Harpel Desiree, Cullen Darron A, Ott Swidbert R, Jiggins Chris D, Walters James R
Department of Ecology and Evolutionary Biology, University of Kansas, Lawrence, KS 66046, USA.
Zoological Institute, KU Leuven, Naamsestraat 59, Box 2465, BE-3000 Leuven, Belgium.
Insect Biochem Mol Biol. 2015 Aug;63:7-13. doi: 10.1016/j.ibmb.2015.04.004. Epub 2015 May 8.
While most adult Lepidoptera use flower nectar as their primary food source, butterflies in the genus Heliconius have evolved the novel ability to acquire amino acids from consuming pollen. Heliconius butterflies collect pollen on their proboscis, moisten the pollen with saliva, and use a combination of mechanical disruption and chemical degradation to release free amino acids that are subsequently re-ingested in the saliva. Little is known about the molecular mechanisms of this complex pollen feeding adaptation. Here we report an initial shotgun proteomic analysis of saliva from Heliconius melpomene. Results from liquid-chromatography tandem mass-spectrometry confidently identified 31 salivary proteins, most of which contained predicted signal peptides, consistent with extracellular secretion. Further bioinformatic annotation of these salivary proteins indicated the presence of four distinct functional classes: proteolysis (10 proteins), carbohydrate hydrolysis (5), immunity (6), and "housekeeping" (4). Additionally, six proteins could not be functionally annotated beyond containing a predicted signal sequence. The presence of several salivary proteases is consistent with previous demonstrations that Heliconius saliva has proteolytic capacity. It is likely that these proteins play a key role in generating free amino acids during pollen digestion. The identification of proteins functioning in carbohydrate hydrolysis is consistent with Heliconius butterflies consuming nectar, like other lepidopterans, as well as pollen. Immune-related proteins in saliva are also expected, given that ingestion of pathogens is a likely route to infection. The few "housekeeping" proteins are likely not true salivary proteins and reflect a modest level of contamination that occurred during saliva collection. Among the unannotated proteins were two sets of paralogs, each seemingly the result of a relatively recent tandem duplication. These results offer a first glimpse into the molecular foundation of Heliconius pollen feeding and provide a substantial advance towards comprehensively understanding this striking evolutionary novelty.
虽然大多数成年鳞翅目昆虫以花蜜作为主要食物来源,但闪蝶属的蝴蝶已经进化出了从食用花粉中获取氨基酸的新能力。闪蝶会用它们的喙收集花粉,用唾液将花粉浸湿,并通过机械破坏和化学降解相结合的方式释放出游离氨基酸,随后这些氨基酸会随着唾液被重新摄入体内。关于这种复杂的花粉摄食适应性的分子机制,我们知之甚少。在此,我们报告了对美凤蝶唾液进行的首次鸟枪法蛋白质组学分析。液相色谱串联质谱分析的结果可靠地鉴定出了31种唾液蛋白,其中大多数都含有预测的信号肽,这与细胞外分泌一致。对这些唾液蛋白的进一步生物信息学注释表明存在四个不同的功能类别:蛋白水解(10种蛋白)、碳水化合物水解(5种)、免疫(6种)和“管家蛋白”(4种)。此外,有6种蛋白除了含有预测的信号序列外,无法进行功能注释。几种唾液蛋白酶的存在与之前关于美凤蝶唾液具有蛋白水解能力的证明一致。这些蛋白可能在花粉消化过程中产生游离氨基酸方面发挥关键作用。鉴定出具有碳水化合物水解功能的蛋白,与美凤蝶像其他鳞翅目昆虫一样食用花蜜以及花粉的情况相符。鉴于摄入病原体是感染的一个可能途径,唾液中存在免疫相关蛋白也在预料之中。少数“管家蛋白”可能并非真正的唾液蛋白,而是反映了在唾液收集过程中发生的适度污染。在未注释的蛋白中有两组旁系同源物,每组似乎都是相对较新的串联重复的结果。这些结果初步揭示了美凤蝶花粉摄食的分子基础,并朝着全面理解这一显著的进化新特性迈出了重要一步。