Literature DB >> 15143041

The genus Spiroplasma and its non-helical descendants: phylogenetic classification, correlation with phenotype and roots of the Mycoplasma mycoides clade.

Gail E Gasparich1, Robert F Whitcomb2, Deborah Dodge3, Frank E French4, John Glass5, David L Williamson6.   

Abstract

The genus Spiroplasma (helical mollicutes: Bacteria: Firmicutes: Mollicutes: Entomoplasmatales: Spiroplasmataceae) is associated primarily with insects. The Mycoplasma mycoides cluster (sensu Weisburg et al. 1989 and Johansson and Pettersson 2002) is a group of mollicutes that includes the type species - Mycoplasma mycoides - of Mycoplasmatales, Mycoplasmataceae and Mycoplasma. This cluster, associated solely with ruminants, contains five other species and subspecies. Earlier phylogenetic reconstructions based on partial 16S rDNA sequences and a limited sample of Spiroplasma and Mycoplasma sequences suggested that the genus Mycoplasma was polyphyletic, as the M. mycoides cluster and the grouping that consisted of the hominis and pneumoniae groups of Mycoplasma species were widely separated phylogenetically and the M. mycoides cluster was allied with Spiroplasma. It is shown here that the M. mycoides cluster arose from Spiroplasma through an intermediate group of non-helical spiroplasmal descendants - the Entomoplasmataceae. As this conclusion has profound implications in the taxonomy of Mollicutes, a detailed phylogenetic study of Spiroplasma and its non-helical descendants was undertaken. These analyses, done with maximum-parsimony, provide cladistic status; a new nomenclature is introduced here, based on 'bottom-up' rather than 'top-down' clade classification. The order Entomoplasmatales consists of four major clades: (i) the Mycoides-Entomoplasmataceae clade, which contains M. mycoides and its allies and Entomoplasma and Mesoplasma species and is a sister lineage to (ii) the Apis clade of Spiroplasma. Spiroplasma and the Entomoplasmataceae are paraphyletic, but this status does not diminish their phylogenetic usefulness. Five species that were previously unclassified phylogenetically are basal to the Apis clade sensu strictu and to the Mycoides clade. One of these species, Spiroplasma sp. TIUS-1, has very poor helicity and a very small genome (840 kbp); this putative species can be envisioned as a 'missing link' in the evolution of the Mycoides-Entomoplasmataceae clade. The other two Spiroplasma clades are: (iii) the Citri-Chrysopicola-Mirum clade (serogroups I, II, V and VIII) and (iv) the ixodetis clade (serogroup VI). As Mesoplasma lactucae represents a basal divergence within the Mycoides-Entomoplasmataceae clade, and as Entomoplasma freundtii is basal to the Mycoides clade, M. mycoides and its allies must have arisen from an ancestor in the Entomoplasmataceae. The paraphyletic grouping that consists of the Hominis and Pneumoniae groups (sensu Johansson & Pettersson 2002) of Mycoplasma species contains the ancestral roots of Ureaplasma spp. and haemoplasmas. This clade is a sister lineage to the Entomoplasmatales clade. Serological classifications of spiroplasma are very highly supported by the trees presented. Genome size and G+C content of micro-organismal DNA were moderately conserved, but there have been frequent and polyphyletically distributed genome reductions. Sterol requirements were polyphyletic, as was the ability to grow in the presence of polyoxyethylene sorbitan-supplemented, but not serum-supplemented, media. As this character is not phylogenetically distributed, Mesoplasma and Entomoplasma should be combined into a single genus. The phylogenetic trees presented here confirm previous reports of polyphyly of the genus Mycoplasma. As both clades of Mycoplasma contain several species of great practical importance, a change of the genus name for species in either clade would have immense practical implications. In addition, a change of the genus name for M. mycoides would have to be approved by the Judicial Commission. For these reasons, the Linnaean and phylogenetic classifications of Mycoplasma must for now be discrepant.

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Year:  2004        PMID: 15143041     DOI: 10.1099/ijs.0.02688-0

Source DB:  PubMed          Journal:  Int J Syst Evol Microbiol        ISSN: 1466-5026            Impact factor:   2.747


  53 in total

1.  Highly dynamic genomic loci drive the synthesis of two types of capsular or secreted polysaccharides within the Mycoplasma mycoides cluster.

Authors:  Clothilde Bertin; Corinne Pau-Roblot; Josiane Courtois; Lucía Manso-Silván; Florence Tardy; François Poumarat; Christine Citti; Pascal Sirand-Pugnet; Patrice Gaurivaud; François Thiaucourt
Journal:  Appl Environ Microbiol       Date:  2014-11-14       Impact factor: 4.792

2.  Evaluation of tRNA gene PCR for identification of mollicutes.

Authors:  Tim Stakenborg; Jo Vicca; Rita Verhelst; Patrick Butaye; Dominiek Maes; Anne Naessens; Geert Claeys; Catharine De Ganck; Freddy Haesebrouck; Mario Vaneechoutte
Journal:  J Clin Microbiol       Date:  2005-09       Impact factor: 5.948

3.  Heritable endosymbionts of Drosophila.

Authors:  Mariana Mateos; Sergio J Castrezana; Becky J Nankivell; Anne M Estes; Therese A Markow; Nancy A Moran
Journal:  Genetics       Date:  2006-06-18       Impact factor: 4.562

4.  Can maternally inherited endosymbionts adapt to a novel host? Direct costs of Spiroplasma infection, but not vertical transmission efficiency, evolve rapidly after horizontal transfer into D. melanogaster.

Authors:  S Nakayama; S R Parratt; K J Hutchence; Z Lewis; T A R Price; G D D Hurst
Journal:  Heredity (Edinb)       Date:  2015-02-04       Impact factor: 3.821

5.  Spiralin-like protein SLP31 from Spiroplasma eriocheiris as a potential antigen for immunodiagnostics of tremor disease in Chinese mitten crab Eriocheir sinensis.

Authors:  Qingguo Meng; Wei Gu; Keran Bi; Huyan Ji; Wen Wang
Journal:  Folia Microbiol (Praha)       Date:  2010-06-06       Impact factor: 2.099

6.  Male killing and incomplete inheritance of a novel spiroplasma in the moth Ostrinia zaguliaevi.

Authors:  Jun Tabata; Yuuki Hattori; Hironori Sakamoto; Fumiko Yukuhiro; Takeshi Fujii; Soichi Kugimiya; Atsushi Mochizuki; Yukio Ishikawa; Daisuke Kageyama
Journal:  Microb Ecol       Date:  2011-01-15       Impact factor: 4.552

7.  First human systemic infection caused by Spiroplasma.

Authors:  Ana Aquilino; Mar Masiá; Pilar López; Antonio J Galiana; Juan Tovar; María Andrés; Félix Gutiérrez
Journal:  J Clin Microbiol       Date:  2014-11-26       Impact factor: 5.948

8.  Detection of Spiroplasma and Wolbachia in the bacterial gonad community of Chorthippus parallelus.

Authors:  P Martínez-Rodríguez; M Hernández-Pérez; J L Bella
Journal:  Microb Ecol       Date:  2013-04-16       Impact factor: 4.552

9.  Prevalence of pathogenic bacteria in Ixodes ricinus ticks in Central Bohemia.

Authors:  Radek Klubal; Jan Kopecky; Marta Nesvorna; Olivier A E Sparagano; Jana Thomayerova; Jan Hubert
Journal:  Exp Appl Acarol       Date:  2015-11-26       Impact factor: 2.132

10.  Interspecific transmission of endosymbiotic Spiroplasma by mites.

Authors:  John Jaenike; Michal Polak; Anna Fiskin; Mada Helou; Miranda Minhas
Journal:  Biol Lett       Date:  2007-02-22       Impact factor: 3.703

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