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1.
通过调查我国已有的4种蜱伯氏疏螺旋体的感染情况,以进一步阐明莱姆病在中国的分布与流行状况。本研究通过筛选扩增伯氏疏螺旋体外膜蛋白A(OspA)基因片段的通用引物,获得1对特异性引物,优化反应条件后建立用于检测蜱体内伯氏疏螺旋体的PCR方法,其扩增片段大小为307 bp。该方法可检测出10 pg的阿氏疏螺旋体(Ba)、1 pg的伽氏疏螺旋体(Bg)和0.01 pg的狭义伯氏疏螺旋体(Bb)的3种不同基因型的伯氏疏螺旋体的OspA基因组DNA,表明其敏感性较好,适用于蜱感染伯氏疏螺旋体状况的调查。本研究从我国7个省采集到的667只蜱,进行伯氏疏螺旋体感染的流行病学调查,分类鉴定表明这些蜱分属革蜱属、血蜱属、牛蜱属和扇头蜱属。PCR检测所获数据表明它们的感染率分别为4%(10/264)、6%(11/137)、31.4%(59/185)和31%  相似文献   

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为建立一种TaqMan-MGB探针实时荧光定量PCR方法,来快速、特异地检测伯氏疏螺旋体,根据GenBank发表的伯氏疏螺旋体16SrRNA序列,应用分子生物学软件进行比对,选取保守序列设计特异性引物及TaqMan-MGB探针,并优化荧光定量PCR反应体系及条件,分别对大肠杆菌、沙门氏菌及钩端螺旋体进行扩增;构建伯氏疏螺旋体标准株16SrRNA基因片段阳性质粒,10倍系列稀释后进行real-time PCR扩增,测定该方法的敏感性。结果可见:仅伯氏疏螺旋体出现阳性扩增,而大肠杆菌、沙门氏菌及钩端螺旋体扩增均为阴性;该方法对阳性质粒的检测限约为100 copies/μL。应用该方法对新疆地区的100份蜱DNA样本进行检测,发现7份为伯氏疏螺旋体阳性。结果表明,本研究建立的TaqMan-MGB探针荧光定量PCR方法具有较高的特异性及良好的敏感性,为今后伯氏疏螺旋体的快速诊断及流行病学调查提供了技术支撑。  相似文献   

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为了解新疆北疆地区鼠类伯氏疏螺旋体携带情况及其基因型分布特征,2021年1—9月在新疆昌吉州吉木萨尔县、伊犁哈萨克自治州新源县、塔城地区乌苏市巴音沟,采集147只野生鼠类的肾脏和膀胱组织样本,采用实时荧光定量PCR和巢式PCR方法,检测鼠类中的伯氏疏螺旋体携带情况;以伯氏疏螺旋体5S—23S基因间隔区进行巢式 PCR检测,对检出的阳性样本进行基因测序及序列分析,确定伯氏疏螺旋体基因型,构建系统发育树。结果显示:在147份鼠类样本中,经实时荧光定量PCR和巢式PCR方法检测,分别检出伯氏疏螺旋体阳性样本11份和13份,阳性率分别为7.48%和8.84%;13份巢式PCR阳性样本中,吉木萨尔县检出1份,新源县检出1份,乌苏市检出11份,通过序列同源性分析确定Borreliella garinii、Borreliella bavariensis为主要致病基因型。结果表明,北疆地区鼠类中存在伯氏疏螺旋体的自然感染,有传播给家畜及人群的风险,应加强该病原体检测和莱姆病防控。  相似文献   

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为了解新疆北疆地区硬蜱携带莱姆病病原伯氏疏螺旋体的流行现状,选择莱姆病病原伯氏疏螺旋体5S-23S rRNA基因间隔区设计嵌套式引物,建立了具有较高敏感性和特异性的伯氏疏螺旋体套式PCR检测方法,应用该方法对2018—2019年在新疆北疆6个地区采集的硬蜱进行伯氏疏螺旋体带菌率检测。结果显示:伯氏疏螺旋体总阳性率为15.17%(81/534),其中青河县阳性率最高,达23.64%(26/110)。提示:应进一步加强及重视北疆地区莱姆病的防控工作。  相似文献   

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根据已有的伯氏疏螺旋体鞭毛基因序列,设计两条特异性引物,PCR扩增该基因,并获得基因全长序列,大小为1 008 bp。采用生物信息学技术,对所获得的伯氏疏螺旋体鞭毛基因序列和拟编码的蛋白序列进行分析,发现其编码336个氨基酸,编码蛋白的理论分子量为35.7 ku,等电点为5.53,具有多个抗原表位序列,其中编码主要抗原位点的片段位于中央区段,该中央区段还具有伯氏疏螺旋体种的保守性。伯氏疏螺旋体鞭毛基因中央区段编码蛋白既是主要的抗原位点又具有保守性,理论上可作为莱姆病的诊断抗原。本文为莱姆病的实验室诊断奠定基础。  相似文献   

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为探索蜱及蜱传病的防控新策略,了解病原与媒介硬蜱相互作用的分子机制,本研究以莱姆病病原伯氏疏螺旋体感染后对长角血蜱4个功能基因的转录影响进行了研究。将不同浓度梯度的伯氏疏螺旋体显微注射到长角血蜱体内,分不同的时间段提取蜱的总RNA,反转录成cDNA后,用实时荧光定量PCR检测蜱基因的表达水平。结果显示:伯氏疏螺旋体感染对蜱半胱氨酸蛋白酶抑制剂1(HLcyst-1)、半胱氨酸蛋白酶抑制剂3(HLcyst-3)、卵泡抑素(FRP)、凝血酶抑制剂(Hemalin)4个功能基因的转录均产生了显著影响,但存在时间和剂量相关性,感染后第4天显著诱导了长角血蜱HLcyst-1基因的表达,抑制了Hemalin基因表达。  相似文献   

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为了解牡丹江地区野生鹿自然感染伯氏疏螺旋体的情况,2019年6月间在牡丹江海林市采集20份野生鹿血标本,应用普通PCR对鹿血标本进行5S-23S基因片段的扩增和测序,并将所得序列与GenBank中的项序列进行分析.结果检出7份阳性样本,阳性率为35%,序列分析发现伯氏疏螺旋体在有2个基因型,分别是Borreliella afzelii和Borreliella garinii.研究结果表明,该地区野生鹿存在伯氏疏螺旋体自然感染.  相似文献   

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应用多聚酶链反应单链构象多态性(PCR-SSCP)技术分析了甘肃地区伯氏疏螺旋体和国际标准株B31的鞭毛基因,发现甘肃不同宿主的2株伯氏疏螺旋体的鞭毛基因是一致的,属间一型螺旋体,而与B31株明显不同,证明甘肃地区分离株与B31株在鞭毛基因上不属同一型螺旋体。  相似文献   

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莱姆病是一种经蜱传播的人兽共患病,随着人们经济的发展,伴侣动物的不断出现增加了人与动物经蜱传播莱姆病的风险,而当前并未有治疗莱姆病的有效方法,因此研制莱姆病疫苗成为一大热点。为了更好地预防莱姆病的发生,本研究通过替换新城疫病毒血凝素-神经氨酸酶蛋白(haemagglutinin-neuraminidase protein,HN)胞外域的方式,利用昆虫杆状病毒表达系统分别构建了含伯氏疏螺旋体候选抗原表位外膜蛋白A(outer surface protein A,OspA)、外膜蛋白C(outer surface protein C,OspC)的新城疫病毒样颗粒(virus-like particles,VLPs),形成了含有伯氏疏螺旋体抗原表位的新城疫病毒样颗粒,为之后研制莱姆病疫苗提供了新思路、新想法。  相似文献   

10.
为了解四川省石渠县牦牛体表寄生蜱携带无形体与疏螺旋体的种类和感染情况。采集牦牛体表寄生蜱,经形态学和分子生物学鉴定,确定蜱种类。再采用巢式PCR分别扩增无形体科16S rRNA基因和疏螺旋体属的16S rRNA与flaB基因片段,并对阳性产物进行测序、比对和系统进化树构建,从而确定无形体和疏螺旋体的种类。结果显示,共采集到818只蜱,其中西藏革蜱占78.97%(646/818)、青海血蜱占21.03%(172/818)。所有蜱中有132只检出无形体,阳性率为16.14%;8只检出疏螺旋体,阳性率为0.98%;3只蜱混合感染牛无形体和疏螺旋体。经进一步分析,仅在青海血蜱中检测到牛无形体(Anaplasma bovis)、埃立克体(Ehrlichia)和疏螺旋体(Borrelia),其阳性率分别为6.98%(12/172),2.33%(4/172)和4.65%(8/172);仅在西藏革蜱中检测到绵羊无形体(Anaplasma ovis),其阳性率为17.96%(116/646)。此外,获得的疏螺旋体16S rRNA和flaB基因序列均与分离自日本大刺血蜱中的Borrelia sp.HM菌株亲缘关系最近。结果提示,四川石渠县存在牛无形体、绵羊无形体、埃立克体未定种以及疏螺旋体未定种,存在感染人的风险。  相似文献   

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Shared flagellar epitopes of Borrelia burgdorferi and Borrelia anserina   总被引:2,自引:0,他引:2  
Antigenic cross-reactivity between Borrelia burgdorferi and Borrelia anserina was studied using mouse immune sera and monoclonal antibodies. With immune sera, significant cross-reactivity between B. burgdorferi and B. anserina was demonstrated by indirect immunofluorescent assay. In immunoblots, most of the cross-reactivity was shown to be associated with the periplasmic flagella. Using monoclonal antibodies in immunoblots, it was shown that B. burgdorferi and B. anserina shared at least two flagellar epitopes, one of which was not shared with Borrelia hermsii or Borrelia coriaceae. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of whole cell lysates and the use of a species-specific monoclonal antibody (H5332) which reacts with a major outer surface protein (Osp A) of B. burgdorferi readily differentiated the two species at the molecular level.  相似文献   

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Arthritis caused by Borrelia burgdorferi in dogs   总被引:11,自引:0,他引:11  
From October 1982 to May 1984, we studied 34 dogs from the Lyme, Conn area that had a history of tick exposure and lameness associated with pain, warmth, and/or swelling in one or more joints. Large numbers of polymorphonuclear leukocytes were seen in Giemsa-stained smears of synovial fluid from 9 dogs, and spirochetes (Borrelia burgdorferi) were found in 1 sample by darkfield microscopy and immunoperoxidase techniques. The geometric mean antibody titer to B burgdorferi in the 34 dogs was 1:2,700, compared with 1:285 in 43 clinically normal dogs from the same area (P less than 0.0001) and 1:50 in 29 dogs from an area in New Jersey that is not endemic for human Lyme disease (P less than 0.00001). We concluded that B burgdorferi in dogs may cause arthritis similar to that in human Lyme disease.  相似文献   

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OBJECTIVE: To evaluate the immune response induced by Borrelia theileri infection and to determine whether B theileri induces cross-reacting antibodies to other bovine borreliae. ANIMALS: Two 3-month-old calves, 1 of which was splenectomized. PROCEDURE: Calves were exposed to Boophilus microplus infected with B theileri. Rectal temperature, PCV, bacteremia, and clinical signs of infection were monitored. Serum was obtained weekly and used to evaluate the humoral response to homologous antigen and B burgdorferi and B coriaceae, using an indirect fluorescent antibody (IFA) test, and to B burgdorferi, using a commercially available ELISA. The identity of cross-reacting antigens was explored, using monoclonal antibodies to genus- and species-specific antigens in an IFA test. RESULTS: B theileri-infected calves produced antibodies that cross-reacted with B burgdorferi and B coriaceae whole-cell antigens. Borrelia theileri whole-cell antigen was recognized by genus-specific monoclonal antibody H9724 but not by species-specific antibody H5332. False-positive reactions were not observed when serum from B theileri-infected calves was tested by use of the ELISA for B burgdorferi. CONCLUSIONS: B theileri induces humoral responses in infected cattle that can be confused with those of other borrelial infections. Care must be taken to definitively distinguish between the various borreliae that may cause disease in cattle. CLINICAL RELEVANCE: Serologic cross-reactivity must be taken into account when making a serodiagnosis of Lyme borreliosis or epizootic abortion in epidemiologic studies involving cattle.  相似文献   

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Using an enzyme-linked immunosorbent assay (ELISA) and Western blotting techniques, cats from the north west of England and North Wales were tested for antibodies to Borrelia burgdorferi. Seropositivity to B burgdorferi in these cats was similar (4.8 per cent) to that found in dogs and horses in the UK from non-endemic areas. Cross-reactive antibodies to Leptospira interrogans serovars did not affect the cat B burgdorferi ELISA data. Clinical signs of Lyme disease were generally absent; lameness was rarely reported. As in other species, it must be considered that high levels of serum anti-borrelia antibodies are not diagnostic for clinical Lyme disease.  相似文献   

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