Acanthocephala (Greek ἄκανθος, akanthos, thorn + κεφαλή, kephale, head) is a phylum of parasitic worms known as acanthocephalans, thorny-headed worms, or spiny-headed worms, characterized by the presence of an eversible proboscis, armed with spines, which it uses to pierce and hold the gut wall of its host. Acanthocephalans have complex life cycles, involving at least two hosts, which may include invertebrates, fish, amphibians, birds, and mammals.  About 1150 species have been described.
The Acanthocephala were thought to be a discrete phylum. Recent genome analysis has shown that they are descended from, and should be considered as, highly modified rotifers. This finding is an example of molecular phylogenetics. This unified taxon is known as Syndermata.
- 1 History
- 2 Phylogeny
- 3 Morphological characteristics
- 4 "Body snatching"
- 5 Life cycles
- 6 Human infections
- 7 See also
- 8 Notes
- 9 References
- 10 External links
The earliest recognisable description of Acanthocephala – a worm with a proboscis armed with hooks – was made by Italian author Francesco Redi (1684). In 1771, Joseph Koelreuter proposed the name Acanthocephala. Philipp Ludwig Statius Müller independently called them Echinorhynchus in 1776. Karl Rudolphi in 1809 formally named them Acanthocephala.
Acanthocephalans are highly adapted to a parasitic mode of life, and have lost many organs and structures through evolutionary processes. This makes determining relationships with other higher taxa through morphological comparison problematic. Phylogenetic analysis of the 18S ribosomal gene has revealed that the Acanthocephala are most closely related to the rotifers. They are possibly closer to the two rotifer classes Bdelloidea and Monogononta than to the other class, Seisonidea, producing the names and relationships shown in the cladogram below.
Currently the phylum is divided into four classes – Palaeacanthocephala, Archiacanthocephala, Polyacanthocephala and Eoacanthocephala. The monophyletic Archiacanthocephala are the sister taxon of a clade comprising Eoacanthocephala and the monophyletic Palaeacanthocephala.
A study of the gene order in the mitochondria suggests that Seisonidea and Acanthocephala are sister clades and that the Bdelloidea are the sister clade to this group.
There are several morphological characteristics that distinguish acanthocephalans from other phyla of parasitic worms.
Acanthocephalans lack a mouth or alimentary canal. This is a feature they share with the cestoda (tapeworms), although the two groups are not closely related. Adult stages live in the intestines of their host and uptake nutrients which have been digested by the host, directly, through their body surface.
The most notable feature of the acanthocephala is the presence of an anterior, protrudible proboscis that is usually covered with spiny hooks (hence the common name: thorny headed worm). The proboscis bears rings of recurved hooks arranged in horizontal rows, and it is by means of these hooks that the animal attaches itself to the tissues of its host. The hooks may be of two or three shapes, usually, longer, more slender hooks are arranged along the length of the proboscis, with several rows of more sturdy, shorter nasal hooks around the base of the proboscis. The proboscis is used to pierce the gut wall of the final host, and hold the parasite fast while it completes its life cycle.
Like the body, the proboscis is hollow, and its cavity is separated from the body cavity by a septum or proboscis sheath. Traversing the cavity of the proboscis are muscle-strands inserted into the tip of the proboscis at one end and into the septum at the other. Their contraction causes the proboscis to be invaginated into its cavity. The whole proboscis apparatus can also be, at least partially, withdrawn into the body cavity, and this is effected by two retractor muscles which run from the posterior aspect of the septum to the body wall.
Some of the acanthocephalans (perforating acanthocephalans) can insert their proboscis in the intestine of the host and open the way to the abdominal cavity.
The size of these animals varies greatly, some are measured to be a few millimetres in length to Gigantorhynchus gigas, which measures from 10 to 65 centimetres (3.9 to 25.6 in).
The body surface of the acanthocephala is peculiar. Externally, the skin has a thin tegument covering the epidermis, which consists of a syncytium with no cell walls. The syncytium is traversed by a series of branching tubules containing fluid and is controlled by a few wandering, amoeboid nuclei. Inside the syncytium is an irregular layer of circular muscle fibres, and within this again some rather scattered longitudinal fibres; there is no endothelium. In their micro-structure the muscular fibres resemble those of nematodes.
Except for the absence of the longitudinal fibres the skin of the proboscis resembles that of the body, but the fluid-containing tubules of the proboscis are shut off from those of the body. The canals of the proboscis open into a circular vessel which runs round its base. From the circular canal two sac-like projections called the lemnisci run into the cavity of the body, alongside the proboscis cavity. Each consists of a prolongation of the syncytial material of the proboscis skin, penetrated by canals and sheathed with a muscular coat. They seem to act as reservoirs into which the fluid which is used to keep the proboscis "erect" can withdraw when it is retracted, and from which the fluid can be driven out when it is wished to expand the proboscis.
The central ganglion of the nervous system lies behind the proboscis sheath or septum. It innervates the proboscis and projects two stout trunks posteriorly which supply the body. Each of these trunks is surrounded by muscles, and this nerve-muscle complex is called a retinaculum. In the male at least there is also a genital ganglion. Some scattered papillae may possibly be sense-organs.
The Acanthocephala are dioecious (an individual organism is either male or female). There is a structure called the genital ligament which runs from the posterior end of the proboscis sheath to the posterior end of the body. In the male, two testes lie on either side of this. Each opens in a vas deferens which bears three diverticula or vesiculae seminales. The male also possesses three pairs of cement glands, found behind the testes, which pour their secretions through a duct into the vasa deferentia. These unite and end in a penis which opens posteriorly.
In the female, the ovaries are found, like the testes, as rounded bodies along the ligament. From the ovaries, masses of ova dehisce into the body cavity, floating in its fluids for fertilization by male's sperm. After fertilization, each egg contains a developing embryo. (These embryos hatch into first stage larva.) The fertilized eggs are brought into the uterus by actions of the uterine bell, a funnel like opening continuous with the uterus. At the junction of the bell and the uterus there is a second, smaller opening situated dorsally. The bell "swallows" the matured eggs and passes them on into the uterus. (Immature embryos are passed back into the body cavity through the dorsal opening.) From the uterus, mature eggs leave the female's body via her oviduct, pass into the host's alimentary canal and are expelled from the host's body within feces.
A curious feature shared by both larva and adult is the large size of many of the cells, e.g. the nerve cells and cells forming the uterine bell. Polyploidy is common, with up to 343n having been recorded in some species. The acanthocephalans lack an excretory system, although some species have been shown to possess flame cells (protonephridia).
Thorny-headed worms begin their life cycle inside invertebrates that reside in marine or freshwater systems. Gammarus lacustris, a small crustacean that feeds near ponds and rivers, is one invertebrate that the thorny-headed worm may occupy. This crustacean is preyed on by ducks and hides by avoiding light and staying away from the surface. However, when infected by a thorny-headed worm it becomes attracted toward light and swims to the surface. Gammarus lacustris will even go so far as to find a rock or a plant on the surface, clamp its mouth down, and latch on, making it easy prey for the duck. The duck is the definitive host for the acanthocephalan parasite. In order to be transmitted to the duck, the parasite's intermediate host (the gammarid) must be eaten by the duck. This modification of gammarid behavior by the acanthocephalan is thought to increase the rate of transmission of the parasite to its next host by increasing the susceptibility of the gammarid to predation.
It is thought that when Gammarus lacustris is infected with a thorny-headed worm, the parasite causes serotonin to be massively expressed. Serotonin is a neurotransmitter involved in emotions and mood. Researchers have found that during mating Gammarus lacustris expresses high levels of serotonin. Also during mating, the male Gammarus lacustris clamps down on the female and holds on for days. Researchers have additionally found that blocking serotonin releases clamping. Another experiment found that serotonin also reduces the photophobic behavior in Gammarus lacustris. Thus, it is thought that the thorny-headed worm physiologically changes the behavior of the Gammarus lacustris in order to enter its final host, the bird.
Acanthocephalans have complex life cycles, involving a number of hosts, for both developmental and resting stages. Complete life cycles have been worked out for only 25 species.
Having been expelled by the female, the acanthocephalan egg is released along with the feces of the host. For development to occur, the egg, containing the acanthor, needs to be ingested by an arthropod, usually a crustacean (there is one known life cycle which uses a mollusc as a first intermediate host). Inside the intermediate host, the acanthor is released from the egg and develops into an acanthella. It then penetrates the gut wall, moves into the body cavity, encysts, and begins transformation into the infective cystacanth stage. This form has all the organs of the adult save the reproductive ones.
The parasite is released when the first intermediate host is ingested. This can be by a suitable final host, in which case the cystacanth develops into a mature adult, or by a paratenic host, in which the parasite again forms a cyst. When consumed by a suitable final host, the cycstacant excysts, everts its proboscis and pierces the gut wall. It then feeds, grows and develops its sexual organs. Adult worms then mate. The male uses the excretions of its cement glands to plug the vagina of the female, preventing subsequent matings from occurring. Embryos develop inside the female, and the life cycle repeats.
An example – Polymorphus spp.
Polymorphus spp. are parasites of seabirds, particularly the eider duck (Somateria mollissima). Heavy infections of up to 750 parasites per bird are common, causing ulceration to the gut, disease and seasonal mortality. Recent research has suggested that there is no evidence of pathogenicity of Polymorphus spp. to intermediate crab hosts. The cystacanth stage is long lived and probably remains infective throughout the life of the crab.
The life cycle of Polymorphus spp. normally occurs between sea ducks (e.g. eiders and scoters) and small crabs. Infections found in commercial-sized lobsters in Canada were probably acquired from crabs that form an important dietary item of lobsters. Cystacanths occurring in lobsters can cause economic loss to fishermen. There are no known methods of prevention or control.
These are considered to be rare. The earliest known infection was found in prehistoric man in Utah. This infection was dated to 1869 ± 160 BC. The species involved was thought to be Moniliformis clarki which is still common in the area. The first report of an isolate in historic times was by Lambl in 1859 when he isolated Macracanthorhynchus hirudinaceus from a child in Prague. Lindemann in 1865 reported that this organism was commonly isolated in Russia. The reason for this was discovered by Schneider in 1871 when he found that an intermediate host, the scarabaeid beetle grub, was commonly eaten raw. The first report of clinical symptoms was by Calandruccio who in 1888 while in Italy infected himself by ingesting larvae. He reported gastrointestinal disturbances and shed eggs in two weeks. Subsequent natural infections have since been reported. Eight species have been isolated from humans to date. Moniliformis moniliformis is the most common isolate. Other isolates include Acanthocephalus bufonis and Corynosoma strumosum.
- Crompton 1985, p. 27
- Koelreuter, I. T. (1770). "Descriptio cyprini rutili, quem halawel russi vocant, historico-anatomica.". Novi commentarii Academiae Scientiarum Imperialis Petropolitanae. 15: 494–503.
- de Buron, I.; Golvan, Y. J. (1986). "Les hôtes des Acanthocéphales. I — Les Hôtes intermédiaires". Annales de Parasitologie Humaine et Comparée. 61 (5): 581–592. doi:10.1051/parasite/1986615581. ISSN 0003-4150.
- Golvan, Y. J.; De Buron, I. (1988). "Les hôtes des Acanthocéphales. II — Les hôtes définitifs. 1. Poissons". Annales de Parasitologie Humaine et Comparée. 63 (5): 349–375. doi:10.1051/parasite/1988635349. ISSN 0003-4150.
- Roberts, Larry S.; Janovy, Jr., John (2009). Foundations of Parasitology (Eighth ed.). McGraw-Hill. p. 502. ISBN 9780073028279.
- Freeman, Scott, Lizabeth Allison, Michael Black, Greg Podgorski, and Kim Quillin. Biological Sciences. 5th ed. Glenview, Il: Pearson, 2014. 638. Print.
- Encyclopedia of Life, retrieved 24 July 2015
- Shimek, Ronald (January 2006). "Nano-Animals, Part I: Rotifers". Reefkeeping.com. Retrieved July 27, 2008.
- Ruppert, Edward E.; Fox, Richard S, & Barnes, Robert D. (2004), Invertebrate zoology : a functional evolutionary approach (7th ed.), Belmont, CA: Thomson-Brooks/Cole, ISBN 978-0-03-025982-1, p. 788ff. – see particularly p. 804
- Weber, M; Wey-Fabrizius Alexandra, R; Podsiadlowski, L; Witek, A; Schill Ralph, O; Sugár, L; Herlyn, H; Hankeln, T (January 2013). "Phylogenetic analysis of endoparasitic Acanthocephala based on mitochondrial genomes suggests secondary loss of sense organs". Mol Phylogenet Evol. 66 (1): 182–189. doi:10.1016/j.ympev.2012.09.017.
- Sielaff, M; Schmidt, H; Struck, TH; Rosenkranz, D; Mark Welch, DB; Hankeln, T; Herlyn, H (March 2016). "Phylogeny of Syndermata (syn. Rotifera): Mitochondrial gene order verifies epizoic Seisonidea as sister to endoparasitic Acanthocephala within monophyletic Hemirotifera". Mol Phylogenet Evol. 96: 79–92. doi:10.1016/j.ympev.2015.11.017.
- Amin, O. A; Heckmann, R. A; Ha, N. V. (2014). "Acanthocephalans from fishes and amphibians in Vietnam, with descriptions of five new species". Parasite. 21: 53. doi:10.1051/parasite/2014052. PMC . PMID 25331738.
- "Acanthocephalans drilling Acipenser stellatus intestine". Parasites World.
- Itämies, J.; Valtonen, E. T.; Fagerholm, H. P. (1980). "Polymorphus minutus (Acanthocephala) infestation in eiders and its role as a possible cause of death". Ann. Zool. Fenn. 17 (4): 285–289.
- Moore, J. G.; Fry, G. F.; Englert, E. (21 March 1969). "Thomy-headed worm infection in North American prehistoric man". Science. 163 (3873): 1324–1325. doi:10.1126/science.163.3873.1324. PMID 17807812.
- Schmidt, Gerald D. (June 1971). "Acanthocephalan infections of man, with two new records". The Journal of Parasitology. Allen Press on behalf of American Society of Parasitologists. 57: 582–584. doi:10.2307/3277920. JSTOR 3277920.
- Tada, I; Otsuji, Y; Kamiya, H; Mimori, T; Sakaguchi, Y; Makizumi, S (February 1983). "The first case of a human infected with an acanthocephalan parasite, Bolbosoma sp.". The Journal of parasitology. 69 (1): 205–8. PMID 6827437.
- Haustein, T; Lawes, M; Harris, E; Chiodini, PL (June 2010). "An eye-catching acanthocephalan.". Clinical microbiology and infection. 16 (6): 787–8. doi:10.1111/j.1469-0691.2009.02896.x. PMID 19689468.
- Amin, O. M. (1987). "Key to the families and subfamilies of Acanthocephala, with erection of a new class (Polyacanthocephala) and a new order (Polyacanthorhynchida)". Journal of Parasitology. 73: 1216–1219. doi:10.2307/3282307.
- Crompton, David; William Thomasson; Nickol, Brent B. (1985.) Biology of the Acanthocephala, Cambridge University Press. p. 27. 
- Lühe, M. (1904). "Geschichte und Ergebnisse der Echinorhynchen – Forschung bis auf Westrumb (1821)". Zoologischer Annalen. 1: 139–250.
- Tain, Luke; Marie-Jeanne Perrot-Minnot; Frank Cézilly (December 22, 2006). "Altered host behaviour and brain serotonergic activity caused by acanthocephalans: evidence for specificity". Proceedings of the Royal Society B. 273 (1605): 3039–3045. doi:10.1098/rspb.2006.3618. PMC . PMID 17015346.
- Zimmer, C. Parasite Rex: Inside the Bizarre World of Nature's Most Dangerous Creatures 92. ISBN 978-0-7432-0011-0 ISBN 0-7432-0011-X.
|Wikimedia Commons has media related to Acanthocephala.|
|Wikispecies has information related to: Acanthocephala|
|Wikisource has the text of the 1911 Encyclopædia Britannica article Acanthocephala.|