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首页> 外文期刊>Ticks and tick-borne diseases >Development of three quantitative real-time PCR assays for the detection of Rickettsia raoultii, Rickettsia slovaca, and Rickettsia aeschlimannii and their validation with ticks from the country of Georgia and the Republic of Azerbaijan
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Development of three quantitative real-time PCR assays for the detection of Rickettsia raoultii, Rickettsia slovaca, and Rickettsia aeschlimannii and their validation with ticks from the country of Georgia and the Republic of Azerbaijan

机译:开发了三种实时定量PCR检测试剂盒,用于检测拉里克氏立克次体,斯洛伐克立克次氏菌和埃希氏立克次体,并用乔治亚州和阿塞拜疆共和国的刻度进行验证

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摘要

A previous surveillance study of human pathogens within ticks collected in the country of Georgia showed a relatively high infection rate for Rickettsia raoultii, R. slovaca, and R. aeschlimannii. These 3 spotted fever group rickettsiae are human pathogens: R. raoultii and R. slovaca cause tick-borne lymphadenopathy (TIBOLA), and R. aeschlimannii causes an infection characterized by fever and maculopapular rash. Three quantitative real-time polymerase chain reaction (qPCR) assays, Rraoul, Rslov, and Raesch were developed and optimized to detect R. raoultii, R. slovaca, and R. aeschlimannii, respectively, by targeting fragments of the outer membrane protein B gene (ompB) using species-specific molecular beacon or TaqMan probes. The 3 qPCR assays showed 100% specificity when tested against a rickettsiae DNA panel (n= 20) and a bacteria DNA panel (n= 12). The limit of detection was found to be at least 3 copies per reaction for all assays. Validation of the assays using previously investigated tick nucleic acid preparations, which included Rickettsia-free tick samples, tick samples that contain R. raoultii, R. slovaca, R. aeschlimannii, and other Rickettsia spp., gave 100% sensitivity for all 3 qPCR assays. In addition, a total of 65 tick nucleic acid preparations (representing 259 individual ticks) collected from the country of Georgia and the Republic of Azerbaijan in 2009 was tested using the 3 qPCR assays. R. raoultii, R. slovaca, and R. aeschlimannii were not detected in any ticks (n= 31) from the Republic of Azerbaijan, but in the ticks from the country of Georgia (n= 228) the minimal infection rate for R. raoultii and R. slovaca in Dermacentor marginatus was 10% and 4%, respectively, and for R. aeschlimannii in Haemaphysalis sulcata and Hyalomma spp. it was 1.9% and 20%, respectively.
机译:先前对格鲁吉亚国家tick中人类病原体的监视研究表明,拉氏立克次体,斯洛伐克R.和埃希里曼氏菌的感染率相对较高。这3个发烧点状立克次体是人类病原体:R. raoultii和R. slovaca引起tick传淋巴结病(TIBOLA),而R. aeschlimannii引起以发烧和斑丘疹为特征的感染。研发了三种定量实时聚合酶链反应(qPCR)检测试剂盒Rraoul,Rslov和Raesch,并对其进行了优化,分别通过靶向外膜蛋白B基因的片段来检测R. raoultii,R。slovaca和Aeschlimannii。 (ompB)使用物种特异性分子信标或TaqMan探针。当针对立克次体DNA组(n = 20)和细菌DNA组(n = 12)进行测试时,3 qPCR分析显示出100%的特异性。对于所有测定,发现每个反应的检测限为至少3个拷贝。使用以前研究过的壁虱核酸制剂(包括无立克次体的壁虱样品,包含拉乌尔蒂伊氏菌,斯洛伐克的R. aeschlimannii和其他立克次氏菌的壁虱样品)对所有3种qPCR的灵敏度均为100%分析。此外,使用3种qPCR分析方法对2009年从乔治亚州和阿塞拜疆共和国采集的65种tick核酸制备物(代表259个individual)进行了测试。 R. raoultii,R。slovaca和R. aeschlimannii在阿塞拜疆共和国的任何壁虱(n = 31)中均未检测到,但在格鲁吉亚国家(n = 228)的壁虱中却未检测到。皮氏囊缘中的raoultii和R. slovaca分别为10%和4%,而伊苏氏红血球中的R. aeschlimannii和透明质酸菌分别为10%和4%。分别是1.9%和20%。

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