Cryptobiosis

(Redirected from Anhydrobiotic)

Cryptobiosis or anabiosis is a metabolic state in extremophilic organisms in response to adverse environmental conditions such as desiccation, freezing, and oxygen deficiency. In the cryptobiotic state, all measurable metabolic processes stop, preventing reproduction, development, and repair. When environmental conditions return to being hospitable, the organism will return to its metabolic state of life as it was prior to cryptobiosis.

Forms

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Anhydrobiosis

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Anhydrobiosis in the tardigrade Richtersius coronifer

Anhydrobiosis is the most studied form of cryptobiosis and occurs in situations of extreme desiccation. The term anhydrobiosis derives from the Greek for "life without water" and is most commonly used for the desiccation tolerance observed in certain invertebrate animals such as bdelloid rotifers, tardigrades, brine shrimp, nematodes, and at least one insect, a species of chironomid (Polypedilum vanderplanki). However, other life forms exhibit desiccation tolerance. These include the resurrection plant Craterostigma plantagineum,[1] the majority of plant seeds, and many microorganisms such as bakers' yeast.[2] Studies have shown that some anhydrobiotic organisms can survive for decades, even centuries, in the dry state.[3]

Invertebrates undergoing anhydrobiosis often contract into a smaller shape and some proceed to form a sugar called trehalose. Desiccation tolerance in plants is associated with the production of another sugar, sucrose. These sugars are thought to protect the organism from desiccation damage.[4] In some creatures, such as bdelloid rotifers, no trehalose has been found, which has led scientists to propose other mechanisms of anhydrobiosis, possibly involving intrinsically disordered proteins.[5]

In 2011, Caenorhabditis elegans, a nematode that is also one of the best-studied model organisms, was shown to undergo anhydrobiosis in the dauer larva stage.[6] Further research taking advantage of genetic and biochemical tools available for this organism revealed that in addition to trehalose biosynthesis, a set of other functional pathways is involved in anhydrobiosis at the molecular level.[7] These are mainly defense mechanisms against reactive oxygen species and xenobiotics, expression of heat shock proteins and intrinsically disordered proteins as well as biosynthesis of polyunsaturated fatty acids and polyamines. Some of them are conserved among anhydrobiotic plants and animals, suggesting that anhydrobiotic ability may depend on a set of common mechanisms. Understanding these mechanisms in detail might enable modification of non-anhydrobiotic cells, tissues, organs or even organisms so that they can be preserved in a dried state of suspended animation over long time periods.

As of 2004, such an application of anhydrobiosis is being applied to vaccines. In vaccines, the process can produce a dry vaccine that reactivates once it is injected into the body. In theory, dry-vaccine technology could be used on any vaccine, including live vaccines such as the one for measles. It could also potentially be adapted to allow a vaccine's slow release, eliminating the need for boosters. This proposes to eliminate the need for refrigerating vaccines, thus making dry vaccines more widely available throughout the developing world where refrigeration, electricity, and proper storage are less accessible.[8]

Based on similar principles, lyopreservation has been developed as a technique for preservation of biological samples at ambient temperatures.[9][10] Lyopreservation is a biomimetic strategy based on anhydrobiosis to preserve cells at ambient temperatures. It has been explored as an alternative technique for cryopreservation. The technique has the advantages of being able to preserve biological samples at ambient temperatures, without the need for refrigeration or use of cryogenic temperatures.[11][12]

Anoxybiosis

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SEM image of Milnesium tardigradum in tun (suspended) state
SEM image of Milnesium tardigradum in active state

In situations lacking oxygen (a.k.a., anoxia), many cryptobionts (such as M. tardigradum) take in water and become turgid and immobile, but can survive for prolonged periods of time. Some ectothermic vertebrates and some invertebrates, such as brine shrimps,[13] copepods,[14] nematodes,[15] and sponge gemmules,[16] are capable of surviving in a seemingly inactive state during anoxic conditions for months to decades.

Studies of the metabolic activity of these idling organisms during anoxia have been mostly inconclusive. This is because it is difficult to measure very small degrees of metabolic activity reliably enough to prove a cryptobiotic state rather than ordinary metabolic rate depression (MRD). Many experts are skeptical of the biological feasibility of anoxybiosis, as the organism is managing to prevent damage to its cellular structures from the environmental negative free energy, despite being both surrounded by plenty of water and thermal energy and without using any free energy of its own. However, there is evidence that the stress-induced protein p26 may act as a protein chaperone that requires no energy in cystic Artemia franciscana (sea monkey) embryos, and most likely an extremely specialized and slow guanine polynucleotide pathway continues to provide metabolic free energy to the A. franciscana embryos during anoxic conditions. It seems that A. franciscana approaches but does not reach true anoxybiosis.[17]

Chemobiosis

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Chemobiosis is the cryptobiotic response to high levels of environmental toxins. It has been observed in tardigrades.[18]

Cryobiosis

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Cryobiosis is a form of cryptobiosis that takes place in reaction to decreased temperature. Cryobiosis begins when the water surrounding the organism's cells has been frozen. Stopping molecule mobility allows the organism to endure the freezing temperatures until more hospitable conditions return. Organisms capable of enduring these conditions typically feature molecules that facilitate freezing of water in preferential locations while also prohibiting the growth of large ice crystals that could otherwise damage cells.[citation needed] One such organism is the lobster.[19]

Osmobiosis

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Osmobiosis is the least studied of all types of cryptobiosis. Osmobiosis occurs in response to increased solute concentration in the solution the organism lives in. Little is known for certain, other than that osmobiosis appears to involve a cessation of metabolism.[18]

Examples

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The brine shrimp Artemia salina, which can be found in the Makgadikgadi Pans in Botswana,[20] survives over the dry season when the water of the pans evaporates, leaving a virtually desiccated lake bed.

The tardigrade, or water bear, can undergo all five types of cryptobiosis. While in a cryptobiotic state, its metabolism reduces to less than 0.01% of what is normal, and its water content can drop to 1% of normal.[21] It can withstand extreme temperature, radiation, and pressure while in a cryptobiotic state.[22]

Some nematodes and rotifers can also undergo cryptobiosis.[23]

See also

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  • Biostasis – Coping with environmental changes without adapting
  • Cryobiology – Study of effects of extreme low temperatures on life
  • Cryonics – Freezing of a human corpse
  • Cryptobiotic soil – Communities of living organisms on the soil surface in arid and semi-arid ecosystems
  • Hibernation – Physiological state of dormant inactivity in order to pass the winter season
  • Lyopreservation – Metabolic state of life

References

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  1. ^ Bartels, Dorothea; Salamini, Francesco (December 2001). "Desiccation Tolerance in the Resurrection Plant Craterostigma plantagineum. A Contribution to the Study of Drought Tolerance at the Molecular Level". Plant Physiology. 127 (4): 1346–1353. doi:10.1104/pp.010765. PMC 1540161. PMID 11743072.
  2. ^ Calahan, Dean; Dunham, Maitreya; DeSevo, Chris; Koshland, Douglas E (October 2011). "Genetic analysis of desiccation tolerance in Sachharomyces cerevisiae". Genetics. 189 (2): 507–519. doi:10.1534/genetics.111.130369. PMC 3189811. PMID 21840858.
  3. ^ Shen-Miller, J; Mudgett, Mary Beth; Schopf, J William; Clarke, Steven; Berger, Rainer (November 1995). "Exceptional seed longevity and robust growth: Ancient sacred lotus from China". American Journal of Botany. 82 (11): 1367–1380. doi:10.2307/2445863. JSTOR 2445863.
  4. ^ Erkut, Cihan; Penkov, Sider; Fahmy, Karim; Kurzchalia, Teymuras V (January 2012). "How worms survive desiccation: Trehalose pro water". Worm. 1 (1): 61–65. doi:10.4161/worm.19040. PMC 3670174. PMID 24058825.
  5. ^ Tunnacliffe, Alan; Lapinski, Jens; McGee, Brian (September 2005). "A putative LEA protein, but no trehalose, is present in anhydrobiotic bdelloid rotifers". Hydrobiologia. 546 (1): 315–321. Bibcode:2005HyBio.546..315T. doi:10.1007/s10750-005-4239-6. S2CID 13072689.
  6. ^ Erkut, Cihan; Penkov, Sider; Khesbak, Hassan; Vorkel, Daniela; Verbavatz, Jean-Marc; Fahmy, Karim; Kurzchalia, Teymuras V (August 2011). "Trehalose renders the dauer larva of Caenorhabditis elegans resistant to extreme desiccation". Current Biology. 21 (15): 1331–1336. Bibcode:2011CBio...21.1331E. doi:10.1016/j.cub.2011.06.064. PMID 21782434. S2CID 18145344.
  7. ^ Erkut, Cihan; Vasilj, Andrej; Boland, Sebastian; Habermann, Bianca; Shevchenko, Andrej; Kurzchalia, Teymuras V (December 2013). "Molecular strategies of the Caenorhabditis elegans dauer larva to survive extreme desiccation". PLOS ONE. 8 (12): e82473. Bibcode:2013PLoSO...882473E. doi:10.1371/journal.pone.0082473. PMC 3853187. PMID 24324795.
  8. ^ "High hopes for fridge-free jabs". BBC News. 2004-10-19.
  9. ^ Yang, Geer; Gilstrap, Kyle; Zhang, Aili; Xu, Lisa X.; He, Xiaoming (1 June 2010). "Collapse temperature of solutions important for lyopreservation of living cells at ambient temperature". Biotechnology and Bioengineering. 106 (2): 247–259. doi:10.1002/bit.22690. PMID 20148402. S2CID 20748794.
  10. ^ Chakraborty, Nilay; Chang, Anthony; Elmoazzen, Heidi; Menze, Michael A.; Hand, Steven C.; Toner, Mehmet (2011). "A Spin-Drying Technique for Lyopreservation of Mammalian Cells". Annals of Biomedical Engineering. 39 (5): 1582–1591. doi:10.1007/s10439-011-0253-1. PMID 21293974. S2CID 11204697.
  11. ^ Yang G, Gilstrap K, Zhang A, Xu LX, He X. "Collapse temperature of solutions important for lyopreservation of living cells at ambient temperatures." Biotechnol Bioeng. 2010 Jun 1;106(2):247–259.
  12. ^ Chakraborty N, Chang A, Elmoazzen H, Menze MA, Hand SC, Toner M. "A spin-drying technique for lyopreservation of mammalian cells". Ann Biomed Eng. 2011 May;39(5):1582–1591.
  13. ^ Clegg et al. 1999
  14. ^ Marcus et al., 1994
  15. ^ Crowe and Cooper, 1971
  16. ^ Reiswig and Miller, 1998
  17. ^ Clegg, James S. (2001). "Cryptobiosis – a peculiar state of biological organization". Comparative Biochemistry and Physiology B. 128 (4): 613–624. doi:10.1016/S1096-4959(01)00300-1. PMID 11290443.  
  18. ^ a b Møbjerg, N.; Halberg, K. A.; Jørgensen, A.; Persson, D.; Bjørn, M.; Ramløv, H.; Kristensen, R. M. (2011). "Survival in extreme environments – on the current knowledge of adaptations in tardigrades". Acta Physiologica. 202 (3): 409–420. doi:10.1111/j.1748-1716.2011.02252.x. PMID 21251237. S2CID 20894284.
  19. ^ "Frozen Lobsters Brought Back to Life". 18 March 2004.
  20. ^ C. Michael Hogan (2008) Makgadikgadi, The Megalithic Portal, ed. A. Burnham
  21. ^ Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
  22. ^ Illinois Wesleyan University Tardigrade Facts
  23. ^ Watanabe, Masahiko (2006). "Anhydrobiosis in invertebrates". Appl. Entomol. Zool. 41 (1): 15–31. Bibcode:2006AppEZ..41...15W. doi:10.1303/aez.2006.15.

Further reading

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  • David A. Wharton, Life at the Limits: Organisms in Extreme Environments, Cambridge University Press, 2002, hardcover, ISBN 0-521-78212-0