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Journal articles on the topic 'Cryptobiosis'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 July 2024

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1

Watanabe, M., T. Kikawada, N. Minagawa, F. Yukuhiro, and T. Okuda. "Mechanism allowing an insect to survive complete dehydration and extreme temperatures." Journal of Experimental Biology 205, no. 18 (2002): 2799–802. http://dx.doi.org/10.1242/jeb.205.18.2799.

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SUMMARY Cryptobiosis describes the state of an organism whose body water is completely dehydrated and metabolic activity has become undetectable. Our study aimed to elucidate the physiological mechanism of cryptobiosis in the highest cryptobiotic invertebrate, Polypedilum vanderplanki. Larvae of this insect rapidly accumulated a large amount of the carbohydrate,trehalose, (18% of dry body mass) during desiccation for 2 days, suggesting that a high level of trehalose accumulation contributed to the successful induction of cryptobiosis in P. vanderplanki as well as in other lower cryptobiotic or

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2

Wright, Jonathan C., Peter Westh, and Hans Ramløv. "CRYPTOBIOSIS IN TARDIGRADA." Biological Reviews 67, no. 1 (2010): 1–29. http://dx.doi.org/10.1111/j.1469-185x.1992.tb01657.x.

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3

Pan, Long, Rong Cui, Yongxia Li, et al. "Third-Stage Dispersal Juveniles of Bursaphelenchus xylophilus Can Resist Low-Temperature Stress by Entering Cryptobiosis." Biology 10, no. 8 (2021): 785. http://dx.doi.org/10.3390/biology10080785.

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Nematodes can enter cryptobiosis by dehydration as an adaptation to low-temperature environments and recover from cryptobiosis by rehydration after environmental improvement. In this work, the survival of Bursaphelenchusxylophilus third-stage dispersal juveniles was studied in response to low-temperature treatment. The average survival rates were 1.7% after −80 °C treatment for 30 d and 82.2% after −20 °C treatment for 30 d. The changes of water content and inorganic salt ions that occur in pine trees during winter gradually alter the osmotic pressure in the liquid environment to dehydrate B.

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4

Shatilovich, Anastasia, Vamshidhar R. Gade, Martin Pippel, et al. "A novel nematode species from the Siberian permafrost shares adaptive mechanisms for cryptobiotic survival with C. elegans dauer larva." PLOS Genetics 19, no. 7 (2023): e1010798. http://dx.doi.org/10.1371/journal.pgen.1010798.

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Some organisms in nature have developed the ability to enter a state of suspended metabolism called cryptobiosis when environmental conditions are unfavorable. This state-transition requires execution of a combination of genetic and biochemical pathways that enable the organism to survive for prolonged periods. Recently, nematode individuals have been reanimated from Siberian permafrost after remaining in cryptobiosis. Preliminary analysis indicates that these nematodes belong to the genera Panagrolaimus and Plectus. Here, we present precise radiocarbon dating indicating that the Panagrolaimus

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5

Stillman, J. H. "CRYPTOBIOSIS VIA SPINDLE CHECKPOINT." Journal of Experimental Biology 207, no. 9 (2004): vi. http://dx.doi.org/10.1242/jeb.00938.

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6

Núñez, Patricia G., Nayeli G. Quevedo, and Roberto Vázquez. "A sustainable culture of tardigrades (Hypsibius dujardini) for astrobiological laboratory activities." EPJ Web of Conferences 200 (2019): 02011. http://dx.doi.org/10.1051/epjconf/201920002011.

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Tardigrades are microscopic organisms that have gained importance in astrobiology in recent years. They have extreme survival ability and can enter into a state of latency for several years called cryptobiosis. Due to our interest in conducting experiments with tardigrades to complement the laboratory exercises with students in the course of astrobiology, we bought samples of tardigrades in the cryptobiotic state. A sample of these were cultured at room temperature (18oC) with an oxygenation system, and fed with Spirulina algae every week. We found that in a few weeks tardigrades were producin

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7

Neuman, Yair. "Cryptobiosis: A new theoretical perspective." Progress in Biophysics and Molecular Biology 92, no. 2 (2006): 258–67. http://dx.doi.org/10.1016/j.pbiomolbio.2005.11.001.

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8

Hakozaki, Shuntaro Hakozaki, Hiroki Yamanobe, Kazuma Yabuki, et al. "ATP accumulation in early resting cyst formation towards cryptobiosis in Colpoda cucullus." Acta Protozoologica 62 (2023): 39–44. http://dx.doi.org/10.4467/16890027ap.23.004.18421.

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Resting cyst formation is a crucial process of cryptobiosis in protists. In colpodid ciliates, cyst formation is accompanied by large-scale morphological changes such as changes of cell shape, resorption of cilia, and formation of a cyst wall; additionally, the cell cycle is arrested. These changes provide acquired tolerance against environmental stresses. During cyst formation, mitochondrial membrane potential is reduced and the level of the ATP synthase beta chain is suppressed, strongly indicating that metabolism has ceased. Here, however, we show that ATP levels are elevated during the ini

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9

Woo, P. T. K. "Cryptobia (Trypanoplasma) salmositica and salmonid cryptobiosis." Journal of Fish Diseases 26, no. 11-12 (2003): 627–46. http://dx.doi.org/10.1046/j.1365-2761.2003.00500.x.

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10

Woo, P. T. K. "On cryptobiosis and infections by Cryptobia." Journal of Fish Diseases 27, no. 8 (2004): 493–94. http://dx.doi.org/10.1111/j.1365-2761.2004.00560.x.

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11

OKUDA, Takashi, Masahiko WATANABE, and Takahiro KIKAWADA. "Organisms with Extraordinary Tolerance to Drought: Cryptobiosis." Seibutsu Butsuri 44, no. 4 (2004): 172–75. http://dx.doi.org/10.2142/biophys.44.172.

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12

Cavalier-Smith, Thomas. "Cryptobiosis, Extremophily, and the Nature of Life." Cell 109, no. 6 (2002): 668–70. http://dx.doi.org/10.1016/s0092-8674(02)00777-8.

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13

Clegg, James S. "Cryptobiosis — a peculiar state of biological organization." Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 128, no. 4 (2001): 613–24. http://dx.doi.org/10.1016/s1096-4959(01)00300-1.

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14

Woo, Patrick T. K. "Immunological and Therapeutic Strategies against Salmonid Cryptobiosis." Journal of Biomedicine and Biotechnology 2010 (2010): 1–9. http://dx.doi.org/10.1155/2010/341783.

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Salmonid cryptobiosis is caused by the haemoflagellate,Cryptobia salmositica. Clinical signs of the disease in salmon (Oncorhynchusspp.) include exophthalmia, general oedema, abdominal distension with ascites, anaemia, and anorexia. The disease-causing factor is a metalloprotease and the monoclonal antibody (mAb-001) against it is therapeutic. MAb-001 does not fix complement but agglutinates the parasite. Some brook charr,Salvelinus fontinaliscannot be infected (Cryptobia-resistant); this resistance is controlled by a dominant Mendelian locus and is inherited. InCryptobia-resistant charr the p

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15

Skowronski, David. "Cryptobiosis and Composition (Presidential Prize Award Winner)." Southwest Philosophy Review 39, no. 1 (2023): 21–29. http://dx.doi.org/10.5840/swphilreview20233913.

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16

Woo, Patrick T. K. "Cryptobiosis and its control in North American fishes." International Journal for Parasitology 31, no. 5-6 (2001): 566–74. http://dx.doi.org/10.1016/s0020-7519(01)00169-2.

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17

Woo, P. T. K. "Protection against Cryptobia (Trypanoplasma) salmositica and Salmonid Cryptobiosis." Parasitology Today 14, no. 7 (1998): 272–77. http://dx.doi.org/10.1016/s0169-4758(98)01265-4.

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18

Gutiérrez, Juan, Sergio Callejas, Sara Borniquel, Laura Benítez, and Ana Martín-González. "Ciliate cryptobiosis: a microbial strategy against environmental starvation." International Microbiology 4, no. 3 (2001): 151–57. http://dx.doi.org/10.1007/s10123-001-0030-3.

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19

Kayastha, Pushpalata, Monika Mioduchowska, Jędrzej Warguła, and Łukasz Kaczmarek. "A Review on the Genus Paramacrobiotus (Tardigrada) with a New Diagnostic Key." Diversity 15, no. 9 (2023): 977. http://dx.doi.org/10.3390/d15090977.

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Paramacrobiotus species have been described in almost every corner of the world. To date, 45 species have been reported from this genus. Among which, 13 belong to the areolatus group (without a microplacoid) and 32 belong to the richtersi group (with a microplacoid). The species’ presence in different climatic conditions and habitats provides evidence of their adaptation to various harsh environments. The species of the genus are both bisexual (diploid) and parthenogenetic (triploid). The bisexual species have external fertilization. And they are omnivorous whose diet consists of certain cyano

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20

Li, Sen, and Patrick T. K. Woo. "Anorexia Reduces the Severity of Cryptobiosis in Oncorhynchus mykiss." Journal of Parasitology 77, no. 3 (1991): 467. http://dx.doi.org/10.2307/3283137.

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21

Woo, Patrick T. K. "The use of monoclonal antibody probes in salmonid cryptobiosis." Aquaculture 177, no. 1-4 (1999): 311–24. http://dx.doi.org/10.1016/s0044-8486(99)00094-0.

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22

Jonsson, K. I. "On the disparate terminological use of the concept cryptobiosis." Journal of Fish Diseases 27, no. 3 (2004): 175–76. http://dx.doi.org/10.1111/j.1365-2761.2004.00534.x.

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23

Koutsovoulos, Georgios, Sujai Kumar, Dominik R. Laetsch, et al. "No evidence for extensive horizontal gene transfer in the genome of the tardigrade Hypsibius dujardini." Proceedings of the National Academy of Sciences 113, no. 18 (2016): 5053–58. http://dx.doi.org/10.1073/pnas.1600338113.

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Tardigrades are meiofaunal ecdysozoans that are key to understanding the origins of Arthropoda. Many species of Tardigrada can survive extreme conditions through cryptobiosis. In a recent paper [Boothby TC, et al. (2015) Proc Natl Acad Sci USA 112(52):15976–15981], the authors concluded that the tardigrade Hypsibius dujardini had an unprecedented proportion (17%) of genes originating through functional horizontal gene transfer (fHGT) and speculated that fHGT was likely formative in the evolution of cryptobiosis. We independently sequenced the genome of H. dujardini. As expected from whole-orga

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24

Huang, Zebo, and Alan Tunnacliffe. "Cryptobiosis, Aging, and Cancer: Yin-Yang Balancing of Signaling Networks." Rejuvenation Research 9, no. 2 (2006): 292–96. http://dx.doi.org/10.1089/rej.2006.9.292.

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25

Metivier, Jean-Christophe, and Frédéric J. J. Chain. "Diversity in Expression Biases of Lineage-Specific Genes During Development and Anhydrobiosis Among Tardigrade Species." Evolutionary Bioinformatics 18 (January 2022): 117693432211402. http://dx.doi.org/10.1177/11769343221140277.

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Lineage-specific genes can contribute to the emergence and evolution of novel traits and adaptations. Tardigrades are animals that have adapted to tolerate extreme conditions by undergoing a form of cryptobiosis called anhydrobiosis, a physical transformation to an inactive desiccated state. While studies to understand the genetics underlying the interspecies diversity in anhydrobiotic transitions have identified tardigrade-specific genes and family expansions involved in this process, the contributions of species-specific genes to the variation in tardigrade development and cryptobiosis are l

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26

WATANABE, Masahiko, Takahiro KIKAWADA, Akihiko FUJITA, Ewa FORCZEK, Taro ADATI, and Takashi OKUDA. "Physiological traits of invertebrates entering cryptobiosis in a post-embryonic stage." European Journal of Entomology 101, no. 3 (2004): 439–44. http://dx.doi.org/10.14411/eje.2004.063.

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27

Morais, Pedro, Jesús Lamas, Manuel L. Sanmartín, Francisco Orallo, and José Leiro. "Resveratrol Induces Mitochondrial Alterations, Autophagy and a Cryptobiosis-like State in Scuticociliates." Protist 160, no. 4 (2009): 552–64. http://dx.doi.org/10.1016/j.protis.2009.04.004.

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28

Tan, Chung-Wei, Palmy Jesudhasan, and Patrick T. K. Woo. "Towards a metalloprotease-DNA vaccine against piscine cryptobiosis caused by Cryptobia salmositica." Parasitology Research 102, no. 2 (2007): 265–75. http://dx.doi.org/10.1007/s00436-007-0757-7.

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29

Clark, Trace, Kayla Tyler, Kara Joseph, et al. "Abstract 2063: Reactive-oxygen-species and Cysteine-oxidation Dependence of Tardigrade Cryptobiosis." Journal of Biological Chemistry 299, no. 3 (2023): S477. http://dx.doi.org/10.1016/j.jbc.2023.103897.

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30

Wang, Chong, Markus A. Grohme, Brahim Mali, Ralph O. Schill, and Marcus Frohme. "Towards Decrypting Cryptobiosis—Analyzing Anhydrobiosis in the Tardigrade Milnesium tardigradum Using Transcriptome Sequencing." PLoS ONE 9, no. 3 (2014): e92663. http://dx.doi.org/10.1371/journal.pone.0092663.

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31

Wright, Jonathan C. "Cryptobiosis 300 Years on from van Leuwenhoek: What Have We Learned about Tardigrades?" Zoologischer Anzeiger - A Journal of Comparative Zoology 240, no. 3-4 (2001): 563–82. http://dx.doi.org/10.1078/0044-5231-00068.

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32

WOO, P. T. K., J. F. LEATHERLAND, and M. S. LEE. "Cryptobia salmositica: cortisol increases the susceptibility of Salmo gairdneri Richardson to experimental cryptobiosis." Journal of Fish Diseases 10, no. 2 (1987): 75–83. http://dx.doi.org/10.1111/j.1365-2761.1987.tb00722.x.

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33

Li, S., and PTK Woo. "A Cryptobia salmositica (Kinetoplastida:Sarcomastigophora) species-specific DNA probe and its uses in salmonid cryptobiosis." Diseases of Aquatic Organisms 25 (1996): 9–14. http://dx.doi.org/10.3354/dao025009.

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34

Hattah Fattah, Muhammad, Siti Rahbiah Busaeri, and Alan Munandar. "Survival Rate and Quality of Phronima Suppa (Phronima sp) Zoea with the Cryptobiosis Application." IOP Conference Series: Earth and Environmental Science 391 (December 19, 2019): 012076. http://dx.doi.org/10.1088/1755-1315/391/1/012076.

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35

Gutiérrez, Juan C., A. Martin-Gonzalez, and T. Matsusaka. "Towards a generalized model of encystment (cryptobiosis) in ciliates: a review and a hypothesis." Biosystems 24, no. 1 (1990): 17–24. http://dx.doi.org/10.1016/0303-2647(90)90025-v.

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36

Schiffer, Philipp H., Etienne G. J. Danchin, Ann M. Burnell, et al. "Signatures of the Evolution of Parthenogenesis and Cryptobiosis in the Genomes of Panagrolaimid Nematodes." iScience 21 (November 2019): 587–602. http://dx.doi.org/10.1016/j.isci.2019.10.039.

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37

Janelt, Kamil, and Łukasz Michalczyk. "15th International Symposium on Tardigrada – Section IV: Physiology, Omics, Cryptobiosis & Astrobiology." Zoological Journal of the Linnean Society 200, no. 1 (2024): 218–19. http://dx.doi.org/10.1093/zoolinnean/zlad127.

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38

ZUO, X., та P. T. K. WOO. "Natural anti-proteases in rainbow trout, Oncorhynchus mykiss and brook charr, Salvelinus fontinalis and the in vitro neutralization of fish α2-macroglobulin by the metalloprotease from the pathogenic haemoflagellate, Cryptobia salmositica". Parasitology 114, № 4 (1997): 375–82. http://dx.doi.org/10.1017/s0031182096008578.

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Natural anti-proteases (α1-protease inhibitor (α1-PI; α1-antitrypsin) and α2-macroglobulin (α2-M)) were found in the blood of rainbow trout, Oncorhynchus mykiss and brook charr, Salvelinus fontinalis. The α2-M inhibited Cryptobia salmositica proteases and was significantly higher in brook charr than in rainbow trout. Under in vitro conditions it took longer for the same number of parasites to neutralize the α2-M in charr than in trout blood. The haemolysis which occurred when C. salmositica was incubated in the blood of rainbow trout was due to neutralization of α2-M. This in vitro study also

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39

Currie, Jaime L. M., and Patrick T. K. Woo. "Susceptibility of sexually mature rainbow trout, Oncorhynchus mykiss to experimental cryptobiosis caused by Cryptobia salmositica." Parasitology Research 101, no. 4 (2007): 1057–67. http://dx.doi.org/10.1007/s00436-007-0586-8.

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40

Watanabe, M. "Increase of internal ion concentration triggers trehalose synthesis associated with cryptobiosis in larvae of Polypedilum vanderplanki." Journal of Experimental Biology 206, no. 13 (2003): 2281–86. http://dx.doi.org/10.1242/jeb.00418.

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41

Ramløv, Hans, and Peter Westh. "Cryptobiosis in the Eutardigrade Adorybiotus (Richtersius) coronifer: Tolerance to Alcohols, Temperature and de novo Protein Synthesis." Zoologischer Anzeiger - A Journal of Comparative Zoology 240, no. 3-4 (2001): 517–23. http://dx.doi.org/10.1078/0044-5231-00062.

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42

ARDELLI, B. F., G. M. FORWARD, and P. T. K. WOO. "Brook charr, Salvelinus fontinalis (Mitchill), and cryptobiosis: a potential salmonid reservoir host for Cryptobia salmositica Katz, 1951." Journal of Fish Diseases 17, no. 6 (1994): 567–77. http://dx.doi.org/10.1111/j.1365-2761.1994.tb00255.x.

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43

Woo, Patrick T. K., and Sen Li. "In vitro Attenuation of Cryptobia salmositica and Its Use as a Live Vaccine against Cryptobiosis in Oncorhynchus mykiss." Journal of Parasitology 76, no. 5 (1990): 752. http://dx.doi.org/10.2307/3283000.

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44

Li, S., and P. T. K. Woo. "Vaccination of rainbow trout, Oncorhynchus mykiss (Walbaum), against cryptobiosis: efficacy of the vaccine in fresh and sea water." Journal of Fish Diseases 20, no. 5 (1997): 369–74. http://dx.doi.org/10.1046/j.1365-2761.1997.00309.x.

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45

Li, S., CB Cowey, and PTK Woo. "Effects of dietary ascorbic acid deficiency on Cryptobia salmositica infection and on vaccination against cryptobiosis in Oncorhynchus mykiss." Diseases of Aquatic Organisms 24 (1996): 11–16. http://dx.doi.org/10.3354/dao024011.

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46

Beamish, FWH, A. Sitja-Bobadilla, JA Jebbink, and PTK Woo. "Bioenergetic cost of cryptobiosis in fish:rainbow trout Oncorhynchus mykiss infected with Cryptobia salmositica and with an attenuated live vaccine." Diseases of Aquatic Organisms 25 (1996): 1–8. http://dx.doi.org/10.3354/dao025001.

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47

THOMAS, P. T., and P. T. K. WOO. "Complement activity in Salmo gairdneri Richardson infected with Cryptobia salmositica (Sarcomastigophora: Kinetoplastida) and its relationship to the anaemia in cryptobiosis." Journal of Fish Diseases 12, no. 4 (1989): 395–97. http://dx.doi.org/10.1111/j.1365-2761.1989.tb00328.x.

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48

Li, S., and P. T. K. Woo. "Efficacy of a live Cryptobia salmositica vaccine, and the mechanism of protection in vaccinated rainbow trout, Oncorhynchus mykiss, against cryptobiosis." Veterinary Immunology and Immunopathology 48, no. 3-4 (1995): 343–53. http://dx.doi.org/10.1016/0165-2427(95)05445-c.

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49

WRIGHT, JONATHAN C. "Desiccation Tolerance and Water-Retentive Mechanisms in Tardigrades." Journal of Experimental Biology 142, no. 1 (1989): 267–92. http://dx.doi.org/10.1242/jeb.142.1.267.

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Tardigrades entering a state of anhydrobiosis (cryptobiosis) show considerable interspecific variation in desiccation tolerance, lower lethal humidities for initial desiccation ranging from 78 to 53 %. Species most tolerant of rapid initial drying also show the most rapid acquisition of tolerance to low humidities (25–31 %) following drying in high humidity. Surface area reduction during tun formation shows a significant positive regression against desiccation tolerance in the Eutardigrada. The most desiccation-tolerant species thus infold the largest areas of cuticle. By comparison, the heter

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50

Laurent, Alexis, Corinne Scaletta, Philippe Abdel-Sayed, Wassim Raffoul, Nathalie Hirt-Burri, and Lee Ann Applegate. "Industrial Biotechnology Conservation Processes: Similarities with Natural Long-Term Preservation of Biological Organisms." BioTech 12, no. 1 (2023): 15. http://dx.doi.org/10.3390/biotech12010015.

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Cryopreservation and lyophilization processes are widely used for conservation purposes in the pharmaceutical, biotechnological, and food industries or in medical transplantation. Such processes deal with extremely low temperatures (e.g., –196 °C) and multiple physical states of water, a universal and essential molecule for many biological lifeforms. This study firstly considers the controlled laboratory/industrial artificial conditions used to favor specific water phase transitions during cellular material cryopreservation and lyophilization under the Swiss progenitor cell transplantation pro

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