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用于检测美国西南部的泥沼米诺鱼(Rhinichthys cobitis)和闪光鱼(Meda fulgida)的定量聚合酶链反应检测法

Quantitative PCR Assays for Detecting Loach Minnow (Rhinichthys cobitis) and Spikedace (Meda fulgida) in the Southwestern United States.

作者信息

Dysthe Joseph C, Carim Kellie J, Paroz Yvette M, McKelvey Kevin S, Young Michael K, Schwartz Michael K

机构信息

United States Department of Agriculture, Forest Service, National Genomics Center for Wildlife and Fish Conservation, Rocky Mountain Research Station, Missoula, MT, United States of America.

United States Department of Agriculture, Forest Service, Southwestern Region, Albuquerque, NM, United States of America.

出版信息

PLoS One. 2016 Sep 1;11(9):e0162200. doi: 10.1371/journal.pone.0162200. eCollection 2016.

Abstract

Loach minnow (Rhinichthys cobitis) and spikedace (Meda fulgida) are legally protected with the status of Endangered under the U.S. Endangered Species Act and are endemic to the Gila River basin of Arizona and New Mexico. Efficient and sensitive methods for monitoring these species' distributions are critical for prioritizing conservation efforts. We developed quantitative PCR assays for detecting loach minnow and spikedace DNA in environmental samples. Each assay reliably detected low concentrations of target DNA without detection of non-target species, including other cyprinid fishes with which they co-occur.

摘要

细尾鳅(Rhinichthys cobitis)和尖尾鱼(Meda fulgida)在美国《濒危物种法》下被列为濒危物种,受到法律保护,它们是亚利桑那州和新墨西哥州吉拉河流域的特有物种。监测这些物种分布的高效且灵敏的方法对于确定保护工作的优先级至关重要。我们开发了定量PCR检测方法,用于检测环境样本中的细尾鳅和尖尾鱼DNA。每种检测方法都能可靠地检测到低浓度的目标DNA,且不会检测到非目标物种,包括与它们共生的其他鲤科鱼类。

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Mitochondrial DNA B Resour. 2020 Jun 8;5(3):2368-2370. doi: 10.1080/23802359.2020.1774435.

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