Ellobiopsis

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Ellobiopsis
Scientific classification
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Ellobiopsis

Caullery, 1910
Species

Ellobiopsis caridarum
Ellobiopsis chattonii
Ellobiopsis elongata
Ellobiopsis eupraxiae
Ellobiopsis fagei
Ellobiopsis racemosus

Contents

Ellobiopsis is a genus of unicellular, ectoparasitic eukaryotes causing disease in crustaceans. [1] This genus is widespread and has been found infecting copepods from both marine and freshwater ecosystems. [2] parasitism has been seen to interfere with fertility in both sexes of copepods. [3] [2]

Taxonomy and History

The Ellobiopsis type species, Ellobiopsis chattoni, was first described in 1910 by Caullery after being isolated from an infected copepod found in the Mediterranean Sea. Ellobiopsis was first classified as a dinoflagellate, but observation of a spore forming organelle concluded that the Ellobiopsis was not a part of this group. Phylogeny based on small subunit (SSU) ribosomal DNA places Ellobiopsis in the Alveolata. [4] In the family Ellobiopsidae, the most closely related genus is Thalassomyces. [4] Three species have been defined in this genus: Ellobiopsis chattoni Caullery (1910), Ellobiopsis elongata Steuer (1932) and Ellobiopsis fagei Hovasse (1951). These species are characterized by morphology of their reproductive structures and their ability to infect species specific hosts.

Description

Morphology

During dispersal, unflagellated spores of Ellobiopsis land on the surface of potential hosts. Once in contact with a host, the cell body of the organism grows and takes on an oval shape. A rhizoid pierces the host cuticle to root the parasite in the copepod tissue. The cell body constricts in the center and differentiate into trophomere and gonomere, proximal and distal to the host body. The cell forms a conical shape. The number of gonomeres is distinguishes species. [2] The cell body has been seen to grows to a length of 700 µm and a width of 350 µm. [5]

Life cycle

The parasitic life cycle of Ellobiopsis chattoni begins with a spore that lands on the surface of a host appendage. A stalk attaches the parasite to the host and it uses an organelle for penetration, called a rhizoid, of the cuticle and to root itself in the host tissue. [2] [5] As the cell grows the root is used for absorption, causing damaging to the local host tissue. [2] Once established at a specific size, approximately 400 µm, [5] the cell body begins to partition itself in half. The half not attached to the host becomes the gonomere and the half attached to the host is named the trophomere. As the gonomere and trophomere partitioning continues to partition, the spore begins to form in the gonomere and it takes on a granulated texture. The pre-spores are released from the reproductive body and form spores for dispersal to the next host. [4]

Host records

Related Research Articles

Apicomplexa Phylum of parasitic alveolates

The Apicomplexa are a large phylum of parasitic alveolates. Most of them possess a unique form of organelle that comprises a type of non-photosynthetic plastid called an apicoplast, and an apical complex structure. The organelle is an adaptation that the apicomplexan applies in penetration of a host cell.

Copepod Subclass of crustaceans

Copepods are a group of small crustaceans found in nearly every freshwater and saltwater habitat. Some species are planktonic, some are benthic, a number of species have parasitic phases, and some continental species may live in limnoterrestrial habitats and other wet terrestrial places, such as swamps, under leaf fall in wet forests, bogs, springs, ephemeral ponds, and puddles, damp moss, or water-filled recesses (phytotelmata) of plants such as bromeliads and pitcher plants. Many live underground in marine and freshwater caves, sinkholes, or stream beds. Copepods are sometimes used as biodiversity indicators.

Perkinsus marinus is a species of alveolates belonging to the phylum Perkinsozoa. It is similar to a dinoflagellate. It is known as a prevalent pathogen of oysters, causing massive mortality in oyster populations. The disease it causes is known as dermo or perkinsosis, and is characterized by the degradation of oyster tissues. The genome of this species has been sequenced.

Velvet (fish disease)

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Gregarinasina Subclass of protists

The gregarines are a group of Apicomplexan alveolates, classified as the Gregarinasina or Gregarinia. The large parasites inhabit the intestines of many invertebrates. They are not found in any vertebrates. However, gregarines are closely related to both Toxoplasma and Plasmodium, which cause toxoplasmosis and malaria, respectively. Both protists use protein complexes similar to those that are formed by the gregarines for gliding motility and invading target cells. This makes them excellent models for studying gliding motility with the goal of developing treatment options for toxoplasmosis and malaria. Thousands of different species of gregarines are expected to be found in insects, and 99% of these gregarines still need to be described. Each insect can be the host of multiple species. One of the most studied gregarines is Gregarina garnhami. In general, gregarines are regarded as very successful parasites, as their hosts are spread over the entire planet.

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Xenoma

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<i>Entomophthora</i>

Entomophthora is a fungal genus in the family Entomophthoraceae. Species in this genus are parasitic on flies and other two-winged insects. The genus was circumscribed by German biologist Ferdinand Cohn in 1856.

Fish disease and parasites Disease that affects fish

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Syndinium is a cosmopolitan genus of parasitic dinoflagellates that infest and kill marine planktonic species of copepods and radiolarians. Syndinium belongs to order Syndiniales, a candidate for the uncultured group I and II marine alveolates. The lifecycle of Syndinium is not well understood beyond the parasitic and zoospore stages.

Hematodinium is a genus of dinoflagellates. Species in this genus, such as Hematodinium perezi, the type species, are internal parasites of the hemolymph of crustaceans such as the Atlantic blue crab and Norway lobster. Species in the genus are economically damaging to commercial crab fisheries, including causing bitter crab disease in the large Tanner or snow crab fisheries of the Bering Sea.

Parvilucifera is a genus of marine alveolates that parasitise dinoflagellates. Parvilucifera is a parasitic genus described in 1999 by Norén et al. It is classified perkinsozoa in the supraphylum of Alveolates. This taxon serves as a sister taxon to the dinoflagellates and apicomplexans. Thus far, five species have been described in this taxon, which include: P.infectans, P.sinerae, P.corolla, P.rostrata, and P.prorocentri. The genus Parvilucifera is morphologically characterized by flagellated zoospore. The life cycle of the species in this genus consist of free-living zoospores, an intracellular stage called trophont, and asexual division to form resting sporangium inside host cell. This taxon has gained more interest in research due to its potential significance in terms of negative regulation for dinoflagellates blooms, that have proved harmful for algal species, humans, and the shellfish industry.

Pasteuria is a genus of mycelial and endospore-forming, nonmotile gram-positive bacteria that are obligate parasites of some nematodes and crustaceans. The genus of Pasteuria was previously classified within the family Alicyclobacillaceae, but has since been moved to the family Pasteuriaceae.

Physoderma is a genus of chytrid fungi. Described by German botanist Karl Friedrich Wilhelm Wallroth in 1833, the genus contains some species that are parasitic on vascular plants, including P. alfalfae and P. maydis, causative agents of crown wart of alfalfa and brown spot of corn, respectively. Of the chytrid genera, Physoderma is the oldest. However, species were confused with the rust fungi, the genus Synchytrium, and the genus Protomyces of Ascomycota. Members of Physoderma are obligate parasites of pteridophytes and angiosperms. There are approximately 80 species within this genus.

Amyloodinium ocellatum is a cosmopolitan ectoparasite dinoflagellate of numerous aquatic organisms living in brackish and seawater environments. The dinoflagellate is endemic in temperate and tropical areas, and is capable of successfully adapting to a variety of different environments and to a great number of hosts, having been identified in four phyla of aquatic organisms: Chordata, Arthropoda, Mollusca and Platyhelminthes. Moreover, it is the only dinoflagellate capable of infecting teleosts and elasmobranchs.

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Coccidinium is a genus of parasitic syndinian dinoflagellates that infect the nucleus and cytoplasm of other marine dinoflagellates. Coccidinium, along with two other dinoflagellate genera, Amoebophyra and Duboscquella, contain species that are the primary endoparasites of marine dinoflagellates. While numerous studies have been conducted on the genus Amoebophyra, specifically Amoebophyra ceratii, little is known about Coccidinium. These microscopic organisms have gone relatively unstudied after the initial observations of Édouard Chatton and Berthe Biecheler in 1934 and 1936.

Ichthyodinium is a monotypic genus of dinoflagellates in the family Dinophysaceae. Ichthyodinium chabelardi (/ɪkθioʊˈdɪniəm/) is currently the sole described species of the genus.

<i>Haplozoon</i> Genus of single-celled organisms

Haplozoon (/hæploʊ’zoʊən/) are unicellular endo-parasites, primarily infecting maldanid polychaetes. They belong to Dinoflagellata but differ from typical dinoflagellates. Most dinoflagellates are free-living and possess two flagella. Instead, Haplozoon belong to a 5% minority of parasitic dinoflagellates that are not free-living. Additionally, the Haplozoon trophont stage is particularly unique due to an apparent lack of flagella. The presence of flagella or remnant structures is the subject of ongoing research.

Nectonema is a genus of marine horsehair worms first described by Addison E. Verrill in 1879. It is the only genus in the family Nectonematidae described by Henry B. Ward in 1892, in the order Nectonematoidea, and in the class Nectonematoida. The genus contains five species; all species have a parasitic larval stage inhabiting crustacean hosts and a free-living adult stage that swims in open water.

References

  1. Gómez F, López-García P, Nowaczyk A, Moreira D (2009). "The crustacean parasites Ellobiopsis Caullery, 1910 and Thalassomyces Niezabitowski, 1913 form a monophyletic divergent clade within the Alveolata". Syst. Parasitol. 74 (1): 65–74. doi:10.1007/s11230-009-9199-1. PMID   19633933. S2CID   3901878.
  2. 1 2 3 4 5 Shields, Jeffrey D. (1994). "The parasitic dinoflagellates of marine crustaceans". Annual Review of Fish Diseases. 4: 241–271. CiteSeerX   10.1.1.520.1367 . doi:10.1016/0959-8030(94)90031-0.
  3. Albaina, A.; Irigoien, X. (2006-04-01). "Fecundity limitation of Calanus helgolandicus, by the parasite Ellobiopsis sp". Journal of Plankton Research. 28 (4): 413–418. doi: 10.1093/plankt/fbi129 . ISSN   0142-7873.
  4. 1 2 3 Gómez, Fernando; López-García, Purificación; Nowaczyk, Antoine; Moreira, David (September 2009). "The crustacean parasites Ellobiopsis Caullery, 1910 and Thalassomyces Niezabitowski, 1913 form a monophyletic divergent clade within the Alveolata". Systematic Parasitology. 74 (1): 65–74. doi:10.1007/s11230-009-9199-1. ISSN   1573-5192. PMID   19633933. S2CID   3901878.
  5. 1 2 3 V., Santhakumari; M., Saraswathy (1979). "On the ellobiopsidae, parasitic protozoa from zooplankton". Mahasagar: Bulletin of the National Institute of Oceanography, India. ISSN   0542-0938.