Made available in DSpace on 2016-01-26T18:56:33Z (GMT). No. of bitstreams: 1 ANA CLAUDIA AMBIEL_Dissertacao Agro.pdf: 1588101 bytes, checksum: 47a54fc705f03fc7d27cd4e4abfdb183 (MD5) Previous issue date: 2007-07-18 / The aim of this work was the determination of intra and intergenetic similarity between three Brachiaria species among germplasm accesses and commercial materials throughout RAPD markers. Seeds were used as DNA source. 10 decamers primers were selected between 120 primers assayed and 107 polymorphic bands were used to perform the molecular variance analysis (AMOVA), Jaccard similarity and species fixation index. 24.4% of the total variability was contained between species and 75.6% inside the species, with a species fixation index (FST) of 0.24. The tree showed that two major branches were formed, one with the three outgroup species and other with the species, this one split in three minor branches one with all B. ruziziensis samples; other with all B. decumbens accessions and three of B. brizantha and the last with two B. brizantha accesses, all commercial cultivars and B. decumbens cv. Basilisk . It was possible to group, throughout RAPD, Brachiaria accesses and cultivars. The genetic variability index between species was considered low and somehow low when faced with autogamous species. B.brizantha showed the highest genetic variability and the lowest FST what means that there is a higher genetic flux intra specific than the others. / O propósito deste trabalho foi determinar a similaridade genética de entre acessos de germoplasma e cultivares comerciais três espécies de Brachiaria (inter e intraespecífica), através de marcadores RAPD. Sementes foram utilizadas como fonte de DNA. 10 primers decâmeros foram selecionados de 120 primers avaliados, produzindo 107 bandas polimórficas, as quais foram utilizados para a análise de variância molecular (AMOVA), o coeficiente de similaridade de Jaccard e índices de fixação gênica. 24,40% da variabilidade genética total está contida entre as espécies e 75,60% dentro destas, com índice de fixação gênica (FST) 0,24. No dendrograma houve a formação de dois ramos, um formado por P. maximum e B. arrecta e o outro subdividido em três: todas amostras de B. ruziziensis; todos os acessos de B. decumbens e três acessos de B. brizantha e o último com dois acessos de B. brizantha mais as B. brizantha comerciais e a B. decumbens cv Basilisk . Foi possível agrupar os acessos e cultivares de Brachiaria através de RAPD. O índice de variabilidade genética entre espécies foi considerado baixo, sendo inferior a valores determinados em algumas espécies autógamas. B. brizantha apresenta maior variabilidade genética e menor FST indicando maior fluxo gênico intra-específico do que as outras.

Made available in DSpace on 2016-07-18T17:51:14Z (GMT). No. of bitstreams: 1 ANA CLAUDIA AMBIEL_Dissertacao Agro.pdf: 1588101 bytes, checksum: 47a54fc705f03fc7d27cd4e4abfdb183 (MD5) Previous issue date: 2007-07-18 / The aim of this work was the determination of intra and intergenetic similarity between three Brachiaria species among germplasm accesses and commercial materials throughout RAPD markers. Seeds were used as DNA source. 10 decamers primers were selected between 120 primers assayed and 107 polymorphic bands were used to perform the molecular variance analysis (AMOVA), Jaccard similarity and species fixation index. 24.4% of the total variability was contained between species and 75.6% inside the species, with a species fixation index (FST) of 0.24. The tree showed that two major branches were formed, one with the three outgroup species and other with the species, this one split in three minor branches one with all B. ruziziensis samples; other with all B. decumbens accessions and three of B. brizantha and the last with two B. brizantha accesses, all commercial cultivars and B. decumbens cv. Basilisk . It was possible to group, throughout RAPD, Brachiaria accesses and cultivars. The genetic variability index between species was considered low and somehow low when faced with autogamous species. B.brizantha showed the highest genetic variability and the lowest FST what means that there is a higher genetic flux intra specific than the others. / O propósito deste trabalho foi determinar a similaridade genética de entre acessos de germoplasma e cultivares comerciais três espécies de Brachiaria (inter e intraespecífica), através de marcadores RAPD. Sementes foram utilizadas como fonte de DNA. 10 primers decâmeros foram selecionados de 120 primers avaliados, produzindo 107 bandas polimórficas, as quais foram utilizados para a análise de variância molecular (AMOVA), o coeficiente de similaridade de Jaccard e índices de fixação gênica. 24,40% da variabilidade genética total está contida entre as espécies e 75,60% dentro destas, com índice de fixação gênica (FST) 0,24. No dendrograma houve a formação de dois ramos, um formado por P. maximum e B. arrecta e o outro subdividido em três: todas amostras de B. ruziziensis; todos os acessos de B. decumbens e três acessos de B. brizantha e o último com dois acessos de B. brizantha mais as B. brizantha comerciais e a B. decumbens cv Basilisk . Foi possível agrupar os acessos e cultivares de Brachiaria através de RAPD. O índice de variabilidade genética entre espécies foi considerado baixo, sendo inferior a valores determinados em algumas espécies autógamas. B. brizantha apresenta maior variabilidade genética e menor FST indicando maior fluxo gênico intra-específico do que as outras.

O vírus respiratório sincicial humano (HRSV) é o principal agente viral causador de doença respiratória em bebês e crianças em idade pré-escolar. A fim de estudar a variabilidade genética de HRSV, grupo B, com inserção de 60 nucleotídeos no gene G, selecionamos amostras de aspirado de nasofaringe de crianças menores de 5 anos de idade, com doença respiratória aguda, admitidas no hospital universitário da Universidade de São Paulo. Testamos 521 amostras, das quais 35,3% foram positivas para HRSV. A região G2 da glicoproteína G foi utilizada para genotipar essas amostras. Todas as amostras do grupo B apresentaram a inserção de 60 nucleotídeos no gene da proteína G, como descrito anteriormente em Buenos Aires, em 1999. As modificações de aminoácidos e nucleotídeos dessas amostras foram comparadas com outras amostras com inserção de 2001-2005. A seqüência de nucleotídeos duplicados foi a cópia exata dos 60 nucleotídeos precedentes em vírus mais antigos, mas as cópias do segmento duplicado acumularam substituições de nucleotídeos em vírus mais recentes. / Human respiratory syncytial virus (HRSV) is the leading viral cause of respiratory illness in infants and young children. In order to study the genetic variability of HRSV group B, with 60-nucleotide duplication in the gene G, we selected nasopharyngeal aspirates samples of children less than five years of age, with acute respiratory illness admitted in the university hospital of São Paulo (USP). We tested 521 samples and the HRSV-detection test positivity rate was 35.3%. The G2 region of glycoprotein G was used as genotyping default. All type B HRSV had a 60-nucleotide duplication in the attachment protein gene like previously described in Buenos Aires, in 1999. Changes in aminoacids and nucleotides in these samples were compaired with other samples with duplication from 2001-2005. The duplicated nucleotide sequence was an exact copy of the preceding 60 nucleotides in early viruses, but copies of the duplicated segment accumulated nucleotide substituions in more recent viruses.

Contexte : Les infections respiratoires aiguës (ARI) sont reconnues comme une cause importante de morbidité, de mortalité et d'hospitalisation chez les enfants dans les pays en développement. Le virus respiratoire syncytial humain (HRSV) est l’agent étiologique principal de maladie sévère des voies respiratoires basses chez les nourrissons, les jeunes enfants et les personnes âgées. Identifié en 2001, le Metapneumovirus humain (HMPV) est un nouveau paramyxovirus. Les études ont montré la cocirculation des sous groupes de ces deux virus avec la domination de l’un des sous groupes selon les zones géographiques et selon les années. Les données restent cependant limitées dans les pays de l’Afrique subsaharienne, sur la prévalence, la saisonnalité et la caractérisation génétique de ces deux virus respiratoires. Au Cameroun, ces deux virus ont été décrits seulement une seule fois (5,7 et 5% pour HRSV et HMPV respectivement) chez des patients présentant des syndromes grippaux en 2012. Objectif : Cette étude rapporte la prévalence, la saisonnalité et la variabilité génétique des souches HRSV et HMPV chez des enfants camerounais pendant 3 saisons épidémiques consécutives (de Septembre 2011 à Octobre 2014). Par ailleurs, la diversité génétique d’autres virus respiratoires détectés au cours de ce travail est présentée comme objectif secondaire.Méthodes : Une surveillance prospective a été menée pour identifier les enfants hospitalisés et ambulatoires âgés de moins de 15 ans présentant des symptômes respiratoires ≤ 5 jours. Les échantillons nasopharyngés ont été testés pour 17 virus respiratoires en utilisant une réaction multiplex de polymérisation en chaîne. La distribution virale et les données démographiques ont été analysées statistiquement. Les échantillons positifs du HRSV et HMPV ont été amplifiés par polymérisation en chaine semi nichée puis séquencés partiellement au niveau du gène G. Des analyses phylogénétiques ont été effectuées sur les séquences nucléotidiques et protéiques partielles du gène G.Résultats : De septembre 2011 à octobre 2014, 822 enfants âgés de moins de 15 ans ont été inscrits dans l’étude. Au moins un virus a été identifié chez chacun des 72,6% (597/822) d'enfants, dont 31,7% (189/597) étaient des codétections; 28,5% (226/822) étaient positifs pour l'adénovirus humain, 21,4% (176/822) pour le virus Influenza, 15,5% (127.822) pour le rhinovirus/entérovirus, 9,4% (77/822) pour le bocavirus, 9% (74/822) pour le HRSV, 8,2% (67/822) pour les coronavirus humain, 6,2% (50/822) pour le parainfluenzavirus humain et 3,9% (32/822) pour le HMPV. L’infection HRSV était plus fréquente chez les enfants de moins de 2 ans (70,3% ; 52/74) et chez les participants hospitalisés (70,3% ; 52/74). Alors que le HRSV a montré un profil saisonnier avec une circulation de septembre à décembre, des cas sporadiques de HMPV ont été détectés tout au long de l'année. HRSV-A (19,1%, 9/47) et HRSV-B (17% ; 8/47) ont été observés relativement à la même fréquence avec (63,8% ; 30/47) de cas en codétection HRSV-A/HRSV-B alors que HMPV-A (71,4% ; 10/14) était majoritaire comparé à HMPV-B (28,6 ; 4/14). L'analyse phylogénétique a révélé que les souches HRSV de l’étude sont groupées au sein du sous groupe NA-1 (pour HRSV-A) et BA-9 (pour HRSV-B). Les souches HMPV camerounaises sont groupés parmi les membres du génotype A2b (pour HMPV-A), B1 et B2 (pour HMPV-B).Conclusion : Cette étude suggère qu’environ 70% des ARI enregistrés chez des enfants au Cameroun sont causés par des virus. La présente étude est également le premier rapport sur la variabilité génétique du gène G des souches de HRSV et HMPV dans la région. Bien que ce travail comble partiellement certaines lacunes d’informations, des études supplémentaires sont requises pour une clarification de l’épidémiologie moléculaire et du mode d’évolution des virus respiratoires présents en Afrique subsaharienne en général et plus singulièrement au Cameroun. / Background: Acute respiratory infections (ARI) are recognized as an important cause of morbidity, mortality and hospitalization among children in developing countries. Human respiratory syncytial virus (HRSV) is the main cause of severe lower respiratory tract disease in infants, young children and the elderly. Identified in 2001, Human Metapneumovirus (HMPV) is a new paramyxovirus. Studies have shown the co-circulation of the subgroups of these two viruses with domination of one of the sub-groups according to the geographical zones and according of years. These two viruses encode two major surface glycoproteins, the highly conserved fusion F protein and the highly variable attachment G protein. Data are still limited in sub-Saharan African countries on prevalence, seasonality and genetic characterization of these two respiratory viruses. In Cameroon, these two viruses have been described only once (5.7 and 5% for HRSV and HMPV respectively) in patients with influenza-like illness in 2012.Objective: This study reports the prevalence, seasonality and the genetic variability of HRSV and HMPV strains in Cameroonian children for 3 consecutive epidemic seasons (September 2011-October 2014). Moreover, the genetic diversity of other respiratory viruses detected during this work is presented as a secondary objective.Methods: A prospective surveillance was conducted to identify inpatient and outpatient children less than 15 years with respiratory symptoms ≤ 5 days. The nasopharyngeal samples were tested for 17 respiratory viruses using a multiplex polymerase chain reaction. Viral distribution and demographic data were analyzed statistically. Positive samples for HRSV and HMPV were amplified by semi-nested polymerize chain reaction and then partially sequenced at the G gene. Phylogenetic analyzes were performed on the partial nucleotide and protein sequences of the G gene.Results: From September 2011 to October 2014, 822 children under 15 years were enrolled in the study. At least one virus was identified in each of 72.6% (577/822) of children, 31.7% (189/597) of whom were co-detections; 28.5% (226/822) were positive for human adenovirus, 21.4% (176/822) for influenza virus, 15.5% (127.822) for rhinovirus/enterovirus, 9.4% (77/822) for bocavirus, 9% (74/822) for HRSV, 8.2% (67/822) for human coronavirus, 6.2% (50/822) for human parainfluenzavirus, and 3.9% (32/822) for HMPV. HRSV infection was more frequent in children under 2 years (70.3%, 52/74) and hospitalized participants (70.3%, 52/74). While HRSV showed a seasonal pattern with circulation from September to December, sporadic cases of HMPV were detected throughout the year. HRSV-A (19.1%, 9/47) and HRSV-B (17%; 8/47) were observed relatively at the same frequency with (63.8%, 30/47) codetections of HRSV-A/HRSV-B. HMPV-A (71.4%; 10/14) was predominant compared to HMPV-B (28.6; 4/14). Phylogenetic analysis revealed that the HRSV strains of the study are grouped within subgroup NA-1 (for HRSV-A) and BA-9 (for HRSV-B). Cameroonian HMPV strains are grouped among the members of genotype A2b (for HMPV-A), B1 and B2 (for HMPV-B).Conclusion: This study suggests that about 70% of ARI recorded in children in Cameroon are caused by viruses. The present study is also the first report on the genetic variability of the G gene of HRSV and HMPV strains in the region. Although this work partially fills gaps for some information, additional studies are required to clarify the molecular epidemiology and evolutionary pattern of respiratory viruses in sub-Saharan Africa in general and more particularly in Cameroon.

Boreal forests are often strongly nitrogen (N) limited. However, human activities are leading to increased N inputs into these ecosystems, through atmospheric N deposition and forest fertilization. N input into boreal forests can promote net primary productivity, increase herbivore and pathogen damage, and shift plant species composition and community structure. Genetic diversity has been suggested as a key mechanism to promote a plant species’ stability within communities in response to environmental change. Within any plant population, specific traits (e.g. growth and defense traits) can vary substantially among individuals, and a greater variation in traits may increase chances for the persistence of at least some individuals of a population, when environmental conditions change. One aspect of plant chemistry that can greatly vary among different genotypes (GTs) are condensed tannin (CTs). These secondary metabolites have been suggested to affect plant performance in many ways, e.g. through influencing plant growth, the interactions of plants with herbivores and pathogens, and through affecting litter decomposition, and hence the return of nutrients to plants. To investigate how genotypic variation in foliar CT production may mediate the effects that anthropogenic N enrichment can have on plant performance and litter decomposition, I performed a series of experiments. For these experiments, aspen (Populus tremula) GTs with contrasting abilities to produce foliar CTs (i.e. low- vs. high-tannin producers) were grown under 3 N conditions, representing ambient N (+0 kg ha-1), upper level atmospheric N deposition (+15 kg ha-1), and forest fertilization rates (+150 kg ha-1). This general experimental set-up was once established in a field-like environment, from which natural enemies were excluded, and once in a field, in which enemies were present. In my first two studies, I investigated tissue chemistry and plant performance in both environments. I observed that foliar CT levels decreased in response to N in the enemy‑free environment (study I), but increased with added N when enemies were present (study II). These opposing responses to N may be explained by differences in soil N availability in the two environments, or by induction of CTs after enemy attack. Enemy damage generally increased in response to N, and was higher in low-tannin than in high-tannin plants across all N levels. Plant growth of high‑tannin plants was restricted under ambient and low N conditions, probably due to a trade-off between growth and defense. This growth constraint for high‑tannin plants was weakened, when high amounts of N were added (study I and II), and when enemy levels were sufficiently high, so that benefits gained through defense could outweigh the costs of defense production (study II). Despite those general responses of low- and high‑tannin producers to added N, I also observed a number of individual responses of GTs to N addition, which in some case were not connected to the intrinsic ability of the GTs to produce foliar CTs. In study III, gene expression levels in young leaves and phenolic pools of the plants that were grown in the enemy‑free environment were studied. This study revealed that gene control over the regulation of the phenylpropanoid pathway (PPP) was distributed across the entire pathway. Moreover, PPP gene expression was higher in high-tannin GTs than in low‑tannin GTs, particularly under ambient N. At the low N level, gene expressions declined for both low- and high-tannin producers, whereas at the high N level expression at the beginning and the end of the PPP was upregulated and difference between tannin groups disappeared. Furthermore, this study showed that phenolic pools were frequently uncorrelated, and that phenolic pools were only to some extent related to tannin production and gene expression. In study IV, I investigated the decomposability of litter from the field plants. I found that N enrichment generally decreased mass loss, but there was substantial genetic variation in decomposition rates, and GTs were differentially responsive to added N. Study IV further showed that CTs only had a weak effect on decomposition, and other traits, such as specific leaf area and the lignin:N ratio, could better explain genotypic difference in mass loss. Furthermore, N addition caused a shift in which traits most strongly influenced decomposition rates. Collectively, the result of these studies highlight the importance of genetic diversity to promote the stability of species in environments that experience anthropogenic change. / Boreala skogar är ofta mycket kväve (N) begränsade. Men mänskliga aktiviteter leder till ökad N tillförsel i dessa ekosystem, både genom depostition av N från atmosfären och skogsgödsling. N-tillförsel i boreala skogar kan främja netto primärproduktionen men även leda till ökade skador från naturliga fiender (herbivorer och patogener) samt skiftningar i växtartsammansättning. Genetisk mångfald har föreslagits som en viktig mekanism för att främja en växtarts stabilitet inom samhällen som upplever miljöförändringar. Inom varje växtpopulation kan specifika egenskaper (t.ex. tillväxt och försvar) varierar kraftigt mellan individer och en större variation i egenskaper kan öka chanserna för att åtminstone några individer från en population överlever ifall miljöförhållandena förändras. En aspekt av växtkemi som i hög grad kan variera mellan olika genotyper (GT) är bladens kondenserade tanniner (KT). Dessa sekundära metaboliter har föreslagits påverka växtens prestationsförmåga på många sätt, t.ex. genom att påverka tillväxt, interaktioner mellan växter och herbivorer eller patogener och genom att påverka förna nedbrytning, och följaktligen återbördandet av näringsämnen till kretsloppet. För att undersöka hur genotypiska variation i KT produktion kan påverka de effekter som antopogent N kan ha på växtens prestationsförmåga och förna nedbrytning, utförde jag en serie experiment. Jag studerade olika asp (Populus tremula) GT med olika förmåga att producera KT (låg- och hög-tannin producenter). Växterna odlades i tre olika N förhållanden, som representerade ambient N nivå (+0 kg ha-1), atmosfärisk N deposition = låg nivå (+15 kg ha-1), och skogsgödsling = hög nivå (150 kg ha‑1). Dessa GT etablerades i en fält-liknande miljö där naturliga fiender uteslutits och i ett fält där naturliga fiender var närvarande. I mina första två studierna undersökte jag vävnadskemi och växternas prestationsförmåga i de båda miljöerna. Jag observerade att KT nivåerna sjönk till följd av N‑tillsats i den fiende-fria miljön (studie I), men ökade med N-tillsats ifall fiender var närvarande (studie II). Dessa motsatta reaktioner på N-tillsats kan förklaras av skillnader i N-tillgång mellan de två odlingsplatserna eller genom ökad KT produktion som respons på angrepp. Skador orsakade av herbivorer och patogener ökade generellt till följd av N‑tillsats och var högre i låg-tannin än i hög‑tannin producerande GT oavsett N‑förhållande. Tillväxten hos växter från hög‑tannin GT begränsades i ambient- och låg N-tillsats förhållanden, troligen på grund av att avvägning mellan tillväxt och försvar förskjutits emot försvar. Den begränsade tillväxten i hög-tannin växter minskade om stora mängder N tillsattes (studie I och II) och om antalet fiender var tillräckligt högt så att nyttan av försvaret kunde uppväga kostnaderna för försvarsproduktionen (studie II). Trots dessa generella respons hos låg- och hög-tannin GT till följd av N‑tillsats observerade jag även ett antal individuella respons hos GT som i vissa fall var orelaterade till växters förmåga att producera KT. I studie III undersöktes genuttrycksnivåer och fenolinnehåll i blad från växter som odladats i en miljö där naturliga fiender exkluderats. Denna studie visade att fenylpropanoidsyntesvägen (FPV) regleras genom kontroll av många av de undersökta FPV-generna. Dessutom var FPV genuttryck högre i hög-tannin GT än i låg-tannin GT, särskilt vid ambient N. Vid låg N-tillsats minskade genuttrycket av FPV-gener i både låg- och hög-tannin producenter, medan hög N-tillgång ledde till att gener i början och slutet av FPV uppreglerades och till att skillnaderna mellan tannin grupperna försvann. Dessutom visade studien att de separata fenol-poolerna ofta var okorrelerade med varandra och att fenol-poolerna bara till viss del var korrelerade med KT produktion och FPV-genutryck. I studie IV undersökte jag nedbrytningshastigheten för förnan från fältodlade aspar. Jag upptäckte att N-tillsats generellt minskade viktförlusten men att det fanns en betydande genetisk variation mellan GT och att dessa även var olika mottagliga för tillsatt N. Studie IV visade vidare att KT endast hade en svag effekt på nedbrytning och att andra egenskaper såsom specifik bladyta och lignin:N ratio kunde bättre förklara den genotypiska skillnaden i viktförlust. Dessutom orsakade N‑tillsats en förskjutning av vilka egenskaper som mest påverkade förnans nedbrytningshastighet. Sammanfattningsvis visar mina studier på vikten av genetisk mångfald för att främja växtartens stabilitet i miljöer som upplever antropogena förändringar.

Ce mémoire analyse l’espérance du temps de fixation conditionnellement à ce qu’elle se produise et la probabilité de fixation d’un nouvel allèle mutant dans des populations soumises à différents phénomènes biologiques en uti- lisant l’approche des processus ancestraux. Tout d’abord, l’article de Tajima (1990) est analysé et les différentes preuves y étant manquantes ou incomplètes sont détaillées, dans le but de se familiariser avec les calculs du temps de fixa- tion. L’étude de cet article permet aussi de démontrer l’importance du temps de fixation sur certains phénomènes biologiques. Par la suite, l’effet de la sé- lection naturelle est introduit au modèle. L’article de Mano (2009) cite un ré- sultat intéressant quant à l’espérance du temps de fixation conditionnellement à ce que celle-ci survienne qui utilise une approximation par un processus de diffusion. Une nouvelle méthode utilisant le processus ancestral est présentée afin d’arriver à une bonne approximation de ce résultat. Des simulations sont faites afin de vérifier l’exactitude de la nouvelle approche. Finalement, un mo- dèle soumis à la conversion génique est analysé, puisque ce phénomène, en présence de biais, a un effet similaire à celui de la sélection. Nous obtenons finalement un résultat analytique pour la probabilité de fixation d’un nouveau mutant dans la population. Enfin, des simulations sont faites afin de détermi- nerlaprobabilitédefixationainsiqueletempsdefixationconditionnellorsque les taux sont trop grands pour pouvoir les calculer analytiquement. / The expected time for fixation given its occurrence, and the probability of fixa- tion of a new mutant allele in populations subject to various biological phe- nomena are analyzed using the approach of the ancestral process. First, the paper of Tajima (1990) is analyzed, and the missing or incomplete proofs are fully worked out in this Master thesis in order to familiarize ourselves with calculations of fixation times. Our study of Tajima’s paper helps to show the importance of the fixation time in some biological phenomena. Thereafter, we extend the work of Tajima (1990) by introducing the effect of natural selec- tion in the model. Using a diffusion approximation, the work of Mano (2009) provides an interesting result about the expected time of fixation given its oc- currence. We derived an alternative method that uses an ancestral process that approximates well Mani’s result. Simulations are made to verify the accuracy ofthenewapproach.Finally,onemodelsubjecttogeneconversionisanalyzed, since this phenomenon, in the presence of bias, has a similar effect as selection. We deduce an analytical result for the probability of fixation of a new mutant in the population. Finally, simulations are made to determine the probability of fixation and the time of fixation given its occurrence when rates are too large to be calculated analytically.

L’optimisation de la biomasse produite par les taillis à courte rotation de peupliers représente un enjeu majeur pour la production de biocarburants de deuxième génération. Dans ce contexte, ce travail vise à faciliter le développement à court terme de nouvelles variétés clonales de peuplier permettant la production d’une ressource de qualité en s’intéressant plus particulièrement à l’architecture génétique de la résistance à la rouille foliaire et de la qualité du bois chez le peuplier noir (Populus nigra), espèce parente des hybrides cultivés. Des marqueurs SNP ont été développés à partir du séquençage de 665 fragments de gènes dans un panel de 21 individus. Ces derniers ont été associés à des marqueurs SSR et AFLP pour construire de nouvelles cartes génétiques sur une famille de 324 plein-frères clonés. Une technique de phénotypage à haut débit basée sur la spectrométrie à proche infrarouge a été développée pour prédire les teneurs en composés chimiques du bois ainsi que le rendement en saccharification. La mise en évidence d’une variabilité génétique importante pour l’ensemble des caractères a permis de cartographier les régions génomiques impliquées dans leur variation. Parmi les 11 QTL détectés pour la résistance, un QTL à effet majeur co-localise avec un QTL majeur associé à la résistance à la rouille foliaire du saule. Pour la qualité du bois, 15 QTL à effet faible à moyen ont été détectés, dont un cartographié sur le chromosome XIII qui colocalise avec des QTL précédemment identifiés chez le peuplier pour les teneurs en sucres et en lignines. Ce travail de thèse ouvre des perspectives d’identification de gènes sous-jacents aux QTL par génétique d’association. / Improvement of lignocellulosic resources from poplar short rotation coppices is a major challenge for the production of second generation biofuels. In this context, the present work aims at optimizing short term creation and deployment of improved poplar clonal varieties through the dissection of genetic control of both leaf rust resistance and wood quality in black poplar (Populus nigra), one of the parental species of cultivated hybrids. SNP markers have been developed from the resequencing of 665 gene fragments in a discovery panel of 21 individuals. These markers were combined with SSRs and AFLPs to build new genetic maps in a pedigree composed of 324 cloned full-sibs. High throughput phenotyping based on near infrared spectroscopy has been used to predict wood chemical contents and saccharification yield. High genetic variability expressed in all traits allowed the identification of genomic regions controlling this variation. Of the 11 QTL mapped for resistance, one major QTL co-localized with a major QTL previously detected for leaf rust resistance in willow. For wood quality, 15 QTL with low to moderate effect have been identified. Interestingly, one QTL mapped on chromosome XIII and colocalized with sugar and lignin contents QTL previously detected in poplar. Present results open perspectives towards the identification of candidate genes underlying the detected QTL through association genetics.

La santé du constitue une préoccupation croissante pour les éleveurs, propriétaires, et le grand public, plusieurs rapports ayant récemment souligné les potentiels impacts négatifs des pratiques d'élevage sur la santé des chiens de race (APGAW 2009, Nicholas 2011), au travers de la diffusion d’affections héréditaires par exemple. Ainsi, l’OFA (Orthopedic Foundation for Animals, http://www.offa.org) considère que la dysplasie de la hanche affecte au moins 163 races de chiens, avec des prévalences allant de 1,2 à 72,1%. La mise en œuvre de stratégie d'élevage afin de réduire l'incidence des maladies héréditaires et leur impact sur le bien-être constitue une priorité pour les éleveurs et les organisations d'élevage. L'efficacité de ces stratégies dépend toutefois fortement de facteurs tels que leur déterminisme génétique, la disponibilité de diagnostics cliniques ou génétiques efficaces, ainsi que les conditions spécifiques au contexte (la prévalence, la démographie, l'existence d'autres affections, la coopération des éleveurs ...). Par exemple, il a été montré que pour une maladie monogénique récessive, à fréquence égale, l'impact d’une stratégie sur la variabilité génétique sera extrêmement différent en fonction de la race (Leroy et Rognon 2012). Il est important de souligner également que le contexte et le cadre réglementaire de l'élevage varient beaucoup en fonction des pays. A titre d'exemple, en Suède, la proportion importante d'animaux de compagnie assurés (environ 50%) permet la mise en place d’enquêtes sur la santé des chiens à grande échelle (Bonnett et al., 2005), facilitant l'identification des affections impactant le bien-être. En fonction des pays, des mesures différentes de luttes contre les affections héréditaires ont pu être mises en place, pouvant aller de l’incitation à utiliser des reproducteurs sains, à l’interdiction de reproduction pour des individus atteints d’affection problématiques. Dans le cas de dysplasie de la hanche, un système d'évaluation génétique a été mis en œuvre dans certains pays (Allemagne, Suède, Royaume-Uni) pour quelques races, alors que dans certains autres pays, il est encore en cours de développement. Notons qu’un projet préliminaire à la thèse sera mise en place à l’échelle des kennels clubs nordiques (KNU) pour s’intéresser à la valeur ajoutée des échanges internationaux de données généalogiques et de santé. / Dog health constitutes a major concern for breeders, owners, as well as the general public, all the more since several study and reports have recently underlined potential impacts of breeding practices on dog health and fitness (APGAW 2009, Nicholas 2011). According to Online Mendelian Inheritance in Animals (OMIA, omia.angis.org.au) more than 586 disorders/traits have been reported in dogs, with various prevalence and consequences for canine health (Collins et al. 2011, Nicholas et al. 2011). As an exemple, Orthopedic Foundation for Animals (OFA 2011, http://www.offa.org) consider that Hip Dysplasia, a polygenetic trait affected by environmental factors, with variable impact on welfare, affects at least 163 dog breeds, with prevalence ranging from 1.2 to 72.1%. Implementation of breeding plans in order to reduce incidence of inherited disorders and their impact on welfare should be a priority for breeders and breeding organizations. Efficiency of such strategies is however highly dependant on several factors such as inheritance pattern, availability of efficient clinical/genetic test, and specific context conditions (prevalence, demography, existence of other disorders, cooperation of breeders…). For instance, it has been showed that for a monogenic recessive disorder with the same frequency, impact of a given strategy on genetic diversity will be completely different depending on the breed (Leroy and Rognon 2012). It is also important to underline that breeding context and breeding rules are very different according to countries. As an exemple, in Sweden the large proportion of pets insured (about 50%) allows the settlement of large surveys on dog health (Bonnett et al. 2005), leading to the identification of disorders critical to breed welfare. Depending on countries, the control of inherited disorders is implemented through various measures, from breeding recommandations to mating ban. In the case of hip dysplasia, a genetic evaluation system has been implemented in some countries (Germany, Sweden, UK) for a few breeds, while in some other countries, it is still under development. The fact that for many breeds there is an exchange of breeding animals between several countries with different breeding policies constitutes also a critical point to be taken into account, when settling a breeding strategy. Moreover it has been showed that efficiency of genetic evaluation for a polygenic trait such a hip dysplasia could be improved by joint evaluation between different countries (Fikse et al. 2012). For this purpose, a preliminary project, starting 2013 in Sweden, will investigate the interest of exchanging pedigree and health data within the framework of Nordic Kennel Union. The aim of this project is to provide operational tools to improve breed health in an international context, concerning both genetic evaluation and implementation of breeding policies.

Este trabalho está inserido no programa de melhoramento genético de Capsicum da Embrapa Hortaliças. Teve como principal objetivo investigar a base genética e a variabilidade de uma população segregante de Capsicum em relação à pungência e a alguns caracteres do fruto para, fornecer informações úteis ao programa. Os genótipos utilizados compreenderam dois genitores homozigóticos contrastantes para o caráter principal, a pungência, bem como as respectivas gerações F1, RC11 e progênies F4.3. Estas últimas num total de 100, foram obtidas pelo método SSD (single seed descent). Empregou-se delineamento em blocos casualizados com três repetições e dez plantas por parcela. As análises biométricas foram feitas com base em médias de parcelas. Os caracteres avaliados foram: pungência, produtividade, largura, comprimento, número e peso médio dos frutos e espessura da polpa. Investigou-se a segregação fenotípica das progênies F4.3, classificando-as em pungentes e doces. Estimou-se o coeficiente de herdabilidade na base de médias de progênies em todos os caracteres. Simulando uma seleção entre progênies somente para a pungência, tanto para aumento como redução deste caráter, estimou-se o ganho esperado (Gs) sob intensidades de 20%, 10% e 5%. Calculou-se a resposta correlacionada desta seleção sobre os demais caracteres. Paralelamente verificou-se a acuidade de avaliar a pungência utilizando métodos sensoriais, em comparação com o processo cromatográfico (CLAE). Estimaram-se os componentes genéticos das médias dos caracteres nas cinco gerações, considerando modelo aditivo-dominante e, quando necessário, incluindo componente epistático aditivo x aditivo. Verificou-se que, os genitores são contrastantes para todos os caracteres com exceção da espessura da polpa. O genitor doce deve conter genes para pungência não expressos. Os dados sugerem que, na população estudada, este caráter deve ser controlado por dois locos epistáticos, duplo-dominantes (9 pungentes : 7 doces em F2) e genes modificadores. Os coeficientes de herdabilidade variaram de intermediários (66%) a altos (92%). Isso explicou os elevados ganhos esperados com a seleção para incrementar ou diminuir a pungência. Pelas respostas correlacionadas, verificou-se que, uma seleção para aumento da pungência deverá levar a uma redução na produtividade, sendo a recíproca também verdadeira. A avaliação da pungência por método cromatográfico foi de aproximadamente 30% mais eficiente do que o método sensorial. Pelos componentes de média observou-se a existência de heterose em todos os caracteres avaliados. O modelo incluindo efeitos epistáticos foi o mais adequado para explicar as médias das gerações, na maioria dos caracteres. Podem surgir indivíduos com frutos pungentes ao cruzar genitores doces. A segregação transgressiva em F4 é indicador de que tipos mais pungentes que o genitor pungente podem ser selecionados a partir desta população segregante. O melhoramento genético deste caráter pode ser estruturado tanto para explorar as variâncias genéticas aditiva e aditiva x aditiva em linhagens superiores como pode ser conduzido para capitalizar a heterose em híbridos de linhagens. Em programas iniciados cruzando-se linhagens, é fundamental identificar a constituição alélica dos genitores. É preciso monitorar a pressão seletiva numa seleção visando a pungência para evitar repostas correlacionadas indesejáveis. Para atingir máximos seletivos, para este caráter, é necessário levar em conta a existência de genes modificadores. / This work is part of the Capsicum plant breeding program at Embrapa Hortaliças. The main objective was to investigate the genetic basis and variability of a segregating population of Capsicum, related to pungency and to some characteristics of the fruit, to provide information for the program. The genotypes that were used had two homozygotic parents, contrasting in their main characteristic, pungency, as well as the respective generations F1, RC11 and progenies F3.4. The latter, totaling 100, were obtained using the SSD method (single seed descent). Randomized complete block design was used with three repetitions and ten plants per plots. The biometric analyses were based on a plot mean basis. The characters evaluated were pungency, productivity, width, length, number and average weight of the fruits and the thickness of the pulp. The fenotypical segregation of the F3.4 progenies were studied, being classified in pungent and sweet. The coefficient of heritability on a progeny mean basis were estimated in all the characters. Simulating a selection among progenies, only for pungency, for the increase as well as the reduction of this character, the expected gain (Gs) was estimated under intensities of 20%, 10% and 5%. The correlated response of this selection was calculated over the remaining characters. Parallel to this, the acuity of evaluating the pungency, using sensorial methods, in comparison to the high pressure liquid chromatographic process (HPLC) was investigated. The genetic components of the trait means of the five generations, were estimated considering the additive dominant model, and, when necessary, including an additive x additive epistatic component. Results indicated that the parents are contrasting for all characters, with the exception of pulp thickness. The sweet parent should contain genes for pungency wich are not expressed. The data suggests that, in the population studied, this character is controlled by two doubly dominant epistatic loci, (9 pungent ones : 7 sweet ones in F2) and modifier genes. Coefficients of heritabilty varied from intermediate (66%) to high (92%). This explained the elevated expected gains from selection, to increase or decrease pungency. From the correlated responses, one could see that, selecting to increase pungency should lead to a reduction in productivity, being the reciprocal also true. The evaluation of pungency by a chromatographic method was approximately 30% more efficient than the sensorial method. By the genetic components of means, the existence of heterosis was observed in all the characters evaluated. The model which included epistatic effects was the most adequate to explain the average generation means in most of the characters. Individuals with pungent fruits can appear on crossing sweet parents. The transgressive segregation in F4 is an indicator that more pungent types than the pungent parent can be selected from this segregating population. Plant breeding of this character can be structured for the exploration of additive and additive x additive genetic variances in superior lines, or to capitalize the heterosis in hybrid of inbred lines. In programs initiated by crossing lines, it is fundamental to identify the allelic constitution of the parents. It is necessary to monitor the selective pressure in selection aiming at pungency, to avoid undesired correlated responses. To attain selective maximums, for this character, it is necessary to take into account the existence of modifier genes.

Dados coletados de experimentos de melhoramento geralmente contêm observações fenotípicas para vários caracteres avaliados em múltiplos ambientes. Especificamente para cana-de-açúcar, medidas repetidas são obtidas para cana-planta e uma ou mais socas. Tal cenário presta-se naturalmente ao uso de modelos mistos para modelagem de variâncias genéticas heterogêneas e correlações entre caracteres, locais e cortes. Essa abordagem também nos permite incluir informações de marcadores moleculares, auxiliando no entendimento da arquitetura genética dos caracteres quantitativos através do mapeamento de QTLs. Este trabalho teve como objetivo detectar QTLs e interação QTL por ambiente pelo método do Mapeamento de Múltiplos Intervalos, o qual também permite a inclusão de epistasia no processo de busca. Nossa população de mapeamento foi composta por 100 indivíduos oriundos de um cruzamento biparental entre os cultivares brasileiros pré-comerciais SP80-180 e SP80-4966, avaliados em duas localidades (Piracicaba e Jaú, SP, Brasil) e três anos (2004 a 2006) para percentual de fibra, conteúdo de sacarose (POL) e toneladas de cana por hectare (TCH). Um mapa genético com 96 grupos de ligação cobrindo 2468,14 cM já estava disponível para esse cruzamento. O modelo fenotípico selecionado conteve matrizes de covariância separadas para caracteres e ambientes, o que resultou em um modelo mais parcimonioso com bom ajuste aos dados. Foram detectados 13 QTLs com efeitos principais e 8 interações epistáticas, cada um deles exibindo interação QTL por local, QTL por corte ou a interação tripla. Assim, nenhum QTL apresentou efeitos estáveis ao longo de todas as combinações de ambientes. No total, 13 dos 21 efeitos apresentaram algum grau de pleiotropia, afetando pelo menos dois dos três caracteres. Além disso, esses QTLs sempre afetaram os caracteres fibra e TCH na mesma direção, enquanto que POL foi afetado no sentido oposto. Não foi observada evidência em favor da hipótese de QTLs ligados em detrimento da hipótese de QTL pleiotrópico para qualquer das posições genômicas detectadas. Esses resultados fornecem valiosas informações sobre a base genética da variação quantitativa em cana-de-açúcar e sobre a relação genética entre caracteres. / Data collected from breeding trials usually comprise phenotypic observations for various traits evaluated at multiple test environments. Specifically for sugarcane, repeated measures are obtained for plant crop and one or more ratoons. Such scenario naturally lends itself to the use of mixed models for modeling heterogeneous genetic variances and correlations between traits, locations and harvests. This modeling approach also enables us to include molecular marker information, aiding in understanding the genetic architecture of quantitative traits through QTL mapping. Our work was aimed at detecting QTL and QTL by environment interaction by the Multiple Interval Mapping method, which also allows the inclusion of epistasis in the search process. Our mapping population was composed of 100 individuals derived from a biparental cross between the Brazilian pre-commercial cultivars SP80-180 and SP80-4966, evaluated at two locations (Piracicaba and Jaú, SP, Brazil) and three harvest years (2004 through 2006) for fiber content, sugar content (POL) and tonnes of cane per hectare (TCH). A genetic linkage map with 96 linkage groups covering 2468.14 cM was already available for this cross. The selected phenotypic model contained separate covariance matrices for traits and environments, which resulted in a more parsimonious model with good fit to the data. We detected 13 QTL with main effects and 8 epistatic interactions, each exhibiting QTL by location, QTL by harvest or the three-way interaction. Thus, no QTL displayed stable effects across all environment combinations. Overall, 13 of the 21 effects presented some degree of pleiotropy, affecting at least two of the three traits. Furthermore, these QTL always affected fiber and TCH in the same direction, while POL was affected in the opposite way. There was no evidence in favor of the linked QTL over the pleiotropic QTL hypothesis for any of the detected genome positions. These results give valuable insights about the genetic basis of quantitative variation in sugarcane and about the genetic relation between traits.