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This thesis examines the costs and benefits of maternal allocation to both mother and offspring in gamebirds, specifically ring necked pheasants (Phasianus colchicus) and the Chinese painted quail (Coturnix chinensis). Maternal allocation of compounds from the mother to the young during early development can potentially have both positive and negative effects. For example the transfer of nutrients to the offspring can help to increase post-partum survival and subsequent life time reproductive success. In contrast, the transfer of stress hormones can potentially have long term negative effects on the offspring’s development. The first part of this thesis investigates the effects of the transfer of immune components from mother to offspring, which are known to have positive short term effects (protection against pathogens in early development). There is therefore considerable interest in whether this response can be induced by maternal vaccination to confer protection to young birds in commercial situations. However, it is unclear how this affects life-history trade offs in the mother and the development of the offspring post-hatching. These effects are especially important in the gamebird industry where birds are commercially reared on a large scale before being released into the wild. Chapter 2 therefore examines the costs and benefits to the mother of producing a maternally transmitted immune response to the CoxAbic vaccine, such as the impact of vaccination on egg laying characteristics and body condition. Chapter 3 looks at these costs and benefits to the chicks by examining growth rates and survival after a challenge of live coccidia in offspring from vaccinated and unvaccinated mothers. Chapter 4 examines the immune response to vaccination in adult pheasants. Finally, chapter 5 considers other factors that have been shown to affect the allocation decisions of females, specifically the effect of male characteristics on female reproductive effort.

Thesis (M.P.H.M.)--Mahidol University, 1999.

Diss. (sammanfattning) Linköping : Univ., 2001. / Härtill 5 uppsatser.

Thesis (Ph. D.)--Ohio State University, 2005. / Title from first page of PDF file. Document formatted into pages; contains xxv, 449 p.; also includes graphics (some col.). Includes bibliographical references (p. 376-449). Available online via OhioLINK's ETD Center

An immunoglobulin-fortified milk replacer and a subcutaneous (SC) injectable solution of immunoglobulins (Ig) were examined as methods of achieving passive immunity in neonatal calves. Bovine Ig, from abattoir blood, were purified by polyphosphate fractionation and ion-exchange chromatography. In experiment 1, carried out at Agriculture Canada Research Station, Agassiz, 37 colostrum-deprived Holstein-Friesian bull calves were allotted to one of four treatments. Col/WM calves were fed colostrum on day 1 and whole milk, days 2 - 42. MR-Nolg calves (control) were fed milk replacer with no Ig, days 1-42. MR-Hi/Lo calves were fed milk replacer with Ig at 50 mg/ml on day 1, and at 10 mg/ml, days 2 -21. MR-Hi/No calves were fed milk replacer with Ig at 50 mg/ml, day 1,'and with no Ig, days 2 - 21. From days 2 2 - 42, MR-Hi/Lo and MR-Hi/No treatment calves received milk replacer with no Ig. In experiment 2, carried out at the University Research Farm at Oyster River, 24 colostrum-deprived Holstein-Friesian bull calves were allotted to one of three treatments. The first two treatments were the same as for experiment 1, Col/WM and MR-Nolg fed for days 1-21. MR-Lo Inj calves were fed milk replacer with Ig at 10 mg/ml, days 1-21, and were also given a SC injection of Ig solution within the first 6 hours of life. For days 2-42, calves were fed WM or MR-Nolg, as per experiment 1. For both experiments, blood samples and calf weights were taken at birth, 24 & 48 hours of age, day 7 and weekly thereafter for six weeks. Diarrhea (scours) levels, rectal temperatures and general health of calves were recorded daily for the first three weeks as well. Experiment 1 survival at 6 weeks of age was 11 out of 11 calves for Col/WM treatment, 8 out of 8 calves for MR-Hi/Lo treatment, 7 out of 8 calves for MR-Hi/No and a significantly lower (P>0.05) 7 out of 9 calves for MR-Nolg. In experiment 2, survival was 7 out of 8 calves for both Col/WM and MR-Lo-Inj treatments and a significantly lower (P>0.05) 4 out of 8 calves for MR-Nolg treatment. Calves on MR-Hi/No had significantly higher diarrhea levels than the other three treatments over weeks one and four in experiment 1. In experiment 2, calves which did not receive any Ig had significantly higher diarrhea levels over weeks three and four than calves which received Ig. Experiment 1 average daily gains (ADG) were significantly higher for calves on Col/WM, MR-Hi/Lo and MR-Hi/No treatments than for calves on MR-Nolg at six weeks of age. In experiment 2, six week ADG were significantly higher for calves on Col/WM and MR-Lo Inj treatments than for MR-Nolg. For both experiments, serum Ig levels of calves on Col/WM were significantly higher than calves on the other treatments at 24 and 48 hours of age. MR-Hi/Lo, MR-Hi/No and MR-Lo Inj calves trended to higher serum Ig levels than MR-Nolg calves but were not significantly different. Calves which received Ig, from colostrum, the Ig-fortified milk replacer or a subcutaneous Ig injection, had higher survival rates, lower diarrhea levels, less antibiotic treatment and higher average daily gains than calves hot receiving any Ig. It was concluded that immunoglobulins, administered either orally or parenterally, are an effective, alternative method, for providing passive immunity in neonatal calves. / Land and Food Systems, Faculty of / Graduate

Parasites have a major impact on host condition and fitness and thereby represent a strong selective force for individuals in wild populations. The main defence against parasite infection and associated morbidity is the host immune response, and consequently it is expected for there to be strong selection eroding genetic variation underlying immune responses in natural populations. However, studies in the wild have found considerable heritable variation underlying immune responses. Few studies have investigated the genetic variants underlying immunity in wild populations and are able to examine how genetic variation is maintained in the face of natural selection. The aim of this thesis is to investigate the selection on, and genetic variation underlying, immunity in a wild Soay sheep population by looking at antibody responses to the prevalent parasite Teladorsagia circumcincta. Anti- T. circumcincta antibody levels (IgA, IgE, IgG) were measured in neonatal plasma samples taken soon after birth, representing maternally-derived antibodies, and in samples from August yearly from four month old lambs and adults, representing endogenous antibodies. All three endogenously produced antibody measures in lambs and adults were repeatable and heritable. In addition, a genome wide association study run on the three antibody traits on August lamb and adult measures found associations between anti-T. circumcincta IgA levels and single nucleotide polymorphisms in a region on chromosome 24. There was evidence for age- and isotype- dependent negative associations between antibody isotypes and strongyle faecal egg counts (FEC). Further, there was evidence for age-dependent selection via positive associations between anti-T. circumcincta IgG and survival in females and annual fecundity in males. In comparison, there was no additive genetic variance underlying maternally-derived (neonatal) anti-T. circumcincta antibody levels in neonates, but maternal and maternal genetic effects explained a considerable proportion of the variance in these traits. There was evidence for associations between neonatal anti-T. circumcincta IgG and later offspring phenotype and fitness, independent of total antibody (IgG) transferred. We found that neonatal anti-T. circumcincta IgG levels positively predicted survival to four months old, as well as weight in August. In addition, neonatal anti-T. circumcincta IgG levels were associated with reduced strongyle FEC in August, and were associated with improved survival over the first winter. In early life, maternally-derived anti-helminth antibodies are important for early growth, survival, and parasite resistance, as well as first winter survival, while fitness benefits in adulthood were associated with higher endogenous anti-helminth antibody levels. This thesis illustrates that maternal effects and genetic variation can have strong effects on variation in immunity in the wild, and this variation in turn can have health and fitness consequences for individuals.

Thesis (Ph.D.(Paediatrics))--University of Pretoria, 2009. / Abstract in English and Afrikaans. Includes bibliographical references.

Mitochondrial diseases are caused by gene mutations in either mitochondrial DNA (mtDNA) or nuclear DNA (nDNA) and they are among one of the most common forms of inherited disorders. It is estimated that 1 out of every 5000 individuals will develop a mitochondrial disease in their lifetime. Due to the crucial and widespread functionality of mitochondria in human cells, prolonged diseases of the mitochondria affect cells of the brain, heart, liver, muscles and kidneys and can lead to multi-organ failure in some patients. Inherited or acquired mitochondrial diseases can present at any stage of life, affecting both children and adults. Since its discovery, the mitochondrial genome has been analyzed and sequenced with increasing ease and this process has helped recognize various mitochondrial disorders as the root of genetic diseases. This paper will explore the unique properties of the mitochondrion and its genome, examine the relationship between mtDNA and some common myopathies such as Leigh syndrome (LS) or maternally inherited Leigh syndrome (MILS), mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) in order to explore commonalities and differences in their inheritance patterns and their effect on mitochondrial function. Although studies have shown that these conditions generally affect the process of oxidative phosphorylation in mitochondria, because of the wide variety of presentations of this disease, further research is needed to understand the different etiologies, as well as to explore novel therapies to treat them.

A transferência passiva de anticorpos da mãe para o filho auxilia na adaptação ao meio externo. No recém-nascido (RN), a colonização pelo Staphylococcus aureus (S. aureus) é precoce, sendo este um importante agente etiológico em infecções neonatais e no lactente jovem, para o qual ainda não se dispõem de vacina. OBJETIVOS: Avaliar as concentrações, títulos e avidez de anticorpos maternos anti-S. aureus do tipo IgG e IgA e a passagem desses anticorpos para os RN por transferência placentária e pelo colostro. MÉTODOS: Estudo caso-controle de 147 parturientes saudáveis. Foram coletadas amostras de soros maternos, de cordão umbilical e colostro. O grupo caso foi definido pela colonização nasal natural pelo S. aureus, sendo que para cada caso (n=49) foram selecionados 2 controles (n=98). Foram utilizadas as metodologias de imunoturbidimetria para dosagem de IgG total, ensaio imunoenzimático para dosagem IgA total e para a aferição das concentrações e títulos de anticorpos específicos anti-S. aureus (IgG sérica, subclasses séricas IgG1 e IgG2, IgA de colostro e os índices de avidez). Foram aplicados testes não paramétricos de Wilcoxon para amostras pareadas e de Mann-Whitney para amostras não pareadas, com intervalo de confiança de 95%, nível de significância p < 0,05. RESULTADOS: No grupo caso, as concentrações séricas de IgG total materna foram maiores mas com menor taxa de transferência placentária de IgG total, ocorrendo o inverso para o grupo controle. Não foram observadas diferenças nas concentrações séricas de IgG materna anti-S. aureus entre os grupos, mas com taxa de transferência placentária significantemente menor no grupo caso. Observou-se que os títulos específicos de IgG1 anti-S. aureus foram mais baixos no soro materno e no cordão do grupo caso, com taxas de transferência similar para os grupos caso e controle. Para os títulos específicos de IgG2 anti-S. aureus, não foram observadas diferenças entre os grupos caso e controle, com taxas de transferência similares entre os grupos. Observou-se que os títulos de IgG2 foram maiores que os de IgG1, tanto no soro materno como no de cordão em ambos os grupos. No soro materno e de cordão, não foram encontradas diferenças entre os grupos nos ensaios de avidez de IgG anti-S. aureus. No estudo de colostro, a concentração de IgA total foi maior no grupo caso, mas sem diferenças entre os grupos para a IgA anti-S. aureus. A comparação da avidez de anticorpos IgA anti-S. aureus do colostro com a de IgG anti-S. aureus do soro materno, em ambos os grupos, mostrou que a avidez de IgA foi maior. CONCLUSÕES: Os resultados demonstraram que a colonização nasal materna por S. aureus não esteve associada com uma maior transferência para o RN de anticorpos IgG ou IgA específicos via placenta ou colostro. A maior transmissão de títulos elevados de IgG2 específicos para o recém-nascido, isto é, anticorpos com uma baixa atividade opsonizante, reitera a maior susceptibilidade neonatal para este agente patogênico. A IgA secretora no colostro apresentou melhor índice de avidez do que a IgG do soro, o que corrobora com a importância da amamentação nos primeiros meses de vida / The passive transfer of antibodies from mother to child assists in adjustment to the external environment. In the newborn (NB), colonization by Staphylococcus aureus (S. aureus) occurs early, which is an important etiologic agent in neonatal and young infant infections, for which no vaccine is available. AIMS: To evaluate concentrations, titers and avidity of anti-S. aureus maternal IgG and IgA antibodies and transmission of these antibodies to the newborns via placental transfer and colostrum. METHODS: Case-control study of 147 healthy pregnant women. Samples of maternal serum, cord blood and colostrum were collected. The case group was defined by natural nasal colonization with S. aureus, and for each case (n = 49) were selected 2 controls (n = 98). Immunoturbidimetric assay was used to measure total IgG, and immunoenzymatic assay to measure total IgA in colostrum and anti-S. aureus concentrations and titers (serum IgG, serum IgG1 and IgG2, colostrum IgA and IgG and IgA avidity indexes). Nonparametric Wilcoxon test for paired samples and the Mann-Whitney test for unpaired samples were applied, with a confidence interval of 95%, significance level of p < 0.05. RESULTS: In the study group, maternal total IgG serum concentrations were higher but with lower total IgG placental transfer ratio, while the opposite occurred for the control group. No differences were observed in anti-staphylococcal maternal IgG serum concentrations between groups, but placental transfer ratio was significantly lower in the case group. It was observed that anti-S. aureus IgG1 titers were lower in maternal and cord serum from the case group, with with similar transfer ratios for case and control groups. Regarding antistaphylococcal IgG2 titers, no differences were observed between case and control groups, with similar transfer ratios between groups. It was observed that specific IgG2 titers were higher than those of IgG1 in both maternal and cord serum from both groups. In maternal and cord blood serum, no differences between groups were found in avidity assays of anti-S. aureus IgG. In colostrum, total IgA concentrations were higher in the case group, but no differences between groups for anti-S. aureus IgA were detected. The comparison of anti-staphylococcal IgA antibodies avidity in colostrum with anti-S. aureus IgG in maternal serum from both groups, showed that IgA presents higher avidity indexes. CONCLUSIONS: The results demonstrated that maternal nasal colonization by S. aureus was not associated with a higher transfer to the NB of specific IgG or IgA antibodies via the placenta or colostrum. The greatest transmission of Sa-specific IgG2 titers to the newborn, i.e., antibodies with low opsonizing activity, reiterates the higher neonatal susceptibility to this pathogen. Secretory IgA in colostrum showed better avidity index than serum IgG, which reinforces the importance of breastfeeding in the early months of life