寄生蜂携带的多DNA病毒的起源及其特性

病毒在通常意义上都是有害的寄生生物,但是有一类特殊的多DNA病毒(PDV)却成为在数量庞大的寄生蜂的生活史中不可或缺的共生病毒.PDV随着寄生蜂的卵一起被注入到寄主的体内,调控寄主的免疫和发育生理,从而确保幼蜂在寄主体内生存发育.PDV的基因组整合在寄生蜂的基因组内,因此PDV病毒粒子的形成并非在寄主受到侵染的组织内,而是位于寄生蜂卵巢的特定细胞(卵萼细胞)中,其编码的蛋白质几乎没有病毒结构性蛋白,主要的表达产物都用于调控寄主的生理活动.PDV基因编码序列比对分析结果显示,茧蜂病毒(BV)与致病性的裸病毒nudivirus和杆状病毒baculovirus存在一定的亲缘关系,然而这些同源基因已高度分化,具有不同的生物学特性,同时也不能确定这些基因是否还具有原始的功能.在寄生蜂基因组中尚有许多与裸病毒和杆状病毒类似的基因,其中一部分基因能够编码BV病毒粒子的结构蛋白,其表达模式亦与PDV病毒粒子的形成有关.由于PDV使用了与这2种病毒类似的传播途径,才使得寄生蜂的PDV基因转入寄主体内发挥作用,虽然这不能说明PDV属于这2种病毒,至少存在PDV从这2种病毒发展而来的可能性.     

多分DNA病毒基因组全序列的测定

在寄生蜂与寄主相互作用关系中,伴随寄生蜂产卵一起注入寄主体内,与寄生蜂“共生的”多分DNA病毒(polydnavirus,PDV)是寄生蜂利用的一种最奇妙的方式。通过抑制寄主的免疫和发育,PDV能够保证寄生蜂的正常发育和羽化。法国Institut de Recherche sur 1a Biologie de I’Insecte,UFR Science et Techniques的科学家测定了茧蜂Cotesia congregate的多分DNA病毒(CeBV)基因组全序列,     

多态DNA病毒对寄生蜂宿主生理功能的影响

多态DNA病毒(polydnavirus, PDV)由一组特异的病毒组成,其生活史与某些寄生蜂种类有着密不可分的联系.大量研究表明该种病毒是决定某些寄生蜂能否在寄主体内成功寄生的关键因子之一[1].本文将综述已有的研究报道,重点阐明PDV随寄生蜂产卵而传递到寄生蜂的寄主体内时所发挥的确切生理功能和作用方式.     

寄生蜂多分DNA病毒的基因表达产物及对寄主昆虫的生理作用

最近有关由多分DNA病毒介导的寄生蜂与寄主关系的研究主要集中在多分DNA病毒基因的表达和伴随寄主生理功能失常的分子机理上 ,本文介绍在寄生蜂作用于寄主时一些重要的PDV基因表达产物 ,包括CsPDV ,MdPDV ,CcPDV ,TrPDV ,HdPDV ,CrPDV和其它PDV的基因表达产物 ,并简叙这些基因表达产物对寄主的生理影响。     

寄生蜂多分DNA病毒对寄主昆虫的免疫抑制作用

多分DNA病毒（PDV）是在膜翅目姬蜂科和茧蜂科寄生蜂体内的一类很独特的病毒,寄生蜂产卵时,PDV随同卵和萼液一起被注射入寄主体内,能干扰寄主的细胞免疫和体液免疫,该病毒直接侵染或间接作用于血细胞,主要是浆细胞和颗粒细胞,导致血细胞变圆或凋亡,PDV也能抑制血淋巴酚氧化酶活性,诱导抗菌因子的大量合成,最近有关研究主要集中在病毒基因的表达和伴随寄主血细胞功能失常的分子事件上,一些寄主蜂的PDV与其他因子,如卵巢蛋白,畸形细胞或蜂毒等协同发挥作用。     

二种寄生蜂寄生对不同虫龄小菜蛾精巢的影响

为探明寄生蜂引起寄主寄生性去势的机制,本文选取携带不同多分DNA病毒(Polydnavirus,PDV)的2种内寄生蜂与共同寄主小菜蛾Plutella xylostella(L.)为寄生体系,研究不同虫龄小菜蛾被寄生后雄性生精细胞、精子束形态和精巢发育体积变化,系统比较寄生性去势程度和分别拥有2类PDV的寄生蜂在寄主精子发生和形成过程中的作用。结果表明:携带Bracovirus PDV的菜蛾盘绒茧蜂Cotesiave stalis(Haliday)或拥有Ichvovirus PDV的半闭弯尾姬蜂Diadegma semiclausum Hellén寄生对不同虫龄小菜蛾的精子发生和形成过程均产生明显的抑制作用,表现为不能产生精子束或精子束数量减少,但抑制程度以寄生低龄寄主时最明显。2种蜂寄生均能抑制小菜蛾精巢体积的增长,但对低龄寄主的抑制程度明显强于高龄寄主,寄生性去势程度取决于寄生时寄主虫龄。相比而言,寄生不同虫龄小菜蛾时,茧蜂引起小菜蛾寄生性去势的程度均强于姬蜂。     

寄生性膜翅目昆虫毒素的生态机制及应用前景

膜翅目昆虫利用高效的毒素进行自身防卫、攻击猎物和调节寄主生长发育.从寄生性膜翅目昆虫毒素的产生、类别、组份、性质、毒素的生态功能以及毒素的作用机制等方面综述了寄生性膜翅目昆虫毒素的研究概况.膜翅目的泌毒器官起源于外胚层,由生殖系统的附腺演化而来.毒液由成熟雌蜂的毒腺或酸腺所分泌,并贮于毒囊中.昆虫毒素是成分复杂的混合物,已知膜翅目昆虫毒素中含有烃类、醇类、醛类、酮类、羧酸类、酯类、内酯类、酶类等多种化合物.寄生性膜翅目昆虫的毒素在提高自身适应能力方面的作用是巨大的,如通过麻痹寄主提高产卵成功的概率、通过抑制寄主的生长发育和免疫功能提高后代的存活率、通过干扰寄主的生理活动改善后代的营养需求等.体外寄生蜂毒素可造成寄主幼虫停止发育、永久性的麻痹甚至死亡,这类毒素常为抑性的、广谱的,一般作用于中枢神经系统或神经-肌肉连接点.而体内寄生蜂多为容性寄生,其毒液中含有多分DNA病毒（PDV）,PDV通过抑制寄主免疫系统而巧妙地调节寄主的生理活动和发育,影响寄主的正常变态,大多数种类直到寄主结茧或做好蛹室时才将其杀死在安全的场所,从而使寄生蜂后代能够顺利完成发育.容性寄生蜂毒素对PDV的功能具有显著的增效或协同作用,而不会使寄主产生永久性麻痹.PDV对寄生蜂本身是非致病性的,与寄生蜂是一种分子水平上的共生或依生关系.寄生性膜翅目昆虫毒素显示了良好的应用前景,特别是在开发人类医药和特异性生物杀虫剂方面.但分离和纯化毒液中各个活性成分是应用的前提,也是生化和毒理研究的需要.     

基于组学的寄生蜂与寄主免疫的相互作用

寄生蜂作为天敌昆虫,在害虫生物防治中起着极其重要的作用。现代分子生物学和第二代测序技术的迅速发展,为筛选寄生蜂与寄主免疫互作的关键分子,阐明寄生蜂逃避或抑制寄主免疫系统攻击的机理提供了新的机遇。昆虫的天然免疫可分为细胞免疫和体液免疫,寄生蜂在与寄主长期的协同进化过程中,依靠毒液(venom)、多分DNA病毒(PDV)、类病毒颗粒(VLP)、畸形细胞(teratocyte)等手段,一方面调控寄主血细胞的增殖和分化,抑制细胞包囊反应,从而破坏寄主的细胞免疫系统;另一方面,通过抑制酚氧化酶原激活干扰寄主的体液免疫,从而逃避黑化反应的攻击。寄生蜂在发育过程中也有相应的免疫防御机制。本文从细胞免疫、体液黑化反应以及免疫信号通路等方面,综述了近年来利用组学手段在寄生蜂调控寄主免疫方面取得的最新进展,以期为阐明天然免疫的分子机制、探索害虫防治新方法提供借鉴。     

蚜小蜂生殖、发育及其与寄主的关系

蚜小蜂是重要的农林作物害虫寄生蜂,被广泛应用于生物防治。文章将国内外对蚜小蜂的生殖与性别决定方式,蚜小蜂的生长和发育以及蚜小蜂对寄主的选择过程,寄生蜂对寄主激素平衡的调节与控制,蚜小蜂与其他寄生蜂之间的竞争作用等蚜小蜂与寄主之间的相互关系的研究概况进行综述。     

寄生蜂抗药性研究进展

植物-植食性昆虫-寄生蜂三级营养结构之间由于长期相互适应和协同进化,产生了一系列独特的相互关系。选择压力将对害虫和寄生蜂的抗药性演化产生影响,但由于寄生蜂具有与植食性昆虫不同的生物学及生态学特性,选择压力对害虫和寄生蜂抗药性演化的影响作用也是不同的。研究结果表明,除体外杀虫剂对寄生蜂的直接汰选因素外,进入寄主昆虫体内的杀虫剂成分、寄主昆虫取食不同植物的特有成分以及气候因子等均会对寄生蜂的抗药性演化产生影响。     

Evolution of polydnaviruses as insect immune suppressors

Polydnaviruses (PDVs) are endogenous particles that are used by some endoparasitic hymenoptera to disrupt host immunity and development. Recent analyses of encapsidated PDV genes have increased the number of known PDV gene families, which are often closely related to insect genes. Several PDV proteins inactivate host haemocytes by damaging their actin cytoskeleton. These proteins share no significant sequence homology and occur in polyphyletic PDV genera, possibly indicating that convergent evolution has produced functionally similar immune-suppressive molecules causing a haemocyte phenotype characterised by damaged cytoskeleton and inactivation. These phenomena provide further insights into the immune-suppressive activity of PDVs and raise interesting questions about PDV evolution, a topic that has puzzled researchers ever since the discovery of PDVs.     

Comparison of three methods of parasitoid polydnavirus genomic DNA isolation to facilitate polydnavirus genomic sequencing

A major long-term goal of polydnavirus (PDV) genome research is to identify novel virally encoded molecules that may serve as biopesticides to target insect pests that threaten agriculture and human health. As PDV viral replication in cell culture in vitro has not yet been achieved, several thousands of wasps must be dissected to yield enough viral DNA from the adult ovaries to carry out PDV genomic sequencing. This study compares three methods of PDV genomic DNA isolation for the PDV of Cotesia flavipes, which parasitizes the sugarcane borer, Diatraea saccharalis, preparatory to sequencing the C. flavipes bracovirus genome. Two of these protocols incorporate phenol-chloroform DNA extraction steps in the procedure and the third protocol uses a modified Qiagen DNA kit method to extract viral DNA. The latter method proved significantly less time-consuming and more cost-effective. Efforts are currently underway to bioengineer insect pathogenic viruses with PDV genes, so that their gene products will enhance baculovirus virulence for agricultural insect pests, either via suppression of the immune system of the host or by PDV-mediated induction of its developmental arrest. Sequencing a growing number of complete PDV genomes will enhance those efforts, which will be facilitated by the study reported here.     

Phocine distemper virus uses phocine and other animal SLAMs as a receptor but not human SLAM

Morbilliviruses use the signaling lymphocyte activation molecule (SLAM) as a receptor to infect their hosts. Seals are almost the only animal species that show apparent infection with phocine distemper virus (PDV). Seal SLAM functioned as a PDV receptor. However, dolphin- and dog-SLAM molecules, but not human SLAM, were also fully functional PDV receptors. These data suggest that the host range of PDV is not simply determined by its SLAM usage. However, human nonsusceptibility to PDV infection may be at least partly attributable to the inability of PDV to use human SLAM as a receptor.     

The evolution of the regulatory mechanism of chloroplast division

Chloroplasts arose from a cyanobacterial endosymbiont and multiply by division, reminiscent of their free-living ancestor. However, chloroplasts can not divide by themselves, and the division is performed and controlled by proteins that are encoded by the host nucleus. The continuity of chloroplasts was originally established by synchronization of endosymbiotic cell division with host cell division, as seen in existent algae. In contrast, land plant cells contain multiple chloroplasts, the division of which is not synchronized, even in the same cell. Land plants have evolved cell and chloroplast differentiation systems in which the size and number of chloroplasts (or other types of plastids) change along with their respective cellular function by changes in the division rate. We recently reported that PLASTID DIVISION (PDV) proteins, land-plant specific components of the chloroplast division apparatus, determined the rate of chloroplast division. The level of PDV protein is regulated by the cell differentiation program based on cytokinin, and the increase or decrease of the PDV level gives rise to an increase or decrease in the chloroplast division rate. Thus, the integration of PDV proteins into the chloroplast division machinery enabled land plant cells to change chloroplast size and number in accord with the fate of cell differentiation.Key words: chloroplast division, cell cycle, cell differentiation, cytokinin, endosymbiosis, evolution     

When parasitic wasps hijacked viruses: genomic and functional evolution of polydnaviruses

The Polydnaviridae (PDV), including the Bracovirus (BV) and Ichnovirus genera, originated from the integration of unrelated viruses in the genomes of two parasitoid wasp lineages, in a remarkable example of convergent evolution. Functionally active PDVs represent the most compelling evolutionary success among endogenous viral elements (EVEs). BV evolved from the domestication by braconid wasps of a nudivirus 100 Ma. The nudivirus genome has become an EVE involved in BV particle production but is not encapsidated. Instead, BV genomes have co-opted virulence genes, used by the wasps to control the immunity and development of their hosts. Gene transfers and duplications have shaped BV genomes, now encoding hundreds of genes. Phylogenomic studies suggest that BVs contribute largely to wasp diversification and adaptation to their hosts. A genome evolution model explains how multidirectional wasp adaptation to different host species could have fostered PDV genome extension. Integrative studies linking ecological data on the wasp to genomic analyses should provide new insights into the adaptive role of particular BV genes. Forthcoming genomic advances should also indicate if the associations between endoparasitoid wasps and symbiotic viruses evolved because of their particularly intimate interactions with their hosts, or if similar domesticated EVEs could be uncovered in other parasites.     

Mechanism of reduction in the number of the circulating hemocytes in the Pseudaletia separata host parasitized by Cotesia kariyai

Larval endoparasitoids can avoid the immune response of the host by the function of polydnavirus (PDV) and venom. PDV infects hemocytes and affects the hemocyte function of the host. In this paper, we investigated how PDV and venom affect the hemocyte population of the host. Cotesia kariyai, the larval endoparasitoid, lowers the hemocyte population of the noctuid host larvae soon after parasitization. The reduction in the number of circulating hemocytes is caused by the breakdown of the circulating hemocytes and of the hematopoietic organ which generates the circulating hemocytes. The decrease in the number of hemocytes shortly after parasitization is a response to the venom. However, the decrease in hemocyte population on and after 6 h post-parasitization appears to be caused by the PDV. Apoptosis in circulating hemocytes was observed on and after 6 h post-injection of PDV plus venom. It was revealed through cytometry that mitosis of circulating hemocytes was halted within 24 h after the injection of PDV plus venom. Apoptosis in the hematopoietic organ was induced 12 h after the injection of PDV plus venom. Furthermore, the plasma from the hosts injected with PDV plus venom depressed the number of hemocytes released from the hemotopoiteic organs.     

Negative-sense RNA viruses: An underexplored platform for examining virus–host lipid interactions

Viruses are pathogenic agents that can infect all varieties of organisms, including plants, animals, and humans. These microscopic particles are genetically simple as they encode a limited number of proteins that undertake a wide range of functions. While structurally distinct, viruses often share common characteristics that have evolved to aid in their infectious life cycles. A commonly underappreciated characteristic of many deadly viruses is a lipid envelope that surrounds their protein and genetic contents. Notably, the lipid envelope is formed from the host cell the virus infects. Lipid-enveloped viruses comprise a diverse range of pathogenic viruses, which often lead to high fatality rates and many lack effective therapeutics and/or vaccines. This perspective primarily focuses on the negative-sense RNA viruses from the order Mononegavirales, which obtain their lipid envelope from the host plasma membrane. Specifically, the perspective highlights the common themes of host cell lipid and membrane biology necessary for virus replication, assembly, and budding.     

Interspecific competition between two endoparasitoids Cotesia vestalis (Hymenoptera: Braconidae) and Oomyzus sokolowskii (Hymenoptera: Eulophidae)

Two endoparasitoids, Cotesia vestalis and Oomyzus sokolowskii, parasitize the same host, larvae of Plutella xylostella. These two species have evolved different parasitization strategies. O. sokolowskii expresses a single factor, venom, and exerts virtually no detrimental effects on the development of its host. C. vestalis, on the other hand, injects polydnavirus (PDV) and venom during oviposition, and teratocytes are released into the host's hemolymph after egg hatching. Parasitization suppresses host immune reactions and redirects its developmental program. Because both these species parasitize the same stage of their hosts, there is the possibility of multiparasitism in nature. Only one species survives multiparasitism and because of its parasitic strategy, we hypothesized that C. vestalis would invariably be the stronger competitor. We designed competition experiments which revealed that C. vestalis is a stronger competitor than O. sokolowskii. We also show that C. vestalis survives intrinsic competition with O. sokolowskii through two mechanisms: physical attack and physiological suppression. We discovered melanized wounds on O. sokolowskii eggs and larvae, which is strong evidence of physical attacks. The physiological suppression is due to PDV and venom injected by C. vestalis. To test this idea more rigorously, we designed a pseudoparasitization experiment which revealed that no O. sokolowskii emerged from multiparasitized hosts when infertile C. vestlais eggs and normal O. sokolowskii larvae are both present inside the same host. These results support our hypothesis that C. vestalis is the stronger competitor and demonstrate two mechanisms that account for the outcome of intrinsic competition between these two endoparasitoids.     

Effects of the polydnavirus of Cotesia congregata on the immune system and development of non-habitual hosts of the parasitoid

Polydnaviruses (PDV) are obligate mutualistic symbionts found in association with some groups of parasitic Hymenoptera. In these groups, they suppress the immune response of the parasitoid’s host and are required for successful parasitoid reproduction. Several PDV effects have been described in different experimental systems, but no clear picture of PDV mode of immunosuppression has emerged. No study to date has directly tested if PDV modes of action are evolutionarily conserved or divergent among parasitoid taxa within the Ichneumonoidea. We hypothesize the divergence in PDV mode of immunosuppression can be detected by identifying points of divergence in the immune response of different host species to PDV from one parasitoid species. This study tests the effects of purified PDV from Cotesia congregata on the immune response of three larval lepidopteran species that naturally are hosts of parasitoid species that differ in taxonomic relatedness to C. congregata. Here we demonstrate that despite associations with distantly related parasitoids (Ichneumonidae and Braconidae), Manduca sexta and Heliothis virescens showed similar patterns of increased glucose dehydrogenase (GLD) activity, suppressed cellular encapsulation in vitro, and increased time to pupation. In contrast, Lymantria dispar showed no response to C. congregata PDV across any of the parameters measured, even though it has an evolutionary association with several parasitoids closely related to C. congregata and within the Microgastrinae. The PDV immunosuppression in H. virescens and M. sexta does not correlate with host molecular phylogeny either. The suborganismal effects shown in M. sexta and H. virescens translated into significantly reduced pupation success in M. sexta only. Results demonstrate that while some PDV modes of immunosuppression in hosts may be divergent, others may be conserved across broad host groups.