猪2型圆环病毒核酸疫苗免疫效应研究

PCR扩增PCV2 ORF2和BVP22基因。将ORF2基因克隆入真核表达载体pCDNA3．1（＋），构建了pCORF2作为核酸疫苗免疫小白鼠。同时将具有蛋白转导功能的BVP22基因分别克隆到ORF2基因的上游和下游，使二者融合表达，命名为pCORF2BVP22和pCBVP220RF2。分4组肌肉免疫BALB/c小白鼠，分别注射pCDNA3．1（＋）、pCORF2、pCORF2BVP22和pCBVP220RF2，共免疫2次，间隔2周，分别于首免后2周和二免后4周采血，ELISA法检测体液抗体。同时为在体外验证ORF2和BVP22基因的真核表达，将ORF2和BVP22基因分别克隆入pEGFP-N1载体，构建了pNORF2和pNBVP22，转染Hela细胞后在荧光显微镜下观察到了ORF2和BVP22在体外的瞬时高效表达。结果显示，通过两次免疫后，各疫苗组均产生了针对ORF2的体液抗体，同时证明BVP22可增强核酸疫苗的免疫效果，其中以BVP22在ORF2上游效果更好。本研究为防制猪2型圆环病毒感染提供了较为理想的侯选疫苗。     

The impact of truncating data on the predictive ability for single‐step genomic best linear unbiased prediction

Simulated and swine industry data sets were utilized to assess the impact of removing older data on the predictive ability of selection candidate estimated breeding values (EBV) when using single‐step genomic best linear unbiased prediction (ssGBLUP). Simulated data included thirty replicates designed to mimic the structure of swine data sets. For the simulated data, varying amounts of data were truncated based on the number of ancestral generations back from the selection candidates. The swine data sets consisted of phenotypic and genotypic records for three traits across two breeds on animals born from 2003 to 2017. Phenotypes and genotypes were iteratively removed 1 year at a time based on the year an animal was born. For the swine data sets, correlations between corrected phenotypes (Cp) and EBV were used to evaluate the predictive ability on young animals born in 2016–2017. In the simulated data set, keeping data two generations back or greater resulted in no statistical difference (p‐value > 0.05) in the reduction in the true breeding value at generation 15 compared to utilizing all available data. Across swine data sets, removing phenotypes from animals born prior to 2011 resulted in a negligible or a slight numerical increase in the correlation between Cp and EBV. Truncating data is a method to alleviate computational issues without negatively impacting the predictive ability of selection candidate EBV.     

叶片开缝对单叶片泵径向力的影响

为了改善单叶片泵的运行特性,降低径向受力不均匀性,采用数值计算与试验相结合的方法分析了单叶片离心泵径向力的动态特性.研究了3个不同流量工况(0.6Q_d,1.0Q_d和1.4Q_d)下径向力的变化规律,结果表明,单叶片离心泵叶轮叶片工作面与背面所受压差是径向力产生的主要原因,并在小流量工况下径向力达到最值.通过对试验与数值模拟结果的分析对比,提出了平衡单叶片泵径向力的新方法-叶片开缝,并在叶片包角方向上选取3个不同位置(0°,90°和270°)布置宽度为1.0 mm的缝隙,分析了不同开缝位置对径向力及泵外特性的影响情况.结果表明:当在叶片尾缘开缝时,对泵的外特性影响较小,并可以较大降低单叶片离心泵叶片工作面和背面的压差,减小叶轮径向受力情况,提高单叶片泵的可靠性和使用寿命.     

氮肥与密度互作对单粒精播花生根系形态、植株性状及产量的影响

为明确花生单粒精播适宜的氮肥水平和种植密度,本研究于2018年和2019年以‘花育22’为供试花生品种,设置3个氮肥水平(0 kg hm~(–2), N0; 60 kg hm~(–2), N1; 120 kg hm~(–2), N2), 3个种植密度(7.93万株hm~(–2), D1; 15.86万株hm~(–2),D2; 23.79万株hm~(–2), D3),采用二因素裂区试验设计,研究氮肥、密度及其互作对单粒精播花生根系形态、植株性状及产量的影响。氮肥对花生根长、根表面积、根体积、根干重的影响不显著,而密度的影响显著。单株根长、根表面积、根体积及根系干重随密度的增加而降低, D1显著高于D2和D3, D2、D3处理间差异不显著;单位面积根长、根表面积、根体积及根系干重随密度的增加而增加, D1显著低于D2和D3, D2、D3处理间差异不显著。氮肥和密度互作对2019年收获期单位面积根长、根表面积的影响显著,与D1相比, N1处理下D3的增幅显著高于N0和N2处理。氮肥及氮肥与密度互作对植株性状的影响存在年度和时期间的差异,主茎叶片数、侧枝数和主茎第一节间粗随密度增加有降低趋势。氮肥对荚果产量的影响不显著,荚果产量随密度的增加呈增加的趋势。产量与根体积、根干重、主茎叶片数、主茎高及侧枝长呈显著正相关。综上所述,在本试验条件下,花生单粒精播适宜的氮肥(N)水平为60 kg hm~(-2),种植密度为18.8万株hm~(-2)。     

Genetic divergence in two tropical maize composites after four cycles of reciprocal recurrent selection

Two tropical maize composites were subjected to four cycles of reciprocal recurrent selection to develop divergent inbred lines with good combining ability. This study was conducted to examine the extent of genetic diversity, changes in allele composition and genetic structure, of 100 randomly selected S₁ lines each from the original (C₀) and advanced (C₄) selection cycles of TZL COMP3 and TZL COMP4, genotyped using single nucleotide polymorphism (SNP) markers. Results revealed that the proportion of alleles at both low and high frequencies decreased from C₀ to C₄, whereas those at intermediate frequencies increased at C₄ in the two composites. More unique and other alleles were lost at C₄ in TZL COMP3 relative to those in TZL COMP4. The changes in different measures of genetic diversity were either small or negligible with selection in the two composites. The proportion of markers departing from Hardy–Weinberg equilibrium (HWE) decreased with selection, whereas the total number of pairs of markers in linkage disequilibrium increased with selection in the two composites. Examination of changes in population structures using a model‐based approach as well as cluster and multivariate analyses found a high degree of concordance in stratifying the 400 S₁ lines into four non‐overlapping groups corresponding to the two selection cycles each within the reciprocal composites. The observed molecular‐based divergence between cycles within the same composite and the clear differentiation between the complementary composites highlight the importance of reciprocal recurrent selection for preserving genetic diversity for long‐term selection. This increases the potential of the advanced selection cycles to sustain genetic gain in productivity of hybrids adapted to the savannas in West and Central Africa.     

Development of a kompetitive allele‐specific PCR marker for selection of the mutated Wx‐D1d allele in wheat breeding

Waxy (Wx) protein is a key enzyme for synthesis of amylose in endosperm. Amylose content in wheat grain influences the quality of end‐use products. Seven alleles have been described at the Wx‐D1 locus, but only two of them (Wx‐D1b, Wx‐D1e) were genotyped with codominant markers. The waxy wheat line K107Wx1 developed by treating ‘Kanto 107’ seeds with ethyl methanesulphonate carries the Wx‐D1d allele. However, no molecular basis supports this nomenclature. In the present study, DNA sequence analysis confirmed that a single nucleotide polymorphism in the sixth exon of Wx‐D1 changed tryptophan at position 301 into a termination codon. Based on this sequence variation, a PCR‐based KASP marker was developed to detect this point mutation using 68 BC₈F₁ plants and 297 BC₈F₂ lines derived from the cross ‘Ningmai 14’*9/K107Wx1. Combined with codominant markers for the Wx‐A1 and Wx‐B1 alleles, waxy and non‐waxy near‐isogenic lines were distinguished. The KASP marker was efficient in identifying the mutant allele and can be used to transfer waxiness to elite lines.     

春蚕一日一回育试养初探

2015年春 ,河南蚕业科学研究院进行了"豫花×湘明"蚕品种全龄一日一回育养蚕试验.结果显示 ,一日一回育龄期经过缩短2d,节约工时 ,节约桑叶 ,通过改进技术措施后产茧量和蚕茧质量能达到普通育基本水平.     

FAHP-GIS在FAST台址单体滑坡危险性评价中的应用

[目的]研究贵州省平塘县500 m口径球面射电望远镜(FAST)工程台址光明顶滑坡的危险性及其区划,为该区及相似地区的滑坡灾害监测与防治提供参考依据。[方法]选取地形地貌、岩性岩组、地质构造、人类工程活动及灾害历史等作为一级评价指标,在此基础上发展二级评价指标,运用GIS技术构建基于模糊层次法(FAHP)的滑坡危险性评价指标体系,并完全参与对指标隶属度矩阵的运算,开展针对喀斯特单体滑坡危险性评价研究。[结果]光明顶坡体总体居于中危险和低危险水平,局部高危险,高危险区域主要位于1 H馈源塔和断层破碎带区域的3个支撑柱附近,高危险区约占研究区面积的4%。[结论]光明顶坡体存在安全隐患,已经对精密的射电望远镜设施的安全运行构成威胁。本文评价结果与实际情况基本相符,评价方法在单体滑坡危险性评价研究方面具有创新性,且可操作。     

亚洲棉EST-SNP的挖掘及其在陆地棉中的验证

【目的】随着不同棉种序列数据库的逐步完善以及高通量测序技术的发展,棉花单核苷酸多态性(Single nucleotide polymorphism,SNP)标记开发可利用的公共数据资源逐步增加。【方法】本研究基于陆地棉祖先基因组的现代种亚洲棉表达序列标签(Expressed sequence tag,EST)数据库,利用CAP3对亚洲棉EST数据库进行拼接。拼接获得7 187个重叠群(Contig),再利用Quality SNP软件进行SNP位点分析。【结果】在807条含有4条以上EST序列的Contig中查找到2 690个SNP位点。通过筛选次要等位基因频率大于30%的位点,获得953个可靠度较高的候选SNP,通过电子筛选,最终获得可用于陆地棉分析的SNP 149个,利用位点特异性聚合酶链式反应以及酶切扩增多态序列验证了EST-SNP的准确性。【结论】本研究证实基于亚洲棉EST数据库挖掘用于陆地棉研究的EST-SNP切实可行,并有望将EST-SNP用于陆地棉遗传图谱构建、重要性状的基因定位以及分子标记辅助育种。     

水稻复合农艺性状QTL剖析

为了解水稻复合性状的数量性状基因座(QTL),在利用单片段代换系进行QTL鉴定的基础上,剖析了水稻株高QTL与主茎高和穗长QTL,主茎高与倒一节间长、倒二节间长、倒三节间长和倒四及以下节间长QTL,谷粒长宽比QTL与粒长和粒宽QTL,每穗粒数QTL与一次枝梗数和二次枝梗数QTL的关系。结果表明:鉴定出株高QTL的6个单片段代换系中有4个只检测出了主茎高QTL,其加性效应百分率为86.00%～99.55%,有1个只检测出了穗长QTL,其加性效应百分率为48.31%,有1个同时检测出了主茎高QTL和穗长QTL,其中主茎高QTL的加性效应百分率为81.72%,穗长QTL加性效应百分率为18.28%;在检测出主茎高QTL的7个单片段代换系中,有1个只检测出倒一节间长QTL,有2个只检测出倒二节间长QTL,有2个检测出倒一节间长QTL和倒二节间长QTL,有2个只检测出倒三节间长QTL;不同的单片段代换系中检测出的节间长的QTL加性效应百分率变化范围为-128.62%～172.07%;7个检测出谷粒长宽比QTL的单片段代换系中,有5个只检测出粒长QTL,1个只检测出粒宽QTL,1个同时检测出了粒长QTL和粒宽QTL;检测出每穗粒数QTL的3个单片段代换系中,有2个只检测出二次枝梗数的QTL,有1个同时检测出一次枝梗数QTL和二次枝梗数的QTL。这些结果表明,代换片段中如能检出复合性状QTL,也可以检出其构成性状QTL;复合性状QTL的加性效应的大部分可由其构成性状QTL的综合效应来解析,但相同的复合性状,不同代换片段检出的构成性状QTL不同。