Construction of a microarray specific to the chicken immune system: profiling gene expression in B cells after lipopolysaccharide stimulation

The objective of this study was to profile gene expression in cells of the chicken immune system. A low-density immune-specific microarray was constructed that contained genes with known functions in the chicken immune system, in addition to chicken-expressed sequence tags (ESTs) homologous with mammalian immune system genes, which were systematically characterized by bioinformatic analyses. Genes and ESTs that met the annotation criteria were amplified and placed on a microarray. The microarray contained 84 immune system gene elements. As a means of calibration, the microarray was then used to examine gene expression in chicken B cells after lipopolysaccharide stimulation. Differential gene expression was observed at 6, 12, and 24 h but not at 48 h after stimulation. The results were validated by semiquantitative polymerase chain reaction. The microarray showed a high degree of reproducibility, as demonstrated by intra- and interassay correlation coefficients of 0.97 and 0.95, respectively. Thus, the low-density microarray developed in this study may be used as a tool for monitoring gene expression in the chicken immune system.     

Microfibril angle non-uniformities within normal and compression wood tracheids

The pattern and extent of variation of microfibril angle (MFA) in normal and compression tracheids of softwood were investigated by using confocal laser scanning microscopy technique. All measurements support the idea that the orientation of microfibrils in single wood tracheids is not uniform. MFA of the radial wall of earlywood tracheids was highly non-uniform and had an approximately circular form of arrangement around the bordered pits (inside the border). Between the bordered pits the measured MFAs were less than the other parts of the tracheid. In the latewood tracheids MFA was less variable. The average orientation of simple pits in the crossfield region was consistent with the mean MFA of the tracheids; however some of the measurements showed a highly variable arrangement in the areas between the simple pits. In many cases the local measured MFAs of compression wood tracheids agreed with the orientation of natural helical cavities of compression wood. Comparing the measured results in different growth rings showed that MFAs in juvenile wood are generally larger than in perfect wood.     

Micromechanics of wood subjected to axial tension

Summary The behaviour of a small group of wood fibers of Sitka spruce during tensile loading is investigated. The load-extension curves for both early and late wood fibers consist of three distinct segments. The first segment is almost a straight line, at some stage of loading a yield point is observed. Beyond this point the specimen becomes less stiff and undergoes a large, mainly irreversible deformation. As the load is increased further, the curve exhibits the third segment showed by a significant change in slope. These curves look different from those obtained on thick specimens. In this respect, the behaviour of a thin wood specimen subjected to cyclic type tensile loading along its longitudinal direction is also illustrated. Based on wood microstructure, a model is presented to interpret the evolution of the Young's modulus of a wood fiber during tensile loading. The model considers wood as an assembly of cylindrical fibers pasted together in a longitudinal direction. We have assumed the cell wall to comprise only an S₂ layer made of a composite material consisting of a lignin and hemicellulose matrix reinforced by helical microfibrils along the fiber. Furthermore, it is assumed that the microfibril angle a in the S₂ layer is not uniform along the fiber axis and matrix degradation occurs in the zones where the microfibril angles are bigger. The validity of this assumption is verified by using holographic interferometry to visualize the displacement field of the specimen's surface under tension.The work reported in this paper is supported by a grant from the Swiss National Science Foundation, and its support is gratefully acknowledged     

Effects of interferon-γ knockdown on vaccine-induced immunity against Marek’s disease in chickens

Interferon (IFN)-γ has been shown to be associated with immunity to Marek’s disease virus (MDV). The overall objective of this study was to investigate the causal relationship between IFN-γ and vaccine-conferred immunity against MDV in chickens. To this end, 3 small interfering RNAs (siRNAs) targeting chicken IFN-γ, which had previously been shown to reduce IFN-γ expression in vitro, and a control siRNA were selected to generate recombinant avian adeno-associated virus (rAAAV) expressing short-hairpin small interfering RNAs (shRNAs). An MDV challenge trial was then conducted: chickens were vaccinated with herpesvirus of turkey (HVT), administered the rAAAV expressing shRNA, and then challenged with MDV. Tumors were observed in 4 out of 10 birds that were vaccinated with HVT and challenged but did not receive any rAAAV, 5 out of 9 birds that were administered the rAAAV containing IFN-γ shRNA, and 2 out of 10 birds that were administered a control enhanced green fluorescent protein siRNA. There was no significant difference in MDV genome load in the feather follicle epithelium of the birds that were cotreated with the vaccine and the rAAAV compared with the vaccinated MDV-infected birds. These results suggest that AAAV-based vectors can be used for the delivery of shRNA into chicken cells. However, administration of the rAAAV expressing shRNA targeting chicken IFN-γ did not seem to fully abrogate vaccine-induced protection.     

Clodronate treatment significantly depletes macrophages in chickens

Macrophages function as phagocytes and antigen-presenting cells in the body. As has been demonstrated in mammals, administration of clodronate [dichloromethylene bisphosphonate (Cl₂MBP)] encapsulated liposomes results in depletion of macrophages. Although this compound has been used in chickens, its effectiveness in depleting macrophages has yet to be fully determined. Here, we show that a single administration of clodronate liposomes to chickens results in a significant depletion of macrophages within the spleen and lungs of chickens up to 4 d post-treatment. This finding suggests that, in order to obtain depletion of macrophages in chickens for greater than 5 d, it is necessary to administer clodronate liposomes 4 d apart. The study also showed that 2 treatments of clodronate liposomes at 4-day intervals resulted in the depletion of macrophages for up to 10 d. The findings of the present study will encourage more precise studies to be done on the potential roles of macrophages in immune responses and in the pathogenesis of microbial infections in chickens.     

Effects of chronic high stocking density on liver proteome of rainbow trout (<Emphasis Type="Italic">Oncorhynchus mykiss</Emphasis>)

The main aim of the present study was to assess the effects of chronic high stocking density on liver proteome of rainbow trout. Rainbow trout juveniles (42.6 ± 2.3 g average body weight) were randomly distributed into six tanks at two stocking densities (low stocking density (LD) = 20 kg m^?3 and high stocking density (HD) = 80 kg m^?3). Both treatments were performed in triplicate tanks for a period of 60 days. High stocking density caused a reduction in the growth performance compared with LD fish. Lysozyme activity increased with stocking density, while serum complement activity presented the opposite pattern. Serum cortisol and total protein levels did not show significant differences (P > 0.05) between experimental groups. The fish reared at high stocking density showed significantly lower osmolality and globulin values but higher albumin level. The HD group had significantly higher activities of catalase, glutathione peroxidase and superoxide dismutase, and malondialdehyde content in the liver when compared to the LD group. Comparative proteomics was used to determine the proteomic responses in livers of rainbow trout reared at high stocking density for 60 days. Out of nine protein spots showing altered abundance (>1.5-folds, P < 0.05), eight spots were successfully identified. Two proteins including apolipoprotein A-I-2 precursor and mitochondrial stress-70 protein were found to increase in HD group. The spots found to decrease in the HD group were identified as follows: 2-peptidylprolyl isomerase A, two isoforms of glyceraldehydes-3-phosphate dehydrogenase, an unnamed protein product similar to fructose-bisphosphate aldolase, 78 kDa glucose-regulated protein, and serum albumin 1 protein.     

The effects of the tank colour on growth performance and physiological responses in fingerling grouper,Epinephelus coioides

In this study, the effects of different background colours on growth performance and physiological parameters of Epinephelus coioides were investigated. One hundred eighty E. coioides (average weight 18.16 ± 0.07 g) were distributed in black, white and blue 300‐L tanks and fed to satiation for 60 days. The tank colour had no significant effect on the weight gain, condition factor, hepatosomatic index and specific growth rate (p > .05). The lowest amount of viscerosomatic index and the highest carcass protein were recorded in the white tank (p < .05). Daily food intake, feed conversion ratio and plasma glucose were significantly higher in the blue tank (p < .05). The highest levels of haematocrit and plasma triglyceride were observed in the white tank, while the total protein and albumin were higher in the black tank compared to the other tanks. The tank colour had no significant effects on the plasma cortisol level (p > .05). Our findings showed that colours used in this study did not evoke stress and thus had no effect on growth, but some metabolic adaptation occurred in each colour to achieve optimum growth.