Bowser A Kirsten, Diamond Antony W, Addison Jason A
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada ; Atlantic Laboratory for Avian Research, University of New Brunswick, Fredericton, New Brunswick, Canada.
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada.
PLoS One. 2013 Dec 16;8(12):e83152. doi: 10.1371/journal.pone.0083152. eCollection 2013.
The predator-prey interactions within food chains are used to both characterize and understand ecosystems. Conventional methods of constructing food chains from visual identification of prey in predator diet can suffer from poor taxonomic resolution, misidentification, and bias against small or completely digestible prey. Next-generation sequencing (NGS) technology has become a powerful tool for diet reconstruction through barcoding of DNA in stomach content or fecal samples. Here we use multi-locus (16S and CO1) next-generation sequencing of DNA barcodes on the feces of Atlantic puffin (Fratercula arctica) chicks (n=65) and adults (n=64) and the stomach contents of their main prey, Atlantic herring (Clupea harengus, n=44) to investigate a previously studied food chain. We compared conventional and molecular-derived chick diet, tested the similarity between the diets of puffin adults and chicks, and determined whether herring prey can be detected in puffin diet samples. There was high variability in the coverage of prey groups between 16S and CO1 markers. We identified more unique prey with our 16S compared to CO1 barcoding markers (51 and 39 taxa respectively) with only 12 taxa identified by both genes. We found no significant difference between the 16S-identified diets of puffin adults (n=17) and chicks (n=41). Our molecular method is more taxonomically resolved and detected chick prey at higher frequencies than conventional field observations. Many likely planktonic prey of herring were detected in feces from puffin adults and chicks, highlighting the impact secondary consumption may have on the interpretation of molecular dietary analysis. This study represents the first simultaneous molecular investigation into the diet of multiple components of a food chain and highlights the utility of a multi-locus approach to diet reconstruction that is broadly applicable to food web analysis.
食物链中的捕食者 - 猎物相互作用被用于描述和理解生态系统。通过视觉识别捕食者饮食中的猎物来构建食物链的传统方法可能存在分类分辨率低、误识别以及对小型或完全可消化猎物的偏见等问题。下一代测序(NGS)技术已成为通过对胃内容物或粪便样本中的DNA进行条形码分析来重建饮食的强大工具。在这里,我们对大西洋海鹦(角嘴海雀)幼鸟(n = 65)和成鸟(n = 64)的粪便以及它们主要猎物大西洋鲱鱼(n = 44)的胃内容物进行多基因座(16S和CO1)DNA条形码的下一代测序,以研究一个先前已研究过的食物链。我们比较了传统方法和分子方法得出的幼鸟饮食,测试了海鹦成鸟和幼鸟饮食之间的相似性,并确定在海鹦饮食样本中是否能检测到鲱鱼猎物。16S和CO1标记之间猎物组的覆盖范围存在很大差异。与CO1条形码标记相比,我们用16S鉴定出了更多独特的猎物(分别为51和39个分类单元),两个基因共同鉴定出的只有12个分类单元。我们发现16S鉴定出的海鹦成鸟(n = 17)和幼鸟(n = 41)的饮食之间没有显著差异。我们的分子方法在分类上分辨率更高,并且比传统的野外观察更频繁地检测到幼鸟猎物。在海鹦成鸟和幼鸟的粪便中检测到了许多可能是鲱鱼的浮游猎物,突出了二次消费可能对分子饮食分析解释产生的影响。这项研究代表了对食物链多个组成部分饮食的首次同时分子研究,并强调了多基因座饮食重建方法在食物网分析中广泛适用的实用性。