Effects of three methionine sources in diets on temporal B0AT1 and ASCT2 mRNA expression in different intestinal segments of cobia,Rachycentron canadum

A 4‐week feeding trial was conducted using five groups of hybrid grouper (61.15 ± 0.15 g) to explore the potential effects of three methionine (Met) sources. Five isonitrogenous and isolipidic diets were formulated that included a fishmeal (FM) diet; nonsupplemented (NS) diet; or NS diets with the addition of the L‐methionine (L‐Met), DL‐methionine (DL‐Met), or coated Met (Co‐Met) to obtain the same Met level as the FM diet. Fish were randomly distributed into sea cages (30 fish per cage). Weight gain and specific growth rate in the DL‐Met group and FM group were significantly higher than those in all other groups (p < .05). In the proximal and distal intestines, of the 20 gene and time combinations (10 per gene), there were 14 combinations (70%) in which there were no significant differences in gene expression levels between the FM and DL‐Met groups (p > .05). The main reason for the same growth effect between the DL‐Met and FM groups may be attributed to the synchronized absorption at most time points after feeding, which had similar expression patterns of B⁰AT1 and ASCT2 of the proximal and distal intestines between two groups.     

牦牛源正呼肠孤病毒2型的检测和分离鉴定

旨在调查川西北牦牛哺乳动物正呼肠孤病毒（MRV）的感染情况并分离病毒。采用RT-PCR方法，对采自川西北15个牧场的72份牦牛腹泻粪便样本和其中5个牧场的15份腹泻牦牛血清样本进行MRV检测，阳性样本进一步用分型PCR确定其血清型。结果显示，粪便样本中MRV检出率为20.83%（15/72），血清2型的比例为60%（9/15）；血清样本中MRV检出率为40%（6/15），血清2型的比例为83.33%（5/6）；未检测到其他血清型。成功地从腹泻粪便中分离到1株MRV血清2型毒株（TCID₅₀为4×10^-8.56·mL^-1），并获得长度为23 587 bp的分离株全基因组，该分离株与中国猪源毒株的遗传关系最近；与GenBank中所有的MRV S1基因相比，该分离株有4个独特的氨基酸突变。本研究从牦牛中检测到MRV，并分离到1株牛源MRV血清2型毒株，为进一步研究MRV血清2型生物学特性奠定了基础。     

“藏粮于地”战略下高标准农田建设模式研究*

高标准农田建设是我国“藏粮于地”战略的重要抓手,是确保粮食产能的重要支撑。在梳理大量参考文献、政策文件和标准规范的基础上,针对现阶段高标准农田建设存在管理体制不完善、空间潜力不足、投资标准偏低、建设质量不高等问题,总结归纳高标准农田建设模式总体构架,通过对我国高标准农田建设综合评价结果排名靠前和提升较快的省份开展高标准农田建设模式调查研究,围绕管理体制、规划布局、建设标准、资金保障以及实施管理方面,提出系统构建高标准农田建设模式的对策建议,为提高高标准农田建设质量作有益参考。     

基于Netty的农业物联网服务器系统设计

为了方便对温室环境的监控和控制,使用Netty网络框架设计了一个农业物联网服务器系统,能够简化物联网服务器端的开发,实现下位机与上位机的实时通信。本文阐述了该系统的工作原理和总体设计,以期为实现大棚农作物生长的智能化和信息化管理。     

饲养系统和日粮对羔羊屠宰性能和肌肉矿物质含量的影响

文章旨在探讨不同饲养系统和日粮对羔羊生长、屠宰性能及肌肉矿物质含量的影响。试验将平均体重为（13.97±0.55）kg的120只羔羊随机分为3组，每组4个重复，每个重复10只。T1组在室内饲喂基础浓缩料，每天补充100 g稻草，T2组在室内饲喂基础浓缩料，每天补充100 g稻草和锌硒复合矿物质（0.2 mg/d硒，50 mg/d锌），T3组在室外放牧，除了采食苜蓿草外，每天额外补充100 g稻草和100 g燕麦。试验时间为9周。结果：T1和T2组羔羊的末重、日增重、半胴体重、下肢深度、下肢重量、眼肌面积、颈、胸肌、肾重量均显著高于T3组（P＜0.05），但骨盆骨重量显著低于T3组（P＜0.05）。各处理组羔羊的可食用部分和骨盆肌肉重量无显著差异（P＞0.05）。T2组63 d羔羊血液硒含量较T1和T3组分别显著提高了19.83%和25.0%（P＜0.05），血液锌含量较T1和T3组分别显著提高了31.71%和45.91%（P＜0.05）。T3组羔羊肌肉钙含量较T1和T2组分别显著提高了8.79%和5.37%（P＜0.05）。T2羔羊肌肉硒和锌含量较T1和T3组分别显著提高了41.18%、65.52%和38.19%、46.15%（P＜0.05），T2和T3组羔羊肌肉钾含量较T1组分别显著提高了3.27%和4.28%（P＜0.05）。结论：在本试验条件下，放牧羔羊胴体的脂肪含量低于室内饲养的羔羊，室外放牧可以提高肌肉钙和钾含量，但肌肉硒含量降低。 [关键词]饲养系统|羔羊|屠宰性能|矿物质     

我国社会救助管理服务体系建设研究

我国社会救助体系不断完善的过程中涉及主体更多元、方式更多样。当前社会救助面临相关部门和组织多、信息复杂、经办分散、分类精准施救难度大等问题。基于我国社会救助模式的合理价值选择，提出管理服务体系建设的重要意义。进而分析社会救助在管理服务上面临的挑战和难题，从组织协调管理、信息网络系统、基层经办机构、社会参与机制四个方面提出构建多层次管理服务体系的思路。力求提高管理服务的效率和效能，促进互助共济社会救助共同体的形成，提升公众满意度，夯实我国民生保障基础。     

白屈菜CmFAD2基因的克隆及植物转化载体构建

通过对白屈菜低温应答过程的转录组分析发现膜脂不饱和化相关基因的表达在一定过程中发生变化,脂肪酸去饱和酶基因FAD2在随温度的变化趋势为正"V"型,且表达量变化显著。利用NCBI等在线软件对序列进行相关生物学信息分析,并对白屈菜FAD家族成员FAD2基因的完整开放阅读框(ORF)进行克隆,并命名为CmFAD2。选用克隆载体pMD-19-T,转化大肠杆菌DH5α,测序验证序列正确性及完整性。将目的基因与植物表达载体pRI-201-AN连接构建重组DNA pRI-201-AN-Cm FAD2,电击法转化农杆菌LBA4404,利用菌液PCR法验证成功。该基因可作为药用植物抗寒品种创制的候选基因。     

Vitrification of mouse two-cell and blastocyst stage embryos in simplified closed system using either a hemi-straw or a hollow fiber device

Two-cell stage and blastocyst stage mouse embryos were equilibrated in a medium containing 7.5% ethylene glycol (EG) and 7.5% dimethyl sulfoxide (DMSO) for 8–15 min. Vitrification was performed in a medium containing 0.5 M sucrose and either 15% EG + 15% DMSO, 17.5% EG + 17.5% DMSO, or 20% EG + 20% DMSO for 30 s. They were then placed either on a hemi-straw (HS) or a hollow fiber vitrification (HFV) device and vitrified by cooled air inside a 0.5-ml straw. In two-cell embryos, a 100% survival rate was obtained from all groups except the 20% HS group (P > .05). All vitrified two-cell groups showed similar rates of blastocyst development to that of fresh control group (P > .05), except 17.5% and 20% HFV groups, which were significantly lower than the other groups (P < .05). In the blastocyst embryos, the HFV groups were divided into two subgroups (non-collapsed; HFV-NC and collapsed; HFV-C blastocyst). Re-expansion rate in 15% HFV-NC, 17.5% HFV-NC, and 15% HFV-C groups was reduced (P < .05), whereas the rest were similar to control. In conclusion, we established a simplified, reliable, and closed system for HFV vitrification applying hemi-straw, which does not require skilled practitioners.     

Protective efficacy of an H5/H7 trivalent inactivated vaccine produced from Re-11, Re-12, and H7-Re2 strains against challenge with different H5 and H7 viruses in chickens

We developed an H5/H7 trivalent inactivated vaccine by using Re-11, Re-12, and H7-Re2 vaccine seed viruses, which were generated by reverse genetics and derived their HA genes from A/duck/Guizhou/S4184/2017(H5 N6)(DK/GZ/S4184/17)(a clade 2.3.4.4 d virus), A/chicken/Liaoning/SD007/2017(H5 N1)(CK/LN/SD007/17)(a clade 2.3.2.1 d virus), and A/chicken/Guangxi/SD098/2017(H7 N9)(CK/GX/SD098/17), respectively. The protective efficacy of this novel vaccine and that of the recently used H5/H7 bivalent inactivated vaccine against different H5 and H7 N9 viruses was evaluated in chickens. We found that the H5/H7 bivalent vaccine provided solid protection against the H7 N9 virus CK/GX/SD098/17, but only 50–60% protection against different H5 viruses. In contrast, the novel H5/H7 trivalent vaccine provided complete protection against the H5 and H7 viruses tested. Our study underscores the importance of timely updating of vaccines for avian influenza control.