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与寄生螨类瓦螨、微孢子虫属病原体以及广泛存在的洛特马利亚菌相关的蜜蜂细菌群落变化。

Changes in the Bacteriome of Honey Bees Associated with the Parasite Varroa destructor, and Pathogens Nosema and Lotmaria passim.

作者信息

Hubert Jan, Bicianova Martina, Ledvinka Ondrej, Kamler Martin, Lester Philip J, Nesvorna Marta, Kopecky Jan, Erban Tomas

机构信息

Crop Research Institute, Drnovska 507/73, CZ-161 06, Prague 6-Ruzyne, Czechia.

Institute for Environmental Studies, Faculty of Science, Charles University, Benatska 2, CZ-128 01, Prague 2, Czechia.

出版信息

Microb Ecol. 2017 Apr;73(3):685-698. doi: 10.1007/s00248-016-0869-7. Epub 2016 Oct 11.

Abstract

The honey bee, Apis mellifera, is a globally important species that suffers from a variety of pathogens and parasites. These parasites and pathogens may have sublethal effects on their bee hosts via an array of mechanisms, including through a change in symbiotic bacterial taxa. Our aim was to assess the influence of four globally widespread parasites and pathogens on the honey bee bacteriome. We examined the effects of the ectoparasitic mite Varroa destructor, the fungal pathogens Nosema apis and Nosema ceranae, and the trypanosome Lotmaria passim. Varroa was detected by acaricidal treatment, Nosema and L. passim by PCR, and the bacteriome using MiSeq 16S rRNA gene sequencing. Overall, the 1,858,850 obtained sequences formed 86 operational taxonomic units (OTUs) at 3 % dissimilarity. Location, time of year, and degree of infestation by Varroa had significant effects on the composition of the bacteriome of honey bee workers. Based on statistical correlations, we found varroosis more important factor than N. ceranae, N. apis, and L. passim infestation influencing the honey bee bacteriome and contributing to the changes in the composition of the bacterial community in adult bees. At the population level, Varroa appeared to modify 20 OTUs. In the colonies with high Varroa infestation levels (varroosis), the relative abundance of the bacteria Bartonella apis and Lactobacillus apis decreased. In contrast, an increase in relative abundance was observed for several taxa including Lactobacillus helsingborgensis, Lactobacillus mellis, Commensalibacter intestini, and Snodgrassella alvi. The results showed that the "normal" bacterial community is altered by eukaryotic parasites as well as displaying temporal changes and changes associated with the geographical origin of the beehive.

摘要

西方蜜蜂(Apis mellifera)是一种在全球具有重要意义的物种,它受到多种病原体和寄生虫的困扰。这些寄生虫和病原体可能通过一系列机制对其蜜蜂宿主产生亚致死效应,包括通过共生细菌类群的变化。我们的目的是评估四种全球广泛存在的寄生虫和病原体对蜜蜂细菌群落的影响。我们研究了外寄生螨狄斯瓦螨(Varroa destructor)、真菌病原体蜜蜂微孢子虫(Nosema apis)和东方蜜蜂微孢子虫(Nosema ceranae)以及锥虫类的巴氏蜜蜂马氏管变形虫(Lotmaria passim)的影响。通过杀螨处理检测狄斯瓦螨,通过聚合酶链反应(PCR)检测微孢子虫和巴氏蜜蜂马氏管变形虫,并使用MiSeq 16S rRNA基因测序分析细菌群落。总体而言,获得的1,858,850个序列在3%的差异水平上形成了86个可操作分类单元(OTU)。地点、年份时间以及狄斯瓦螨的侵染程度对蜜蜂工蜂的细菌群落组成有显著影响。基于统计相关性,我们发现蜂螨病比东方蜜蜂微孢子虫、蜜蜂微孢子虫和巴氏蜜蜂马氏管变形虫侵染更重要,它影响蜜蜂细菌群落并导致成年蜜蜂细菌群落组成的变化。在种群水平上,狄斯瓦螨似乎改变了20个OTU。在狄斯瓦螨侵染水平高(蜂螨病)的蜂群中,蜜蜂巴尔通体(Bartonella apis)和蜜蜂乳杆菌(Lactobacillus apis)的相对丰度降低。相反,包括赫尔辛堡乳杆菌(Lactobacillus helsingborgensis)、蜜蜂乳杆菌(Lactobacillus mellis)、肠道共生杆菌(Commensalibacter intestini)和阿尔维氏蜜蜂球菌(Snodgrassella alvi)在内的几个分类群的相对丰度有所增加。结果表明,“正常”细菌群落会受到真核寄生虫的改变,同时也会表现出时间变化以及与蜂巢地理来源相关的变化。

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