Paramecium

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"Paramecia" redirects here. For the prehistoric protist, see Paramecia (alga).

Paramecium
"Paramecium aurelia"
Paramecium aurelia
Scientific classification Edit this classification
Domain: Eukaryota
Clade: Diaphoretickes
Clade: SAR
Clade: Alveolata
Phylum: Ciliophora
Class: Oligohymenophorea
Order:
Peniculida
Family: Parameciidae
Genus: Paramecium
Müller, 1773
Species

See text

Synonyms[1]
  • Paramoecium Hermann, 1783
  • Paramœcium Hermann, 1783
  • Chloroparamecium Fokin, Przybos, Chivilev, Beier, Horn, Skotarczak, Wodecka & Fujishima, 2004
  • Viridoparamecium Kreutz, Stoeck & Foissner, 2012

Paramecium (

Ciliophora.[3]

Historical background

Paramecia, illustrated by Otto Müller, 1773
Earliest known illustration of Paramecium
"Slipper animalcule," illustrated by Louis Joblot, 1718

Paramecium were among the first ciliates to be observed by

protozoology, Antonie van Leeuwenhoek, and were clearly described by his contemporary Christiaan Huygens in a letter from 1678.[4] The earliest known illustration of a Paramecium species was published anonymously in Philosophical Transactions of the Royal Society in 1703.[5]

In 1718, the French mathematics teacher and microscopist Louis Joblot published a description and illustration of a microscopic poisson (fish), which he discovered in an infusion of oak bark in water. Joblot gave this creature the name "Chausson", or "slipper", and the phrase "slipper animalcule" remained in use as a colloquial epithet for Paramecium, throughout the 18th and 19th centuries.[6]

The name "Paramecium" – constructed from the Greek παραμήκης (paramēkēs, "oblong") – was coined in 1752 by the English microscopist John Hill, who applied the name generally to "Animalcules which have no visible limbs or tails, and are of an irregularly oblong figure."[7] In 1773, O. F. Müller, the first researcher to place the genus within the Linnaean system of taxonomy, adopted the name Paramecium but changed the spelling to Paramæcium.[8] In 1783, Johann Hermann changed the spelling once more, to Paramœcium.[9] C. G. Ehrenberg, in a major study of the infusoria published in 1838, restored Hill's original spelling for the name, and most researchers have followed his lead.[10]

Description

A diagram of Paramecium caudatum
A diagram of Paramecium caudatum

Species of Paramecium range in size from 50 to 330 μm in length. Cells are typically ovoid, elongate, or foot- or cigar-shaped.

The body of the cell is enclosed by a stiff but elastic structure called the

pellicle. The pellicle consists of an outer cell membrane (plasma membrane), a layer of flattened membrane-bound sacs called alveoli, and an inner membrane called the epiplasm. The pellicle is not smooth, but textured with hexagonal or rectangular depressions. Each of these polygons is perforated by a central aperture through which a single cilium projects. Between the alveolar sacs of the pellicle, most species of Paramecium have closely spaced spindle-shaped trichocysts, explosive organelles that discharge thin, non-toxic filaments, often used for defensive purposes.[11][12]

Typically, an

anterior of the cell to its midpoint. This is lined with inconspicuous cilia which beat continuously, drawing food into the cell.[13] Paramecium are primarily heterotrophic, feeding on bacteria and other small organisms. A few species are mixotrophs, deriving some nutrients from endosymbiotic algae (chlorella) carried in the cytoplasm of the cell.[14]

Osmoregulation is carried out by contractile vacuoles, which actively expel water from the cell to compensate for fluid absorbed by osmosis from its surroundings.[15] The number of contractile vacuoles varies depending on the species.[13]

Movement

A Paramecium propels itself by whip-like movements of the cilia, which are arranged in tightly spaced rows around the outside of the body. The beat of each cilium has two phases: a fast "effective stroke," during which the cilium is relatively stiff, followed by a slow "recovery stroke," during which the cilium curls loosely to one side and sweeps forward in a counter-clockwise fashion. The densely arrayed cilia move in a coordinated fashion, with waves of activity moving across the "ciliary carpet," creating an effect sometimes likened to that of the wind blowing across a field of grain.[16]

The Paramecium spirals through the water as it progresses. When it happens to encounter an obstacle, the "effective stroke" of its cilia is reversed and the organism swims backward for a brief time, before resuming its forward progress. This is called the avoidance reaction. If it runs into the solid object again, it repeats this process, until it can get past the object.[17]

It has been calculated that a Paramecium expends more than half of its energy in propelling itself through the water.[18] This ciliary method of locomotion has been found to be less than 1% efficient. This low percentage is nevertheless close to the maximum theoretical efficiency that can be achieved by an organism equipped with cilia as short as those of the members of Paramecium.[19]

Gathering food

Paramecium feeding on Bacteria

Paramecium feed on microorganisms like bacteria, algae, and yeasts. To gather food, the Paramecium makes movements with cilia to sweep prey organisms, along with some water, through the oral groove (vestibulum, or vestibule), and into the cell. The food passes from the cilia-lined oral groove into a narrower structure known as the buccal cavity (gullet). From there, food particles pass through a small opening called the cytostome, or cell mouth, and move into the interior of the cell. As food enters the cell, it is gathered into food vacuoles, which are periodically closed off and released into the cytoplasm, where they begin circulating through the cell body by the streaming movement of the cell contents, a process called cyclosis or cytoplasmic streaming. As a food vacuole moves along, enzymes from the cytoplasm enter it, to digest the contents. As enzymatic digestion proceeds, the vacuole contents become more acidic. Within five minutes of a vacuole's formation, the pH of its contents drops from 7 to 3.[20] As digested nutrients pass into the cytoplasm, the vacuole shrinks. When the fully digested vacuole reaches the anal pore, it ruptures, expelling its waste contents outside the cell.[21][22][23]

Symbiosis

Some species of Paramecium form

kappa particles, give Paramecium the ability to kill other strains of Paramecium that lack kappa particles.[26]

Genome

The

genome duplications.[27]

In some ciliates, like Stylonychia and Paramecium, only UGA is decoded as a stop codon, while UAG and UAA are reassigned as sense codons (that is, codons that code for standard amino acids), coding for the amino acid glutamic acid.[28]

Learning

The question of whether Paramecium exhibit learning has been the object of a great deal of experimentation, yielding equivocal results. However, a study published in 2006 seems to show that Paramecium caudatum may be trained, through the application of a 6.5 volt electric current, to discriminate between brightness levels.[29] This experiment has been cited as a possible instance of cell memory, or epigenetic learning in organisms with no nervous system.[30]

Reproduction and sexual phenomena

Reproduction

Like all ciliates, Paramecium have a dual

micronuclei. The macronucleus controls non-reproductive cell functions, expressing the genes needed for daily functioning. The micronucleus is the generative, or germline nucleus, containing the genetic material that is passed along from one generation to the next.[31]

Paramecium reproduction is asexual, by binary fission, which has been characterized as "the sole mode of reproduction in ciliates" (conjugation being a sexual phenomenon, not directly resulting in increase of numbers).[3][32] During fission, the macronucleus splits by a type of amitosis, and the micronuclei undergo mitosis. The cell then divides transversally, and each new cell obtains a copy of the micronucleus and the macronucleus.[3]

Fission may occur spontaneously, in the course of the vegetative cell cycle. Under certain conditions, it may be preceded by self-fertilization (autogamy),[33] or it may immediately follow conjugation, in which Paramecium of compatible mating types fuse temporarily and exchange genetic material.

Conjugation

In ciliates such as Paramecium, conjugation is a sexual phenomenon that results in

haploid micronuclei are exchanged over the bridge. Following conjugation, the cells separate. The old macronuclei are destroyed, and both post-conjugants form new macronuclei, by amplification of DNA in their micronuclei.[31] Conjugation is followed by one or more "exconjugant divisions."[34]

Stages of conjugation
Stages of conjugation in Paramecium caudatum

In Paramecium caudatum, the stages of conjugation are as follows (see diagram at right):

  1. Compatible mating strains meet and partly fuse
  2. The micronuclei undergo meiosis, producing four haploid micronuclei per cell.
  3. Three of these micronuclei disintegrate. The fourth undergoes mitosis.
  4. The two cells exchange a micronucleus.
  5. The cells then separate.
  6. The micronuclei in each cell fuse, forming a diploid micronucleus.
  7. Mitosis occurs three times, giving rise to eight micronuclei.
  8. Four of the new micronuclei transform into macronuclei, and the old macronucleus disintegrates.
  9. Binary fission occurs twice, yielding four identical daughter cells.

Aging

In the asexual fission phase of growth, during which cell divisions occur by mitosis rather than meiosis, clonal aging occurs leading to a gradual loss of vitality. In some species, such as the well studied Paramecium tetraurelia, the asexual line of clonally aging Paramecium loses vitality and expires after about 200 fissions if the cells fail to undergo autogamy or conjugation. The basis for clonal aging was clarified by

DNA damage increases dramatically.[39] Thus, DNA damage in the macronucleus appears to be the cause of aging in P. tetraurelia. In this single-celled protist, aging appears to proceed as it does in multicellular eukaryotes, as described in DNA damage theory of aging
.

Meiosis and rejuvenation

When clonally aged P. tetraurelia are stimulated to undergo meiosis in association with either conjugation or automixis, the genetic descendants are rejuvenated, and are able to have many more mitotic binary fission divisions. During either of these processes, the micronuclei of the cell(s) undergo meiosis, the old macronucleus disintegrates and a new macronucleus is formed by replication of the micronuclear DNA that had recently undergone meiosis. There is apparently little, if any, DNA damage in the new macronucleus. These findings further solidify that clonal aging is due, in large part, to a progressive accumulation of DNA damage; and that rejuvenation is due to the repair of this damage in the micronucleus during meiosis. Meiosis appears to be an adaptation for DNA repair and rejuvenation in P. tetraurelia.[40] In P. tetraurelia, CtlP protein is a key factor needed for the completion of meiosis during sexual reproduction and recovery of viable sexual progeny.[40] The CtlP and Mre11 nuclease complex are essential for accurate processing and repair of double-strand breaks during homologous recombination.[40]

Video gallery

  • Paramecium bursaria, a species with symbiotic algae
  • Paramecium putrinum
  • Paramecium binary fission
  • Paramecium in conjugation
  • Paramecium caudatum

List of species

Paramecium aurelia species complex:

Other species:

References

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  6. ^ Joblot, Louis (1718). Description et usages de Plusieurs Nouveaux Microscopes, tant simple que composez (in French). Vol. 2. Paris: Jacques Collombat. p. 79.
  7. ^ Hill, John (1752). An History of Animals. Paris: Thomas Osborne. p. 5.
  8. ^ Müller, Otto Frederik; Müller, Otto Frederik (1773). Vermivm terrestrium et fluviatilium, seu, Animalium infusoriorum, helminthicorum et testaceorum, non marinorum, succincta historia. Vol. v.1 (1773-1774). et Lipsiae: apud Heineck et Faber.
  9. ^ Paramoecium Hermann, 1783
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  13. ^ a b Curds, Colin R.; Gates, Michael; Roberts, David McL. (1983). British and other freshwater ciliated protozoa. Vol. 2. Cambridge University Press. p. 126.
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External links
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