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实时宿主-寄生虫协同进化:蜜蜂抗性机制与螨类繁殖策略的变化

Host-Parasite Co-Evolution in Real-Time: Changes in Honey Bee Resistance Mechanisms and Mite Reproductive Strategies.

作者信息

Moro Arrigo, Blacquière Tjeerd, Panziera Delphine, Dietemann Vincent, Neumann Peter

机构信息

Institute of Bee Health, Vetsuisse Faculty, University of Bern, CH-3097 Bern, Switzerland.

Agroscope, Swiss Bee Research Center, CH-3003 Bern, Switzerland.

出版信息

Insects. 2021 Jan 29;12(2):120. doi: 10.3390/insects12020120.

Abstract

Co-evolution is a major driving force shaping the outcome of host-parasite interactions over time. After host shifts, the lack of co-evolution can have a drastic impact on novel host populations. Nevertheless, it is known that Western honey bee () populations can cope with host-shifted ectoparasitic mites () by means of natural selection. However, adaptive phenotypic traits of the parasites and temporal variations in host resistance behavior are poorly understood. Here, we show that mites made adaptive shifts in reproductive strategy when associated with resistant hosts and that host resistance traits can change over time. In a fully-crossed field experiment, worker brood cells of local adapted and non-adapted (control) host colonies were infested with mites originating from both types of host colonies. Then, mite reproduction as well as recapping of cells and removal of infested brood (i.e., Varroa Sensitive Hygiene, VSH) by host workers were investigated and compared to data from the same groups of host colonies three years earlier. The data suggest adaptive shifts in mite reproductive strategies, because mites from adapted hosts have higher probabilities of reproduction, but lower fecundity, when infesting their associated hosts than mites in treated colonies. The results confirm that adapted hosts can reduce mite reproductive success. However, neither recapping of cells nor VSH were significantly expressed, even though the latter was significantly expressed in this adapted population three years earlier. This suggests temporal variation in the expression of adaptive host traits. It also appears as if mechanisms not investigated here were responsible for the reduced mite reproduction in the adapted hosts. In conclusion, a holistic view including mite adaptations and studies of the same parasite/host populations over time appears overdue to finally understand the mechanisms enabling survival of -infested honey bee host colonies.

摘要

协同进化是随着时间推移塑造宿主 - 寄生虫相互作用结果的主要驱动力。宿主转移后,缺乏协同进化会对新宿主种群产生巨大影响。然而,已知西方蜜蜂(Apis mellifera)种群能够通过自然选择应对宿主转移的体外寄生螨(Varroa destructor)。然而,寄生虫的适应性表型特征以及宿主抗性行为的时间变化却知之甚少。在这里,我们表明,当与抗性宿主相关联时,螨在繁殖策略上发生了适应性转变,并且宿主抗性特征会随时间变化。在一项完全交叉的田间实验中,将来自本地适应型和非适应型(对照)宿主蜂群的工蜂幼虫巢房用源自这两种类型宿主蜂群的螨进行侵染。然后,研究了螨的繁殖以及宿主工蜂对巢房的重新覆盖和受侵染幼虫的清除(即瓦螨敏感卫生行为,VSH),并与三年前同一组宿主蜂群的数据进行比较。数据表明螨的繁殖策略发生了适应性转变,因为来自适应型宿主的螨在侵染其相关宿主时比处理过的蜂群中的螨具有更高的繁殖概率,但繁殖力较低。结果证实适应型宿主可以降低螨的繁殖成功率。然而,巢房重新覆盖和VSH均未显著表现出来,尽管三年前在这个适应型种群中VSH显著表现。这表明适应性宿主特征的表达存在时间变化。似乎也是这里未研究的机制导致了适应型宿主中螨繁殖的减少。总之,为了最终理解使感染瓦螨的蜜蜂宿主蜂群得以存活的机制,早就应该采用包括螨的适应性以及对同一寄生虫/宿主种群随时间进行研究的整体观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59c1/7911685/f8987fa4fa2f/insects-12-00120-g001.jpg

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