4.5 Article

Amplicon Sequencing of Variable 16S rRNA from Bacteria and ITS2 Regions from Fungi and Plants, Reveals Honeybee Susceptibility to Diseases Results from Their Forage Availability under Anthropogenic Landscapes

期刊

PATHOGENS
卷 10, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/pathogens10030381

关键词

Apis mellifera; 16S rRNA; ITR2; NGS; Nosema apis; Nosema ceranae; Nosema bombi; Acarapis woodi; Trypanosomatida; Crithidia spp; neogregarines; Apicystis spp; antropocene; insectageddon; urban area; urban environment; bee biology

资金

  1. Polish National Agency for Academic Exchange under the Foreign Promotion Programme (NAWA) [UMCS PPI/PZA/2019/1/00039]
  2. NCN [418332]
  3. EMBO Installation Grants 2017
  4. BBSRC [BB/L023164/1]
  5. EU: SYNTHESYS project [GB-TAF7137]
  6. [POIR. 04.04.00-00-3E9C/17-00]
  7. BBSRC [BB/L023164/1] Funding Source: UKRI

向作者/读者索取更多资源

The microbiome study provides complex information on the health status of bees and reveals a close relationship between bee diet and pathogen infection. The composition of microbial communities and pathogen infections in bees are influenced by factors such as environmental changes and plant availability.
European Apis mellifera and Asian Apis cerana honeybees are essential crop pollinators. Microbiome studies can provide complex information on health and fitness of these insects in relation to environmental changes, and plant availability. Amplicon sequencing of variable regions of the 16S rRNA from bacteria and the internally transcribed spacer (ITS) regions from fungi and plants allow identification of the metabiome. These methods provide a tool for monitoring otherwise uncultured microbes isolated from the gut of the honeybees. They also help monitor the composition of the gut fungi and, intriguingly, pollen collected by the insect. Here, we present data from amplicon sequencing of the 16S rRNA from bacteria and ITS2 regions from fungi and plants derived from honeybees collected at various time points from anthropogenic landscapes such as urban areas in Poland, UK, Spain, Greece, and Thailand. We have analysed microbial content of honeybee intestine as well as fungi and pollens. Furthermore, isolated DNA was used as the template for screening pathogens: Nosema apis, N. ceranae, N. bombi, tracheal mite (Acarapis woodi), any organism in the parasitic order Trypanosomatida, including Crithidia spp. (i.e., Crithidia mellificae), neogregarines including Mattesia and Apicystis spp. (i.e., Apicistis bombi). We conclude that differences between samples were mainly influenced by the bacteria, plant pollen and fungi, respectively. Moreover, honeybees feeding on a sugar based diet were more prone to fungal pathogens (Nosema ceranae) and neogregarines. In most samples Nosema sp. and neogregarines parasitized the host bee at the same time. A higher load of fungi, and bacteria groups such as Firmicutes (Lactobacillus); gamma-proteobacteria, Neisseriaceae, and other unidentified bacteria was observed for Nosema ceranae and neogregarine infected honeybees. Healthy honeybees had a higher load of plant pollen, and bacteria groups such as: Orbales, Gilliamella, Snodgrassella, and Enterobacteriaceae. Finally, the period when honeybees switch to the winter generation (longer-lived forager honeybees) is the most sensitive to diet perturbations, and hence pathogen attack, for the whole beekeeping season. It is possible that evolutionary adaptation of bees fails to benefit them in the modern anthropomorphised environment.

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