe biofortification of potato is a promising strategy to prevent Fe deficiency worldwide either through traditional breeding or biotechnological approaches. These approaches require the identification of candidate genes to uptake, transport and store Fe in potato tubers. We employed multiple approaches including SNP genotyping, QTL analysis, identifying genes orthologous to Arabidopsis ferrome, yeast complementation assay and genetic transformation to avoid the limitation from a single approach. We revealed several candidate genes potentially associated with potato plant Fe acquisition, PGSC0003DMG400024976 (metal transporter), PGSC0003DMG400013297 (oligopeptide transporter), PGSC0003DMG400021155 (IRT1) and IRTunannotated (an ortholog to the IRT gene that is not annotated in the potato genome). The microorganisms in the rhizosphere react intensely with the various metabolites released by plant roots in a variety of ways such as positive, negative, and neutral. These interactions can influence the uptake and transport of micronutrients in the plant roots. Therefore, the contribution of soil microorganisms in the rhizosphere to improve Fe supply of plants may play a key role in Fe biofortification, especially under real world field-based soil scenarios. We thus investigated rhizosphere microbial community diversity in Andean potato landraces to understand the role of plant-microbial interaction in potato Fe nutrient cycling. From the analysis of the high-throughput Illumina sequences of 16S and ITS region of ribosomal RNA gene, we found that both potato landraces with low and high Fe content in tubers and a landrace on which low or high Fe content fertilizer was applied to the leaf surface had large impacts on the rhizosphere fungal community composition. Indicator species analysis (ISA) indicated that Operational Taxonomic Units (OTUs) contributing most to these impacts were closely related to Eurotiomycetes and Leotiomycetes in the phylum Ascomycota, Glomeromycetes in the phylum Glomeromycota and Microbotryomycetes in the phylum Basidiomycota. Lots of species from these groups have been shown to regulate plant mineral nutrient cycling. Our research revealed potential candidate genes and fungal taxa involved in the potato plant Fe nutrient dynamics, which provides new insights into crop management and breeding strategies for sustainable Fe fortification in agricultural production. / Ph. D.

The variation for embryo production in anther culture of Solanum phureja was examined as a function of maximum greenhouse temperature prior to bud harvest and innate responsiveness among anthers within a bud. S. phureja clones PP5, AD2-4, A3P2-6 and AD3-4 were grown in a greenhouse under a 16 h photoperiod. The temperature was monitored continuously using a thermograph. Buds were collected from PPS and AD2-4 and the anthers were cultured in two groups of five flasks. In the first group, each flask contained the 30 anthers from 6 buds; the second group, each flask contained 1 anther from each of 30 buds -- a total of 30 anthers per flask. Significantly smaller coefficients of variation were observed for the second group, suggesting that the variation for embryogenic capacity among buds was greater than that among anthers within a bud. Variation in embryo yield as a function of greenhouse temperature for clones A3P2-6 and AD3-4 was examined by stepwise regression analysis. Embryogenic capacity of clone A3P2-6 was adversely affected by high temperatures (31-37°C) that occurred 2 and 7 days before bud harvest. However similarly high temperatures appeared to enhance the androgenic response of clone AD3-4. Regeneration rate of anther-derived embryos over three subcultures to fresh regeneration medium was examined as a function of anther donor or clone, cold pretreatment of embryos, and morphological classification of embryos. Only clonal origin significantly affected regeneration. Regeneration rate declined on each serial subculture. The frequency of regenerable embryos varied from 12.5% for clone BARD 1-3 to 46.0% for clone A3P2-6. Flow cytometric analyses were performed on several anther-derived monoploids of S. phureja to examine the frequency of nuclei at the 1x, 2x, and 4x levels within and among clones. Significant variation was found among duplicate cultures of the individual clones, but this variation was small enough to allow the detection of significant differences among the clones. Monoploid cell frequency ranged from 22.3% to 35.7%. Diploid cell frequency ranged from 48.6% to 59.9%. Tetraploid cell frequency ranged from 11.9% to 25.3%. Several families of anther-derived monoploid clones of S. phureja were analyzed for differences among clones within a family and among families. Significant differences were found in both categories. Finally, unstained protoplasts of monoploid S. phureja clone AM3 were sorted based on forward angle light scatter (FALS) and autofluorescence. Fractions selected for low FALS and weak autofluorescence appeared to be selectively enriched for monoploid protoplasts. / Master of Science

The potential benefits of plant genetic engineering for disease and pest resistance have been widely acknowledged in many studies, and although genetically modified crops are still encountering public wariness, these benefits warrant continued exploration. Because of its intrinsic economic benefits, the development of true potato seed (TPS) cropping systems has been instituted in many regions of the world. The incorporation of transgenic resistance could further the economic gain of farmers who are seeking ways to sustain their livelihood in the most efficient way possible. It is, however, largely unresearched how sexual hybridization of a transgenic crop would affect the behavior of a transgene in the resultant progeny. In the initial part of this study, transgenic lines were developed with a Cry3Aa transgene. These plants were then used in 4x-4x reciprocal crosses and 4x-2x hybridization schemes to determine the stability of the transgene after sexual hybridization. There was no observed parent of origin effect on transgene expression; however, a highly significant, non-mendelian inheritance of the Cry3Aa transgene was seen in the maternally inherited transgene of one set of progeny from a reciprocal cross. Additional transgenic lines of potato were developed with a PVY-O coat protein transgene. These plants were challenged with PVY-O and monitored for symptoms visually and for virus serologically. One transgenic line exhibited complete resistance to PVY-O while two others showed a delay in symptom occurrence. Further examination of the expression levels of the PVY-O coat protein transgene will be necessary to determine the type and usefulness of the observed resistance. / Master of Science

Pour cette étude, dans un premier temps, une caractérisation physico-chimique et rhéologique des amidons natifs de deux cultivars locaux de pomme de terre (Sipiera et Tselefou) et de trois de manioc (2425, 4115 et Seedling) a été faite avant leur incorporation dans du pâté de bœuf à 20, 30, 40 et 50g/kg de mêlée. L’influence du type d’amidon et de leur taux d’incorporation sur les propriétés physico-chimiques et texturales des pâtés a été évaluée. Les résultats ont montré que les propriétés physiques, fonctionnelles et rhéologiques des amidons sont étroitement liées à leur origine botanique. L’Analyse en Composantes Principales (ACP) laisse paraître que de tous les amidons natifs, celui du cultivar de pomme de terre Sipiera se rapproche le plus du témoin. Une fois incorporé dans les pâtés ; l’ACP de tous les paramètres texturaux des pâtés aux amidons natifs indique que le pâté à l’amidon du cultivar de manioc Seedling à de 40g/kg de mêlée (PS40), est celui qui se rapproche le plus du pâté témoin. Dans un deuxième temps, les amidons de pomme de terre (Sipiera) et de manioc (2425) ont été sélectionnés pour la modification (acétylation). Ces amidons acétylés ont par la suite fait l’objet des mêmes analyses que les amidons natifs et incorporés dans les pâtés aux mêmes taux que les amidons natifs. Des résultats, il ressort que les propriétés fonctionnelles des amidons natifs sont fortement influencées par l’acétylation et le temps d’acétylation. Les essais d’incorporation des amidons acétylés dans les pâtés montrent que l’amidon Sipiera/20 à un taux d’incorporation de 40g/kg de mêlée ne se distingue pas significativement (p>0,05) du pâté témoin / The first part of this work deals with the physico-chemical and rheological characterisation of native starches of two local cultivars of Irish potatoes (Sipiera and Tselefou) and three cultivars of cassava (2425, 4115 and Seedling) before they are incorporated into beef patty at 20, 30, 40 and 50g/kg ground meat. The influence of the type of starch and the amount of incorporation on the physico-chemical and textural properties of patties was evaluated. Results show that the physical, functional and rheological properties of starches are closely related to their botanical origin. Principal Component Analysis (PCA) showed that Irish potato cultivar Sipiera had properties that were close to reference. The PCA of all the textural properties of patties with native starches show that patty from starch of cassava cultivar Seedling at 40g/kg (PS40) was closest to the reference. In the second part of the work, the starch Sipiera and 2425 were selected for modification. These two starches were then acetylated for 10 and 20min. and this permitted us to have Sipiera/10, Sipiera/20, 2425/10 and 2425/20. The functional properties of the native starches were however strongly influenced by acetylation and the time of acetylation. Incorporation trials of this acetylated starches at different amounts in patty showed that Sipiera/20 starch at an incorporation rate of 40g/kg ground meat is not significantly different from the reference patty