| Drosophila innubila | |
|---|---|
| |
| A Drosophila innubila female on mushroom | |
Scientific classification 
| |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Diptera |
| Family: | Drosophilidae |
| Genus: | Drosophila |
| Subgenus: | Drosophila |
| Species: | D. innubila
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| Binomial name | |
| Drosophila innubila Spencer in Patterson, 1943
| |
Drosophila innubila is a species of vinegar fly restricted to high-elevation woodlands in the mountains of the southern USA and Mexico,[1] which it likely colonized during the last glacial period.[2] Drosophila innubila is a kind of mushroom-breeding Drosophila, and member of the Drosophila quinaria species group. Drosophila innubila is best known for its association with a strain of male-killing Wolbachia bacteria. These bacteria are parasitic, as they drain resources from the host and cause half the infected female's eggs to abort. However Wolbachia may offer benefits to the fly's fitness in certain circumstances.[3] The D. innubila genome was sequenced in 2019.[4][5]
Symbiosis
Drosophila innubila is stably infected by a strain of male-killing Wolbachia bacteria. The association between Drosophila innubila and Wolbachia can vary greatly within local populations. However, their relationship is very consistent across the overall Drosophila innubila species.[3]
Male-killing by these Wolbachia results in the offspring of flies being entirely female, the biological sex with the higher reproductive output. Thus, this Wolbachia spreads in the population owing to the increased reproductive advantage of females it infects.[1] However bacterial density varies over development. Bacterial density is lowest in the embryo and increases over the lifespan of the fly, reaching its highest densities in the ovaries of females. Bacterial density directly affects the efficiency of Wolbachia inheritance, as females with lower Wolbachia density also produce daughters with a low bacterial density.[6] The forces driving differences in bacterial density may be epigenetic. If bacterial densities are low enough, females begin to produce males in spite of being infected with male-killing Wolbachia.[6] There is no evidence that a Wolbachia infection can be transmitted horizontally from an infected female fly to an uninfected female fly. Unlike extracellular symbiotic bacteria (e.g. Spiroplasma), Wolbachia live inside their host cells, which likely reduces its ability to move between hosts.[5]
Infected sons are less likely to die from Wolbachia infection if their mother possessed a smaller bacterial density.[6] It is speculated that the bacterial density of Wolbachia inside a host can vary, depending on the antibiotic activity of larval or adult food sources, possible host defense mechanisms, the age of the host, bacterial interactions within the host, as well as the environmental conditions that the fly experiences.[6] Currently, there is no evidence for a mechanism in Drosophila innubila that suppresses or inhibits the male-killing effect of Wolbachia.[6]
Additionally, an unknown factor contributes to increased fitness benefits of Wolbachia infection.[5] The presence of a Wolbachia infection can increase the fitness of a female fly by increasing her size and enhancing her fertility.[5] Moreover, the D. innubila DNA nudivirus "DiNV" is a common viral infection amongst this species.[7] It has been shown that certain Wolbachia can protect their hosts against viral infection, even leading to biocontrol strategies that use Wolbachia infection to suppress the spread of viral diseases.[8] What role (if any) Wolbachia plays in defense against viruses is unclear. However, other studies that investigated the contribution of Wolbachia infection to the fitness of Drosophila species suggested that the bacteria can enhance survival of its host in the presence of oxidative stressors as well as prevent other pathogens from infecting the host by outcompeting them for host-derived resources like cholesterol.[9][10] In addition, it is also suspected that Wolbachia may also be able to manipulate the expression of its host's DNA through utilization of host microRNA.[11]
Immunity
The genome of D. innubila was sequenced for a study in 2019, and boasts a very high quality of assembly, rivalling that of the classic genetic model Drosophila melanogaster. This study highlighted the importance of the interaction between D. innubila and its viruses as implied by patterns of immune evolution in antiviral genes. Notably, natural selection on the immunity and antiviral pathways in D. innubila differ markedly from D. melanogaster, implying divergent evolutionary pressures.[4] The D. innubila DNA virus is similar to the D. melanogaster Kallithea virus.[12] As such, comparisons between D. melanogaster and D. innubila and their viruses promise to inform on the nature of host-virus interactions.[4]
In some mushroom-feeding Drosophila species, such as D. guttifera and D. neotestacea, the antimicrobial peptide gene Diptericin B has been pseudogenized. However this gene is maintained in D. innubila, and is activated upon infection.[13]
See also
References
- ^ a b Dyer KA, Jaenike J (November 2004). "Evolutionarily stable infection by a male-killing endosymbiont in Drosophila innubila: molecular evidence from the host and parasite genomes". Genetics. 168 (3): 1443–55. doi:10.1534/genetics.104.027854. PMC 1448788. PMID 15579697.
- ^ Jaenike J, Dyer KA, Reed LK (2003). "Within-population structure of competition and the dynamics of male-killing Wolbachia". Evolutionary Ecology Research. 5 (7): 1023–36.
- ^ a b Dyer KA, Jaenike J (July 2005). "Evolutionary dynamics of a spatially structured host-parasite association: Drosophila innubila and male-killing Wolbachia". Evolution; International Journal of Organic Evolution. 59 (7): 1518–28. doi:10.1554/04-666. PMID 16153037. S2CID 198154919.
- ^ a b c Hill T, Koseva BS, Unckless RL (March 2019). "The genome of Drosophila innubila reveals lineage-specific patterns of selection in immune genes". Molecular Biology and Evolution. 36 (7): 1405–1417. doi:10.1093/molbev/msz059. PMC 6573480. PMID 30865231.
- ^ a b c d Unckless RL, Jaenike J (March 2012). "Maintenance of a male-killing Wolbachia in Drosophila innubila by male-killing dependent and male-killing independent mechanisms". Evolution; International Journal of Organic Evolution. 66 (3): 678–689. doi:10.1111/j.1558-5646.2011.01485.x. PMID 22380432. S2CID 11559837.
- ^ a b c d e Dyer KA, Minhas MS, Jaenike J (April 2005). "Expression and modulation of embryonic male-killing in Drosophila innubila: opportunities for multilevel selection". Evolution; International Journal of Organic Evolution. 59 (4): 838–48. doi:10.1554/04-527. PMID 15926693. S2CID 198159022.
- ^ Hill T, Unckless RL (January 2018). "The dynamic evolution of Drosophila innubila Nudivirus". Infection, Genetics and Evolution. 57: 151–157. doi:10.1016/j.meegid.2017.11.013. PMC 5725240. PMID 29155284.
- ^ Hoffmann AA, Montgomery BL, Popovici J, Iturbe-Ormaetxe I, Johnson PH, Muzzi F, Greenfield M, Durkan M, Leong YS, Dong Y, Cook H, Axford J, Callahan AG, Kenny N, Omodei C, McGraw EA, Ryan PA, Ritchie SA, Turelli M, O'Neill SL (August 2011). "Successful establishment of Wolbachia in Aedes populations to suppress dengue transmission". Nature. 476 (7361): 454–7. Bibcode:2011Natur.476..454H. doi:10.1038/nature10356. PMID 21866160. S2CID 4316652.
- ^ Capobianco III F, Nandkumar S, Parker JD (September 2018). "Wolbachia affects survival to different oxidative stressors dependent upon the genetic background in Drosophila melanogaster: Wolbachia and oxidative stress". Physiological Entomology. 43 (3): 239–244. doi:10.1111/phen.12252. S2CID 89663286.
- ^ Caragata EP, Rancès E, Hedges LM, Gofton AW, Johnson KN, O'Neill SL, McGraw EA (2013-06-27). Vernick KD (ed.). "Dietary cholesterol modulates pathogen blocking by Wolbachia". PLOS Pathogens. 9 (6): e1003459. doi:10.1371/journal.ppat.1003459. PMC 3694857. PMID 23825950.
- ^ Zhang G, Hussain M, O'Neill SL, Asgari S (June 2013). "Wolbachia uses a host microRNA to regulate transcripts of a methyltransferase, contributing to dengue virus inhibition in Aedes aegypti". Proceedings of the National Academy of Sciences of the United States of America. 110 (25): 10276–81. Bibcode:2013PNAS..11010276Z. doi:10.1073/pnas.1303603110. PMC 3690878. PMID 23733960.
- ^ Webster CL, Waldron FM, Robertson S, Crowson D, Ferrari G, Quintana JF, Brouqui JM, Bayne EH, Longdon B, Buck AH, Lazzaro BP, Akorli J, Haddrill PR, Obbard DJ (July 2015). "The Discovery, Distribution, and Evolution of Viruses Associated with Drosophila melanogaster". PLOS Biology. 13 (7): e1002210. doi:10.1371/journal.pbio.1002210. PMC 4501690. PMID 26172158.
- ^ Hanson, Mark Austin; Lemaitre, Bruno; Unckless, Robert L. (2019). "Dynamic evolution of antimicrobial peptides underscores trade-offs between immunity and ecological fitness". Frontiers in Immunology. 10: 2620. doi:10.3389/fimmu.2019.02620. ISSN 1664-3224. PMC 6857651. PMID 31781114.
This page was last edited on 4 December 2023, at 00:29