Cyanobiont
Cyanobionts are
Currently, cyanobionts have been found to form symbiosis with various organisms in marine environments such as
Role in symbiosis
Cyanobionts play a variety of roles in their symbiotic relationships with the host organism.
By entering into a symbiosis with nitrogen-fixing cyanobacteria, organisms that otherwise cannot inhabit low-nitrogen environments are provided with adequate levels of fixed nitrogen to carry out life functions.
Cyanobacteria are also photosynthetically active and can therefore meet carbon requirements independently.
Maintenance of successful symbioses
In order to maintain a successful symbiosis following host infection, cyanobacteria need to match their life cycles with those of their hosts’.[8] In other words, cyanobacterial cell division must be done at a rate matching their host in order to divide at similar times. As free living organisms, cyanobacteria typically divide more frequently compared to eukaryotic cells, but as symbionts, cyanobionts slow down division times so they do not overwhelm their host.[8] It is unknown how cyanobionts are able to adjust their growth rates, but it is not a result of nutrient limitation by the host. Instead, cyanobionts appear to limit their own nutrient uptake in order to delay cell division, while the excess nutrients are diverted to the host for uptake.[8]
As the host continues to grow and reproduce, the cyanobiont will continue to infect and replicate in the new cells. This is known as vertical transmission, where new daughter cells of the host will be quickly infected by the cyanobionts in order to maintain their symbiotic relationship. This is most commonly seen when hosts reproduce asexually.[9] In the water fern Azolla, cyanobacteria colonize the cavities within dorsal leaves.[8] As new leaves form and begin to grow, the new leaf cavities that develop will quickly become colonized by new incoming cyanobacteria.[8]
An alternative mode of transmission is known as horizontal transmission, where hosts acquire new cyanobacteria from the surrounding environment between each host generation.[10] This mode of transmission is commonly seen when hosts reproduce sexually, as it tends to increase the genetic diversity of both host and cyanobiont.[9] Hosts that use horizontal transmission in order to obtain cyanobacteria will typically acquire a large and diverse cyanobiont population.[9] This may be used as a survival strategy in open oceans as indiscriminate uptake of cyanobacteria may guarantee capture of appropriate cyanobionts for each successive generation.[10]
Genetic modifications within host
Following infection and establishment of an endosymbiotic relationship, the new cyanobionts will no longer be free living and autonomous, but rather begin to dedicate their physiological activities in tandem with their hosts'.[11] Over time and evolution, the cyanobiont will begin to lose portions of their genome in a process known as genome erosion. As the relationship between the cyanobacteria and host evolves, the cyanobiont genome will develop signs of degradation, particularly in the form of pseudogenes.[11] A genome undergoing reduction will typically have a large proportion of pseudogenes and transposable elements dispersed throughout the genome.[11] Furthermore, cyanobacteria involved in symbiosis will begin to accumulate these mutations in specific genes, particularly those involved in DNA repair, glycolysis, and nutrient uptake.[11] These gene sets are critical for organisms that live independently, however as cyanobionts living in symbiosis with their hosts, there may not be any evolutionary need to continue maintaining the integrity of these genes. As the major function of a cyanobiont is to provide their host with fixed nitrogen, genes involved in nitrogen fixation or cell differentiation are observed to remain relatively untouched.[11] This may suggest that cyanobacteria involved in symbiotic relationships can selectively stream line their genetic information in order to best perform their functions as cyanobiont-host relationships continue to evolve over time.[11]
Examples of symbioses
Cyanobacteria have been documented to form symbioses with a large range of eukaryotes in both marine and terrestrial environments. Cyanobionts provide benefit through dissolved organic carbon (DOC) production or nitrogen fixation but vary in function depending on their host.[12] Organisms that depend on cyanobacteria often live in nitrogen-limited, oligotrophic environments and can significantly alter marine composition leading to blooms.[12][13]
Diatoms
Commonly found in
Other genera of diatoms can form symbioses with cyanobacteria; however, their relationships are less known. Spheroid cyanobacteria have been found within the diatom Rhopalodia gibba and have been found to possess genes for nitrogen fixation, but do not possess the proper pigments for photosynthesis.[20]
Dinoflagellates
Heterotrophic dinoflagellates can form symbioses with cyanobacteria (phaeosomes), most often in tropical marine environments.[12] The function of the cyanobiont depends on its host species. Abundant marine cyanobacteria in the genus Synechococcus form symbionts with dinoflagellates in the genera Ornithocercus, Histionesis and Citharistes, where it is hypothesized to benefit its host through the provision of fixed nitrogen in oligotrophic, subtropical waters.[22] Increased instances of phaeosome symbiosis have been documented in a stratified, nitrogen-limited environment, and living within a host can provide an anaerobic environment for nitrogen fixation to occur.[23] However, there is conflicting evidence of this. One study on phaeosomes in cells of Ornithocercus spp. has provided evidence that symbionts belonging to the genus Synechococcus, supply organic carbon rather than nitrogen, due to the absence of nitrogenase within these cyanobacteria.[24]
Sponges
One hundred species within the classes
Lichens
Bryophytes
Bryophytes are non-vascular plants encompassing mosses, liverworts, and hornworts, which most often form symbioses with members from the cyanobacterial genus Nostoc.[31] Depending on the host, the cyanobiont can be inside (endophytic) or outside the host (epiphytic).[31] In mosses, cyanobacteria are major nitrogen fixers and grow mostly epiphytically, aside from two species of Sphagnum which protect the cyanobiont from an acidic-bog environment.[32] In terrestrial Arctic environments, cyanobionts are the primary supplier of nitrogen to the ecosystem whether free-living or epiphytic with mosses.[33] Cyanobacterial associations with liverworts are rare, with only four of 340 genera of liverworts harbouring symbionts.[31] Two of the genera, Marchantia and Porella, are epiphytic, while the genera Blasia and Cavicularia are endophytic.[34] In hornworts however, endophytic cyanobionts have been described in more than triple the number of genera relative to liverworts.[35] Bryophytes and their cyanobacterial symbionts possess different structures depending on the nature of the symbiosis.[34] For instance, colonies of cyanobacterial symbionts in the liverwort Blasia spp. are present as auricles (small dots) between the inner and outer papillae near the ventral surface of the liverworts; whereas, cyanobionts in the hornworts Anthoceros and Phaeoceros are present within the thallus', in specialized slime cavities.[31] However, cyanobacteria first must locate and physically interact with their host in order to form a symbiotic relationship. Members of the cyanobacterial genus Nostoc can become motile through the use of hormogonia, while the host plant excretes chemicals to guide the cyanobacteria via chemotaxis.[31] For instance, liverworts in the genus Blasia can secrete HIF, a strong chemo-attractant for nitrogen-starved and symbiotic cyanobacteria. Cells of Nostoc punctiforme, which have been shown to possess genes encoding proteins that complement chemotaxis-related proteins within flowering plants belonging to the genus Gunnera.[36][37]
Ascidians
Filamentous cyanobacteria within the genera Synechocystis and Prochloron has been found within the tunic cavity of didemnid sea squirts. The symbiosis is proposed to have originated through the intake of a combination of sand and cyanobacteria which eventually proliferated.[38] The hosts benefit from receiving fixed carbon from the cyanobiont while the cyanobiont may benefit by protection from harsh environments.[38][39]
Echiuroid worms
Little is known about the symbiotic relationship between echiuroid worms and cyanobacteria. Unspecified cyanobacteria have been found within the subepidermal connective tissue of the worms Ikedosoma gogoshimense and Bonellia fuliginosa.[40]
Coral
Unicellular and symbiotic cyanobacteria were discovered in cells of coral belonging to the species
References
- PMID 20459320.
- ^ ISBN 9781466575196.
- PMID 18319454.
- ^ ISBN 9781904455158.
- ^ S2CID 5074495.
- PMID 11121783.
- ^ a b MicrobeWiki Kenyon. "Ecological impacts of symbiotic cyanobacteria (cyanobionts) living in marine environment".
- ^ S2CID 839086.
- ^ S2CID 15841778.
- ^ PMID 23071304.
- ^ PMID 20628610.
- ^ ISBN 978-0-306-46855-1.
- S2CID 84134683.
- ^ ISBN 9789048141265.
- ^ .
- ^ .
- S2CID 84962782.
- S2CID 53504106.
- ^ Villareal, Tracy (1994). "Widespread Occurrence of the Hemiaulus-cyanobacterial Symbiosis in the Southwest North Atlantic Ocean". Bulletin of Marine Science. 7: 1–7.
- PMID 14963089.
- PMID 33947914. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
- .
- ^ R., Jyothibabu; N.V., Madhu; P.A., Maheswaran; C.R.A., Devi; T., Balasubramanian; K.K.C., Nair; C.T., Achuthankutty (2006-01-01). "Environmentally-related seasonal variation in symbiotic associations of heterotrophic dinoflagellates with cyanobacteria in the western Bay of Bengal".
{{cite journal}}
: Cite journal requires|journal=
(help) - .
- ^ ISSN 1439-0485.
- ^ Wilkinson, Clive (1979). "Nutrient translocation from symbiotic cyanobacteria to coral reef sponges". Biologie des Spongiaires. 291: 373–380.
- ^ Wilkinson, Clive; Trott, Lindsay (1985). "Light as a factor determining the distribution of sponges across the central Great Barrier Reef". Australian Institute of Marine Science. 5: 125–130.
- ^ Usher, Kaley M.; Simon, T.; Fromont, J.; Kuo, J.; Sutton, D.C. (2004). "A new species of cyanobacterial symbiont from the marine sponge Chondrilla nucula". Symbiosis. 36 (2): 183–192.
- PMID 15797223.
- ISBN 9789401084468.
- ^ PMID 18267939.
- ISBN 978-0-306-48005-8.
- JSTOR 1552487.
- ^ ISBN 978-0849332753.
- S2CID 85582943.
- ^ Babic, S. "Hormogonia formation and the establishment of symbiotic associations between cyanobacteria and the bryophytes Blasia and Phaeoceros." University of Leeds. Leeds, UK (1996).
- S2CID 8752382.
- ^ JSTOR 3226942.
- ^ Pardy, R. L., and C. L. Royce. "Ascidians with algal symbionts." Algae and Symbioses, plants, Animals, Fungi, Viruses, interactions explored. Biopress Ltd, England (1992): 215-230.
- ^ Rai, Amar N., and Amar N. Rai. CRC Handbook of symbiotic cynobacteria. No. 04; QR99. 63, R3.. 1990.
- S2CID 37612615.