The nematodes ( or ; ; ), roundworms or eelworms constitute the phylum Nematoda. Species in the phylum inhabit a broad range of environments. Most species are free-living, feeding on , but many are parasitism. Parasitic worms (helminths) are the cause of soil-transmitted helminthiases.
They are classified along with , and other moulting animalia in the clade Ecdysozoa. Unlike the , nematodes have a tubular digestion, with openings at both ends. Like tardigrades, they have a reduced number of , but their sister phylum Nematomorpha has kept the ancestral protostome Hox genotype, which shows that the reduction has occurred within the nematode phylum.
Nematode species can be difficult to distinguish from one another. Consequently, estimates of the number of nematode species are uncertain. A 2013 survey of animal biodiversity suggested there are over 25,000. Estimates of the total number of extant species are subject to even greater variation. A widely referenced 1993 article estimated there might be over a million species of nematode. A subsequent publication challenged this claim, estimating the figure to be at least 40,000 species. Although the highest estimates (up to 100 million species) have since been deprecated, estimates supported by rarefaction curves, together with the use of DNA barcoding and the increasing acknowledgment of widespread cryptic species among nematodes, have placed the figure closer to one million species.
Nematodes have successfully adapted to nearly every ecosystem: from marine (salt) to fresh water, soils, from the polar regions to the tropics, as well as the highest to the lowest of elevations. They are ubiquitous in freshwater, marine, and terrestrial environments, where they often outnumber other animals in both individual and species counts, and are found in locations as diverse as mountains, deserts, and . They are found in every part of the Earth's lithosphere,
even at great depths, below the surface of the Earth in gold mines in South Africa. They represent 90% of all animals on the Seabed. In total, 4.4 × 1020 nematodes inhabit the Earth's topsoil, or approximately 60 billion for each human, with the highest densities observed in tundra and boreal forests. Their numerical dominance, often exceeding a million individuals per square meter and accounting for about 80% of all individual animals on Earth, their diversity of lifecycles, and their presence at various trophic levels point to an important role in many ecosystems. They play crucial roles in polar ecosystems. The roughly 2,271 genera are placed in 256 families. The many parasitic forms include in most plants and animals. A third of the genera occur as of ; about 35 nematode species are .
The name of the group Nematoda, informally called "nematodes", came from Nematoidea, originally defined by Karl Rudolphi in 1808, from Ancient Greek νῆμα ( nêma, nêmatos, 'thread') and -ειδἠς ( -eidēs, 'species'). It was treated as family Nematodes by Burmeister in 1837.
At its origin, the "Nematoidea" erroneously included Nematodes and Nematomorpha, attributed by Karl Theodor Ernst von Siebold in 1843. Along with Acanthocephala, Trematoda, and Cestoidea, it formed the obsolete group Entozoa, created by Rudolphi in 1808. They were classed along with Acanthocephala in the obsolete phylum Aschelminth by Gegenbaur in 1859.
In 1861, Karl Moriz Diesing treated the group as order Nematoda. In 1877, the taxon Nematoidea, including the family Gordiidae (horsehair worms), was promoted to the rank of phylum by Ray Lankester. The first clear distinction between the nemas and gordiids was realized by František Vejdovsky when he named the group containing the horsehair worms the order Nematomorpha in 1886.
In 1910, Grobben proposed the phylum Aschelminthes, and the nematodes were included as class Nematoda alongside the classes , , Kinorhyncha, Priapulida, and Nematomorpha.
In 1919, Nathan Cobb proposed that nematodes should be recognized alone as a phylum. He argued they should be called "nema" in English rather than "nematodes" and defined the taxon Nemates (later emended as Nemata, Latin plural of nema), listing Nematoidea sensu restricto as a synonym.
In 1932, Potts elevated the class Nematoda to the level of phylum, leaving the name the same. Although Potts' and Cobb's classifications are equivalent, both names are used, and Nematode became a popular term in zoological science.
Initial studies of incomplete DNA sequences suggested the existence of five :
The Secernentea seem to be a natural group of close relatives, while the Adenophorea appear to be a paraphyletic assemblage of roundworms that retain a good number of plesiomorph. The old Enoplia do not seem to be monophyletic, either, but do contain two distinct lineages. The old group Chromadorea seems to be another paraphyletic assemblage, with the Monhysterida representing a very ancient minor group of nematodes. Among the Secernentea, the Diplogasteria may need to be united with the Rhabditia, while the Tylenchia might be paraphyletic with the Rhabditia.
The understanding of roundworm systematics and phylogeny as of 2002 is summarised below:
Phylum Nematoda
Later work has suggested the presence of 12 clades. In 2019, a study identified one conserved signature indel (CSI) found exclusively in members of the phylum Nematoda through comparative genetic analyses. The CSI consists of a single amino acid insertion within a conserved region of a Na(+)/H(+) exchange regulatory factor protein NRFL-1 and is a molecular marker that distinguishes the phylum from other species. An analysis of the mitochondrial DNA suggests that the following groupings are valid
In 2022 a new classification of the entire phylum Nematoda was presented by M. Hodda. It was based on current molecular, developmental and morphological evidence. Under this classification, the classes and subclasses are:
The body is often ornamented with ridges, rings, bristles, or other distinctive structures.
The head is relatively distinct. Whereas the rest of the body is bilaterally symmetrical, the head is radially symmetrical, with sensory bristles and, in many cases, solid 'head-shields' radiating outwards around the mouth. The mouth has either three or six lips, which often bear a series of teeth on their inner edges. An adhesive 'caudal gland' is often found at the tip of the tail. The epidermis is either a syncytium or a single layer of cells, and is covered by a thick cuticle. The cuticle is often of a complex structure and may have two or three distinct layers. Underneath the epidermis lies a layer of longitudinal muscle cells. The relatively rigid cuticle works with the muscles to create a hydroskeleton, as nematodes lack circumferential muscles. Projections run from the inner surface of muscle cells towards the nerve cords; this is a unique arrangement in the animal kingdom, in which nerve cells normally extend fibers into the muscles rather than vice versa.
No stomach is present, with the pharynx connecting directly to a muscleless intestine that forms the main length of the gut. This produces further enzymes and also absorbs nutrients through its single-cell-thick lining. The last portion of the intestine is lined by a cuticle, forming a rectum, which expels waste through the anus just below and in front of the tip of the tail. The movement of food through the digestive system is the result of the body movements of the worm. The intestine has valves or at either end to help control food movement through the body.
There is an excretory gland, also known as a ventral cell, or renette cell in all species of Adenophorea. In Secernentia there is an excretory canal system that may or may not use a gland cell.
The nervous system is the only place in the body that contains cilia; these are all nonmotile and with a sensory function.
The body is covered in numerous sensory and papillae that together provide a sense of touch. Behind the sensory bristles on the head lie two small pits, or ''. These are well supplied with nerve cells and are probably chemoreceptor organs. A few aquatic nematodes possess what appear to be eye-spots, but whether or not these are actually sensory in nature is unclear.
Reproduction is usually sexual, though hermaphrodites are capable of self-fertilization. Males are usually smaller than females or hermaphrodites (often much smaller) and often have a characteristically bent or fan-shaped tail. During copulation, one or more spicules move out of the cloaca and are inserted into the genital pore of the female. Amoeboid sperm crawl along the spicule into the female worm. Nematode sperm is thought to be the only eukaryotic cell without the globular protein G-actin.
Eggs may be embryonated or unembryonated when passed by the female, meaning their fertilized eggs may not yet be developed. A few species are known to be ovoviviparous. The eggs are protected by an outer shell, secreted by the uterus. In free-living roundworms, the eggs hatch into , which appear essentially identical to the adults, except for an underdeveloped reproductive system; in parasitic roundworms, the lifecycle is often much more complicated. The structure of the eggshell is complicated and includes several layers; a detailed anatomical and terminological framework has been proposed for these layers in 2023.
Nematodes as a whole possess a wide range of modes of reproduction. Some nematodes, such as Heterorhabditis spp., undergo a process called endotokia matricida: intrauterine birth causing maternal death. Some nematodes are hermaphrodite, and keep their self-fertilized eggs inside the uterus until they hatch. The juvenile nematodes then ingest the parent nematode. This process is significantly promoted in environments with a low food supply.
The nematode model species C. elegans, C. briggsae, and Pristionchus pacificus, among other species, exhibit androdioecy,
The genus Mesorhabditis exhibits an unusual form of parthenogenesis, in which sperm-producing males copulate with females, but the sperm do not fuse with the ovum. Contact with the sperm is essential for the ovum to begin dividing, but because no fusion of the cells occurs, the male contributes no genetic material to the offspring, which are essentially cloning of the female.
One form of nematode is entirely dependent upon , which are the sole source of ficus fertilization. They prey upon the wasps, riding them from the ripe fig of the wasp's birth to the fig flower of its death, where they kill the wasp, and their offspring await the birth of the next generation of wasps as the fig ripens.
A parasitic Tetradonematidae nematode discovered in 2005, Myrmeconema neotropicum, induces fruit mimicry in the tropical ant Cephalotes atratus. Infected ants develop bright red gasters (abdomens), tend to be more sluggish, and walk with their gasters in a conspicuous elevated position. These changes likely cause frugivorous birds to confuse the infected ants for berries, and eat them. Parasite eggs passed in the bird's feces are subsequently collected by foraging C. atratus and are fed to their , thus completing the lifecycle of M. neotropicum.
Similarly, multiple varieties of nematodes have been found in the abdominal cavities of the primitively social sweat bee, Lasioglossum zephyrus. Inside the female body, the nematode hinders ovarian development and renders the bee less active, thus less effective in pollen collection.
Greenhouse growers use entomopathogenic nematodes as beneficial agents to control . The nematodes enter the larvae of the gnats by way of their anus, mouth, and spiracles (breathing pores) and then release bacteria which kills the gnat larvae. Commonly used nematode species to control pests on greenhouse crops include Steinernema feltiae for fungus gnats and western flower thrips, Steinernema carpocapsae used to control shore flies, Steinernema kraussei for control of Vine weevil, and Heterorhabditis bacteriophora to control beetle larvae.
Rotations of plants with nematode-resistant species or varieties is one means of managing parasitic nematode infestations. For example, planting Tagetes as a cover crop just prior to planting a nematode-susceptible plant, has been shown to suppress nematodes. Another approach involves using natural antagonists, particularly bacteria and fungi, which have proven effective in suppressing plant-parasitic nematodes, such as the fungus Gliocladium roseum. Chitosan, a natural biocontrol, elicits plant defense responses to destroy parasitic cyst nematodes on roots of soybean, corn, sugar beet, potato, and tomato crops without harming beneficial nematodes in the soil. Soil steaming is an efficient method to kill nematodes before planting a crop, but indiscriminately eliminates both harmful and beneficial soil fauna.
The golden nematode Globodera rostochiensis is a particularly harmful pest that has resulted in quarantines and crop failures worldwide. It can be controlled, however. CSIRO, the scientific research body of the Australian government, found a 13- to 14-fold reduction of nematode population densities in plots having Chinese mustard Brassica juncea green manure or seed meal in the soil.
Trichinosis starts in the intestines but larvae can migrate to muscle. nematodes cause filariasis.
Toxocariasis is a zoonotic infection caused by roundworms passed from dogs, and sometimes cats. It can give rise to different types of larva migrans such as visceral larva migrans, and ocular larva migrans.
Studies have shown that parasitic nematodes infect causing damage to the eel's swim bladder, dairy animals like cattle and buffalo, and all species of sheep.
One group of carnivorous fungi, the nematophagous fungi, are predators of soil nematodes. They can set enticements for the nematodes in the form of lassos or adhesive structures. They can also release powerful toxins when in contact with nematodes.
Etymology
Taxonomy and systematics
History
Phylogeny
Systematics
Fossil record
Anatomy
Digestive system
Excretory system
Nervous system
Reproduction
Aging
Free-living species
Parasitic species
Agriculture and horticulture
Disease in humans
Soil ecosystems
Survivability
See also
External links
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