加拿大披碱草-野大麦三倍体杂种加倍植株同工酶分析

分析了加拿大披碱草-野大麦三倍体属间杂种F₁加倍植株的同工酶酶谱特征。结果显示:同一生育阶段杂种自然加倍植株与加倍F₁代植株在EST、POD和SOD酶带的数目、位点及强弱方面具有一致性和遗传稳定性,而与杂种F₁代及亲本的酶带表型差异显著,从酶蛋白分子水平证明该杂种F₁染色体加倍是真实的;加倍植株抽穗期旗叶的EST、POD酶谱中分别呈现9和4条酶带,分蘖期幼叶的EST、POD、SOD酶谱内分别呈现8、4和4条酶带,有多态性位点的特征酶带可作为杂种加倍后代育性恢复鉴定的遗传标记的候选位点;对供试材料不同生育阶段做同工酶酶谱对比分析,比单一生育阶段更能反映其酶带表型的遗传差异性,提高同工酶电泳技术鉴定结果的准确性。     

H5N1亚型禽流感病毒A/Guangxi/1/2005株抗药机制的研究

为研究H5N1亚型禽流感病毒(AIV)的抗药机制,本研究选取Clade2.3.4亚群中一株对金刚烷胺敏感的人源AIV A/Guangxi/1/2005(H5N1)(S-GX05),用抗流感病毒药物金刚烷胺对其进行定向诱导,筛选出一株抗药性病毒株,命名为R-A/Guangxi/1/2005(R-GX05)。通过全基因测序并与S-GX05全基因序列进行对比,结果显示S-GX05只在其M2蛋白中有一个氨基酸位点发生突变,即A30P;抗药性鉴定这两株病毒的半数药物抑制浓度(IC50)分别为0.9μM和48.9μM,表明R-GX05对金刚烷胺表现出一定程度的抗性。动物实验证实,这两株病毒对BALB/c小鼠的致病性基本一致,均表现出高致病性,其MLD50分别为4.7 log10 EID50和5.0 log10 EID50,两株病毒在小鼠体内各组织脏器中的分布及增殖能力也基本相同。这些结果表明,S-GX05在药物压力下产生抗药性后,并未引起其它生物学特性的改变。A30P的发现为进一步从分子水平上研究H5N1亚型AIV的抗药机制及新型抗流感新药的研发奠定了基础。     

A Case of Metastatic Adrenocortical Carcinoma Diagnosed with Steroidogenic Factor-1 in a Sprague-Dawley Rat

This report describes the morphological and immunohistochemical characteristics of an adrenocortical carcinoma with distant metastasis in a Sprague-Dawley rat. Macroscopically, a single large mass was observed in the adrenal gland, and multiple nodules were noted in the lung, liver and thyroid. Histologically, the adrenal tumor consisted of a solid growth of eosinophilic round cells with nuclear atypia. Vascular invasion was present, and multiple metastatic lesions were also observed in the lungs, liver, and mediastinal lymph nodes. Immunohistochemically, the nuclei of these tumor cells were positive for Steroidogenic Factor-1 (SF-1). In the thyroid, tumor cells histologically resembling adrenal cells were immunohistochemically negative for SF-1 but positive for calcitonin; thus the lesion was diagnosed as thyroid C-cell carcinoma. From these results, the present case was diagnosed as adrenocortical carcinoma with distant metastases. SF-1 could be a valuable marker for the differential diagnosis of adrenocortical tumors versus other endocrine tumors such as C-cell carcinoma.     

黄羽肉鸡IGF-1基因单核苷酸多态性与生长性状的相关研究

本试验将类胰岛素生长因子1(IGF-1)作为研究肉鸡生长的候选基因,以海门京海集团的第二世代黄羽肉鸡为试验材料,根据鸡IGF-1基因DNA序列设计引物,采用PCR-SSCP方法进行SNP检测和基因型分析,探讨IGF-1基因多态性与鸡生长性状之间的关系。于IGF-1基因外显子1上发现一处突变。这个突变产生的不同基因型与鸡生长性状进行的统计分析结果表明,个体的1日龄初生重、4周龄、12周龄及300日龄成年体重在不同基因型之间均存在显著差异(P<0.05)。AA基因型1日龄初生重、4周龄、8周龄及300日龄成年体重均显著高于BB基因型个体(P<0.05)。推测可以将IGF-1基因应用于鸡生长的标记辅助选择育种实践。     

6种植密度对玉草1号产量与品质的影响

研究了种植密度对玉草1号产量、品质及植株性状的影响。结果表明,45 000与52 500株/hm2 2种密度的总鲜草产量差异不显著（分别为128 944和133 167 kg/hm2）,但二者均显著的高于密度为37 500株/hm2的总鲜草产量（117 370 kg/hm2）;但这3种密度处理的总干草产量差异不显著。分析这3种密度间各品质指标、植株性状指标总体表现,结果密度为37 500株/hm2的粗蛋白（CP）含量、CP产量、相对饲用价值（RFV）、分蘖数、总茎粗、干物率均为最高,密度为45 000株/hm2次之,处理52 500株/hm2最低;中性洗涤纤维（NDF）含量密度为37 500株/hm2最低,52 500株/hm2最高。综合产量与饲用品质比较研究表明,玉草1号种植密度为45 000株/hm2左右在我国南方最适宜。     

鹅IDH1基因的分离、序列分析及表达特征研究

为阐明鹅肥肝形成的机制,使用mRNA差异显示技术研究朗德鹅和淑浦鹅在超饲养和正常饲养条件下肝脏基因表达差异.基因IDH1被证实在2个品种鹅肝脏中表达受到显著抑制(P<0.05).结果,得到了该基因1269 bp的CDS序列,与鸡IDHI有95%的同源性.序列分析表明,该序列含有1个1 248 bp的开放读码框(ORF),编码含415个氨基酸的蛋白质,该蛋白质序列存在1个保守结构域Icd,与其它物种该蛋白的同源性分别为:鸡99%、大鼠89%、人90%、猿90%、牛88%、小鼠88%.应用生物信息学的方法对该蛋白质的功能和结构进行了分析.组织表达分析表明,鹅IDH1基因在肝脏中表达丰富,在脾、肾和肌胃中中等表达,在其它组织中表达量较低.研究结果显示,超饲可以抑制鹅肝脏IDH1基因mRNA的表达.     

Changes in growth performance, digestive enzyme activities and nutrient digestibility of cherry valley ducks in response to aflatoxin B1 levels

The objective of this study was to investigate toxic effects of aflatoxin B1(AFB₁) on growth performance, organs, hepatic enzyme activities, apparent digestibility of nutrients and digestive enzyme activities in ducks. Ninety 1-day-old Cherry Valley commercial ducks were designed to three treatment groups with three replicates of ten birds each. Group I (control) was fed conventional feed free of AFB₁, group II or III was fed the diets containing 20 μg/kg or 40 μg/kg AFB₁-contaminated rice respectively. The feeding trial lasted 6 weeks. The results were that decreased body weight gain and feed intake, increased feed to gain ratio and selected organ weights (liver, kidney and pancreas) were observed in AFB₁-treated groups. The activities of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were significantly increased in AFB₁-contamined groups. The apparent digestibility of crude protein (CP) was significantly lower while activities of digestive enzyme from duodenum contents including protease, chymotrypsin, trypsin and amylase were increased in AFB₁-treated group. These results indicated that AFB₁ of feed could decrease growth performance and apparent digestibility of nutrients, change digestive enzyme activities of duodenum contents in duck.     

Cytokine response in Balb/c mice infected with Francisella tularensis LVS and the Pohang isolate

We investigated the immune response induced by the Francisella (F.) tularensis live vaccine strain (LVS) and the Pohang isolate. After the Balb/c mice were infected intradermally (i.d) with 2 × 10⁴ cfu of F. tularensis LVS and Pohang, respectively, their blood and organs were collected at different times; 0, 3, 6, 24, 72, 96, 120 and 168 h after infection. Using these samples, RT-PCR and ELISA analysis were carried out for the comparative study of the cytokines, including TNF-α, INF-γ, IL-2, IL-4, IL-10 and IL-12. In the Pohang-infected mice at 120 h, the liver showed a 53 times higher level of TNF-α and a 42 times higher level of IFN-γ than the respective levels at the early time points after infection. The levels of TNF-α and IFN-γ induced by LVS were 5 times lower than those induced by the Pohang isolate. Also, the organs from the Pohang-infected mice showed higher levels of TNF-α, IFN-γ, IL-10 and IL-12 than the levels in the LVS-infected mice. The blood from the Pohang-infected mice at 120 h revealed about a 40 times increased level of IFN-γ, and IL-10 was also increased by 4 times at 96 h compared to an early infection time point, while IL-4 was not induced during the whole infection period. These results suggest that F. tularensis may induce a Th1-mediated immune response to in vivo infection and the Pohang isolate has a higher capacity than the LVS to induce an acute immune response in Blab/c mice.     

Distribution of the neurokinin-1 receptor in equine intestinal smooth muscle

REASON FOR PERFORMING STUDY: Tachykinins have profound effects on equine intestinal motility, but the distribution of the neurokinin receptors (NKRs) through which they act is unknown. This study reports the distribution of one of these receptors, the neurokinin-1 receptor (NK1R), in smooth muscle throughout the equine intestinal tract. OBJECTIVES: To quantify the distribution of the NK1R, based upon mRNA expression, in smooth muscle of different regions of the equine intestinal tract. METHODS: Nine regions of the intestinal tract were sampled in 5 mature horses. Total RNA was isolated from smooth muscle and reverse transcribed; NK1R mRNA was then quantified using real-time PCR. RESULTS: NK1R mRNA was found at all levels of the sampled intestinal tract. The smooth muscle of the proximal small intestine and the ventral colon exhibited the highest level of NK1R mRNA expression in the equine intestinal tract. CONCLUSIONS: Tachykinins probably affect intestinal contractility and propulsion in the proximal small intestine and in the ventral colon.