Farming termites determine the genetic population structure of Termitomyces fungal symbionts

DC FieldValueLanguage
dc.contributor.authorNobre, Tania
dc.contributor.authorFernandes, Cecilia
dc.contributor.authorBoomsma, Jacobus J.
dc.contributor.authorKorb, Judith
dc.contributor.authorAanen, Duur K.
dc.date.accessioned2021-12-23T16:15:53Z-
dc.date.available2021-12-23T16:15:53Z-
dc.date.issued2011
dc.identifier.issn09621083
dc.identifier.urihttps://osnascholar.ub.uni-osnabrueck.de/handle/unios/11632-
dc.description.abstractSymbiotic interactions between macrotermitine termites and their fungal symbionts have a moderate degree of specificity. Consistent with horizontal symbiont transmission, host switching has been frequent over evolutionary time so that single termite species can often be associated with several fungal symbionts. However, even in the few termite lineages that secondarily adopted vertical symbiont transmission, the fungal symbionts are not monophyletic. We addressed this paradox by studying differential transmission of fungal symbionts by alate male and female reproductives, and the genetic population structure of Termitomyces fungus gardens across 74 colonies of Macrotermes bellicosus in four west and central African countries. We confirm earlier, more limited, studies showing that the Termitomyces symbionts of M. bellicosus are normally transmitted vertically and clonally by dispersing males. We also document that the symbionts associated with this termite species belong to three main lineages that do not constitute a monophyletic group. The most common lineage occurs over the entire geographical region that we studied, including west, central and southern Africa, where it is also associated with the alternative termite hosts Macrotermes subhyalinus and Macrotermes natalensis. While Termitomyces associated with these alternative hosts are horizontally transmitted and recombine freely, the genetic population structure of the same Termitomyces associated with M. bellicosus is consistent with predominantly clonal reproduction and only occasional recombination. This implies that the genetic population structure of Termitomyces is controlled by the termite host and not by the Termitomyces symbiont.
dc.description.sponsorshipMarie CurieEuropean Commission; European CommunityEuropean Commission [220077]; Netherlands Organization for Scientific Research (VIDI)Netherlands Organization for Scientific Research (NWO); N. was supported by a Marie Curie Intra European Fellowship within the 7th European Community Framework Programme (IEF Project No 220077). C. F. was supported by a grant under the programme ERASMUS. D. K. A. was supported by the Netherlands Organization for Scientific Research (VIDI).
dc.language.isoen
dc.publisherWILEY
dc.relation.ispartofMOLECULAR ECOLOGY
dc.subjectBiochemistry & Molecular Biology
dc.subjectclonality
dc.subjectCOMB
dc.subjectEcology
dc.subjectEnvironmental Sciences & Ecology
dc.subjectESTABLISHMENT
dc.subjectEvolutionary Biology
dc.subjectGROWING TERMITES
dc.subjectISOPTERA
dc.subjectLABORATORY COLONIES
dc.subjectMacrotermes bellicosus
dc.subjectMACROTERMES-MICHAELSENI
dc.subjectMOLECULAR MARKERS REVEAL
dc.subjectPHYLOGENETIC-RELATIONSHIPS
dc.subjectRECOMBINATION
dc.subjectsymbiont transmission
dc.subjectTermitomyces
dc.subjectTRANSMISSION
dc.titleFarming termites determine the genetic population structure of Termitomyces fungal symbionts
dc.typejournal article
dc.identifier.doi10.1111/j.1365-294X.2011.05064.x
dc.identifier.isiISI:000289522400021
dc.description.volume20
dc.description.issue9
dc.description.startpage2023
dc.description.endpage2033
dc.contributor.orcid0000-0002-1855-7451
dc.contributor.orcid0000-0002-3598-1609
dc.contributor.researcheridC-9925-2012
dc.contributor.researcheridM-2785-2014
dc.identifier.eissn1365294X
dc.publisher.place111 RIVER ST, HOBOKEN 07030-5774, NJ USA
dcterms.isPartOf.abbreviationMol. Ecol.
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