Biology:Schellackia

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Short description: Genus of single-celled organisms


Schellackia
Scientific classification
Domain:
Eukaryota
(unranked):
(unranked):
Alveolata
Phylum:
Class:
Subclass:
Coccidiasina
Order:
Eucoccidiorida
Suborder:
Family:
Lankesterellidae
Genus:
Schellackia
Species

Schellackia balli [1]
Schellackia bolivari
Schellackia brugooi
Schellackia calotesi [2]
Schellackia cf agamae
Schellackia golvani
Schellackia iguanae
Schellackia landauae [3]
Schellackia legeri
Schellackia occidentalis [4]
Schellackia orientalis
Schellackia ptyodacryli
Schellackia weinbergi

The genus Schellackia comprises obligate unicellular eukaryotic parasites within the phylum Apicomplexa, and infects numerous species of lizards and amphibians worldwide. Schellackia is transmitted via insect vectors, primarily mites and mosquitoes, which take up the parasite in blood meals. These vectors then subsequently infect reptilian and amphibian which consume the infected insects.[5] The parasites deform erythrocytes of the host into crescents, and can be visualized using a blood smear.

The type species, Schellackia bolivari, was described by Anton Reichenow in 1919.

History of knowledge

Schellackia was first described by Anton Reichenow in 1919, with the type species Schellackia bolivari having been discovered parasitizing the spiny-footed lizard Acanthodactylus erythrurus and the Spanish Psammodromus hispanicus within the Iberian Peninsula.

At first, many difficulties in describing new species were present – very few characteristics could be described from blood sporozoites within the primary host, with most defining characteristics being restricted to the parasite’s endogenous stages within the gut epithelium of the host. This led to relatively few described species for a parasite genus that was supposedly very geographically widespread.[6]

In more recent years, however, molecular characterization methods have allowed a more precise determination of species identity and their phylogenetic relationship.[6]

Life cycle

As is typical of Apicomplexans, Schellackia replicates via multiple fission. The parasite utilizes both merogony (asexual) and gametogony (sexual), with both processes occurring within the mucosal epithelium of the duodenum of infected hosts.[7]

Young meronts can be expected to be around 6 μm in diameter, growing up to around 30 μm as they mature before they divide into merozoites. However, these figures and the time required for maturation can vary between species. The meronts subsequently split via cytokinesis, dividing into usually around 8 to 32 merozoites which are released as the host cell ruptures. Post-merogony, the development of merozoites produces a residual body of variable size. Merozoites are non-motile and proceed to infect other cells in order to rapidly reproduce.[7]

Gametogony occurs later in infection, generally after the majority of merogony activity. Male gametocytes (microgamonts) divide to form flagellated microgametes, while female gametocytes (macrogamonts) concurrently differentiate into macrogametes, sometimes even within the same host cell. These gametes then fuse forming zygotes within the epithelial layer of the duodenum of the host.[7]

Subsequently, zygotes transition to an oocyst stage. This transition is marked by the formation of large refractile bodies within the oocysts, soon followed by the appearance of developing sporozoites. The mature octonucleate oocyst is a characteristic phase of Schellackia’s lifecycle. Eventually, the oocyst divides by endopolygeny into eight sporozoites which combine with extensions of the refractory body as they exit the ruptured oocyst. This process leaves behind empty spaces within the epithelium and lamina propria of the host.[7]

The sporozoites then make their way into the host’s blood cells including erythrocytes, leucocytes and macrophages. The sporozoites often exist within a common parasitophorous vacuole which is shared with other sporozoites, although some also dwell within their own individual vacuole.[7]

The presence of sporozoites within the blood cells of the host allows the parasite to proliferate to additional hosts via blood-consuming insect vectors such as mites, ticks and mosquitos.[5]

Hosts and habitat

Schellackia species infect reptiles and amphibians all around the world, and are present in all continents except Antarctica. Although they have primarily been studied in lizards, they have been found to infect other animals including the Brazilian tree-frog, Phrynohyas venulosa.[8] The parasites are highly host specific, tending to infect a single host genus even when other lizard genera are present within the same geographical area.[6] Multiple species of Schellackia are named after their archetypal host, such as Schellackia occidentalis[5] and Schellackia agama.[7]

Description of the organism

Schellackia gametocytes are contained within parasitophorous vacuoles consisting of two membranes that are connected by numerous points of contact. The outer layer is thicker and bilaminate, while the inner layer comprises a single thinner structure. The vacuoles containing macrogametocytes are dense with fine granular material, while such material is largely absent from vacuoles containing microgametocytes.[9]

The microgametocytes and microgametes are contained within their own membrane within the vacuole. Developing microgametocytes have a peripheral nucleus without a visible nucleolus but contain dense patches of peripheral chromatin. The surface of the microgametocyte is covered in deep invaginations which provide increased surface area. Microgametes have flagella with a typical 9+2 axoneme structure, and five microtubules run parallel to the nucleus along the length of the gamete.[9]

Macrogametocytes are bound by a pellicle comprising two membranes perforated by multiple micropores. Two shapes of mitochondria are present – large, rounded mitochondria with tubular cristae are located beneath the pellicle, while smaller elongated mitochondria with a single row of cristae are present in aggregates. The nucleus is larger than the one found in microgametocytes and contains a large, compact nucleolus. The cytoplasm contains a dense RER network, as well as food, lipid, and other various vesicles. The presence of a high density of amylopectin granules in the cytoplasm causes it to have a foamy appearance, a characteristic maintained in the zygote.[7]

Schellackia sporozoites exist either free-floating or within a parasitophorous vacuole within a host cell. On occasion, multiple sporozoites have been observed to fit into a single expanded parasitophorous vacuole. The space within the vacuole surrounding the sporozoites contains a fine granular substance, and sometimes membranous residues. The sporozoites themselves are bound by a pellicle and contain a nucleus with a nucleolus and peripheral chromatin. One or two refractile bodies are also present, as well as multiple large mitochondria, amylopectin granules, and micronemes that extend from the apical tip along the length of the sporozoites.[10]

An important defining characteristic of the genus Schellackia is its octonucleate oocyst stage within the small intestine of a primary host – a combination of the presence of such oocysts as well as a lack of other parasites within the geographical area which share similar characteristics is sufficient to identify the genus.[11] The oocysts are enclosed in a translucent wall that is partially impermeable to Giemsa stain, and the cells leave behind empty rounded spaces upon expiration.[9]

References

  1. Le Bail O, Landau I (1974) Description and experimental life cycle of Schellackia balli n. sp. (Lankesterellidae) a parasite of toads in Guyana. Ann Parasitol Hum Comp 49(6):663-668
  2. Finkelman, S.; Paperna, I. (2014). "Schellackia calotesi n. sp. from agamid lizards of the genus Calotes in Thailand". Parasite 5 (1): 23–26. doi:10.1051/parasite/1998051023. ISSN 1252-607X. PMID 9754293.  open access
  3. Lainson, R, Shaw JJ, Ward RD (1976) Schellackia landauae sp. nov. (Eimeriorina: Lankesterellidae) in the Brazilian lizard Polychrus marmoratus (Iguanidae): experimental transmission by Culex pipiens fatigans. Parasitol 11 (2)
  4. Bonorris, J.S., Ball, G.H.1955. Schellackia occidentalis n. sp., a blood-inhabiting coccidian found in lizards in Southern California. J Protozool 2: 31-34
  5. 5.0 5.1 5.2 BONORRIS, JIM S.; BALL, GORDON H. (February 1955). "Schellackia occidentalisn.sp., a Blood-inhabiting Coccidian Found in Lizards in Southern California". The Journal of Protozoology 2 (1): 31–34. doi:10.1111/j.1550-7408.1955.tb02393.x. ISSN 0022-3921. 
  6. 6.0 6.1 6.2 Megía-Palma, Rodrigo; Martínez, Javier; Cuervo, José J.; Jiménez-Robles, O.; Gomes, Verónica; Cabidof, C.; Fitzed, P.S.; Martina, J. et al. (2016). "Molecular diversity of the genus Schellackia (Apicomplexa: Schellackiidae) parasitizing lizards of the family lacertidae (squamata)". Molecular: 79. 
  7. 7.0 7.1 7.2 7.3 7.4 7.5 7.6 Bristovetzky, Mariana; Paperna, Ilan (November 1990). "Life cycle and transmission of Schellackia cf. agamae, a parasite of the starred lizard Agama stellio". International Journal for Parasitology 20 (7): 883–892. doi:10.1016/0020-7519(90)90026-j. ISSN 0020-7519. 
  8. Paperna, I.; Lainson, R. (October 1995). "Schellackia (Apicomplexa: Eimeriidae) of the brazilian tree-frog, Phrynohyas venulosa (Amphibia: Anura) from Amazonian Brazil". Memórias do Instituto Oswaldo Cruz 90 (5): 589–592. doi:10.1590/s0074-02761995000500008. ISSN 0074-0276. 
  9. 9.0 9.1 9.2 Ostrovska, K.; Paperna, I. (1987). "Fine structure of gamont stages of Schellackia cf. agamae (Lankesterellidae, Eucoccidia) from the starred lizard Agama stellio". Parasitology Research 73 (6): 492–499. doi:10.1007/bf00535322. ISSN 0044-3255. 
  10. Paperna, I. (April 1993). "Electron microscopic study of Schellackia cf. agamae sporozoite infection in mosquitoes". International Journal for Parasitology 23 (2): 187–190. doi:10.1016/0020-7519(93)90140-t. ISSN 0020-7519. 
  11. Telford, Sam R. (June 1993). "A species of Schellackia (Apicomplexa: Lankesterellidae) parasitising east and southeast Asian lizards". Systematic Parasitology 25 (2): 109–117. doi:10.1007/bf00009980. ISSN 0165-5752. 

Wikidata ☰ Q7431106 entry