Artigo Revisado por pares

Molecular phylogeny of the South American land slug Phyllocaulis (Mollusca, Soleolifera, Veronicellidae)

2009; Wiley; Volume: 39; Issue: 2 Linguagem: Inglês

10.1111/j.1463-6409.2009.00412.x

ISSN

1463-6409

Autores

Suzete Rodrigues Gomes, Fernanda Britto da Silva, Inga Ludmila Veitenheimer Mendes, José Willibaldo Thomé, Sandro L. Bonatto,

Tópico(s)

Marine Biology and Ecology Research

Resumo

Zoologica ScriptaVolume 39, Issue 2 p. 177-186 Molecular phylogeny of the South American land slug Phyllocaulis (Mollusca, Soleolifera, Veronicellidae) Suzete Rodrigues Gomes, Suzete Rodrigues GomesSearch for more papers by this authorFernanda Britto da Silva, Fernanda Britto da SilvaSearch for more papers by this authorInga L. Veitenheimer Mendes, Inga L. Veitenheimer MendesSearch for more papers by this authorJosé Willibaldo Thomé, José Willibaldo ThoméSearch for more papers by this authorSandro L. Bonatto, Sandro L. BonattoSearch for more papers by this author Suzete Rodrigues Gomes, Suzete Rodrigues GomesSearch for more papers by this authorFernanda Britto da Silva, Fernanda Britto da SilvaSearch for more papers by this authorInga L. Veitenheimer Mendes, Inga L. Veitenheimer MendesSearch for more papers by this authorJosé Willibaldo Thomé, José Willibaldo ThoméSearch for more papers by this authorSandro L. Bonatto, Sandro L. BonattoSearch for more papers by this author First published: 12 February 2010 https://doi.org/10.1111/j.1463-6409.2009.00412.xCitations: 12 Suzete Rodrigues Gomes, Instituto Butantan, Laboratório de Parasitologia/Malacologia, Av. Vital Brasil, 1500, Bairro Butantã, Cep. 05503-900, Sao Paulo, SP, Brazil. E-mail: [email protected]Suzete Rodrigues Gomes and Inga L. Veitenheimer Mendes, Laboratório de Malacologia, Departamento de Zoologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Cep. 91501-970, RS, Brazil. E-mails: [email protected], [email protected]Fernanda Britto da Silva and Sandro L. Bonatto, Laboratório de Biologia Genômica e Molecular, Faculdade de Biociências, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Cep. 90.619-900, RS, Brazil. E-mails: [email protected], [email protected]José Willibaldo Thomé, Escritório de Malacologia e de Biofilosofia, Praça Dom Feliciano, 39, Sala 1303, Ed. Guanabara, Porto Alegre, Cep. 90020-160, RS, Brazil. E-mail: [email protected] Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Abstract Gomes, S. R., Britto da Silva, F., Mendes, I. L. V., Thomé, J. W. & Bonatto, S. L. (2009). Molecular phylogeny of the South American land slug Phyllocaulis (Mollusca, Soleolifera, Veronicellidae). —Zoologica Scripta, 39, 177–186. Our main objectives were investigate the phylogenetic relationships between the species of the land slug Phyllocaulis and the monophyly of the genus based on mitochondrial (16S and COI) and nuclear (ITS2) DNA sequences from multiple individuals from each species. Evolutionary trees were constructed using Bayesian inference, maximum likelihood, maximum parsimony and neighbor-joining methods. All species accepted in the current taxonomy based on penial characteristics and radular measurements were reciprocally monophyletic. Five species out of six formed a clade with the following highly supported relationship: Phyllocaulis gayi, Phyllocaulis soleiformis, Phyllocaulis renschi, Phyllocaulis variegatus, Phyllocaulis boraceiensis. The position of Vaginulus taunaisii changed according to the analysis, appearing as sister-group of Phyllocaulis or as sister-group of Phyllocaulis tuberculosus. Divergence times estimated from the 16S tree indicated that the extant species of Phyllocaulis shared a common ancestor around 1.3 Ma and that most species originated between 0.8 and 0.6 Ma. References Ant, H. (1966). Die Bedeutung der Eiszeiten für die rezente Verbreitung der europäischen Landgastropoden. Malacologia, 5, 61– 62. Barker, G. M. (2001). The Biology of Terrestrial Molluscs. Willingford: CABI Publishing. Caldeira, R. L., Mendonça, C. L. G. F., Goveia, C. O., Lenzi, H., Graeff-Teixeira, C., Lima, W. S., Mota, E. M., Pecora, I. L., Medeiros, A. M. Z. & Carvalho, O. S. (2007). First record of molluscs naturally infected with Angiostrongylus cantonensis (Chen, 1935) (Nematoda: Metastrongylidae) in Brazil. Memórias do Instituto Oswaldo Cruz, 102, 887– 889. Chiba, S. (1999). Accelerated evolution of land snails Mandarina in the oceanic Bonin Islands: evidence from mitochondrial DNA sequences. Evolution, 53, 460– 471. Dayrat, B., Tillier, A., Lecointre, G. & Tillier, S. (2001). New clades of Euthyneuran Gastropods (Mollusca) from 28S rRNA sequences. Molecular Phylogenetics and Evolution, 19, 225– 235. Dick, C. W., Roubik, D. W., Gruber, K. F. & Bermingham, E. (2004). Long-distance gene flow and cross-Andean dispersal of lowland rainforest bees (Apidae: Euglossini) revealed by comparative mitochondrial DNA phylogeography. Molecular Ecology, 13, 3775– 3785. Doyle, J. J. & Doyle, J. L. (1987). A rapid DNA isolation procedure from small quantities of fresh leaf tissues. Phytochemistry Bulletin, 19, 11– 15. Felsenstein, J. (1981). Evolutionary trees from DNA sequences: a maximum likelihood approach. Journal of Molecular Evolution, 17, 368– 376. Fitch, W. M. (1971). Toward defining the course of evolution: minimum change for a specific tree topology. Systematic Zoology, 20, 406– 416. Folmer, O., Black, M., Hoen, W., Lutz, R. & Vrijenhoek, R. (1994). DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Molecular Marine Biology and Biotechnology, 3, 294– 299. Forcart, L. (1953). The Veronicellidae of Africa (Mollusca, Pulmonata). Annales du Musee Royal du Congo Belge, 23, 1– 110. Gomes, S. R. & Thomé, J. W. (2004). Diversity and distribution of the Veronicellidae (Gastropoda; Soleolifera) in the Oriental and Australian biogeographical regions. Memoirs of the Queensland Museum, 49, 589– 601. Götting, K. J. (1985). Kiefer und Radula in der Gattung Phyllocaulis Colosi (Pulmonata: Soleolifera: Veronicellidae). Archiv für Molluskenkunde, 116, 47– 56. Graeff-Teixeira, C., Thomé, J. W., Pinto, S. C. C., Camillo-Coura, L. & Lenzi, H. L. (1989). Phyllocaulis variegatus– an intermediate host of Angiostrongylus costaricensis in south Brazil. Memórias do Instituto Oswaldo Cruz, 84, 65– 68. Graeff-Teixeira, C., Pinto, V. M., Júnior, E. B. & Agostini, A. A. (1994). Natural infection of Phyllocaulis soleiformis with larvae morphologically similar to L2 of Angiostrongylus costaricensis. Memórias do Instituto Oswaldo Cruz, 89, 121. Hall, T. A. (1999). Bioedit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series, 41, 95– 98. Hayashi, M. & Chiba, S. (2000). Intraspecific diversity of mitochondrial DNA in the land snail Euhadra peliomphala (Bradybaenidae). Biological Journal of the Linnean Society, 70, 391– 401. Hoffmann, H. (1925). Die Vaginuliden. Ein Beitrag zur Kenntnis ihre Biologie, Anatomie, Systematik, geographischen Verbreitung und Phylogenie. Jenaische Zeitschrift für Naturwissenschaft, 61, 1– 374. Hoffmann, F. G. & Baker, R. J. (2003). Comparative phylogeography of short-tailed bats (Carollia: Phyllostomidae). Molecular Ecology, 12, 3403– 3414. Huelsenbeck, J. P. & Ronquist, F. (2001). Mr. Bayes: Bayesian inference of phylogeny. Bioinformatics, 17, 754– 755. Kimura, M. (1980). A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution, 16, 111– 120. Mansur, G. G. & Thomé, J. W. (2008). Revalidation of Phyllocaulis renschi (Mollusca: Gastropoda: Veronicellidae) based on radula and mandible structures of taxonomic significance for the genus. Studies on Neotropical Fauna and Environment, 43, 77– 84. Martins, R. S. (1999). Aspectos da morfologia e biometria de cinco formas de Phyllocaulis soleiformis (Orbigny, 1835) (Gastropoda, Soleolifera, Veronicellidae). Master Dissertation. Departamento de Biociências, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre. Morrone, J. (2004). Panbiogeografia, componentes bióticos y zonas de transición. Revista Brasileira de Entomologia, 48, 149– 162. Nylander, J. A. A. (2004). Mr. Modeltest 2.2. [Computer software and manual]. Program distributed by the author. Uppsala: Uppsala University. Palumbi, S. R. (1996). Nucleic acids II: the polymerase chain reaction. In D. M. Hillis, C. Moritz & B. K. Mable (Eds) Molecular Systematics (pp. 205– 247). Sunderland, MA: Sinauer Associates. Pfenninger, M. & Posada, D. (2002). Phylogeographic history of the land snail Candidula unifasciata (Poiret 1801) (Helicellinae, Stylommatophora): fragmentation, corridor migration and secondary contact. Evolution, 56, 1776– 1788. Pfenninger, M., Eppenstein, A. & Magnin, F. (2003). Evidence for ecological speciation in the sister species Candidula unifasciata (Poiret, 1801) and C. rugosiuscula (Michaud, 1831) (Helicellinae, Gastropoda). Biological Journal of the Linnean Society, 79, 611– 628. Pinceel, J., Jordaens, K. & Backeljau, T. (2005). Extreme mtDNA divergence in a terrestrial slug (Gastropoda, Pulmonata, Arionidae): accelerated evolution, allopatric divergence and secondary contact. Journal of Evolutionary Biology, 18, 1264– 1280. Posada, D. & Crandall, K. A. (1998). Modeltest: testing the model of DNA substitution. Bioinformatics, 14, 817– 818. Rambo, R. P., Agostini, A. A. & Graeff-Teixeira, C. (1997). Abdominal angiostrongylosis in southern Brazil – prevalence and parasitic burden in molluscs intermediate hosts from eighteen endemic foci. Memórias do Instituto Oswaldo Cruz, 92, 9– 14. Ribas, C. C. & Miyaki, C. Y. (2004). Molecular systematics in Aratinga parakeets: species limits and historical biogeography in the "solstitialis" group, and the systematic position of Nandayus nenday. Molecular Phylogenetics and Evolution, 30, 663– 675. Rodriguez, F., Oliver, J. F., Marin, A. & Medina, J. R. (1990). The general stochastic model of nucleotide substitutions. Journal of Theoretical Biology, 142, 485– 501. Saitou, N. & Nei, M. (1987). The neighbor-joining method: a new method for reconstructing phylogenetic trees. Molecular Biology and Evolution, 4, 406– 425. Soares, B. M. & Thomé, J. W. (2002). Variabilidade morfológica de Phyllocaulis variegatus (Mollusca, Gastropoda, Veronicellidae) no Rio Grande do Sul, Brasil. Biociências, 10, 149– 168. Stuardo, J. R. & Vargas-Almonacid, P. (2000). Moluscos terrestres de Chile. Sinonimia y problemas relacionados: 1. Familias Veronicellidae, Pupillidae y Achatinellidae (Gastropoda: Pulmonata). Gayana, 64, 171– 188. Swofford, D. L. (1998). PAUP*: Phylogenetic Analysis Using Parsimony (and Other Methods). Version 4 [Computer software and manual]. Sunderland, MA: Sinauer. Tamura, K., Dudley, J., Nei, M. & Kumar, S. (2007). MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Molecular Biology and Evolution, 24, 1596– 1599. Thomaz, D., Guiller, A. & Clarke, B. (1996). Extreme divergence of mitochondrial DNA within species of pulmonate land snails. Proceedings of the Royal Society of London B: Biological Sciences, 263, 363– 368. Thomé, J. W. (1969). Erneute Beschreibung neotropischer Veronicellidae-Typen (Mollusca, Gastropoda). II. Arten aus der Sammlung des Senckenberg-Museums in Frankfurt a. M. Archiv für Molluskenkunde, 99, 331– 363. Thomé, J. W. (1975). Os gêneros da família Veronicellidae nas Américas (Mollusca; Gastropoda). Iheringia, 48, 3– 56. Thomé, J. W. (1976). Revisão do gênero Phyllocaulis (Colosi, 1922) (Mollusca, Veronicellidae). Iheringia, 49, 67– 90. Thomé, J. W., Gomes, S. R. & Silva, R. S. (1999). Ocorrência e distribuição da família Veronicellidae Gray, 1840 (Mollusca, Gastropoda) no Rio Grande do Sul, Brasil. Biociências, 7, 157– 165. Thompson, J. D., Gibson, T. J., Plewniak, F., Jeanmougin, F. & Higgins, D. G. (1997). The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Research, 25, 4876– 4882. Valdovinos, C., Olmos, V. & Moya, C. (2005). Moluscos terrestres y dulceacuícolas de la Cordillera de la Costa chilena. In C. Smith-Ramírez, J. Armesto & C. Valdovinos (Eds) Historia, biodiversidad y ecologia de los bosques costeros de Chile (pp. 292– 306). Santiago: Editorial Universitaria. Wade, C. M. & Mordan, P. B. (2000). Evolution within the gastropod molluscs using the ribosomal RNA gene-cluster as an indicator of phylogenetic relationships. Journal of Molluscan Studies, 66, 565– 570. Wade, C. M., Mordan, P. B. & Naggs, F. (2006). Evolutionary relationships among the Pulmonate land snails and slugs (Pulmonata, Stylommatophora). Biological Journal of the Linnean Society, 87, 593– 610. Winnepenninckx, B., Backeljau, T. & Wachter, R. (1998). Investigation of molluscan phylogeny on the basis of 18S rRNA sequences. Molecular Biology and Evolution, 13, 1306– 1317. Wüster, W., Ferguson, J. E., Quijada-Mascareñas, A., Pook, C. E., Salomão, M. G. & Thorpe, R. S. (2005). Tracing an invasion: landbridges, refugia, and the phylogeography of the Neotropical rattlesnake (Serpentes: Viperidae: Crotalus durissus). Molecular Ecology, 14, 1095– 1108. Xia, X. & Xie, Z. (2001). DAMBE: software package for data analysis in molecular biology and evolution. Journal of Heredity, 92, 371– 373. Yang, Z. & Rannala, B. (1997). Bayesian phylogenetic inference using DNA sequences: a Markov chain Monte Carlo method. Molecular Biology and Evolution, 14, 717– 724. Yoon, S. H. & Kim, W. (2000). Phylogeny of some gastropod mollusks derived from 18S rDNA sequences with emphasis on the Euthyneura. The Nautilus, 114, 84– 92. Citing Literature Supporting Information Fig. S1 A–F. Photographs of live specimens of the species of Phyllocaulis.—A. Phyllocaulis soleiformis.—B. Phyllocaulis renschi.—C. Phyllocaulis gayi.—D. Phyllocaulis variegates.—E. Phyllocaulis boraceiensis.—F. Phyllocaulis tuberculosus. Please note: Wiley-Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. Filename Description ZSC_412_sm_FigS1.jpg2.4 MB Supporting info item Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article. Volume39, Issue2March 2010Pages 177-186 ReferencesRelatedInformation

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