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1.
为了解不同风险因素对陕北白绒山羊布鲁氏菌病个体阳性率的影响,通过对陕北某9个市县的1 138个白绒山羊养殖场、养殖户进行问卷调查,并结合所调查养殖场的34 841份血液样本的血清学检测结果进行统计、单因素分析.结果显示,引种前不进行检疫与引种前进行检疫的养殖场,布鲁氏菌病的个体阳性率分别为2.61%和1.89%,差异显...  相似文献   

2.
为了解新疆南北疆部分疫区马匹携带驽巴贝斯虫(Babesia caballi)抗体情况,运用实验室已构建保存的地方虫株重组Bc48为靶抗原,将重组原核表达质粒pGEX4T-1-Bc48转化至BL21表达系统中,诱导表达出36 KDa的重组蛋白。经KCl法切胶纯化重组蛋白后作为rELISA包被抗原,对阿克苏、伊犁、和硕等7个区域的随机采集样品(n=256)进行马驽巴贝斯虫抗体检测。结果显示,Bc48重组抗原能够精确识别马驽巴贝斯虫标准阳性和阴性血清;所检测的临床样品中,驽巴贝斯虫抗体阳性率为19.5%,其中,南疆2个地区(和硕、阿克苏)马驽巴贝斯虫病阳性率分别为30%、9%;北疆5个地区(昭苏种马场、伊犁卡拉苏、洪纳海乡、阿尕什敖包乡和富蕴县区域)马驽巴贝斯虫抗体阳性率分别为17%、12.5%、17%、5%和35%。本次调查结果为新疆驽巴贝斯虫防控措施及疫苗和驱虫药的使用提供必要的理论依据。  相似文献   

3.
OBJECTIVE: To estimate the specificity of an absorbed enzyme-linked immunosorbent assay kit for Johne's disease (JD) when used in mature cattle populations resident in northern Australia. DESIGN: Blood samples were collected from beef cattle in northern Queensland, the Northern Territory and northern Western Australia, and from dairy cattle in northern Queensland. The specificity of a serological test for JD was estimated by testing the blood samples with an absorbed ELISA kit. Further samples were collected from cattle with positive ELISA results to determine the presence or absence of infection with Mycobacterium avium subsp paratuberculosis. PROCEDURE: During 1995 and 1996, blood, tissue and gut contents were collected from beef cattle at abattoirs in Queensland and the Northern Territory; and blood and faecal samples were collected from dairy cattle in herds assessed to be most at risk for JD in northern Queensland. The blood samples were tested using an absorbed ELISA kit. Tissues and gut contents from beef cattle that had positive ELISA results were cultured for M. avium subsp paratuberculosis, and tissues were examined histologically. Faecal samples from dairy cattle with positive ELISA results were cultured for M. avium subsp paratuberculosis. RESULTS: Estimates of specificity for this absorbed ELISA in mature northern Australian cattle were 98.0% (97.0 to 98.8%, 95% CI) in beef cattle, and 98.3% (96.7 to 99.3%, 95% CI) in dairy cattle. CONCLUSION: Estimates of specificity in this study were lower for beef cattle from the Northern Territory and northern Western Australia and for dairy cattle from northern Queensland than those quoted from studies on cattle in southern Western Australia. This should be considered when serological testing using the JD ELISA is carried out on northern Australian cattle.  相似文献   

4.
Objective To estimate the specificity of an absorbed enzyme-linked immuno-sorbent assay kitd for Johne's disease (JD) when used in mature cattle populations resident in northern Australia.
Design Blood samples were collected from beef cattle in northern Queensland, the Northern Territory and northern Western Australia, and from dairy cattle in northern Queensland. The specificity of a serological test for JD was estimated by testing the blood samples with an absorbed ELISA kit. Further samples were collected from cattle with positive ELISA results to determine the presence or absence of infection with Mycobacterium avium subsp paratuberculosis .
Procedure During 1995 and 1996, blood, tissue and gut contents were collected from beef cattle at abattoirs in Queensland and the Northern Territory; and blood and faecal samples were collected from dairy cattle in herds assessed to be most at risk for JD in northern Queensland. The blood samples were tested using an absorbed ELISA kit. Tissues and gut contents from beef cattle that had positive ELISA results were cultured for M avium subsp paratuberculosis , and tissues were examined histo-logically. Faecal samples from dairy cattle with positive ELISA results were cultured for M avium subsp paratuberculosis .
Results Estimates of specificity for this absorbed ELISA in mature northern Australian cattle were 98.0% (97.0 to 98.8%, 95% CI) in beef cattle, and 98.3% (96.7 to 99.3%, 95% CI) in dairy cattle.
Conclusion Estimates of specificity in this study were lower for beef cattle from the Northern Territory and northern Western Australia and for dairy cattle from northern Queensland than those quoted from studies on cattle in southern Western Australia. This should be considered when serological testing using the JD ELISA is carried out on northern Australian cattle.  相似文献   

5.
为了解新疆南疆部分地方品种绵羊嗜血支原体和泰勒虫的感染情况,采用PCR法检测新疆南疆5个地方品种绵羊共100份血液DNA样本.结果表明:新疆南疆部分地方品种绵羊泰勒虫和嗜血支原体感染率分别为35.0%(35/100)和3.0%(3/100).仅和田羊和多浪羊上检测到嗜血支原体感染,感染率分别为8.0%(2/25)和5....  相似文献   

6.
Survey for Trichinella spp. in red foxes (Vulpes vulpes) in Belgium.   总被引:3,自引:0,他引:3  
Concurrently with a survey for Echinococcus multilocularis in the red fox (Vulpes vulpes) in Flanders, northern Belgium, serological and parasitological analyses for Trichinella spp. were carried out from 1996 to 1999. Muscle samples from foxes in Wallonia, southern Belgium, were obtained during a survey for rabies and alveolar echinococcosis from 1998 to 2000.In muscle samples from tongue, diaphragm, hindlegs and tail of 179 Flemish foxes no larvae were found by trichinoscopy. Serum and muscle juice of, respectively 176 and 26 animals were examined using an ELISA for the detection of antibodies against excretory-secretory (ES) antigen. There were eight (4.5%) positive sera, but no positive muscle juice samples.All muscle samples from 639 foxes in Wallonia proved to be negative for larvae in artificial digestion. Serum and muscle juice of 130 and 478 foxes, respectively were examined in ES-ELISA. There were 61 (46.9%) positive sera and 90 (18.8%) positive muscle juice samples. A comparison between 88 serum and muscle juice samples of the same foxes showed that only half of the serum-positive animals were detected using muscle juice. However, for establishing the true meaning of these results, a more profound epidemiological study on the vulpine population in Belgium is necessary.  相似文献   

7.
为了解伊犁河谷区域新疆褐牛隐孢子虫病流行情况,从该地区的伊宁市和察布查尔锡伯自治县的4个养殖场采集356份粪便样品,提取基因组DNA,以隐孢子虫小亚基核糖体DNA(SSU rDNA)为靶基因,进行套式PCR扩增,并对阳性样品进行序列分析.结果显示:伊宁市和察布查尔锡伯自治县各有1个养殖场的新疆褐牛发现隐孢子虫感染,总的...  相似文献   

8.
The polymerase chain reaction (PCR) was used to diagnose goat brucellosis and compare its sensitivity against some of the most commonly used serological and bacteriological techniques. Twenty two female and one male out of 300 clinically healthy, mixed-breed goats were randomly chosen from a ranch located at Marín, Nuevo León, Mexico. Milk and blood samples were taken from each animal and used to obtain both microbiological cultures and DNA of the pathogen, and sera was tested against Rose Bengal antigen (RBT). Results showed that 86% of the blood samples were positive on the PCR test, while 60% were positive on the serological test. The pathogen was isolated from only one blood culture. Sixty four percent of the milk samples were positive on PCR tests, but failed to yield bacteria in culture. Biochemical and PCR specific assay demonstrated that Brucella abortus biovar 1 was associated with the infection. This study demonstrates the higher sensitivity of PCR over RBT and blood culture and its potential towards a rapid identification of Brucella strains.  相似文献   

9.
The single nucleotide polymorphisms (SNPs) of ovine lymphocyte antigen DQB1 (OLA-DQB1) gene exon 2 was amplified by PCR-SSCP method from 148 healthy and 60 infected with Brucella Chinese Merino sheep and then PCR products of different alleles were sequenced to determine the polymorphism loci of the gene.The differences in gene frequency and genotype frequency of each SNP loci were analyzed statistically to analyze its correlation with brucellosis susceptibility.The sequencing result showed that 43 SNPs were detected in 270 bp DNA sequence,the gene frequencies of G196A allele had extremely significant difference in case and control samples (P< 0.01),and its genotype frequencies presented significant difference (P< 0.05).Similarly,C211T allele was significantly different in case and control samples (P< 0.05).The results showed that the polymorphism of OLA-DQB1 gene exon 2 might be a significant association gene with brucellosis susceptibility.  相似文献   

10.
In total, 582 sera from 116 black goat herds were analyzed by a commercially available ELISA kit to monitor the seroprevalence of Mycobacterium avium subspecies paratuberculosis (Mpt) in Korean black goats (Capra hircus aegagrus). The mean number of goats sampled per herd was 5.11, 4.66, and 5.38 for the northern, central, and southern regions of Korea, respectively. The apparent regional prevalence of Mpt was estimated at 18.2-38.2% and 4.6-15.3% for herds and goats, respectively. The Mpt-positive goats were predominantly detected in the south (n=28), compared to either the northern (n=9) or central (n=11) regions (chi=14.459, P<0.05). Our findings indicate that Mpt is prevalent among the goat population, but regional variation exists.  相似文献   

11.
Killer whales and sea otters maintained in captivity are the subjects of routine health monitoring programs, and interest in immunologic studies in sea otters has been rising recently in response to potential impacts from infectious disease and environmental pollution on the threatened southern sea otter population. Development of species-specific reagents for immunologic studies in these two marine mammals is currently in its infancy. In this study, killer whale and sea otter immunoglobulin-specific polyclonal antibodies were generated, and used to develop tests for serum Ig concentration in the killer whale (Orcinus orca) and the southern (Enhydra lutris nereis) and northern sea otter (Enhydra lutris lutris). Killer whale serum IgG was purified using caprylic acid/ammonium sulfate precipitation. Sea otter plasma IgG was purified using protein-A-agarose. Polyclonal anti-Ig antisera were produced in rabbits, and specificity confirmed by immunoelectrophoresis. Radial immunodiffusion was used to measure Ig concentration in serum or plasma samples derived from 21 captive killer whales, 18 wild and 4 captive southern sea otters and 15 wild and 4 captive northern sea otters grouped by age. Mean killer whale serum Ig concentration (+/-95% confidence interval) ranged from 15.04 +/- 3.97 g/l for animals aged 0-5 years to 26.65 +/- 9.8 g/l for animals aged >10 years. Mean sea otter serum Ig concentration (+/-95% confidence interval) ranged from 28.39 +/- 11.00 g/l for southern sub-adults to 32.76 +/- 11.58 g/l for southern adults. No significant difference in serum Ig concentration was found between southern and northern sea otters. Serum Ig concentrations in two northern sea otter pups were low compared to those of adult sea otters. The two serum Ig quantitation assays produced were highly specific and reproducible and will be useful additions to the limited number of tests available for immune function in these marine mammal species.  相似文献   

12.
猪细环病毒1型是近年来发现的又一种环状DNA病毒,可能存在潜在致病作用。为了初步了解其流行情况,用PCR技术和ELISA技术对来自京津冀、华东与华南地区578头保育猪血清样品进行了检测。结果显示,猪细环病毒1型的核酸与抗体的猪场阳性率均为100%;核酸阳性率为73.88%,抗体阳性率为78.72%,二者之间无显著差异(P>0.05)。进一步分析发现,猪细环病毒1型的核酸阳性率和抗体阳性率都超过50%的猪场达到86.67%,都超过80%的占53.33%。调查结果表明,猪细环病毒1型感染在我国部分地区普遍流行,其在多数猪场的感染率很高。  相似文献   

13.
The aim of this study was to evaluate the performance of commercial heartworm antigen tests in dogs harbouring Dirofilaria immitis microfilariae near its distribution limit in South America. A total of 4934 blood samples of adult dogs from Southern Greater Buenos Aires were examined to detect circulating microfilariae in the buffy coat interface between December 2005 and April 2006. Microfilariae were detected in 88 (1.8%) blood samples and all the microfilariae observed were identified as D. immitis by acid phosphatase stain technique. In a first trial, 69 (78.4%) out of the 88 serum were positive by Speed((R)) Diro. Then, a new test was performed over 25 microfilariae-positive serum samples randomly selected among the 88 previously tested samples and using simultaneously Speed((R)) Diro, Witness((R)) Dirofilaria and Snap((R)) 3dx. This second trial showed identical results for the three different tests, in which 19 (76%) samples were positive. Therefore, more than 20% of microfilaremic dogs were antigen negative. The main hypothesis that could explain our finding is a low worm burden in the study area. According to our preliminary results, it is highly recommendable the complementary use of antigen tests and other procedures to obtain an accurate diagnostic near the distribution limit of the parasite.  相似文献   

14.
15.
为了解2020年1—12月北疆部分地区猪伪狂犬病野毒株(PRV-gE)感染情况,采用间接酶联免疫吸附试验(ELISA)法对从北疆4个地区采集的657份猪血样进行PRV-gE蛋白抗体水平检测.结果显示,4个地区PRV-gE抗体阳性率为29.83%(196/657),乌苏地区与其他地区的抗体水平存在一定差异(P<0.05)...  相似文献   

16.
半干旱黄土丘陵沟壑区封禁流域植被枯落物分布规律研究   总被引:6,自引:1,他引:6  
通过对陕北半干旱黄土丘陵沟壑区封育流域内不同立地条件下枯落物现存量的测定与分析,研究了枯落物的影响因子及分布规律。对60个样地调查研究结果表明:枯落物现存量与坡度呈二次回归关系,枯落物现存量最小值出现在坡度25.5°的位置;阴坡枯落物现存量比阳坡高25.1%,沟坡枯落物现存量比梁坡高41.7%;地表生物量与枯落物现存量呈显著的正相关性(P0.05);土壤含水量与枯落物现存量呈正相关性;土壤含水量与地表生物量两者的共同作用对枯落物现存量影响明显。  相似文献   

17.
为全面了解吉林省某规模化牛场牛病毒性腹泻(BVD)的流行情况,试验采集临床血清样品157份,粪便样品18份,肝脏、精液等组织样品17份,应用BVDV抗体检测试剂盒进行血清抗体检测,利用BVDV1型引物,采用纳米PCR方法对血清及临床样品进行BVDV抗原检测,对抗原阳性样品进行测序分析;将抗原阳性样品经研磨、稀释后用0.22μm滤膜过滤除菌,接入牛肾细胞(MDBK)进行病毒分离培养,盲传3代后再次进行抗原检测;采用免疫荧光技术检测病毒对MDBK细胞的侵染作用;利用Mega软件绘制系统进化树并进行同源性比对分析。结果显示,该牛场临床血清BVDV抗体阳性率为77.1%,血清抗原阳性率为12.1%,临床粪便等样品抗原阳性率为74.3%;病料接入细胞未观察到细胞病变,分离毒株PCR产物测序分析结果与样品抗原检测结果一致;免疫荧光检测结果显示,分离株毒液正常吸附于MDBK细胞中,有明显荧光反应;抗原测序分析显示,该牛场BVD主要流行毒株与BVDV JL-1株同源性高达99.0%,且均为BVDV 1型毒株。本研究对该牛场BVDV流行情况进行了全面调查,为开展净化工作奠定了基础。  相似文献   

18.
Bulk milk samples from 2236 dairy herds randomly selected throughout Sweden in proportion to region and herd size were analysed for antibodies to bovine coronavirus (BCV) in an ELISA. The results were expressed as optical density (OD) values and an OD > 0.04 was considered positive. Eighty-nine per cent of the samples were antibody-positive and 52 per cent had high levels of antibodies to BCV (an OD > 0.70). There were significantly higher OD values (P < 0.001) and fewer antibody-negative samples (P < 0.001) from larger herds than from smaller herds. There were also significantly higher OD values and fewer antibody-negative samples from herds in southern Sweden than from herds in northern Sweden (P < 0.001 and P < 0.001, respectively). These results indicate a higher frequency of BCV infections in larger herds and in herds in southern Sweden.  相似文献   

19.
[目的]牛病毒性腹泻—黏膜病(bovine viral diarrhea-mucosal disease, BVD)引起牛腹泻、呼吸系统疾病、生殖功能障碍、免疫抑制、母畜流产、死胎等,对牛产业发展危害严重。牛病毒性腹泻—黏膜病病毒(bovine viral diarrhea-mucosal disease virus, BVDV)在我国大部分牛群中普遍存在,各地流行情况严重程度不同,本调查旨在调查云南省BVDV的流行情况。[方法]调查通过采用商品化的酶联免疫吸附试验(ELISA)试剂盒对BVDV感染和流行情况进行调查,采集了云南省4个州10个县(市)的部分规模牛场及散养户的牛血清样品456份。[结果]结果发现,云南省不同地区所检的牛血清样品总抗体阳性率为16.45%(75/456),抗原阳性率为0.53%(2/378),其中抗体阳性率以大理州洱源县60.0%(9/15)最高,而丽江市华坪县的血清样品中未检测到抗体阳性,大理州宾川县和丽江市宁蒗县的抗原阳性率较低,分别为7.69%(1/13)和4.00%(1/25)。云南省规模场牛的血清样品抗体总阳性率为27.27%(45/165),抗原阳性率为1.15%(1/87),散养户牛的分别为10.31%(30/291)和0.34%(1/291)。[结论]云南省的牛群中存在着BVDV感染的情况,其抗体抗原的阳性率水平跟地区有着紧密的联系,不同的养殖方式抗原抗体水平存在着一定差异,必须要加强云南省BVDV监测与防控,减少其造成的经济损失。  相似文献   

20.
Serum samples were collected from 372 sheep and same number of goats from the three geopolitical zones of Borno state, Nigeria. The samples were tested for the presences of Toxoplasma gondii antibodies by enzyme-linked immunosorbent assay. Of these, 6.7% (25/372) and 4.6% (17/372) of sheep and goats, respectively, were found to be seropositive to T. gondii antibodies, both far less than the estimated global average of 31%. Results were statistically analyzed by chi-square (χ2) test. The results showed that age, environmental conditions, and farm location are the main determinants of prevalence of antibodies against T. gondii in the study area. Older animals (>3 years) are significantly more infected than younger animals (between 6 months and 1 year).The prevalence of anti T. gondii antibodies is significantly higher (P < 0.05) in both sheep and goats sampled from the southern zone than the northern zone. Animals from the southern zones are about four times more likely to be exposed to T. gondii infection than those in the northern zone, (sheep; odds ratio (OR) = 4.25, 95% confidence interval (CI) = 1.177–15.36, P = 0.018), (goats; OR = 4.38, 95% CI = 0.925–20.73, P = 0.04). Farm location in urban area was identified as a risk factor for sheep (OR = 6.06, 95% CI = 2.53–14.54, P = 0.000), and goats (OR = 4.99, 95% CI = 1.59–15.62, P = 0.004). Current data on prevalence of ovine and caprine T. gondii in Borno state are provided by the study as well as identifying the main risk factors associated with T. gondii infection in the area.  相似文献   

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