雅库特地区硬蜱及其病原体的鉴定与分子分析

A. Barashkova, A. Reshetnikov, E. Popov
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引用次数: 0

摘要

本研究的目的是鉴定雅库特中部左岸地区的伊索迪德蜱及其病原体。材料和方法。这项工作于2019-2020年在雅库特中部左岸地区进行。2019年采集了9只蜱虫,2020年采集了27只。我们研究了森林灌木站、草原站、草地站、近水站和定居点站。为了确定该地区体外寄生虫的区系和生态特征,我们使用了标准的收集方法。蜱种由N.A.Filippova使用形态学键确定;通过PCR方法确认了测定的正确性。采用聚合酶链式反应分析法对采集的蜱虫进行了巴贝斯虫病和蜱传病毒性脑炎病原体的研究。结果和讨论。全沟硬蜱是硬蜱的一种,栖息在雅库特中部左岸地区。雅库特地区未发现康氏血蜱。2008年,在其中心地带的雅库特,首次出现了家养驯鹿血液原生动物疾病的自然焦点。最近,人们观察到全溃疡伊蚊的数量有所增加。蜱虫活动记录在5月的第二个十年到8月的第二十年。地松鼠Parriii嗜精细胞是胚胎前期的主要宿主。用聚合酶链式反应分析法检测蜱虫感染巴贝斯虫病和蜱传病毒性脑炎的病原体时,没有检测到病原体。
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Identification and molecular analysis of ixodid ticks (Acari: Ixodidae) and their pathogens in Yakutia
The purpose of the research is to identify ixodid ticks and their pathogens in the left bank area of Central Yakutia. Materials and methods. The work was carried out in 2019–2020 in the left bank area of Central Yakutia. Nine ticks were collected in 2019, and 27 ticks in 2020. We studied forest shrub stations, steppe stations, meadow field stations, near-water stations and stations of settlements. To determine faunal and ecological characteristics of ectoparasites in the territory, we used standard collection methods. The tick species was determined using morphological keys by N. A. Filippova; the determination correctness was confirmed by the PCR method. The collected ticks were studied for causative agents of babesiosis and tick-borne viral encephalitis using PCR analysis. Results and discussion. One species of ixodid ticks, Ixodes persulcatus, inhabits the left bank area of Central Yakutia. Haemaphysalis concinna was not found in Yakutia. In 2008, a natural focus of blood protozoan disease of domestic reindeer appeared for the first time in Yakutia in its central zone. Recently, an increase in the number of I. persulcatus has been observed. Tick activity is recorded from the second decade of May to the second decade of August. The ground-squirrel Spermophilus parryii is the main host for the preimaginal stages. Pathogens were not detected when ticks were examined for causative agents of babesiosis and tick-borne viral encephalitis using PCR analysisd.
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