O conhecimento da diversidade genética e da estrutura populacional das variedades mantidas em bancos de germoplasma é de fundamental importância para sua efetiva utilização em programas de melhoramento. O mapeamento por associação, também conhecido como mapeamento por desequilíbrio de ligação, é um dos principais métodos para relacionar genes e alelos às características de interesse, através da co-segregação de marcadores genéticos polimórficos com os genes envolvidos na variação das características em estudo. O Banco de Germoplasma de Arroz do Departamento de Genética da ESALQ contém 192 acessos japoneses que foram estudados com o objetivo de entender sua diversidade, estruturação genética e determinar a associação genômica de caracteres agronômicos relacionados a produção de grãos. A caracterização molecular foi conduzida através da tecnologia DArT-seq, que gerou dados de marcadores SNPs (single-nucleotide polymorphism) e silico DArTs. Em seguida, após a filtragem, 5.578 SNPs de alta qualidade foram utilizados para calcular as estimativas de diversidade no pacote hierfstat e a estrutura do painel de acessos através da análise discriminante de componentes principais (DAPC), que consiste em determinar existência de cluster em um grupo de genótipos em que não há informação a priori sobre existência de grupos. A diversidade genética nos acessos foi evidenciada pelo valor de heterozigosidade esperada (HS) (0,0279) e a estruturação foi evidenciada pela formação de três subgrupos. O mapeamento associativo foi realizado com o uso do pacote GAPIT, sendo considerados seis caracteres: número de dias para florescimento (NDF), estatura de planta (EP), comprimento da panícula (CP), peso de parcela (PP), massa de mil grãos (MMG) e CICLO, bem como 24.266 marcadores silico DArTs e 1.965 marcadores SNPs. Foram detectadas um total de 113 associações significativas genótipo-fenótipo (P<0,001) quando utilizado marcadores silico DArTs em todas as seis características analisadas e, um total de 21 associações significativas genótipo-fenótipo (P<0,001) quando utilizado marcadores SNPs para apenas quatro das seis características analisadas: EP, CICLO, MMG e PP. Considerando-se os 113 silico DArTs associados significativamente na análise, 90 foram localizados em regiões intergênicas e 23 foram localizados dentro de genes. Enquanto que, dos 21 SNPs significativos, 11 foram localizados em regiões intergênicas e 10 foram localizados dentro de genes. A informação gerada neste estudo foi útil para testar associações ao longo do genoma do arroz. O modelo linear misto (MLM) empregado no mapeamento associativo acredita-se ter conseguido controlar eficientemente os falsos positivos no mapeamento utilizando os marcadores SNPs. As informações geradas neste estudo servem de base para avaliações mais aprofundadas, utilizando o conjunto de marcadores significativos como ponto de partida para determinação dos genes mais importantes para a produtividade em arroz. / The knowledge of the genetic diversity and population structure of varieties maintained in germplasm banks is crucial for their effective use in breeding programs. Association mapping, also known as linkage disequilibrium mapping, is one of the main methods for relating genes and alleles to the characteristics of interest, through the co-segregation of polymorphic genetic markers with the genes involved in the variation of the characteristics under study. The Rice Germplasm Bank of the Department of Genetics of ESALQ contains 192 Japanese accessions that were studied with the purpose of understanding its diversity, genetic structuring and determining the genomic association of agronomic traits related to grain production. The molecular characterization was conducted by DArTseq technology, which generated data of SNPs (single-nucleotide polymorphism) markers and silico DArTs. Then, after filtering, 5,578 high-quality SNPs were used to calculate the diversity estimates in hierfstat package and the accession panel structure through discriminant analysis of principal components (DAPC), which consists of determining the cluster existence in a group of genotypes where there is no a priori information about the existence of groups. The genetic diversity in the accessions was evidenced by the expected heterozygosity value (HS) (0.0279) and the population structure was evidenced by the formation of three clusters. The association mapping was performed using the GAPIT package, considering six characters: number of days for flowering (NDF), plant height (EP), panicle length (CP), plot weight (PP), mass of thousand grains (MMG) and CYCLE, as well as 24.266 silico DArTs markers and 1.965 SNPs markers. We detected a total of 113 significant associations genotype-phenotype (P <0.001) when used silico DArTs markers in all six analyzed characteristics and a total of 21 significant associations genotype-phenotype (P<0.001) when used SNPs markers for only four of the six analyzed characteristics: EP, CYCLE, MMG and PP. Considering the 113 silico DArTs significantly associated in the analysis, 90 were located in intergenic regions and 23 were localized within genes. While of the 21 significant SNPs, 11 were located in intergenic regions and 10 were located within genes. The information generated in this study was useful for testing associations throughout the rice genome. The mixed linear model (MLM) used in association mapping is believed to have been able to efficiently control false positives in the mapping using the SNPs markers. The information generated in this study serves as a basis for further evaluation using the set of significant markers as a starting point for determining the most important genes for rice yield.

Submitted by isabela.moljf@hotmail.com (isabela.moljf@hotmail.com) on 2017-04-27T13:44:40Z No. of bitstreams: 1 julianamainentileallopes.pdf: 2178130 bytes, checksum: ac4968430d3e36932e81380861925cd4 (MD5) / Approved for entry into archive by Adriana Oliveira (adriana.oliveira@ufjf.edu.br) on 2017-05-12T15:49:17Z (GMT) No. of bitstreams: 1 julianamainentileallopes.pdf: 2178130 bytes, checksum: ac4968430d3e36932e81380861925cd4 (MD5) / Made available in DSpace on 2017-05-12T15:49:17Z (GMT). No. of bitstreams: 1 julianamainentileallopes.pdf: 2178130 bytes, checksum: ac4968430d3e36932e81380861925cd4 (MD5) Previous issue date: 2015-03-03 / CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico / FAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais / Estudos recentes sugerem que a duplicação completa dos genomas é muito mais comum do que sua estabilidade, ocorrendo em todas as angiospermas. Nesse contexto, Lippia alba (Mill.) N.E.Br. (Verbenaceae) constitui um modelo interessante de estudo, pois além de ser a espécie mais estudada dentro do gênero Lippia, é amplamente utilizada na medicina popular apresentando importância econômica, sobretudo em função da riqueza de seus óleos essenciais. Estudos recentes demonstraram a existência de pelo menos cinco diferentes níveis de ploidia em Lippia alba, revelando grande plasticidade do genoma. A fim de contribuir para entender a variação genética e o processo de poliploidização em Lippia alba, o presente trabalho objetivou identificar novos marcadores genéticos do tipo microssatélite e estimar a diversidade genética em 100 acessos de Lippia alba. Foram avaliados nove loci já descritos e 16 novos marcadores. O tamanho dos fragmentos foi detectado por eletroforese capilar usando o sequenciador MegaBACE1000 (GE Healthcare, Buckinghamshire, UK). A identificação dos alelos foi inferida utilizando o software Fragment Profile (GE Healthcare, Buckinghamshire, UK). Os dados finais foram exportados para uma planilha do Excel® e foram transformados nos arquivos de entrada específicos para cada programa computacional. Os valores de PIC (polymorphism information content) e heterozigosidade foram calculados por meio do programa Cervus v3.0.7. Os coeficientes de similaridades de Jaccard e Dice foram calculados para construir um dendrograma de acordo com o algoritmo UPGMA (Unweighted Pair Group Method with Arithmetic Mean) por meio dos softwares NTSYS e PAST. Para a análise por inferência Bayesiana, foi utilizado o programa STRUCTURE v 2.3.4. Foi possível observar a formação de grupos de acordo com o nível de ploidia e inferir a possível origem de alguns citótipos baseada na similaridade genética entre os acessos. Os resultados contribuem para fortalecer a hipótese de que os acessos tenham surgido por autopoliploidia. / Recent studies suggest that complete genome duplication is much more common than its stability, occurring in almost all angiosperms. Lippia alba (Mill.) N.E.Br. (Verbenaceae), is the most studied species within the genus Lippia, and it is widely used in folk medicine presenting economic importance mainly due to the richness of their essential oils. Recent studies have demonstrated the existence of at least five different ploidy levels in Lippia alba revealing a large genome plasticity making the species an interesting model of study. To better understand the genetic variation and the polyploidization process in Lippia alba, this study aimed to identify new genetic microsatellite markers and estimate the genetic diversity for 100 Lippia alba accessions. We assessed 9 loci already described and 16 new markers. The size of the fragments was detected by capillary electrophoresis using MegaBACE1000 sequencer (GE Healthcare, Buckinghamshire, UK). The identification of alleles was inferred using the Fragment Profile software (GE Healthcare, Buckinghamshire, UK). Final data were exported to an Excel spreadsheet according to the input files of each software used. PIC values (polymorphism information content) and heterozygosity were calculated using Cervus v3.0.7 software. Jaccard and Dice similarity coefficient were calculated to construct a dendrogram according to UPGMA algorithm (Unweighted Pair Group Method with Arithmetic Mean) using NTSYS and PAST softwares. Bayesian inference analysis was performed using STRUCTURE v 2.3.4 program. It was possible to observe the formation of groups according to the ploidy level and infer the possible origin of some cytotypes based on genetic similarity among accessions. Results contribute to support the hypothesis that the cytotypes have emerged by autopolyploidy.

Abstract Spatial and temporal variation is a universal feature in most organisms in nature, commonly reflecting the past evolutionary history of the species as well as the prevailing environmental conditions. The purpose of this doctoral thesis study was to investigate the genetic and phenotypic variation, and to assess the roles of the different processes affecting them in the moose (Alces alces). Altogether 809 DNA samples of moose, gathered throughout Finland and the Republic of Karelia in Russia, were analysed with a variety of population genetic methods. Furthermore, the shape of the moose mandible was investigated with the help of geometric morphometrics using a subset of samples gathered from 179 moose in Finland. This study showed that the Finnish and especially the Karelian moose population harboured relatively high genetic diversity, albeit with clear regional differences in its spatial distribution. In the northern half of Finland, a secondary contact of two diverged mitochondrial lineages was revealed. The presence of the two lineages was interpreted to reflect the existence of allopatric refugia of moose during the Last Glacial Maximum and the subsequent bi-directional recolonisation of Fennoscandia. Furthermore, a spatially explicit Bayesian clustering analysis suggested existence of three genetic clusters, which were estimated to have split after the post-glacial recolonisation. The results also showed that past declines in the moose numbers during the 18th and 19th centuries led to population bottlenecks, leaving a genetic imprint. Thus, the present moose population in eastern Fennoscandia carries the signs of both ancient and more recent events in its genetic composition. Finally, a significant latitudinal shift was revealed in the shape of the moose mandible. The pattern was considered independent of the genetic clustering of the population. The main changes included an enlargement of the attachment surfaces of the muscles controlling biting and mastication, implying more effective mastication in the north compared with the south, possibly an adaptive response to a longer period of hard wintertime diet. The results of this thesis encourage continuation of studies on the moose in order to fully reveal the impact of particular historical events and especially anthropogenic factors on the genetic and phenotypic variation of this species. They also provide the starting point for ‘genetically enlightened’ moose management and conservation in Finland. / Tiivistelmä Lähes kaikilla eliölajeilla esiintyy ajallista ja paikallista muuntelua, joka on seurausta lajin evolutiivisesta historiasta ja vallitsevista ympäristöoloista. Tässä väitöskirjatutkimuksessa tutkin hirven (Alces alces) geneettistä ja fenotyyppistä muuntelua sekä niitä selittäviä taustatekijöitä populaatiogeneettisillä ja geometrisen morfometrian menetelmillä. Geneettisen aineiston muodostivat Suomesta ja Venäjän Karjalasta kerätyt 809 hirven DNA-näytteet. Fenotyyppisenä ominaisuutena tutkittiin hirven leukaluun muotoa yhteensä 179 alaleuasta. Geneettinen monimuotoisuus oli tutkimuksen mukaan Suomen ja erityisesti Karjalan hirvipopulaatiossa verrattain korkea, joskin alueelliset erot olivat varsin selviä. Pohjoisesta Suomesta löytyi kahta erilaistunutta mitokondrion DNA:n sukulinjaa, joiden arvioin erilaistuneen viimeisen jääkauden aikana, todennäköisesti erillisissä refugioissa, ja saapuneen aikoinaan Suomeen eri reittejä pitkin. Tämän ohella tuman DNA paljasti lisää alueellisia rakenteita; bayesilainen ryhmittelyanalyysi havaitsi hirvellä kolme erillistä alapopulaatiota. Näiden ryhmien arvioin kehittyneen vasta Suomen uudelleenasuttamisen jälkeen. Tämän tutkimuksen tulokset osoittivat myös, että historiallisesti tunnetut kannanromahdukset 1700- ja 1800-luvuilla johtivat populaation pullonkaulaan, joka jätti jälkensä hirven perimään. Itäisen Fennoskandian hirvipopulaation geneettiseen muunteluun ovat siis vaikuttaneet sen historian aikana niin jääkauden aikaiset kuin tuoreemmatkin tapahtumat. Tämän lisäksi hirven alaleuan muodossa havaittiin merkitsevä etelä-pohjoissuuntainen muutos. Tulosten mukaan purentaa ohjaavien lihasten kiinnityspinnat laajenevat pohjoista kohti siirryttäessä, mikä viittaisi siihen, että hirven leukojen puruvoima on pohjoisessa suurempi kuin etelässä. Ilmiö oli riippumaton populaation geneettisestä ryhmittyneisyydestä, ja se on mahdollisesti seurausta kovemman talviruokavalion aiheuttamasta adaptiivisesta vasteesta. Tämän väitöskirjan tulokset rohkaisevat jatkamaan aiheen tutkimusta, jotta eri historiallisten tapahtumien sekä eritoten ihmisvaikutuksen merkitys lajin geneettiseen ja fenotyyppiseen muunteluun voitaisiin selvittää perin pohjin. Lisäksi tulokset muodostavat lähtökohdan ’geneettisesti valistuneelle’ hirvikannan hoidolle Suomessa.

La sélection des nouveaux porte-greffes du genre Prunus a pour principal objectif d’utiliser lavariabilité génétique existant au sein des différentes espèces de Prunus afin de créer un matérielvégétal innovant, performant au plan agronomique et résistant à différentes contraintes biotiques etabiotiques. L’exploitation de la variabilité génétique s'appuie sur le phénotypage des différentsindividus présents dans les collections de ressources génétiques pour les caractères recherchés. Celapermet de sélectionner des génotypes spécifiques pour améliorer un trait donné.Dans cette étude constituée de deux parties, nous avons exploré la diversité génétique au seindu genre Prunus pour ce qui concerne deux traits importants : l’aptitude au bouturage et les réponsesde certains porte-greffes à la contrainte hydrique.Dans la première partie l’aptitude au bouturage ligneux a été explorée dans une collectiongénétique de 222 génotypes. Les résultats obtenus montrent une variabilité considérable entre les sousgenresAmygdalus et Prunophora et également une variabilité interspécifique au sein de chaque sousgenre.La réussite au bouturage est nettement améliorée chez les hybrides interspécifiques dont un desparents appartient à l’espèce P cerasifera.Dans la deuxième partie nous avons étudié les réponses à la contrainte hydrique chez neufgénotypes couramment utilisés comme porte-greffes. Nous avons comparé trois régimes hydriquesdifférents : témoins, stressés et recouvrés. L’humidité du substrat est maintenue à la capacité au champtout au long de l’expérience pour les plants témoins, par contre l’arrosage a été arrêté pendant 14 jourspour les plants stressés, puis il a été repris pendant 10 jours pour les plants recouvrés. Durant cetteexpérience, nous avons effectué des mesures morphologiques et physiologiques sur la partie aérienneainsi que des excavations à la fin de chaque phase pour examiner les modifications au niveau dusystème racinaire. Sur la partie aérienne, la contrainte hydrique a provoqué une diminutionsignificative de la photosynthèse nette, de la transpiration totale, de la conductance stomatique, et del’expansion des feuilles.Le système racinaire a répondu à cette contrainte par plusieurs modifications. D’abord, le ratio racines/pousses a augmenté pour 4 génotypes (GF305, GF677, Montclar et Myrobolan1254). Ensuite, lesdifférents traits de l’architecture racinaire ont montré des modifications sous l’effet de la contraintehydrique : la longueur de la zone apicale non ramifiée (LZANR) qui traduit l’élongation racinaire,ainsi que les diamètres apicaux des racines ont diminué chez tous les génotypes. Par conséquent lesracines se sont affinées et ont réduit leur croissance en longueur. Produire des racines plus finesaugmente la surface de contact entre les racines et le sol et améliore la capacité d’absorption. Unediminution de la distance inter-ramification a été observée chez les plants stressés. Cette modificationpourrait s’expliquer par le fait que les plantes produisent plus de racines latérales en profondeur oùl’eau est souvent plus disponible. De plus, les racines latérales produites étaient également plus fines.Au plan qualitatif, les génotypes ont eu des réponses semblables, mais l’intensité de la réponse a variéselon les génotypes. / In breeding programs of Prunus rootstocks the aim is to use the existing genetic variabilitywithin Prunus species in order to create new rootstock genotypes with excellent agronomic traits, andimproved resistance to biotic and abiotic stresses.Exploitation of the genetic variability is based on the evaluation of phenotypic variation amongindividuals within genetic collections for desirable traits. This make possible to select specificgenotypes to improve a given trait.This study consists of two parts; we explored the genetic diversity within the genus Prunusregarding two important characteristics: rooting ability of hardwood cuttings and responses of somerootstocks to water stress.In the first part, rooting ability of hardwood cuttings was evaluated among 222 genotypespreserved in genetic collection. The results show considerable variability among the sub genusAmygdalus, Prunophora, and also an interspecific variability within each of them. Rooting ability byhardwood cutting was significantly improved in interspecific hybrids if one parent belongs to Pcerasifera species.In the second part of this study we studied the responses of nine genotypes, commonly usedrootstocks, to water stress. We applied three treatments: control, water stress and recovering.Soil moisture was maintained at field capacity through all stages of the experiment for the controlplants. On the contrary we stopped watering during 14 days for the stressed plants, and then we rewateredthe recovered plants for 10 days.During this experience, we performed morphological and physiological measurements on the aboveground parts of plants and we excavated plants at the end of each phase to observe root systemmodifications.Aboveground parts of plant responded to water stress by a significant decrease in net photosynthesis,total transpiration, stomatal conductance and leaf expansion.Root system responded to water stress by several modifications:Four genotypes (GF305, Montclar, GF677 and Myrobolan) showed a significant increase in root toshoot ratio under drought conditions. We also detected morphological modifications on the differenttraits of root architecture in response to water stress.The length of the apical unbranched zone LAUZ and the apical diameter were decreased forall genotypes, consequently, roots became finer and reduced their rate of elongation. Fine rootsenhance the surface of contact between roots and soil which in turn improve the acquisition of waterunder drought condition.The inter-branch distance also responded, and it tended to decrease under the water stress treatment.The decrease in inter-branch distance can be explained by a production of more lateral roots in deeplayers, where water was more available, moreover these new laterals roots were also finer.Qualitatively, a common response to water stress was observed on the different traits of the rootsystem architecture, but we showed a genotypic effect determining the level of the response.

Une approche a plusieurs echelles a été développé afin de vérifier si les différences de Δ13C entre les genotypes de peuplier représentaient les différences d'efficience de transpiration à l'échelle des feuilles et la plante entière. Nous avons également vérifié la stabilité des différences génotypiques pour Δ13C dans le temps. Nous avons constaté que les différences génotypiques pour Δ13C pouvaient etre traduites comme la difference d efficience de transpiration a l echelle des feuilles ainsi qu au niveau de la plante entière. L amplitude de la variabilité de l efficience de transpiration a l echelle du plant etait plus grand par rapport à la variabilite a l echelle de la feuille, demontrant le rôle de la perte du carbone lors de la respiration diurne et nocturne (Φc) ainsi que l'eau perdue pendant la transpiration nocturne (Φw). La productivité génotypique augmentait avec l efficience de transpiration chez Populus deltoides × nigra, mais restait stable chez Populus nigra. Les valeurs absolues de l efficience de transpiration observees lors de cette etude etaient plus elevees que chez les autres especes. L enrichissement en 18O de la matiere organique (Δ18Olb) et de l eau (Δ18Olw) des feuilles correlait avec la variation de la conductance stomatique (gs) soit au niveau de l individu ou au niveau génotypique. Lors d une premiere experience nous avons montre que les valeurs de Δ13C restaient stables pour les genotypes Populus deltoides × nigra ages de 5 a 15 ans, avec un classement génotypique particulierement conservé pendant l etude. Toutefois, une seconde experience nous a permis de demontre que des arbres ages de 4 a 7 ans presentaient des valeurs de Δ13C significativement plus faibles que celles observees lors de la premiere experimentation, avec une augmentation progressive de ces valeurs avec l age. Nous concluons que, chez le peuplier, le Δ13C peut etre considere comme un estimateur fiable de l efficience de transpiration a l echelle du plant entier, et le classement genotypique établi chez de jeunes arbres pour Δ13C reste stable avec l'âge. / Up scaling approach was developed to check whether genotype differences in Δ13C represent the differences in transpiration efficiency at leaf and whole plant scale. We also verified the stability genotype difference in Δ13C with age. We found that genotype differences in Δ13C were as such translated as the difference in transpiration efficiency at both leaf and whole plant scale. Magnitude of variability of whole plant transpiration efficiency was higher as compared to at leaf level highlighting the role of carbon lost during photo and dark respiration (Φc) and water lost during night transpiration (Φw). Genotype productivity increased with increase in transpiration efficiency in Populus deltoides × nigra genotypes but remained unchanged in Populus nigra genotypes. Values of whole plant transpiration efficiency were found higher as compared to other species.18O enrichment in both leaf bulk (Δ18Olb) and leaf water (Δ18Olw) reflected variation in stomatal conductance (gs) either at individual level or at genotypic level. In Populus deltoides × nigra genotypes, no increase or decreasing trend was found in Δ13C between the age of 5-15 years and genotypic ranking was conserved over the tested period. However, significantly lower Δ13C values were evidenced between the age of 4-7, which increased with age. We conclude that in poplar, Δ13C is a reliable estimator of whole plant transpiration efficiency and the ranking made in young plant for Δ13C remain stable with age.

Les interventions de lutte contre le paludisme, comme la distribution massive de moustiquaires imprégnées et les polythérapies à base d’artémisinine, ont permis depuis les années 2000 de réduire le nombre de décès d’environ 60% au plan mondial, avec de grandes disparités d’un pays à l’autre. Si certains pays sont entrés en phase d’élimination, d’autres, et particulièrement en Afrique sub-Saharienne, doivent encore contrôler la maladie. La mise au point d’un vaccin contre le paludisme reste l’une des voies prioritaires pour la lutte contre la maladie. Parmi les différents candidats vaccins, les vaccins visant à bloquer la transmission chez le moustique vecteur connaissent un intérêt croissant. Dans ce travail de thèse, j’ai évalué l’efficacité d’anticorps anti-AnAPN1 à bloquer la transmission d’isolats naturels de Plasmodium falciparum chez An. coluzzii. L’aminopeptidase 1 est une protéine qui tapisse l’épithélium intestinal du moustique et qui servirait de récepteur aux ookinètes. Nous avons réalisé des essais d’infections expérimentales sur la plateforme d’entomologie de l’OCEAC à Yaoundé. Les anticorps anti-AnAPN1, 4H5B7, ont montré une activité bloquante dose-dépendante et l’inhibition de la transmission varie selon le donneur de gamétocytes. Nous avons alors modélisé les différents paramètres qui pouvaient moduler l’efficacité de l’anticorps et nous avons montré que la multiplicité de l’infection du donneur avait un effet significatif. Nous avons ensuite étudié la dynamique de transmission des génotypes de P. falciparum sous pression d’anticorps à des doses non bloquantes afin d’identifier les génotypes qui ne sont pas sensibles à l’anticorps. Le traitement réduit la diversité génétique de la population de parasites mais nous n’avons pas observé de sélection de génotypes particuliers de P. falciparum suite à l’exposition des moustiques aux anticorps anti-AnAPN1. Les analyses de génétique des populations ont révélé une corrélation positive entre le FIS et la multiplicité d’infection, les gamètes de P. falciparum tendent à s’apparier entre génotypes apparentés dans les populations de forte complexité génétique. Les résultats de ce travail soulignent l’importance de la diversité génétique de la population de gamétocytes pour la transmission chez le moustique vecteur. / Malaria control interventions over the last 15 years have lead to reduce malaria mortality by about 60% worldwide. This large reduction in malaria burden results mostly from effective mass distribution of insecticide-treated mosquito nets and artemisinin-based combination therapies. Some countries have already entered into elimination stage but others, particularly in sub-Saharan Africa, have yet to control the disease. The development of a vaccine against malaria remains a major priority for the fight against the disease. Among the different candidate vaccines, transmission-blocking vaccines have gained interest in the recent years. These vaccines would interrupt transmission from humans to mosquitoes. The anopheline alanyl aminopeptidase N (AnAPN1) is a mosquito-based malaria transmission-blocking vaccine candidate. In this PhD work, we evaluated the efficacy of anti-AnAPN1 antibodies against field isolates of Plasmodium falciparum in Anopheles coluzzii. Anti-AnAPN1 antibodies delivered to mosquitoes through artificial feedings showed a dose-dependent blocking activity and the transmission inhibition varied according to gametocytes donors. We modeled the different parameters that could modulate the antibody efficiency and we showed that the multiplicity of infection in the blood donor has a significant effect. We further explored the transmission dynamics of the co-infecting P. falciparum genotypes at non-blocking doses of antibodies. The mAb treatment reduced the genetic diversity of the parasite population but we did not detect any trace of selection on parasite genotypes. Genetic analyses revealed a positive correlation between FIS and multiplicity of infection, thus P. falciparum gametes mate with close relatives in infections with high genetic complexity. The results of this work highlight the importance of the genetic diversity of gametocyte population for transmission in the mosquito vector

Toxoplasma gondii, protozoaire ubiquitaire chez les mammifères et les oiseaux, est l’agent étiologique de la toxoplasmose, une maladie posant un réel problème de santé publique dans le monde avec environ 200 000 nouveaux cas de toxoplasmose congénitale chaque année. Il a été montré que la sévérité clinique de la toxoplasmose variait en fonction des régions géographiques, avec en particulier l’Amérique du Sud qui paie le plus lourd tribu de cette maladie. Malheureusement, les mécanismes de ces disparités géographiques sont encore peu compris et l’origine géographique ainsi que l'histoire évolutive du pathogène sont encore incertaines. Une collection mondiale de 168 isolats de T. gondii recueillis dans 13 populations de 5 continents a été séquencée pour cinq fragments de gènes (140 single nucleotide polymorphisms à partir de 3153 bp par isolat). La phylogénie basée sur les méthodes de Maximum de vraisemblance avec une estimation de l’âge du plus récent ancêtre commun (TMRCA) et des analyses géostatistiques ont été réalisées afin d’inférer l’origine hypothétique de T. gondii. Nous montrons que les souches actuelles de ce parasite ont vraisemblablement évolué à partir d’un ancêtre Sud-Américain il y a environ 1,5 million d’années et avons reconstruit la propagation mondiale du pathogène qui a suivi. Cette émergence est beaucoup plus récente que l’apparition de la forme ancestrale de T. gondii il y a environ 11 Ma et est postérieure à l’arrivée des félidés dans cette partie du monde. Nous proposons que la lignée ancestrale de T. gondii ait été introduite en Amérique du Sud avec les félidés et que l’évolution de l’infectivité orale des kystes tissulaires à travers le carnivorisme ainsi que la diversification des félidés dans cette région du monde a permis l'apparition d'une nouvelle souche ayant une capacité de transmission beaucoup plus efficace que la lignée ancestrale, ce qui lui a permis de la supplanter et d’avoir une distribution pandémique. / Toxoplasma gondii, a protozoan found ubiquitously in mammals and birds, is the etiologic agent of toxoplasmosis, a disease causing substantial Public Health burden worldwide, including about 200,000 new cases of congenital toxoplasmosis each year. Clinical severity has been shown to vary across geographical regions with South America exhibiting the highest burden. Unfortunately, the drivers of these heterogeneities are still poorly understood, and the geographical origin and historical spread of the pathogen worldwide are currently uncertain. A worldwide sample of 168 T. gondii isolates gathered in 13 populations was sequenced for five fragments of genes (140 single nucleotide polymorphisms from 3,153 bp per isolate). Phylogeny based on Maximum likelihood methods with estimation of the time to the most recent common ancestor (TMRCA) and geostatistical analyses were performed for inferring the putative origin of T. gondii. We show that extant strains of the pathogen likely evolved from a South American ancestor, around 1.5 million years ago, and reconstruct the subsequent spread of the pathogen worldwide. This emergence is much more recent than the appearance of ancestral T. gondii, believed to have taken place about 11 My ago, and follows the arrival of felids in this part of the world. We posit that an ancestral lineage of T. gondii likely arrived in South America with felids and that the evolution of oral infectivity through carnivorism and the radiation of felids in this region enabled a new strain to outcompete the ancestral lineage and undergo a pandemic radiation.

The oceanic whitetip shark, Carcharhinus longimanus, is a circumtropical pelagic shark of high conservation concern (IUCN Red List: “Critically Endangered” in the Western North and Western Central Atlantic and “Vulnerable” globally). I present the first, population genetic assessment of the oceanic whitetip shark on a global scale, based on analysis of two mitochondrial genome regions (entire 1066-1067 bp control region and 784 bp partial ND4 gene), and nine nuclear microsatellite loci. No population structure was detected within the Western Atlantic. However, highly significant population structure was detected between Western Atlantic and Indo-Pacific Ocean sharks across all markers. Additionally, a nominally significant signal of matrilineal structure between the Indian and Pacific Ocean sharks was detected by AMOVA and pairwise tests of the ND4 gene only (pairwise ΦST = 0.051, P = 0.046; pairwise Jost’s D = 0.311, 95% CI = 0.020, 0.0614). Although significant inter-basin population structure was evident, it was associated with deep phylogeographic mixing of mitochondrial haplotypes and evidence of contemporary migration between the Western Atlantic and Indo-Pacific Oceans. I theorize that semi-permeable thermal barriers are responsible for the differentiation between the Western Atlantic and Indo-Pacific set in a framework of global phylogeographic mixing. Relatively low mtDNA genetic diversity (concatenated mtCR-ND4 nucleotide diversity π = 0.32% ± 0.17%) compared to other circumtropical elasmobranch species raises potential concern for the future genetic health of this species. Overall, significant population structure exists, at a minimum, between the Western Atlantic and Indo-Pacific Ocean, and effective management strategies must take this into consideration.

Abstract Wild populations of large carnivores in Europe were almost wiped out during the last centuries. Nowadays, the number of brown bears in North and Eastern Europe has increased, and the current situation suggests that these populations have recovered or are in the process of recovery. Knowledge of the population genetic consequences of demographic recovery in large carnivores, especially across national borders and on broader geographical scales, is still limited. In this study, we collected 3,757 fecal and hair samples as well as 881 tissue samples from brown bears across Northern Europe, with a focus on the Finnish population and neighboring areas, to investigate the population structure, connectivity, and genetic diversity on a spatial as well as a temporal scale. Bayesian clustering analysis of the population structure suggested the division of brown bears in Northern Europe into several genetic clusters, and the subdivision of the Finnish population into a northern and southern subpopulation. The estimation of gene flow pointed to better connectivity of the bears between Southern Finland and Western Russia, while migration between Scandinavia and Northern Finland as well as between Scandinavia and Southern Finland/Western Russia appeared to be restricted. Genetic clusters identified in Finland, Russia and Northern Norway displayed high genetic diversity, which was among the highest reported in wild brown bears. Recovery of the Finnish population has been accompanied by a detected range expansion towards the north, while genetic differentiation between clusters has decreased and genetic diversity has increased in the southern population, suggesting expansion from the south. Our results demonstrated that the immigration of bears from Russia still plays a major role in the Finnish bear population; however, connectivity between the Finnish-Russian population and Scandinavian bears appears to be restricted and should be improved, as well as regularly monitored. / Tiivistelmä Suurpetojen luonnonpopulaatiot hävisivät Euroopasta melkein kokonaan viimeisten vuosisatojen aikana. Ruskeakarhujen määrä on viime aikoina kasvanut Pohjois- ja Itä-Euroopassa, ja karhupopulaatiot ovat toipuneet tai toipumassa. Tieto demografisen toipumisen geneettisistä seurauksista populaatioissa on varsin rajoittunutta etenkin laajemmassa maantieteellisessä mittakaavassa, yli valtiorajojen. Keräsimme tätä tutkimusta varten 3757 uloste- ja karvanäytettä ja 881 kudosnäytettä Suomesta ja sen lähialueilta. Tarkoituksenamme oli kartoittaa Pohjois-Euroopan karhupopulaatioiden geneettistä rakennetta ja monimuotoisuutta, sekä populaatioiden välisiä yhteyksiä huomioiden ajallinen ja maantieteellinen ulottuvuus. Bayesiläisen ryhmittelyanalyysin perusteella Pohjois-Euroopan karhut jakaantuvat useaan geneettiseen ryhmään. Suomen populaatiossa erottuivat eteläinen ja pohjoinen alapopulaatio. Analyysit geenivirran määrästä osoittivat, että Etelä-Suomen ja Länsi-Venäjän karhupopulaatiot ovat yhteneväisemmät, kun taas migraatio Skandinavian ja Pohjois-Suomen sekä Etelä-Suomen ja Länsi-Venäjän välillä vaikuttaisi olevan rajoittunutta. Suomesta, Venäjältä ja Pohjois-Norjasta tunnistetut alaryhmät olivat geneettisesti hyvin monimuotoisia, ja muuntelu oli korkeampaa kuin koskaan aiemmin karhuilla havaittu. Suomen karhupopulaation toipuessa ja levitessä pohjoiseen, geneettinen erilaistuminen maan sisällä on vähentynyt ja eteläisen alapopulaation monimuotoisuus kasvanut. Tämä viittaa populaation laajentumiseen etelästä käsin. Tulosten perusteella karhujen tulomuutto Venäjältä on yhä tärkeää Suomen populaatiolle. Suomen ja Venäjän karhupopulaatioiden yhteyttä Skandinavian karhupopulaatioihin tulisi seurata ja parantaa.

Abstract Hosts and pathogens are involved in a continuous evolutionary arms race, where pathogens attack and hosts defend themselves. The main tools for winning the race are natural selection and the genetic diversity that selection acts on. However, in small populations natural selection may be ineffective. Therefore, the genes taking part in immune defense may lack adaptability to new or changing pathogens. Major histocompatibility complex (MHC) is an important genomic region that includes highly polymorphic immune defense genes. In this doctoral thesis, I studied the natural selection and genetic diversity of MHC class II genes in dogs and Finnish wolves. I also used dog MHC diversity to estimate the number of founding wolves in dog domestication. The Finnish wolf population declined rapidly in size due to excessive hunting from the late 19th century until the early 20th century. After decades of a very small population size, the population started recovering in the mid-1990s. This study shows that, despite the fluctuations in population size, the diversity of the MHC loci in the Finnish wolf has remained high and comparable to the larger neighboring Russian Karelian wolf population. Unlike the neutral genetic markers, the MHC loci of the Finnish and Russian Karelian populations have not differentiated. These results indicate similar balancing selection acting on the MHC loci of the two wolf populations. In dogs, the strength of natural selection is likely weakened by artificial selection and veterinary care. The potential phases of natural selection would be during embryogenesis and fetal development. However, no strong signs of prenatal selection were found in this study. MHC diversity was estimated to be higher in Asian dogs than in dogs from Europe. A simulation study indicated a minimum of 500 founding wolves for the modern dog population. Dog MHC diversity implies an Asian origin for domestication from a large and diverse wolf population. Both natural selection and demography have an influence on the genetic diversity of a species. In small populations, random genetic drift is enforced. However, in loci with important fitness impacts, selection may be particularly strong and outweigh drift, as demonstrated in the MHC loci of a small wolf population in this study. / Tiivistelmä Isäntä ja taudinaiheuttajat käyvät jatkuvaa kaksinkamppailua, jossa taudinaiheuttajat hyökkäävät ja isäntä puolustautuu. Kamppailussa menestymiseen tarvitaan geneettistä monimuotoisuutta sekä sen pohjalta toimivaa luonnonvalintaa. Pienissä populaatioissa luonnonvalinnan teho voi kuitenkin heikentyä, jolloin immuunipuolustukseen osallistuvat geenit eivät kykene sopeutumaan uusiin tai muuttuneisiin taudinaiheuttajiin. MHC-alueella (major histocompatibility complex) sijaitsee suuri joukko monimuotoisia immuunipuolustukseen osallistuvia geenejä. Väitöskirjassani tutkin luokan II MHC-geeneihin kohdistuvaa luonnonvalintaa ja niiden geneettistä monimuotoisuutta koirilla ja Suomen susilla. Arvioin myös koiran kesyttämisprosessiin osallistuneiden susien määrää nykykoiran MHC-monimuotoisuuden pohjalta. Suomen susipopulaation koko pieneni nopeasti voimakkaan metsästyksen vuoksi 1800-luvun lopulta 1900-luvun alkuun. Populaatio pysyi hyvin pienenä useita vuosikymmeniä, kunnes se alkoi elpyä 1990-luvun puolivälissä. Tutkimus osoitti, että populaatiokoon vaihteluista huolimatta Suomen susien MHC-geenien monimuotoisuus on säilynyt korkeana ja on vastaavalla tasolla kuin Venäjän Karjalan susipopulaatiossa. Suomen ja Venäjän Karjalan susipopulaatioiden MHC-geenit eivät ole erilaistuneet, vaikka populaatiot poikkeavat toisistaan neutraalien geenimerkkien suhteen. Samanlainen tasapainottava valinta näyttäisi kohdistuvan näiden susipopulaatioiden MHC-geeneihin. Keinotekoinen valinta ja eläinlääketieteellinen hoito todennäköisesti heikentävät koirien MHC-geeneihin kohdistuvaa luonnonvalintaa. Luonnonvalinta voisi yhä vaikuttaa alkion- ja sikiönkehityksen aikana, mutta tästä ei tutkimuksessa löytynyt todisteita. MHC-muuntelun määrän arvioitiin olevan suurempaa aasialaisissa kuin eurooppalaisissa koirissa. Simulaatiotutkimuksen mukaan nykyisen koirapopulaation perustamiseen olisi tarvittu vähintään 500 sutta. Tulokset viittaavat koiran kesyttämisen tapahtuneen Aasiassa suuresta ja monimuotoisesta susipopulaatiosta. Sekä luonnonvalinta että demografia vaikuttavat lajien geneettiseen monimuotoisuuteen. Pienissä populaatioissa satunnaisajautuminen voimistuu. Valinta voi kuitenkin olla erityisen voimakasta ja voittaa satunnaisajautumisen geeneissä, joilla on erityisen tärkeä vaikutus yksilön kelpoisuuteen, kuten tutkimuksessa osoitettiin pienen susipopulaation MHC-geenien kohdalla.