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1.
Nat Commun ; 12(1): 5489, 2021 09 16.
Article in English | MEDLINE | ID: mdl-34531391

ABSTRACT

Intraspecific competition is a major force in mediating population dynamics, fuelling adaptation, and potentially leading to evolutionary diversification. Among the evolutionary arms races between parasites, one of the most fundamental and intriguing behavioural adaptations and counter-adaptations are superparasitism and superparasitism avoidance. However, the underlying mechanisms and ecological contexts of these phenomena remain underexplored. Here, we apply the Drosophila parasite Leptopilina boulardi as a study system and find that this solitary endoparasitic wasp provokes a host escape response for superparasitism avoidance. We combine multi-omics and in vivo functional studies to characterize a small set of RhoGAP domain-containing genes that mediate the parasite's manipulation of host escape behaviour by inducing reactive oxygen species in the host central nervous system. We further uncover an evolutionary scenario in which neofunctionalization and specialization gave rise to the novel role of RhoGAP domain in avoiding superparasitism, with an ancestral origin prior to the divergence between Leptopilina specialist and generalist species. Our study suggests that superparasitism avoidance is adaptive for a parasite and adds to our understanding of how the molecular manipulation of host behaviour has evolved in this system.


Subject(s)
Drosophila melanogaster/parasitology , GTPase-Activating Proteins/genetics , Host-Parasite Interactions/genetics , Insect Proteins/genetics , Wasps/genetics , Wasps/pathogenicity , Animals , Avoidance Learning , Behavior, Animal , Biological Coevolution , Central Nervous System/parasitology , Eating , Female , GTPase-Activating Proteins/classification , GTPase-Activating Proteins/metabolism , Gene Expression , Insect Proteins/classification , Insect Proteins/metabolism , Larva/parasitology , Male , Multigene Family , Reactive Oxygen Species/metabolism , Wasps/metabolism
2.
PLoS One ; 16(8): e0256246, 2021.
Article in English | MEDLINE | ID: mdl-34411169

ABSTRACT

Different factitious hosts were used to mass rear Trichogramma japonicum Ashmead in different parts of the globe because thorough details were lacking in both the laboratory and the field. The objective of this study was to compare, parasitoid, T. japonicum reared in different factitious hosts. Three commonly used factitious host eggs, Corcyra cephalonica (Stainton), Ephestia kuehniella Zeller and Sitotroga cerealella Olivier were tested under laboratory conditions and then in the field over a yellow stem borer, Scirpophaga incertulus (Walker) of rice. The highest parasitism by T. japonicum was observed on E. kuehniella eggs. The parasitoid's highest emergence (88.99%) was observed on S. cerealella eggs at 24 h exposure, whereas at 48 h it was on E. kuehniella eggs (94.66%). Trichogramma japonicum females that emerged from E. kuehniella eggs were significantly long-lived. The days of oviposition by hosts and the host species were significant individually, but not their interaction. Higher proportions of flying T. japonicum were observed when reared on E. kuehniella and C. cephalonica eggs. Field results showed that T. japonicum mass-reared on E. kuehniella showed higher parasitism of its natural host, S. incertulus eggs. Hence, by considering these biological characteristics and field results, E. kuehniella could be leveraged for the mass rearing of quality parasitoids of T. japonicum in India, the Asian continent and beyond.


Subject(s)
Host-Parasite Interactions/genetics , Hymenoptera/genetics , Lepidoptera/parasitology , Pest Control, Biological , Animals , Eggs/parasitology , Female , Host Specificity/genetics , Hymenoptera/pathogenicity , India , Larva/pathogenicity , Lepidoptera/genetics , Moths/parasitology , Oryza/parasitology , Oviposition/genetics , Wasps/pathogenicity
3.
Article in English | MEDLINE | ID: mdl-34120097

ABSTRACT

Parasitoids have been extensively found to manipulate nutrient amounts of their hosts to benefit their own development and survival, but the underlying mechanisms are largely unknown. Leptopilina boulardi (Hymenoptera: Figitidae) is a larval-pupal endoparasitoid wasp of Drosophila melanogaster whose survival relies on the nutrients provided by its Drosophila host. Here, we used RNA-seq to compare the gene expression levels of the host midgut at 24 h and 48 h post L. boulardi parasitization. We obtained 95 and 191 differentially expressed genes (DEGs) in the parasitized host midgut at 24 h and 48 h post L. boulardi parasitization, respectively. A KEGG analysis revealed that several metabolic pathways were significantly enriched in the upregulated DEGs, and these pathways included "starch and sucrose metabolism" and "galactose metabolism". A functional annotation analysis showed that four classes of genes involved in carbohydrate digestion process had increased expression levels in the midgut post L.boulardi parasitization than nonparasitized groups: glucosidase, mannosidase, chitinase and amylase. Genes involved in protein digestion process were also found among the DEGs, and most of these genes, which belonged to the metallopeptidase and serine-type endopeptidase families, were found at higher expression levels in the parasitized host midgut comparing with nonparasitized hosts. Moreover, some immune genes, particularly those involved in the Toll and Imd pathways, also exhibited high expression levels after L.boulardi parasitization. Our study provides large-scale transcriptome data and identifies sets of DEGs between parasitized and nonparasitized host midgut tissues at 24 h and 48 h post L. boulardi parasitization. These resources help improve our understanding of how parasitoid infection affects the nutrient components in the hosts.


Subject(s)
Animal Nutritional Physiological Phenomena , Drosophila melanogaster/genetics , Host-Parasite Interactions , Transcriptome , Wasps/pathogenicity , Animals , Drosophila melanogaster/parasitology , Female
4.
Nat Commun ; 12(1): 2453, 2021 04 27.
Article in English | MEDLINE | ID: mdl-33907186

ABSTRACT

Parasitoid wasps inflict widespread death upon the insect world. Hundreds of thousands of parasitoid wasp species kill a vast range of insect species. Insects have evolved defensive responses to the threat of wasps, some cellular and some behavioral. Here we find an unexpected response of adult Drosophila to the presence of certain parasitoid wasps: accelerated mating behavior. Flies exposed to certain wasp species begin mating more quickly. The effect is mediated via changes in the behavior of the female fly and depends on visual perception. The sight of wasps induces the dramatic upregulation in the fly nervous system of a gene that encodes a 41-amino acid micropeptide. Mutational analysis reveals that the gene is essential to the behavioral response of the fly. Our work provides a foundation for further exploration of how the activation of visual circuits by the sight of a wasp alters both sexual behavior and gene expression.


Subject(s)
Drosophila Proteins/genetics , Drosophila melanogaster/genetics , Drosophila simulans/genetics , Drosophila/genetics , Receptors, Ionotropic Glutamate/genetics , Receptors, Odorant/genetics , Sexual Behavior, Animal/physiology , Wasps/pathogenicity , Adaptation, Physiological , Animals , Animals, Genetically Modified , Carnivory/physiology , Drosophila/metabolism , Drosophila/parasitology , Drosophila Proteins/deficiency , Drosophila Proteins/metabolism , Drosophila melanogaster/metabolism , Drosophila melanogaster/parasitology , Drosophila simulans/metabolism , Drosophila simulans/parasitology , Female , Fertility/genetics , Gene Expression Regulation , Male , Neurons/cytology , Neurons/metabolism , Pattern Recognition, Visual/physiology , Receptors, Ionotropic Glutamate/deficiency , Receptors, Odorant/deficiency , Wasps/physiology , beta-Carotene 15,15'-Monooxygenase/genetics , beta-Carotene 15,15'-Monooxygenase/metabolism
5.
Arch Insect Biochem Physiol ; 107(2): e21786, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33818830

ABSTRACT

Cotesia kariyai (Ck) larvae implanted into the body cavity of the Mythimna separata (armyworm) larvae get melanized and encapsulated after adhesion by hemocytes called hyperspread cells (HSCs). The present study showed that HSCs could not adhere to the implanted Ck larvae in armyworm larvae after injection of Ck polydnavirus (CkPDV) + venom (V), thus melanization and encapsulation could not occur. A C-type lectin called Mys-IML of the host armyworm larvae was considered to be involved in the recognition of foreign substances which always expressed in hemocytes. The CkPDV DNA encodes a C-type lectin called Cky811 that has high amino acid homology to Mys-IML. HSCs did not adhere when CkPDV + V was mixed with the hemolymph of armyworm larvae on glass slides and incubated in vitro, but the addition of anti-Cky811 antibody enabled HSCs to adhere. The messenger RNA (mRNA) expression of Mys-IML in armyworm larvae injected with CkPDV + V became undetectable by 6 h. On the contrary, Cky811 mRNA was well expressed in the hemocytes of armyworm larvae injected with CkPDV + V from 0.5 to 6 h. Cky811 protein was also detected in the crude extracts from Ck venom gland + Ck venom reservoir, suggesting that these proteins regulate foreign substance recognition by the armyworm within 0.5 h. These results suggest that CkPDV + V suppresses mRNA expression of Mys-IML, and that Cky811 protein expressed in hemocytes regulates foreign substance recognition of Mys-IML, resulting in inhibition of the downstream reaction steps: HSCs adhesion, melanization, and encapsulation.


Subject(s)
Lectins, C-Type/immunology , Moths/parasitology , Polydnaviridae , Wasps , Animals , Antibodies, Viral/metabolism , Hemocytes/immunology , Hemocytes/metabolism , Host-Parasite Interactions/immunology , Immunity , Larva/immunology , Larva/metabolism , Larva/parasitology , Lectins, C-Type/metabolism , Moths/immunology , Polydnaviridae/metabolism , Viral Proteins/immunology , Viral Proteins/metabolism , Wasps/pathogenicity , Wasps/virology
6.
Sci Rep ; 11(1): 5032, 2021 03 03.
Article in English | MEDLINE | ID: mdl-33658582

ABSTRACT

During oviposition, ectoparasitoid wasps not only inject their eggs but also a complex mixture of proteins and peptides (venom) in order to regulate the host physiology to benefit their progeny. Although several endoparasitoid venom proteins have been identified, little is known about the components of ectoparasitoid venom. To characterize the protein composition of Torymus sinensis Kamijo (Hymenoptera: Torymidae) venom, we used an integrated transcriptomic and proteomic approach and identified 143 venom proteins. Moreover, focusing on venom gland transcriptome, we selected additional 52 transcripts encoding putative venom proteins. As in other parasitoid venoms, hydrolases, including proteases, phosphatases, esterases, and nucleases, constitute the most abundant families in T. sinensis venom, followed by protease inhibitors. These proteins are potentially involved in the complex parasitic syndrome, with different effects on the immune system, physiological processes and development of the host, and contribute to provide nutrients to the parasitoid progeny. Although additional in vivo studies are needed, initial findings offer important information about venom factors and their putative host effects, which are essential to ensure the success of parasitism.


Subject(s)
Deoxyribonucleases/genetics , Esterases/genetics , Insect Proteins/genetics , Peptide Hydrolases/genetics , Phosphoric Monoester Hydrolases/genetics , Proteome/genetics , Wasp Venoms/chemistry , Animals , Deoxyribonucleases/classification , Deoxyribonucleases/isolation & purification , Deoxyribonucleases/metabolism , Esterases/classification , Esterases/isolation & purification , Esterases/metabolism , Gene Ontology , Insect Proteins/classification , Insect Proteins/isolation & purification , Insect Proteins/metabolism , Molecular Sequence Annotation , Oviposition/physiology , Peptide Hydrolases/classification , Peptide Hydrolases/isolation & purification , Peptide Hydrolases/metabolism , Phosphoric Monoester Hydrolases/classification , Phosphoric Monoester Hydrolases/isolation & purification , Phosphoric Monoester Hydrolases/metabolism , Protease Inhibitors/classification , Protease Inhibitors/isolation & purification , Protease Inhibitors/metabolism , Proteome/classification , Proteome/isolation & purification , Proteome/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Transcriptome , Wasp Venoms/toxicity , Wasps/chemistry , Wasps/pathogenicity , Wasps/physiology
7.
PLoS One ; 15(12): e0241530, 2020.
Article in English | MEDLINE | ID: mdl-33332420

ABSTRACT

Maize, Zea mays L., is the most abundant field crop in China. Aphids are the most economically damaging pest on maize, particularly in the maize agri-ecosystems of Jilin Province, northeastern China. Parasitic wasps are important natural enemies of aphids, but limited information exists about their species composition, richness and seasonal dynamics in northeastern China. In this study, the population dynamics of maize aphids and parasitoid wasps were assessed in relation to each other during the summer seasons of two consecutive years, 2018 and 2019. We selected maize fields in the Changchun, Songyuan, Huinan and Gongzhuling areas of Jilin Province. Four species of aphids were recorded from these maize fields: Rhopalosiphum padi (L), Rhopalosiphum maidis (Fitch), Aphis gossypii Glover and Macrosiphum miscanthi (Takahashi). The dominant species in each of the four areas were R. maids (Filch) and R. padi in Changchun, R. padi in Songyuan, A. gossypii and R. padi in Huinan, and A.gossypii and R. padi in Gongzhuling. We delineated a species complex made up of primary parasitoids and hyperparasitoids associated with maize aphids. The primary parasitoids Lysiphlebus testaceipes, Binodoxys communis and Aphelinus albipodus together formed approximately 85.3% of the parasitoid complex. Pachyneuron aphidis, Phaenoglyphis villosa, Syrphophagus taeniatus and Asaphes suspensus made up the hyperparasitoids. Of the primary parasitoids, L. testaceipes was the dominant species (81.31%). Of the hyperparasitoid group, P. villosa was the dominant species (68.42%). Parasitism rates followed the fluctuation of the aphid population. The highest parasitic rate was observed during the peak period of cotton aphids. In this paper, the occurrence dynamics and dominant species of aphids and the dynamics of parasitic natural enemies of aphids in maize fields in Jilin Province are, for the first time, systematically reported. This study provides important information for the establishment and promotion of aphid biological control in maize fields.


Subject(s)
Aphids/parasitology , Aphids/pathogenicity , Wasps/pathogenicity , Zea mays/parasitology , Animals , Aphids/classification , China , Ecosystem , Host-Parasite Interactions , Pest Control, Biological , Population Dynamics , Seasons , Species Specificity , Wasps/classification
8.
Sci Rep ; 10(1): 19096, 2020 11 05.
Article in English | MEDLINE | ID: mdl-33154398

ABSTRACT

Uncertainty about the taxonomic status and the specificity of a species commonly prevent its consideration as a candidate for biological control of pest organisms. Here we use a combination of molecular analysis and crossing experiments to gather evidence that the parasitoid wasp Ganaspis brasiliensis, a candidate for biological control of the invasive spotted wing drosophila Drosophila suzukii, is a complex of at least two cryptic species. Complementary experiments demonstrate that individuals from one genetic group readily parasitize several drosophila species regardless of their food source while individuals from the other one are almost exclusively specific to larvae feeding in ripening fruits. Because only D. suzukii attacks ripening fruits in its area of invasion, parasitoids from this second group appear to be well suited as a biological control agent. Our study demonstrates the need for a combination of biosystematics with biological and ecological investigations for the development of safe and efficient biological control programs.


Subject(s)
Biological Control Agents , Drosophila/parasitology , Drosophila/pathogenicity , Wasps/physiology , Wasps/pathogenicity , Animals , China , Ecosystem , Female , Fruit/parasitology , Genetics, Population , Genome, Insect , Haplotypes , Host-Parasite Interactions/genetics , Introduced Species , Japan , Male , Species Specificity , Wasps/genetics
9.
Nat Commun ; 11(1): 4483, 2020 09 08.
Article in English | MEDLINE | ID: mdl-32900993

ABSTRACT

The Drosophila lymph gland, the larval hematopoietic organ comprised of prohemocytes and mature hemocytes, has been a valuable model for understanding mechanisms underlying hematopoiesis and immunity. Three types of mature hemocytes have been characterized in the lymph gland: plasmatocytes, lamellocytes, and crystal cells, which are analogous to vertebrate myeloid cells, yet molecular underpinnings of the lymph gland hemocytes have been less investigated. Here, we use single-cell RNA sequencing to comprehensively analyze heterogeneity of developing hemocytes in the lymph gland, and discover previously undescribed hemocyte types including adipohemocytes, stem-like prohemocytes, and intermediate prohemocytes. Additionally, we identify the developmental trajectory of hemocytes during normal development as well as the emergence of the lamellocyte lineage following active cellular immunity caused by wasp infestation. Finally, we establish similarities and differences between embryonically derived- and larval lymph gland hemocytes. Altogether, our study provides detailed insights into the hemocyte development and cellular immune responses at single-cell resolution.


Subject(s)
Drosophila melanogaster/cytology , Drosophila melanogaster/genetics , Hemocytes/cytology , Hemocytes/metabolism , Transcriptome , Animals , Animals, Genetically Modified , Cell Differentiation/genetics , Cell Lineage/genetics , Drosophila melanogaster/metabolism , Ectoparasitic Infestations/genetics , Ectoparasitic Infestations/metabolism , Ectoparasitic Infestations/pathology , Gene Expression Profiling , Hematopoiesis/genetics , Host-Parasite Interactions/genetics , Host-Parasite Interactions/physiology , Lymphoid Tissue/cytology , Lymphoid Tissue/metabolism , Lymphoid Tissue/parasitology , RNA-Seq , Single-Cell Analysis , Wasps/pathogenicity
10.
Heredity (Edinb) ; 124(4): 592-602, 2020 04.
Article in English | MEDLINE | ID: mdl-31896821

ABSTRACT

The ability of an insect to survive attack by natural enemies can be modulated by the presence of defensive symbionts. Study of aphid-symbiont-enemy interactions has indicated that protection may depend on the interplay of symbiont, host and attacking parasite genotypes. However, the importance of these interactions is poorly understood outside of this model system. Here, we study interactions within a Drosophila model system, in which Spiroplasma protect their host against parasitoid wasps and nematodes. We examine whether the strength of protection conferred by Spiroplasma to its host, Drosophila melanogaster varies with strain of attacking Leptopilina heterotoma wasp. We perform this analysis in the presence and absence of ethanol, an environmental factor that also impacts the outcome of parasitism. We observed that Spiroplasma killed all strains of wasp. However, the protection produced by Spiroplasma following wasp attack depended on wasp strain. A composite measure of protection, including both the chance of the fly surviving attack and the relative fecundity/fertility of the survivors, varied from a <4% positive effect of the symbiont following attack of the fly host by the Lh14 strain of wasp to 21% for the Lh-Fr strain in the absence of ethanol. We also observed that environmental ethanol altered the pattern of protection against wasp strains. These data indicate that the dynamics of the Spiroplasma-Drosophila-wasp tripartite interaction depend upon the genetic diversity within the attacking wasp population, and that prediction of symbiont dynamics in natural systems will thus require analysis across natural enemy genotypes and levels of environmental ethanol.


Subject(s)
Drosophila melanogaster/microbiology , Spiroplasma , Symbiosis , Wasps , Animals , Drosophila melanogaster/parasitology , Ethanol , Genotype , Spiroplasma/physiology , Wasps/genetics , Wasps/pathogenicity
11.
Mol Genet Genomics ; 295(1): 107-120, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31506717

ABSTRACT

The oriental gall wasp Dryocosmus kuriphilus represents a limiting pest for the European Chestnut (Castanea sativa, Fagaceae) as it creates severe yield losses. The European Chestnut is a deciduous tree, having major social, economic and environmental importance in Southern Europe, covering an area of 2.53 million hectares, including 75,000 ha devoted to fruit production. Cultivars show different susceptibility and very few are resistant to gall wasp. To deeply investigate the plant response and understand which factors can lead the plant to develop or not the gall, the study of transcriptome is basic (fundamental). To date, little transcriptomic information are available for C. sativa species. Hence, we present a de novo assembly of the chestnut transcriptome of the resistant Euro-Japanese hybrid 'Bouche de Bétizac' (BB) and the susceptible cultivar 'Madonna' (M), collecting RNA from buds at different stages of budburst. The two transcriptomes were assembled into 34,081 (BB) and 30,605 (M) unigenes, respectively. The former was used as a reference sequence for further characterization analyses, highlighting the presence of 1444 putative resistance gene analogs (RGAs) and about 1135 unigenes, as putative MiRNA targets. A global quantitative transcriptome profiling comparing the resistant and the susceptible cultivars, in the presence or not of the gall wasp, revealed some GO enrichments as "response to stimulus" (GO:0050896), and "developmental processes" (e.g., post-embryonic development, GO:0009791). Many up-regulated genes appeared to be transcription factors (e.g., RAV1, AP2/ERF, WRKY33) or protein regulators (e.g., RAPTOR1B) and storage proteins (e.g., LEA D29) involved in "post-embryonic development". Our analysis was able to provide a large amount of information, including 7k simple sequence repeat (SSR) and 335k single-nucleotide polymorphism (SNP)/INDEL markers, and generated the first reference unigene catalog for the European Chestnut. The transcriptome data for C. sativa will contribute to understand the genetic basis of the resistance to gall wasp and will provide useful information for next molecular genetic studies of this species and its relatives.


Subject(s)
Fagaceae/genetics , Transcriptome/genetics , Wasps/pathogenicity , Animals , Europe , Fagaceae/parasitology , Gene Expression Profiling/methods , Microsatellite Repeats/genetics , Molecular Sequence Annotation/methods , Plant Diseases/parasitology , Polymorphism, Single Nucleotide/genetics , Transcription Factors/genetics , Trees/genetics , Trees/parasitology , Up-Regulation/genetics
12.
Genomics ; 112(2): 1096-1104, 2020 03.
Article in English | MEDLINE | ID: mdl-31247332

ABSTRACT

Hymenopteran parasitoid wasps are a diverse collection of species that infect arthropod hosts and use factors found in their venoms to manipulate host immune responses, physiology, and behaviour. Whole parasitoid venoms have been profiled using proteomic approaches, and here we present a bioinformatic characterization of the venom protein content from Ganaspis sp. 1, a parasitoid that infects flies of the genus Drosophila. We find evidence that diverse evolutionary processes including multifunctionalization, co-option, gene duplication, and horizontal gene transfer may be acting in concert to drive venom gene evolution in Ganaspis sp.1. One major role of parasitoid wasp venom is host immune evasion. We previously demonstrated that Ganaspis sp. 1 venom inhibits immune cell activation in infected Drosophila melanogaster hosts, and our current analysis has uncovered additional predicted virulence functions. Overall, this analysis represents an important step towards understanding the composition and activity of parasitoid wasp venoms.


Subject(s)
Arthropod Venoms/genetics , Evolution, Molecular , Wasps/genetics , Animals , Arthropod Venoms/metabolism , Drosophila melanogaster/immunology , Drosophila melanogaster/parasitology , Gene Duplication , Gene Transfer, Horizontal , Immune Evasion , Proteome/genetics , Proteome/metabolism , Wasps/pathogenicity
13.
G3 (Bethesda) ; 10(1): 1-12, 2020 01 07.
Article in English | MEDLINE | ID: mdl-31676506

ABSTRACT

Leptopilina heterotoma are obligate parasitoid wasps that develop in the body of their Drosophila hosts. During oviposition, female wasps introduce venom into the larval hosts' body cavity. The venom contains discrete, 300 nm-wide, mixed-strategy extracellular vesicles (MSEVs), until recently referred to as virus-like particles. While the crucial immune suppressive functions of L. heterotoma MSEVs have remained undisputed, their biotic nature and origin still remain controversial. In recent proteomics analyses of L. heterotoma MSEVs, we identified 161 proteins in three classes: conserved eukaryotic proteins, infection and immunity related proteins, and proteins without clear annotation. Here we report 246 additional proteins from the L. heterotoma MSEV proteome. An enrichment analysis of the entire proteome supports vesicular nature of these structures. Sequences for more than 90% of these proteins are present in the whole-body transcriptome. Sequencing and de novo assembly of the 460 Mb-sized L. heterotoma genome revealed 90% of MSEV proteins have coding regions within the genomic scaffolds. Altogether, these results explain the stable association of MSEVs with their wasps, and like other wasp structures, their vertical inheritance. While our results do not rule out a viral origin of MSEVs, they suggest that a similar strategy for co-opting cellular machinery for immune suppression may be shared by other wasps to gain advantage over their hosts. These results are relevant to our understanding of the evolution of figitid and related wasp species.


Subject(s)
Extracellular Vesicles/genetics , Insect Proteins/genetics , Wasp Venoms/genetics , Wasps/genetics , Animals , Drosophila/immunology , Drosophila/parasitology , Extracellular Vesicles/metabolism , Female , Insect Proteins/metabolism , Male , Proteome/genetics , Proteome/metabolism , Transcriptome , Wasp Venoms/metabolism , Wasps/pathogenicity
14.
G3 (Bethesda) ; 10(1): 165-175, 2020 01 07.
Article in English | MEDLINE | ID: mdl-31685524

ABSTRACT

Immune priming occurs when a past infection experience leads to a more effective immune response upon a secondary exposure to the infection or pathogen. In some instances, parents are able to transmit immune priming to their offspring, creating a subsequent generation with a superior immune capability, through processes that are not yet fully understood. Using a parasitoid wasp, which infects larval stages of Drosophila melanogaster, we describe an example of an intergenerational inheritance of immune priming. This phenomenon is anticipatory in nature and does not rely on parental infection, but rather, when adult fruit flies are cohabitated with a parasitic wasp, they produce offspring that are more capable of mounting a successful immune response against a parasitic macro-infection. This increase in offspring survival correlates with a more rapid induction of lamellocytes, a specialized immune cell. RNA-sequencing of the female germline identifies several differentially expressed genes following wasp exposure, including the peptiodoglycan recognition protein-LB (PGRP-LB). We find that genetic manipulation of maternal PGRP-LB identifies this gene as a key element in this intergenerational phenotype.


Subject(s)
Disease Resistance/genetics , Drosophila melanogaster/genetics , Maternal Inheritance , Animals , Carrier Proteins/genetics , Carrier Proteins/metabolism , Drosophila melanogaster/immunology , Drosophila melanogaster/parasitology , Female , Oogonia/metabolism , Wasps/pathogenicity
15.
PLoS One ; 14(12): e0226485, 2019.
Article in English | MEDLINE | ID: mdl-31869362

ABSTRACT

Body size reduction, also known as miniaturization, is an important evolutionary process that affects a number of physiological and phenotypic traits and helps animals conquer new ecological niches. However, this process is poorly understood at the molecular level. Here, we report genomic and transcriptomic features of arguably the smallest known insect-the parasitoid wasp, Megaphragma amalphitanum (Hymenoptera: Trichogrammatidae). In contrast to expectations, we find that the genome and transcriptome sizes of this parasitoid wasp are comparable to other members of the Chalcidoidea superfamily. Moreover, compared to other chalcid wasps the gene content of M. amalphitanum is remarkably conserved. Intriguingly, we observed significant changes in M. amalphitanum transposable element dynamics over time, in which an initial burst was followed by suppression of activity, possibly due to a recent reinforcement of the genome defense machinery. Overall, while the M. amalphitanum genomic data reveal certain features that may be linked to the unusual biological properties of this organism, miniaturization is not associated with a large decrease in genome complexity.


Subject(s)
Body Size/genetics , Genome, Insect , Wasps/genetics , Adaptation, Biological/genetics , Animals , Chromosome Mapping , Ecosystem , Evolution, Molecular , Genes, Insect , Genetic Speciation , Host-Parasite Interactions/genetics , Immune System/metabolism , Molecular Sequence Annotation , Sequence Analysis, DNA , Transcriptome/genetics , Venoms/genetics , Wasps/anatomy & histology , Wasps/immunology , Wasps/pathogenicity
16.
PLoS Genet ; 15(11): e1008398, 2019 11.
Article in English | MEDLINE | ID: mdl-31682601

ABSTRACT

Galls are plant tissues whose development is induced by another organism for the inducer's benefit. 30,000 arthropod species induce galls, and in most cases the inducing effectors and target plant systems are unknown. Cynipid gall wasps are a speciose monophyletic radiation that induce structurally complex galls on oaks and other plants. We used a model system comprising the gall wasp Biorhiza pallida and the oak Quercus robur to characterise inducer and host plant gene expression at defined stages through the development of galled and ungalled plant tissues, and tested alternative hypotheses for the origin and type of galling effectors and plant metabolic pathways involved. Oak gene expression patterns diverged markedly during development of galled and normal buds. Young galls showed elevated expression of oak genes similar to legume root nodule Nod factor-induced early nodulin (ENOD) genes and developmental parallels with oak buds. In contrast, mature galls showed substantially different patterns of gene expression to mature leaves. While most oak transcripts could be functionally annotated, many gall wasp transcripts of interest were novel. We found no evidence in the gall wasp for involvement of third-party symbionts in gall induction, for effector delivery using virus-like-particles, or for gallwasp expression of genes coding for plant hormones. Many differentially and highly expressed genes in young larvae encoded secretory peptides, which we hypothesise are effector proteins exported to plant tissues. Specifically, we propose that host arabinogalactan proteins and gall wasp chitinases interact in young galls to generate a somatic embryogenesis-like process in oak tissues surrounding the gall wasp larvae. Gall wasp larvae also expressed genes encoding multiple plant cell wall degrading enzymes (PCWDEs). These have functional orthologues in other gall inducing cynipids but not in figitid parasitoid sister groups, suggesting that they may be evolutionary innovations associated with cynipid gall induction.


Subject(s)
Host-Parasite Interactions/genetics , Plant Tumors/genetics , Quercus/genetics , Wasps/genetics , Animals , Gene Expression Regulation, Plant/genetics , Genomics , Larva/genetics , Metabolic Networks and Pathways/genetics , Phenotype , Plant Growth Regulators/genetics , Plant Leaves , Plant Tumors/parasitology , Quercus/parasitology , Wasps/pathogenicity
17.
PLoS Pathog ; 15(10): e1008084, 2019 10.
Article in English | MEDLINE | ID: mdl-31589659

ABSTRACT

It is common to find abundant genetic variation in host resistance and parasite infectivity within populations, with the outcome of infection frequently depending on genotype-specific interactions. Underlying these effects are complex immune defenses that are under the control of both host and parasite genes. We have found extensive variation in Drosophila melanogaster's immune response against the parasitoid wasp Leptopilina boulardi. Some aspects of the immune response, such as phenoloxidase activity, are predominantly affected by the host genotype. Some, such as upregulation of the complement-like protein Tep1, are controlled by the parasite genotype. Others, like the differentiation of immune cells called lamellocytes, depend on the specific combination of host and parasite genotypes. These observations illustrate how the outcome of infection depends on independent genetic effects on different aspects of host immunity. As parasite-killing results from the concerted action of different components of the immune response, these observations provide a physiological mechanism to generate phenomena like epistasis and genotype-interactions that underlie models of coevolution.


Subject(s)
Drosophila melanogaster/immunology , Drosophila melanogaster/parasitology , Hemocytes/immunology , Host-Parasite Interactions , Immunity, Humoral/immunology , Wasps/immunology , Animals , Drosophila melanogaster/genetics , Female , Genotype , Hemocytes/parasitology , Male , Monophenol Monooxygenase/metabolism , Wasps/genetics , Wasps/pathogenicity
18.
Eur Cytokine Netw ; 30(1): 34-38, 2019 Mar 01.
Article in English | MEDLINE | ID: mdl-31074416

ABSTRACT

This study mainly to explore the change of serum cytokines in wasp sting patients and the potential correlation between cytokines and acute kidney injury (AKI) due to wasp stings. The levels of IL-2, IL-4, IL-6, IL-10, TNF-α, and IFN-γ in 33 wasp sting and 24 healthy people were measured by flow cytometry, the level of IL-17 was detected by enzyme-linked immunosorbent assay and the laboratory examination including inflammatory indicators, muscle enzyme markers, and renal function were detected by automatic biochemical analyzer, blood analyzer, and urine analyzer. The wasp sting patients were divided into AKI (n = 10) and non-AKI groups (n = 23). The correlation between the levels of serum cytokines and laboratory examination results was analyzed. The levels of IL-2, IL-6, IL-10, IFN-γ, and IL-17 were statistically increased in wasp sting patients compared with the controls (P < 0.05). IL-6, IL-10, and IL-17 levels were markedly increased in the AKI group compared with the non-AKI group (P < 0.05). Moreover, compared with non-AKI group, inflammatory markers and muscle enzyme markers were more abnormal in the AKI group. The positive rate of urinary occult blood in the AKI group was higher than that in the non-AKI group. The levels of IL-2, IL-4, IL-6, IFN-γ, and IL-17 correlated positively with white blood cell counts. The levels of IL-2, IL-4, IL-10, IFN-γ, and IL-17 correlated positively with the levels of serum creatinine. The levels of IL-2, IL-4, IL-10, IL-10, and IFN-γ correlated positively with the levels of C-reactive protein. The levels of IL-10, and IFN-γ correlated positively with urinary occult blood. Conclusion: Elevated levels of cytokines in wasp sting patients might be involved in the development and progression of acute kidney injury.


Subject(s)
Acute Kidney Injury/blood , C-Reactive Protein/analysis , Creatinine/blood , Cytokines/blood , Insect Bites and Stings/blood , Acute Kidney Injury/pathology , Adult , Aged , Aged, 80 and over , Animals , Female , Humans , Interferon-gamma/blood , Interleukin-10/blood , Interleukin-2/blood , Interleukin-4/blood , Interleukin-6/blood , Leukocyte Count , Male , Middle Aged , Muscle, Skeletal/enzymology , Occult Blood , Tumor Necrosis Factor-alpha/blood , Wasps/pathogenicity , Young Adult
19.
Biochem Biophys Res Commun ; 502(3): 415-421, 2018 07 20.
Article in English | MEDLINE | ID: mdl-29856996

ABSTRACT

Acute inflammation can cause serious tissue damage and disease in physiologically-challenged organisms. The precise mechanisms leading to these detrimental effects remain to be determined. In this study, we utilize a reproducible means to induce cellular immune activity in Drosophila larvae in response to mechanical stress. That is, forceps squeeze-administered stress induces lamellocytes, a defensive hemocyte type that normally appears in response to wasp infestation of larvae. The posterior signaling center (PSC) is a cellular microenvironment in the larval hematopoietic lymph gland that is vital for lamellocyte induction upon parasitoid attack. However, we found the PSC was not required for mechanical stress-induced lamellocyte production. In addition, we observed that mechanical injury caused a systemic expression of Unpaired3. This cytokine is both necessary and sufficient to activate the cellular immune response to the imposed stress. These findings provide new insights into the communication between injured tissues and immune system induction, using stress-challenged Drosophila larvae as a tractable model system.


Subject(s)
Drosophila melanogaster/immunology , Drosophila melanogaster/metabolism , Animals , Animals, Genetically Modified , Cellular Microenvironment , Drosophila Proteins/metabolism , Drosophila melanogaster/parasitology , Hemocytes/cytology , Hemocytes/immunology , Immunity, Cellular , Janus Kinases/metabolism , Larva/immunology , Larva/metabolism , Larva/parasitology , STAT Transcription Factors/metabolism , Signal Transduction , Stress, Mechanical , Transcription Factors/metabolism , Wasps/immunology , Wasps/pathogenicity
20.
BMC Biol ; 16(1): 54, 2018 05 18.
Article in English | MEDLINE | ID: mdl-29776407

ABSTRACT

BACKGROUND: Trichogrammatids are minute parasitoid wasps that develop within other insect eggs. They are less than half a millimeter long, smaller than some protozoans. The Trichogrammatidae are one of the earliest branching families of Chalcidoidea: a diverse superfamily of approximately half a million species of parasitoid wasps, proposed to have evolved from a miniaturized ancestor. Trichogramma are frequently used in agriculture, released as biological control agents against major moth and butterfly pests. Additionally, Trichogramma are well known for their symbiotic bacteria that induce asexual reproduction in infected females. Knowledge of the genome sequence of Trichogramma is a major step towards further understanding its biology and potential applications in pest control. RESULTS: We report the 195-Mb genome sequence of Trichogramma pretiosum and uncover signatures of miniaturization and adaptation in Trichogramma and related parasitoids. Comparative analyses reveal relatively rapid evolution of proteins involved in ribosome biogenesis and function, transcriptional regulation, and ploidy regulation. Chalcids also show loss or especially rapid evolution of 285 gene clusters conserved in other Hymenoptera, including many that are involved in signal transduction and embryonic development. Comparisons between sexual and asexual lineages of Trichogramma pretiosum reveal that there is no strong evidence for genome degradation (e.g., gene loss) in the asexual lineage, although it does contain a lower repeat content than the sexual lineage. Trichogramma shows particularly rapid genome evolution compared to other hymenopterans. We speculate these changes reflect adaptations to miniaturization, and to life as a specialized egg parasitoid. CONCLUSIONS: The genomes of Trichogramma and related parasitoids are a valuable resource for future studies of these diverse and economically important insects, including explorations of parasitoid biology, symbiosis, asexuality, biological control, and the evolution of miniaturization. Understanding the molecular determinants of parasitism can also inform mass rearing of Trichogramma and other parasitoids for biological control.


Subject(s)
Evolution, Molecular , Pest Control, Biological , Wasps/classification , Wasps/genetics , Animals , Genomics , Moths/parasitology , Phylogeny , Wasps/pathogenicity , Whole Genome Sequencing/methods
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