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基于分子的实验室检测在蜱虫鉴定方面比显微镜检测更具准确性。

Molecular-based laboratory testing confer accuracy over microscopical testing for tick identification.

作者信息

Singh Isaac, Lee Min-Kuang, Kon Emily, Chahil Navdeep, Cheung Martin, Hogan Catherine, Morshed Muhammad

机构信息

British Columbia Centre for Disease Control, 655 W 12th Ave, Vancouver, British Columbia, V5Z 4R4, Canada.

University of British Columbia, Vancouver, British Columbia, V6T 1Z4, Canada.

出版信息

Int J Parasitol Parasites Wildl. 2024 Dec 11;26:101031. doi: 10.1016/j.ijppaw.2024.101031. eCollection 2025 Apr.

Abstract

As per published literature, the tick is the primary Lyme disease vector in British Columbia (BC), while the tick species is the dominant vector on the East Coast of Canada, with no . presence seen in BC. However, a recent publication reported presence of in BC which initiated this study to determine the accuracy of the microscopic identification of ticks received in the BC Centre for Disease Control (BCCDC) Public Health Laboratory and compare morphologic methods to molecular methods. Molecular testing uses a real-time PCR assay to amplify the internal transcribed spacer 2 region as a screening method for ; while Sanger sequencing tests the cytochrome c oxidase subunit 1 gene for species confirmation. Of the 209 ticks tested, 74% were , 3.8% were , and 22% were other genus including . Phylogenetic analysis was achieved through Sanger sequencing, confirming the accuracy of the real-time PCR assay. Notably, 6 of 8 tick's hosts had clear travel history outside BC, while the 2 remaining have no confirmed travel. Both the microscopic and molecular identification methods suggest that ticks are dominant in BC and ticks identified as have host travel history outside of BC. This study further underscores the importance of tick surveillance as global human travel and sometimes along with their pets facilitate tick migration.

摘要

根据已发表的文献,蜱是不列颠哥伦比亚省(BC)莱姆病的主要传播媒介,而该蜱种是加拿大东海岸的主要传播媒介,在BC省未发现。然而,最近的一篇出版物报道了BC省存在该蜱种,这引发了本研究,以确定BC省疾病控制中心(BCCDC)公共卫生实验室收到的蜱的显微镜鉴定的准确性,并将形态学方法与分子方法进行比较。分子检测使用实时PCR测定法扩增内部转录间隔区2区域作为该蜱种的筛选方法;而桑格测序检测细胞色素c氧化酶亚基1基因以进行物种确认。在测试的209只蜱中,74%是该蜱种,3.8%是另一种蜱,22%是其他属,包括某属。通过桑格测序进行系统发育分析,证实了实时PCR测定法的准确性。值得注意的是,8只该蜱种的宿主中有6只在BC省以外有明确的旅行史,而其余2只没有确认的旅行史。显微镜和分子鉴定方法均表明该蜱种在BC省占主导地位,被鉴定为该蜱种的蜱的宿主在BC省以外有旅行史。这项研究进一步强调了蜱监测的重要性,因为全球人类旅行,有时还带着他们的宠物,促进了蜱的迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d5b/11720100/b7d244e1ed95/ga1.jpg

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