Order of single-celled organisms From Wikipedia, the free encyclopedia
The vampyrellids (orderVampyrellida, class Vampyrellidea), colloquially known as vampire amoebae, are a group of free-living predatoryamoebae classified as part of the lineage Endomyxa. They are distinguished from other groups of amoebae by their irregular cell shape with propensity to fuse and split like plasmodial organisms, and their life cycle with a digestive cyst stage that digests the gathered food. They appear worldwide in marine, brackish, freshwater and soil habitats. They are important predators of an enormous variety of microscopic organisms, from algae to fungi and animals.[3] They are also known as aconchulinid amoebae (order Aconchulinida).[4]
Vampyrellids are traditionally considered filose amoebae, i.e. they generate slender pseudopodia (filopodia). They are naked, devoid of external structures such as scales, cell coats or a glycocalyx, although there may be a temporary mucilage coat in the trophozoite stage. The trophozoites vary greatly in shape, size and color between species, but can be grouped into three cell states or 'morphotypes': isodiametric, expanded, and 'filoflabellate'.[2][3]
Isodiametric (spherical) morphotype, common in algivorous Vampyrella and Lateromyxa, with radiating filopodia. Some species float in the water column, resembling heliozoa in shape. Others crawl on the surface by concentrating stiff filopodia at the anterior region of the cell, attaching them to the surface, retracting and moving them towards the posterior region.[3]
Expanded morphotype, the most common, bound to the surface, with a variety of shapes (for example, either fan-shaped or branched in Leptophrys; with large, hyaline lamellae with thread-like filopodia in Sericomyxa; highly branched or reticulate, in Platyreta and Thalassomyxa). [3]
Filoflabellate morphotype, only found in Placopus, with flattened elliptical, spherical or fan-shaped cells that exhibit a clear separation between the granuloplasmic cell hump and the hyaloplasmic lamellae, sometimes called 'lamellipodia'. There are numerous filopodia on the ventral side of the cell. Some of these trophozoites resemble amoebozoans such as vannellids, except for the presence of filopodia. They move by rolling over the filopodia that are anchored to the substrate.[3]
The three distinct morphotypes of vampyrellid amoebaeMotile cell after feeding (J), early (K) and mature (L) digestive cysts, cyst with daughter cells after internal plasmotomy (M)Large, bulky plasmodium of Vampyrella lateritiaVampyrella lateritia resting cyst with four envelopes
Nutrition stages
All known vampyrellids are heterotrophicamoebae with a free-living (non-parasitic) life cycle that lacks flagellate stages, except for Lateromyxa gallica, and is characterized by an alternation between mobile and immobile cellular stages:[3]
The mobile, amoeboid cells, called 'trophozoites' or 'swarmers'[a] in old literature. Their main activity is to disperse, search and gather food through phagocytosis.[3]
The immobile but highly metabolically active 'digestive cyst' stage, that appears after the feeding. In some species it is called a 'resting phase', but it is different from a true resting cyst (or spore) that is metabollically inactive to survive adverse conditions. To reach this stage, the trophozoite retracts its filopodia, secretes a layered cell wall, and strongly attaches itself to the substrate or floats freely. Either a central main vacuole or multiple separate vacuoles appear to digest the food. The cytoplasm color may change to a bright red, orange or yellow color, or remain colorless. When the digestive phase is finished, one or multiple trophozoites hatch from the cyst through holes in the cell wall.[3]
Reproduction
In some species, near the end of the digestive cyst stage, asexual reproduction takes place inside the cyst through a cell division (called 'internal plasmotomy'), resulting in 2–4 daughter cells. These cells are released as young trophozoites through the holes. Other species do not divide inside the closed cyst, and instead divide during or after the hatching process ('external plasmotomy'). Lateromyxa gallica shows an unusual mode of reproduction: while feeding on the inside of algal cells, the plasmodiashed and develop into digestive cysts.[3]
There is a lack of evidence for sexual reproduction in vampyrellids, except for some meiotic stages in resting cysts revealed in Lateromyxa gallica through ultrastructural studies.[5]
Plasmodial behavior
Many vampyrellid species have more than one nucleus and behave like plasmodia. They can fuse their cells upon contact, and split apart when moving in opposite directions. Some species readily grow plasmodia as large as a Petri dish under laboratory conditions, while others only fuse when the cell density is high and the food availability is low. It is uncertain to what extend this can happen in the natural environment. In contrast, Placopus species are rarely ever seen with more than two nuclei.[3]
Resting stages
Under adverse environmental conditions, vampyrellids can transform into several types of resting stages:[3]
Hypnocysts, thin-walled and devoid of food content, formed when the trophozoite is disturbed by external stress.[3]
Secondary cysts, thin-walled and devoid of food content, formed as a result of starvation.[3]
True resting cysts, also called 'sporocysts' or 'spores' in old literature. They form in natural samples and old cultures, when there is no food or the conditions are unfavorable. They build several cyst walls and condense their cellular contents. They can survive events of desiccation or freezing, up to at least three years.[3]
Vampyrellids have evolved strategies to deal with relatively large bulky prey that are difficult to consume. They display at least four different feeding strategies to engulf entire prey or to devour the contents of other eukaryoticcells. These feeding strategies are not mutually exclusive, and the same species can display each with a different type of prey.[3]
Free capture. Similarly to amoebae of other supergroups, they catch and enclose their prey within a food vacuole by usual phagocytosis. Some can paralyse their prey before the enclosement. The size of the enveloping is widely varied, from numerous small cells at the same time to entire nematodes or colonial green algae.[3]
Colony invasion. They attach to the colonies of volvocalean algae, dissolve and penetrate the extracellular gelatinous mucilage matrix, and phagocytose individual cells inside the colony. Possibly for protection against predators, they transform into digestive cysts inside of the colony.[3]
Protoplast extraction, the most famous strategy. They specifically remove, ingest and digest the cellular contents of their prey, always by dissolving the prey's organic cell wall or simply displacing the prey's siliceous wall, and invading through pseudopodia (called 'calyculopodia') to remove the cell contents . Some species eject the prey cytoplasm by applying pressure, a process known as 'plasmoptysis', which is followed by a rapid formation of a large vacuole. This process resembles a sucking motion, and is likely the reason for their comparison to vampires. In marine species no plasmoptysis is observed, which suggests that the osmotic pressure given by salinity is important for plasmoptysis.[3]
Prey infiltration. Similarly to protoplast extractors, they perforate the cell wall of an algal prey, but invade the cell itself and completes the cycle within it. Some are able to move laterally from one cell to the next in filamentous prey. They divide into smaller portions that turn into digestive cysts.[3]
Vampyrellids have a long history of research. They are known for the vampire-like feeding habit of several vampyrellid amoebae, which pierce the cell walls of other eukaryotic cells to feed specifically on the cell contents, a feeding mechanism known as protoplast extraction. This similarity lead to the origin of the name for their most popular genus, Vampyrella, and their colloquial name 'vampire amoebae'.[3]
One of the earliest unambiguous reports of a vampyrellid is the mid-19th century description of Amoeba lateritia (now known as Vampyrella lateritia) by the German botanist Georg Fresenius.[13] The first extensive documentation of their life history and feeding behavior was provided in 1865 by the Polish protozoologist Leon Cienkowski, who created the genus Vampyrella and classified it in a subgroup of the 'monads',[14] a polyphyletic assemblage of parasitoidprotists. Posterior works and monographs described numerous aquatic vampyrellid species, with important observations of their behaviour and ecology. In 1885, the German mycologist Wilhelm Zopf demonstrated the presence of nuclei in vampyrellids and erected the first family, Vampyrellidae.[15][16][3]
In the mid-20th century the first discoveries of soil-dwelling Vampyrellida were made. The first vampyrellid laboratory culture was established, containing the soil amoeba Theratomyxa weberi that fed on nematodes. Similar soil amoebae were isolated later, and studied as possible pest control against plant-pathogenic nematodes.[17] Other studies identified a giant soil vampyrellid as the organism responsible for perforations found in fungalspores.[18][3]
Vampyrellida represents one of the major groups of free-living amoebae, phylogenetically separate from other groups of amoebae such as Amoebozoa, Heterolobosea and Nucleariidae. Instead, Vampyrellida is an isolated clade within the Rhizariasupergroup.[26] They are the closest relatives of the Phytomyxea, parasites of plants and algae that, unlike vampyrellids, disperse through flagellated stages during their life cycle and spend most of their active life within host cells.[3] Current classifications place both Vampyrellida and Phytomyxea, along with other small groups of Rhizaria, within the phylum Endomyxa.[4] Several phylogenetic analyses have recovered a sister group relationship between Vampyrellida and Phytomyxea and have named their clade Proteomyxia[1] or Phytorhiza.[27]
There are currently 48 credible vampyrellid species distributed in 10 genera, scattered across five well-established clades found through genetic data, four of which are families. Despite the advances, most of the vampyrellid diversity is still unknown or undescribed.[3]
Family VampyrellidaeZopf 1885 emend. Hess, Sausen et Melkonian 2012[2]
The term 'swarmers' is more specially used for ciliated, swimming cells such as gametes, so trophozoites is a more appropriate term.[3]
Not to be confused with the diatom genus HyalodiscusEhrenberg 1845, which takes preference in the biological nomenclature for being described earlier.[3]
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