Evaluating food web interactions among microcrustaceans and insect in a tropical shallow lake using DNA-based protocol.

Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis Pub Date : 2021-07-01 Epub Date: 2023-11-28
Andrés R Domingos, Abner Carvalho-Batista, Rafael Robles, Marlene S Arcifa, Fernando L Mantelatto
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Abstract

We developed species-specific primers of five microcrustacean preys, Ceriodaphnia richardi, Diaphanosoma cf. brevireme, Daphnia gessneri, Simocephalus serrulatus, Thermocyclops decipiens and Mesocyclops sp., to analyze food-web interactions involving their two insect predators Rheumatobates crassifemur and Martarega uruguayensis distributed in a tropical shallow lake. We designed internal primers of the COI gene (177-282 bp), and tested them, by means of PCR, for specificity and sensitivity. In our tests for specificity, all primers successfully amplified the DNA target but were species-specific failing to amplify the biomarker from any of the other species tested, even in a mixed DNA sample, including predators' DNA. In tests for sensitivity, primers successfully amplified zooplankton biomarkers from low concentration of DNA extractions and also from digestive tract of predators, even after many hours of ingestion. This technique provides a framework as an efficient tool for evaluation of food-web research in natural aquatic environments, where it is impossible to observe if predation occurs. Furthermore, this technique provides an effective solution for the identification of zooplankton species from the predator's digestive tract, where morphological identification alone is sometimes difficult because predators do not consume the prey but feeds using extra-oral digestion, such is the case of heteropterans.

使用基于DNA的协议评估热带浅水湖中微型鲸目动物和昆虫之间的食物网相互作用。
我们开发了五种微小水豚猎物的物种特异性引物,即Ceriodaphnia richardi、Diaphanosoma cf.brevreme、Daphnia gessneri、Simocephalus serrulatus、Thermocycops decipiens和Mesocyclops sp.,以分析分布在热带浅水湖中的两种昆虫捕食者Rheumatobates crassifemur和Martarega uruguayensis的食物网相互作用。我们设计了COI基因的内部引物(177-282 bp),并通过PCR检测它们的特异性和敏感性。在我们的特异性测试中,所有引物都成功地扩增了DNA靶点,但都是物种特异性的,即使在混合DNA样本中,包括捕食者的DNA中,也无法扩增出其他测试物种的生物标志物。在敏感性测试中,引物成功地从低浓度的DNA提取物和捕食者的消化道中扩增了浮游动物生物标志物,即使在摄入数小时后也是如此。这项技术提供了一个框架,作为评估自然水生环境中食物网研究的有效工具,在那里无法观察是否发生捕食。此外,这项技术为从捕食者的消化道中识别浮游动物物种提供了一个有效的解决方案,在这种情况下,单凭形态学识别有时很困难,因为捕食者不消耗猎物,而是通过口外消化来进食,比如异翼虫。
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