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The enrichment of egg with folate is a viable option for supplying the general population of a food product rich in natural folates. However, attempts to increase the concentration of folate in egg beyond the achieved level of enrichment had been unsuccessful because egg folate reached a maximum plateau when folic acid (FA) was increased in the diet. Thus, experiments were conducted to determine the factors regulating the deposition of dietary FA into the eggs. In the first study, the effect of feeding equimolar intake of FA and 5-methyltetrahydrofolate (5-methylTHF), the biologically active form of folate; on egg folate concentrations, indices of folate status, and activities of folate-dependent enzymes was evaluated. Folic acid and 5-methylTHF demonstrated equivalent effects in enhancing the egg folate concentrations and improving the indices of folate status in the laying hen. The activities of folate-dependent enzymes were similar between the two forms of folate except for hepatic dihydrofolate reductase (DHFR) activity which increased in FA-fed birds compared to 5-methylTHF-fed birds. However, this demonstrated the ability of the laying hen to metabolically convert FA into its biologically active forms. Therefore, the influence of intestinal FA absorption in the regulation of FA deposition in the egg was subsequently evaluated. Using the in vitro everted intestinal sac technique, FA was absorbed in all regions of the intestine. Absorption was maximum at acidic pH 6.0, and increased in the duodenum and jejunum compared to the ileum and cecum. The rate of FA absorption in the jejunum diminished at higher FA concentrations. Therefore, further study was conducted to determine the regulation of FA absorption when levels of FA in the laying hen diet are increased. Supplementation of increased FA levels resulted to a down-regulation of FA absorption in the duodenum, but not in the jejunum of the laying hen. This down-regulation was not associated to a decreased mRNA gene expression of the duodenal folate transporters. Overall, decreased intestinal rate of FA absorption possibly associated to a post-transcriptional or translational regulation of specific folate transporters in the intestine of the laying hen may contribute to the saturation in the egg folate concentration.

A study was undertaken to evaluate and compare the effectiveness of three anthelmintics, ivermectin, fenbendazole, and a combination of ivermectin and pyrantel pamoate, on fecal egg count reductions of cyathostomes and Parascaris equorum in 30 foals at the Texas A&M Horse Center. The foals were reared under standard horse center practices and were naturally infected with both cyathostomes and Parascaris. The foals were randomized into three treatment groups with individuals being rerandomized after each eight week observation period. The treatments of ivermectin and fenbendazole were given at the manufacturer's recommended doses and the pyrantel treatment was given at two times the manufacturer's recommended dose. All doses were based on weights taken prior to treatment. Fecal egg counts were performed at the time of treatment and at two week intervals after treatment for a total of eight weeks. Each foal received a total of three treatments during the course of the study along with the most effective treatment at the conclusion of the study. Fecal egg counts were performed by a modified McMaster's test with a sensitivity of 25 eggs per gram of feces and by the modified Wisconsin double centrifugal floatation with a sensitivity of 0.2 eggs per gram of feces. Fecal egg reduction percentages were calculated for each two week interval. Analysis of the results showed that ivermectin, either used alone or with pyrantel was a more effective anthelmintic for cyathostome (small strongyle) control than fenbendazole. Fenbendazole and pyrantel showed a higher initial reduction in Parascasris eggs when compared to the ivermectin only treated group, but ivermectin showed improved egg reduction over time. At the conclusion of this study, a primary treatment of ivermectin at the manufacturer's recommended dose and treatment of pyrantel at two times the manufacturer's recommended dose was recommended to control cyathostome egg production and severely reduce the initial number of Parascaris adults in the foals at this facility. Subsequent monthly does of ivermectin at the manufacturer's recommended dose was also recommended to continue to control both parasites. Follow up fecal examinations were also recommended to test the continued effectiveness of the recommended treatment protocol.

The following morphological structures of the ovipositor of Homolobus truncator (Say) (Hymenoptera : Braconidae) are described and hypotheses of their functions are proposed: a series of sharp ridges on the distal surface of the notch helps maintain a grip on the inner surface of the host cuticle; the sperone directs eggs away from the inner surface of the ventral valves; a flap-like structure on each ventral valve covers the portal through which eggs pass; the valvillus maintains position of the egg within the ovipositor and acts against the egg to force it out; ctenidia on the inner surface of the ventral valves move eggs along the basal half of the egg canal; recurved barbs at the apex of each ventral valve hook into the inner surface of the host cuticle to maintain purchase while the thick dorsal valve is inserted into the host. The tribe Maxfischeriini (Hymenoptera : Braconidae) is emended to subfamily status based on morphological and biological evidence. A novel egg morphology is described for Maxfischeria, representing a new life history strategy among Braconidae. Based on egg and ovipositor morphology, I suggest that Maxfischeria is a proovigenic, koinobiont ectoparasitoid. Five new species of Maxfischeria are described (M. ameliae sp. nov., M. anic sp. nov. M. briggsi sp. nov., M. folkertsorum sp. nov., and M. ovumancora sp. nov.). A phylogenetic analysis of morphological and molecular characters for the braconid subfamily Euphorinae is presented. The results imply a revised classification that recognizes 9 tribes and 44 genera. Proposed changes include: Meteorus and Zele are recognized as Meteorinae. Planitorus and Mannokeraia are included among Euphorinae and comprise the tribe Planitorini. Cosmophorini, Euphorini, Helorimorphini, Perilitini, Leiophron, and Perilitus are redefined. The following synonyms are proposed: Cryptoxilonini and Dinocampini with Cosmophorini; Myiocephalini and Proclithrophorini with Perilitini; Myiocephalus with Microctonus; Bracteodes, Falcosyntretus, Sculptosyntretus, Syntretellus, Syntretomorpha, and Syntretoriana with Syntretus and are recognized as subgenera; Perilitus (Townesilitus) with Microctonus and are recognized as a subgenus. Transitions in host associations are examined with ancestral state reconstruction. Some ambiguous nodes in the reconstruction are reconciled by examining the overlap in host associations.

Pseudomonas Aeruginosa is a common gram-negative bacterium present in the environment. It causes severe infections in immunosuppressed patients. Cystic fibrosis patients are especially at risk of being infected with Pseudomonas Aeruginosa. Ongoing studies are preformed to find alternative therapies to antibiotics, due to increased resistance. One new treatment is intake of specific IgY antibodies against Pseudomonas Aeruginosa as an oral therapy. The problem today is that IgY solutions must be kept frozen until consumed.  In this study we examined the possibility to freeze-dry specific IgY antibodies without losing any activity or specificity of the antibodies. This would be more convenient of patients, as well as it makes transportation and storage easier.  The methods used were ELISA for control of activity, western blot analysis and SDS-PAGE gel for control of specificity. Three different batches of the IgY anti-Pseudomonas Aeruginosa solution were tested. The results showed that no loss in activity occurred that would affect clinical outcome or change of specificity in the antibodies after freeze-drying appears. This indicates that it is possible to replace the liquid antibody to a freeze-dried powder.

The Australian Zebra Finch (Taeniopygia guttata) is an important animal model for vertebrate development and behavior. New research initiatives in the fields of epigenetics rely heavily on injecting hormones and environmental toxins directly into the eggs of different bird species such as zebra finches and other passerine songbirds to replicate the effects maternal condition on offspring. However, the widely used method of egg-injections does not accurately replicate physiological conditions, as the injected substances remain concentrated at the injection site for extended periods and do not diffuse into the developing tissues. Therefore, we propose an alternative method to injection protocols that takes advantage of the porous nature of eggs. Corticosterone (CORT), a major vertebrate stress hormone, dissolved in ethyl alcohol was applied to the surface of zebra finch eggs daily. The effect of this treatment on decreasing hatching success shows that topical hormonal treatments are a viable alternative to egg injection.

The enrichment of egg with folate is a viable option for supplying the general population of a food product rich in natural folates. However, attempts to increase the concentration of folate in egg beyond the achieved level of enrichment had been unsuccessful because egg folate reached a maximum plateau when folic acid (FA) was increased in the diet. Thus, experiments were conducted to determine the factors regulating the deposition of dietary FA into the eggs. In the first study, the effect of feeding equimolar intake of FA and 5-methyltetrahydrofolate (5-methylTHF), the biologically active form of folate; on egg folate concentrations, indices of folate status, and activities of folate-dependent enzymes was evaluated. Folic acid and 5-methylTHF demonstrated equivalent effects in enhancing the egg folate concentrations and improving the indices of folate status in the laying hen. The activities of folate-dependent enzymes were similar between the two forms of folate except for hepatic dihydrofolate reductase (DHFR) activity which increased in FA-fed birds compared to 5-methylTHF-fed birds. However, this demonstrated the ability of the laying hen to metabolically convert FA into its biologically active forms. Therefore, the influence of intestinal FA absorption in the regulation of FA deposition in the egg was subsequently evaluated. Using the in vitro everted intestinal sac technique, FA was absorbed in all regions of the intestine. Absorption was maximum at acidic pH 6.0, and increased in the duodenum and jejunum compared to the ileum and cecum. The rate of FA absorption in the jejunum diminished at higher FA concentrations. Therefore, further study was conducted to determine the regulation of FA absorption when levels of FA in the laying hen diet are increased. Supplementation of increased FA levels resulted to a down-regulation of FA absorption in the duodenum, but not in the jejunum of the laying hen. This down-regulation was not associated to a decreased mRNA gene expression of the duodenal folate transporters. Overall, decreased intestinal rate of FA absorption possibly associated to a post-transcriptional or translational regulation of specific folate transporters in the intestine of the laying hen may contribute to the saturation in the egg folate concentration.

Egg is one of the major food allergens that affects 1.6~3.2% of the infants and young children population. The objective of this study is to reduce the egg white IgE binding ability by lactobacilli or Aspergillus oryzae fermentation. Modifications of egg white proteins during fermentation were analyzed by Ninhydrin method, Ellman method, SDS-PAGE, ELISA, and MALDI-TOF-MS. Tryptone supplementation and acidification are necessary to grow lactobacilli in egg white. Egg whites were fermented by L sanfranciscensis, L. sakei, and L. delbrueckii subsp. delbrueckii individually for 96 h; and Aspergillus oryzae for 120 h. The IgE binding ability of egg white was significantly reduced (~50%) by L. delbrueckii subsp. delbrueckii after 48 h of incubation and almost eliminated by Aspergillus oryzae after 24 h of inoculation. In addition to slight modification of ovomucoid (the dominant egg allergen), no substantial protein degradation was observed during fermentation. / Food Science and Technology