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使用多标记分析法提高华支睾吸虫环境DNA检测灵敏度

Improved environmental DNA detection sensitivity of Opisthorchis viverrini using a multi-marker assay.

作者信息

Matsuo Riko, Togetani Ayana, Adisakwattana Poom, Yoonuan Tippayarat, Phuphisut Orawan, Limpanont Yanin, Sakata Masayuki K, Sato Marcello Otake, Sato Megumi, Minamoto Toshifumi

机构信息

Graduate School of Human Development and Environment, Kobe University, 3-11, Tsurukabuto, Nada-ku, Kobe, Hyogo, 657-8501, Japan.

Faculty of Global Human Sciences, Kobe University, Kobe, Japan.

出版信息

Parasitol Res. 2024 Dec 26;123(12):419. doi: 10.1007/s00436-024-08423-7.

Abstract

Opisthorchiasis, caused by the liver fluke Opisthorchis viverrini, is endemic to Southeast Asian countries and constitutes a major health problem as it increases the risk of cholangiocarcinoma. However, owing to the complicated life cycle of O. viverrini, there is no rapid method for monitoring the risk of infection in the environment. The inability to identify water sources at risk of infection presents a challenge in implementing preventive measures in areas where fish are a significant component of the local diet. Using the environmental DNA (eDNA) approach to detect parasitic DNA in water samples, it is possible to understand the distribution of O. viverrini and the dynamics of infection with high accuracy. However, the sensitivity of environmental samples remains a bottleneck. In this study, we developed a highly sensitive method for detecting O. viverrini eDNA by designing a multi-marker assay targeting two mitochondrial and two nuclear genes. We compared its performance with single-marker assays using tissue-derived DNA. The multi-marker assay exhibited the highest detection sensitivity. We also collected data from 56 sites in Sakon Nakhon, Thailand, in October 2022, and tested them for eDNA detection of O. viverrini. Eleven sites were positive in the multi-marker assay, whereas five sites were positive in the single-marker assay. This multi-marker assay can be used in the field to detect small organisms and rare species, other than parasites, that are expected to have low levels of eDNA.

摘要

由肝吸虫华支睾吸虫引起的华支睾吸虫病在东南亚国家流行,由于它会增加胆管癌风险,因此构成了一个重大的健康问题。然而,由于华支睾吸虫复杂的生命周期,目前尚无快速监测环境中感染风险的方法。在鱼类是当地饮食重要组成部分的地区,无法识别有感染风险的水源给实施预防措施带来了挑战。利用环境DNA(eDNA)方法检测水样中的寄生虫DNA,能够高精度地了解华支睾吸虫的分布和感染动态。然而,环境样本的灵敏度仍然是一个瓶颈。在本研究中,我们通过设计针对两个线粒体基因和两个核基因的多标记检测方法,开发了一种高度灵敏的检测华支睾吸虫eDNA的方法。我们将其性能与使用组织来源DNA的单标记检测方法进行了比较。多标记检测方法表现出最高的检测灵敏度。我们还于2022年10月从泰国呵叻府的56个地点收集了数据,并对其进行华支睾吸虫eDNA检测。多标记检测方法中有11个地点呈阳性,而单标记检测方法中有5个地点呈阳性。这种多标记检测方法可用于野外检测除寄生虫外预计eDNA水平较低的小型生物和稀有物种。

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