Literature DB >> 19017064

Morphology, conjugation, and postconjugational reorganization of Dileptus tirjakovae n. sp. (Ciliophora, Haptoria).

Peter Vdacný1, Wilhelm Foissner.   

Abstract

We studied the morphology, conjugation, and postconjugational reorganization of a new haptorid ciliate, Dileptus tirjakovae n. sp., using conventional methods. Dileptus tirjakovae is characterized by two abutting, globular macronuclear nodules and scattered brush kinetids. Conjugation is similar to that in congeners, that is, it is temporary, heteropolar, and the partners unite bulge-to-bulge with the proboscis. Some peculiarities occur in the nuclear processes: there are two synkaryon divisions producing four synkaryon derivatives, of which two become macronuclear anlagen, one becomes the micronucleus, and one degenerates. Unlike spathidiids, D. tirjakovae shows massive changes in body shape and ciliary pattern before, during, and after conjugation: early and late conjugants as well as early exconjugants resemble Spathidium, while mid-conjugants resemble Enchelyodon. These data give support to the hypothesis that spathidiids evolved from a Dileptus-like ancestor by reduction of the proboscis. Dileptus tirjakovae exconjugants differ from vegetative cells by their smaller size, stouter body, shorter proboscis, and by the lower number of ciliary rows, suggesting one or several postconjugation divisions. Although 83% of the exconjugants have the vegetative nuclear pattern, some strongly deviating specimens occur and might be mistaken for distinct species, especially because exconjugants are less than half as long as vegetative cells.

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Year:  2008        PMID: 19017064      PMCID: PMC2917757          DOI: 10.1111/j.1550-7408.2008.00343.x

Source DB:  PubMed          Journal:  J Eukaryot Microbiol        ISSN: 1066-5234            Impact factor:   3.346


  4 in total

1.  Body, nuclear, and ciliary changes during conjugation of Protospathidium serpens (Ciliophora, Haptoria).

Authors:  Kuidong Xu; Wilhelm Foissner
Journal:  J Eukaryot Microbiol       Date:  2004 Nov-Dec       Impact factor: 3.346

2.  Basic light and scanning electron microscopic methods for taxonomic studies of ciliated protozoa.

Authors:  W Foissner
Journal:  Eur J Protistol       Date:  2011-11-02       Impact factor: 3.020

3.  Molecular phylogeny of litostome ciliates (Ciliophora, Litostomatea) with emphasis on free-living haptorian genera.

Authors:  Michaela C Strüder-Kypke; Andre-Denis G Wright; Wilhelm Foissner; Antonis Chatzinotas; Denis H Lynn
Journal:  Protist       Date:  2006-07-13

4.  Regulation of ciliary pattern in dileptus (Ciliata). II. Formation of a cortical domain of sensory cilia from a domain of locomotor cilia.

Authors:  K Golinska
Journal:  J Cell Sci       Date:  1983-07       Impact factor: 5.285

  4 in total
  4 in total

1.  Ontogenesis of Dileptus terrenus and Pseudomonilicaryon brachyproboscis (Ciliophora, Haptoria).

Authors:  Peter Vdacný; Wilhelm Foissner
Journal:  J Eukaryot Microbiol       Date:  2009 May-Jun       Impact factor: 3.346

2.  Description of Four New Soil Dileptids (Ciliophora, Haptoria), with Notes on Adaptations to the Soil Environment.

Authors:  Peter Vďačný; Wilhelm Foissner
Journal:  Acta Protozool       Date:  2008       Impact factor: 0.892

3.  Genealogical analyses of multiple loci of litostomatean ciliates (Protista, Ciliophora, Litostomatea).

Authors:  Peter Vd'ačný; William A Bourland; William Orsi; Slava S Epstein; Wilhelm Foissner
Journal:  Mol Phylogenet Evol       Date:  2012-07-10       Impact factor: 4.286

4.  Morphological and molecular phylogeny of dileptid and tracheliid ciliates: resolution at the base of the class Litostomatea (Ciliophora, Rhynchostomatia).

Authors:  Peter Vďačný; William Orsi; William A Bourland; Satoshi Shimano; Slava S Epstein; Wilhelm Foissner
Journal:  Eur J Protistol       Date:  2011-06-08       Impact factor: 3.020

  4 in total

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