Borba Renata S, Hoover Shelley E, Currie Robert W, Giovenazzo Pierre, Guarna M Marta, Foster Leonard J, Zayed Amro, Pernal Stephen F
Agriculture & Agri-Food Canada, Beaverlodge Research Farm, Beaverlodge, Alberta, Canada.
Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada.
PLoS One. 2022 Jan 31;17(1):e0263273. doi: 10.1371/journal.pone.0263273. eCollection 2022.
Many pathogens and parasites have evolved to overwhelm and suppress their host's immune system. Nevertheless, the interactive effects of these agents on colony productivity and wintering success have been relatively unexplored, particularly in large-scale phenomic studies. As a defense mechanism, honey bees have evolved remarkable social behaviors to defend against pathogen and parasite challenges, which reduce the impact of disease and improve colony health. To investigate the complex role of pathogens, parasites and social immunity behaviors in relation to colony productivity and outcomes, we extensively studied colonies at several locations across Canada for two years. In 2016 and 2017, colonies founded with 1-year-old queens of diverse genetic origin were evaluated, which represented a generalized subset of the Canadian bee population. During each experimental year (May through April), we collected phenotypic data and sampled colonies for pathogen analysis in a standardized manner. Measures included: colony size and productivity (colony weight, cluster size, honey production, and sealed brood population), social immunity traits (hygienic behavior, instantaneous mite population growth rate, and grooming behavior), as well as quantification of gut parasites (Nosema spp., and Lotmaria passim), viruses (DWV-A, DWV-B, BQCV and SBV) and external parasites (Varroa destructor). Our goal was to examine: 1) correlations between pathogens and colony phenotypes; 2) the dynamics of pathogens and parasites on colony phenotypes and productivity traits; and 3) the effects of social immunity behaviors on colony pathogen load. Our results show that colonies expressing high levels of some social immunity behaviors were associated with low levels of pathogens/parasites, including viruses, Nosema spp., and V. destructor. In addition, we determined that elevated viral and Nosema spp. levels were associated with low levels of colony productivity, and that five out of six pathogenic factors measured were negatively associated with colony size and weight in both fall and spring periods. Finally, this study also provides information about the incidence and abundance of pathogens, colony phenotypes, and further disentangles their inter-correlation, so as to better understand drivers of honey bee colony health and productivity.
许多病原体和寄生虫已经进化到能够压倒并抑制宿主的免疫系统。然而,这些病原体和寄生虫对蜂群生产力和越冬成功率的交互作用相对而言尚未得到充分研究,尤其是在大规模表型组学研究中。作为一种防御机制,蜜蜂进化出了非凡的社会行为来抵御病原体和寄生虫的挑战,从而减少疾病的影响并改善蜂群健康状况。为了研究病原体、寄生虫和社会免疫行为在蜂群生产力及结果方面的复杂作用,我们在加拿大的多个地点对蜂群进行了为期两年的广泛研究。在2016年和2017年,我们评估了由不同遗传来源的1岁蜂王建立的蜂群,这些蜂群代表了加拿大蜜蜂种群的一个广义子集。在每个实验年份(5月至次年4月),我们以标准化方式收集表型数据并对蜂群进行采样以进行病原体分析。测量指标包括:蜂群大小和生产力(蜂群重量、蜂团大小、蜂蜜产量和封盖子脾数量)、社会免疫特征(卫生行为、螨虫瞬时种群增长率和梳理行为),以及肠道寄生虫(微孢子虫属和洛氏蜜蜂微孢子虫)、病毒(DWV - A、DWV - B、BQCV和SBV)和体外寄生虫(狄斯瓦螨)的定量分析。我们的目标是研究:1)病原体与蜂群表型之间的相关性;2)病原体和寄生虫对蜂群表型及生产力特征的动态影响;3)社会免疫行为对蜂群病原体负荷的影响。我们的研究结果表明,表现出高水平某些社会免疫行为的蜂群与低水平的病原体/寄生虫相关,包括病毒、微孢子虫属和狄斯瓦螨。此外,我们确定病毒和微孢子虫属水平升高与蜂群生产力水平低下有关,并且在秋季和春季测量的六个致病因素中有五个与蜂群大小和重量呈负相关。最后,本研究还提供了有关病原体的发病率和丰度、蜂群表型的信息,并进一步理清了它们之间的相互关系,以便更好地了解蜜蜂蜂群健康和生产力的驱动因素。