Armophorea

Armophorea is a class of ciliates in the subphylum Intramacronucleata.[1][2] .[3] It was first resolved in 2004[4] and comprises three orders: Metopida, Clevelandellida,[5] and Armophorida.[6] Previously members of this class were thought to be heterotrichs because of similarities in morphology, most notably a characteristic dense arrangement of cilia surrounding their oral structures.[7] However, the development of genetic tools and subsequent incorporation of DNA sequence information has led to major revisions in the evolutionary relationships of many protists, including ciliates.[8] Metopids, clevelandellids, and armophorids were grouped into this class based on similarities in their small subunit rRNA sequences, making them one of two so-called "riboclasses" of ciliates, however, recent analyses suggest that Armophorida may not be related to the other two orders.[9]

Armophorea
Sicuophora multigranularis (Clevelandellida)
Scientific classification
(unranked): Diaphoretickes
Clade: TSAR
Clade: SAR
Infrakingdom: Alveolata
Phylum: Ciliophora
Subphylum: Intramacronucleata
Class: Armophorea
Lynn, 2004
Orders
  • Metopida
  • Clevelandellida
  • Armophorida

Etymology

The name Armophorea is thought to be derived from the Latin word arma, meaning weapons, or armus, meaning shoulder. This name refers to the caenomorphid members of this class, which have a characteristic military helmet-like morphology, and also a twisted appearance that looks like a shoulder.[7]

Habitat and ecology

Free-living armophoreans live in anoxic or microaerobic habitats, in the sediment or water column where there is reduced or absent oxygen. Thus their distribution is quite limited, although they are found globally in both marine and freshwater habitats, as well as in terrestrial sediment. Clevelandellids live as commensal symbionts inside of the digestive tracts of terrestrial and aquatic animals.[7]

Armophoreans can survive by encystment when in unfavorable environmental conditions. This is quite important for clevelandellids because it facilitates their transmission between hosts.[7]

Like most anaerobic ciliates, armophoreans have mitochondria-derived organelles called hydrogenosomes. These specialized organelles produce energy for the cell in absence of oxygen by the fermentation of pyruvate into acetate and hydrogen. Armophoreans harbor methanogenic endosymbiotic archaea that have been located in the cytoplasm adjacent to their hydrogenosomes. Host cells can contain up to 10,000 methanogens, and they are thought to play roles in host growth and metabolism.[10] It is hypothesized that these symbionts consume the hydrogen that is produced as an end-product of fermentation, making it a more favorable reaction and increasing its energetic yield.[11] Marine armophoreans also harbor ectosymbiotic bacteria that are sulfate reducers, which are thought to play a similar role as the endosymbiotic methanogens in that they also consume hydrogen as a metabolite of host fermentation.[10]

Methanogenesis by these encosymbiotic archaea can contribute substantially to the production of methane in sulphate-rich, anoxic detrital sediments and the anoxic water column, but the contribution is modest (>2%) in sandy sediments where the ciliates are lower in number.[12] This is in contrast to clevelandellids: over 80% of the methane produced by the American cockroach can be attributed to these ciliates via their methanogenic endosymbionts.[7] There are a lot of things that are going to be diffencnt in the way thay you would have to do things in the mean in the liffr ,[13]

References
  1. Gao, Feng; Warren, Alan; Zhang, Qianqian; Gong, Jun; Miao, Miao; Sun, Ping; Xu, Dapeng; Huang, Jie; Yi, Zhenzhen; Song, Weibo (2016). "The all-data-based evolutionary hypothesis of ciliated protists with a revised classification of the Phylum Ciliophora (Eukaryota, Alveolata)". Scientific Reports. 6: 24874. doi:10.1038/srep24874. PMC 4850378. PMID 27126745.
  2. Da Silva Paiva, T; Do Nascimento Borges, B; Da Silva-Neto, I. D. (2013). "Phylogenetic study of Class Armophorea (Alveolata, Ciliophora) based on 18S-rDNA data". Genetics and Molecular Biology. 36 (4): 571–585. doi:10.1590/S1415-47572013000400017. PMC 3873190. PMID 24385862.
  3. Li, Can; Zhao, Weishan; Zhang, Dong; Wang, Runqiu; Wang, Guitang; Zou, Hong; Li, Wenxiang; Wu, Shangong; Li, Ming (2018). "Sicuophora (Syn. Wichtermania) multigranularis from Quasipaa spinosa (Anura): morphological and molecular study, with emphasis on validity of Sicuophora (Armophorea, Clevelandellida)". Parasite. 25: 38. doi:10.1051/parasite/2018035. ISSN 1776-1042. PMC 6063722. PMID 30052499.
  4. AFFA'A, FELIX-MARIE; HICKEY, DONAL A.; STRUDER-KYPKE, MICHAELA; LYNN, DENIS H. (May 2004). "Phylogenetic Position of Species in the Genera Anoplophrya, Plagiotoma, and Nyctotheroides (Phylum Ciliophora), Endosymbiotic Ciliates of Annelids and Anurans". The Journal of Eukaryotic Microbiology. 51 (3): 301–306. doi:10.1111/j.1550-7408.2004.tb00570.x. ISSN 1066-5234. PMID 15218698.
  5. De Puytorac, P; Grain, J (1976). "Ultrastructure du cortex buccal et évolution chez les ciliés". Protistologica. 12: 49–67.
  6. Jankowski, AW (1964). "Morphology and evolution of Ciliophora. III. Diagnoses and phylogenesis of 53 sapropelobionts, mainly of the order Heterotrichida". Protist. 107: 185–294.
  7. Lynn, Denis H.. (2008). The Ciliated Protozoa : Characterization, Classification, and Guide to the Literature. Springer Science + Business Media B.V. ISBN 9781402082399. OCLC 758317642.
  8. Caron, David A.; Countway, Peter D.; Jones, Adriane C.; Kim, Diane Y.; Schnetzer, Astrid (2012-01-15). "Marine Protistan Diversity". Annual Review of Marine Science. 4 (1): 467–493. doi:10.1146/annurev-marine-120709-142802. ISSN 1941-1405. PMID 22457984.
  9. Li, Song; Bourland, William A.; Al-Farraj, Saleh A.; Li, Lifang; Hu, Xiaozhong (October 2017). "Description of two species of caenomorphid ciliates (Ciliophora, Armophorea): Morphology and molecular phylogeny". European Journal of Protistology. 61: 29–40. doi:10.1016/j.ejop.2017.08.001.
  10. Fenchel, Tom; Finlay, Bland J. (2010), "Free-Living Protozoa with Endosymbiotic Methanogens", (Endo)symbiotic Methanogenic Archaea, Springer Berlin Heidelberg, pp. 1–11, doi:10.1007/978-3-642-13615-3_1, ISBN 9783642136146
  11. Worm, Petra; Müller, Nicolai; Plugge, Caroline M.; Stams, Alfons J. M.; Schink, Bernhard (2010), "Syntrophy in Methanogenic Degradation", (Endo)symbiotic Methanogenic Archaea, Springer Berlin Heidelberg, pp. 143–173, doi:10.1007/978-3-642-13615-3_9, ISBN 9783642136146
  12. Fenchel, T. (January 1993). "Methanogenesis in marine shallow water sediments: The quantitative role of anaerobic protozoa with endosymbiotic methanogenic bacteria". Ophelia. 37 (1): 67–82. doi:10.1080/00785326.1993.10430378. ISSN 0078-5326.
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