感染鸡贫血病毒雏鸡接种新城疫疫苗后免疫保护效应及其机理研究

 雏鸡 1日龄人工感染鸡贫血病毒 (CAV) ,于 8日龄接种 L asota疫苗 ,免疫后 2 8d进行新城疫强毒 (v NDV)攻击 ,以同龄未感染 CAV和用 L asota疫苗免疫并经 v NDV攻毒雏鸡为对照 ,检测其免疫保护效应 ,胸腺和脾脏 T细胞数量及 T细胞增殖反应 ,法氏囊和脾脏 Ig G+、Ig M+、Ig A+抗体生成细胞数量 ,血清免疫球蛋白 Ig G、Ig M、Ig A含量 ,血凝抑制抗体 (HI)滴度等。结果表明 ,CAV人工感染并用新城疫 (ND)疫苗免疫雏鸡经 v NDV攻击后的免疫保护率为 6 0 % ,对照组雏鸡 v NDV攻击后免疫保护率为 10 0 % ,胸腺和脾脏 T细胞数量和 T细胞增殖反应、法氏囊和脾脏Ig G+ 、Ig M+ 、Ig A+ 抗体生成细胞数量、血清 Ig G、Ig M、Ig A含量及 HI抗体滴度 ,均较对照组雏鸡显著降低。说明感染鸡贫血病毒雏鸡接种新城疫疫苗后的免疫保护效应及免疫功能明显降低。     

微波处理松材线虫病疫木技术研究

该文对利用微波处理松材线虫病疫木技术进行了研究，结果表明：不论木材厚薄大小、含水量多少、在微波处理炉腔内怎样堆放，以及环境温度、微波功率等因素的如何变化，只要SWB-Ⅱ型隧道式微波除害处理设备显示的木材表面温度大于68℃，持续30min，就能有效地杀死松木中的松褐天牛和松材线虫。     

舟山海岛松材线虫病疫区迹地晚稻杨梅更新技术

在定海区岑港镇烟墩椗次何家山松材线虫病为害迹地上,试用晚稻杨梅进行树种更替,5年生幼林株高普遍在2m以上,冠幅2m×2m左右,最大植株树高达3m,冠幅2.7m×2.7m,幼林生长正常,试验初见成效.     

Proteomic analysis of intestinal mucosa responses to Salmonella enterica serovar typhimurium in naturally infected pig

Salmonella enterica serovar typhimurium (S. typhimurium) is one of the most frequent Salmonella serotypes isolated from European pigs. Despite the advances in understanding the mechanisms involved in host–pathogen interactions and host cell responses to S. typhimurium, the global change that occurs in naturally exposed populations has been poorly characterized. Here, we present a proteomics study on intestinal mucosa of pigs naturally infected with S. typhimurium, in order to better understand the pathogenesis of salmonellosis and the pathways which might be affected after infection. Samples were analyzed by 2D-DIGE and 44 different proteins exhibited statistically significant differences. The data set was analyzed by employing the Ingenuity Pathway Analysis and the physiological function most significantly perturbed were immunological and infectious disease, cellular assembly and organization and metabolism. The pathways implicated in the porcine immune response to S. typhimurium were gluconeogenesis and Rho GDI/RhoA signaling, and our results suggest that keratins and the intermediate filaments could play an important role in the damage of the mucosa and in the success of infection. The role of these findings in salmonellosis has been discussed, as well as the importance of analyzing naturally infected animals to have a complete picture of the infection. Also, we compared the results found in this work with those obtained in a similar study using experimentally infected animals.     

Detection of calves persistently infected with bovine pestivirus in a sample of dairy calves in south-eastern Queensland

Objective To determine the proportion and incidence of calves persistently infected with bovine pestivirus in calves (n = 1521) supplied to the Tick Fever Research Centre and to assess the test regime to detect calves persistently infected with bovine pestivirus.
Design Calves, 1 to 6 weeks old, selected for use in the production of the tick fever vaccine were collected from 21 properties in 56 separate groups between October 1990 and December 1996. Each group was examined for the presence of calves persistently infected with bovine pestivirus.
Procedure All calves were routinely tested for antibody to bovine pestivirus and bovine pestivirus antigen using a serum neutralisation test and an antigen-capture ELISA, respectively. Pooled lymphocyte samples from calves were also monitored for bovine pestivirus by inoculation of sheep. Whole herd testing was carried out in eight herds, using a serum neutralisation test as a screen test followed by an antigen-capture ELISA of cattle with a serum neutralisation test titre of less than 32.
Results Fourteen of the 1521 calves tested (0.9%), were detected as persistently infected and the incidence ranged from 0.0 to 3.0 % per year over 6 years. Persistently infected calves were found in 13 of the 59 groups and originated from 7 of the 21 herds used. In whole herd testing on the properties of origin, cattle persistently infected with bovine pestivirus were detected in four of the eight herds tested
Conclusions The proportion of calves persistently infected with bovine pestivirus is similar to that in other countries and indicates that bovine pestivirus could be a significant cause of economic loss in Australian cattle herds. In detecting calves persistently infected with bovine pestivirus, the combination of sheep inoculation, paired antigen-capture ELISA and serum neutralisation tests appeared to be highly sensitive and specific.     

不同育秧方式水稻恶苗病发生规律研究

种子带菌量的高低和催芽时间的长短 ,对水稻恶苗病发生的轻重具有重要的影响。在不同的育秧方式条件下 ,水稻恶苗病的侵染具有不同过程     

Effect of Date of Planting, Genotype and Source of Seed on Disease Incidence, Yield, and Agronomic Performance of Soybean

Four soybean genotypes chosen from four seed sources were planted in a factorial arrangement on four dates in a split-plot design at the Alabama A & M Experimental Station on a Decatur silt clay loam soil. The highest vigor index was recorded from seeds harvested from the 4th date of planting. These seeds had the lowest level of Diaporthe phaseolorum var. caulivora infection, indicating that vigor index, as a measurement of seed quality, was negatively correlated with the level of infection by soybean stem canker pathogen. Seed yield was highest at the 2nd date of planting and lowest at the 4th date of planting. Tracy-M and Bedford confirmed previous reports on their resistance and susceptibility, respectively, to soybean stem canker. All the genotypes performed their best at the 2nd date of planting. Source of seeds appeared to have little effect on the performance of the plant in the field.     

Brucella abortus detection by PCR assay in blood, milk and lymph tissue of serologically positive cows

Brucellosis is a highly infectious disease which is diagnosed using serological and microbiological methods. The objective of this study was to assess the viability of using conventional and real-time PCR assays as potential diagnostic tools for the detection of Brucella abortus in naturally infected cows. PCR assays that amplify various regions of the Brucella genome, IS711 genetic element, 31kDa outer membrane protein and 16S rRNA, were optimised using nine known Brucella strains. Real-time PCR was used to examine the detection efficiency of the IS711 assay which was estimated at 10 gene copies. Milk, blood and lymph tissue samples were collected from naturally infected animals. B. abortus was not detected in blood samples collected from naturally infected cows by conventional or real-time PCR, but was detected in a proportion of the culture-positive milk (44%) and lymph tissue (66% - retropharyngeal, 75% - supramammary) samples by the same methods. There was no difference between PCR and bacteriological detection methods. It is unlikely that conventional or real-time PCR will supersede current diagnostic methods for detection of B. abortus in clinical samples.     

RNA干扰技术抑制新家坡石斑鱼虹彩病毒感染细胞多肽ICP46与绿色荧光蛋白融合基因的表达

新加坡石斑鱼虹彩病毒（singapore grouper iridovirus,SGIV）是一种严重的能引起全身性疾病的病原体,对石斑鱼养殖造成了重大的经济损失。将含有SGIV感染细胞多肽ICP46（infected cell polypeptides 46）基因的真核表达载体pEGFP-ICP46转染到胖头鲤细胞（fathead minnow cells,FHM）中进行融合表达,用荧光显微镜观察到ICP46-GFP融合蛋白主要分布于FHM细胞的细胞质中。根据SGIV-ICP46的序列,设计并体外化学合成了特异性干扰SGIV-ICP46的siRNA（siRNA-ICP46）,与pEGFP-ICP46共转染到FHM细胞中,通过荧光显微镜观察不同时间点荧光强度的变化。转染后24~48 h,实验细胞（共转染siRNA-ICP46和pEGFP-ICP46）和阳性对照细胞（共转染siRNA-GFP和pEGFP-ICP46）中的荧光微弱,发荧光的细胞数量较阴性对照（共转染siRNA-Negative和pEGFP-ICP46）少70%左右,但其后实验细胞和阳性对照细胞的荧光强度开始增强,在转染后72 h其与阴性对照组已差别不大。说明体外化学合成的siRNA-ICP46转染后24~48 h可有效抑制FHM细胞中外源导入SGIV-ICP46基因的表达。     

贡柑黑腐病发生规律研究

2011—2012年采用盆栽苗人工接种和田间调查相结合的方法,研究了贡柑产区近年为害严重的黑腐病(病原菌为Alternaria citri)的发生规律。结果表明:在人工接种条件下,其病原菌可以从没有伤口的叶面侵入,但更易从伤口入侵;贡柑和默科特桔最感病,其次是椪柑和南丰蜜桔,在有伤口和连续下雨的条件下马水桔、沙糖桔和温州蜜柑的嫩芽也偶被感染,橙类、柚类、柠檬和金柑抗病。在田间,贡柑、默科特桔最感病,其次是南丰蜜桔、椪柑,马水桔、沙糖桔、温州蜜柑未见发病。刚抽发的嫩梢和幼果易感病,组织越嫩越易感病,老叶、成熟果实感病少,幼树和刚结果树以及嫩梢多的树发病重。该病原菌孢子萌发需要高湿,下雨、高温、高湿有利于该病的发生和流行。夏梢发病最重,其次是春梢和幼果,秋梢发病轻。在人工接种条件下,只要下雨和温度达到15～30℃,1～3天即可显症,病斑沿着叶脉快速扩展。发病快、扩展快是其难防治的最大原因。