Gomes Sofia I F, Kielak Anna M, Hannula S Emilia, Heinen Robin, Jongen Renske, Keesmaat Ivor, De Long Jonathan R, Bezemer T Martijn
Department of Terrestrial Ecology, The Netherlands Institute of Ecology (NIOO-KNAW), Droevendaalsesteeg 10, 6708 PB, Wageningen, The Netherlands.
Present Address: Lehrstuhl für Terrestrische Ökologie, Wissenschaftszentrum Weihenstephan für Ernährung, Landnutzung und Umwelt, Technische Universität München, Hans-Carl-von-Carlowitz-Platz 2, 85354, Freising, Germany.
Anim Microbiome. 2020 Oct 7;2(1):37. doi: 10.1186/s42523-020-00055-3.
Insect-associated microorganisms can provide a wide range of benefits to their host, but insect dependency on these microbes varies greatly. The origin and functionality of insect microbiomes is not well understood. Many caterpillars can harbor symbionts in their gut that impact host metabolism, nutrient uptake and pathogen protection. Despite our lack of knowledge on the ecological factors driving microbiome assemblages of wild caterpillars, they seem to be highly variable and influenced by diet and environment. Several recent studies have shown that shoot-feeding caterpillars acquire part of their microbiome from the soil. Here, we examine microbiomes of a monophagous caterpillar (Tyria jacobaeae) collected from their natural host plant (Jacobaea vulgaris) growing in three different environments: coastal dunes, natural inland grasslands and riverine grasslands, and compare the bacterial communities of the wild caterpillars to those of soil samples collected from underneath each of the host plants from which the caterpillars were collected.
The microbiomes of the caterpillars were dominated by Proteobacteria, Actinobacteria, Firmicutes and Bacteroidetes. Only 5% of the total bacterial diversity represented 86.2% of the total caterpillar's microbiome. Interestingly, we found a high consistency of dominant bacteria within the family Burkholderiaceae in all caterpillar samples across the three habitats. There was one amplicon sequence variant belonging to the genus Ralstonia that represented on average 53% of total community composition across all caterpillars. On average, one quarter of the caterpillar microbiome was shared with the soil.
We found that the monophagous caterpillars collected from fields located more than 100 km apart were all dominated by a single Ralstonia. The remainder of the bacterial communities that were present resembled the local microbial communities in the soil in which the host plant was growing. Our findings provide an example of a caterpillar that has just a few key associated bacteria, but that also contains a community of low abundant bacteria characteristic of soil communities.
与昆虫相关的微生物能为其宿主带来广泛益处,但昆虫对这些微生物的依赖程度差异很大。昆虫微生物组的起源和功能尚未得到充分了解。许多毛虫的肠道中可携带共生体,这些共生体影响宿主代谢、养分吸收和病原体防护。尽管我们对驱动野生毛虫微生物组组装的生态因素缺乏了解,但它们似乎高度可变,并受饮食和环境影响。最近的几项研究表明,以嫩枝为食的毛虫从土壤中获取部分微生物组。在此,我们研究了从生长在三种不同环境(沿海沙丘、天然内陆草原和河滨草原)的天然宿主植物(普通千里光)上采集的单食性毛虫(黄褐天幕毛虫)的微生物组,并将野生毛虫的细菌群落与从采集毛虫的每种宿主植物下方采集的土壤样本的细菌群落进行比较。
毛虫的微生物组以变形菌门、放线菌门、厚壁菌门和拟杆菌门为主。仅5%的总细菌多样性占毛虫微生物组总量的86.2%。有趣的是,我们发现三个栖息地所有毛虫样本中伯克霍尔德菌科内优势细菌具有高度一致性。有一个属于劳尔氏菌属的扩增子序列变体,平均占所有毛虫群落组成的53%。平均而言,毛虫微生物组的四分之一与土壤共有。
我们发现,从相距100多公里的田野采集的单食性毛虫均由单一的劳尔氏菌主导。其余存在的细菌群落类似于宿主植物生长土壤中的当地微生物群落。我们的研究结果提供了一个例子,即一种毛虫只有少数几种关键的相关细菌,但也包含一个具有土壤群落特征的低丰度细菌群落。