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1.
Wambura P.N. Mollel J.O. Moshy D.W. Mbise A.N. Taylor W.P. 《Tropical animal health and production》1999,31(1):9-14
In January 1997, serum samples from 1346 adult sheep and goats were tested by a competitive ELISA to determine the prevalence of rinderpest in the northern zone of Tanzania. Seroconversion rates of 20%, 13%, 9%, 7% and 3% in sheep and goats were recorded in Ngorongoro, Monduli, Hai, Arumeru and Simanjiro districts, respectively. The low profile and insidious nature of the rinderpest virus involved caused very mild disease in cattle in some of these area. The mild signs associated with this outbreak of rinderpest resulted in difficulty in its diagnosis. In these circumstances, the presence of rinderpest antibody in sheep and goats served as a valuable and effective indicator of the rinderpest outbreak in cattle. 相似文献
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Seroprevalence of, and risk factors for, peste des petits ruminants in sheep and goats in Northern Jordan 总被引：1，自引：0，他引：1
Peste des petits ruminants (PPR) is an economically important disease that affect sheep and goat industry in Asia and Africa. In this study, we investigated the seroprevalence, and risk factors, of PPR in sheep and goat flocks from five different governorates (Irbid, Jarash, Ajloun, Mafraq and Zarka) located in Northern Jordan. Serum samples from 929 and 400 sheep and goats, respectively, corresponding to 122 sheep flock and 60 goats flock were collected. Seroprevalence was determined using PPR competitive ELISA. Health status and management information were collected using a semi-structured pre-tested questionnaire. The individual true prevalence of PPR in sheep and goats was 29 and 49%, respectively. The flock level true prevalence of PPR was 60 and 74% in sheep and goats, respectively. In both sheep and goat flocks, large flock size, visiting live animals market and inadequate veterinary services were identified as risk factors for PPR seropositivity. Mixed (sheep and goats) raising was identified as a risk factor for PPR seropositivity in sheep flocks only. 相似文献
3.
Hammouchi M Loutfi C Sebbar G Touil N Chaffai N Batten C Harif B Oura C El Harrak M 《Veterinary microbiology》2012,160(1-2):240-244
Peste des petits ruminants virus (PPRV) recently caused a serious outbreak of disease in Moroccan sheep and goats. Alpine goats were highly susceptible to PPRV with mortality rates approaching 100%, as opposed to local breeds of sheep which were less susceptible to the disease. The relative susceptibility of alpine goats was investigated through an experimental infection study with the Moroccan strain of PPRV. Severe clinical signs were observed in the alpine goats with virus being excreted through ocular, nasal and oral routes. No difference in the severity of the disease in goats was observed with different inoculation routes and transmission of the virus by direct contact was confirmed. This study confirmed the susceptibility of the alpine goat to PPRV infection and describes a challenge protocol that effectively and consistently reproduced severe clinical signs of PPR in experimentally infected goats. 相似文献
4.
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
5.
Seroprevalence of Peste des petits ruminants in cattle and buffaloes from Southern Peninsular India 总被引：1，自引：1，他引：0
Balamurugan V Krishnamoorthy P Veeregowda BM Sen A Rajak KK Bhanuprakash V Gajendragad MR Prabhudas K 《Tropical animal health and production》2012,44(2):301-306
This study describes seroprevalence of Peste des petits ruminants (PPR) in cattle and buffaloes carried out during the period 2009–2010 using the randomly collected serum samples from different
parts of Southern peninsular India. The report presents the results of PPR virus (PPRV)—specific antibodies in situations
where either the subclinical or inapparent or non-lethal infection was there in cattle and buffaloes. A total of 2,548 serum
samples [cattle = 1,158, buffaloes = 1,001, sheep = 303 and goat = 86] were collected and screened for PPRV antibodies by
using a PPR monoclonal antibody-based competitive ELISA kit. Analysis of 2,159 serum samples indicates an overall 4.58% prevalence
of PPRV antibody in cattle and buffaloes. The presence of PPRV-specific antibodies demonstrates that cattle and buffaloes
are exposed to PPR infection naturally, and the transmission mode may be direct or indirect. Further, it implies the importance
of bovines as subclinical hosts for the virus besides widespread presence of the disease in sheep and goats in the country. 相似文献
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2007年小反刍兽疫(PPR)在我国西藏首次暴发,在西藏和新疆部分地区使用PPR Nigeria 75/1疫苗株制造的疫苗进行免疫接种。为明确疫苗的安全性,中国兽医药品监察所国家牛瘟参考实验室对其安全性能进行了系统评价。健康易感山羊、绵羊及怀孕山羊、怀孕绵羊按不同剂量接种疫苗后,均未观察到异常临床反应;怀孕母羊所产羔羊数量与对照组无明显差异。疫苗对小白鼠、豚鼠的非特异性安全试验表明,所有接种动物均健活。结果表明该疫苗安全性良好,可在田间大规模使用。 相似文献
9.
小反刍兽疫分子生物学研究进展 总被引：2，自引：1，他引：1
小反刍兽疫(peste des petits ruminants,PPR)是由小反刍兽疫病毒(peste des petits ruminants virus,PPRV)引起的一种急性、烈性、接触性传染病。山羊高度易感;牛、猪等动物也可以感染带毒,野生动物偶有发生。作者主要介绍了小反刍兽疫病毒各基因结构特点,6种结构蛋白的功能,以及小反刍兽疫的诊断技术等方面的最新研究进展。 相似文献
10.
N. Mishra K. Rajukumar A. Tiwari R. K. Nema S. P. Behera J. S. Satav S. C. Dubey 《Tropical animal health and production》2009,41(7):1231-1239
The aim of this study was to determine the prevalence of pestivirus antibodies in sheep and goats in India. A total of 2803 serum samples collected between 2004 and 2008 from 1777 sheep in 92 flocks and 1026 goats in 63 flocks belonging to 13 states were tested by competition ELISA for detection of pestivirus antibodies. In sheep, the true prevalence rate was 23.4% (95% confidence interval: 22.9%–27.0%) and in goats it was 16.9% (95% CI: 16.4%–21.3%). The flock level seroprevalence was 66.3% for sheep and 54.0% for goats. Geographical variation in individual and flock prevalence was highly significant. A significant association (p?<?0.05) was found between sheep and goat flocks having cattle contact and the flock level seroprevalence. The seroprevalence was lower in 6 months–1 year age group compared to the 1–2 year and >2 year age groups in both sheep and goats. Cross neutralization studies on 61 seropositive sheep and 34 seropositive goat samples representing all positive flocks, exhibited > four fold higher titre to bovine viral diarrhoea virus type 1 (BVDV-1) in 41 sheep and 23 goat samples and to BVDV-2 in one sheep and goat each. This study for the first time showed serological evidence of wide spread BVDV infections in Indian sheep and goats, with BVDV-1 predominating and BVDV-2 occasionally besides highlighting the potential risk of infection to other species, which needs to be considered whenever BVD control measures are initiated. 相似文献
11.
小反刍兽疫病毒(PPRV)是副黏病毒科(Paramyxoviridae)麻疹病毒属(Morbolivirus)的成员,主要感染山羊、绵羊等小反刍动物,引起一种高度接触性病毒性传染病。小反刍兽疫为一种重大的外来性疾病,2007年在中国西藏自治区日土县首次发生。自2013年末以来中国新疆、青海、甘肃、宁夏、内蒙、湖南、辽宁等地频繁暴发小反兽疫疫情,给中国的畜牧业带来了巨大的损失,引起极大的重视。为更好的分析小反刍兽疫的病原特性及采取有效的防控措施,文章对小反刍兽疫的病原学及疫苗研究进展进行论述。 相似文献
12.
During the period from January 2002 to December 2003, serum samples were collected from 104 small ruminant flocks consisting
of 18 sheep flocks, 27 goat flocks, and 59 mixed flocks containing both sheep and goats in northern Jordan. Only female sheep
and goats were sampled. At least five females aged over 2 years per flock per species were sampled and examined for Mycoplasma mycoides subspecies capri using the latex agglutination test. To increase the chances of detecting positive flocks, sick or older ewes were sampled.
Specific information was obtained using a questionnaire to identify potential risk factors for M. mycoides subsp. capri seropositivity in small ruminants. The true flock-level seroprevalences of M. mycoides subsp. capri were 34%, 32%, and 38% in small ruminants (sheep and goats), sheep, and goats, respectively. Differences between flock-level
seroprevalences in sheep and goats were not significant (p = 0.7). Multivariable logistic regression analysis of 21 production and health management practices showed four to be associated
with M. mycoides subsp. capri seropositivity including flocks which were grazed and fed concentrate supplement (OR = 4.6), improper cleaning of milking
utensils (OR = 4.7), buying new animals to replace culled ones (OR = 0.3), and treating against helminths when clinical signs
of helminth infections appear (OR = 0.4). 相似文献
13.
Peste des petits ruminants (PPR) is an important viral disease of sheep and goats, endemic in India. The study was undertaken to characterize the local PPRV by sequencing fusion (F) protein and nucleoprotein (N) gene segments and phylogenetic analysis, so as to focus on genetic variation in the field viruses. Selected regions of PPRV genome were amplified from clinical samples collected from 32 sheep and goats by RT-PCR and the resulting amplicons were sequenced for phylogenetic analysis. The phylogenetic tree based on the 322bp F gene sequences of PPRV from five different locations clustered them into lineage 4 along with other Asian isolates. While the 425bp N gene sequences revealed a different pattern of branching, yielding three distinct clusters for Nigerian, Turkey and Indian isolates. Thus, classification of PPRV into lineages based on the N gene sequences appeared to yield better picture of molecular epidemiology for PPRV. 相似文献
14.
K. S. Intisar Y. H. Ali M. A. Haj M. A. T. Sahar M. M. Shaza A. M. Baraa O. M. Ishag Y. M. Nouri K. M. Taha E. M. Nada A. M. Ahmed A. I. Khalafalla G. Libeau A. Diallo 《Tropical animal health and production》2017,49(4):747-754
The existence of peste des petits ruminants (PPR) in domestic ruminants and camels in Sudan during 2008–2012 was investigated. Lung tissues and serum samples were randomly collected from sheep, goats, cattle, and camels at different areas of Sudan. A total of 12,384 serum samples were collected from clinically healthy 7413 sheep, 1988 camels, 1501 cattle, 1459 goats, and 23 gazelles at different areas in the Sudan. They were examined for PPR antibodies using competitive ELISA (cELISA). The overall detected seroprevalence of PPR in tested sera was 49.4%; seroprevalence values within species were 67.1, 48.2, 25.8, 2.1, and 21.7% in sheep, goat, cattle, camels, and gazelles, respectively. The highest seroprevalence (68.1%) was observed in sera collected from Darfur states, then the central states (54.3%). A total of 1276 lung tissue samples (623 sheep, 324 cattle, 220 camels, and 109 goats) were collected. The majority of lung samples were collected from clinically healthy animals that showed lesions on PM in slaughterhouses (95%) and during PPR outbreaks; samples were tested for PPR antigen using immunocapture ELISA (IcELISA). PPR antigen was detected in 233 out of the 1276 tested samples (18.3%). Positive results were observed in samples collected from clinically healthy and diseased animals. The observed prevalence values in each species were 33.6, 21.1, 15.4, and 12.3% in camel, goat, sheep, and cattle, respectively. PPR antigen was detected in samples from different areas; however, the highest prevalence (63.9%) was found in samples collected from the eastern states, then Khartoum state (28%). Trials for virus isolation were done in different cell cultures. Out of 30 IcELISA-positive samples inoculated in primary bovine and ovine kidney cells, Vero cells, the PPR virus was successfully isolated from 15 (eight sheep, five camels, and two goats) samples in the three cell culture types. Using RT-PCR, PPRV nucleic acid was detected in all 25 IcELISA-positive tested samples. 相似文献
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为了解河南省长垣市奶山羊小反刍兽疫疫情流行情况和免疫抗体水平,2018—2020年,采用阻断酶联免疫吸附剂测定（ELISA）法和实时荧光聚合酶链式反应（PCR）法,对长垣市32 家奶山羊散养户采集羊血清和鼻拭子样品,进行羊小反刍兽疫免疫抗体及病原学检测。结果表明,2018年、2019年和2020年的血清抗体合格率分别为83.13%、85.64%和86.67%,平均85.17%,高于国家规定的70.00%。病原学监测全部样品为阴性。提示长垣市总体疫苗免疫效果良好,羊群具有抵抗小反刍兽疫侵袭的基本能力。为长垣市制定科学合理的防控措施、逐步消灭小反刍兽疫和退出小反刍兽疫免疫计划提供参考依据。 相似文献
16.
E. S. Swai W. Moshy P. F. Mtui S. Bwanga G. Machange P. Sanka 《Tropical animal health and production》2009,41(6):959-967
Sera from 497 sheep and 555 goats collected in a cross sectional study from different geographical locations in north-eastern
Tanzania were examined for antibodies to Ehrlichia ruminantium using MAP 1-B ELISA technique. E. ruminantium antibodies were found in 68.6% (341/497) of sheep and 64.7% (359/555) of goats. Overall seroprevalence was 66.5% (700/1052).
Infection rates were higher in sheep than goats (P < 0.05), in pastoral than in agro-pastoral production systems (P < 0.05)
and in female sheep than males (P < 0.05). (131/143) 91.6% of the farms/flocks tested revealed sero-positive animals. E.ruminantium infections were found in all the geographical villages and districts tested. The infection rates per administrative district
varied from 36.4% (Muheza) to 90% (Mkinga) in goats and from 11.9% (Muheza) to 94.6% (Mkinga) in sheep. The results shows
E. ruminantium infection was prevalent and widely but unevenly distributed throughout the eight districts under study. These findings should
be taken into consideration when future disease control and livestock upgrading programs are implemented. 相似文献
17.
Abubakar M Rajput ZI Arshed MJ Sarwar G Ali Q 《Tropical animal health and production》2011,43(4):745-747
An outbreak resulting in mortality in Sindh Ibex (Capra aegagrus blythi) was investigated. There was a history of about 36 deaths (both young and adult) during the period of 1 month. Disease appeared
in a generalized form, affecting the respiratory and digestive systems. Major lesions were respiratory distress, pustules
on and in the mouth, ocular–nasal discharges, and severe diarrhea. The most significant lesion was the oculonasal discharges
and diarrhea. Deaths were mainly due to blindness, anorexia, diarrhea, and respiratory arrest. Both adult (mortality = 21)
and young (mortality = 15) animals were affected with the disease. Peste des petits ruminants virus (PPRV) antigen was detected
in the spleen, lung, lymph node, and swab samples by immunocapture enzyme-linked immunosorbent assay. Spleen and lung samples
were also tested and found positive for the presence of F-gene of PPRV by polymerase chain reaction. Thirteen of 20 serum
samples from nearby sheep and goats were found positive for antibodies to PPRV. The disease threatened the huge population
of ibex in the wild life park, which was spread over a large area, but vaccination of the domestic population of sheep and
goats in the surrounding villages appeared to control the disease. 相似文献
18.
One hundred and ninety-five goat and 67 sheep sera collected from various parts of southern Nigeria were screened for neutralising antibodies to both the peste des petits ruminants (PPR) and rinderpest viruses. Neutralising antibodies against both viruses were found in the sheep and goat sera examined. Parallel titration of samples which neutralised both viruses indicated a primary infection with the PPR virus (PPRV). However, some samples which failed to neutralise PPRV neutralised the rinderpest virus (RV) indicating RV activity in sheep and goats in Nigeria. These findings are discussed in relation to the diagnosis of PPRV infection and the recent reappearance of bovine rinderpest in Nigeria. 相似文献
19.
Risk factors associated with Mycoplasma agalactiae infection of small ruminants in northern Jordan 总被引：1，自引：0，他引：1
Serological detection of Mycoplasma agalactiae was carried out in 104 small ruminants flocks consisting of 18 sheep, 27 goat and 59 flocks containing both sheep and goats in northern Jordan between 2002 and 2003. At least 5 serum samples per flock were tested using an indirect ELISA for antibodies to M. agalactiae. To increase the chances of detecting this mycoplasma, sick or older animals were sampled. A high seropositivity to M. agalactiae was found in small ruminants suggesting a major role for M. agalactiae in contagious agalactia in northern Jordan. There was no significant difference in the seroprevalence of M. agalactiae in sheep and goats at flock level (X(2)=0.14, d.f.=1, p=0.7). A total of 31 variables including production and health management practices were tested as risk factors for seropositive flocks and analyzed using logistic regression analysis. Increasing risk factors for M. agalactiae seropositive flocks were: using outsider rams, improper cleaning of the milking utensils and separating young from dam, with odds ratios of 5, 3, 4.2, respectively; having mastitis problems in the flock was negatively associated (p=0.04) with M. agalactiae seropositivity. Educating small ruminant farmers to avoid the use of outsider rams, ensuring adequate cleaning of milking utensils and separating the young from dams would enhance the health of small ruminants. 相似文献