Department of Entomology, University of Kentucky, Agricultural Science Center, Lexington, Kentucky, USA.
Integr Zool. 2024 Sep;19(5):790-806. doi: 10.1111/1749-4877.12806. Epub 2024 Jan 31.
Metabarcoding-based diet analysis is a valuable tool for understanding the feeding behavior of a wide range of species. However, many studies using these methods for wild animals assume accuracy and precision without experimental evaluation with known positive control food items. Here, we conducted a feeding trial experiment with a positive control community in pasture-raised chickens and assessed the efficacy of several commonly used DNA extraction kits and primer sets. We hand-fed 22 known food items, including insects and plants, to six backyard laying hens and collected their excreta for eight h. We evaluated the efficacy of three DNA extraction kits, three primer sets for plant identification (targeting rbcL, trnL, and internal transcribed spacer 2 [ITS2]), and three primer sets for arthropod identification (targeting cytochrome oxidase subunit I [COI]). The detection success rate of our positive control food items was highly variable, ranging from 2.04% to 93.88% for all kit/primer combinations and averaging 37.35% and 43.57% for the most effective kit/primer combination for plants and insects, respectively. Extraction kits using bead-based homogenization positively affected the recovery proportion of plant and insect DNA in excreta samples. The minimum time to detect known food items was 44 min post-feeding. Two COI primer sets significantly outperformed the third, and both recovery proportion and taxonomic resolution from ITS2 were significantly higher than those from rbcL and trnL. Taken together, these results display the potential variability that can be inherently present in DNA-based diet analyses and highlight the utility of experimental feeding trials in validating such approaches, particularly for omnivores with diverse diets.
基于代谢条码的饮食分析是一种了解广泛物种摄食行为的有价值工具。然而,许多使用这些方法研究野生动物的研究都假设准确性和精密度,而没有使用已知阳性对照食物进行实验评估。在这里,我们在牧场饲养的鸡中进行了阳性对照群落的喂养试验实验,并评估了几种常用 DNA 提取试剂盒和引物对的功效。我们向六只后院产蛋鸡人工投喂 22 种已知食物,包括昆虫和植物,并在 8 小时内收集它们的粪便。我们评估了三种 DNA 提取试剂盒、三种植物鉴定引物对(靶向 rbcL、trnL 和内部转录间隔区 2[ITS2])和三种节肢动物鉴定引物对(靶向细胞色素氧化酶亚基 I[COI])的功效。我们的阳性对照食物的检测成功率差异很大,所有试剂盒/引物组合的检测成功率从 2.04%到 93.88%不等,植物和昆虫最有效的试剂盒/引物组合的平均检测成功率分别为 37.35%和 43.57%。使用基于珠粒的均化的提取试剂盒对植物和昆虫 DNA 在粪便样本中的回收比例有积极影响。检测已知食物的最短时间为喂食后 44 分钟。两个 COI 引物对明显优于第三个,ITS2 的回收比例和分类分辨率明显高于 rbcL 和 trnL。总的来说,这些结果显示了 DNA 饮食分析中可能存在的潜在变异性,并强调了实验喂养试验在验证这些方法,特别是对具有多样化饮食的杂食动物的有用性。