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

机译:来自临床和环境样品Coxiella Burnetii的分子方法:西班牙基因型的变异性

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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 a multiplex (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 characterization 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 those adaA 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:背景技术Coxiella Burnetii是一种难以培养的高克隆微生物,需要BSL3的传播条件。这导致全球孤立的可用性稀缺。另一方面,已发表的表征方法已经描绘了高达8种不同的基因组和36种基因型。然而,除了表现出有限的歧视性(3基因型)的情况下,所有这些方法,依赖于在10到20个PCR扩增或测序DNA的长片段中,这使其直接应用于临床样品不切实际并导致a稀缺关于C. Burnetii基因型循环数据的可访问性。结果评估西班牙这种生物体的可变性,我们开发了一种新的方法,包括多重(8个靶标)PCR和杂交,所述特定探针繁殖该生物体成8种基因组,最多16种基因型。它允许以单一的运行从临床和环境样品中进行直接表征,这将有助于研究在野生和国内循环中循环的不同基因型以及散发性人类病例和爆发。该方法已用参考隔离验证。在Spain中发现了C. Burnetii的高可变性,在测试的90个样品中,检测10种不同的基因型,是与急性Q发热病例相关的那些adaa阴性,其作为肝脏受累和慢性病例的中间持续时间的发烧。感染人类的​​基因型也被发现在绵羊,山羊,大鼠,野猪和蜱中,并且在我们的临床样本中从未发现过牛的唯一基因型。结论这种新开发的方法允许证明C.Burnetii在西班牙的变化很大。通过这里提出的数据,牛似乎不参与研究的样品中的C. Burnetii的传播,而羊,山羊,野猪,大鼠和蜱虫与人口培养基因型。

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