Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria

Background: Cryptic population structure can be an indicator of incipient speciation or historical processes. We investigated a previously documented deep break in the mitochondrial haplotypes of Heliconius erato chestertonii to explore the possibility of cryptic speciation, and also the possible pr...

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Fecha de publicación:
2011
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/21893
Acceso en línea:
https://doi.org/10.1186/1471-2148-11-358
https://repository.urosario.edu.co/handle/10336/21893
Palabra clave:
Invertebrados
Cryptic Speciation
Hybrid zone
Amplify fragment length polymorphism
Endosymbiotic bacterium
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dc.title.spa.fl_str_mv Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
title Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
spellingShingle Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
Invertebrados
Cryptic Speciation
Hybrid zone
Amplify fragment length polymorphism
Endosymbiotic bacterium
title_short Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
title_full Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
title_fullStr Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
title_full_unstemmed Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
title_sort Deep mitochondrial divergence within a Heliconius butterfly species is not explained by cryptic speciation or endosymbiotic bacteria
dc.subject.ddc.spa.fl_str_mv Invertebrados
topic Invertebrados
Cryptic Speciation
Hybrid zone
Amplify fragment length polymorphism
Endosymbiotic bacterium
dc.subject.keyword.spa.fl_str_mv Cryptic Speciation
Hybrid zone
Amplify fragment length polymorphism
Endosymbiotic bacterium
description Background: Cryptic population structure can be an indicator of incipient speciation or historical processes. We investigated a previously documented deep break in the mitochondrial haplotypes of Heliconius erato chestertonii to explore the possibility of cryptic speciation, and also the possible presence of endosymbiont bacteria that might drive mitochondrial population structure. Results: Among a sample of 315 individuals from 16 populations of western Colombia, two principal mtDNA clades were detected with 2.15% divergence and we confirmed this structure was weakly associated with geography. The first mtDNA clade included 87% of individuals from northern populations and was the sister group of H. erato members of Andes western, while the second clade contained most individuals from southern populations (78%), which shared haplotypes with an Ecuadorian race of H. erato. In contrast, analysis using AFLP markers showed H. e. chestertonii to be a genetically homogeneous species with no association between mitochondrial divergence and AFLP structure. The lack of congruence between molecular markers suggests that cryptic speciation is not a plausible explanation for the deep mitochondrial divergence in H. e chestertonii. We also carried out the first tests for the presence of endosymbiontic bacteria in Heliconius, and identified two distinct lineages of Wolbachia within H. e. chestertonii. However, neither of the principal mitochondrial clades of H. e. chestertonii was directly associated with the patterns of infection. Conclusions: We conclude that historical demographic processes are the most likely explanation for the high mitochondrial differentiation in H. e. chestertonii, perhaps due to gene flow between Cauca valley H. e. chestertonii and west Pacific slope populations of H. erato. © 2011 Mũoz et al; licensee BioMed Central Ltd.
publishDate 2011
dc.date.created.none.fl_str_mv 2011
dc.date.issued.none.fl_str_mv 2011
dc.date.accessioned.none.fl_str_mv 2020-05-07T14:29:23Z
dc.date.available.none.fl_str_mv 2020-05-07T14:29:23Z
dc.type.eng.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1186/1471-2148-11-358
dc.identifier.issn.none.fl_str_mv 1471-2148
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/21893
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https://repository.urosario.edu.co/handle/10336/21893
identifier_str_mv 1471-2148
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationIssue.none.fl_str_mv No. 1
dc.relation.citationTitle.none.fl_str_mv BMC Evolutionary Biology
dc.relation.citationVolume.none.fl_str_mv Vol. 11
dc.relation.ispartof.spa.fl_str_mv BMC Evolutionary Biology, ISSN: 1471-2148 Vol. 11, No. 1 (2011)
dc.relation.uri.spa.fl_str_mv https://bmcevolbiol.biomedcentral.com/articles/10.1186/1471-2148-11-358
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rights_invalid_str_mv Abierto (Texto Completo)
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institution Universidad del Rosario
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