The flagella are arranged in one or more clusters near the anterior of the cell. Their basal bodies are linked to parabasal fibers that are associated with a prominent Golgi complex, together forming a parabasal apparatus distinctive to the group.[5] Attachment of a parabasal fiber to the first Golgi cisterna by thin filaments has been reported in Tritrichomonas foetus.[6] Usually they also give rise to a sheet of cross-like microtubules that runs down the center of the cell and in some cases projects past the end. This is called the axostyle, but is different in structure from the axostyles of oxymonads.[citation needed]
Parabasalids are anaerobic, and lack mitochondria, but this is now known to be a result of secondary loss, and they contain small hydrogenosomes which apparently developed from reduced mitochondria.[7] Similar relics have been found in other amitochondriate flagellates, and the parabasalids are probably related to them, forming a group called the metamonads. They lack the feeding grooves found in most others, but this is probably a secondary loss as well.[citation needed]
Classification
Before reclassification, the parabasalids were divided into about seven[9] to 10 orders depending on sources. Present classification divides Parabasalia into four orders, that is, Trichonymphida, Spirotrichonymphida, Cristamonadida, and Trichomonadida.
[1]
The trichomonads have one group of 4–6 flagella, one of which is attached to the side of the cell and often forms an undulating membrane. Many are found in vertebrate hosts, including Trichomonas vaginalis, which causes a sexually transmitted disease in humans.
The other orders, formerly grouped as the hypermastigids, have a large number of flagellar clusters and are found exclusively in the guts of insects. (The term "Hypermastigida" is still occasionally encountered.[10])
Evolution
The parabasalid Trichomonas vaginalis is not known to undergo meiosis. However, Malik et al.[11] examined T. vaginalis for the presence of 29 genes that function in meiosis and found 27 such genes, including eight genes specific to meiosis in model organisms. These findings suggested that the capability for meiosis, and hence sexual reproduction, was likely present in a recent parabasalid ancestor of T. vaginalis.[11]
References
^ abAdl, Sina M.; Simpson, Alastair G. B.; Farmer, Mark A.; Andersen, Robert A.; Anderson, O. Roger; Barta, John R.; Bowser, Samuel S.; Brugerolle, Guy; Fensome, Robert A.; Fredericq, Suzanne; James, Timothy Y.; Karpov, Sergei; Kugrens, Paul; Krug, John; Lane, Christopher E.; Lewis, Louise A.; Lodge, Jean; Lynn, Denis H.; Mann, David G.; Mccourt, Richard M.; Mendoza, Leonel; Moestrup, Ojvind; Mozley-Standridge, Sharon E.; Nerad, Thomas A.; Shearer, Carol A.; Smirnov, Alexey V.; Spiegel, Frederick W.; Taylor, Max F. J. R. (October 2005). "The New Higher Level Classification of Eukaryotes with Emphasis on the Taxonomy of Protists". The Journal of Eukaryotic Microbiology. 52 (5): 399–451. doi:10.1111/j.1550-7408.2005.00053.x. PMID16248873.
^Ohkuma, Moriya; Iida, Toshiya; Ohtoko, Kuniyo; Yuzawa, Hiroe; Noda, Satoko; Viscogliosi, Eric; Kudo, Toshiaki (June 2005). "Molecular phylogeny of parabasalids inferred from small subunit rRNA sequences, with emphasis on the Hypermastigea". Molecular Phylogenetics and Evolution. 35 (3): 646–655. doi:10.1016/j.ympev.2005.02.013. PMID15878133.
^Benchimol, Marlene; Ribeiro, Karla Consort; Mariante, Rafael Meyer; Alderete, John F. (2001). "Structure and division of the Golgi complex in Trichomonas vaginalis and Tritrichomonas foetus". European Journal of Cell Biology. 80 (9): 593–607. doi:10.1078/0171-9335-00191. PMID11675935.
^Yubuki, Naoji; Céza, VÍT; Cepicka, Ivan; Yabuki, Akinori; Inagaki, Yuji; Nakayama, Takeshi; Inouye, Isao; Leander, Brian S (2010). "Cryptic Diversity of Free-Living Parabasalids, Pseudotrichomonas keilini and Lacusteria cypriaca n. G., n. Sp., as Inferred from Small Subunit rDNA Sequences". Journal of Eukaryotic Microbiology. 57 (6): 554–61. doi:10.1111/j.1550-7408.2010.00509.x. PMID20880033. S2CID4195962.
^Carpenter, Kevin J.; Keeling, Patrick J. (July 2007). "Morphology and Phylogenetic Position of Eucomonympha imla (Parabasalia: Hypermastigida)". Journal of Eukaryotic Microbiology. 54 (4): 325–332. doi:10.1111/j.1550-7408.2007.00263.x. PMID17669157.