病毒杀虫剂在我国无公害茶园防治中的应用现状与展望     

刘阳  陆建良  郑新强 《茶叶》2013,39(3):130-133

茶叶作为一种食品，其安全问题受到越来越高的关注。病毒杀虫剂具有专一性强、安全性高、持效作用长、能有效地控制害虫种群密度等特点，成为生物防治的研究热点。现就病毒杀虫剂在我国无公害茶园中的应用现状进行综述，并展望未来发展趋势。  相似文献   

Genetic diversity and mixed infections of begomoviruses infecting tomato, pepper and cucurbit crops in Nicaragua   总被引：1，自引：0，他引：1  

M. Ala-Poikela  E. Svensson ‡  A. Rojas  T. Horko  L. Paulin  J. P. T. Valkonen  A. Kvarnheden † 《Plant pathology》2005,54(4):448-459

Begomoviruses were detected in Nicaraguan fields of tomato ( Lycopersicon esculentum ) and adjacently growing plants of pepper ( Capsicum annuum ), chilli pepper ( C . baccatum ), cushaw ( Cucurbita argyrosperma ) and Mexican fireplant ( Euphorbia heterophylla ) using polymerase chain reaction (PCR) and universal begomovirus primers. All tomato and Mexican fireplant plants showing symptoms were infected with begomoviruses, while only 30–46% of the pepper, chilli pepper and cushaw plants showing symptoms tested virus-positive. No begomoviruses were found in potato. The virus species were provisionally identified by sequencing 533 bp of the viral coat protein gene ( AV1 ). Tomato severe leaf curl virus (ToSLCV), Tomato leaf curl Sinaloa virus (ToLCSinV) and Pepper golden mosaic virus (PepGMV) were found to infect both tomato and pepper. A new provisional species designated Tomato leaf curl Las Playitas virus (ToLCLPV) was detected in a tomato plant. Squash yellow mottle virus (SYMoV) and PepGMV were found in cucurbits, the latter for the first time in this host. Euphorbia mosaic virus (EuMV) was detected in Mexican fireplant. Sequencing of a larger number of PCR-amplified clones from selected plants revealed intraspecific viral sequence variability, and also multiple begomovirus infections which could represent up to three species in a single tomato or cushaw plant. Phylogenetic grouping of virus sequences did not correlate with the host of origin.  相似文献   

人工感染雏鹅新型病毒性肠炎的病理形态学发展规律的研究   总被引：5，自引：0，他引：5  

程安春 《畜牧兽医学报》2001,32(4):362-370

40只2日龄四川白鹅口服感染雏鹅新型病毒性肠炎病毒，在不同阶段解剖发病和死亡雏鹅，电镜观察组织器官的病理变化发展规律，接种后第2天，十二指肠绒毛顶部上皮细胞发生坏死、脱落。随着感染时间延长，上皮细胞的坏死、脱落迅速向绒毛基部发展，并伴随固有膜炎性细胞浸润和坏死，病变向着空肠段发展，进一步发展为纤维素性坏死性肠炎，于小肠中后段形成假膜包裹肠内容物的栓塞物或直接由纤维素性渗出物与地不死肠粘膜混合凝固形成栓塞物阻塞肠腔，使外观膨大，肺充血和出血，肾充血、出血及肾小管上皮细胞变性。部分病例肝颗粒变性、脂肪变性，后期部分病例气管、腺胃上皮细胞脱落，早期部分病例心充血和出血，食道、胰腺及脑正常，电镜下可观察到小肠上皮细胞核畸形、固缩、核仁消失、核膜模糊和胞核崩解；胞浆严重空化，形成含有很多病毒粒子的“封入体”；粗面内质网扩张呈囊状，其上的核蛋白体严重脱落；线粒体外膜破裂或嵴断裂及空化，部分受到损害的线凿全充满大量的病毒粒子；形成肠道栓子的外层假膜有大量的病毒粒子、细菌以及坏死的肠上皮细胞，肝脏细胞粗面内质网严重扩张及部分线粒体肿胀、脊断裂；而心肌细胞粗面内质网的轻度扩张及胞核畸形。本文还对雏鹅新型病毒性肠炎与小鹅瘟的病理变化进行了比较分析。  相似文献   

An oculo-cerebellar syndrome caused by congenital bovine viral diarrhoea virus-infection   总被引：1，自引：0，他引：1  

H Bielefeldt Ohmann 《Acta veterinaria Scandinavica》1984,25(1):36-49

An epizootic characterized by birth of calves severly ataxic and blind were encountered in 3 herds 7–8 months after outbreaks of bovine virus diarrhoea. Serological and virological investigations indicated introduction of bovine viral diarrhoea virus (BVDV) into previously virus-free herds, followed by transplacental virus infection of the fetuses of cows in the first trimester. Clinical, pathological, serological, and microbiological examinations were performed on 10 calves. Pathological findings included microcephaly and cerebellar hypoplasia, ocular malformations, and thymic hypoplasia. BVDV was isolated from tissue and blood of 7 calves, and 4 calves, 1 of which had not received colostrum, had virus-specific neutralizing antibodies.This is the first report on natural occurrence of congenital bovine infection with BVDV among Danish cattle herds resulting in abortion and birth of calves with severe debilitating congenital anomalies. It draws attention to the importance of this virus for bovines of all age groups.  相似文献   

A Universal `One-tube' RT-PCR Protocol for Amplifying Isolates of Bovine Viral Diarrhoea Virus     

Pfeffer M  Freyburg MV  Kaaden OR  Beer M 《Veterinary research communications》2000,24(7):491-503

The increase in the knowledge of the genetic variability of BVDV and the identification of some of the genetic determinants of its pathogenicity require robust and practical tools for rapid molecular characterization of the various genotypes of this virus. This study was undertaken to develop a standard protocol for RT-PCR that allows the amplification of various parts of the genome of BVDV without the need for optimizing each individual reaction. The reaction set-up is very flexible because it consists of two pre-mixes. These are a master mix, with all the required reagents except the desired primers, which are the components of the second pre-mix and are therefore easily interchangeable between the different reactions. After adding any primer-containing pre-mix to the fixed master mix, a non-interrupted cycling protocol led to the generation of amplicons of up to 4 kbp in size in amounts sufficient for subsequent sequencing reactions. The method was applied to five different regions of the BVDV genome: (i) the well-known 5-UTR to differentiate genotypes I and II; (ii) the entire E2 gene, or an approximately 550 bp region within the E2 gene, in order to find the molecular equivalent of antigenic varieties; (iii) the entire structural protein coding region covering the Npro, capsid, E ^RNS, E1 and E2 genes; (iv) a 2.1 kbp region embracing the NS2/3 junction which is known to be cleaved in cytopathic biotypes of BVDV; and (v) the region covering the entire NS4B and NS5A/B genes. All six RT-PCRs were successfully applied using (i) primers with lengths of between 20 and 52 nucleotides, (ii) an aliquot of RNA extracted from either 10⁶ infected bovine embryonal lung cells or the same number of leukocytes from viraemic cattle, and (iii) all the genotype I and II strains of BVDV tested. The technique described was used to generate various Sindbis virus/BVDV recombinants. The correct processing of the amplicon-derived E2 glycoprotein of BVDV strain PT810 was demonstrated by its reaction with a monoclonal antibody in an immunofluorescence assay. Given the variety of RT-PCRs tested, we conclude that this universal protocol may be useful with other RNA viruses.  相似文献   

鸡病毒性关节炎病毒C-98分离株S1基因的克隆与序列分析     

常继涛关平原  乌日罕马立峰于富丽  特木尔巴根 《中国兽医科技》2006,36(4):287-291

提取鸡病毒性关节炎病毒（AVAV）内蒙古分离株（C-98株）总RNA，参考GenBank中禽呼肠孤病毒（ARV）S1133株S1基因序列设计了2对引物，应用RT—PCR技术扩增了病毒S1基因，将S1基因cDNA克隆到pGEM—T Easy载体后测序。将测定序列拼接后与参考毒株ARV-176、ARV-138、ARV-S1133、MDRV—YJL的S1基因序列进行了比较。结果显示，AVAV C-98分离株的S1基因与强毒株ARV-176株的同源性最高，达99．9％；与MDRV—YJL的同源性为99．3％，与弱毒疫苗株ARV—S1133的同源性也达97．9％；与ARV-138株的同源性最低，为81．2％。表明，AVAVC-98株与参考毒株的差异较小，与疫苗株ARV-S1133有很高的同源性。  相似文献   

低聚木糖和酸化剂对断奶仔猪生产性能的影响   总被引：6，自引：0，他引：6  

郭雪峰  边连全  付亮亮 《中国饲料》2006,(17):20-21

本试验研究了低聚木糖及其与酸化剂合用对断奶仔猪生产性能的影响。选择72头35±1日龄、平均断奶体重(10.33±0.34)kg的健康三元(杜×长×大)杂交仔猪,按体重和性别分成4个处理组,每处理组3个重复。第1组为对照组,饲喂玉米-豆粕型基础日粮;第2组为低聚木糖(200mg/kg)组;第3组为酸化剂(8g/kg)组;第4组为合用组,添加低聚木糖(200mg/kg)和酸化剂(8g/kg)。研究结果表明,各试验组日增重、料重比得到显著改善(P<0.05),腹泻率显著下降(P<0.01)。  相似文献   

牛病毒性腹泻病毒持续感染的免疫学研究进展     

钟发刚  王新华  程安春 《动物医学进展》2006,27(Z1):13-15

牛病毒性腹泻病毒(BVDV)是危害养牛业的重要病原之一。BVDV感染能够引起广泛的临床症状,包括牛病毒性腹泻-黏膜病、持续感染、免疫耐受、繁殖障碍、血小板减少与出血综合征等。由于其病原的复杂性,给该病的控制及疫苗研制带来了一定的困难。近年来,对其免疫学的研究取得了一定进展,特别是在病原的基本免疫学特征、体液免疫、细胞免疫、免疫耐受和免疫调节方面做了深入研究,同时也在参与免疫应答的细胞因子方面做了研究,这些都为牛病毒性腹泻-黏膜病的预防和控制研究提供了新的思路。  相似文献   

Development of a monoclonal antibody-based co-agglutination test to detect enterotoxigenic Escherichia coli isolated from diarrheic neonatal calves     

Brajesh C. Varshney  N.M. Ponnanna  Pranati A. Sarkar  Pragna Rehman  Jigar H. Shah 《Journal of veterinary science (Suw?n-si, Korea)》2007,8(1):57-64

Escherichia coli (E. coli) strains were collected from young diarrheic calves in farms and field. Strains that expressed the K99 (F5) antigen were identified by agglutination tests using reference antibodies to K99 antigen and electron microscopy. The K99 antigen from a selected field strain (SAR-14) was heat-extracted and fractionated on a Sepharose CL-4B column. Further purification was carried out by sodium deoxycholate treatment and/or ion-exchange chromatography. Monoclonal antibodies to purified K99 antigen were produced by the hybridoma technique, and a specific clone, NEK99-5.6.12, was selected for propagation in tissue culture. The antibodies, thus obtained, were affinity-purified, characterized and coated onto Giemsa-stained Cowan-I strain of Staphylococcus aureus (S. aureus). The antibody-coated S. aureus were used in a co-agglutination test to detect K99+ E. coli isolated from feces of diarrheic calves. The specificity of the test was validated against reference monoclonal antibodies used in co-agglutination tests, as well as in ELISA. Specificity of the monoclonal antibodies was also tested against various Gram negative bacteria. The developed antibodies specifically detected purified K99 antigen in immunoblots, as well as K99+ E. coli in ELISA and co-agglutination tests. The co-agglutination test was specific and convenient for large-scale screening of K99+ E. coli isolates.  相似文献   

Isolation and Identification of a Variant Porcine Epidemic Diarrhea Virus and the Immune Efficacy of Its Inactivated Vaccine     

CHANG Xianyun  ZHAO Runze  TONG Ke  CHEN Shaoxian  LIU Guoping 《中国畜牧兽医》2007,47(11):3651-3658

This study was aimed to isolate a mutant strain of porcine epidemic diarrhea virus and prepare a PEDV inactivated vaccine with high valence by suspension culture process for immunizing against PEDV effectively in China.200 small intestines and theirs contents of diarrhea piglets died of diarrhea,collected from many large-scale pig farms in China,were detected by RT-PCR and sequenced,a mutant strain of porcine epidemic diarrhea virus was selected and put on the suspension-cultured Vero cells in a 2 L reactor for virus isolation and continuous cell culture,the harvested virus suspension,which was identified and determined TCID₅₀,was inactivated by formaldehyde and mixed with aluminum hydroxide gel adjuvant to prepare PEDV inactivated vaccine.After its physical behavior,stability viscosity,sterility test were checked out,the safety and immune efficacy were studied by immunizing the pregnant pigs and theirs piglets.The results were as follows:86 samples were detected positive in 200 samples,cytopathy occurred after the mutant strain samples screened were passaged to 5th generation,the virus suspension was harvested in 10th generation and identified as a mutant strain of PEDV,named PEDV-GF10 strain.The virus titer of harvested virus suspension was measured up to 1×10^8.0 TCID₅₀/mL after concentrated.After the vaccine was checked out,the sows,40 and 25 days before delivery in experimental groups,were injected into Xuehai acupoint with 4 mL vaccine and the pigs in blank group were free of immunifications.The results showed that there were no obvious differences in the production status of the sows in experimental groups and blank group and the temperature of theirs 3-day-old healthy piglets injected different doses of vaccine,and the vaccine was safe to the sows and piglets.Forty 3-day-old piglets producted by pregnant sows in experimental groups and blank group were randomly selected and taken 4 mL 1×10^8.0TCID₅₀/mL F10 virus culture.The PEDV morbidity of piglets in blank group was 100% after injection and the antibodies were negative;10% piglets in blank group had mild diarrhea symptoms,the protection rate was up to 90%,antibody of passive immunity in piglets lasted for more than 35 days.Virus titer of mutant strain of PEDV-GF10 improved a lot by suspension cell culture,the PEDV-GF10 inactivated vaccine was safe,and could effectively prevent and control the variation strain of PEDV in China.  相似文献