蜜蜂抗狄斯瓦螨机制的研究进展

狄斯瓦螨Varroa destructor已蔓延至世界各地,给养蜂生产带来巨大挑战,被认为是世界养蜂业的主要威胁。因此,抗螨机制的研究和抗螨蜂种的培育显得尤为重要,而掌握蜜蜂的抗螨机制则是成功培育抗螨蜂种的前提条件。本文从行为、生理及分子机制等多个不同角度对国内外蜜蜂抗狄斯瓦螨机制研究的最新进展进行了详细的阐述。尤其是从分子水平研究蜜蜂的抗螨机制对选育抗螨蜂种具有重要意义,将为利用分子遗传辅助标记筛选方法和先进的生物工程技术并结合传统的育种手段成功培育出具有抗螨性能的优良蜜蜂品系奠定基础。     

蜜蜂寄生螨—狄斯瓦螨的研究进展

狄斯瓦螨Varroa destructor是对世界养蜂业危害最大的蜜蜂寄生虫,严重危害蜜蜂封盖幼虫、蛹和成蜂,并携带和传播蜜蜂病毒,造成蜂群生产力严重下降乃至全群毁灭。狄斯瓦螨的有效防治措施的研发有赖于对其研究进展的了解,本文综述了以下3方面的研究概况:1)狄斯瓦螨的繁殖特性;2)对蜜蜂的危害;3)主要防治方法。以期为蜂螨相关的研究和应用奠定基础。     

狄斯瓦螨和蜜蜂病毒对意大利蜜蜂蜂群越冬的影响

越冬期是蜂群损失最主要的阶段.通过比较分析45个意大利蜜蜂Apis mellifera ligustica蜂群在繁殖越冬蜂前的狄斯瓦螨Varroa destructor寄生率和病毒感染情况、越冬表现及越冬期存活蜂群的病毒感染情况等,探究与越冬期蜜蜂健康紧密相关的影响因素.结果表明,繁殖越冬蜂前蜂群的狄斯瓦螨寄生率与蜜蜂残翅病毒(DWV)和以色列急性麻痹病毒(IAPV)基因组拷贝数呈中等线性相关关系(pDWV=0.003,pIAPV=0.001),且狄斯瓦螨寄生率低于9％的蜂群与DWV感染程度相关性更高,而寄生率高于9％的蜂群与IAPV的相关性更高.越冬期死亡蜂群在繁殖越冬蜂前的狄斯瓦螨寄生率和IAPV病毒基因组拷贝数均显著高于存活蜂群.狄斯瓦螨和IAPV是本次实验中意蜂蜂群越冬期健康的首要影响因素.结合狄斯瓦螨寄生率和IAPV基因组拷贝数的正相关性,本研究认为在繁殖越冬蜂前将蜂螨寄生率控制在较低水平(9％以下)能有效减少越冬期意蜂蜂群损失.     

蜜蜂幼虫血淋巴游离氨基酸和微量元素含量的差异对其抗螨特性的影响

重新界定的外寄生螨类---狄斯瓦螨Varroa destructor(Anderson and Trueman),严重危害全世界的西方蜜蜂Apis mellifera。但是对其原始寄主东方蜜蜂Apis cerana不构成可见的危害。在西方蜜蜂群中,狄斯瓦螨在雄蜂房和工蜂房都能进行繁殖。在其亚洲的原始寄主东方蜜蜂群中,它们可以寄生于雄蜂和工蜂,但在工蜂房中不育。蜜蜂的血淋巴是狄斯瓦螨生存和繁殖需要摄取的惟一食物来源,推测血淋巴中的某种物质含量会影响狄斯瓦螨的繁殖。对中华蜜蜂Apis ceranaFabricius和意大利蜜蜂ApismelliferaL.工蜂和雄蜂封盖幼虫血淋巴中游离氨基酸和与营养有关的微量元素含量进行了比较,发现其存在明显差异,并推测这些差异与东方蜜蜂抗螨能力强有关。     

狄斯瓦螨和蜜蜂残翅病毒对蜜蜂健康的协同影响

世界各地大范围的西方蜜蜂Apis mellifera蜂群损失现象已引起科学界和公众的持续关注。狄斯瓦螨Varroa destructor和蜜蜂残翅病毒(Deformed wing virus,DWV)是西方蜜蜂群中最主要的两大生物威胁。尽管二者侵害蜜蜂均已有较长历史,但直至近十年来的研究才发现两者间的协同效应对蜂群健康的影响远超过其单独作用时所造成的危害:(1)蜜蜂残翅病毒可在狄斯瓦螨体内大量复制,继而进一步传播;(2)狄斯瓦螨的刺吸行为使病毒粒子跨越寄主的生理屏障而直接进入蜜蜂血淋巴;(3)狄斯瓦螨的寄生促使蜜蜂残翅病毒的高毒力毒株在蜂群中优势扩增和盛行;(4)狄斯瓦螨影响蜜蜂个体发育与免疫系统等生理机能,以致降低了蜂群对病毒的抵抗力;(5)蜜蜂残翅病毒对宿主造成的免疫抑制有利于狄斯瓦螨的寄生与繁殖。狄斯瓦螨、蜜蜂残翅病毒和西方蜜蜂间的关系已经成为昆虫外寄生物、病原体与寄主相互作用研究的一个典型模型。本文对近十年该领域的相关研究进行综述,以期为蜂群损失的原因调查以及昆虫寄生虫、病原微生物与寄主间关系的研究提供参考和借鉴。     

外寄生诱导的寄主蜜蜂免疫和病理学反应

了解外寄生物一病原体一寄主三者之间的关系,不仅有重要的理论意义也有广阔的应用前景。狄斯瓦螨（Varroa）是蜜蜂的外寄生螨,可以导致蜜蜂后代的大量死亡,同时也可以携带和诱导很多病毒的发生。蜜蜂蛹感染狄斯瓦螨后,残翅病毒（deformed wings virus,DWV）的扩增水平明显增加,     

狄斯瓦螨与蜜蜂的寄生关系

蜜蜂Apis spp.是重要的经济昆虫,也是研究最为深入和广泛的社会性昆虫。狄斯瓦螨Varroa destructor是蜜蜂的体外寄生虫,是对西方蜜蜂Apis mellifera蜂群健康危害最为严重的生物因子。近十多年来,由于全球蜂群损失现象严重,而同时以蜜蜂为代表的授粉昆虫的健康直接关系到农业生产和生态安全,关于狄斯瓦螨与蜜蜂的寄生关系的研究受到极大关注。作为社会性昆虫的一种体外寄生虫,狄斯瓦螨不仅需要适应蜜蜂个体的生长发育,借助蜜蜂化蛹期间的封盖期完成繁殖,同时还要能够逃避蜜蜂社会性行为的清理。本文从狄斯瓦螨的生物学特性以及其与寄主间的互作关系等方面进行论述,以期进一步理解寄生虫-无脊椎动物寄主(特别是社会性昆虫寄主)的相互作用,为寄生虫病学研究提供借鉴。     

信息素介导的西方蜜蜂与狄斯瓦螨互作研究进展

狄斯瓦螨是一种严重危害西方蜜蜂的体外寄生螨,是世界养蜂业的最大威胁.人们广泛采用化学方法防治狄斯瓦螨,但易引起狄斯瓦螨的抗药性、蜜蜂中毒和蜂产品药物残留等问题.为此,人们尝试了多种蜂螨绿色防控技术.其中利用蜜蜂信息素防治狄斯瓦螨是一个重要的研究方向.研究表明,狄斯瓦螨能利用蜜蜂信息素识别处于不同发育阶段的寄主,并对特定时期的寄主表现出高度的选择性.近年来,多种能作用于狄斯瓦螨的蜜蜂信息素相继被报道.这些信息素包括成蜂、蛹和幼虫信息素.有的信息素对狄斯瓦螨表现出驱避作用,有的则表现出引诱作用.本文对这些信息素的种类、主要组成成分、对狄斯瓦螨的作用等进行了综述,旨在为今后的研究与应用提供参考.     

狄斯瓦螨对杀螨剂抗性机制的研究进展

狄斯瓦螨Varroa destructor是严重危害西方蜜蜂Apis mellifera的主要寄生螨之一,由于杀螨剂长期大量、单一和连续使用,狄斯瓦螨对杀螨剂的抗性发展日趋严重,探明狄斯瓦螨抗性机制对于治理狄斯瓦螨具有重要意义。狄斯瓦螨抗性形成受遗传因素、人为操作因素及其他生态因素的影响,其抗性机制与化学杀螨剂的种类有关,目前研究较多的是靶标不敏感性机制和解毒代谢增强机制,对拟除虫菊酯类杀螨剂抗性机制研究较为透彻,而对有机磷类和甲咪类杀螨剂抗性机制研究有限。本文基于文献,阐述了狄斯瓦螨对拟除虫菊酯类、有机磷类和甲咪类杀螨剂抗性机制的最新研究进展,讨论了抗性治理的最新研究成果及该领域未来的研究方向,以期为狄斯瓦螨有效治理、杀螨剂的安全有效使用及新型杀螨剂开发等研究提供参考。     

中草药精油对蜜蜂狄斯瓦螨的熏杀效果

在实验室条件下测定10种中草药精油对蜜蜂狄斯瓦螨Varroa destructor Anderson&Trueman的熏蒸效果,通过测定中草药精油对蜜蜂和螨的毒性,筛选出具有杀螨活性而对蜜蜂较安全的中草药精油。结果表明:中草药精油对蜜蜂都有一定的毒害;而在对蜜蜂无毒性的剂量下,48h时茴香油、丁香油、肉桂油分别能引起92.5%、54%和12%的螨死亡,显著高于对照组(P<0.05);根据初步筛选结果,选择茴香油和丁香油进行进一步毒力测定,结果表明48h时茴香油对螨的LD50为0.949μL,蜜蜂的LD50为4.033μL;丁香油对螨的LD50为0.795μL,蜜蜂的LD50为1.965μL。茴香油在48h时有着较高的选择比(蜜蜂的LD50/螨的LD50=4.250);GC-MS鉴定茴香油最主要成分是茴香脑(占总成分的88.72%),丁香油的主要成分是丁香酚(68.28%)和石竹烯(20.79%)。可见,茴香油和丁香油在控制狄斯瓦螨的应用上具有很大潜力。     

Development of a 44K SNP assay focussing on the analysis of a varroa-specific defence behaviour in honey bees (Apis mellifera carnica)

Honey bees are exposed to a number of damaging pathogens and parasites. The most destructive among them, affecting mainly the brood, is Varroa destructor. A promising approach to prevent its spread is to breed for Varroa-tolerant honey bees. A trait that has been shown to provide significant resistance against the Varroa mite is hygienic behaviour, a behavioural response of honey bee workers to brood diseases in general. This study reports the development of a 44K SNP assay, specifically designed for the analysis of hygienic behaviour of individual worker bees (Apis mellifera carnica) directed against V. destructor. Initially, 70,000 SNPs chosen from a large set of SNPs published by the Honey Bee Genome Project were validated for their suitability in the analysis of the Varroa resistance trait 'uncapping of Varroa-infested brood'. This was achieved by genotyping of pooled DNA samples of trait bearers and two trait-negative controls using next-generation sequencing. Approximately 36,000 of these validated SNPs and another 8000 SNPs not validated in this study were selected for the construction of a SNP assay. This assay will be employed in following experiments to analyse individualized DNA samples in order to identify quantitative trait loci (QTL) involved in the control of the investigated trait and to evaluate and possibly confirm QTL found in other studies. However, this assay is not just suitable to study Varroa tolerance, it is as well applicable to analyse any other trait in honey bees. In addition, because of its high density, this assay provides access into genomic selection with respect to several traits considered in honey bee breeding. It will become publicly available via AROS Applied Biotechnology AS, Aarhus, Denmark, before the end of the year 2011.     

Resistance of the honey bee, Apis mellifera to the acarian parasite Varroa destructor: behavioural and electroantennographic data

Abstract. One way in which Apis mellifera honey bees resist Varroa destructor is by detection and elimination of nestmates. This study uses behavioural tests and electroanntennography to assess the role of chemostimuli in recognition by honey bees of this acarian ectoparasite. Behavioural tests using living or dead parasites involved observation of honey bee grooming activity (antennation) under controlled conditions in Petri dishes, and removal behaviour (uncapping and elimination of parasitized and unparasitized control brood cells) under natural conditions. Some bees from colonies with both small and large parasite populations showed aggressive behaviour (biting). No difference was observed according to whether the mite was dead or alive. Under natural conditions, bees uncapped more parasitized cells than control cells. Electroantennographic tests were performed to measure sensitivity to various Varroa extracts at three concentrations (10, 20 and 30 Varroa Equivalents). Only 30 Varroa Equivalent methanol extracts made from Varroa collected from brood cells elicited significantly greater antennal response than controls (pure solvent). All three methanol extracts elicited significantly greater antennal response than controls. No response was observed using Varroa extracts made with acetone or hexane. These findings suggest that polar products may act as chemostimuli for recognition of V. destructor by honey bees. Further study will be necessary to determine which polar products are involved in this recognition and assess grooming and removal behaviour using these products.     

大蜂螨对一些气味物质的趋性

狄斯瓦螨Varroa destructor Anderson & Trueman是意大利蜜蜂Apis mellifera Spinola的主要外寄生螨。雌成螨在幼虫巢房封盖前不久侵入幼虫巢房,并开始繁殖为害。从雌成螨在一个很短的时间内进入蜜蜂幼虫巢房,以及雄蜂幼虫巢房蜂螨的寄生率明显高于工蜂幼虫巢房的现象,表明蜜蜂幼虫体表一些信息素(semiochemicals)可能起着重要的引诱作用。作者对与大蜂螨相关的19种气味物质进行筛选,并对封盖前工蜂幼虫和雄蜂幼虫表皮挥发物进行气谱及气-质联谱测定。结果表明:雄蜂6龄幼虫对大蜂螨的引诱作用显著高于丁香水等10种气味物质。工蜂和雄蜂末龄幼虫体表挥发物的共有组份是9-二十三烯(C23H46),但它在雄蜂幼虫中所占的比例要明显高于工蜂幼虫。工蜂幼虫的特有主要组分是十八烷(C18H38)和9-甲基十九烷(C19H40);而雄蜂幼虫的特有主要组分是二十五烷(C25H52)和二十三烷(C23H48)。     

Functionality of Varroa-resistant honey bees (Hymenoptera: Apidae) when used in migratory beekeeping for crop pollination

Two types of honey bees, Apis mellifera L. (Hymenoptera: Apidae), bred for resistance to Varroa destructor Anderson & Trueman were evaluated for performance when used in migratory crop pollination. Colonies of Russian honey bees (RHB) and outcrossed bees with Varroa-sensitive hygiene (VSH) were managed without miticide treatments and compared with colonies of Italian honey bees that served as controls. Control colonies were managed as groups which either were treated twice each year against V. destructor (CT) or kept untreated (CU). Totals of 240 and 247 colonies were established initially for trials in 2008 and 2009, respectively. RHB and VSH colonies generally had adult and brood populations similar to those of the standard CT group regarding pollination requirements. For pollination of almonds [Prunus dulcis (Mill.) D.A.Webb] in February, percentages of colonies meeting the required six or more frames of adult bees were 57% (VSH), 56% (CT), 39% (RHB), and 34% (CU). RHB are known to have small colonies in early spring, but this can be overcome with appropriate feeding. For later pollination requirements in May to July, 94-100% of colonies in the four groups met pollination size requirements for apples (Malus domestica Borkh.), cranberries (Vaccinium macrocarpon Aiton), and lowbush blueberries (Vaccinium angustifolium Aiton). Infestations with V. destructor usually were lowest in CT colonies and tended to be lower in VSH colonies than in RHB and CU colonies. This study demonstrates that bees with the VSH trait and pure RHB offer alternatives for beekeepers to use for commercial crop pollination while reducing reliance on miticides. The high frequency of queen loss (only approximately one fourth of original queens survived each year) suggests that frequent requeening is necessary to maintain desired genetics.     

Acute contact toxicity of oxalic acid to Varroa destructor (Acari: Varroidae) and their Apis mellifera (Hymenoptera: Apidae) hosts in laboratory bioassays

Laboratory bioassays were performed to characterize the acute contact toxicity of oxalic acid (OA) to Varroa destructor (Anderson and Trueman) and their honey bee hosts (Apis mellifera L.). Specifically, glass-vial residual bioassays were conducted to determine the lethal concentration of OA for V. destructor, and topical applications of OA in acetone were conducted to determine the lethal dose for honey bees. The results indicate that OA has a low acute toxicity to honey bees and a high acute toxicity to mites. The toxicity data will help guide scientists in delivering optimum dosages of OA to the parasite and its host, and will be useful in making treatment recommendations. The data will also facilitate future comparisons of toxicity if mite resistance to OA becomes evident.     

Varroa mites in the apiaries of Campania region

Mites in the genus Varroa are obligate ectoparasites of honey bee populations worldwide. Recent evidence from morphological, geographical, and especially genetic variation has spurred an important revision of Varroa taxonomy. Specifically, mitochondrial DNA (mtDNA) evidence suggests that the main mite pest on western honey bees (Apis mellifera) is not Varroa jacobsoni, as first described, but a distinct species now named Varroa destructor. Genetic markers also have been used to support a taxonomic basis for regional differences in how Varroa mites impact honey bees. Recent morphometric and molecular studies confirmed the presence of the species V. destructor also in the apiaries of the Campania region of southern Italy. In the three-year period 2001-2003 a survey was conducted in 118 municipalities of the five provinces of the Campania region in order to add data to the limited epidemiological information available regarding Varroa destructor in this zone. The level of infestation by the mite was assessed on a total of 521 apiaries (241 apiaries were inspected on 2001, 154 on 2002, and 126 on 2003). In each apiary, 100 comb cells were examined and in each province the level of infestation was calculated using the following formula: (number of Varroa specimens/number of open comb cells) x 100. In order to display the level of infestation, Geographical Information Systems were used in order to draw parasitological maps.     

Expression of Varroa sensitive hygiene (VSH) in commercial VSH honey bees (Hymenoptera: Apidae)

We tested six commercial sources of honey bees, Apis mellifera L. (Hymenoptera: Apidae), whose breeding incorporated the trait of Varroa sensitive hygiene (VSH). VSH confers resistance to the parasitic mite Varroa destructor Anderson & Trueman by enhancing the ability of the bees to hygienically remove mite-infested brood. VSH production queens (i.e., queens commercially available for use in beekeepers' production colonies) from the six sources were established in colonies which later were measured for VSH. Their responses were compared with those of colonies with three other types of queens, as follows: VSH queens from the selected closed population maintained by USDA-ARS for research and as a source of breeding germplasm, queens from the cooperating commercial distributor of this germplasm, and queens of a commercial, mite-susceptible source. The reduction of mite infestation in brood combs exposed to test colonies for 1 wk differed significantly between groups. On average, colonies with VSH production queens reduced infestation by 44%. This group average was intermediate between the greater removal by pure ARS VSH (76%) and the cooperators' breeding colonies (64%), and the lesser removal by susceptible colonies (7%). VSH production colonies from the different sources had variable expression of hygiene against mites, with average reduced infestations ranging from 22 to 74%. In addition, infertility was high among mites that remained in infested cells in VSH breeder colonies from ARS and the commercial distributor but was lower and more variable in VSH production colonies and susceptible colonies. Commercial VSH production colonies supply mite resistance that generally seems to be useful for beekeeping. Resistance probably could be improved if more VSH drones sources were supplied when VSH production queens are being mated.     

微孢子虫和狄斯瓦螨分别侵染后的意蜂血淋巴蛋白质含量变化

微孢子虫Nosema apis和狄斯瓦螨微孢子虫Nosema apis和狄斯瓦螨 Varroa destructor (Acari: Varroidae)均为危害意蜂Apis mellifera的重要寄生虫,该文对其危害后意蜂血淋巴蛋白质含量的变化进行了研究。用考马斯亮蓝法测定了意蜂受侵染后血淋巴的蛋白质总量,并用高压超薄层等电点聚焦法进行血淋巴蛋白质分类。结果显示,病蜂血淋巴蛋白质总量,在人工感染微孢子虫后1～10天呈微孢子虫Nosema apis和狄斯瓦螨 Varroa destructor (Acari: Varroidae)均为危害意蜂Apis mellifera的重要寄生虫,该文对其危害后意蜂血淋巴蛋白质含量的变化进行了研究。用考马斯亮蓝法测定了意蜂受侵染后血淋巴的蛋白质总量,并用高压超薄层等电点聚焦法进行血淋巴蛋白质分类。结果显示,病蜂血淋巴蛋白质总量,在人工感染微孢子虫后1～10天呈上升趋势,然后逐渐下降,感染后12～27天保持在感染前意蜂血淋巴总蛋白质含量水平以下。螨侵染后意蜂血淋巴蛋白质含量明显增高,与健康意蜂相比差异极显著。高压超薄层等电点聚焦分析表明：狄斯瓦螨自然侵染意蜂后,意蜂血淋巴蛋白质组分与健康对照组相比发生了明显改变。这些结果提示,意蜂对于微孢子虫或狄斯瓦螨的侵染产生了一定的免疫反应。     

Hirsutella thompsonii and Metarhizium anisopliae as potential microbial control agents of Varroa destructor,a honey bee parasite

The potential of Hirsutella thompsonii Fisher and Metarhizium anisopliae (Metschinkoff) as biological control agents of the parasitic mite, Varroa destructor Anderson and Trueman was evaluated in the laboratory and in observation hives. In the laboratory, time required for 90% cumulative mortality of mites (LT(90)) was 4.16 (3.98-4.42) days for H. thompsonii and 5.85 (5.48-7.43) days for M. anisopliae at 1.1 x 10(3) conidia mm(-2). At a temperature (34+/-1 degrees C) similar to that of the broodnest in a honey bee colony, Apis mellifera L., H. thompsonii [LC(90)=9.90 x 10(1) (5.86-19.35) conidia mm(-2) at Day 7] and M. anisopliae [LC(90)=7.13 x 10(3) (2.80-23.45) conidia mm(-2) at Day 7] both showed significant virulence against V. destructor. The applications of H. thompsonii to observation hives resulted in significant mortality of mites, and reduction of the number of mites per bee 21 and 42 days post-treatments. The treatments did not significantly affect the mite population in sealed brood. However, the fungus must have persisted because infected mites were still observed [82.97+/-(0.6)%] 42 days post-treatment. In addition, the fungus was found to sporulate on the host. A small percentage [2.86+/-(0.2)%] of dead mites found in the control hives also showed fungal infection, suggesting that adult bees drifted between hives and disseminated the fungus. H. thompsonii was harmless to the honey bees at the concentrations applied and did not have any deleterious effects on the fecundity of the queens. Microbial control with fungal pathogens provides promising new avenues for control of V. destructor and could be a useful component of an integrated pest management program for the honey bee industry.