vanEngelsdorp Dennis, Traynor Kirsten S, Andree Michael, Lichtenberg Elinor M, Chen Yanping, Saegerman Claude, Cox-Foster Diana L
Department of Entomology, Plant Science Building University of Maryland, College Park, Maryland, United States of America.
Cooperative Extension Butte County, University of California Cooperative Extension, Oroville, California, United States of America.
PLoS One. 2017 Jul 17;12(7):e0179535. doi: 10.1371/journal.pone.0179535. eCollection 2017.
Honey bee (Apis mellifera) colonies continue to experience high annual losses that remain poorly explained. Numerous interacting factors have been linked to colony declines. Understanding the pathways linking pathophysiology with symptoms is an important step in understanding the mechanisms of disease. In this study we examined the specific pathologies associated with honey bees collected from colonies suffering from Colony Collapse Disorder (CCD) and compared these with bees collected from apparently healthy colonies. We identified a set of pathological physical characteristics that occurred at different rates in CCD diagnosed colonies prior to their collapse: rectum distension, Malpighian tubule iridescence, fecal matter consistency, rectal enteroliths (hard concretions), and venom sac color. The multiple differences in rectum symptomology in bees from CCD apiaries and colonies suggest effected bees had trouble regulating water. To ensure that pathologies we found associated with CCD were indeed pathologies and not due to normal changes in physical appearances that occur as an adult bee ages (CCD colonies are assumed to be composed mostly of young bees), we documented the changes in bees of different ages taken from healthy colonies. We found that young bees had much greater incidences of white nodules than older cohorts. Prevalent in newly-emerged bees, these white nodules or cellular encapsulations indicate an active immune response. Comparing the two sets of characteristics, we determined a subset of pathologies that reliably predict CCD status rather than bee age (fecal matter consistency, rectal distension size, rectal enteroliths and Malpighian tubule iridescence) and that may serve as biomarkers for colony health. In addition, these pathologies suggest that CCD bees are experiencing disrupted excretory physiology. Our identification of these symptoms is an important first step in understanding the physiological pathways that underlie CCD and factors impacting bee health.
蜜蜂(西方蜜蜂)蜂群每年仍持续遭受高损失率,原因仍不清楚。众多相互作用的因素与蜂群数量减少有关。了解病理生理学与症状之间的联系途径是理解疾病机制的重要一步。在本研究中,我们检查了从患有蜂群崩溃失调(CCD)的蜂群中采集的蜜蜂所具有的特定病理特征,并将其与从看似健康的蜂群中采集的蜜蜂进行比较。我们确定了一组病理生理特征,这些特征在被诊断患有CCD的蜂群崩溃前以不同的发生率出现:直肠扩张、马氏管虹彩、粪便稠度、直肠肠结石(硬结块)和毒囊颜色。来自CCD养蜂场和蜂群的蜜蜂在直肠症状方面的多种差异表明,受影响的蜜蜂在调节水分方面存在问题。为确保我们发现的与CCD相关的病理特征确实是病理特征,而非成年蜜蜂衰老过程中身体外观的正常变化(假设CCD蜂群主要由年轻蜜蜂组成),我们记录了从健康蜂群中采集的不同年龄蜜蜂的变化情况。我们发现,幼蜂出现白色结节的发生率比年长的蜂群高得多。这些白色结节或细胞包裹体在新羽化的蜜蜂中很常见,表明存在活跃的免疫反应。通过比较这两组特征,我们确定了一组病理特征子集,这些特征能够可靠地预测CCD状态而非蜜蜂年龄(粪便稠度、直肠扩张大小、直肠肠结石和马氏管虹彩),并且可能作为蜂群健康的生物标志物。此外,这些病理特征表明,患有CCD的蜜蜂正经历排泄生理紊乱。我们对这些症状的识别是理解CCD背后的生理途径以及影响蜜蜂健康的因素的重要第一步。