[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/kleptoplasty-wikipedia\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/wiki41\/kleptoplasty-wikipedia\/","headline":"Kleptoplasty – Wikipedia","name":"Kleptoplasty – Wikipedia","description":"before-content-x4 From Wikipedia, the free encyclopedia after-content-x4 Form of algae symbiosis Kleptoplasty or kleptoplastidy is a symbiotic phenomenon whereby plastids,","datePublished":"2020-10-08","dateModified":"2020-10-08","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/wiki41\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/c9645c498c9701c88b89b8537773dd7c?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/c\/c7\/Elysia_clarki_digestive_tubule_cell.png\/260px-Elysia_clarki_digestive_tubule_cell.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/c\/c7\/Elysia_clarki_digestive_tubule_cell.png\/260px-Elysia_clarki_digestive_tubule_cell.png","height":"280","width":"260"},"url":"https:\/\/wiki.edu.vn\/en\/wiki41\/kleptoplasty-wikipedia\/","about":["Wiki"],"wordCount":5308,"articleBody":"     (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4From Wikipedia, the free encyclopedia       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Form of algae symbiosis  Kleptoplasty or kleptoplastidy is a symbiotic phenomenon whereby plastids, notably chloroplasts from algae, are sequestered by host organisms. The word is derived from Kleptes (\u03ba\u03bb\u03ad\u03c0\u03c4\u03b7\u03c2) which is Greek for thief. The alga is eaten normally and partially digested, leaving the plastid intact. The plastids are maintained within the host, temporarily continuing photosynthesis and benefiting the predator.[1] The term was coined in 1990 to describe chloroplast symbiosis.[2][3]       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Table of ContentsCiliates[edit]Dinoflagellates[edit]Sacoglossan sea slugs[edit]Nudibranch sea slugs[edit]Foraminifera[edit]Rhabdocoel flatworms[edit]See also[edit]References[edit]External links[edit]Ciliates[edit]  Mesodinium rubrum is a ciliate that steals chloroplasts from the cryptomonad Geminigera cryophila.[4]M. rubrum participates in additional endosymbiosis by transferring its plastids to its predators, the dinoflagellate planktons belonging to the genus Dinophysis.[5]Karyoklepty is a related process in which the nucleus of the prey cell is kept by the predator as well. This was first described in 2007 in M. rubrum.[6]       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4Dinoflagellates[edit]The stability of transient plastids varies considerably across plastid-retaining species. In the dinoflagellates Gymnodinium spp. and Pfisteria piscicida, kleptoplastids are photosynthetically active for only a few days, while kleptoplastids in Dinophysis spp. can be stable for 2 months.[1] In other dinoflagellates, kleptoplasty has been hypothesized to represent either a mechanism permitting functional flexibility, or perhaps an early evolutionary stage in the permanent acquisition of chloroplasts.[7]Sacoglossan sea slugs[edit]  Some of the only known animals that practice kleptoplasty are sea slugs in the clade Sacoglossa.[8] Several species of Sacoglossan sea slugs capture intact, functional chloroplasts from algal food sources, retaining them within specialized cells lining the mollusc’s digestive diverticula. The longest known kleptoplastic association, which can last up to ten months, is found in Elysia chlorotica,[2] which acquires chloroplasts by eating the alga Vaucheria litorea, storing the chloroplasts in the cells that line its gut.[9] Juvenile sea slugs establish the kleptoplastic endosymbiosis when feeding on algal cells, sucking out the cell contents, and discarding everything except the chloroplasts. The chloroplasts are phagocytosed by digestive cells, filling extensively branched digestive tubules, providing their host with the products of photosynthesis.[10] It is not resolved, however, whether the stolen plastids actively secrete photosynthate or whether the slugs profit indirectly from slowly degrading kleptoplasts.[11]Due to this unusual ability, the sacoglossans are sometimes referred to as “solar-powered sea slugs,” though the actual benefit from photosynthesis on the survival of some of the species that have been analyzed seems to be marginal at best.[12] In fact, some species may even die in the presence of the carbon dioxide-fixing kleptoplasts as a result of elevated levels of reactive oxygen species.[13]Changes in temperature have been shown to negatively affect kleptoplastic abilities in sacoglossans. Rates of photosynthetic efficiency as well as kleptoplast abundance have been shown to decrease in correlation to a decrease in temperature. The patterns and rate of these changes, however, varies between different species of sea slug.[14]Nudibranch sea slugs[edit]Some species of nudibranchs, another group of sea slugs, such as Pteraeolidia ianthina sequester whole living symbiotic zooxanthellae within their digestive diverticula, and thus are also “solar-powered”.[citation needed]Foraminifera[edit]Some species of the foraminiferan genera Bulimina, Elphidium, Haynesina, Nonion, Nonionella, Nonionellina, Reophax, and Stainforthia have been shown to sequester diatom chloroplasts.[15]Rhabdocoel flatworms[edit]Two species from the group of marine flatworms known as the rhabdocoels, Baicalellia solaris and Pogaina paranygulgus, have been found to constitute another type of animal that displays kleptoplasty. The group was previously classified as having algal endosymbionts, though it was already discovered that the endosymbionts did not contain nuclei.[16]While consuming diatoms, B. solaris and P. paranygulus, in a process not yet discovered, extract plastids from their prey, incorporating them subepidermally, while separating and digesting the frustule and remainder of the diatom. In B. solaris the extracted plastids, or kleptoplasts, continue to exhibit functional photosynthesis for a short period of roughly 7 days. As the two groups are not sister taxa, and the trait is not shared among groups more closely related, there is evidence that kleptoplasty evolved independently within the two taxa.[17]See also[edit]References[edit]^ a b Minnhagen S, Carvalho WF, Salomon PS, Janson S (September 2008). “Chloroplast DNA content in Dinophysis (Dinophyceae) from different cell cycle stages is consistent with kleptoplasty”. Environ. Microbiol. 10 (9): 2411\u20137. doi:10.1111\/j.1462-2920.2008.01666.x. PMID\u00a018518896.^ a b S. K. Pierce; S. E. Massey; J. J. Hanten; N. E. Curtis (June 1, 2003). “Horizontal Transfer of Functional Nuclear Genes Between Multicellular Organisms”. Biol. Bull. 204 (3): 237\u2013240. doi:10.2307\/1543594. JSTOR\u00a01543594. PMID\u00a012807700. S2CID\u00a09671982. Retrieved 2008-11-24.^ Clark, K. B.; Jensen, K. R.; Strits, H. M. (1990). “Survey for Functional Kleptoplasty Among West Atlantic Ascoglossa (=Sacoglossa) (Mollusca: Opisthobranchia)”. The Veliger. 33: 339\u2013345. ISSN\u00a00042-3211. S2CID\u00a087182226.^ Johnson, Matthew D.; Oldach, David; Charles, F. Delwiche; Stoecker, Diane K. (Jan 2007). “Retention of transcriptionally active cryptophyte nuclei by the ciliate Myrionecta rubra”. Nature. 445 (7126): 426\u20138. Bibcode:2007Natur.445..426J. doi:10.1038\/nature05496. PMID\u00a017251979. S2CID\u00a04410812.^ Nishitani, G.; Nagai, S.; Baba, K.; Kiyokawa, S.; Kosaka, Y.; Miyamura, K.; Nishikawa, T.; Sakurada, K.; Shinada, A.; Kamiyama, T. (2010). “High-level congruence of Myrionecta rubra prey and Dinophysis species plastid identities as revealed by genetic analyses of isolates from Japanese coastal waters”. Applied and Environmental Microbiology. 76 (9): 2791\u20132798. doi:10.1128\/AEM.02566-09. PMC\u00a02863437. PMID\u00a020305031.^ Johnson, Matthew D.; Oldach, David;  et\u00a0al. (25 January 2007). “Retention of transcriptionally active cryptophyte nuclei by the ciliate Myrionecta rubra“. Nature. 445 (7126): 426\u2013428. Bibcode:2007Natur.445..426J. doi:10.1038\/nature05496. PMID\u00a017251979. S2CID\u00a04410812. Retrieved 4 February 2015.^ Gast RJ, Moran DM, Dennett MR, Caron DA (January 2007). “Kleptoplasty in an Antarctic dinoflagellate: caught in evolutionary transition?”. Environ. Microbiol. 9 (1): 39\u201345. CiteSeerX\u00a010.1.1.490.54. doi:10.1111\/j.1462-2920.2006.01109.x. PMID\u00a017227410.^ H\u00e4ndeler, K.; Grzymbowski, Y. P.; Krug, P. J.; W\u00e4gele, H. (2009). “Functional chloroplasts in metazoan cells – a unique evolutionary strategy in animal life”. Frontiers in Zoology. 6: 28. doi:10.1186\/1742-9994-6-28. PMC\u00a02790442. PMID\u00a019951407.^ Catherine Brahic (24 November 2008). “Solar-powered sea slug harnesses stolen plant genes”. New Scientist. Retrieved 24 November 2008.^ “SymBio: Introduction-Kleptoplasty”. University of Maine. Archived from the original on 2008-12-02. Retrieved 2008-11-24.^ de Vries, Jan; Christa, Gregor; Gould, Sven B. (2014). “Plastid survival in the cytosol of animal cells”. Trends in Plant Science. 19 (6): 347\u2013350. doi:10.1016\/j.tplants.2014.03.010. ISSN\u00a01360-1385. PMID\u00a024767983.^ De Vries, Jan; Rauch, Cessa; Christa, Gregor; Gould, Sven B. (2014). “A sea slug’s guide to plastid symbiosis”. Acta Societatis Botanicorum Poloniae. 83 (4): 415\u2013421. doi:10.5586\/asbp.2014.042. ISSN\u00a02083-9480.^ de Vries, J.; Woehle, C.; Christa, G.; Wagele, H.; Tielens, A. G. M.; Jahns, P.; Gould, S. B. (2015). “Comparison of sister species identifies factors underpinning plastid compatibility in green sea slugs”. Proceedings of the Royal Society B: Biological Sciences. 282 (1802): 20142519. doi:10.1098\/rspb.2014.2519. ISSN\u00a00962-8452. PMC\u00a04344150. PMID\u00a025652835.^ Laetz, Elise; Wagele, Heike (2018). “How does temperature affect functional kleptoplasty? Comparing populations of the solar-powered sister-species Elysia timida Risso, 1818 and Elysa cornigera Nuttall, 1989 (Gastopoda: Sacoglossa)”. Frontiers in Zoology. 15: 17. doi:10.1186\/s12983-018-0264-y. PMC\u00a05937827. PMID\u00a029760759.^ Bernhard, Joan M.; Bowser, Samuel S. (1999). “Benthic foraminifera of dysoxic sediments: chloroplast sequestration and functional morphology”. Earth-Science Reviews. 46 (1\u20134): 149\u2013165. Bibcode:1999ESRv…46..149B. doi:10.1016\/s0012-8252(99)00017-3.^ E. Marcus, Turbellaria Brasileiros (9). Bol. Fac. Fil. Ci. Letras Univ. S\u00e3o Paulo 16, 5\u2013215 (1951).^ Van Steenkiste, Niels W. L.; Stephenson, India; Herranz, Mar\u00eda; Husnik, Filip; Keeling, Patrick J.; Leander, Brian S. (2019). “A new case of kleptoplasty in animals: Marine flatworms steal functional plastids from diatoms”. Science Advances. 5 (7): eaaw4337. Bibcode:2019SciA….5.4337V. doi:10.1126\/sciadv.aaw4337. PMC\u00a06636991. PMID\u00a031328166.External links[edit]     (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4"},{"@context":"http:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/wiki41\/kleptoplasty-wikipedia\/#breadcrumbitem","name":"Kleptoplasty – Wikipedia"}}]}]