Literature DB >> 21402076

On dormancy strategies in tardigrades.

Roberto Guidetti1, Tiziana Altiero, Lorena Rebecchi.   

Abstract

In this review we analyze the dormancy strategies of metazoans inhabiting "hostile to life" habitats, which have a strong impact on their ecology and in particular on the traits of their life history. Tardigrades are here considered a model animal, being aquatic organisms colonizing terrestrial habitats. Tardigrades evolved a large variety of dormant stages that can be ascribed to diapause (encystment, cyclomorphosis, resting eggs) and cryptobiosis (anhydrobiosis, cryobiosis, anoxibiosis). In tardigrades, diapause and cryptobiosis can occur separately or simultaneously, consequently the adoption of one adaptive strategy is not necessarily an alternative to the adoption of the other. Encystment and cyclomorphosis are characterized by seasonal cyclic changes in morphology and physiology of the animals. They share several common features and their evolution is strictly linked to the molting process. A bet-hedging strategy with different patterns of egg hatching time has been observed in a tardigrade species. Four categories of eggs have been identified: subitaneous, delayed-hatching, abortive and diapause resting eggs, which needs a stimulus to hatch (rehydration after a period of desiccation). Cryptobiotic tardigrades are able to withstand desiccation (anhydrobiosis) and freezing (cryobiosis) at any stage of their life-cycle. This ability involves a complex array of factors working at molecular (bioprotectans), physiological and structural levels. Animal survival and the accumulation of molecular damage are related to the time spent in the cryptobiotic state, to the abiotic parameters during the cryptobiotic state, and to the conditions during initial and final phases of the process. Cryptobiosis evolved independently at least two times in tardigrades, in eutardigrades and in echiniscoids. Within each evolutionary line, the absence of cryptobiotic abilities is more related to selective pressures to local habitat adaptation than to phylogenetic relationships. The selective advantages of cryptobiosis (e.g. persistency in "hostile to life" habitats, reduction of competitors, parasites and predators, escaping in time from stressful conditions) could explain the high tardigrade species diversity and number of specimens found in habitats that dry out compared to freshwater habitats.
Copyright © 2011 Elsevier Ltd. All rights reserved.

Mesh:

Year:  2011        PMID: 21402076     DOI: 10.1016/j.jinsphys.2011.03.003

Source DB:  PubMed          Journal:  J Insect Physiol        ISSN: 0022-1910            Impact factor:   2.354


  35 in total

1.  A thin polymer membrane, nano-suit, enhancing survival across the continuum between air and high vacuum.

Authors:  Yasuharu Takaku; Hiroshi Suzuki; Isao Ohta; Daisuke Ishii; Yoshinori Muranaka; Masatsugu Shimomura; Takahiko Hariyama
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-15       Impact factor: 11.205

2.  The Microbial Community of Tardigrades: Environmental Influence and Species Specificity of Microbiome Structure and Composition.

Authors:  Matteo Vecchi; Irene L G Newton; Michele Cesari; Lorena Rebecchi; Roberto Guidetti
Journal:  Microb Ecol       Date:  2018-01-15       Impact factor: 4.552

3.  Tardigrada: An Emerging Animal Model to Study the Endoplasmic Reticulum Stress Response to Environmental Extremes.

Authors:  Łukasz Kaczmarek
Journal:  Prog Mol Subcell Biol       Date:  2021

Review 4.  Suspended animation, diapause and quiescence: arresting the cell cycle in C. elegans.

Authors:  Pamela A Padilla; Mary L Ladage
Journal:  Cell Cycle       Date:  2012-05-01       Impact factor: 4.534

5.  Tardigrades Use Intrinsically Disordered Proteins to Survive Desiccation.

Authors:  Thomas C Boothby; Hugo Tapia; Alexandra H Brozena; Samantha Piszkiewicz; Austin E Smith; Ilaria Giovannini; Lorena Rebecchi; Gary J Pielak; Doug Koshland; Bob Goldstein
Journal:  Mol Cell       Date:  2017-03-16       Impact factor: 17.970

6.  Tolerance to Anhydrobiotic Conditions Among Two Coexisting Tardigrade Species Differing in Life Strategies.

Authors:  Milena Roszkowska; Bartłomiej Gołdyn; Daria Wojciechowska; Jakub Z Kosicki; Edyta Fiałkowska; Hanna Kmita; Łukasz Kaczmarek
Journal:  Zool Stud       Date:  2021-12-07       Impact factor: 1.904

7.  RNA interference can be used to disrupt gene function in tardigrades.

Authors:  Jennifer R Tenlen; Shaina McCaskill; Bob Goldstein
Journal:  Dev Genes Evol       Date:  2012-11-28       Impact factor: 0.900

8.  The toughest animals of the Earth versus global warming: Effects of long-term experimental warming on tardigrade community structure of a temperate deciduous forest.

Authors:  Matteo Vecchi; Laurent Kossi Adakpo; Robert R Dunn; Lauren M Nichols; Clint A Penick; Nathan J Sanders; Lorena Rebecchi; Roberto Guidetti
Journal:  Ecol Evol       Date:  2021-06-29       Impact factor: 2.912

9.  The Aquaporin Channel Repertoire of the Tardigrade Milnesium tardigradum.

Authors:  Markus A Grohme; Brahim Mali; Weronika Wełnicz; Stephanie Michel; Ralph O Schill; Marcus Frohme
Journal:  Bioinform Biol Insights       Date:  2013-05-26

10.  Nature, source and function of pigments in tardigrades: in vivo raman imaging of carotenoids in Echiniscus blumi.

Authors:  Alois Bonifacio; Roberto Guidetti; Tiziana Altiero; Valter Sergo; Lorena Rebecchi
Journal:  PLoS One       Date:  2012-11-21       Impact factor: 3.240

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