Incorporating mitogenome sequencing into integrative taxonomy: The multidisciplinary redescription of the ciliate Thuricola similis (Peritrichia, Vaginicolidae) provides new insights into the evolutionary relationships among Oligohymenophorea subclasses.


Journal

Molecular phylogenetics and evolution
ISSN: 1095-9513
Titre abrégé: Mol Phylogenet Evol
Pays: United States
ID NLM: 9304400

Informations de publication

Date de publication:
05 2021
Historique:
received: 14 11 2020
revised: 13 01 2021
accepted: 26 01 2021
pubmed: 6 2 2021
medline: 22 6 2021
entrez: 5 2 2021
Statut: ppublish

Résumé

The evolutionary relationships among Oligohymenophorea subclasses are under debate as the phylogenomic analysis using a large dataset of nuclear coding genes is significantly different to the 18S rDNA phylogeny, and it is unfortunately not stable within and across different published studies. In addition to nuclear genes, the faster-evolving mitochondrial genes have also shown the ability to solve phylogenetic problems in many ciliated taxa. However, due to the paucity of mitochondrial data, the corresponding work is scarce, let alone the phylogenomic analysis based on mitochondrial gene dataset. In this work, we presented the characterization on Thuricola similis Bock, 1963, a loricate peritrich (Oligohymenophorea), incorporating mitogenome sequencing into integrative taxonomy. As the first mitogenome for the subclass Peritrichia, it is linear, 38,802 bp long, and contains two rRNAs, 12 tRNAs, and 43 open reading frames (ORFs). As a peculiarity, it includes a central repeated region composed of tandemly repeated A-T rich units working as a bi-transcriptional start. Moreover, taking this opportunity, the phylogenomic analyses based on a set of mitochondrial genes were also performed, revealing that T. similis, as a representative of Peritrichia subclass, branches basally to other three Oligohymenophorea subclasses, namely Hymenostomatia, Peniculia, and Scuticociliatia. Evolutionary relationships among those Oligohymenophorea subclasses were discussed, also in the light of recent phylogenomic reconstructions based on a set of nuclear genes. Besides, as a little-known species, T. similis was also redescribed and neotypified based on data from two populations collected from wastewater treatment plants (WWTPs) in Brazil and Italy, by means of integrative methods (i.e., living observation, silver staining methods, scanning and transmission electron microscopy, and 18S rDNA phylogeny). After emended diagnosis, it is characterized by: (1) the sewage habitat; (2) the lorica with a single valve and small undulations; (3) the 7-22 µm-long inner stalk; and (4) the presence of only a single postciliary microtubule on the left side of the aciliferous row in the haplokinety. Among Vaginicolidae family, our 18S rRNA gene-based phylogenetic analysis revealed that Thuricola and Cothurnia are monophyletic genera, and Vaginicola could be a polyphyletic genus.

Identifiants

pubmed: 33545277
pii: S1055-7903(21)00022-1
doi: 10.1016/j.ympev.2021.107089
pii:
doi:

Substances chimiques

RNA, Ribosomal, 18S 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107089

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Wanying Liao (W)

Department of Biology, University of Pisa, Via A. Volta 4/6, 56126 Pisa, Italy.

Pedro Henrique Campello-Nunes (PH)

Laboratório de Protistologia, Instituto de Biologia, Departamento de Zoologia, Universidade Federal do Rio de Janeiro, CEP: 21941-902 Ilha do Fundão, Rio de Janeiro, Brazil.

Leandro Gammuto (L)

Department of Biology, University of Pisa, Via A. Volta 4/6, 56126 Pisa, Italy.

Tiago Abreu Viana (T)

Laboratório de Protistologia, Instituto de Biologia, Departamento de Zoologia, Universidade Federal do Rio de Janeiro, CEP: 21941-902 Ilha do Fundão, Rio de Janeiro, Brazil.

Roberto de Oliveira Marchesini (R)

Laboratório de Protistologia, Instituto de Biologia, Departamento de Zoologia, Universidade Federal do Rio de Janeiro, CEP: 21941-902 Ilha do Fundão, Rio de Janeiro, Brazil.

Thiago da Silva Paiva (T)

Laboratório de Protistologia, Instituto de Biologia, Departamento de Zoologia, Universidade Federal do Rio de Janeiro, CEP: 21941-902 Ilha do Fundão, Rio de Janeiro, Brazil.

Inácio Domingos da Silva-Neto (ID)

Laboratório de Protistologia, Instituto de Biologia, Departamento de Zoologia, Universidade Federal do Rio de Janeiro, CEP: 21941-902 Ilha do Fundão, Rio de Janeiro, Brazil.

Letizia Modeo (L)

Department of Biology, University of Pisa, Via A. Volta 4/6, 56126 Pisa, Italy; CISUP, Centro per l'Integrazione della Strumentazione Scientifica dell'Università di Pisa, Lungarno Pacinotti 43, 56126 Pisa, Italy. Electronic address: letizia.modeo@unipi.it.

Giulio Petroni (G)

Department of Biology, University of Pisa, Via A. Volta 4/6, 56126 Pisa, Italy; CISUP, Centro per l'Integrazione della Strumentazione Scientifica dell'Università di Pisa, Lungarno Pacinotti 43, 56126 Pisa, Italy. Electronic address: giulio.petroni@unipi.it.

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