首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到18条相似文献,搜索用时 437 毫秒
1.
为了解云南省部分地区规模化猪场种公猪精液繁殖障碍病毒性病原的感染状况,应用PCR对2014年—2016年间云南省部分地区规模化猪场212份种公猪精液进行了猪繁殖与呼吸综合征病毒(PRRSV)、猪瘟病毒(CSFV)、猪伪狂犬病病毒(PRV)、猪圆环病毒2型(PCV2)和猪细小病毒(PPV)5种与猪繁殖障碍有关的病原检测。结果表明,PPRSV阳性率为7.08%,CSFV阳性率为3.77%,PCV2阳性率为6.60%,PRV阳性率为3.30%,没有检测出PPV,PRRSV和PCV2的感染率呈上升趋势,其他疫病保持相对平稳态势。所有的混合感染样品中,均检测出了PRRSV,其中PRRSV和PCV2的混合感染最为常见。结果提示,控制猪场疫病发生的关键是控制PRRSV和PCV2的流行,有必要加强对种猪群的疫病病毒检测,推行种猪场主要疫病的控制与净化工作。  相似文献   

2.
种公猪精液中与繁殖障碍有关的6种病毒的检测   总被引:1,自引:1,他引:1  
采用PCR和RT-PCR技术,于2006年4月~10月对上海及其周边地区的30个猪场和人工授精站的生产公猪精液样品355份进行了猪繁殖与呼吸综合征病毒(PRRSV)、猪伪狂犬病病毒(PRV)、猪细小病毒(PPV)、猪圆环病毒(PCV)、猪瘟病毒(CSFV)和日本脑炎病毒(JEV)等6种与猪繁殖障碍有关的病毒的检测,结果表明,日本脑炎病毒检测为阴性,检出PRRSV、PRV、CSFV、PPV和PCV阳性数和阳性率分别为6份(1.69%)、9份(2.54%)、5份(1.41%)、75份(21.1%)、6份(1.69%),有一个猪场的5份样品存在PRV和PPV混合感染.  相似文献   

3.
广西猪细小病毒与PRRSV、CSFV、PCV2、PRV混合感染的检测   总被引:7,自引:0,他引:7  
应用PCR技术,对广西南宁、玉林、贵港、柳州、钦州和桂林6个市的10个规模化猪场送检的141份病猪组织样品进行猪细小病毒(PPV)的检测;同时,对鉴定为PPV阳性的样品进行了猪繁殖与呼吸综合征病毒(PRRSV)、猪瘟病毒(CS-FV)、猪圆环病毒2型(PCV2)和猪伪狂犬病毒(PRV)的检测,以确定猪群中PPV与其它病毒混和感染情况。结果,所有样品诸病毒的阳性检出率达17.73%(25/141);流产胎儿PPV阳性率为19.57%(9/46),繁殖障碍母猪扁桃体的PPV阳性率为17.74%(11/62),发病断奶仔猪组织病料的PPV阳性率为15.15%(5/33),PPV与PRRSV、CSFV、PCV2和/或PRV4种病毒均有混合感染现象,混合感染样品占PPV阳性样品的48.00%(12/25)。  相似文献   

4.
为了解细环病毒(Torque teno virus,TTV)在广西猪群中的感染情况,本研究运用Nest-PCR方法,对2009—2011年采自广西140个规模猪场的156份血液、流产胎儿及肺脏、脾脏、肾脏、肝脏、淋巴结等组织样品进行检测,并对阳性样品的非编码区(UTR)进行克隆测序及遗传进化分析;同时对部分样品进行猪圆环病毒2型(PCV2)、猪繁殖与呼吸综合征病毒(PRRSV)、典型猪瘟病毒(CSFV)、伪狂犬病病毒(PRV)检测及细菌的分离鉴定。结果发现,广西猪群中TTV总感染率达到93.6%,TTV2的感染率(76.9%)不仅明显高于TTV1(16.7%),且毒株间遗传变异较大。TTV多与PCV2和PRRSV混合感染,且以与PRRSV混合感染率更高(64.29%)。猪群中存在2重、3重,甚至4重TTV与其他病毒的混合感染。临床上TTV与细菌的混合感染(或细菌继发感染)以链球菌和副猪嗜血杆菌多见。本研究证实在广西猪群中存在TTV感染,且存在普遍的TTV与PRRSV、PCV2和CSFV混合感染。  相似文献   

5.
应用PCR技术,结合,临床观察、病理解剖对福建省不同地区断乳多系统衰竭综合征(PMws)发病猪群采集的病料进行多重病原检测与分离。结果表明50份病料中猪圆环病毒2型(PCV2)、猪繁殖与呼吸综合征病毒(PRRSV)、猪瘟病毒(CSFV)、猪伪狂犬病病毒(PRV)阳性率分别为40%、26%、4%、0,不同地区各病原检出率差别不大。病毒性混合感染以PCV2和PRRSV为主,感染率为22%;PCV2与CFSV混合感染率为4%;PRRSV与CFSV混合感染率为4%;PCV2、CFSV、PRRSV三种病原混合感染率为4%。研究结果表明福建大部分地区猪群PMWS的发生是PCV2、PRRSV、CSFV等多种病原混合感染的结果,其主要病原为PCV2,该病的发生没有明显地域性。  相似文献   

6.
猪圆环病毒(PCV)病是近几年新发现的一种猪的传染病,由猪圆环病毒(PCV)引起猪的一种多系统功能障碍性疾病.猪圆环病毒病临床上以断奶仔猪多系统衰竭综合征(PMWS)等为主要特征,该病原体已被确认为猪圆环病毒Ⅱ型(PCV2).研究表明,猪圆环病毒Ⅱ型不仅是断奶仔猪多系统衰竭综合征(PMWS)的病原而且能够引起多种猪病,主要有新生仔猪先天性脑震颤、猪皮炎及肾衰综合征、猪增生性坏死性肺炎等,并常与猪细小病毒(PPV)、猪繁殖与呼吸综合征病毒(PRRSV)等病原合并感染使病情加重和复杂化,也是引起母猪繁殖障碍的病原之一.  相似文献   

7.
付春青 《北方牧业》2005,(10):13-13
<正> 猪断奶后多系统衰弱综合征(PMWS)是一种严重影响养猪生产的疾病综合征,是由圆环病毒2型(PCV2)感染引起的,主要发生于断奶仔猪。同时 PCV2经常和猪繁殖与呼吸综合征病毒(PRRSV)、细小病毒(PPV)混合感染,PMWS 的发生还常常有其他细菌如:副猪嗜血杆菌、衣原体、支原体、胸膜肺炎放线杆菌、多杀性巴氏杆菌以及链球菌等继发感染。除此之外,PMWS  相似文献   

8.
为探明2014年广西猪群主要疫病的感染情况,本研究从发病猪场和屠宰场采集猪组织样品共325份,应用RT-PCR方法检测猪瘟病毒(CSFV)、猪繁殖与呼吸综合征病毒(PRRSV)、猪流行性腹泻病毒(PEDV),并应用PCR方法检测猪圆环病毒2型(PCV2)和猪伪狂犬病病毒(PRV)。结果发现,发病猪场中,这5种病毒感染率分别为12.00%、28.57%、19.43%、53.71%和9.71%,而屠宰场的感染率分别为5.33%、2.67%、5.33%、59.33%和11.33%。对猪群混合感染情况分析发现,PCV2和其他病原的混合感染率最高。其中,发病猪场二重感染最高的为PRRSV+PCV2,达到11.43%,其次为PEDV+PCV2、CSFV+PCV2和PCV2+PRV,阳性率分别为5.71%、4.00%和4.00%;三重感染率最高的为PRRSV+PEDV+PCV2以及PRRSV+PCV2+PRV,阳性率均为2.29%。屠宰场二重感染最高的是PCV2+PRV,达到3.33%;三重感染最高的是CSFV+PCV2+PRV,阳性率为0.67%。结果表明,在发病猪场和屠宰场中,PCV2的感染率最高,且常与其他病原发生混合感染,PRV感染率呈上升趋势,加强对这2种病毒的监控对控制广西地区猪群发病具有重要意义。  相似文献   

9.
断奶仔猪多系统消耗综合症 ( PMWS)是一种新的猪传染病 ,主要侵害 6~ 8周龄仔猪 ,引起淋巴系统疾病、渐进性体重下降、呼吸道症状及黄疸 ,造成患猪免疫机能下降、生产性能降低。1 病原据报道 ,PMWS与感染猪圆环病毒( PCV)有关 ,分为二型 ,分别为 PCV- 1和PCV- 2。PCV- 2是 PMWS的主要病因 ,但不是唯一病因。PMWS很可能是 PCV与猪细小病毒 ( PPV)、猪繁殖与呼吸综合症 (蓝耳病 )病毒 ( PRRSV)等病原混合感染的结果 ,消瘦和呼吸困难是 PMWS的特征。2 流行病学PMWS主要侵害 6~ 8周龄仔猪 ,发病率4%~ 1 0 % ,死亡率 5 0…  相似文献   

10.
本试验采用多重PCR方法,对来检于贵州省清镇市某猪场送检病料进行猪病毒性疫病的病原快速检测,诊断结果表明该例患病猪为猪细小病毒(PPV)、猪圆环病毒2型(PCV2)、猪繁殖与呼吸综合征病毒(PRRSV) 3种病毒的混合感染。  相似文献   

11.
To investigate the epidemiology of multi-pathogens related with post-weaning multi-systemic wasting syndrome (PMWS) in Jiangsu province and surrounding areas,125 healthy samples and 261 diseased samples which obtained in Jiangsu,Anhui and Zhejiang provinces from the January 2014 to May 2015 were screened by PCR for the presence of PCV2,PRRSV,PPV,TTV and P1.These results revealed the following infection rates of PCV2,PRRSV,PPV,TTV1,TTV2 and P1 were 39.38%,21.76%,3.11%,15.80%,16.32% and 10.10%,respectively.In comparison,the co-infection of several viruses occurred in the diseased pigs,and the main co-infections were PCV2+TTV2 (15.32%) and PCV2+PRRSV (11.87%).These observations indicated that the phenomenon of co-infection with multi-pathogens had been widely existing in swine,which increased the difficulty of prevention and controlling of the PMWS.  相似文献   

12.
A comparative serologic and virologic study was performed in pigs from 5 herds with postweaning multisystemic wasting syndrome (PMWS) and 2 herds without PMWS in Quebec. In each herd, 60 blood samples were collected at 4-wk intervals from pigs from 3 to 23 wk of age. The serum was evaluated for the presence of antibodies to porcine circovirus type 2 (PCV2) and porcine reproductive and respiratory syndrome virus (PRRSV), as well as for the presence of nucleic acid of PCV2, PRRSV, and porcine parvovirus (PPV), by means of the polymerase chain reaction (PCR). Serologic profiles for PCV2 were very similar in 6 of the 7 herds, including the 2 without PMWS, and were characterized by a gradual decrease in antibody titres from 3 until 11 wk of age, followed by seroconversion at 15 wk, and high PCV2 antibody titres thereafter in all pigs. Only starting at 11 to 15 wk of age could PCV2 viremia be detected, except in 1 herd, in which clinical signs were observed at 6 to 7 wk of age. A PCV2 viremia could be detected within the same pigs for a minimum of 8 wk, and the virus could still be detected in 41% of the serum samples obtained at 23 wk of age. The antibody level did not appear to influence the occurrence of disease, since titres were similar in pigs in the herds with or without PMWS. Infection with PRRSV, as demonstrated by PCR and seroconversion, preceded that of PCV2 by at least 1 mo in both types of herd. Both PRRSV and PCV2 were detected in some pigs in 5 of the 7 herds, including 1 herd without PMWS. Porcine parvovirus could be detected in serum by PCR in 2 herds with PMWS after the onset of clinical signs and also in 1 herd without PMWS. Genomic analysis of PCV2 strains identified in the herds without PMWS indicated complete or very high homology (99.4% to 100%) with the PCV2 strains identified in 4 herds with PMWS. In our field study, the triggering of PMWS in the herds could not be linked to coinfection with either PRRSV or PPV or to the use of a specific immunostimulant, such as vaccines, or to particular genomic differences between the PCV2 strains identified.  相似文献   

13.
随着规模化养猪业的发展,传染性疾病越来越多,混合感染或多重感染十分普遍,给疾病的诊断和预防带来很大困难。本文将我们实验室2010年分别采自福建、广西、河南、上海、内蒙、浙江、江苏和山西等地发病猪场的185份病料,通过RT-PCR和PCR方法对其进行猪繁殖与呼吸综合征病毒(Porcine reproductive and respiratory syndrome virus,PRRSV)、猪繁殖障碍的猪瘟病毒(Classical swine fever virus,CSFV)、猪圆环病毒2(Porcine circovirus type 2,PCV2)、猪细小病毒(Porcine parvovirus,PPV)、猪伪狂犬病毒(Pseudorabies virus,PRV)、细环病毒2(Torque teno virus 2,TTV2)等病毒检测。结果表明在所检的病料中PRRSV、PCV2和TTV2的阳性率比较高,分别为49.2%、62.2%和95.1%。有些地方TTV2的阳性率高达100%;同时,还存在很普遍的PRRSV与PCV2、PRRSV与TTV2、PCV2与TTV2等混合感染,混合感染率分别为27.6%、45.4%、58.4%;以及PRRSV、PCV2与TTV2的三重感染率为24.9%。同时对部分PRRSV阳性病料的PRRSV GP5和nsp2基因分别进行测序,分析测序结果表明病料中的PRRSV的GP5和nsp2序列与PRRSV HuN4株的相应序列的亲缘关系分别在98.2%和96.2%以上,且在nsp2区域都存在30个不连续氨基酸的缺失,说明现在临床中所流行的PRRSV可能仍是与高致病性PRRSV基因型相似的病毒。通过本文可以及时了解当前养猪场的病毒性疾病的流行情况,为猪场病毒性疾病的防控提供依据。  相似文献   

14.
根据GenBank_h发表的猪圆环病毒2型(Porcinecircovirustype2,PCV2)基因组序列和TTV(Torquetenovirus)1、2型的UTR序列设计合成引物,建立了分别用于检测PCV2和TTV1、TTV2的PCR及巢式PCR方法。应用建立的PCR方法对送检的广东、福建和江西等7个省份258份血液和组织样品进行了PCV2、TTV1和TTV2的检测,确定猪群中PCV2与TTV1和/或TTV2混合感染情况。结果表明,94份样品表现为PCV2和TTV1的混合感染,占样品总数的36.4%;193份样品表现为PCV2和TTV2的混合感染,占74.8%;另外,还有一些样品为三重感染,占34.5%。由此可以看出,猪群中PCV2和/或TTV1和/或TTV2的混合感染很普遍。  相似文献   

15.
为了解我国猪群中猪输血传播病毒(TTV)与猪圆环病毒(PCV)混合感染情况,本研究采用PCR方法对采自14个省280份病料样品进行检测,结果显示,TTV1和TTV2阳性检出率分别为51.8%和28.2%,TTV1与TTV2混合感染率为18.2%;PCV1和PCV2阳性率分别为41.1%和37.5%,PCV1与PCV2混合感染率为19.6%;PCV2阳性样品中TTV1和TTV2混合感染率达75.0%。此外,对2株TTV1基因组进行测序,与GenBank中登录的6个TTV1序列比对,相似性结果为67.3%~95.1%;对4株TTV2基因组测序,与GenBank登录的4条TTV2序列比对,相似性为84.7%~90.4%;将TTV1与TTV2进行序列比对,相似性仅为44.0%。TTV1和TTV2基因高变区分别位于520 nt~2 594 nt和720 nt~2 170 nt;TTV1基因保守区位于1 nt~520 nt和2 595 nt~2 800 nt;而TTV2基因保守区位于1 nt~719 nt和2 171 nt~2 800 nt。以上结果表明,我国猪群中存在TTV与PCV2的混合感染,并且两种病毒混合感染引起...  相似文献   

16.
Currently virus surveillance in swine herds is constrained by the cost-effectiveness and efficiency of sampling methods. The objective of this study was to assess the value of using oral fluids collected by barn personnel as a method of surveillance based on PCR testing. Approximately 12,150 pigs in 10 wean-to-finish barns on 10 farms were monitored for the presence of porcine circovirus type 2 (PCV2), porcine reproductive and respiratory syndrome virus (PRRSV), influenza A virus (IAV), and Torque teno virus genogroups 1 (TTV1) and 2 (TTV2) by sampling oral fluid specimens. Oral fluid samples were collected from 6 pens at each site starting at the time of pig placement (~3 weeks of age) and continuing thereafter at 2-week intervals for a period of 18 weeks. Data were analyzed both on a pen basis and barn basis. Overall, 508 (85%) samples were positive for PCV2, 73 (12%) for PRRSV, 46 (8%) for IAV, 483 (81%) for TTV2, and 155 (26%) for TTV1 during the study period. The estimated arithmetic means of the quantitative PCR-positive oral fluids for PCV2, PRRSV, and IAV were 1×10(4.62), 1×10(4.97), and 1×10(5.49)per ml. With a single exception, all barns were positive for PCV2 and TTV2 at every sampling point in the study. Virus detection varied among barns, particularly for IAV and PRRSV. The pen level, cumulative distribution of agent combinations between all 10 barns were statistically different. The most commonly observed patterns were PCV2+TTV2 (239 pen samples, 40%), PCV2+TTV1+TTV2 (88 pen samples, 15%), and PCV2 alone (66 pen samples, 11%). This "proof-of-concept" project showed that a variety of viruses could be detected either intermittently or continuously in pig populations and demonstrated that barn herd virus status is highly variable, even among barns in the same production system. Oral fluid sampling is a promising approach for increasing the efficiency and cost effectiveness of virus surveillance in swine herds.  相似文献   

17.
This work aimed to detect and study natural co-infection of Circoviridae torque teno virus (TTV) and porcine circovirus 2 (PCV2) in the swine reproductive apparatus. Semen and organs from 17 boars were tested by nested and real-time PCR. PCV2 was amplified from semen (47%), lymph nodes (84.6%) and testicles (35.3%). TTV2 was amplified from 16/17 testis and 13/13 lymph nodes. TTV1 DNA was detected in fewer testicle samples (2/17), which were also TTV2 positive. Analyzed ovaries, follicular fluid and uteri of 83 culled sows showed TTV2, TTV1 and PCV2 from 49.3%, 30.1% and 6.0% of the sows, respectively. Sperm analysis indicated insignificant differences between PCV2 and TTVs positive and negative boars. The most frequent pathologic lesion in sows was endometritis (28.9%), but this was unassociated with PCV2 or TTVs detection. These findings question the importance of PCV2 and TTV2 natural co-infection in the pathology of porcine reproductive failures.  相似文献   

18.
根据GenBank登录的猪伪狂犬病毒(PRV)、猪圆环病毒2型(PCV2)和猪繁殖与呼吸综合征病毒(PRRSV)的参考基因序列,设计3对引物分别用于扩增PCV2的ORF2基因、PRV的gE基因、PRRSV的N基因的目的片段,通过优化反应中各个影响因素,建立了PRV、PCV2、PRRSV的多重PCR(mPCR)检测方法。敏感性和特异性的结果表明,该方法对这3种病毒的最低核酸检出量分别为32.5(PRV)、25.2(PCV2)、35.9pg(PRRSV)。该方法对猪流感病毒(SIV)、猪圆环病毒1型(PCV1)、大肠杆菌、猪瘟病毒(CSFV)、猪流行性腹泻病毒(TGE)等病毒的检测结果均为阴性。200份临床样品的多重PCR结果表明,PCV2感染率为80%(160/200),PRV感染率为21%(42/200),PRRSV的感染率为78%(156/200)。200份临床样品主要为PCV2和PRRSV混合感染,阳性率达56.0%(112/200)。该方法的建立对这3种病毒病的早期快速检测和指导临床实践具有十分重要的意义。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号