Leucochloridium paradoxum explained

Leucochloridium paradoxum, the green-banded broodsac, is a parasitic flatworm (or helminth). Its intermediate hosts are land snails, usually of the genus Succinea. The pulsating, green broodsacs fill the eye stalks of the snail, thereby attracting predation by birds, the primary host. These broodsacs visually imitate caterpillars, a prey of birds. The adult parasite lives in the bird's cloaca, releasing its eggs into the faeces.

Life cycle

The species in Leucochloridium share a similar life cycle.[1] [2] They are parasites of snails and birds. This is a truncated life cycle compared with typical trematodes, because the snail acts as both the first and second intermediate host.[3]

Eggs ingested by the snail hatch into miracidia, which develop in the snail's hepatopancreas into the next stage, a sporocyst. The mature sporocyst consists of a number of branches spreading through the haemocoel and may make up a fifth or more of the snail's weight. Some of the branches develop into long tubes ending in a swollen broodsac, but these are staggered in their states of development, so that normally only 2 or 3 are mature simultaneously.[4] One or both of the snail's tentacles become occupied by a mature broodsac, which transforms the appearance. The tentacle is swollen and the pulsating, colourful, banded broodsac visible inside mimics the appearance of an insect larva like a caterpillar. This encourages their consumption by the next host, insectivorous birds. Observations in captivity indicated that birds tore the broodsac out of the snail before eating it,[5] so the snail may survive this. Birds may also become infected by eating broodsacs that have spontaneously burst from the tentacle, surviving for an hour whilst they continue to pulsate.[4] [6]

At their base,[7] the sporocysts produce asexually many tail-less cercariae, which develop directly into metacercariae within the sporocyst, depositing a thick mucoid coat around themselves. The mature metacercariae are oval in shape, 1.2 × 0.8 mm; typically 100–250 such metacercariae accumulate in a broodsac.[7] If the broodsac is eaten by a bird, the metacercariae pass along its alimentary tract, and lodge in the cloaca. Having lost the mucoid coat, they develop into adult distomes, long. This form has two suckers on the ventral side, which anchor it to the cloacal wall, and a smooth dorsal surface. The adults are hermaphroditic and release eggs into the bird's faeces. Some will be eaten by a snail, thus completing the life cycle.[6]

In a study in Russia, snails became infected in spring and summer. The resultant sporocysts were producing infective metacercariae in the following spring but then died in late summer.[4] The lifetime of the adult stage in its bird host is believed to be of the order of weeks or months.

Behaviour of the broodsacs and infected snails

The pulsations of the broodsacs typically vary from 40 to 75 times a minute depending on temperature, but they cease in the dark.

The parasite manipulates the snail host's behaviour in a way likely to make it more conspicuous to birds. In one study of Succinea putris hosts, infected snails stayed in better lit places for longer, sat on higher vegetation, and were more mobile. Whereas 53% of infected snails remained fully exposed for the 45 minutes of the observation period, the figure was only 28% for the controls (nearby snails without Leucochloridium broodsacs).[8] Infected snails may survive for at least a year and continue to be able to use the eyes on the ends of their tentacles. Although snails infected by other Leucochloridium species are reported to continue to reproduce,[1] snails infected by L. paradoxum often show a reduction of the sexual organs.[9]

The appearance and behaviour of the sporocysts is a case of aggressive mimicry, where the parasite vaguely resembles the food of the host, thereby gaining the parasite entry into the host's body by being eaten. This is unlike most other cases of aggressive mimicry, in which the mimic eats the duped animal.[10]

Taxonomy

In older literature, L. paradoxum may be referred to as L. macrostomum, derived from Rudolphi's 1803 description of Fasciola macrostoma, which he later (1809) renamed Distomum macrostomum. Zeller (1874) misidentified specimens of L. paradoxum as D. macrostomum. Rudolphi's species is now in the genus Urogonimus.[11] Leucochloridium heckerti Kagan, 1951 is also considered a synonym of L. paradoxum.

Identification

The easiest way to differentiate between Leucochloridium species is from the appearance of the broodsacs in the tentacle of the host snail. Leucochloridium paradoxum exhibits broodsacs that have green bands with dark brown and black spots, and with a dark-brown or reddish-brown tip.[12] [9] Nowadays this method of identification may be supported with ribosomal DNA sequences. A snail may be simultaneously infected by more than one species of Leucochloridium.

The adults, found in the cloaca of birds, are less well known, so that distinguishing the species is less straightforward.

Habitat

Leucochlordium paradoxum is found in moist areas, such as marshes, where the usual intermediate host Succinea snails are found.

Distribution

Leucochloridium paradoxum was originally described based on its sporocyst stage, collected from an island in the river Elbe at Pillnitz, near Dresden, Germany. Other known locations are Poland, Belarus, the Saint Petersburg area of Russia, Denmark, Sweden, Norway, the Netherlands, the United Kingdom and Japan.[13] [14] [12] [15] It is believed to be the species of Leuchochloridium infecting an endemic species of semi-slug on Robinson Crusoe Island in the Pacific, the only record from the Southern Hemisphere.[16]

Hosts

Intermediate hosts:

Hosts:

External links

Notes and References

  1. Kagan . I.G. . Aspects in the life history of Neoleucochloridium problematicum (Magath, 1920) New Comb. and Leucochloridium cyanocittae McIntosh, 1932 (Trematoda:Brachylaemidae) . Transactions of the American Microscopical Society . 1951 . 70 . 281-3184 . 10.2307/3223567.
  2. Lewis . P.D. . Helminths of terrestrial molluscs in Nebraska. II. Life cycle of Leucochloridium variae McIntosh, 1932 (Digenea: Leucochloridiidae) . Journal of Parasitology . 1974 . 60 . 2 . 251 . 10.2307/3278459.
  3. Poulin . R. . Cribb . T. H. . Trematode life cycles: short is sweet? . Trends in Parasitology . 2002 . 18 . 4 . 176–183 . 10.1016/S1471-4922(02)02262-6.
  4. Tokmakova . A.S. . Ataev . G.L. . Сезонные изменения в биологии Leucochloridium paradoxum (Trematoda, Leucochlomorphidae) . Parazitologiya . 2015 . 49 . 3 . 200-207 . Seasonal changes in the biology of Leucochloridium paradoxum (Trematoda, Leucochlomorphidae) . Russian.
  5. Zeller . E. . Über Leucochloridium paradoxum Carus und die weitere Entwickung seiner Distomenbrut. . Zeitschrift für wissenschaftliche Zoologie . 1874 . 24 . 564–578 + Pl. XLVIII.
  6. Heckert . G.A. . Leucochloridium paradoxam. Monographische darstellung der entwicklungs- und Lebensgeschichte des Distomum macmstomum . Bibliotheca Zoologica . 1889 . 4 . 1-66 + Pls I-IV .
  7. Ataev . G.L. . Dobrovolskij . A.A. . Tokmakova . A.S. . Размножение партенит трематод Leucochloridium paradoxum (Trematoda: Leucochloridiidae) . Parazitologiya . 2014 . 47 . 2 . 178-182 . Reproduction of trematode Leucochloridium paradoxum sporocysts (Trematoda: Leucochloridiidae) . Russian.
  8. Wesołowska . W. . Wesołowski . T. . Do Leucochloridium sporocysts manipulate the behaviour of their snail hosts?. Journal of Zoology . March 2014 . 292 . 3 . 151–155 . 10.1111/jzo.12094.
  9. Wesenberg-Lund . C. . Contributions to the development of the Trematoda Digenea. I. The biology of Leucochloridium paradoxum. . Det Kongelike Danske Videnskakbernes Selskab, Naturvidenskabelig-mathematisk Afdeling . 1931 . 4 . 90–142.
  10. Jackson . R. R. . Cross . F. R. . A cognitive perspective on aggressive mimicry . Journal of Zoology . 2013 . 290 . 3 . 161–171 . 10.1111/jzo.12036. 3748996 .
  11. Kagan . I.G. . Revision of the subfamily Leucochloridiinae Poche, 1907 (Trematoda: Brachylaemidae) . American Midland Naturalist . 1952 . 48 . 2 . 257 . 10.2307/2422256.
  12. Bakke . T. A. . A revision of the family Leucochloridiidae Poche (Digenea) and studies on the morphology of Leucochloridium paradoxum Carus, 1835 . Systematic Parasitology . April 1980 . 1 . 3-4 . 189–202 . 10.1007/BF00009845.
  13. Casey . S.P. . Bakke . T.A. . Harris . P.D. . Cable . J. . Use of ITS rDNA for discrimination of European green- and brown-banded sporocysts within the genus Leucochloridium Carus, 1835 (Digenea: Leucochloriidae) . Systematic Parasitology . 2003 . 56 . 163–168. 10.1023/B:SYPA.0000003809.15982.ca.
  14. Ataev . G. L. . Zhukova . A. A. . Tokmakova . А. S. . Prokhorova . Е. E. . Multiple infection of amber Succinea putris snails with sporocysts of Leucochloridium spp. (Trematoda) . Parasitology Research . August 2016 . 115 . 8 . 3203–3208 . 10.1007/s00436-016-5082-6.
  15. Nakao . Minoru . Sasaki . Mizuki . Waki . Tsukasa . Iwaki . Takashi . Morii . Yuta . Yanagida . Kazumi . Watanabe . Megumi . Tsuchitani . Yoshikazu . Saito . Takumi . Asakawa . Mitsuhiko . Distribution records of three species of Leucochloridium (Trematoda: Leucochloridiidae) in Japan, with comments on their microtaxonomy and ecology . Parasitology International . October 2019 . 72 . 101936 . 10.1016/j.parint.2019.101936.
  16. Castillo . V.M. . González . H. . Evidence of parasitism in the semi-slug Omalonyx gayana d’Orbigny, 1835 with Leucochloridium paradoxum (Carus, 1835) sporocysts on Robinson Crusoe Island . Tentacle . 2021 . 29 . 34-35 .