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Molecular Detection and Characterization of Borrelia garinii (Spirochaetales: Borreliaceae) in Ixodes nipponensis (Ixodida: Ixodidae) Parasitizing a Dog in Korea

机译:日本寄生虫(Ixodes nipponensisIxodida:Ixodidae)中寄生于狗中的garreii garreii(Spirochaetales:Borreliaceae)的分子检测和表征

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摘要

The present study aimed to detect and characterize spp. in ticks attached to dogs in Korea. Overall, 562 ticks (276 pools) attached to dogs were collected and tested for infection by PCR targeting the 5S-23S rRNA intergenic spacer region (rrf-rrl). One tick larva (pool level, 0.4%; individual level, 0.2%) was confirmed by sequencing , a zoonotic pathogen. For molecular characterization, the outer surface protein A ( ) and genes were analyzed. Phylogenetic analysis distinguished from , which has been recently identified as a novel species. On the other hand, phylogenetic analysis showed that single gene analysis involving rrf-rrl or was not sufficient to differentiate from . In addition, the -infected tick was identified as by sequencing according to mitochondrial 16S rRNA and the second transcribed spacer region. To our knowledge, this is the first study to report the molecular detection of in parasitizing a dog in Korea. Continuous monitoring of tick-borne pathogens in ticks attached to animals is required to avoid disease distribution and possible transmission to humans.
机译:本研究旨在检测和表征spp。在韩国的狗身上s。总体上,收集了与狗连接的562个s(276个池),并通过针对5S-23S rRNA基因间隔区(rrf-rrl)的PCR进行了感染检测。通过对人畜共患病原体的测序确定了一个tick幼虫(池水平为0.4%;个体水平为0.2%)。为了进行分子表征,分析了外表面蛋白A()和基因。系统发育分析不同于,最近已被鉴定为新物种。另一方面,系统发育分析表明,涉及rrf-rrl或的单基因分析不足以区分。另外,如通过根据线粒体16S rRNA和第二转录间隔区的测序来鉴定感染的tick。据我们所知,这是韩国首例报道对寄生犬进行分子检测的研究。需要连续监测附着在动物身上的tick中的tick传播病原体,以避免疾病分布和可能传播给人类。

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