Dogs have lived with us for thousands of years, so we have learned to understand one another. Dogs have been shown to synchronize their behavior with humans. Behavioral synchronization is characterizes by doing the same thing at the same time and in the same place as someone else. This synchronization is often dependent on the relationship and the emotional state of the individuals. The main aim in this study was to develop a method to test behavioral synchronization and also to investigate how this, but also other behaviors, are effect by preceding human-dog interactions. Privately owned dogs (N=21) were tested with three different treatments (play, pet or ignore). The test procedure consisted of the owner walking or standing still in a predefined pattern, while their dog was freely roaming. This study showed that dogs adapted their movement pattern to their owners. This was similar to previous studies showing that the method developed can be used to test behavioral synchronization between owner and dog. Dogs explored the test arena less after play interaction and they also tended to seek more eye contact with their owners, but the interactions did not affect how much time spent in human proximity, how much they followed them or on dogs movement pattern.

The black-tailed prairie dog (Cynomys ludovicianus) has experienced dramatic declines over much of its historical range due to habitat loss, plague, poisonings, and shootings. Many populations now occur as isolated genetic relicts. A multiple locus genetic profile was obtained using microsatellite analyses of six polymorphic nucleotide repeats from 319 black-tailed prairie dogs collected from 16 colonies throughout the state of Texas. This assessment revealed that existing populations have sufficient variation at all six loci to verify the usefulness of this approach as a primary genetic tool in conservation and preservation. The data reveals regional-dependent frequency patterns as well as support for founder/bottleneck effects for several of the 16 sites. Although the prairie dog population in Texas as a whole may appear genetically diverse, considerable genetic divergence has already occurred among the subpopulations (FST = 0.164). Isolation by distance is supported by genic differentiation analysis (P < 0.001) and pairwise correlation analysis between genetic distance and geographic distance (P < 0.001). Prairie dogs from six (COC, LUBA, LUBC, LUBD, LUBE, and TAR) of the original 16 sites have been relocated or exterminated, or were in the process of being relocated. Results indicated the following colonies (COT, DAL, HOW, and HUD) are of sufficient size and possess ample genetic diversity to be characterized as candidate foundation populations for future preservation efforts. The proximity of small colonies (< 20 hectares) such as HEMB, LUBB, and PEC, to other colonies should be examined to determine if they are isolated or part of a metapopulation. Colonies (HAR, HEMA, and SCH) with low genetic diversity would be ideal candidates for supplementation. Alternatively, these colonies could be relocated or blended with other similar but genetically distinct colonies. Baselines for healthy, pet prairie dog hematology and blood chemistries were also established. Results signify that data gathered from pet prairie dog blood analyses should be referenced against hematology and blood chemistry baselines established using pet prairie dog subjects.

The Utah prairie dog (Cynomys parvidens) was listed by the U.S. Fish and Wildlife Service as an endangered species in 1973 because of range-wide population declines. The species was reclassified as threatened in 1984 because of population increases on private lands. Habitat fragmentation coupled with a lack of suitable habitat has impeded species recovery. Desired species habitat conditions include 0-8% shrub cover, 12-40% cool-season grass cover, and 1-10% perennial forb cover. Cool-season grasses are critical for Utah prairie dogs because of high spring energy requirements. Past research suggested that reducing shrub cover may increase cover of desired grasses and forbs. From 2008-2010, I evaluated the effects of high intensity fall sheep grazing and low application of herbicide (tebuthiuron) as tools to reduce shrub cover and enhance grass and forb cover on the Awapa Plateau Utah prairie dog recovery area in south-central Utah. I placed 1700 ewes in 4 ha stratified and randomly selected plots until >70% vegetation utilization was achieved. Five additional randomly-selected plots were treated with tebuthiuron at a rate of ~1.68 kg/ha. Percent cover of grass, forbs, and shrubs was recorded on treatments and paired control plots in June 2009 and 2010 to determine treatment vegetation responses. I also affixed 22 juvenile Utah prairie dogs with radio transmitters to determine if over-winter survival differed relative to treatment. Live shrub cover was lower on grazed plots in year 1 (P<0.001) and in year 2 (P=0.015). Dead shrub cover in grazed plots was higher in year 1 (P<0.001). Grazed plots exhibited increased forb cover from year 1 (P=0.104) to year 2 (P=0.008). Live shrub cover was lower in herbicide plots in year 2 (P=0.002). Dead shrub cover in herbicide plots was higher in year 2 (P=0.006). Tebuthiuron and grazed plots exhibited a reduction in shrub height (P=0.010, P=0.026, respectively). Tebuthiron plots exhibited less grass cover (P=0.034). Intensive sheep grazing and a low application of tebuthiuron reduced both shrub cover and vertical structure, but failed to increase the percent of grass cover when compared to the control plots. All plots exhibited reduced grass cover in 2010 in response to below normal precipitation. However, percent grass cover was higher on the grazed plots. It is possible that low inherent site productivity in combination with below normal average precipitation compromised treatment effects. Because of radio transmitter failure, I was not able to obtain survival data after hibernation. Prairie dog counts and weights did not differ by treatment type. If climate change reduces overall precipitation on the Awapa Plateau, recovery of the Utah prairie dog on this site will be problematic.

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The capacity of zoonotic pathogens to infect multiple hosts creates surveillance challenges but also provides opportunities to gather data from animal species that can be used to understand risks to human health. This thesis presents a conceptual and practical assessment of the utility of domestic dog serosurveillance for the detection and surveillance of two pathogens, influenza A and Leptospira spp. The first chapter gives a theoretical framework that can be used to explore the attributes of animal sentinels and assess their utility in different contexts. In subsequent chapters, this framework is applied in a practical assessment of the utility of a domestic dog serosurveillance approach for the detection and surveillance influenza A and Leptospira spp. at two sites in Africa. Two cross-sectional surveys of the avian and mammal populations at a site in Northern Cameroon were conducted in early 2006 to determine if H5N1 influenza A viruses had circulated in this area and in which species that presence could be detected. Serological and molecular evidence of extensive H5 virus circulation in the domestic duck population was identified. 47% of domestic ducks at the Maga site were cELISA positive for anti-influenza A antibodies and 20% were HI test positive against an H5N1 antigen. There was also evidence of exposure to H5 subtype viruses in the local dog and pig populations. At the Kibera site in Nairobi, a cohort study was established to carry out surveillance of influenza A and Leptospira spp. in the domestic dog population and cross-sectional surveys of the domestic poultry and rodent populations were completed. There was no indication of influenza A circulation in any of the animal species surveyed, indicating low risk of zoonotic influenza A infection in the human population of Kibera. In contrast, there was extensive molecular and serological evidence of the presence of Leptospira spp. in both the rodent and dog populations. 18% of 236 trapped rodents were PCR positive for kidney carriage of pathogenic leptospires and the estimated seroprevalence of anti- Leptospira antibodies in the dog population ranged from 5-36% during the course of the study, indicating high potential risk of leptospirosis infection in the human population. The results indicate that dog serosurveillance can be used as useful tool for the determination of broad-scale patterns of pathogen presence and relative levels of population exposure. However, there are limitations of the data that can be gathered from animal sentinels and the complexities introduced particularly by incomplete understanding of diagnostic test performance must be recognized. Animal sentinel surveillance may be of most use for addressing fundamental questions of what pathogens are present where. In the developing world particularly where disease burden data are still lacking, dog sentinel serosurveillance can provide essential baseline data that can be used to target future research and resource allocation.

The retriever breeds have the same origin and have long been used as a gundog for hunting of game, mostly birds. However, recently the retriever breeds have become a popular pet and show dog. This have affected the breeding of the dogs as the same traits are not bred for a gundog and a pet or show dog. Breeds as the Labrador retriever consists of a field- and common-type. The aim of this study is to investigate any differences between and within five of the retriever breeds in behaviours as retrieving, search and game reaction. 64 dogs undergoing the field trial Description of Function- Retriever was video recorded and scores from 430 dogs that have undergone field trials was obtained. Both differences between and within breeds were found when analysing both the videos and scores. In the video analysis, the Flatcoated retriever showed the most retrieving behaviours and was the most passive. The Nova scotia duck tolling retriever was in both the video and score analyses the most active breed. The Labrador retriever scored high in game reaction. The field- and mixed-types had almost always higher scores in behaviours linked to hunting, compared to the common-type. This supports findings that recent selection in breeding have a larger effect on behaviour than the origin uses of the dogs.

The cost of drug development is high with many drugs failing during toxicity testing. This is a particular problem in veterinary medicine where the pharmaceutical market size is so small that it may not be economically viable to develop drugs. The liver and specifically hepatocytes have a crucial role in drug metabolism via oxidation by cytochrome enzymes (CYP), conjugation and excretion into the biliary system. This drug metabolism is unpredictable between species as each has unique CYP profiles. Furthermore there is breed variation of CYP profiles within the canine species. The ability to produce an in vitro source of canine hepatocytes to model drug metabolism in this species and in different breeds would greatly reduce the expense of candidate drug testing. If an unlimited supply could be produced in vitro this would reduce the number of animals required in pre-clinical testing. The aim of this thesis was to produce an in vitro supply of canine hepatocyte-like cells from stem cell sources, namely hepatic progenitor cells (HPC), mesenchymal stem cells (MSC) or induced pluripotent stem cells (iPSC). Cultures of canine primary hepatocytes were produced to use as a gold standard, but also to develop and refine tests of hepatocyte characterisation and function. A panel of primers was developed for use in real time polymerase chain reaction (PCR) as well as optimising tests for low density lipoprotein (LDL) and indocyanine green uptake, albumin production, periodic acid- Schiff staining for glycogen and CYP activity using a luciferase-based system. As primary hepatocytes rapidly lost their defining characteristics and function in vitro, methods of maintaining function using CYP inducers and culture substrates were assessed. Isodensity centrifugation and magnetic-activated cell sorting was employed to isolate HPCs. Selection of cells from the non-parenchymal cell fraction with stem cell marker Prominin 1 demonstrated that these were keratin 7 positive, a HPC marker. Cells morphologically consistent with HPC appeared and expanded in culture after 2 weeks. On passaging, these cells failed to continue expanding, despite plating onto collagen, laminin, SNL feeder cells or using Kubota’s medium (known to allow rapid expansion of rodent and human HPCs). Canine adipose (Ad-MSC) and bone marrow-derived mesenchymal stromal cells (BM-MSC) were isolated post mortem. These were characterised as CD45, 105 and STRO-1 positive, CD11b, 19 and 45 negative cells which could be differentiated into adipocytes, chondrocytes and osteocytes based on staining characteristics and relative gene expression. Protocols published for other species were used to differentiate both Ad-MSC and BM-MSC towards a hepatocyte phenotype. Although a dramatic change in morphology and a reduction in vimentin gene expression were noted, suggesting a loss of mesenchymal phenotype, these protocols did not induce a hepatocyte phenotype. Pre-treatment with 5-Aza-2′-deoxycytidine to cause DNA demethylation and valproic acid to inhibit histone deacetylation also failed to allow transdifferentiation. A polycistronic vector containing Oct-4, c-Myc, Sox2 and Klf4 was successfully transfected into canine epidermal keratinocyte progenitor cells which became alkaline phosphatase positive and assumed a morphology consistent with iPSC. After colony selection and expansion, PCR evidence of plasmid presence was lost, colony morphology changed, and alkaline phosphatase activity reduced, consistent with vector expression factor and pluripotency loss. Canine iPSCs produced by lentiviral method were then differentiated towards hepatocyte phenotype using a published protocol for mouse and human iPSC. These cells were then assessed for hepatocyte characteristics using the developed reagents and primers. These cells demonstrated increased gene expression and morphology consistent with differentiation towards a hepatocyte-like phenotype. This thesis demonstrates successful culture of canine primary hepatocytes and validation of tests of hepatocyte phenotype. This provides a basis for optimising primary hepatocyte function in vitro and assessment of the success of differentiation protocols on stem cell sources. Canine mesenchymal stromal cells do not appear to transdifferentiate towards a hepatocyte-like phenotype using published protocols for other species. Canine iPSC are a promising candidate for an in-vitro source of hepatocyte-like cells.

Orientador: Rosemeri de Oliveira Vasconcelos / Coorientador: Gisele Fabrino Machado / Banca: Daniel Cortes Beretta / Banca: Rosangela Zacarias Machado / Resumo: Os cães infectados pelo protozoário Leishmania (Leishmania) chagasi podem ou não apresentar sinais clínicos dessa zoonose e são a principal fonte de infecção para o homem. A pele é o primeiro órgão infectado pelo parasito na LVC. As enzimas metaloproteinases da matriz (MMPs) atuam na degradação da matriz extracelular (MEC) e na modulação da resposta inflamatória, frente a vários tipos de injúrias. O objetivo deste estudo foi avaliar a expressão de MMP-2 e MMP-9, por meio da técnica de imuno-histoquímica e zimografia na pele de cães naturalmente acometidos por LVC e comparar estes resultados com a imunodetecção das citocinas TNF- e TGF- e do protozoário Leishmania, com as possíveis alterações da matriz extracelular dermal. A alteração da composição de fibras colágenas da derme foi avaliada pela coloração PicroSirius. O método foi usado para diferenciar fibras colágenas dos tipos I e III, nas regiões do focinho, orelha e abdômen. A carga parasitária, intensidade de inflamação e a produção de MMP 2 e 9 foram maiores nas regiões cutâneas da orelha e focinho. Os macrófagos, linfócitos e plasmócitos predominaram no infiltrado inflamatório da derme superficial, formando granulomas, associados a degradação do colágeno maduro (tipo I) e a discreta deposição de colágeno jovem (tipo III), com maior intensidade nos cães com elevada carga parasitária cutânea. O TGF-β foi detectado nos três grupos de cães infectados (assintomático, oligossintomático e sintomático), sem diferenças significativas entre eles. O TNF-α não foi detectado na maioria dos animais infectados e no grupo controle. Conclui-se que quanto maior a carga parasitária e a intensidade de inflamação na pele, maior a degradação do colágeno maduro, produção de MMPs 2 e 9 e produção de TGF-β. A MMP-9 ativa poderia ser utilizada... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Dogs infected by Leishmania (Leishmania) chagasi may or may not show clinical signs of the zoonosis and they are the main source of infection for man. The skin is the first organ infected by the parasite in the LVC. The enzyme matrix metalloproteinases (MMPs) act on the degradation of extracellular matrix (ECM) and in the inflammatory response modulation against many kinds of injuries. The aim of this study was to evaluate the expression of MMP-2 and MMP-9 by immuno-histochemistry and zymography in the skin of dogs naturally affected by LVC and the immunodetection of TNF- and TGF- and of Leishmania and compare these results with the possible alterations of dermal extracellular matrix. The method was used to differentiate collagen fibers in the dermis was evaluated by Picrosirius red staining to differentiate collagen types I and III, in regions of the nose, ear and abdomen. The parasite load, intensity of inflammation, increased production of MMP 2 and 9 were higher in regions of the ear and muzzle. Macrophages, lymphocytes and plasma cells predominated in the inflammatory infiltrate of the superficial dermis, forming granulomas, associated with degradation of mature collagen (type I) and the discrete deposition of the young collagen (type III), with greater intensity in dogs with high parasite load skin. The TGF-β was detected in all groups of infected dogs (asymptomatic, oligosymptomatic and symptomatic), no significant differences among them. The TNF-α was not detected in most infected animals and the control group. It follows that the greater is the intensity of parasitic load and inflammation of the skin, the greater is the degradation of mature collagen, the production of MMPs and 2 and 9, production of TGF-β. Active MMP-9 could be used as a marker of inflammation in infected dogs. This profile of the... (Complete abstract click electronic access below) / Mestre