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• W2019833246 abstract "Diverse insect species harbor symbiotic bacteria, which play important roles such as provisioning nutrients and providing defense against natural enemies [1Moran N.A. McCutcheon J.P. Nakabachi A. Genomics and evolution of heritable bacterial symbionts.Annu. Rev. Genet. 2008; 42: 165-190Crossref PubMed Scopus (1113) Google Scholar, 2Werren J.H. Baldo L. Clark M.E. Wolbachia: master manipulators of invertebrate biology.Nat. Rev. Microbiol. 2008; 6: 741-751Crossref PubMed Scopus (1817) Google Scholar, 3Oliver K.M. Degnan P.H. Burke G.R. Moran N.A. Facultative symbionts in aphids and the horizontal transfer of ecologically important traits.Annu. Rev. Entomol. 2010; 55: 247-266Crossref PubMed Scopus (643) Google Scholar, 4Haine E.R. Symbiont-mediated protection.Proc. Biol. Sci. 2008; 275: 353-361Crossref PubMed Scopus (213) Google Scholar, 5Brownlie J.C. Johnson K.N. Symbiont-mediated protection in insect hosts.Trends Microbiol. 2009; 17: 348-354Abstract Full Text Full Text PDF PubMed Scopus (240) Google Scholar, 6Kaltenpoth M. Actinobacteria as mutualists: general healthcare for insects?.Trends Microbiol. 2009; 17: 529-535Abstract Full Text Full Text PDF PubMed Scopus (183) Google Scholar]. Whereas nutritional symbioses are often indispensable for both partners, defensive symbioses tend to be of a facultative nature [1Moran N.A. McCutcheon J.P. Nakabachi A. Genomics and evolution of heritable bacterial symbionts.Annu. Rev. Genet. 2008; 42: 165-190Crossref PubMed Scopus (1113) Google Scholar, 2Werren J.H. Baldo L. Clark M.E. Wolbachia: master manipulators of invertebrate biology.Nat. Rev. Microbiol. 2008; 6: 741-751Crossref PubMed Scopus (1817) Google Scholar, 3Oliver K.M. Degnan P.H. Burke G.R. Moran N.A. Facultative symbionts in aphids and the horizontal transfer of ecologically important traits.Annu. Rev. Entomol. 2010; 55: 247-266Crossref PubMed Scopus (643) Google Scholar, 4Haine E.R. Symbiont-mediated protection.Proc. Biol. Sci. 2008; 275: 353-361Crossref PubMed Scopus (213) Google Scholar, 5Brownlie J.C. Johnson K.N. Symbiont-mediated protection in insect hosts.Trends Microbiol. 2009; 17: 348-354Abstract Full Text Full Text PDF PubMed Scopus (240) Google Scholar, 6Kaltenpoth M. Actinobacteria as mutualists: general healthcare for insects?.Trends Microbiol. 2009; 17: 529-535Abstract Full Text Full Text PDF PubMed Scopus (183) Google Scholar, 7Kellner R.L.L. Dettner K. Differential efficacy of toxic pederin in deterring potential arthropod predators of Paederus (Coleoptera: Staphylinidae) offspring.Oecologia. 1996; 107: 293-300Crossref Scopus (108) Google Scholar, 8Oliver K.M. Russell J.A. Moran N.A. Hunter M.S. Facultative bacterial symbionts in aphids confer resistance to parasitic wasps.Proc. Natl. Acad. Sci. USA. 2003; 100: 1803-1807Crossref PubMed Scopus (924) Google Scholar, 9Scarborough C.L. Ferrari J. Godfray H.C. Aphid protected from pathogen by endosymbiont.Science. 2005; 310: 1781Crossref PubMed Scopus (535) Google Scholar, 10Hedges L.M. Brownlie J.C. O’Neill S.L. Johnson K.N. Wolbachia and virus protection in insects.Science. 2008; 322: 702Crossref PubMed Scopus (808) Google Scholar, 11Teixeira L. Ferreira A. Ashburner M. The bacterial symbiont Wolbachia induces resistance to RNA viral infections in Drosophila melanogaster.PLoS Biol. 2008; 6: e2Crossref PubMed Scopus (798) Google Scholar, 12Jaenike J. Unckless R. Cockburn S.N. Boelio L.M. Perlman S.J. Adaptation via symbiosis: recent spread of a Drosophila defensive symbiont.Science. 2010; 329: 212-215Crossref PubMed Scopus (369) Google Scholar]. The Asian citrus psyllid Diaphorina citri is a notorious agricultural pest that transmits Liberibacter spp. (Alphaproteobacteria), causing the devastating citrus greening disease or Huanglongbing [13Halbert S.E. Manjunath K.L. Asian citrus psyllids (Sternorrhyncha: Psyllidae) and greening disease in citrus: a literature review and assessment of risk in Florida.Fla. Entomol. 2004; 87: 330-353Crossref Scopus (745) Google Scholar, 14Bové J.M. Huanglongbing: a destructive, newly-emerging, century-old disease of citrus.J. Plant Pathol. 2006; 88: 7-37Google Scholar]. In a symbiotic organ called the bacteriome, D. citri harbors two distinct intracellular symbionts: a putative nutrition provider, Carsonella_DC (Gammaproteobacteria), and an unnamed betaproteobacterium with unknown function [15Subandiyah S. Nikoh N. Tsuyumu S. Somowiyarjo S. Fukatsu T. Complex endosymbiotic microbiota of the citrus psyllid Diaphorina citri (Homoptera: Psylloidea).Zoolog. Sci. 2000; 17: 983-989Crossref Scopus (90) Google Scholar], for which we propose the name “Candidatus Profftella armatura.” Here we report that Profftella is a defensive symbiont presumably of an obligate nature with an extremely streamlined genome. The genomes of Profftella and Carsonella_DC were drastically reduced to 464,857 bp and 174,014 bp, respectively, suggesting their ancient and mutually indispensible association with the host. Strikingly, 15% of the small Profftella genome encoded horizontally acquired genes for synthesizing a novel polyketide toxin. The toxin was extracted, pharmacologically and structurally characterized, and designated diaphorin. The presence of Profftella and its diaphorin-biosynthetic genes was perfectly conserved in the world’s D. citri populations." @default.
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• W2019833246 date "2013-08-01" @default.
• W2019833246 modified "2023-10-16" @default.
• W2019833246 title "Defensive Bacteriome Symbiont with a Drastically Reduced Genome" @default.
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• W2019833246 doi "https://doi.org/10.1016/j.cub.2013.06.027" @default.
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