Copidosoma floridanum
 | This article's lead section may be too short to adequately summarize the key points. (November 2013) |
| Copidosoma floridanum | |
|---|---|
Scientific classification 
| |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Hymenoptera |
| Family: | Encyrtidae |
| Genus: | Copidosoma |
| Species: | C. floridanum
|
| Binomial name | |
| Copidosoma floridanum Ashmead, 1900
| |
| Synonyms[1] | |
| |
Copidosoma floridanum is a species of wasp in the family Encyrtidae and is primarily a parasitoid of moths in the subfamily Plusiinae. It has the largest recorded brood of any parasitoidal insect, at 3,055 individuals.[2] The life cycle begins when a female oviposits into the eggs of a suitable host species, laying one or two eggs per host. Each egg divides repeatedly and develops into a brood of multiple individuals, a phenomenon called polyembryony. The larvae grow inside their host, breaking free at the end of the host's own larval stage.[2]
A cosmopolitan species, Copidosoma floridanum is distributed worldwide. Because of its significance to agriculture as pest control and its phylogenic relationship with other important species, the wasp's genome is being sequenced by the Human Genome Sequencing Center as part of the i5K project,[3] which aims to sequence the genomes of 5,000 arthropods.[4]
Description
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Taxonomy
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Behavior
Reproductive altruism
As a putatively eusocial species, C. floridanum embodies only two of the four behavioral characteristics that characterize genuine eusociality: larvae live in groups, and there is reproductive division of labor, or reproductive altruism.[5] The second characteristic, reproductive altruism, is, in these wasps, manifested as a sterile soldier caste that has the sole purpose of protecting their reproductive clonal siblings throughout their larval stage. Reproductive altruism behavior plays a major role in the survival and reproductive success of C. floridanum. This species displays haplodiploid sex determination, which increases relatedness among females from 0.5 to 0.75 because males develop from unfertilized eggs and are therefore haploid while females develop from normally fertilized eggs and are therefore diploid. So, as a result of eusocial progeny allocation and a distinctive type of clonal development in parasitized hosts, polyembryonic wasps including C. floridanum are able to thrive.[6][7][8] Additionally, these wasps modify their caste ratios in response to interspecific competition, creating a trade-off between reproduction and defense, as the wasps adapt to the levels of competition within the group.[6]
Aggression and spite
C. floridanum produce eggs that divide clonally to produce larger broods. The polyembryonic wasp caste system consists of two separate groups: some of the embryos in a clone mature into reproductive larvae that ultimately develop into adults, while the other group consists of sterile soldier larvae that protect siblings from competitors.[9] At this ecological level, the soldiers’ reproductive altruism is tied to clone-level allocation to defense; thus, in order to maximize the reproductive success of the siblings, soldiers risk their own chances of reproductive success (with no conflict between the soldiers themselves) [9] In his study, Giron argues that soldier aggression in this wasp species is inversely related to competitors’ genetic relatedness, without respect to levels of resource competition.[9] In a later study, Giron sought to differentiate between the aggression of female and male soldiers, finding that the latter group is non-aggressive toward all competitors.[9]
Polyembryonic wasps, including C. floridanum, exhibit spite through instances of precocious larval development.[10] Spite provides an explanation for how natural selection can favor harmful behaviors that are costly to both the actor and the recipient; spite is typically considered a form of altruism that benefits a secondary recipient.[11] Two criteria demonstrate that spite is truly occurring: (i) the behavior is truly costly to the actor and does not provide a long-term direct benefit; and (ii) harming behaviors are directed toward relatively unrelated individuals.[11]
In C. floridanum, the process takes place in the following manner: the host insect lays two eggs in the eggs of moths, usually one male and one female, which proceed to divide asexually to produce a brood of clonal brothers and clonal sisters.[7] The wasp larvae then mature within the moth caterpillar, utilizing the moth as food throughout growth. Competition for resources limits how many adult wasps can emerge from the host; this indicates that negative relatedness likely exists within the brood. A portion of the larvae do not emerge, who serve as adults who forgo future reproduction in order to kill relatively unrelated opposite-sex siblings maturing in the same host before dying themselves; this special group of adult killers developed precociously.[12] Asymmetrical dispersal (defined as the sex differences in the scale of competition) and asymmetrical relatedness (brothers tend to be more related to sisters than the reverse) most likely serve as the evolutionary resolution of this conflict, in favor of the sisters.[12] This process, most importantly, frees up resources for closer relatives.
Soldier's spite behavior
C. floridanum gain interspecific competitive advantage over other competitors, including Glyptapanteles pallipes and Microplitis demolitor, primarily due to the presence of their soldier caste, whose fitness is limited to the survival of their clonal siblings. Uka studied the interspecific competition between C. floridanum male broods and G. pallipes in order to perceive the defensive strategies of the former group. The C. floridanum progeny survival rate was greater than that of G. pallipes, regardless of the interval of oviposition.[13] C. floridanum gains a competitive advantage through its ability to physiologically suppress or putatively attack its adversaries. First off, they secrete a physiologically suppressive factor form in their labial glands as embryos or even in the tissue of the host and steadily supplied to the hemolymph. This toxic factor causes damage to G. pallipes larvae and ultimately leads to death. More specifically, C. floridanum induces a delay in competitor maturation, along with generating paralysis and weakness (Uki). Physical attack, on the other hand, has not been proven to be effective as a means of killing competitors.[14]
Cellular compatibility of wasp within host
The morula-stage embryo of C. floridanum invades the embryo of the host, utilizing adherent junctions to host cells. This is an effective evolutionary strategy, as other approaches could leave obvious wounds on the host cells, alerting competitors to the presence of this wasp species. As a result, these embryos can invade a phylogenetically distant host embryo (the moth) by taking advantage of the compatibility of its cells with host tissues.[15]
Kin discrimination
During larval development, an extraembryonic membrane surrounds each organism during maturation with the caterpillar host. A series of experiments performed by Giron and Strand proved that this membrane serves as the cue for kin selection; they demonstrated that attack rates were less common with kinship when the membrane was present. When the membrane was removed, attack rates between kin increased.[8] This study additionally demonstrated how the membrane functions as a cue for kin discrimination by switching the membranes between larvae. Researchers found that the soldiers were fooled into not killing relatively unrelated larvae that were encased by an transplanted membrane.
Caste-based identity: genetic and development influences
Recently, studies have been conducted to identify differentially expressed genes in C. floridanum castes that code for identifiable ions and proteins that the sterile soldiers, for instance, share. Soldiers and reproductive larvae express enzymes with the differential usage of proteinase inhibitors and ribosomal proteins.[16] More specifically, odorant binding proteins (OBPs) are utilized for kin recognition, along with the likely usage of toxin-like and SP genes in the ability of soldiers to murder competitors or as immune defense against potential pathogens.[16] The host's molting cycle plays a significant role in determining the identity of precocious and reproductive larvae. More specifically, the C. floridanum young mature in synchrony with specific phases within the moth’s molting cycle. In the early stages of embryonic development, changes within the host’s developmental program intrinsically influence caste determination.[17]
References
- ^ "Synonyms for Copidosoma floridanum". GBIF.org. Retrieved 29 May 2017.
- ^ a b Alvarez, Juan Manuel (15 April 1997). "Chapter 26: Largest Parasitoid Brood". Book of Insect Records. University of Florida. Retrieved 3 September 2013.
- ^ Strand, Michael. "i5K: Copidosoma floridanum". Human Genome Sequencing Center. Baylor College of Medicine. Retrieved 3 September 2013.
- ^ "i5k Project Summary". Human Genome Sequencing Center. Baylor College of Medicine. Retrieved 3 September 2013.
- ^ Wilson and Foster, George F., Edward O. (1978). Caste and Ecology in the Social Insects. Princeton, NJ: Princeton University Press. pp. 3–25.
- ^ a b Harvey, Jeffrey A.; Laura S. Corley; Michael R. Strand (13 July 2000). "Competition induces adaptive shifts in caste ratios of a polyembryonic wasp". Nature. 406: 183–186. doi:10.1038/35018074. PMID 10910357.
- ^ a b Giron, David; Derek W. Dunn; Ian C.W. Hardy; Michael Strand (5 August 2005). "Aggression by polyembryonic wasp soldiers correlates with kinship but not resource competition". Nature. 430: 676–679. doi:10.1038/nature02721. PMID 15295600.
- ^ a b Giron, David; Michael R. Strand (4 May 2004). "Host resistance and the evolution of kin recognition in polyembryonic wasps". The Royal Society: Biology Letters: 395–399.
- ^ a b c d Giron, David; Jeffrey A. Harvey; Jena Anne Johnson; Michael Strand (22 August 2007). "Male soldier caste larvae are non-aggressive in the polyembryonic wasp Copidosoma floridanum". Biology Letters. 3 (4): 431–434. doi:10.1098/rsbl.2007.0199. PMC 2390675. PMID 17535791.
- ^ Gardner, Andy; Ian C. W. Hardy; Peter D. Taylor; Stuart A. West (April 2007). "Spiteful Soldiers and Sex Ratio Conflict in Polyembryonic Parasitoid Wasps". The American Naturalist. 169 (4): 519–533. doi:10.1086/512107.
- ^ a b West, Nicholas B. Davies and John R. Krebs, Stuart A., (1981). An Introduction to Behavioural Ecology. Oxford: Wiley-Blackwell. pp. 308–333, 360–393.
{{cite book}}: CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link) - ^ a b Gardner, Adam A.; S.A. West (2004). "Spite and the scale of competition". J. Evol. Biol.: 1195–1203.
- ^ Uka, Daisuke; Tsuyoshi Hiraoka; Kikuo Iwabuchi (November–December 2006). "Physiological suppression of the larval parasitoid Glyptapanteles pallipes by the polyembryonic parasitoid Copidosoma floridanum". Journal of Insect Physiology. 52 (11–12): 1137–1142. doi:10.1016/j.jinsphys.2006.08.002.
- ^ Uka, Daisuke; Tsuyoshi Hiraoka; Kikuo Iwabuchi (November–December 2006). "Physiological suppression of the larval parasitoid Glyptapanteles pallipes by the polyembryonic parasitoid Copidosoma floridanum". Journal of Insect Physiology. 52 (11–12): 1137–1142. doi:10.1016/j.jinsphys.2006.08.002.
- ^ Nakaguchi, Azusa (12 January 2006). "Compatible invasion of a phylogenetically distant host embryo by a hymenopteran parasitoid embryo". Cell Tissue Res. 324: 167–173. doi:10.1007/s00441-005-0111-2.
- ^ a b Donnell, David M.; Michael R. Strand (February 2006). "Caste-based differences in gene expression in the polyembryonic wasp Copidosoma floridanum". Insect Biochemistry and Molecular Biology. 36 (2): 141–153. doi:10.1016/j.ibmb.2005.11.009.
- ^ Grbc, Miodrag; David Rivers; Michael R Strand (June 1997). "Caste formation in the polyembryonic wasp Copidosoma floridanum (Hymenoptera: Encyrtidae): in vivo and in vitro analysis". Journal of Insect Physiology. 43 (6): 553–565. doi:10.1016/s0022-1910(97)00004-8.
External links
- Zimmer, Carl (14 August 2007). "Lessons From an Insect's Life Cycle: Extreme Sibling Rivalry". NYTimes.com. The New York Times Company. Retrieved 4 September 2013.