A Tuberculose vem acometendo animais selvagens desde o surgimento das primeiras coleções organizadas. Particularmente, macacos são altamente suscetíveis as micobactérias, gerando grandes perdas econômicas para as instituições, além do risco de transmissão para o homem e animais. As principais micobatérias, que causam a doença em primatas em cativeiro, são o Mycobacterium tuberculosis e Mycobacterium bovis. Acredita-se que primatas do "novo mundo" são menos suscetíveis do que os do "velho mundo", entretanto observa-se que tuberculose tem sido documentada em várias espécies. A principal forma de transmissão é através de aerossóis contendo os bacilos. A doença pode evoluir para a forma ativa ou latente, dependendo do estado imunológico do animal. Os sinais clínicos podem ser insidiosos, com somente uma alteração comportamental, seguido por anorexia e letargia, alterações respiratórias ou simplesmente o animal pode aparecer morto no recinto. O diagnóstico clínico é difícil e problemático, sendo que muitas vezes as lesões consistentes com a doença só são observadas na necropsia. Por isso o uso de outras ferramentas de diagnóstico é importante, como o teste de tuberculinização, cultivo e isolamento bacteriano, que são os mais usados na rotina das instituições, e os exames radiográficos do tórax e abdômen, testes moleculares e sorológicos. Toda instituição que mantém primatas em cativeiro deveriam possuir programas de prevenção para evitar a entrada da micobactéria dentro da coleção, principalmente ao se adquirir novos animais. Por isso, o emprego de medidas de biossegurança é essencial para diminuir o risco de doenças para o homem e para os animais dentro das instituições. Essas medidas consistem na implantação de uma série de procedimentos e normas operacionais rígidas, como programas de quarentena, programas de saúde para os funcionários e formação de equipe capacitada e treinada. / Tuberculosis has been affecting wild animals since the arising of the first organized collections. Specially, monkeys are highly susceptible to mycobacteria, which cause great economic losses in the institutions, beyond the risk of transmission to man and animals. The main species of mycobacteria, that cause disease in nonhuman primates in captivity, are Mycobacerium tuberculosis and Mycobacterium bovis. It is believed that nonhuman primates from the "new world" are less susceptible than the "old world" ones, however it is noted that tuberculosis has been continually documented in several species. Aerosols that contain infectious bacilli are the main transmission mode. The disease can progress to active or latent form, which depends on the animal's immune status. The clinical signs can be insidious, with only a behavior change, followed by anorexia and lethargy, respiratory alteration or the animal can appear dead in the room. The clinical diagnostic is difficult and problematic, and often lesions are only observed at necropsy. Therefore, the use of other diagnostic tools is important, as the tuberculin skin test, bacterial culture and isolation, that are most used during the routine of institutions, and radiography of the chest and abdomen, molecular and serological tests. Every institution that maintains nonhuman primates in captivity should have prevention programs to avoid the entry of mycobacteria inside of collection, mainly when new animals are acquired. Thus, the use of biosecurity measures is essential to reduce the risk of disease in humans and animals within institutions. These measures consist in implanting series of rigid procedures and operational standards, like quarantine programs, health programs for employees and formation of the qualified team.

The acquisition of relational concepts plays an integral role and is assumed to be a prerequisite for analogical reasoning. Language and token-trained apes (e.g. Premack, 1976; Thompson, Oden, and Boysen, 1997) are the only nonhuman animals to succeed in solving and completing analogies, thus implicating language as the mechanism enabling the phenomenon. In the present study, I examine the role of meaning in the analogical reasoning abilities of three different primate species. Humans, chimpanzees, and rhesus monkeys completed relational match-to-sample (RMTS) tasks with either meaningful or nonmeaningful stimuli. For human participants, meaningfulness facilitated the acquisition of analogical rules. Individual differences were evident amongst the chimpanzees suggesting that meaning can either enable or hinder their ability to complete analogies. Rhesus monkeys did not succeed in either condition, suggesting that their ability to reason analogically, if present at all, may be dependent upon a dimension other than the representational value of stimuli.

The purpose for the present study was to examine working memory for what, where, and when information in rhesus monkeys (Macaca mulatta) and adult humans using a computerized task. In Experiment 1, monkeys and humans completed three delayed matching-to-sample (DMTS) tasks: 1) identity DMTS, 2) spatial DMTS, and 3) temporal DMTS. In Experiments 2, the identity and spatial tasks were combined so that monkeys had to report both what and where information about an event. In Experiment 3, the identity, spatial, and temporal tasks were combined in order to examine what-where-when memory integration. In Experiment 4, monkeys and humans were presented with two sequential events, and a memory cue indicated which event they were required to report. The rhesus monkeys and human participants were able to report all three components of the events and there was some evidence suggesting that these components were integrated in memory for the rhesus monkeys.

Ebola virus (EBOV) is a zoonotic pathogen which causes a fulminant hemorrhagic fever and results in up to 90% fatality. Despite efforts over the past 38 years, a licensed prophylactic or post-exposure option remains unavailable. Several experimental vaccines have already demonstrated protection from lethal EBOV disease in nonhuman primates (NHPs). However, attempts to translate this research from bench to bedside have been hampered, since the immune responses that correlate with protection against EBOV are not well-defined. Without this information, it is not possible to reliably predict the efficacy of vaccines or treatments in humans without lethal challenge. The goal of this thesis is to determine the immune parameters that are predictive of protection against EBOV. Due to the rapid speed of EBOV pathogenesis, it was originally hypothesized that a rapid and robust CD8+ T-cell response must be crucial for survival. Using a previously-characterized adenovirus-vectored Ebola vaccine (Ad5-optGP), transgenic/knockout C57BL/6J mice with ablation for selected immune responses were vaccinated and challenged 28 days later. Surprisingly, while CD8+ T-cell knockout mice survived infection, B-cell knockout mice did not, indicating that the antibody response played a critical role in protection. Humoral and cell-mediated responses were compared between survivor and moribund guinea pigs and NHPs from previous vaccination and post-exposure therapy experiments, either with Ad5-optGP or a vesicular stomatitis virus (VSV)-vectored vaccine (VSVΔG/EBOVGP). Circulating EBOV glycoprotein (GP)-specific IgG antibody levels were the best correlation for protection independent of vaccine platform or timing of exposure (p<0.0001), strongly supporting the role of antibody responses in the control of EBOV infection. To demonstrate that antibodies are also responsible for protection, three previously-characterized monoclonal antibodies recognizing different GP epitopes were combined into a cocktail (ZMAb). Initiation of ZMAb treatment 1 and 2 days post infection (dpi) with EBOV protected 100% and 50% of NHPs, respectively. These results provide a reliable measure for predicting protection from EBOV in three commonly used animal models, and present a strong case for the use of antibodies as an effective post-exposure treatment. This knowledge will ultimately help in the development and validation of a clinical product against EBOV infection.

This thesis reports on cross-sectional surveys aimed at detecting and characterizing haemoprotozoan parasites infecting wild free-ranging non human primates (NHPs) in Kenya, East Africa. Blood samples from olive baboons (Papio cynocephalus anubis), vervet monkeys or African green monkeys (AGMs, Chlorocebus aethiops) and Syke's monkeys (Cercopithecus mitis) from five provinces of Kenya were analyzed. The haemoprotozoan parasites survey was performed with microscopic evaluation of blood smears, serological techniques and molecular tools. Blood specimens and serum samples from 121 NHPs were tested for the presence of Trypanosoma brucei (Study I). Indirect antibody enzyme-linked immunosorbent assay (Ab-ELISA) detected titers of anti-T. brucei antibodies in 19% (23/121) of the sera sampled. Subsequent field-oriented latex agglutination test (LAT) detected presence of T. brucei antigens in 16% (19/121) of the sera. However, there were no active infections detected on fixed blood smears, or wet blood films. Of the 378 NHPs sera samples tested for Leishmania major exposure using Ab-ELISA, 66% had detectable anti-L. major antibodies (study II). Western blot (WB) assay detected anti-L. major antibodies in sera from 46% (175/378) of the NHPs samples. Specific proliferation of peripheral blood mononuclear cells to L. major antigen was demonstrated in 23% (17/57) of AGMs samples. Haemoprotozoan parasites, Entopolypoides macaci and Hepatocystis kochi were detected by microscopic evaluation of Giemsa-stained blood smears from 179 NHPs (study III). The prevalence rate of E. macaci was 43% in African green monkeys, 35% in Syke’s monkeys and 33% in baboons. H. kochi infection rate was 18% in African green monkeys, 23% in baboons and 25% in Syke’s monkeys. Subsequent indirect immunofluorescent antibody test (IFAT) supported the morphologic appearance of E. macaci observed by microscopy. Molecular tools were used to detect and identify haemoprotozoan parasites in wild free-ranging NHPs (study IV). Nested polymerase chain reaction (PCR) targeting Babesia β-tubulin gene detected a 22% (27/125) B. microti infections in free-ranging NHPs in Kenya. PCR also detected 22% mixed infections by Hepatocystis and Entopolypoides, 12% Hepatocystis and Babesia and 7% Entopolypoides and Babesia (study V). Phylogenetic analysis inferred from mitochondrial cytochrome b (Cyt-b) gene confirmed the presence of Hepatocystis kochi whereas analysis of 18SS rRNA gene confirmed presence of two piroplasms, Babesia sp. and Entopolypoides macaci. In conclusion, epidemiological results from sero-prevalence studies provide strong circumstantial evidence that some species of Kenyan NHPs are naturally exposed to L. major and T. brucei infections and could be potential reservoir hosts for these haemoparasites. Molecular diagnosis revealed the occurrence of mixed parasite infections and confirmed the circulation of Babesia and Entopolypoides species in the same populations of Kenyan NHPs.

abstract: Within the primate lineage, skeletal traits that contribute to inter-specific anatomical variation and enable varied niche occupations and forms of locomotion are often described as the result of environmental adaptations. However, skeletal phenotypes are more accurately defined as complex traits, and environmental, genetic, and epigenetic mechanisms, such as DNA methylation which regulates gene expression, all contribute to these phenotypes. Nevertheless, skeletal complexity in relation to epigenetic variation has not been assessed across the primate order. In order to gain a complete understanding of the evolution of skeletal phenotypes across primates, it is necessary to study skeletal epigenetics in primates. This study attempts to fill this gap by identifying intra- and inter-specific variation in primate skeletal tissue methylation in order to test whether specific features of skeletal form are related to specific variations in methylation. Specifically, methylation arrays and gene-specific methylation sequencing are used to identify DNA methylation patterns in femoral trabecular bone and cartilage of several nonhuman primate species. Samples include baboons (Papio spp.), macaques (Macaca mulatta), vervets (Chlorocebus aethiops), chimpanzees (Pan troglodytes), and marmosets (Callithrix jacchus), and the efficiencies of these methods are validated in each taxon. Within one nonhuman primate species (baboons), intra-specific variations in methylation patterns are identified across a range of comparative levels, including skeletal tissue differences (bone vs. cartilage), age cohort differences (adults vs. juveniles), and skeletal disease state differences (osteoarthritic vs. healthy), and some of the identified patterns are evolutionarily conserved with those known in humans. Additionally, in all nonhuman primate species, intra-specific methylation variation in association with nonpathological femur morphologies is assessed. Lastly, inter-specific changes in methylation are evaluated among all nonhuman primate taxa and used to provide a phylogenetic framework for methylation changes previously identified in the hominin lineage. Overall, findings from this work reveal how skeletal DNA methylation patterns vary within and among primate species and relate to skeletal phenotypes, and together they inform our understanding of epigenetic regulation and complex skeletal trait evolution in primates. / Dissertation/Thesis / Doctoral Dissertation Anthropology 2017

A Tuberculose vem acometendo animais selvagens desde o surgimento das primeiras coleções organizadas. Particularmente, macacos são altamente suscetíveis as micobactérias, gerando grandes perdas econômicas para as instituições, além do risco de transmissão para o homem e animais. As principais micobatérias, que causam a doença em primatas em cativeiro, são o Mycobacterium tuberculosis e Mycobacterium bovis. Acredita-se que primatas do &quot;novo mundo&quot; são menos suscetíveis do que os do &quot;velho mundo&quot;, entretanto observa-se que tuberculose tem sido documentada em várias espécies. A principal forma de transmissão é através de aerossóis contendo os bacilos. A doença pode evoluir para a forma ativa ou latente, dependendo do estado imunológico do animal. Os sinais clínicos podem ser insidiosos, com somente uma alteração comportamental, seguido por anorexia e letargia, alterações respiratórias ou simplesmente o animal pode aparecer morto no recinto. O diagnóstico clínico é difícil e problemático, sendo que muitas vezes as lesões consistentes com a doença só são observadas na necropsia. Por isso o uso de outras ferramentas de diagnóstico é importante, como o teste de tuberculinização, cultivo e isolamento bacteriano, que são os mais usados na rotina das instituições, e os exames radiográficos do tórax e abdômen, testes moleculares e sorológicos. Toda instituição que mantém primatas em cativeiro deveriam possuir programas de prevenção para evitar a entrada da micobactéria dentro da coleção, principalmente ao se adquirir novos animais. Por isso, o emprego de medidas de biossegurança é essencial para diminuir o risco de doenças para o homem e para os animais dentro das instituições. Essas medidas consistem na implantação de uma série de procedimentos e normas operacionais rígidas, como programas de quarentena, programas de saúde para os funcionários e formação de equipe capacitada e treinada. / Tuberculosis has been affecting wild animals since the arising of the first organized collections. Specially, monkeys are highly susceptible to mycobacteria, which cause great economic losses in the institutions, beyond the risk of transmission to man and animals. The main species of mycobacteria, that cause disease in nonhuman primates in captivity, are Mycobacerium tuberculosis and Mycobacterium bovis. It is believed that nonhuman primates from the &quot;new world&quot; are less susceptible than the &quot;old world&quot; ones, however it is noted that tuberculosis has been continually documented in several species. Aerosols that contain infectious bacilli are the main transmission mode. The disease can progress to active or latent form, which depends on the animal&#39;s immune status. The clinical signs can be insidious, with only a behavior change, followed by anorexia and lethargy, respiratory alteration or the animal can appear dead in the room. The clinical diagnostic is difficult and problematic, and often lesions are only observed at necropsy. Therefore, the use of other diagnostic tools is important, as the tuberculin skin test, bacterial culture and isolation, that are most used during the routine of institutions, and radiography of the chest and abdomen, molecular and serological tests. Every institution that maintains nonhuman primates in captivity should have prevention programs to avoid the entry of mycobacteria inside of collection, mainly when new animals are acquired. Thus, the use of biosecurity measures is essential to reduce the risk of disease in humans and animals within institutions. These measures consist in implanting series of rigid procedures and operational standards, like quarantine programs, health programs for employees and formation of the qualified team.

The evolutionary origins of human handedness are not yet fully understood as evidence of lateralized behavior in nonhuman primates is inconclusive. In the present study, lateralized behavior in both spontaneously occurring motor patterns and a tube task was examined in 15 white-handed gibbons (Hylobates lar). Significant side preferences at the individual level were found within all 15 studied motor patterns. However, no population-level side bias was found for any of the spontaneously occurring or task-related motor patterns and none of the gibbons were consistent in their hand preference across all motor patterns. When only considering the individuals with a significant preference, a significant majority was left-preferent for resting foot. Strength of side preference was significantly higher for the tube task than for all spontaneously occurring motor patterns. Side preferences for manipulation and resting position were significantly stronger than those for supporting hand. Additionally, the preferences for manipulation were significantly stronger than those for leading limb. In the bimanual tube task, females displayed a tendency towards a left-side bias, while males tended to display a bias to the right. Furthermore, females had a significantly stronger hand preference for supporting hand than males. No other sex differences were found. Age, posture, and kinship had no significant effect on lateralized behavior for any of the motor patterns. As in other nonhuman primates, the white-handed gibbons were only consistent in their hand preference across tasks that required similar movements. Altogether, these findings support the notion that population-level handedness may be restricted to human subjects.

No description available.

No description available.