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Molecular method for the characterization of Coxiella burnetii from clinical and environmental samples: variability of genotypes in Spain

机译:从临床和环境样品中表征柯氏柯克斯体的分子方法:西班牙基因型的变异性

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摘要

Background: Coxiella burnetii is a highly clonal microorganism which is difficult to culture, requiring BSL3 conditions for its propagation. This leads to a scarce availability of isolates worldwide. On the other hand, published methods of characterization have delineated up to 8 different genomic groups and 36 genotypes. However, all these methodologies, with the exception of one that exhibited limited discriminatory power (3 genotypes), rely on performing between 10 and 20 PCR amplifications or sequencing long fragments of DNA, which make their direct application to clinical samples impracticable and leads to a scarce accessibility of data on the circulation of C. burnetii genotypes. Results: To assess the variability of this organism in Spain, we have developed a novel method that consists of amultiplex (8 targets) PCR and hybridization with specific probes that reproduce the previous classification of this organism into 8 genomic groups, and up to 16 genotypes. It allows for a direct haracterization from clinical and environmental samples in a single run, which will help in the study of the different genotypes circulating in wild and domestic cycles as well as from sporadic human cases and outbreaks. The method has been validated with reference isolates. A high variability of C. burnetii has been found in Spain among 90 samples tested, detecting 10 different genotypes, being thoseadaA negative associated with acute Q fever cases presenting as fever of intermediate duration with liver involvement and with chronic cases. Genotypes infecting humans are also found in sheep, goats, rats, wild boar and ticks, and the only genotype found in cattle has never been found among our clinical samples. Conclusions: This newly developed methodology has permitted to demonstrate that C. burnetii is highly variable in Spain. With the data presented here, cattle seem not to participate in the transmission of C. burnetii to humans in the samples studied, while sheep, goats, wild boar, rats and ticks share genotypes with the human population.
机译:背景:伯氏柯氏杆菌是一种高度克隆的微生物,难以培养,需要BSL3条件才能繁殖。这导致全球分离株的稀缺性。另一方面,已公开的表征方法描述了多达8个不同的基因组和36个基因型。但是,所有这些方法,除了一种方法显示出有限的区分能力(3个基因型)外,都依赖于执行10到20次PCR扩增或对DNA的长片段进行测序,这使得将其直接应用于临床样品不可行,并导致伯氏梭菌基因型循环数据缺乏可及性。结果:为了评估该生物在西班牙的变异性,我们开发了一种新方法,该方法由多重PCR(8个靶标)组成,并与特定探针杂交,可将该生物先前的分类重现为8个基因组,最多16种基因型。它允许一次性从临床和环境样本中直接抽血,这将有助于研究野生和家养循环中散发的不同基因型以及人间零星病例和暴发。该方法已通过参考菌株验证。西班牙的90个样本中发现了伯氏梭菌的高变异性,检测到10种不同的基因型,即那些与急性Q发热病例呈阴性,伴有肝脏受累中期和慢性病例的发热的adasadaA阴性。在绵羊,山羊,大鼠,野猪和tick中也发现了感染人类的​​基因型,在我们的临床样本中从未发现过在牛中发现的唯一基因型。结论:这种新开发的方法已经证明西班牙伯氏梭菌的变异性很大。根据此处提供的数据,在所研究的样本中,牛似乎不参与伯氏梭菌向人类的传播,而绵羊,山羊,野猪,大鼠和壁虱与人类共有基因型。

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