Hydra (genus)

Hydra (/ˈhaɪdrə/ h-EYE-drə) is a genus of small, fresh-water organisms of the phylum Cnidaria and class Hydrozoa. They are native to the temperate and tropical regions.[2][3] Biologists are especially interested in Hydra because of their regenerative ability – they do not appear to die of old age, or indeed to age at all.

This article is about the aquatic animal. For mythological monster, see Lernaean Hydra. For other uses, see Hydra (disambiguation).

Hydra
Hydra species
Scientific classification
Kingdom: Animalia
Phylum: Cnidaria
Class: Hydrozoa
Order: Anthoathecata
Family: Hydridae
Dana, 1846
Genus: Hydra
Linnaeus, 1758[1]
Species[1]

Morphology
Schematic drawing of a discharging nematocyst

Hydra has a tubular, radially symmetric body up to 10 mm (0.39 in) long when extended, secured by a simple adhesive foot called the basal disc. Gland cells in the basal disc secrete a sticky fluid that accounts for its adhesive properties.

At the free end of the body is a mouth opening surrounded by one to twelve thin, mobile tentacles. Each tentacle, or cnida (plural: cnidae), is clothed with highly specialised stinging cells called cnidocytes. Cnidocytes contain specialized structures called nematocysts, which look like miniature light bulbs with a coiled thread inside. At the narrow outer edge of the cnidocyte is a short trigger hair called a cnidocil. Upon contact with prey, the contents of the nematocyst are explosively discharged, firing a dart-like thread containing neurotoxins into whatever triggered the release. This can paralyze the prey, especially if many hundreds of nematocysts are fired.

Hydra has two main body layers, which makes it "diploblastic". The layers are separated by mesoglea, a gel-like substance. The outer layer is the epidermis, and the inner layer is called the gastrodermis, because it lines the stomach. The cells making up these two body layers are relatively simple. Hydramacin[4] is a bactericide recently discovered in Hydra; it protects the outer layer against infection. A single Hydra is composed of 50,000 to 100,000 cells which consist of three specific stem cell populations that will create many different cell types. These stem cells will continually renew themselves in the body column.[5] Hydras have two significant structures on their body: the "head" and the "foot". When a Hydra is cut in half, each half will regenerate and form into a small Hydra; the "head" will regenerate a "foot" and the "foot" will regenerate a "head". If the Hydra is sliced into many segments then the middle slices will form both a "head" and a "foot".[6]

Respiration and excretion occur by diffusion throughout the surface of the epidermis, while larger excreta are discharged through the mouth.[7][8]

Nervous system

The nervous system of Hydra is a nerve net, which is structurally simple compared to more derived animal nervous systems. Hydra does not have a recognizable brain or true muscles. Nerve nets connect sensory photoreceptors and touch-sensitive nerve cells located in the body wall and tentacles.

The structure of the nerve net has two levels:

  • level 1 – sensory cells or internal cells; and,
  • level 2 – interconnected ganglion cells synapsed to epithelial or motor cells.

Some have only two sheets of neurons.[9]

Motion and locomotion
Hydra attached to a substrate

If Hydra are alarmed or attacked, the tentacles can be retracted to small buds, and the body column itself can be retracted to a small gelatinous sphere. Hydra generally react in the same way regardless of the direction of the stimulus, and this may be due to the simplicity of the nerve nets.

Hydra are generally sedentary or sessile, but do occasionally move quite readily, especially when hunting. They have two distinct methods for moving – 'looping' and 'somersaulting'. They do this by bending over and attaching themselves to the substrate with the mouth and tentacles and then relocate the foot, which provides the usual attachment, this process is called looping. In somersaulting, the body then bends over and makes a new place of attachment with the foot. By this process of "looping" or "somersaulting", a Hydra can move several inches (c. 100 mm) in a day. Hydra may also move by amoeboid motion of their bases or by detaching from the substrate and floating away in the current.

Reproduction and life cycle
Hydra budding:
  1. Non-reproducing
  2. Creating a bud
  3. Daughter growing out
  4. Beginning to cleave
  5. Daughter broken off
  6. Daughter clone of parent

When food is plentiful, many Hydra reproduce asexually by producing buds in the body wall, which grow to be miniature adults and break away when they are mature.

When a hydra is well fed, a new bud can form every two days.[10] When conditions are harsh, often before winter or in poor feeding conditions, sexual reproduction occurs in some Hydra. Swellings in the body wall develop into either ovaries or testes. The testes release free-swimming gametes into the water, and these can fertilize the egg in the ovary of another individual. The fertilized eggs secrete a tough outer coating, and, as the adult dies (due to starvation or cold), these resting eggs fall to the bottom of the lake or pond to await better conditions, whereupon they hatch into nymph Hydra. Some Hydra species, like Hydra circumcincta and Hydra viridissima, are hermaphrodites[11] and may produce both testes and ovaries at the same time.

Many members of the Hydrozoa go through a body change from a polyp to an adult form called a medusa, which is usually the life stage where sexual reproduction occurs, but Hydra do not progress beyond the polyp phase.

Feeding

Hydra mainly feed on aquatic invertebrates such as Daphnia and Cyclops.

While feeding, Hydra extend their body to maximum length and then slowly extend their tentacles. Despite their simple construction, the tentacles of Hydra are extraordinarily extensible and can be four to five times the length of the body. Once fully extended, the tentacles are slowly manoeuvred around waiting for contact with a suitable prey animal. Upon contact, nematocysts on the tentacle fire into the prey, and the tentacle itself coils around the prey. Within 30 seconds, most of the remaining tentacles will have already joined in the attack to subdue the struggling prey. Within two minutes, the tentacles will have surrounded the prey and moved it into the opened mouth aperture. Within ten minutes, the prey will have been engulfed within the body cavity, and digestion will have started. Hydra are able to stretch their body wall considerably in order to digest prey more than twice their size. After two or three days, the indigestible remains of the prey will be discharged through the mouth aperture via contractions.

The feeding behaviour of Hydra demonstrates the sophistication of what appears to be a simple nervous system.

Some species of Hydra exist in a mutual relationship with various types of unicellular algae. The algae are protected from predators by Hydra and, in return, photosynthetic products from the algae are beneficial as a food source to Hydra.

Measuring the feeding response
Addition of glutathione causes reduction in the tentacle spread in hydra.

The feeding response in Hydra is induced by glutathione (specifically in the reduced state as GSH) released from damaged tissue of injured prey.[12] There are several methods conventionally used for quantification of the feeding response. In some, the duration for which the mouth remains open is measured.[13] Other methods rely on counting the number of Hydra among a small population showing the feeding response after addition of glutathione.[14] Recently, an assay for measuring the feeding response in hydra has been developed.[15] In this method, the linear two-dimensional distance between the tip of the tentacle and the mouth of hydra was shown to be a direct measure of the extent of the feeding response. This method has been validated using a starvation model, as starvation is known to cause enhancement of the Hydra feeding response.[15]

Tissue regeneration

Hydra undergoes morphallaxis (tissue regeneration) when injured or severed. Typically, Hydras will reproduce by just budding off a whole new individual, the bud will occur around two-thirds of the way down the body axis. When a Hydra is cut in half, each half will regenerate and form into a small Hydra; the "head" will regenerate a "foot" and the "foot" will regenerate a "head". This regeneration occurs without cell division. If the Hydra is sliced into many segments then the middle slices will form both a "head" and a "foot".[6] The polarity of the regeneration is explained by two pairs of positional value gradients. There is both a head and foot activation and inhibition gradient. The head activation and inhibition works in an opposite direction of the pair of foot gradients.[16] The evidence for these gradients was shown in the early 1900s with grafting experiments. The inhibitors for both gradients have shown to be important to block the bud formation. The location that the bud will form is where the gradients are low for both the head and foot.[6] Hydras are capable of regenerating from pieces of tissue from the body and additionally after tissue dissociation from reaggregates.[16]

Non-senescence

Daniel Martinez claimed in a 1998 article in Experimental Gerontology that Hydra are biologically immortal.[17] This publication has been widely cited as evidence that Hydra do not senesce (do not age), and that they are proof of the existence of non-senescing organisms generally. In 2010, Preston Estep published (also in Experimental Gerontology) a letter to the editor arguing that the Martinez data refute the hypothesis that Hydra do not senesce.[18]

The controversial unlimited life span of Hydra has attracted much attention from scientists. Research today appears to confirm Martinez' study.[19] Hydra stem cells have a capacity for indefinite self-renewal. The transcription factor "forkhead box O" (FoxO) has been identified as a critical driver of the continuous self-renewal of Hydra.[19] In experiments, a drastically reduced population growth resulted from FoxO down-regulation.[19]

In bilaterally symmetrical organisms (Bilateria), the transcription factor FoxO impacts stress response, lifespan, and increase in stem cells. If this transcription factor is knocked down in bilaterian model organisms, such as fruit flies and nematodes, their lifespan is significantly decreased. In experiments on H. vulgaris (a radially symmetrical member of phylum Cnidaria), when FoxO levels were decreased, there was a negative impact of many key features of the Hydra, but no death was observed, thus it is believed other factors may contribute to the apparent lack of aging in these creatures.[5]

While Hydra immortality is well-supported today, the implications for human aging are still controversial. There is much optimism;[19] however, it appears that researchers still have a long way to go before they are able to understand how the results of their work might apply to the reduction or elimination of human senescence.[20]

Genomics

An ortholog comparison analysis done within the last decade demonstrated that Hydra share a minimum of 6,071 genes with humans. Hydra is becoming an increasingly better model system as more genetic approaches become available.[5] A draft of the genome of Hydra magnipapillata was reported in 2010.[21]

gollark: !hwdyk msg
gollark: Sinthorion
gollark: !hwdyk msg
gollark: IFcoltransG
gollark: !hwdyk msg

See also
  • Lernaean Hydra, a Greek mythological aquatic creature after which the genus is named
  • Turritopsis dohrnii, another cnidarian (a jellyfish) that scientists believe to be immortal

References
  1. Schuchert P (2011). Schuchert P (ed.). "Hydra Linnaeus, 1758". World Hydrozoa database. World Register of Marine Species. Retrieved 20 December 2011.
  2. Gilberson L (1999). Zoology Lab Manual (4th ed.). Primis Custom Publishing.
  3. Solomon E, Berg L, Martin D (2002). Biology (6th ed.). Brooks/Cole Publishing.
  4. Jung S, Dingley AJ, Augustin R, Anton-Erxleben F, Stanisak M, Gelhaus C, Gutsmann T, Hammer MU, Podschun R, Bonvin AM, Leippe M, Bosch TC, Grötzinger J (January 2009). "Hydramacin-1, structure and antibacterial activity of a protein from the basal metazoan Hydra" (PDF). The Journal of Biological Chemistry. 284 (3): 1896–905. doi:10.1074/jbc.M804713200. PMID 19019828.
  5. Tomczyk S, Fischer K, Austad S, Galliot B (January 2015). "Hydra, a powerful model for aging studies". Invertebrate Reproduction & Development. 59 (sup1): 11–16. doi:10.1080/07924259.2014.927805. PMC 4463768. PMID 26120246.
  6. Gilbert SF (2000). "Regeneration". Developmental Biology (6th ed.).
  7. "Olympus Microscopy Resource Center | Pond Life Video Gallery – Hydra (Coelenterata)". olympus.magnet.fsu.edu. Retrieved 21 September 2019.
  8. Cantor, Marvin H.; Rahat, Menachem (1982). "Regulation of Respiration and Photosynthesis in Hydra viridis and in Its Separate Cosymbionts: Effect of Nutrients". Physiological Zoology. The University of Chicago Press. 55 (3): 281–288. doi:10.1086/physzool.55.3.30157891. ISSN 0031-935X. JSTOR 30157891.
  9. Ji N, Flavell SW (April 2017). "Hydra: Imaging Nerve Nets in Action". Current Biology. 27 (8): R294–R295. doi:10.1016/j.cub.2017.03.040. PMID 28441559.
  10. Patton WK (August 2014). "Hydra (coelenterate)". Grolier Multimedia Encyclopedia. Grolier Online.
  11. Holstein T, Emschermann P (1995). Cnidaria: Hydrozoa Süsswasserfauna von Mitteleuropa. Bd 1/2+ 3. Stuttgart: Spektrum Akademischer Verlag. ISBN 978-3-8274-0836-5.
  12. Loomis WF (October 1955). "Glutathione control of the specific feeding reactions of hydra". Annals of the New York Academy of Sciences. 62 (9): 211–27. Bibcode:1955NYASA..62..211L. doi:10.1111/j.1749-6632.1955.tb35372.x.
  13. Bellis SL, Laux DC, Rhoads DE (November 1994). "Affinity purification of Hydra glutathione binding proteins". FEBS Letters. 354 (3): 320–4. doi:10.1016/0014-5793(94)01154-0. PMID 7957948.
  14. Venturini G (1987). "The hydra GSH receptor. Pharmacological and radioligand binding studies". Comparative Biochemistry and Physiology. C, Comparative Pharmacology and Toxicology. 87 (2): 321–4. doi:10.1016/0742-8413(87)90015-6. PMID 2888575.
  15. Kulkarni R, Galande S (November 2014). "Measuring glutathione-induced feeding response in hydra". Journal of Visualized Experiments (93): e52178. doi:10.3791/52178. PMC 4354099. PMID 25490534.
  16. Fujisawa T (February 2003). "Hydra regeneration and epitheliopeptides". Developmental Dynamics. 226 (2): 182–9. doi:10.1002/dvdy.10221. PMID 12557197.
  17. Martínez DE (May 1998). "Mortality patterns suggest lack of senescence in hydra". Experimental Gerontology. 33 (3): 217–25. doi:10.1016/S0531-5565(97)00113-7. PMID 9615920.
  18. Estep PW (September 2010). "Declining asexual reproduction is suggestive of senescence in hydra: comment on Martinez, D., "Mortality patterns suggest lack of senescence in hydra." Exp Gerontol 33, 217–25". Experimental Gerontology. 45 (9): 645–6. doi:10.1016/j.exger.2010.03.017. PMID 20398746.
  19. Boehm AM, Khalturin K, Anton-Erxleben F, Hemmrich G, Klostermeier UC, Lopez-Quintero JA, Oberg HH, Puchert M, Rosenstiel P, Wittlieb J, Bosch TC (November 2012). "FoxO is a critical regulator of stem cell maintenance in immortal Hydra". Proceedings of the National Academy of Sciences of the United States of America. 109 (48): 19697–702. Bibcode:2012PNAS..10919697B. doi:10.1073/pnas.1209714109. PMC 3511741. PMID 23150562.
  20. "Investigating the Agelessness of Hydra". Reason. FightAging.org. November 2012. Retrieved 23 November 2012.
  21. Chapman JA, Kirkness EF, Simakov O, Hampson SE, Mitros T, Weinmaier T, et al. (March 2010). "The dynamic genome of Hydra". Nature. 464 (7288): 592–6. Bibcode:2010Natur.464..592C. doi:10.1038/nature08830. PMC 4479502. PMID 20228792.
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