scholarly journals Quantifying the unquantifiable: why Hymenoptera – not Coleoptera – is the most speciose animal order

2018 ◽  
Author(s):  
Andrew A. Forbes ◽  
Robin K. Bagley ◽  
Marc A. Beer ◽  
Alaine C. Hippee ◽  
Heather A. Widmayer

AbstractBackgroundWe challenge the oft-repeated claim that the beetles (Coleoptera) are the most species-rich order of animals. Instead, we assert that another order of insects, the Hymenoptera, are more speciose, due in large part to the massively diverse but relatively poorly known parasitoid wasps. The idea that the beetles have more species than other orders is primarily based on their respective collection histories and the relative availability of taxonomic resources, which both disfavor parasitoid wasps. Though it is unreasonable to directly compare numbers of described species in each order, the ecology of parasitic wasps – specifically, their intimate interactions with their hosts – allows for estimation of relative richness. We present a simple logical model that shows how the specialization of many parasitic wasps on their hosts suggests few scenarios in which there would be more beetle species than parasitic wasp species. We couple this model with an accounting of what we call the “genus-specific parasitoid-host ratio” from four well-studied genera of insect hosts, a metric by which to generate extremely conservative estimates of the average number of parasitic wasp species attacking a given beetle or other insect host species. Synthesis of our model with data from real host systems suggests that the Hymenoptera may have 2.5 - 3.2× more species than the Coleoptera. While there are more described species of beetles than all other animals, the Hymenoptera are almost certainly the larger order.

2021 ◽  
Author(s):  
Bertanne Visser ◽  
Cécile Le Lann ◽  
Caroline M. Nieberding ◽  
Mark Lammers ◽  
Daniel A. Hahn ◽  
...  

Ruther et al (2021) evaluated fatty acid synthesis in several parasitic wasp species to test if the general finding that lipogenesis in parasitoids is lacking is upheld (Visser et al 2010 PNAS). As proposed by Visser & Ellers (2008), parasitoids can readily assimilate the triglyceride stores produced by their host. When large triglyceride stores are carried over from larval feeding into adulthood (i.e., up to 30 to 40% of the parasitoid’s dry body weight; Visser et al., 2018, 2021), de novo lipid synthesis from adult feeding is either unnecessary or too costly to maintain, leading to trait loss (Ellers et al., 2012). To test the hypothesis that many parasitoids do not synthesize substantial quantities of fat stores as adults, a previous study used feeding experiments on a wide taxonomic range of insects, including parasitoid wasps, parasitoid flies, a parasitoid beetle, and 65 non-parasitoid species (Visser et al., 2010 and references therein). What is striking is that when compared to non-parasitoid insects, 24 out of 29 evolutionarily distinct parasitoid lineages (Coleoptera, Diptera and Hymenoptera; Visser et al., 2010) did not accumulate significant lipid quantities in adulthood even when fed surplus carbohydrates. When little to no lipids are synthesized de novo by adult parasitoid wasps, this can lead to significant constraints on energy allocation toward key adult functions, such as maintenance, dispersal, and reproduction (Jervis et al., 2008). To our minds, the most important question is ‘why don’t parasitoids accumulate substantial quantities of fat as adults like other insects do, and what does this mean for their life histories?’


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Shimaa A. M. Ebrahim ◽  
Gaëlle J. S. Talross ◽  
John R. Carlson

AbstractParasitoid 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.


2008 ◽  
Vol 98 (4) ◽  
pp. 379-387 ◽  
Author(s):  
T. Klug ◽  
R. Meyhöfer ◽  
M. Kreye ◽  
M. Hommes

AbstractIn spite of the fact that since the end of the eighties, the horse chestnut leafminer,Cameraria ohridella, has established itself throughout Europe, native predators such as ants and birds are not attuned to this neozoic species. In contrast, several parasitic wasp species already started to exploit the invasive horse chestnut leafminer, but until now parasitation rates are quite low, mainly because of asynchrony in the lifecycles of parasitoids and host. Only the removal of leaf litter, in which pupae hibernate, is at the moment a strategy to reduce the infestation level in the next year. Unfortunately, not only hibernating horse chestnut leafminers but also parasitoids are removed, and important resources for biocontrol are unused. In the current study, we investigated the potential efficiency of the horse chestnut leafminer parasitoid complex extracted from leaf litter in defined environments. Parasitoids were released at different densities to investigate density dependence in parasitation rates.Although seven different species were released in our experiments, onlyPnigalio agraulesturned out to be responsible for biocontrol ofC. ohridella. We recorded parasitation rates of up to 35%. Overall, parasitation rates were independent of the leafminer density but increased fourfold if ten times more parasitoid individuals were released. Unfortunately, none of the parasitoid species could be established in the experimental units in the long run. Results are compared to other parasitoid-leafminer systems, and promotion of horse chestnut leafminer parasitoids to support natural selection and biological control of the horse chestnut leafminer is discussed.


2021 ◽  
Author(s):  
Johnny R. Ramroop ◽  
Mary Ellen Heavner ◽  
Zubaidul H. Razzak ◽  
Shubha Govind

AbstractThe wasps Leptopilina heterotoma parasitize and ingest their Drosophila hosts. They produce extracellular vesicles (EVs) in the venom that are packed with proteins, some of which perform immune suppressive functions. EV interactions with blood cells of host larvae are linked to hematopoietic depletion, immune suppression, and parasite success. But how EVs disperse within the host, enter and kill hematopoietic cells are not well understood. Using an antibody marker for L. heterotoma EVs, we show that these parasite-derived structures are readily distributed within the hosts’ hemolymphatic system. EVs converge around the tightly clustered cells of the posterior signaling center (PSC) of the larval lymph gland, a small hematopoietic organ in Drosophila. The PSC serves as a source of developmental signals in naïve animals. In wasp-infected animals, the PSC directs the differentiation of lymph gland progenitors into lamellocytes. These lamellocytes are needed to encapsulate the wasp egg and block parasite development. We found that L. heterotoma infection disassembles the PSC and PSC cells disperse into the disintegrating lymph gland lobes. Genetically manipulated PSC-less lymph glands remain non-responsive and largely intact in the face of L. heterotoma infection. We also show that the larval lymph gland progenitors use the endocytic machinery to internalize EVs. Once inside, L. heterotoma EVs damage the Rab7- and LAMP1-positive late endocytic and phagolysosomal compartments. Rab5 maintains hematopoietic and immune quiescence as Rab5 knockdown results in hematopoietic over-proliferation and ectopic lamellocyte differentiation. Thus, both aspects of anti-parasite immunity, i.e., (a) phagocytosis of the wasp’s immune-suppressive EVs, and (b) progenitor differentiation for wasp egg encapsulation reside in the lymph gland. These results help explain why the lymph gland is specifically and precisely targeted for destruction. The parasite’s simultaneous and multipronged approach to block cellular immunity not only eliminates blood cells, but also tactically blocks the genetic programming needed for supplementary hematopoietic differentiation necessary for host success. In addition to its known functions in hematopoiesis, our results highlight a previously unrecognized phagocytic role of the lymph gland in cellular immunity. EV-mediated virulence strategies described for L. heterotoma are likely to be shared by other parasitoid wasps; their understanding can improve the design and development of novel therapeutics and biopesticides as well as help protect biodiversity.Author summaryParasitoid wasps serve as biological control agents of agricultural insect pests and are worthy of study. Many parasitic wasps develop inside their hosts to emerge as free-living adults. To overcome the resistance of their hosts, parasitic wasps use varied and ingenious strategies such as mimicry, evasion, bioactive venom, virus-like particles, viruses, and extracellular vesicles (EVs). We describe the effects of a unique class of EVs containing virulence proteins and produced in the venom of wasps that parasitize fruit flies of Drosophila species. EVs from Leptopilina heterotoma are widely distributed throughout the Drosophila hosts’ circulatory system after infection. They enter and kill macrophages by destroying the very same subcellular machinery that facilitates their uptake. An important protein in this process, Rab5, is needed to maintain the identity of the macrophage; when Rab5 function is reduced, macrophages turn into a different cell type called lamellocytes. Activities in the EVs can eliminate lamellocytes as well. EVs also interfere with the hosts’ genetic program that promotes lamellocyte differentiation needed to block parasite development. Thus, wasps combine specific preemptive and reactive strategies to deplete their hosts of the very cells that would otherwise sequester and kill them. These findings have applied value in agricultural pest control and medical therapeutics.


2018 ◽  
Author(s):  
Deborah Di Giovanni ◽  
David Lepetit ◽  
Matthieu Boulesteix ◽  
Yohann Coute ◽  
Marc Ravallec ◽  
...  

To circumvent host immune response, some hymenopteran endo-parasitoids produce virus-like structures in their reproductive apparatus that are injected into the host together with the eggs. These viral-like structures are absolutely necessary for the reproduction of these wasps. The viral evolutionary origin of these viral-like particles has been demonstrated in only a few cases of wasp species all belonging to the Ichneumonoidea superfamily. In addition, the nature of the initial virus-wasp association remains unknown for all. This is either because no closely related descendant infects the wasps, because it has not been sampled yet, or because the virus lineage went extinct. In this paper, we show that the virus-like particles (VLPs) produced by endoparasitoids of Drosophila belonging to the Leptopilina genus (superfamily Cynipoidea) do have a viral origin, solving the debate on their origin. Furthermore, the ancestral donor virus still has close relatives infecting one of the wasp species, thus giving us insights on the ecological interaction that possibly allowed the domestication process. Intriguingly, this contemporary virus is both vertically and horizontally transmitted and has the particularity to manipulate the superparasitism behavior of the wasp. This raises the possibility that behavior manipulation has been instrumental in the birth of such association between wasps and viruses.


1998 ◽  
Vol 14 (2) ◽  
pp. 153-176 ◽  
Author(s):  
BJARTE H. JORDAL ◽  
LAWRENCE R. KIRKENDALL

Petioles are not usually thought of as a habitat for wood-boring insects. The large, woody leaf petioles of Neotropical Cecropia trees, however, have a diverse coleopterous fauna: 36 beetle species in three subfamilies of Cerambycidae and Curculionidae were recorded from Cecropia leafstalks in Costa Rica. A high percentage of the petioles were colonized by beetles in many patches, though fewer were colonized in sun-exposed sites. Community composition was dependent on forest type, petiole moisture and geographical location, but not on the species of Cecropia. Species of Scolytinae were most abundant though species of Zygopinae and Lamiinae were found regularly. The host-specific scolytine genus Scolytodes dominated in most localities, although species of Hypothenemus, Coccotrypes and Xylosandrus morigerus occurred frequently. Sympatric species of Scolytodes clearly used different parts of the petioles. Brood sizes of scolytine beetles were extremely low, ranging from two to ten offspring on average. However, mortality due to parasitoid wasps or predators was low, and since fresh leaves fall close to the previously fallen ones, mortality due to dispersal may also be low. Thus, large beetle populations can exist despite extremely low brood sizes.


1983 ◽  
Vol 29 (5) ◽  
pp. 576-583 ◽  
Author(s):  
Jacques F. Fargues ◽  
Pierre H. Robert

The effects on pathogenicity of Metarhizium anisopliae (Metsch.) Sor. following one or more passages through the original and the heterologous insect host species were investigated by using two pathotypes specific for Cetonia aurata L. and Oryctes rhinoceros L., respectively. A significant increase in virulence occurred after a single host passage. Thus, the infection potential of host-passed inocula could be increased by a factor of 10 to 100, and its host-induced adaptation was almost complete after the first in vivo passage. Bacteria located on the integument of the host cadaver were not implicated in this phenomenon. When the fungus was again grown on artificial medium, the loss in virulence was also very fast. Consequently, changes in virulence of the two tested strains seemed to be phenotypic responses implicating inducible enzymatic mechanisms. Nevertheless, the parasitic behaviour of the two pathotypes toward the larvae of the nonsusceptible species was not modified by host passaging through their respective insect hosts. It is concluded that changes in entomopathogenic hyphomycete virulence, resulting from host passage, concern only the naturally susceptible host species.


2010 ◽  
Vol 19 (3) ◽  
pp. 367-379 ◽  
Author(s):  
M. Van Den Berg ◽  
P. Verbaarschot ◽  
S. Hontelez ◽  
L. E. M. Vet ◽  
M. Dicke ◽  
...  

mSphere ◽  
2021 ◽  
Vol 6 (3) ◽  
Author(s):  
Fei Wang ◽  
Bo Yuan ◽  
Shan Xiao ◽  
Jiao Zhang ◽  
Wenxi Jia ◽  
...  

ABSTRACT In this study, many virus-like fragments were obtained from transcriptomes of three wasp species, including Anisopteromalus calandrae (8), Lariophagus distinguendus (3), and Theocolax elegans (18), which can parasitize and control rice weevil Sitophilus oryzae, a serious insect pest of farm-stored grains. By further bioinformatic analysis and sequencing, we identified six novel RNA viruses with complete genomes and named them WWPSRV-1, WWPSRV-2, AcPSRV-1, AcNSRV-1, AcNSRV-2, and LdNSRV-1. PCR-based detection revealed that WWPSRV-1 and WWPSRV-2 had the possibility of interspecies virus transmission, especially WWPSRV-2, which was also present in the rice weevil adults. Phylogenetically, three out of these six viruses appeared to be members of order Picornavirales: WWPSRV-1 belonged to unassigned virus families of this order, whereas WWPSRV-2 and AcPSRV-1 belonged to families Iflaviridae and Dicistroviridae, respectively. The conserved picornavirus-typical domains helicase, protease, and RNA-dependent RNA polymerase could be found in the nonstructural protein encoded by the three viruses, whose genomes consisted of the different numbers of open reading frames (ORFs). The other three RNA viruses could be classified to order Mononegavirales: AcNSRV-1 and AcNSRV-2 belonged to family Lispiviridae, whereas LdNSRV-1 belonged to a big family Rhabdoviridae. The genomes of the three viruses contained at least five ORFs, encoding deduced proteins in the following order: 3′-N-P-M-G-L-5′. All the ORFs were separated by conserved intergenic sequences which likely regulated the transcription termination and initiation. Our findings enhance the understanding of RNA viruses in weevil wasps and set the foundation for the future study of the association among weevils, weevil wasps, and RNA viruses. IMPORTANCE The enormous diversity of RNA viruses in insects is continuously validated. Parasitoid wasps, as biocontrol insects which are widely used against insect pests in agroecosystems, may also carry many “good” RNA viruses. Some RNA viruses in parasitoid wasps have been reported to affect the host wasps or the wasps’ host. Here, six novel RNA viruses with complete genomes were identified in three parasitoid wasps of the rice weevil. One of these viruses was also detected in the rice weevil adults. Phylogenetically, WWPSRV-1 was the first unambiguous detection of Nora-like virus in insect parasitoids. WWPSRV-2 and AcPSRV-1 belong to families Iflaviridae and Dicistroviridae, some viruses of which can result in lethal infections in silkworms and honeybees. The other three RNA viruses belong to order Mononegavirales, which comprises many well-known insect-associated viruses.


2020 ◽  
Author(s):  
Jérémy Gauthier ◽  
Hélène Boulain ◽  
Joke J.F.A. van Vugt ◽  
Lyam Baudry ◽  
Emma Persyn ◽  
...  

AbstractMost endogenous viruses, an important proportion of eukaryote genomes, are doomed to slowly decay. Little is known, however, on how they evolve when they confer a benefit to their host. Bracoviruses are essential for the parasitism success of parasitoid wasps, whose genomes they integrated ~103 million years ago. Here we show, from the assembly of a parasitoid wasp genome, for the first time at a chromosomal scale, that symbiotic bracovirus genes spread to and colonized all the chromosomes. Moreover, large viral clusters are stably maintained suggesting strong evolutionary constraints. Genomic comparison with another wasps revealed that this organization was already established ~53 mya. Transcriptomic analyses highlight temporal synchronization of viral gene expression, leading to particle production. Immune genes are not induced, however, indicating the virus is not perceived as foreign by the wasp. This recognition suggests that no conflicts remain between symbiotic partners when benefits to them converge.


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