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。     

基于气流脉冲和结构光成像的牛肉嫩度检测方法

针对传统牛肉嫩度检测速度慢、精度低的问题，提出了基于气流脉冲结合结构光3D成像的牛肉嫩度快速无损检测方法。首先，利用脉冲气流对牛肉表面进行冲击，同时通过结构光3D成像获取待测牛肉表面凹陷区域的三维点云信息；然后，采用去噪、点云分割、贪婪投影三角化、Delaunay三角化、曲面拟合等算法进行点云处理，获得牛肉表面凹陷区域的深度、映射面积、表面积和体积等信息；基于此,分别建立基于最小二乘支持向量机回归（LS-SVR）、BP神经网络和广义回归神经网络（GRNN）的生鲜牛肉剪切力预测模型；结果表明，GRNN模型预测表现最佳，预测集相关系数为0.975，均方根误差为5.307N。采用基于K-fold交叉验证的GRNN神经网络对牛肉嫩度等级进行预测，结果显示该方法对较嫩牛肉分级效果较好，为100%，对较老牛肉分级效果稍差，为91.3%。研究表明，基于气流脉冲结合结构光3D成像进行牛肉剪切力以及嫩度快速、无损检测是可行的。     

“食品添加剂”课程教学模式改革研究

在当今“慕课”和“金课”日益盛行的教学模式下,针对“食品添加剂”课程传统教学“以教师讲授为主”、教学模式陈旧、学生被动接受知识、课程考核方式单一、学习成效不显著等缺点,从教学方式、考核方式进行初步改革探讨,使课前预习和课堂听课有机融合,推进翻转课堂,逐步向“金课”建设过渡,提升学生自主学习能力,促进教学质量提高。     

零耦合度空间2T1R并联机构运动学与刚度建模分析

根据基于方位特征(POC)方程的并联机构拓扑设计理论与方法，提出一种零耦合度、含1条冗余支链的三自由度两平移一转动(2T1R)并联机构，并对该机构进行拓扑分析。结果表明：该机构具有符号式位置正解和部分运动解耦特性，其被动冗余支链能避免奇异位置，改善刚度；因机构耦合度为零，易求解出其符号式位置正解，并分析了机构可能产生的3种奇异位置；运用虚拟弹簧法建立了每条支链的刚度模型并进行求解，给出并分析了机构笛卡尔刚度矩阵中扭转刚度和线性刚度的变化趋势，讨论了冗余支链对整体刚度性能的影响，验证了冗余支链可使机构整体刚度性能提升约22%。     

miR-140-3p inhibits viability,invasion and migration of non-small-cell lung cancer A549 cells by targeting PD-L1

AIM: To explore the target relationship between microRNA-140-3p (miR-140-3p) and programmed cell death ligand 1 (PD-L1) and their effect on the viability, migration and invasion of non-small-cell lung cancer A549 cells.METHODS: RT-qPCR was used to detect the miR-140-3p expression in HLF-1, A549 and H1299 cells, and then the A549 cells with the most significant difference were selected as the subsequent research object. TargetScan software and dual-luciferase reporter assay were performed to predict and confirm the target relationship between miR-140-3p and PD-L1. RT-qPCR and Western blot were used to determine the effects of miR-140-3p mimic and inhibitor on PD-L1 expression level. MTT assay was used to detect the viability of A549 cells. Transwell assay was performed to detect the migration and invasion abilities of the A549 cells.RESULTS: miR-140-3p was significantly down-regulated in the A549 cells and H1299 cells (P<0.05). Transfection with miR-140-3p mimic decreased the expression of PD-L1 and inhibited the viability, migration and invasion of the A549 cells. Transfection with pcDNA3.0-PD-L1 reversed the inhibitory effect of miR-140-3p on the viability, migration and invasion of the A549 cells.CONCLUSION: miR-140-3p inhibits the viability, migration and invasion of A549 cells by targeting PD-L1.     

长链酰胺化纳米纤维素增强聚乳酸复合材料

以纳米纤维素(NCC)为原料,先采用四甲基哌啶氮氧化物(TEMPO)氧化制备氧化纳米纤维素(TONC),再与不同链长脂肪胺在催化剂作用下发生反应,得到脂肪胺改性纳米纤维素,当脂肪胺为十二胺(DOA)、十四胺(TEA)、十六胺(HEA)、十八胺(OCA)时,分别制得DOATONC、TEATONC、HEATONC和OCATONC。傅里叶变换红外光谱(FT-IR)、X射线衍射(XRD)和元素分析表明:脂肪链接枝成功,改性后纳米纤维素的晶形没有发生改变,为原有Ⅰ型晶型;接触角和分散性测试表明:随着脂肪链的增长,改性纳米纤维素表面的亲水性明显下降(接触角由65.8°上升至93.9°),而分散率由25.17%先降至11.97%,再升至71.71%。将1%的改性纳米纤维素添加到聚乳酸(PLA)中制得复合膜,机械性能测试结果表明:随着脂肪链的增长,复合膜的机械性能明显提高,其中PLA/OCATONC复合膜的拉伸强度和断裂伸长率分别达到40.2 MPa和6.39%。     

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.     

软枣猕猴桃叶片愈伤组织诱导技术的研究

[目的]由于软枣猕猴桃在初代培养中外植体诱导率极低且快繁效果差,因此进行其组织培养技术体系的研究,以期解决其人工种植的难题.[方法]本研究以软枣猕猴桃展叶为外植体,通过采用不同消毒试剂及消毒处理时间,筛选出最佳的灭菌程序;将不同培养基与不同浓度的KT、2,4-D组合,筛选出最佳的初代培养基配方.[结果]选用展叶为外植体,75％CH3CH2OH处理30 s后以10％NaClO处理20 min,0.1％HgCl2处理15 min后无菌水冲洗3～4次,接至pH=5.8的MS+1 mg·L-1 KT+0.5 mg·L-12,4-D+3％白糖+0.55％琼脂培养基上,置于光照2500 lx、8 h·d-1,26℃下培养8 d后有少部分愈伤组织出现,60 d后平均单芽愈伤组织达0.8 g以上,平均单个愈伤组织长度0.7～1.4 cm,属中块愈伤组织.[结论]以本实验得出的愈伤组织培养方法进行培养,可有效提高诱导率,达到快繁的目的.