The environmental physiology of Antarctic terrestrial nematodes: a review

The environmental physiology of terrestrial Antarctic nematodes is reviewed with an emphasis on their cold-tolerance strategies. These nematodes are living in one of the most extreme environments on Earth and face a variety of stresses, including low temperatures and desiccation. Their diversity is low and declines with latitude. They show resistance adaptation, surviving freezing and desiccation in a dormant state but reproducing when conditions are favourable. At high freezing rates in the surrounding medium the Antarctic nematode Panagrolaimus davidi freezes by inoculative freezing but can survive intracellular freezing. At slow freezing rates this nematode does not freeze but undergoes cryoprotective dehydration. Cold tolerance may be aided by rapid freezing, the production of trehalose and by an ice-active protein that inhibits recrystallisation. P. davidi relies on slow rates of water loss from its habitat, and can survive in a state of anhydrobiosis, perhaps aided by the ability to synthesise trehalose. Teratocephalus tilbrooki and Ditylenchus parcevivens are fast-dehydration strategists. Little is known of the osmoregulatory mechanisms of Antarctic nematodes. Freezing rates are likely to vary with water content in Antarctic soils. Saturated soils may produce slow freezing rates and favour cryoprotective dehydration. As the soil dries freezing rates may become faster, favouring freezing tolerance. When the soil dries completely the nematodes survive anhydrobiotically. Terrestrial Antarctic nematodes thus have a variety of strategies that ensure their survival in a harsh and variable environment. We need to more fully understand the conditions to which they are exposed in Antarctic soils and to apply more natural rates of freezing and desiccation to our studies.Communicated by: I.D. Hume     

Dehydration-inducible changes in expression of two aquaporins in the sleeping chironomid, Polypedilum vanderplanki

Aquaporin, AQP, is a channel protein that allows water to permeate across cell membranes. Larvae of the sleeping chironomid, Polypedilum vanderplanki, can withstand complete dehydration by entering anhydrobiosis, a state of suspended animation; however, the mechanism by which water flows out of the larval body during dehydration is still unclear. We isolated two cDNAs (PvAqp1 and PvAqp2) encoding water-selective aquaporins from the chironomid. When expressed in Xenopus oocytes, PvAQP1 and PvAQP2 facilitated permeation of water but not glycerol. Northern blots and in situ hybridization showed that expression of PvAqp1 was dehydration-inducible and ubiquitous whereas that of PvAqp2 was dehydration-repressive and fat body-specific. These data suggest distinct roles for these aquaporins in P. vanderplanki, i.e., PvAqp2 controls water homeostasis of fat body during normal conditions and PvAqp1 is involved in the removal of water during induction of anhydrobiosis.     

Resistance of a recombinant Escherichia coli to dehydration

Dehydration of microorganisms, rendering them anhydrobiotic, is often an efficient method for the short and long term conservation of different strain-producers. However, some biotechnologically important recombinant bacterial strains are extremely sensitive to conventional treatment. We describe appropriate conditions during dehydration of the recombinant Escherichia coli strain HB 101 (GAPDH) that can result dry cells having a ∼88% viability on rehydration. The methods entails air-drying after addition of 100 mM trehalose to the cultivation medium or distilled water (for short term incubation).     

Distribution of Tardigrades within a Moss Cushion: Do Tardigrades Migrate in Response to Changing Moisture Conditions?

The distribution of tardigrades within the layers of the cushion moss Grimmia alpicola Hedwig, 1801 was investigated. The aim of this study was to determine the tardigrade species present within the moss layers during both wet and dry periods and to determine if migration occurred in response to changing moisture conditions. Samples of the moss were removed from concrete caps on brick fence posts before and after rainfall and separated into two sections (top and bottom). The tardigrades from each layer and moisture condition were identified to species. Data for each species were statistically analyzed with a two-way analysis of variance (ANOVA) to compare the numbers of individuals present in the top and bottom layers of the moss under both wet and dry conditions.

Five tardigrade species were identified, including two species new to science: Macrobiotus sp. n.; Milnesium tardigradum Doyère, 1840; Echiniscus viridissimus Peterfi, 1956; Echiniscus perviridis Ramazzotti, 1959; and Echiniscus sp. n. The new species will be described in a forthcoming paper. No significant differences were found in the numbers of individuals of four of the five species in each layer within the moss or for each moisture condition. Only one species, E. viridissimus, was significantly more frequent in the top layer of the moss, regardless of moisture condition.

Migration within the moss cushion was not detected in any of these five species as a result of changes in moisture conditions. In xeric moss species, it may not be beneficial for tardigrades to migrate to avoid desiccation. Instead, they apparently undergo anhydrobiosis in both the top and bottom layers of the moss cushion.     

Effects of host desiccation on development, survival, and infectivity of entomopathogenic nematode Steinernema carpocapsae

This study investigates the effect of host desiccation on entomopathogenic nematode (EPN) development, emergence, infectivity, and cross-protection against secondary environmental stress. Galleria mellonella hosts infected with the EPN Steinernema carpocapsae A10 were allowed to dehydrate in an environmental chamber for up to 56 days at 23 degrees C achieving a weight loss of approximately 86% by day 44 post-infection. Host carcasses were rehydrated on water-saturated filter paper in White traps to collect emergent infective juveniles (IJ) at specific time intervals. Populations were counted with an apparent peak coinciding with desiccated hosts rehydrated at 24-day post-infection. Desiccation-stressed IJ populations from each time interval were tested for infectivity, and cross-resistance to secondary temperature and pH stresses and were found to have significant increases in both infectivity and protection from extremes of temperature and pH compared with controls. Total aqueous soluble protein profiles from control and desiccation-stressed IJs were analyzed using 10% SDS Laemmli gels. Several novel proteins were over-expressed in EPN from hosts subjected to desiccation suggesting the induction and expression of stress response genes.     

Intracellular localization of group 3 LEA proteins in embryos of Artemia franciscana

Late embryogenesis abundant (LEA) proteins are accumulated by anhydrobiotic organisms in response to desiccation and improve survivorship during water stress. In this study we provide the first direct evidence for the subcellular localizations of AfrLEA2 and AfrLEA3m (and its subforms) in anhydrobiotic embryos of Artemia franciscana. Immunohistochemistry shows AfrLEA2 to reside in the cytoplasm and nucleus, and the four AfrLEA3m proteins to be localized to the mitochondrion. Cellular locations are supported by Western blots of mitochondrial, nuclear and cytoplasmic fractions. The presence of LEA proteins in multiple subcellular compartments of A. franciscana embryos suggests the need to protect biological structures in many areas of a cell in order for an organism to survive desiccation stress, and may explain in part why a multitude of different LEA proteins are expressed by a single organism.     

Cryptobiosis--a peculiar state of biological organization

David Keilin (Proc. Roy. Soc. Lond. B, 150, 1959, 149–191) coined the term ‘cryptobiosis’ (hidden life) and defined it as ‘the state of an organism when it shows no visible signs of life and when its metabolic activity becomes hardly measurable, or comes reversibly to a standstill.’ I consider selected aspects of the 300 year history of research on this unusual state of biological organization. Cryptobiosis is peculiar in the sense that organisms capable of achieving it exhibit characteristics that differ dramatically from those of living ones, yet they are not dead either, so one may propose that cryptobiosis is a unique state of biological organization. I focus chiefly on animal anhydrobiosis, achieved by the reversible loss of almost all the organism's water. The adaptive biochemical and biophysical mechanisms allowing this to take place involve the participation of large concentrations of polyhydroxy compounds, chiefly the disaccharides trehalose or sucrose. Stress (heat shock) proteins might also be involved, although the details are poorly understood and seem to be organism-specific. Whether the removal of molecular oxygen (anoxybiosis) results in the reversible cessation of metabolism in adapted organisms is considered, with the result being ‘yes and no’, depending on how one defines metabolism. Basic research on cryptobiosis has resulted in unpredicted applications that are of substantial benefit to the human condition and a few of these are described briefly.