Pentastomida
Pentastomida Temporal range:
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Adult female Linguatula serrata | |
Scientific classification ![]() | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Arthropoda |
Class: | Ichthyostraca |
Subclass: | Pentastomida Diesing, 1836 |
Orders | |
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The Pentastomida are an enigmatic group of parasitic arthropods commonly known as tongue worms due to the resemblance of the species of the genus Linguatula to a vertebrate tongue; molecular studies point to them being degenerate crustaceans.[1]
About 130 species of pentastomids are known; all are obligate parasites with correspondingly degenerate anatomy. Adult tongue worms vary from about 1 to 14 cm (0.4 to 5.5 in) in length, and parasitise the respiratory tracts of vertebrates. They have five anterior appendages. One is the mouth; the others are two pairs of hooks, which they use to attach to the host. This arrangement led to their scientific name, meaning "five openings", but although the appendages are similar in some species, only one is a mouth.
Alternative names for the Pentastomida include Pentastoma (strictly a genus name), Linguatulida, and Acanthotheca.
Biology
Historically significant accounts of tongue worm biology and systematics include early work by Josef Aloys Frölich,[2] Alexander von Humboldt,[3] Karl Asmund Rudolphi,[4] Karl Moriz Diesing[5] and Rudolph Leuckart.[6]
Other important summaries have been published by Louis Westenra Sambon,[7] Richard Heymons[8] and John Riley,[9] and a review of their evolutionary relationships with a bibliography up to 1969 was published by J. T. Self.[10]
Anatomy
Pentastomids are worm-like animals ranging from 1 to 14 centimetres (0.39 to 5.51 in) in length. The female is larger than the male. The anterior end of the body bears five protuberances, four of which are clawed legs, while the fifth bears the mouth. The body is segmented and covered in a chitinous cuticle. The digestive tract is simple and tubular since the animal feeds entirely on blood, except from genus Linguatula which lives in the nasal cavity of carnivorous mammals where they feed mainly on mucus and dead cells,[11][12] although the mouth is somewhat modified as a muscular pump.[13]
The nervous system is similar to that of other arthropods, including a ventral nerve cord with ganglia in each segment. Although the body contains a haemocoel, no circulatory, respiratory, or excretory organs are present.[13]
Life cycle
Pentastomids live in the upper respiratory tract of reptiles, birds, and mammals, where they lay eggs. They are gonochoric (having two sexes), and employ internal fertilisation. The eggs are either coughed out by the host or leave the host body through the digestive system. The eggs are then ingested by an intermediate host, which is commonly either a fish or a small herbivorous mammal.[13]
The larva hatches in the intermediate host and breaks through the wall of the intestine. It then forms a cyst in the intermediate host's body. The larva is initially rounded in form, with four or six short legs, but moults several times to achieve the adult form. At least one species has a free living larva. There is both indirect development with nymphal stages and direct development. The pentastomid reaches the main host when the intermediate host is eaten by the main host, and crawls into the respiratory tract from the oesophagus.[13][14]
Human infestation
Tongue worms occasionally parasitise humans.[15] While a report exists of Sebekia inducing dermatitis,[16][17] the two genera responsible for most internal human infestation are Linguatula and Armillifer. Visceral pentastomiasis can be caused by Linguatula serrata, Armillifer armillatus, Armillifer moniliformis, Armillifer grandis, and Porocephalus crotali.[18]
The terms associated with infections can vary:
- Linguatula disease can be called linguatuliasis or linguatulosis.
- Porocephalus disease can be called porocephaliasis or porocephalosis.
- Armillifer disease can also be called porocephalosis.[19] (An alternate name for Armillifer moniliformis is Porocephalus moniliformis.)[20]
- "Pentastomiasis" can refer to any infection of Pentastomida.
Porocephalus and Armillifer (which are all cylindrical and all inhabit snakes) have much more in common with each other than they do with Linguatula (which is flat and inhabits dogs and wolves).
Affinities
The affinities of tongue worms have long proved controversial. Historically, they were initially compared to various groups of parasitic worms. Once the arthropod-like nature of their cuticle was recognised, similarities were drawn with mites,[21] particularly gall mites (Eriophyidae). Although gall mites are much smaller than tongue worms, they also have a long, segmented body and only two pairs of legs. Later work[citation needed] drew comparisons with millipedes and centipedes (Myriapoda), with velvet worms (Onychophora) and water bears (Tardigrada). Some authors[citation needed] interpreted tongue worms as essentially intermediate between annelids and arthropods, while others suggested that they deserved a phylum of their own. Tongue worms grow by moulting, which suggests they belong to Ecdysozoa, while other work has identified the arthropod-like nature of their larvae.[22] In general, the two current alternative interpretations are: pentastomids are highly modified and parasitic crustaceans, probably related to fish lice, or they are an ancient group of stem-arthropods, close to the origins of Arthropoda.
Crustaceans
The possibility that tongue worms are crustaceans can be traced back to the work of Pierre-Joseph Van Beneden,[23] who compared them to parasitic copepods. The modern form of this hypothesis dates from Karl Georg Wingstrand's study of sperm morphology,[24] which recognised similarities in sperm structure between tongue worms and fish lice (Argulidae) – a group of maxillopod crustaceans which live as parasites on fish and occasionally amphibians. John Riley and colleagues also offered a detailed justification for the inclusion of the tongue worms among the crustaceans.[25] The fish louse model received significant further support from the molecular work of Lawrence G. Abele and colleagues.[26] A number of subsequent molecular phylogenies have corroborated these results,[27][28][29] and the name Ichthyostraca has been proposed for a (Pentastomida + Branchiura) clade.[30] Thus a number of important standard works and databases on crustaceans now include the pentastomids as members of this group.[31]
Stem-arthropods
Critics of the Ichthyostraca hypothesis have pointed out that even parasitic crustaceans can still be recognised as crustaceans based on their larvae; but that tongue worms and their larvae do not express typical characters for Crustacea or even Euarthropoda. An alternative model notes the extremely ancient Cambrian origins of these animals and interprets tongue worms as stem-group arthropods.[32] A recent morphological analysis recovered Pentastomida outside the arthropods, as sister group to a clade including nematodes, priapulids and similar ecdysozoan 'worm' groups.[33] Adding fossils, they suggested an extinct animal called Facivermis could be closely related to tongue worms. However it should be stressed that these authors did not explicitly test pentastomid/crustacean relationships.
Fossil record
Exceptionally preserved, three-dimensional and phosphatised fossils from the Upper Cambrian Orsten of Sweden[34] and the Cambrian/Ordovician boundary of Canada[35] have been identified as pentastomids. Also one from the Wuluian (middle Cambrian) of Greenland.[36] Four fossil genera have been identified from the Cambrian so far: Aengapentastomum, Bockelericambria, Haffnericambria and Heymonsicambria. These fossils suggest that pentastomids evolved very early and raise questions about whether these animals were parasites at this time, and if so, on which hosts. Conodonts (primitive fish) have sometimes been mentioned as possible hosts in this context.[35] A fifth genus, Invavita, is from Silurian-aged marine strata of England: fossil specimens of Invavita are found firmly attached to their ostracod hosts of the species Nymphatelina gravida.[37][38] It possessed a head, a worm-like body, and two pairs of limbs.[39]
Classification
This article follows Martin and Davis[31] in placing the Pentastomida in the class Maxillopoda within the subphylum Crustacea. The subclass contains these extant orders, superfamilies, families, genera, and species:[40]
![](http://upload.wikimedia.org/wikipedia/commons/thumb/a/ae/Armillifer_armillatus.jpg/220px-Armillifer_armillatus.jpg)
![](http://upload.wikimedia.org/wikipedia/commons/thumb/f/fe/Armillifer.jpg/220px-Armillifer.jpg)
- †Aengapentastomum (Waloszek, Repetksi & Maas 2006)
- †Aengapentastomum andresi (Waloszek, Repetksi & Maas 2006)
- †Boeckelericambria (Walossek & Müller 1994)
- †Boeckelericambria pelturae (Walossek & Müller 1994)
- †Haffnericambria (Walossek & Müller 1994)
- †Haffnericambria trolmeniensis (Walossek & Müller 1994)
- †Heymonsicambria (Walossek & Müller 1994)
- †Heymonsicambria ahlgreni (Castellani et al. 2011)
- †Heymonsicambria gossmannae (Walossek & Müller 1994)
- †Heymonsicambria kinnekullensis (Walossek & Müller 1994)
- †Heymonsicambria repetskii (Walossek & Müller 1994)
- †Heymonsicambria scandica (Walossek & Müller 1994)
- †Heymonsicambria taylori (Walossek, Repetski & Müller 1994)
- Eupentastomida Waloszek, (Repetski & Mass 2006)
- Cephalobaenida (Heymons, 1935)
- Cephalobaenidae (Heymons, 1922)
- Bothropsiella (Cavalieri, 1967) species inquirendum
- Bothropsiella cornuta (Cavalieri, 1967)
- Cephalobaena (Heymons, 1922)
- Cephalobaena tetrapoda (Heymons, 1922)
- †Invavita (Siveter et al. 2015)
- †Invavita piratica (Siveter et al. 2015)
- Reighardiida (Almeida & Christoffersen, 1999)
- Reighardiidae (Heymons, 1926)
- Hispania (Martínez et al., 2004)
- Hispania vulturis (Martínez et al., 2004)
- Reighardia (Ward, 1899)
- Reighardia lomviae (Dyck, 1975)
- Reighardia sternae (Diesing, 1864)
- Raillietiellida (Almeida & Christoffersen, 1999)
- Raillietiellidae (Sambon, 1922)
- Raillietiella (Sambon, 1910)
- Raillietiella aegypti (Ali, Riley & Self, 1982)
- Raillietiella affinis (Bovien, 1927)
- Raillietiella agcoi (Tubangui & Masiluñgan, 1936)
- Raillietiella ampanihyensis (Gretillat, Brygoo & Domergue, 1962)
- Raillietiella amphiboluri (Mahon, 1954)
- Raillietiella belohaensis (McAllister, Riley, Freed & Freed, 1993)
- Raillietiella bicaudata (Heymons & Vitzthum, 1935)
- Raillietiella boulengeri (Vaney & Sambon, 1910)
- Raillietiella bufonis (Ali, Riley & Self, 1982)
- Raillietiella cartagenensis (Ali, Riley & Self, 1985)
- Raillietiella chamaeleonis (Gretillat & Brygoo, 1959)
- Raillietiella colubrilineati (Leuckart, 1860)
- Raillietiella congolensis (Fain, 1961)
- Raillietiella crotali (Ali, Riley & Self, 1984)
- Raillietiella freitasi (Motta & Gomes, 1968)
- Raillietiella furcocercum (Diesing, 1836)
- Raillietiella gehyrae (Bovien, 1927)
- Raillietiella gigliolii (Hett, 1924)
- Raillietiella gowrii (Rajalu & Rajendran, 1970)
- Raillietiella hebitihamata (Self & Kuntz, 1960)
- Raillietiella hemidactyli (Hett, 1934)
- Raillietiella indica (Gedoelst, 1921)
- Raillietiella kochi (Heymons, 1926)
- Raillietiella mabuiae (Heymons, 1922)
- Raillietiella maculatus (Rao & Hiregaudar, 1962)
- Raillietiella maculilabris (Ali, Riley & Self, 1984)
- Raillietiella madagascariensis (McAllister et al., 1993)
- Raillietiella mediterranea (Hett, 1915)
- Raillietiella monarchus (Ali, Riley & Self, 1984)
- Raillietiella morenoi (Abreu-Acosta et al., 2006)
- Raillietiella mottae (Almeida, Freire & Lopes, 2008)
- Raillietiella namibiensis (Riley & Heideman 1998)
- Raillietiella orientalis (Hett, 1915)
- Raillietiella piscator (Nair, 1967)
- Raillietiella rileyi (Krishnasamy et al., 1995)
- Raillietiella schoutedeni (Fain, 1960)
- Raillietiella scincoides (Ali, Riley & Self, 1984)
- Raillietiella spiralis (Hett, 1924)
- Raillietiella teagueselfi (Riley, McAllister & Freed, 1988)
- Raillietiella tetrapoda (Gretillat, Brygoo & Domergue, 1962)
- Raillietiella trachea (Riley, Oaks & Gilbert, 2003)
- Raillietiella venteli (Motta, 1965)
- Yelirella (Spratt, 2010)[41]
- Yelirella petauri (Spratt, 2003) (Spratt 2010)
- Porocephalida (Heymons 1935)
- Linguatuloidea (Haldeman 1851)
- Linguatulidae (Haldeman, 1851)
- Linguatula (Frölich, 1789)
- Linguatula arctica (Riley, Haugerud & Nilssen, 1987)
- Linguatula multiannulata (Haffner & Rack in Haffner, Rack & Sachs, 1969)
- Linguatula recurvata (Diesing, 1850)
- Linguatula serrata (Frölich, 1789)
- Neolinguatula (Haffner & Rack in Haffner, Rack & Sachs, 1969)
- Neolinguatula nuttalli (Sambon, 1922)
- Subtriquetridae (Fain, 1961)
- Subtriquetra (Sambon, 1922)
- Subtriquetra megacephalum (Baird, 1853)
- Subtriquetra rileyi (Junker, Boomker & Booyse, 1998)
- Subtriquetra shipleyi (Hett, 1924)
- Subtriquetra subtriquetra (Diesing, 1836)
- Porocephaloidea (Sambon 1922)
- Porocephalidae (Sambon, 1922)
- Armillifer (Sambon, 1922)
- Armillifer aborealis (Riley & Self, 1981)
- Armillifer agkistrodontis (Self & Kuntz, 1966)
- Armillifer armillatus (Wyman, 1845)
- Armillifer australis (Heymons, 1935)
- Armillifer grandis (Hett, 1915)
- Armillifer mazzai (Sambon, 1922)
- Armillifer moniliformis (Diesing, 1836)
- Armillifer yoshidai (Kishida, 1928)
- Cubirea (Kishida, 1928)
- Cubirea annulata (Baird, 1853)
- Cubirea pomeroyi (Woodland, 1921)
- Elenia (Heymons, 1932)
- Elenia australis (Heymons, 1932)
- Gigliolella (Chabaud & Choquet, 1954)
- Gigliolella brumpti (Giglioli, 1922)
- Kiricephalus (Sambon, 1922)
- Kiricephalus clelii (Riley & Self, 1980)
- Kiricephalus coarctatus (Diesing, 1850)
- Kiricephalus constrictor (Riley & Self, 1980)
- Kiricephalus gabonensis (Riley & Self, 1980)
- Kiricephalus pattoni (Stephens, 1908)
- Kiricephalus tortus (Shipley, 1898)
- Parasambonia (Stunkard & Gandal, 1968)
- Parasambonia bridgesi (Stunkard & Gandal, 1968)
- Parasambonia minor (Riley & Self, 1982)
- Porocephalus (Humboldt, 1812)
- Porocephalus basiliscus (Riley & Self, 1979)
- Porocephalus benoiti (Fain, 1960)
- Porocephalus bifurcatus
- Porocephalus clavatus (Wyman, 1845)
- Porocephalus crotali (Humboldt, 1812)
- Porocephalus dominicana (Riley & Walters, 1980)
- Porocephalus stilesi (Sambon in Vaney & Sambon, 1910)
- Porocephalus subuliferum (Leuckart, 1860)
- Porocephalus taiwana (Qiu, Ma, Fan & Lu, 2005)
- Porocephalus tortugensis (Riley & Self, 1979)
- Waddycephalus (Sambon, 1922)
- Waddycephalus calligaster (Riley & Self, 1981)
- Waddycephalus komodoensis (Riley & Self, 1981)
- Waddycephalus longicauda (Riley & Self, 1981)
- Waddycephalus porphyriacus (Riley & Self, 1981)
- Waddycephalus punctulatus (Riley & Self, 1981)
- Waddycephalus radiata (Riley & Self, 1981)
- Waddycephalus scutata (Riley & Self, 1981)
- Waddycephalus superbus (Riley & Self, 1981)
- Waddycephalus teretiusculus (Baird, 1862)
- Waddycephalus vitiensis (Heymons, 1932)
- Sebekidae (Sambon, 1922)
- Alofia (Giglioli in Sambon, 1922)
- Alofia ginae (Giglioli in Sambon, 1922)
- Alofia indica (von Linstow, 1906)
- Alofia merki (Giglioli 'in Sambon, 1922)
- Alofia nilotici (Riley & Huchzermeyer, 1995)
- Alofia parva (Riley & Huchzermeyer, 1995)
- Alofia platycephalum (Lohrmann, 1889)
- Alofia simpsoni (Riley, 1994)
- Alofia travassosi (Heymons, 1932)
- Diesingia (Sambon, 1922)
- Diesingia kachugensis (Shipley, 1910)
- Diesingia megastomum (Diesing, 1836)
- Selfia (Riley, 1994)
- Selfia porosus (Riley, 1994)
- Leiperia (Sambon, 1922)
- Leiperia australiensis (Riley & Huchzermeyer, 1996)
- Leiperia cincinnalis (Sambon in Vaney & Sambon, 1910)
- Leiperia gracilis (Diesing, 1836)
- Sambonia (Noc & Giglioli, 1922)
- Sambonia clavata (Lohrmann, 1889)
- Sambonia parapodum (Self & Kuntz, 1966)
- Sambonia solomenensis (Self & Kuntz, 1957)
- Sambonia varani (Self & Kuntz, 1957)
- Sambonia wardi (Sambon in Vaney & Sambon, 1910)
- Agema (Riley et al., 1997)
- Agema silvaepalustris (Riley et al., 1997)
- Pelonia (Junker & Boomker, 2002)
- Pelonia africana (Junker & Boomker, 2002)
- Sebekia (Sambon, 1922)
- Sebekia cesarisi (Giglioli in Sambon, 1922)
- Sebekia divestei (Giglioli in Sambon, 1922)
- Sebekia johnstoni (Riley, Spratt & Winch, 1990)
- Sebekia microhamus (Self & Rego, 1985)
- Sebekia minor (Wedl, 1861)
- Sebekia mississippiensis (Overstreet, Self & Vliet, 1985)
- Sebekia multiannulata (Riley, Spratt & Winch, 1990)
- Sebekia novaeguineae (Riley, Spratt & Winch, 1990)
- Sebekia okavangoensis (Riley & Huchzermeyer, 1995)
- Sebekia oxycephalum (Diesing, 1836)
- Sebekia purdieae (Riley, Spratt & Winch, 1990)
- Sebekia trinitatis (Riley, Spratt & Winch, 1990)
References
- ^ Lavrov, Dennis V.; Brown, Wesley M.; Boore, Jeffrey L. (7 March 2004). "Phylogenetic position of the Pentastomida and (pan)crustacean relationships". Proceedings of the Royal Society of London. Series B: Biological Sciences. 271 (1538): 537–544. doi:10.1098/rspb.2003.2631.
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(help) - ^ J. A. Frölich (1789). "Beschreibung einiger neuer Eingeweidewürmer". Der Naturforscher. 24: 101–162.
- ^ A. von Humboldt (1811). "Sur un ver intestin trouvé dans les poumons du serpent à sonnettes, de Cumana". Voyage de Humboldt et Bonpand 2. Ptie. F. Schoell et G. Dufour, Paris. pp. 298–304.
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- ^ R. Leuckart (1860). "Bau und Entwicklungsgeschichte der Pentastomen nach Untersuchungen besonders von Pent. taenoides und P. denticulatum". C. F. Winter'sche Verlagshandlung, Leipzig: vi + 160.
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- ^ Encyclopedic Reference of Parasitology: Biology, Structure, Function
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- ^ Correct spelling: Sebakia --> Sebekia, See "Sebekia Sambon, 1922". WoRMS. World Register of Marine Species.
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- ^ P. J. van Beneden (1849). "Recherches sur l'organisation et le développement des Lingatules (Pentastoma Rud.), suivies de la description d'une espèce nouvelle provenant d'un Mandrill". Annales des Sciences Naturelles Zoologie Series. 3 (11): 313–348.
- ^ K. G. Wingstrand (1972). "Comparative spermatology of a pentastomid, Raillietiella hemidactyli, and a branchiuran crustacean, Argulus foliaceus, with a discussion of pentastomid relationships". Det Kongelige Danske Videnskabernes Selskab Biologiske Skrifter. 19 (4): 1–72.
- ^ J. Riley, A. A. Banaja & J. L. James (1978). "The phylogenetic relationships of the Pentastomida: the case for their inclusion within the Crustacea". International Journal for Parasitology. 8 (4): 245–254. doi:10.1016/0020-7519(78)90087-5.
- ^ L. G. Abele, W. Kim & B. E. Felgenhauer (1989). "Molecular evidence for inclusion of the Phylum Pentastomida in the Crustacea" (PDF). Molecular Biology and Evolution. 6 (6): 685–691.[dead link]
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- ^ Todd H. Oakley; Joanna M. Wolfe; Annie R. Lindgren; Alexander K. Zaharoff (2013). "Phylotranscriptomics to bring the understudied into the fold: monophyletic Ostracoda, fossil placement, and Pancrustacean phylogeny". Molecular Biology and Evolution. 30 (1): 215–233. doi:10.1093/molbev/mss216. PMID 22977117.
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- ^ a b J. W. Martin & G. E. Davis (2001). An Updated Classification of the Recent Crustacea (PDF). Natural History Museum of Los Angeles County. pp. 132 pp.
- ^ Dieter Waloszek, John E. Repetski & Andreas Maas (2006). "A new Late Cambrian pentastomid and a review of the relationships of this parasitic group". Transactions of the Royal Society of Edinburgh: Earth Sciences. 96 (2): 163–176. doi:10.1017/S0263593300001280. S2CID 84859920.
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- ^ a b Dieter Walossek, John E. Repetski & Klaus J. Müller (1994). "An exceptionally preserved parasitic arthropod, Heymonsicambria taylori n. sp. (Arthropoda increate sedis: Pentastomida) from Cambrian – Ordovician boundary beds of Newfoundland". Canadian Journal of Earth Sciences. 31 (11): 1664–1671. doi:10.1139/e94-149.
- ^ Peel, John S. (2022). "The oldest tongue worm: A stem-group pentastomid arthropod from the early middle Cambrian (Wuliuan Stage) of North Greenland (Laurentia)". GFF: 1–9. doi:10.1080/11035897.2022.2064543. S2CID 249028918.
- ^ Gill, Victoria (22 May 2015). "A 425-million-year-old parasite found attached to host". BBC Online. Retrieved 22 May 2015.
- ^ Siveter, David J.; Briggs, Derek E.G.; Siveter, Derek J.; Sutton, Mark D. (2015). "A 425-Million-Year-Old Silurian Pentastomid Parasitic on Ostracods". Current Biology. 25 (12): 1632–1637. doi:10.1016/j.cub.2015.04.035. PMID 26004764.
- ^ "Requiem for an ancient tongue worm". Yale News. 21 May 2015. Retrieved 5 June 2015.
- ^ Geoff Boxshall (2013). "Pentastomida". WoRMS. World Register of Marine Species. Retrieved May 13, 2013.
- ^ Spratt, D.M. (2010). "Yelirella nomen novum for Rileyella Spratt, 2003 (Pentastomida: Cephalobaenida), a junior homonym of Rileyella Townsend, 1909 (Diptera: Tachinidae)". Parasite. 17 (4): 319. doi:10.1051/parasite/2010174319. ISSN 1252-607X. PMID 21275237.
External links
- Encyclopædia Britannica (11th ed.). 1911. .