Pseudoceratina Explained

Pseudoceratina is a genus of sponge within the family Pseudoceratinidae. They are characterized by possession of a dendritic fiber skeleton lacking laminar bark but containing pith. They have been found in a variety of habitats including the Great Barrier reef (Queensland, Australia), the Red Sea, and Jamaica. Sponges of this genus have a microbiome known to produce a variety of chemicals that are used in pharmaceutical and anti-fouling activities. Notably, a species in this genus produces a chemical that is effective in inhibiting the migration of metastatic breast cancer cells.

Description

Sponges within the genus Pseudoceratina (originally named Psammaplysilla) are identified by possession of a dendritic fiber skeleton containing only pith elements while lacking the laminar bark that can be found in other sponges.[1] Several species have been described as yellow in color, but oxidizes in air and turns a dark yellowish-green, with variations in growth type including plates, tubes, and spikey branching arms.[2] [3] [4] [5] Pseudoceratina crassa has been described as having conical-shaped mounds, which divide as it grows, and only containing one oscule. In 2013, a proposition of a new species of Pseudoceratina was proposed.[4] This sponge was found to have a high density of collagen fibrills, which is considered a synapomorphy for the genus Pseudoceratina, but lacks the typical skeletal framework observed in other species of this genus. Instead, this species was found within the structure of a coral. This may indicate plasticity when building a fibrous skeleton for species in the genus Pseudoceratina.

Ecology

Pseudoceratina clavata can be found in patchy distributions within the Great Barrier Reef at around 15–20 meters deep. The species Pseudoceratina crassa is a brooder which releases its larvae once a year during daylight hours which are yellow and between 1.5–2.0 millimeters. Larvae of this species will settle and begin metamorphizing within 24 hours of being released. It is unsure why, but the larvae are considered distasteful by fish species thus survival rate is not significantly affected by predation. The larvae are released during daylight hours because the juvenile sponges are more susceptible to UV radiation. Adult sponges of the species Pseudoceratina crassa also have mechanisms to prevent predation as it was found that hermit crabs would avoid feeding on samples of this species.[6] Pseudoceratina crassa is one of the most prevalent species of sponges found on the north coast of Jamaica in Discovery Bay Reef where their growth rate was measured following Hurricane Allen in 1980.[7] Following settlement, the sponges can double in size after roughly 257 days during the initial exponential growth period after which growth begins to slow.

Symbionts

Symbiotic bacteria forming microbiomes within sponges is fairly standard across Porifera.[8] They can provide chemical defenses for the sponge, a necessity for a soft-bodied, sessile creature.[9] Pseudoceratina has been found to produce a number of different brominated alkaloids.[10] The microbiomes of the genus Pseudoceratina are distinctively different compared to other sponges that produce a subclass of bromotyrosine alkaloids indicating that microbiomes are not conserved between taxa and across geography.[11] However, the metabolomes produced are significantly correlated to the composition of the microbiome. A different study that compared the symbionts found in the species Pseudoceratina clavata to Rhabdastrella globostellata, both found on the Great Barrier Reef, showed a similar community structure on both the phylum- and species-level.

The natural products of their symbiotic bacteria can also be utilized for human purposes. Three different species in particular have been studied for their chemical production: Pseudoceratina arabica, Pseudoceratina clavata,[12] and Pseudoceratina purpurpea.[13] Pseudoceratina clavata is the first reported marine invertebrate to contain the genus Salinispora which had previously only been found in marine sediments. The ten strains of bacteria isolated from this species of sponge may control the structure of the sponge's microbial community through antagonistic activity inhibiting the growth of non-Salinospora bacteria. These strains may be useful in biopharmaceutical screenings. The natural products of Pseudoceratina have been used for enzyme inhibition,[14] antimicrobial,[15] parasympatholytic, cytotoxic,[16] and antifouling bioactivites.[17] Five new brominated alkaloids were isolated from the species Pseudoceratina arabica, found in the Red Sea, and were found to be effective in inhibiting the migration of metastatic breast cancer cells in vitro.

Notes and References

  1. Erwin . M . Thacker . W . 2016 . Phylogenetic analyses of marine sponges within the order Verongida: a comparison of morphological and molecular data (project) . 2022-03-14 . MorphoBank datasets. 10.7934/p2448 .
  2. Lafi . Feras F. . Garson . Mary J. . Fuerst . John A. . August 2005 . Culturable Bacterial Symbionts Isolated from Two Distinct Sponge Species (Pseudoceratina clavata and Rhabdastrella globostellata) from the Great Barrier Reef Display Similar Phylogenetic Diversity . Microbial Ecology . 50 . 2 . 213–220 . 10.1007/s00248-004-0202-8 . 16215644 . 29466131 . 0095-3628.
  3. Lindquist . Niels . Hay . Mark E. . November 1996 . Palatability and Chemical Defense of Marine Invertebrate Larvae . Ecological Monographs . 66 . 4 . 431–450 . 10.2307/2963489 . 2963489 . 0012-9615. 1853/36769 . free .
  4. Diaz . M. C. . Thacker . R. W. . Redmond . N. E. . Matterson . K. O. . Collins . A. G. . 2013-04-26 . Phylogenetic Novelties and Geographic Anomalies among Tropical Verongida . Integrative and Comparative Biology . 53 . 3 . 482–494 . 10.1093/icb/ict033 . 23624868 . 1540-7063. free .
  5. Web site: Yellow prickly encrusting sponges (Pseudoceratina purpurea) on the Shores of Singapore . 2022-03-14 . www.wildsingapore.com.
  6. Waddell . B . Pawlik . JR . 2000 . Defenses of Caribbean sponges against invertebrate predators. I. Assays with hermit crabs . Marine Ecology Progress Series . 195 . 125–132 . 10.3354/meps195125 . 2000MEPS..195..125W . 0171-8630. free .
  7. Wilkinson . Clive R. . Cheshire . Anthony C. . August 1988 . Growth rate of Jamaican coral reef sponges after hurricane Allen . The Biological Bulletin . 175 . 1 . 175–179 . 10.2307/1541905 . 1541905 . 0006-3185.
  8. Vogel . Gretchen . 2008-05-23 . The Inner Lives of Sponges . Science . 320 . 5879 . 1028–1030 . 10.1126/science.320.5879.1028 . 18497285 . 6296682 . 0036-8075.
  9. Raveendran . T. V. . Mol . V. P. Limna . 2009 . Natural product antifoulants . Current Science . 97 . 4 . 508–520 . 24111879 . 0011-3891.
  10. Shaala . Lamiaa . Youssef . Diaa . Sulaiman . Mansour . Behery . Fathy . Foudah . Ahmed . Sayed . Khalid . 2012-11-08 . Subereamolline A as a Potent Breast Cancer Migration, Invasion and Proliferation Inhibitor and Bioactive Dibrominated Alkaloids from the Red Sea Sponge Pseudoceratina arabica . Marine Drugs . 10 . 12 . 2492–2508 . 10.3390/md10112492 . 23203273 . 3509531 . 1660-3397. free .
  11. Mohanty . Ipsita . Tapadar . Subhasish . Moore . Samuel G. . Biggs . Jason S. . Freeman . Christopher J. . Gaul . David A. . Garg . Neha . Agarwal . Vinayak . 2021-04-27 . Presence of Bromotyrosine Alkaloids in Marine Sponges Is Independent of Metabolomic and Microbiome Architectures . mSystems . 6 . 2 . 10.1128/msystems.01387-20 . 33727403 . 8547014 . 2379-5077.
  12. Book: A., Kim, T. K. Garson, M. J. Fuerst, J. . Marine actinomycetes related to the 'Salinospora' group from the Great Barrier Reef sponge Pseudoceratina clavata . 2005-01-01 . Blackwell Publishing Ltd . 828752580.
  13. Jang . Jae-Hyuk . van Soest . Rob W. M. . Fusetani . Nobuhiro . Matsunaga . Shigeki . 2007-07-03 . Pseudoceratins A (Ia) and B (Ib), Antifungal Bicyclic Bromotyrosine-Derived Metabolites from the Marine Sponge Pseudoceratina purpurea. . ChemInform . 38 . 27 . 10.1002/chin.200727169 . 0931-7597.
  14. 2003-08-12 . Psammaplins from the Sponge Pseudoceratina purpurea: Inhibition of Both Histone Deacetylase and DNA Methyltransferase . ChemInform . 34 . 32 . 10.1002/chin.200332143 . 0931-7597. Crews . Phillip . etal .
  15. Badr . Jihan M. . Shaala . Lamiaa A. . Abou-Shoer . Mohamed I. . Tawfik . Mona K. . Habib . Abdel-Azim M. . 2008-07-04 . Bioactive Brominated Metabolites from the Red Sea Sponge Pseudoceratina arabica . Journal of Natural Products . 71 . 8 . 1472–1474 . 10.1021/np8002113 . 18598078 . 0163-3864.
  16. Kijjoa . Anake . Bessa . Júlia . Wattanadilok . Rawiwan . Sawangwong . Pichan . Nascimento . Maria São José . Pedro . Madalena . Silva . Artur M. S. . Eaton . Graham . Soest . Rob van . Herz . Werner . 2005-08-01 . Dibromotyrosine Derivatives, a Maleimide, Aplysamine-2 and Other Constituents of the Marine Sponge Pseudoceratina purpurea . Zeitschrift für Naturforschung B . 60 . 8 . 904–908 . 10.1515/znb-2005-0815 . 53394219 . 1865-7117. free .
  17. Tsukamoto . Sachiko . Kato . Haruko . Hirota . Hiroshi . Fusetani . Nobuhiro . June 1996 . Ceratinamides A and B: New antifouling dibromotyrosine derivatives from the marine sponge Pseudoceratina purpurea . Tetrahedron . 52 . 24 . 8181–8186 . 10.1016/0040-4020(96)00387-0 . 0040-4020.