Swine fever. Immunisation of piglets   总被引：4，自引：0，他引：4  

P Precausta  F Kato  A Brun 《Comparative immunology, microbiology and infectious diseases》1983,6(4):281-289

Vaccination against Swine Fever using the CL Chinese strain can be done in 7-day-old piglets if they are born of non-immune sows. The simultaneous weaning and vaccination emphasises the safety of this strain. The excellent immunity observed confirms the immunocompetence of 7-day-old piglets. In piglets born of immune sows and also weaned at 7 days, passive protection can extend beyond the age of 2 months if the sow is vaccinated several months prior to gestation. The immune level of the piglets would seem to depend on the interval between vaccination of the sow and farrowing and can be attributed to the quality of the antibodies transmitted by the colostrum. Piglets born of sows vaccinated 10 months prior to farrowing can be vaccinated as early as 5 weeks; the protection percentage observed at the age of about 6 months is over 80%. A booster injection at this age then confers immunity to future breeders throughout their economic life, i.e. 4 years in the reported experiment.  相似文献   

Infectious bovine keratoconjunctivitis: Bacteriologic,immunologic, and clinical responses of cattle to experimental exposure with Moraxella bovis     

Guy M Weech  Harland W Renshaw 《Comparative immunology, microbiology and infectious diseases》1983,6(1):81-94

The bacteriologic, immunologic, and clinical responses of 3- to 4-month old Holstein-Friesian calves to experimental exposure with Moraxella bovis type 10900 has been investigated. After u.v. radiation and intraconjunctival exposure with 1.9 × 10⁷ microorganisms, each eye of 16 calves exhibited signs of blepharospasm, photophobia, and increased lacrimation. Bacteria were recovered from exposed eyes for 2–7 consecutive weeks before maximal clinical response occurred. The severity of the cases varied from eyes that exhibited mild signs to severe clinical cases with profuse lacrimation, conjunctival swelling, corneal opacity, and ulceration. By 70 days after exposure, M. bovis could not be recovered from any conjunctival swabs, and clinical signs were not observed. Four non-exposed control animals did not develop clinical signs nor was M. bovis recovered from conjunctival swabs.Lacrimal secretions collected at the time of and 1 week after maximal clinical response had significantly elevated levels of total protein as compared to those collected 3, 2, and 1 week before, and 2 and 3 weeks after maximal clinical response. A passive hemagglutination test, using tanned formalized sheep erythrocytes sensitized with M. bovis sonicate antigen, detected antibody in lacrimal secretions from 22 of 32 eyes. The appearance of specific antibody in lacrimal secretions correlated with the amelioration of clinical signs and the decline in numbers of M. bovis microorganisms recovered from conjunctival swabs.  相似文献   

Towards sustainable control of Lepidopterous pests in olive cultivation     

Annette Herz  Sherif A. Hassan  Esmat Hegazi  Feeby N. Nasr  Ali A. Youssef  W. E. Khafagi  Essam Agamy  Mohieddine Ksantini  Taieb Jardak  Basilis E. Mazomenos  Maria A. Konstantopoulou  Laura Torres  Fátima Gonçalves  Albino Bento  José A. Pereira 《Gesunde Pflanzen》2005,57(5):117-128

Zusammenfassung Traditionelle, extensiv bearbeitete Olivenhaine, aber auch moderne Intensiv-Plantagen mit künstlicher Bewässerung und hohem Einsatz von Düngern bzw. chemischen Pflanzenschutzmitteln kennzeichnen die derzeitigen verschiedenen Anbauformen der Olive im Mittelmeerraum. Schadlepidopteren wie die Olivenmotte (Prays oleae, Lep.: Yponomeutidae) und die Jasminmotte (Palpita unionalis, Lep.: Pyralidae) werden durch regelmässigen Insektizideinsatz bekämpft. Das von der EU geförderte internationale Forschungsprojekt TRIPHELIO zielte auf die Entwicklung insektizidfreier Alternativmethoden durch (1) die Optimierung der pheromongestützten Überwachung und Verwirrtechnik, (2) der Anwendung von Habitatmanagement-Strategien zur Förderung natürlicher Gegenspieler, und (3) dem Einsatz von Trichogramma-Schlupfwespen. Zusätzlich wurden Module für eine optimale Anwendung biotechnischer und biologischer Methoden bezüglich der Phänologie der Schadinsekten und möglicher Nebenwirkungen von Pestiziden erarbeitet. Die intensive Kooperation zwischen Wissenschaftlern und Praktikern aus mehreren Ländern Europas und Nordafrikas erlaubte den Entwurf möglicher Lösungsansätze für verschiedene Anbaubedingungen und klimatische Regionen des Mittelmeerraumes. Die wichtigsten Ergebnisse und Ausblicke für eine zukünftige praktische Umsetzung werden in dieser Veröffentlichung beschrieben.  相似文献   

Comparative nucleotide sequence analysis of the phosphoprotein gene of peste des petits ruminants vaccine virus of Indian origin   总被引：2，自引：0，他引：2  

Muthuchelvan D  Sanyal A  Sarkar J  Sreenivasa BP  Bandyopadhyay SK 《Research in veterinary science》2006,81(1):158-164

The nucleotide sequences of the phosphoprotein (P) gene of peste des petits ruminants (PPRV) vaccine virus (PPRV Sungri/96) belongs to Asian lineage have been determined and the deduced amino acid sequences were compared with another vaccine strain PPRV/Nigeria75/1 and with those of the other morbilliviruses. The 1652 nucleotides of the P gene encode a phosphoprotein of 509 amino acid residues (from nucleotide numbers 60 to 1587), which is 91% identical to that of PPRV/Nigeria75/1. The C protein consists of 177 amino acid residues and is 91% identical with that of PPRV/Nigeria75/1. The conserved mRNA editing site (5'TTAAAAGGGCACAG) was present at positions 742-756 in the P gene, which is conserved in all other morbilliviruses. The CTT trinucleotide sequence is present at the N/P and P/M intergenic region, which is totally conserved in morbilliviruses. This will be the third sequence for the P gene of PPRV since that of the vaccine strain and a wild-type Turkish isolate has been published already.  相似文献   

World Association for the Advancement of Veterinary Parasitology (W.A.A.V.P.) guidelines for evaluating the efficacy of ectoparasiticides against biting and nuisance flies on ruminants     

Holdsworth PA  Vercruysse J  Rehbein S  Peter RJ  De Bruin C  Letonja T  Green P;World Association for the Advancement of Veterinary Parasitology 《Veterinary parasitology》2006,136(1):3-13

These guidelines have been prepared to assist in the planning, conduct and interpretation of studies for the assessment of the efficacy of ectoparasiticides (excluding repellents) against the biting and nuisance dipteran flies of ruminants. Information is provided on the selection of animals, dose determination and dose confirmation studies, field studies, record keeping and result interpretation. These guidelines advocate the use of pen facilities for dose determination and dose confirmation studies. These guidelines also are intended to assist investigators on how to conduct specific studies, to provide specific information for registration authorities involved in the decision-making process, to assist in the approval and registration of new ectoparasiticides, and to facilitate the worldwide adoption of standard procedures.  相似文献   

小反刍兽疫病毒细胞膜受体的鉴定     

蒙学莲  窦永喜  翟军军 《西北农林科技大学学报(自然科学版)》2012,40(9):13-18,23

【目的】对小反刍兽疫病毒（Peste des petits ruminants virus,PPRV）H蛋白胞外区（tH）细胞膜受体进行鉴定,为PPRV致病机制的研究奠定基础。【方法】克隆PPRV H基因胞外区（tH）,在毕赤酵母(Pichia pastoris)中进行真核表达,纯化后免疫家兔,获得兔抗PPRVtH蛋白特异性抗体;提取山羊外周血淋巴细胞膜蛋白,经SDS-PAGE检测后,湿转印法转印至NC膜,分别利用纯化的重组tH蛋白和PPRV进行病毒铺覆蛋白结合试验（VOPBA）,对受体进行鉴定。【结果】成功克隆了1 653 bp的PPRV tH基因,构建其重组酵母表达质粒pPIC9K-tH,诱导表达后获得了60 ku目的蛋白。重组tH蛋白免疫家兔后获得了效价为1∶200的抗血清。Westernblotting分析发现,该重组蛋白可与PPRV多克隆抗体发生特异性反应,山羊外周血淋巴细胞膜蛋白上有2个与PPRV和重组tH蛋白结合的蛋白带,分子质量约为38和100 ku。【结论】从山羊外周血淋巴细胞膜蛋白上鉴定到了2种与PPRV结合的蛋白组分,其特性有待于进一步研究。  相似文献   

小反刍兽疫病毒M基因截短表达及鉴定     

黄华欣  李刚  王勇  金红岩  陶春爱  程朝飞  隋修锟 《中国动物检疫》2012,29(10):40-45

目的将小反刍兽疫病毒M蛋白基因截短表达后用于特异性单抗制备及临床抗体水平检测。方法:用在线分析软件BepiPred分析小反刍兽疫病毒M蛋白潜在的B细胞线性表位,以本实验室构建的pCR2.1T-PPRV M质粒为模板,扩增三段截短的M基因,纯化后的PCR产物分别与克隆载体pCR2.1T连接,筛选出的阳性重组质粒经双酶切后,分别与表达载体pET-32a(+)及pGEX-6p-1连接,再将鉴定为阳性的重组质粒转化入E.coli BL21(DE3)菌株诱导表达,并用SDS-PAGE及Western blot验证。结果 PCR产物电泳,得到与预期大小相符的特异性片段。对连接克隆载体及表达载体的重组质粒双酶切后,均出现与预期一致的片段,DNA测序表明,插入片段序列与小反刍兽疫Nigeria75/1株M蛋白基因完全一致。重组蛋白经SDS-PAGE及Western blot鉴定,证明所构建的重组蛋白均获得高效表达,并均具有良好的反应原性。结论成功表达了小反刍兽疫截短M基因的蛋白,为制备特异性单抗及小反刍兽疫抗体检测奠定了一定基础。  相似文献   

我国首例小反刍兽疫诊断报告   总被引：30，自引：10，他引：30  

王志亮  包静月  吴晓东  刘雨田  李林  刘佩兰  赵永刚  刘春菊  肖肖 《中国动物检疫》2007,24(8):24-26

2007年7月我国西藏发生不明山羊疫情,国家外来动物病诊断中心对当地动物疫病控制中心送检的14只病死山羊病料和一批血清样品分别进行病原学和血清学检测。利用较敏感的小反刍兽疫病毒(PPRV)特异性荧光定量RT-PCR方法,在11只病羊组织中检测到小反刍兽疫病毒核酸。利用次敏感的PPRV普通RT-PCR方法,从8只病羊组织中检测到PPRV核酸。针对1号样本病原核酸N基因和F基因片段进行遗传发生分析,该病原属于4系。利用竞争ELISA试剂盒对送检的13份血清样本进行抗体检测,结果全部阳性。将1号组织样本接种Vero细胞分离病毒,透射电镜观察下,发现了500纳米左右的病毒粒子。对分离毒株进行PCR检测同样证实其为PPRV。  相似文献   

Regional Conservation in the Virunga-Bwindi Region     

《Journal of Sustainable Forestry》2013,32(1-2):189-204

SUMMARY

Bwindi Impenetrable National Park and the Virunga Volcano region are the last remaining habitats of the highly endangered mountain gorilla (Gorilla beringei beringei). This conservation area, shared by Uganda, Rwanda and the Democratic Republic of Congo, also acts as a refuge for biodiversity and high endemism in the Albertine Rift of Central East Africa. This particular region has suffered from a number of years of civil strife, which have severely affected the management of these forests. This paper will explore the experiences of the International Gorilla Conservation Programme (IGCP) obtained throughout the development of regional processes that are working towards establishing a transboundary-protected area. The establishment of a regional framework and tools utilized are described. The costs and constraints incurred by the IGCP and the resulting positive impacts on conservation are also highlighted.  相似文献   

小反刍兽疫病毒及山羊痘病毒N-ITR基因二联实时荧光定量RT-PCR检测方法的建立     

赵文华  杨仕标  高华峰 《中国畜牧兽医》2014,41(3):65-71

Peste des petits ruminants virus (PPRV) and goat pox virus (GTPV) are the causative agents of two kinds of goats’ diseases-peste des petits ruminants and goat pox which can cause disaster economic losses. In order to detect the two viruses simultaneously and quickly, two sets of primers and relative probes were designed based on the nucleoprotein (N) gene of PPRV and the inverted terminal repeat (ITR) segment of GTPV， respectively. In order to work together in the same reaction, the probes were labeled with different fluorescent materials 5′FAM-TAMRA3′and 5′JOE-Eclipse3′，respectively. Results showed that the duplex Real-time RT-PCR assay was identified to be specific for PPRV and GTPV only and specific fluorescent signal could be detected, but the related viruses including fowl pox virus（FPV）and canine distemper virus (CDV) had no specific fluorescent signal. Positive recombinant plasmids (PPRV pMD18-T-N and GTPV pMD18-T-ITR) were built and used for positive quantitative templates to establish duplex standard curves. The developed assay based on the probe N-ITR was found to be highly specific and sensitive with a detection limit of 10² copies/μL cDNA and 10³ copies/μL DNA for PPRV and GTPV， respectively. Finally, the duplex Real-time RT-PCR assay for simultaneous detection of PPRV and GTPV was established preliminarily in the study.  相似文献