Topic
Epixenosomes
About: Epixenosomes is a research topic. Over the lifetime, 16 publications have been published within this topic receiving 363 citations. The topic is also known as: Epixenosoma & Epixenosomes.
Papers
TL;DR: This work characterized the ultrastructure and molecular phylogenetic position of B. bacati, a novel (uncultivated) lineage of heterotrophic euglenozoan that belongs to the Euglenozoa and currently branches as the earliest diverging member of the Symbiontida
Abstract: Poorly understood but highly diverse microbial communities exist within anoxic and oxygen-depleted marine sediments. These communities often harbour single-celled eukaryotes that form symbiotic associations with different prokaryotes. During low tides in South-western British Columbia, Canada, vast areas of marine sand become exposed, forming tidal pools. Oxygen-depleted sediments within these pools are distinctively black at only 2-3 cm depth; these layers contain a rich variety of microorganisms, many of which are undescribed. We discovered and characterized a novel (uncultivated) lineage of heterotrophic euglenozoan within these environments using light microscopy, scanning and transmission electron microscopy, serial sectioning and ultrastructural reconstruction, and molecular phylogenetic analyses of small subunit rDNA sequences. Bihospites bacati n. gen. et sp. is a biflagellated microbial eukaryote that lives within low-oxygen intertidal sands and dies within a few hours of exposure to atmospheric oxygen. The cells are enveloped by two different prokaryotic episymbionts: (1) rod-shaped bacteria and (2) longitudinal strings of spherical bacteria, capable of ejecting an internal, tightly wound thread. Ultrastructural data showed that B. bacati possesses all of the euglenozoan synapomorphies. Moreover, phylogenetic analyses of SSU rDNA sequences demonstrated that B. bacati groups strongly with the Symbiontida: a newly established subclade within the Euglenozoa that includes Calkinsia aureus and other unidentified organisms living in low-oxygen sediments. B. bacati also possessed novel features, such as a compact C-shaped rod apparatus encircling the nucleus, a cytostomal funnel and a distinctive cell surface organization reminiscent of the pellicle strips in phagotrophic euglenids. We characterized the ultrastructure and molecular phylogenetic position of B. bacati n. gen. et sp. Molecular phylogenetic analyses demonstrated that this species belongs to the Euglenozoa and currently branches as the earliest diverging member of the Symbiontida. This is concordant with ultrastructural features of B. bacati that are intermediate between C. aureus and phagotrophic euglenids, indicating that the most recent ancestor of the Symbiontida descended from phagotrophic euglenids. Additionally, the extrusive episymbionts in B. bacati are strikingly similar to so-called "epixenosomes", prokaryotes previously described in a ciliate species and identified as members of the Verrucomicrobia. These parallel symbioses increase the comparative context for understanding the origin(s) of extrusive organelles in eukaryotes and underscores how little we know about the symbiotic communities of marine benthic environments.
53 citations
TL;DR: A new symbiotic hypothesis is proposed: that the mid-ancestor of eukaryotic cells obtained epixenosomelike verrucomicrobia as defensive ectosYmbionts and the ectosymbiont later became endosyMBiotic, and some of the protrusions took on a new role in cell movement, which led to evolve into flagella.
Abstract: The origin of eukaryotic flagella has long been a mystery. Here we review the possibility that flagella sprouted evolutionarily from the eukaryotic cell proper seems very unlikely because it is hard to imagine what function and benefit in natural selection the flagella would have provided to the cells when they first emerged as simple buds. Lynn Margulis' 1970 spirochete hypothesis, though popular still, has never been confirmed. Moreover, the absence of tubulin and axonemal dynein in the spirochetes and the incapability of the bacterial and eukaryotic membranes' making a continuum now suggest that the hypothesis is outdated. Tubulin genes were recently identified in a new bacteria division, verrucomicrobia, and microtubules have also been found in one of these species, epixenosomes, the defensive ectosymbionts. On the basis of these data, we propose a new symbiotic hypothesis: that the mid-ancestor of eukaryotic cells obtained epixenosomelike verrucomicrobia as defensive ectosymbionts and the ectosymbionts later became endosymbiotic. They still, however, protruded from the surface of their host to play their role. Later, many genes were lost or incorporated into the host genome. Finally, the genome, the bacterial membrane, and the endosymbiotic vesicle membrane were totally lost, and fingerlike protrusions with microtubules formed. As the cells grew larger, the defensive function of the protrusions eventually weakened and then vanished. Some of the protrusions took on a new role in cell movement, which led them to evolve into flagella. The key step in this process was that the dynein obtained from the host evolved into axonemal dyneins, attaching onto the microtubules and forming motile axonemes. Our hypothesis is unproven, but it offers a possible explanation that is consistent with current scientific thought. We hope that our ideas will stimulate additional studies on the origin of eukaryotic flagella and on investigations of verrucomicrobia. Whether such studies confirm, refine, or replace our hypothesis, they should nevertheless further our understanding of the origin of eukaryotic cells.
44 citations
TL;DR: It has been found that BT, besides being well preserved when fixed in the presence of tannic acid, are sensitive to factors known to depolymerize cytoplasmic microtubules in a variety of cells such as nocodazole and cold and show a positive immunoreaction against different antitubulin antibodies.
29 citations
TL;DR: The hypothesis that epixenosomes play a defensive role against predators was tested by comparing the behavior of Litonotus lamella when preying upon Euplotes crassus, E. itoi without epIXenosomes, and to a certain extent, Euplotidium with epixenesomes whose ejecting capability has been inhibited, and the involvement of the epxenosome's ejecting apparatus in a defensive function was suggested.
Abstract: . Euplotidium itoi harbors on its dorsal surface peculiar episymbionts (referred to as epixenosomes) equipped with a complex extrusive apparatus. In the laboratory. E. itoi stocks without epixenosomes behave and reproduce like symbiotized stocks. the hypothesis that epixenosomes play a defensive role against predators was tested by comparing the behavior of Litonotus lamella when preying upon Euplotes crassus, E. itoi without epixenosomes. and E. itoi with epixenosomes. Litonotus discharges its toxicysts upon direct-cell-to cell contact, and paralyzes the three types of prey with the same efficiency. Nevertheless, Litonotus can ingest Euplotes, Euplotidium without epixenosomes, and to a certain extent, Euplotidium with epixenosomes whose ejecting capability has been inhibited. while it never eats Euplotidium with unaltered epixenosomes. In each prey-type, about 60% of the individuals attacked by Litonotus toxicyst discharge are able to recover their normal behavior once transferred into pure sea water. This percentage for E. itoi with epixenosomes that are never eaten by the predator corresponds to the probability of survival. This probability is lower for the other two prey-types in which the prey engulfed by the predator do not have the chance to recover. These data support the hypothesis and suggest the involvement of the epixenosome's ejecting apparatus in a defensive function.
27 citations
TL;DR: In this article, the ultrastructure of the extrusive apparatus of epixenosomes has been analyzed by means of SEM observations, thin sectioning and negative staining, and it is shown that this structure gradually acquires its definitive appearance.
17 citations
Related Topics (5)
Performance Metrics
| Year | Papers |
|---|---|
| 2010 | 2 |
| 2005 | 1 |
| 2003 | 1 |
| 2000 | 1 |
| 1999 | 3 |
| 1998 | 1 |