绿色富硒生物猪饲料中AFB1达标生产工艺优化研究

饲料中黄曲霉毒素(AFB₁)容易超标,检出率达80%~100%,毒性大,具强致癌性,可抑制生猪免疫机能,降低动物生产性能,引起动物继发感染,还会在动物产品中残留而威胁人类健康,给生猪养殖带来经济损失,降低猪肉食品安全性。本文通过使用先进固体发酵系统设备和益生菌发酵技术,采用单因素试验和响应面中试优化,获得发酵降解猪饲料AFB₁的最佳工艺参数为硒浓度0.3 mg/kg,发酵时间12 h,量子波强度30 Hz,益生菌菌种组合CGMCC NO.17328混合CGMCC NO.15611。该工艺将猪饲料AFB₁量从63.41μg/kg降解到2.98μg/kg,降解率达到95.30%,AFB₁含量达到国家饲料安全标准。生产工艺适合养猪场低成本快速生产AFB₁达标猪饲料。     

Comparison of flagellin and an oil-emulsion adjuvant in inactivated Newcastle disease vaccine in stimulation of immunogenic parameters

The present study was designed to investigate the potential application of native (N) and recombinant (truncated modified [tmFliC] and full-length [flFliC]) flagellin proteins along with inactivated Newcastle disease virus (NDV). Fifty six SPF chickens were immunized twice with PBS (control), inactivated NDV (Ag), inactivated NDV/flFliC (AgF), inactivated NDV/tmFliC (AgT), inactivated NDV/N (AgN), commercial vaccine containing Montanide (Vac) and Vac/N (VacN), with a two-week interval. Blood was collected weekly and spleens were harvested after chickens were sacrificed. Interleukin-6 (IL-6) and tumor necrotic factor-α (TNF-α) gene expression in peripheral blood mononuclear cells were analyzed by Real-Time PCR. Antibody response was assessed by haemagglutination inhibition (HI). Cellular activity was quantified by MTT assay. Results showed that the most IL-6 and TNF-α gene expression was observed in AgF group (P < 0.01). The lowest gene expression among vaccinated groups was observed in Ag group for IL-6 and Ag and Vac group for TNF-α. The highest HI titer was observed in Vac, VacN, AgF and AgT groups. The AgF group showed the highest cellular activity (P < 0.01). In conclusion, flagellin-adjuvanted groups showed a pro-inflammatory effect and acted similarly to or better than the Vac group. Hence, flagellin can be proposed as a potential adjuvant for ND vaccine.     

Genome wide association studies (GWAS) of element contents in grain with a special focus on zinc and iron in a world collection of barley (Hordeum vulgare L.)

Genome wide association studies (GWAS) were carried out to map Quantitative Trait Loci (QTL) associated with element contents in the grain using 336 spring barley. Of the elements analyzed, Fe content ranged from 21.9 to 91.0 mg kg⁻¹, Zn from 10.4 to 54.5 mg kg⁻¹, Ba from 0.2 to 8.9, Ca from 186.4 to 977.5, Cu from 1.5 to 9.8, K from 353.2 to 7721.5, Mg from 1049.8 to 2024.2, Mn from 8.1 to 22.9, Na from 55.9 to 627.9, P from 2272.9 to 5428.8, S from 880.7 to 1898.0, Si from 19.1 to 663.2, and Sr from 0.35 to 2.62 mg kg⁻¹. GWAS were carried out using 6519 SNP markers and multiple elements in MLM:PCA + K model in TASSEL software. Population analyses showed two sub-populations, primarily based on row types. GWAS for row types showed association with INTERMEDIUM-C, a modifier gene for lateral spikelet fertility in the 4H chromosome, validating current GWAS approach. GWAS also showed that 2 QTL for Ba, 2 for Ca, 4 for Cu, 11 for Fe, 2 for K, 3 for Mg, 6 for Mn, 4 for Na, 3 for S, 5 for Si, and 3 for Zn were mapped in barley chromosomes. The QTL identified in the current study are valuable for breeding nutrient dense barley cultivars in the future, especially Zn and Fe.     

Effects of Large Saddle Panels on the Biomechanics of the Equine Back During Rising Trot: Preliminary Results

The saddle panels, directly in contact with the horse's back, are likely an important element to optimize the fitting of the saddle, the comfort of the horse, and subsequently, the pain management in dorsalgic horses. The aim of this study was to better understand the effect of the saddle panels on the horse's back, by evaluating a prototype saddle (comfort panels: CP) compared to a standard saddle (STD). The horse's back movements were measured using inertial measurement units (IMUs) fixed at the levels of thoracic vertebrae T6, T12, T16 (under the saddle) and lumbar vertebrae L2 and L5. The centers of mass (COMs) of the horse and the rider and limb's protraction-retraction angles, pressure between saddle and horse's back, and force on the stirrups were measured using respectively 2D motion capture, pressure mat and force sensors in the stirrup leather. Three horses were trotted at the rising trot (sitting: left diagonal-rider seated; standing: right diagonal-rider standing) by the same rider. To compare saddles, linear mixed-effects regression models were used. The estimated means (SE) were calculated. During sitting phase, pressure in the cranial and middle areas of the saddle significantly increased for CP compared to STD (+0.9 (0.2) kPa and +1.0 (0.1) kPa, respectively) whereas caudal pressure decreased (−1.8 (0.4) kPa). Concurrently, the range of motion of angles T12-T16 and T16-L2 under the saddle significantly increased (+1.8 (0.2)° and +2.3 (0.3)°, respectively). The results showed that modifications of the panels' shape not only affect the pressure distribution but also the kinematics of the thoracic and lumbar regions of the equine back.     

Intrinsic influence of various plasticizers on functional properties and reactivity of wheat gluten thermoplastic materials

Various compounds, differing in their chemical functions, number of functional group and degree of hydrophobicity, were tested as wheat gluten plasticizers in a thermoplastic process. A low melting point and a moderate hydrophobicity were found to be critical characteristics of a good wheat gluten plasticizer. The influence of five selected plasticizers (water, glycerol, 1,4-butanediol, lactic and octanoic acids) on functional properties of the wheat gluten network was investigated. Dried gluten was used to avoid any plasticization due to hydration water (usually around 10% for commercial gluten). The influence of plasticizer properties and content was studied by dynamic mechanical thermal analysis, size exclusion-high performance liquid chromatography, tensile and water swelling tests. The plasticizing effect, at the same molar content, was found to be identical for water, glycerol and 1,4-butanediol. Lactic and octanoic acids were found to have higher and lower plasticizing effects, respectively. Mechanical properties were mainly related to the thermoplastic state of the materials. Water and lactic acid were found to confer smaller and larger extensibilities, respectively, to gluten materials. Thermo-mechanical reactivity also depended on plasticizer properties. Gluten aggregation, normally induced by heating, was prevented by the acidic environment produced by lactic acid. Water swelling behaviour was found to depend on the hydrophobicity of the plasticizer used, on the degree of gluten crosslinking and on the pH of the gluten-plasticizer blend.     

Passive protection of mice with antiserum to neuraminidase fromPasteurella multocida serotype A:3

Antiserum to a partially purified neuraminidase fromPasteurella multocida, type A:3, was adsorbed with protease-digestedP. multocida type 3 lipopolysaccharide (LPS) to remove LPS immunoreactivity. The LPS-adsorbed antineuraminidase caused a 77% reduction in the neuraminidase activity of homologousP. multocida in anin vitro enzyme neutralization test. All 14 mice passively immunized with the adsorbed antineuraminidase were protected against challenge infection with homologousP. multocida in a mouse protection test. Ten out of 14 mice in one group that received antisera containing antibodies to both neuraminidase and LPS were protected. In contrast, only 1 out of 14 mice that were immunized with pre-immune serum survived the challenge. These results suggest that antiserum toP. multocida neuraminidase was, at least partly, responsible for the protection observed in this study. Neuraminidase may be one of the immunogenic protective proteins present in aqueous extracts ofPasteurella multocida.     

Comparisons of physiological and biochemical responses between milkfish (Chanos chanos) and grass carp (Ctenopharyngodon idella) to cold shock

Temporal changes in physiological parameters and enzyme activities related to carbohydrate metabolism in the milkfish (Chanos chanos) and the grass carp (Ctenopharyngodon idella) under cold shock at 15 °C were examined in order to better understand thermal compensation mechanisms of teleosts with different cold tolerances. The plasma glucose, lactate, and lipid contents as well as enzyme activities of citrate synthase, glucose-6-phosphate dehydrogenase, fructose-1,6-bisphosphatase, phosphorylase a, and lactate dehydrogenase at varying time intervals were monitored. The results show that changes in plasma glucose and lipid contents of the milkfish were more notable than those of the grass carp, but the elevation in plasma lactate contents in the grass carp occurred earlier and was much greater than that in the milkfish. Furthermore, changes in plasma glucose contents in the milkfish were correlated with the enzyme activities of phosphorylase a and fructose-1,6-bisphosphatase, but in the grass carp they were correlated with glucose-6-phosphate dehydrogenase and lactate dehydrogenase activities instead. In addition, the change in lactate dehydrogenase activity in the grass carp was more notable than those of other enzymes, but lactate dehydrogenase activities in the milkfish steadily decreased during cold compensation. The results demonstrate that the two species (milkfish and grass carp) respond quite differently to cold shock, and this may be related to their differences in cold tolerance.     

Effects of pesticides and fertilizer on invertebrate populations of grass and wheat plots in Kent in relation to productivity and yield

At a site in Kent, perennial ryegrass (Lolium perenne) variety S24 and Italian ryegrass (L. multiflorum) variety RVP, wheat varieties Armada and Norman, and the original mixed grass ley were grown in small plots during 1982–84. Two toxic pesticides (phorate and aldicarb) were applied to half the total number of plots three times each year to eliminate soil invertebrate populations. Fertilizer was also applied to most plots. The yields of the crops, grown with and without pesticide, and the effects of the fertilizer were compared. Grass herbage yield was measured on three occasions during the summers of 1983 and 1984. Wheat grain yields were also determined in 1983. During the first year significant differences were not apparent in grass dry matter yield between pesticide-treated and non-treated plots, but significant differences were found in the second year. The perennial ryegrass was more susceptible to pest damage than the Italian ryegrass or the grass ley. Grass yields varied between cuts and in relation to variety and pesticide treatment, yields tending to be greater in untreated plots. Fertilizer treatment greatly increased grass dry matter yields, particularly with the Italian ryegrass. The effects of pesticide treatment on both wheat varieties varied although some yield enhancement was evident. Invertebrate animal populations in pesticide and fertilizer-treated plots were also assessed in autumn 1982, spring and autumn 1983 and spring 1984. In contrast to pesticide treatment, fertilizer treatment had little effect on soil invertebrate populations. Nematode populations were reduced at each sampling occasion by the pesticide treatment. Slug populations were initially unaffected but were subsequently reduced. Leatherjackets, by far the most abundant pest in both grass and wheat plots, were markedly affected by pesticides on all sampling occasions. Generally, fewer soil-dwelling dipterous larvae were recovered in spring than in autumn. Stem-boring dipterous larvae were virtually absent.     

Cloning of plasma membrane H-ATPase gene in Populus euphratica Oliv.

For this paper, the plasma membrane (PM) H -ATPase gene has been cloned from Populus euphratica Oliv. through a homology based strategy. The isolated 3,210 bp cDNA contains a single 2,862 bp open reading frame (ORF) which encodes a putative H -ATPase protein of 953 amino acid residues, with a significant homology to plasma membrane H -ATPase of Primus persica, Phaseolus vulgaris, Sesbania rostrata and Daucus carota. The predicted protein has a molecular weight of 104,553 Da. The copy number analysis revealed multiple copies of the PM H -ATPase in the P. euphratica genome after digestion of their genomic DNA by the restriction enzymes EcoRI, NdeⅠ, FbaⅠand BglⅡ, and Southern blot.