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1.
小反刍兽疫(PPR)是一种由小反刍兽疫病毒引起的疾病,主要感染山羊和绵羊。2021年为加快推进小反刍兽疫无疫区建设,实现小反刍兽疫非免疫无疫区建设标准,长沙市某县拟在本地开展小反刍兽疫退出强制免疫风险评估。通过对小反刍兽疫监测流调、危害识别、风险路径的确定和风险因素层级评估等方法进行的定性风险评估初步显示,在该地取消小反刍兽疫强制免疫后可能会发生小反刍兽疫的风险等级为中。在风险管理措施上,提出该地退出强制免疫应推迟一年,重点完善政策支持、加强监测排查、加强检疫监管、强化培训宣传等建议。 相似文献
2.
Zahur AB Ullah A Hussain M Irshad H Hameed A Jahangir M Farooq MS 《Preventive veterinary medicine》2011,102(1):87-92
A sero survey was conducted during 2005-2006 to estimate the sero prevalence of PPR in the small ruminant population of Pakistan. A total of 2798 samples were collected including goats (1979) and sheep (819) from villages in 27 randomly selected districts. These were tested by cELISA for PPRV and true prevalence estimates were calculated by Rogan and Gladen estimator. Overall, 1273 (45.5%) were found positive; 980 (49.5%) of 1979 samples from goats and 293 (35.8%) of 819 serum samples from sheep were positive. The true sero-prevalence of PPR was estimated to be 48.5% (95% CI, 46.6-50.3), and 52.9% (95% CI, 50.7-55.1) and 37.7 (95% CI, 34.4-41.0) for goats and sheep, respectively. PPR virus is widely distributed all across Pakistan and has become an endemic infection of small ruminants. Since it is one of the leading causes of morbidity and mortality in small ruminants, it poses a serious threat to food security and the rural economy in Pakistan. 相似文献
3.
Production and Characterization of Monoclonal Antibodies to Peste des Petits Ruminants (PPR) Virus 总被引：1，自引：0，他引：1
Singh RP Bandyopadhyay SK Sreenivasa BP Dhar P 《Veterinary research communications》2004,28(7):623-639
Peste des petits ruminants (PPR) is an acute, febrile viral disease of small ruminants, caused by a virus of the genus Morbillivirus. PPR and rinderpest viruses are antigenically related and need to be differentiated serologically. In the present study, 23 mouse monoclonal antibodies were produced by polyethyleneglycol (PEG)-mediated fusion of sensitized lymphocytes and myeloma cells. Among these, two belong to the IgM class and the remaining 21 to various subclasses of IgG. The MAbs from the IgG class designated 4B6 and 4B11 neutralized PPR virus in vitro. In radioimmunoprecipitation assay, 10 MAbs recognized nucleoprotein, 4 recognized the matrix protein and one each haemagglutinin and phosphoprotein. The remaining 7 MAbs failed to precipitate any defined viral protein. The reactivity pattern of the monoclonal antibodies in indirect ELISA indicated a close antigenic relationship within three Indian PPR (lineage 4) virus isolates and also within two rinderpest vaccine strains. All PPR virus isolates could be distinguished from rinderpest vaccine viruses on the basis of the reactivity pattern of all MAbs and anti-N protein MAbs. A set of six monoclonal antibodies specific to PPR virus could also be identified from the panel. From the panel of MAbs available, two MAbs were selected for diagnostic applications, one each for the detection of antigens and antibodies to PPR virus. 相似文献
4.
Intisar K. Saeed Yahia H. Ali AbdelMelik I. Khalafalla E. A. Rahman-Mahasin 《Tropical animal health and production》2010,42(1):89-93
The current situation of PPR in Sudan was investigated. A total of 61 tissue samples were collected from various PPR suspected
outbreaks in sheep in Sudan during 2008. Collected tissue samples were tested for PPR antigen using IcELISA, PPR antigen was
detected in 26 out of 61 samples (42.6%). Highest antigen detection rate was in specimens collected from western Sudan. A
total of 1198 serum samples were collected from sheep (n = 500), camels (n = 392), and goats (n = 306) from different areas
in Sudan (Khartoum, Gezira, Tambool, River Nile, Kordofan, White Nile, Blue Nile, Gedarif, Kassala, Halfa ElGadida, Port Sudan).
Collected sera were examined for PPR antibodies using cELISA, a total of 336 (67.2%) sheep, 170 (55.6%) goat and 1 (0.3%)
camel samples were found to be positive. 相似文献
5.
Pankaj Kumar Amitava Dey Abhay Kumar Pradeep Kumar Ray Poolangulam Chinnakkan Chandran Rashmi Rekha Kumari Manish Kumar 《Tropical animal health and production》2018,50(7):1441-1447
Outbreaks of Peste des petits ruminants (PPR) viral disease in Black Bengal goats were investigated from the middle Indo-Gangetic Plains of India. Clinical profile of PPR-affected flocks was recorded from four different outbreak sites of the region. The PPR outbreak was diagnosed serologically using commercially available sandwich ELISA kit. Relatively, low mortality rate (mean 26.75%) for PPR outbreak was recorded due to the endemic status of the disease. To understand the role of oxidative stress in PPR virus pathogenesis, various oxidant and antioxidant parameters in goats infected with PPR were estimated and compared with the uninfected/healthy goats of the same flock. The measured high level of pro-oxidant malondialdehyde (MDA) obtained from lipid peroxidation along with lower levels of anti-oxidants viz. superoxide dismutase (SOD), glutathione peroxidase (GPx) and catalase (CAT) in PPR-affected Black Bengal goats suggests oxidative stress as one of the mechanism of pathogenesis of PPR virus. In addition, the correlation of oxidative stress due to PPR and the resulting reproductive disorders in the female goats were evaluated. The abortion in pregnant does observed during PPR outbreak was proportional to debility and oxidative stress manifested during PPR infection. The reproductive performance of recovered female goats in the period of 18 months of monitoring was significantly compromised in terms of kidding and twinning frequency. The mortality rate in kids born from PPR-recovered goats was significantly higher compared to those from health goats in the first 9 months post-recovery. From the present study, it may be concluded that together with the PPR virus, infection in goats and the resulting oxidative stress play a vital role for abortion and reduced post-reproductive performance in Black Bengal female goat. 相似文献
6.
Experimental studies on immunosuppressive effects of peste des petits ruminants (PPR) virus in goats
Rajak KK Sreenivasa BP Hosamani M Singh RP Singh SK Singh RK Bandyopadhyay SK 《Comparative immunology, microbiology and infectious diseases》2005,28(4):287-296
Effect of virulent and attenuated peste des petits ruminants (PPR) virus on the immune response to nonspecific antigen (ovalbumin) was investigated. Clinical and serological responses were monitored in goats administered with ovalbumin concurrently with either PPR vaccine or virulent virus. Study showed that PPR virulent virus causes marked immunosuppression as evidenced by leukopenia, lymphopenia, and reduced early antibody response to both specific and nonspecific antigen. These observations were predominant particularly during acute phase of disease (4-10 days post-infection). On the other hand, the vaccine virus induced only a transient lymphopenia without significantly affecting the immune response to nonspecific antigen or to itself during this period. Further, the antibody levels to ovalbumin in the group administered with virulent PPRV increased significantly between days 28 and 35 post-infection in comparison to the titers in other two groups given with either ovalbumin alone or in combination with vaccine. 相似文献
7.
Development of a monoclonal antibody based competitive-ELISA for detection and titration of antibodies to peste des petits ruminants (PPR) virus 总被引：6，自引：0，他引：6
Peste des petits ruminants (PPR) is an acute febrile, viral, disease of small ruminants with great economic importance. A competitive-ELISA (c-ELISA) test was developed for detection of antibodies to PPR virus in the sera samples of goats and sheep. The test uses monoclonal antibody to a neutralizing epitope of haemagglutinin protein of the virus. Based on the distribution of known negative sera samples (n=933) in respect of PPR virus antibodies in the test, a cut-off value was set as 38%. This value was the result of mean of negative population added with two times the standard deviations. A total of 1668 sera samples from goat and sheep and 32 sera from cattle were screened by c-ELISA and virus neutralization test (VNT). Efficacy of c-ELISA compared very well with VNT having high relative specificity (98.4%) and sensitivity (92.4%). The sensitivity of c-ELISA for PPR sero-surveillance could further be increased (95.4%), if the target population is non-vaccinated. c-ELISA test correlated well with VNT (r=0.845) for end-point titration of PPR virus antibody in 64 goat sera samples. It could clearly separate infected population from uninfected in field sera. Using c-ELISA test paired sera samples from 13 goats provided a clear diagnosis of PPR virus infection. Furthermore, antibodies to PPR virus could be successfully detected during 1 year after vaccination in four goats inoculated with an experimental PPR vaccine. Findings suggest that the c-ELISA test developed can easily replace VNT for sero-surveillance, sero-monitoring, diagnosis from paired sera samples and end-point titration of PPR virus antibodies. 相似文献
8.
Muhammad Khalid Mansoor Abdullmajeed Hamood Al-Rawahi Hatim Ali El-Tahir Badar Al-Faraei Muhammad Hammad Hussain Muhammad Nadeem Asi Ibrahim Al-Hussani Safwat Sabar 《Tropical animal health and production》2018,50(1):1-3
Foot and mouth disease (FMD) remains subclinical and self-limiting in small ruminants, but risk of spread of infection to susceptible cohorts is of great epidemiological significance; therefore, small ruminants must be included in vaccination campaigns in FMD endemic regions. Three groups of goats already immunized against peste des petits ruminants (PPR) were vaccinated with FMD and PPR vaccines alone or concurrently. The specific antibody response against three FMD virus strains and PPR virus were evaluated by competitive enzyme-linked immunosorbent assay (cELISA). Goats concurrently vaccinated with PPR + FMD vaccines had significantly (p < 0.05) higher antibody titers to two serotypes of FMD virus at 28, 45, and 60 days post-immunization compared to goats vaccinated with FMD vaccine alone, while goats vaccinated with PPR vaccines alone or PPR + FMD vaccines concurrently showed similar antibody kinetics against PPR virus up till 60 days post-vaccination. Overall, antibody kinetic curves for all three tested strains of FMD virus and PPR virus were similar in vaccinated groups during the course of experiment. 相似文献
9.
10.
This paper constitutes the first record of utilizing the S. aureus protein-A (PA), conjugated to peroxidase enzyme, for the detection of the Peste des Petits Ruminants (PPR) virus antigens
in tissues of experimentally infected goats. The goats were experimentally infected with a virulent PPR virus, which was previously
isolated from a severe natural disease outbreak in gazelles, during 2002 in Saudi Arabia. The technique is rapid, and has
the superiority over the peroxidase –anti-peroxidase (PAP) test in that, inactivation of the indigenous peroxidase in the
tissues is not required and that it can be used against a wide range of animal species. An advantage over the other immunolabelled
conjugates is that PA attaches specifically to the crystalizable fraction (Fc) of the IgG molecule, thus allowing the antigen
binding fraction (Fab) of the molecule, free to interact specifically with the antigen. So, it doesn't actually compete with
the antigen for the Fab portion of the IgG molecule. In the present study, PA conjugate detected the PPR virus antigens in
various tissues of the experimentally infected goats. 相似文献
11.
Nussieba A. Osman A. S. Ali Mahasin E. A/Rahman M. A. Fadol 《Tropical animal health and production》2009,41(7):1449-1453
Counter immnuo-electrophoresis (CIEP) and Competitive ELISA (C-ELISA) tests were employed for seroprevalence of Peste des Petits Ruminants (PPR) infection in Sudan. The result of both tests showed high prevalence of PPRV antibodies in sheep and goats sera collected from six different regions of Sudan. Of the 519 serum samples examined for the presence of PPRV antibodies 307(59.15%) were positive by CIEP while 263(50.67%) were positive by C-ELISA. CIEP technique was shown to be more sensitive than C-ELISA technique for detection of PPRV antibodies (Kappa statistics 0.259). C-ELISA allowed rapid, simple, specific, sensitive and differential sero-diagnosis of PPRV and RPV in sheep, goats and cattle. CIEP is, unlike competitive ELISA, is group-specific test and can not differentiate between PPR and RP infections. Despite its low specificity CIEP can be a useful indicative screening test for PPRV antibodies in flocks that neither been vaccinated nor otherwise exposed to PPR or RP virus. Results obtained suggest that CIEP, like the HI test, could be a useful screening test where it is not possible to use C-ELISA. 相似文献
12.
利用投影寻踪回归技术进行草地产量预报的研究 总被引：3，自引：0，他引：3
本文利用1991～1992年在新疆阜康县不同类型草地上观测的牧草产量、环境因子和卫星遥感资料运用投影寻踪回归(PPR)技术,探讨了草地产量预报的原理与方法,建立了产量预报综合模型,其预报精度达到83.5%以上,并克服传统预报方法的一些不足,科学地提示其内在关系,进而对影响产量预报精度和产量形成的因素进行分析与实验验证。因而研究结果表明利用PPR技术基本实现了科学预报草地产量的目的。 相似文献
13.
Antibody seroprevalences against peste des petits ruminants (PPR) virus in camels, cattle, goats and sheep in Ethiopia 总被引：1，自引：0，他引：1
Abraham G Sintayehu A Libeau G Albina E Roger F Laekemariam Y Abayneh D Awoke KM 《Preventive veterinary medicine》2005,70(1-2):51-57
A questionnaire-survey data indicated that 26% of 276 farmers reported the presence of respiratory disease in their herds in 2001. The incidence was perceived as "high" in small ruminants and camels, but as "low" in cattle. Simultaneously, 2815 serum samples from camels (n=628), cattle (n=910), goats (n=442) and sheep (n=835) were tested. The peste des petits ruminants (PPR) antibody seroprevalence was 3% in camels, 9% in cattle, 9% in goats and 13% in sheep. The highest locality-specific seroprevalences were: camels 10%, cattle 16%, goats 22% and sheep 23%. The animals had not been vaccinated against rinderpest or PPR. Antibody seroprevalences detected in camels, cattle, goats and sheep confirmed natural transmission of PPR virus under field conditions. 相似文献
14.
Khan HA Siddique M Arshad M Abubakar M Akhtar M Arshad MJ Ashraf M 《Tropical animal health and production》2009,41(4):427-430
A total of 70 sheep and 330 goats were selected randomly. All the animals were kept under same housing and management conditions.
Serum samples were collected from all the animals and tested for the presence of antibodies against Peste des petits ruminants
(PPR) virus using competitive ELISA (cELISA). All the animals were found negative showing percentage inhibition (PI) values
<50. The animals were vaccinated against PPR with Nig/75/1 strain vaccine of PPR Serum samples were collected from randomly
selected 12 sheep and 30 goats at 10, 30 and 45 days post-vaccination. The samples were subjected to cELISA to determine the
presence of antibodies against PPRV. The samples with PI >50 were considered as sero-positive. The sheep found positive at
10, 30 and 45 days post-vaccination were 1(8.3%), 7(58.3%) and 12(100%) respectively. In case of goats 3(10.0%), 29(96.6%)
and 27(90.0%) animals gave positive results at 10, 30 and 45 days post-vaccination respectively. Mean PI values in sheep at
10, 30 and 45 days post-vaccination were recorded as 37, 65 and 91 respectively, whereas in goats these values were 43, 78
and 86 respectively. 相似文献
15.
16.
17.
AGPT and HA tests were employed for rapid diagnosis of PPRV infection in sheep and goats in Sudan. Forty lymph nodes and spleen
samples from suspected cases of PPR in both sheep and goats were examined by AGPT and HA tests for detection of PPRV antigen.
Viral antigen was detected from (77.5%) of the samples tested by AGPT and (92.5%) tested by HA test. The results of both tests
revealed that HA test was more sensitive than AGPT for detection of PPRV antigen (Kappa statistics 0.4366). Another advantage
of the HA test over AGPT was that it can differentiate PPRV from RPV. Thus the HA test represents a quick, easy, simple, cheap
and reliable confirmatory test for the diagnosis of PPR and differential diagnosis of PPRV and RPV. The HA test was carried
out using chicken, goat and pig RBCs. Chicken RBCs were found to be the most sensitive for detection of PPRV antigen, followed
by goat then pig RBCs. The HA time when using chicken RBCs was 20–25 minutes, using goat RBCs was 25–30 minutes and using
pig RBCs was 40–45 minutes. The distribution of PPR infection in four different regions of Sudan was investigated. 相似文献
18.
E. Couacy-Hymann S.C. Bodjo M.Y. Koffi C. Kouakou T. Danho 《Research in veterinary science》2009,87(2):332-335
Goats were infected subcutaneously with different African and Indian isolates of peste-des-petits-ruminants virus. Typical signs of disease were recorded from day 6 post infection for all isolates. Ocular, nasal and mouth samples were tested for the presence of virus antigen or nucleic acid using the immunocapture ELISA (ICE) and the RT-PCR technique. Using ICE, virus antigen was detected at day 4 in ocular and nasal samples of goats infected with Côte-d’Ivoire 89 and in the ocular, nasal and mouth samples with the India, Calcutta strains. By day 5, all samples from both these groups were positive while ocular and nasal samples from groups with Sudan-Sennar and Nigeria 75/1 strains became positive. With the RT-PCR technique virus nucleic acid, presumed to be associated with infectious virus excretion, was detected at day 3 in oral and nasal samples in groups infected with Côte-d’Ivoire 89 and India-Calcutta strains. From day 6–9, all samples from all groups were positive with both techniques. This experiment demonstrated that PPR virus antigens and nucleic acid, presumed to be related to infectious virus, is excreted 2–3 days before the appearance of clinical signs whatever the technique used which is of epidemiological importance in controlling the spread of the disease. The ICE being easier to perform in developing countries can be recommended as a useful method to investigate PPR in small ruminants flocks at an early stage to prevent the diffusion of the disease. 相似文献
19.
Vinayagamurthy Balamurugan Paramasivam Saravanan Arnab Sen Kaushal Kishor Rajak Gnanavel Venkatesan Paramanandham Krishnamoorthy Veerakyathappa Bhanuprakash Raj Kumar Singh 《Journal of veterinary science (Suw?n-si, Korea)》2012,13(3):279-285
This study measured the clinical prevalence of peste des petits ruminants (PPR) among sheep and goats in India between 2003 and 2009 by analyzing clinical samples from suspected cases of PPR that were submitted to the Rinderpest and Allied Disease Laboratory, Division of Virology, IVRI, Mukteswar for PPR diagnosis. PPR outbreaks were confirmed by detecting PPR virus (PPRV)-specific antigen in the clinical samples. Clinical samples (blood, nasal swabs, spleen, lymph node, kidney, liver, intestine, and pooled tissue materials) were taken from a total of 592 sheep and 912 goats in different states of India and screened for the presence of PPRV antigen using a monoclonal antibody-based sandwich ELISA kit. A total of 20, 38, and 11 laboratory-confirmed PPR outbreaks occurred among sheep, goat, and combined sheep and goat populations, respectively. Our findings provide evidence of widespread PPR endemicity in India. The underlying reasons could be variations in husbandry practices in different geographical regions, agro-climatic conditions, and livestock migration. Furthermore, decrease in the number of PPR outbreaks over time might be due to the effectiveness of current live PPR vaccines and timely vaccination of target species. Vaccination against PPR has been practiced in India since 2002 to control this disease. 相似文献
20.
小反刍兽疫流行病学及防控研究进展 总被引：1，自引：0，他引：1
小反刍兽疫是山羊、绵羊以及一些野生小反刍动物的一种急性或亚急性接触性传染病,自从首次发生以来一直呈扩大趋势,成为了严重危害畜牧业生产安全的重大跨国动物疫病之一。诊断技术和疫苗接种是预防控制小反刍兽疫的重要手段,根据小反刍兽疫典型的临床症状可初步做出假设性诊断,但确诊需要实验室诊断技术的支持。论文从小反刍兽疫目前的世界分布情况、小反刍兽疫病毒的起源以及易感动物等方面阐述了该病的流行病学特征,介绍了小反刍兽疫病毒实验室诊断技术的研究进展及几种具有应用前景的小反刍兽疫疫苗,为该病的研究和有效防控提供依据。 相似文献