Physiological and proteomic changes suggest an important role of cell walls in the high tolerance to metals of Elodea nuttallii

Journal of Hazardous Materials

Volumn 263, Issue , 2013, Pages 575-583

  Larras, Floriane ^a   Regier, Nicole ^a   Planchon, Sébastien ^b   Poté, John ^a   Renaut, Jenny ^b   Cosio, Claudia ^a  

^a UNIVERSITY OF GENEVA   (Switzerland)

^b LUXEMBOURG INSTITUTE OF SCIENCE AND TECHNOLOGY   (Luxembourg)

Author keywords

Cadmium; Inorganic mercury; Lignin; Methyl mercury; Toxicokinetics

Indexed keywords

BIOACCUMULATION; BIOREMEDIATION; CADMIUM; CELLS; LIGNIN; MACHINERY; MERCURY (METAL); METALS; MOLECULAR BIOLOGY; PLANTS (BOTANY);

ANTIOXIDANT ENZYME; DIFFERENT MECHANISMS; ENVIRONMENTAL CONCENTRATION; INORGANIC MERCURY; METAL ACCUMULATION; METHYL MERCURY; SUBCELLULAR DISTRIBUTION; TOXICOKINETICS;

CYTOLOGY;

CADMIUM; MERCURY;

ANTIOXIDANT; BIOACCUMULATION; CELL ORGANELLE; ENZYME ACTIVITY; HEAVY METAL; HISTOLOGY; MACROPHYTE; METAL; PHOTOSYNTHESIS; PHYSIOLOGY; PHYTOREMEDIATION; POLLUTION EXPOSURE; PROTEOMICS; TOLERANCE; TOXICITY; WEED;

ADAPTATION; ARTICLE; BIOACCUMULATION; CELL FUNCTION; CELL STRUCTURE; CELL WALL; CELLULAR DISTRIBUTION; CONTROLLED STUDY; ELODEA; ELODEA NUTTALLII; ENERGY RESOURCE; LIGNIFICATION; MACROPHYTE; METAL TOLERANCE; NONHUMAN; PHOTOSYNTHESIS; PHYTOREMEDIATION; PROTEOMICS; ROOT GROWTH; SHOOT GROWTH;

ELODEA NUTTALLII;

CADMIUM; INORGANIC MERCURY; LIGNIN; METHYL-MERCURY; TOXICOKINETICS;

ANTIOXIDANTS; BIODEGRADATION, ENVIRONMENTAL; BUTHIONINE SULFOXIMINE; CADMIUM; CADMIUM CHLORIDE; CELL WALL; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; GELS; HYDROCHARITACEAE; KINETICS; LIGNIN; MERCURIC CHLORIDE; MERCURY; METALS; PEROXIDASE; PHOTOSYNTHESIS; PHYTOCHELATINS; PLANT PROTEINS; PLANT ROOTS; PLANT SHOOTS; PROTEOMICS; SOIL POLLUTANTS; SUPEROXIDE DISMUTASE;

EID: 84889078903     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2013.10.016     Document Type: Article

References (53)

1. Croteau M.-N., Luoma S.N., Stewart A.R. Trophic transfer of metals along freshwater food webs: evidence of cadmium biomagnification in nature. Limnology and Oceanography 2005, 50:1511-1519.
2. Bravo A.G., Loizeau J.L., Bouchet S., Richard A., Rubin J.F., Ungureanu V.G., Amouroux D., Dominik J. Mercury human exposure through fish consumption in a reservoir contaminated by a chlor-alkali plant: Babeni reservoir (Romania). Environmental Science and Pollution Research 2010, 17:1422-1432.
3. Owen R., Plant J.A., Ragnarsdottir K.V., Voulvoulis N. Conclusions: pollutants, risk and society. Pollutants, Human Health and the Environment 2011, 319-326. John Wiley & Sons, Ltd, London, UK.
4. Bonanno G., Lo Giudice R. Heavy metal bioaccumulation by the organs of Phragmites australis (common reed) and their potential use as contamination indicators. Ecological Indicators 2010, 10:639-645.
5. Noges T., Luup H., Feldmann T. Primary production of aquatic macrophytes and their epiphytes in two shallow lakes (Peipsi and Vrtsjarv) in Estonia. Aquatic Ecology 2010, 44:83-92.
6. Wetzel R.G. Limnology - Lake and River Ecosystems 2001, Academic Press, San Diego. 3rd ed.
7. Chambers P.A., Lacoul P., Murphy K.J., Thomaz S.M. Global diversity of aquatic macrophytes in freshwater. Hydrobiologia 2008, 595:9-26.
8. Weiss J.V., Emerson D., Megonigal J.P. Geochemical control of microbial Fe(III) reduction potential in wetlands: comparison of the rhizosphere to non-rhizosphere soil. FEMS Microbiology Ecology 2004, 48:89-100.
9. Castro R., Pereira S., Lima A., Corticeiro S., Valega M., Pereira E., Duarte A., Figueira E. Accumulation, distribution and cellular partitioning of mercury in several halophytes of a contaminated salt marsh. Chemosphere 2009, 76:1348-1355.
10. Valega M., Lima A.I.G., Figueira E., Pereira E., Pardal M.A., Duarte A.C. Mercury intracellular partitioning and chelation in a salt marsh plant, Halimione portulacoides (L.) Aellen: strategies underlying tolerance in environmental exposure. Chemosphere 2009, 74:530-536.
11. Regier N., Frey B., Converse B., Roden E., Grosse-Honebrick A., Bravo A.G., Cosio C. Elodea nuttallii roots effect on bacterial communities and MMHg proportion in a Hg polluted sediment. PloS ONE 2012, 7:e45565.
12. Regier N., Larras F., Bravo A.G., Ungereanu V.G., Cosio C. Hg bioaccumulation in the macrophyte Elodea nuttallii in the field and in microcosm: Hg in shoots accumulated from the water might involve Cu transporters. Chemosphere 2013, 90:595-602.
13. Samecka-Cymerman A., Kempers A.J. Biomonitoring of water pollution with Elodea canadensis. A case study of three small Polish rivers with different levels of pollution. Water, Air, & Soil Pollution 2003, 145:139-153.
14. Mishra V.K., Tripathi B.D., Kim K.H. Removal and accumulation of mercury by aquatic macrophytes from an open cast coal mine effluent. Journal of Hazardous Materials 2009, 172:749-754.
15. Minouflet M. Etude du modèle végétal aquatique, Elodea nuttallii pour l'évaluation du risque des métaux: Bioaccumulation et effets biologiques. Earth Science 2008, 297. Geneva University, Geneva.
16. Hassler C.S., Slaveykova V.I., Wilkinson K.J. Discriminating between intra- and extracellular metals using chemical extractions. Limnology and Oceanography, Methods 2004, 2:237-247.
17. Chyla M.A., Zyrnicki W. Determination of metal concentrations in animal hair by the ICP method - comparison of various washing procedures. Biological Trace Element Research 2000, 75:187-194.
18. Li Y.F., Chen C.Y., Li B., Wang J.X., Gao Y.X., Zhao Y.L., Chai Z.F. Scalp hair as a biomarker in environmental and occupational mercury exposed populations: suitable or not?. Environmental Research 2008, 107:39-44.
19. Lodenius A., Tulisalo E., Soltanpour-Gargari A. Exchange of mercury between atmosphere and vegetation under contaminated conditions. Science of the Total Environment 2003, 304:169-174.
20. Le Faucheur S., Tremblay Y., Fortin C., Campbell P.G.C. Acidification increases mercury uptake by a freshwater alga, Chlamydomonas reinhardtii. Environmental Chemistry 2011, 8:612-622.
21. Schaefer J.K., Morel F.M.M. High methylation rates of mercury bound to cysteine by Geobacter sulfurreducens. Nature Geoscience 2009, 2:123-126.
22. Ben Ammar W., Mediouni C., Tray B., Ghorbel M.H., Jemal F. Glutathione and phytochelatin contents in tomato plants exposed to cadmium. Biology of Plants 2008, 52:314-320.
23. Hunt R. Studies in Biology 1978, Edward Arnold Ltd, London.
24. Cosio C., Dunand C. Transcriptome analysis of various flower and silique development stages indicates a set of class III peroxidase genes potentially involved in pod shattering in Arabidopsis thaliana. BMC Genomics 2010, 11:16.
25. Bloom N., Fitzgerald W.F. Determination of volatile mercury species at the picogram level by low-temperature gas-chromatography with cold-vapor atomic fluorescence detection. Analytica Chimica Acta 1988, 208:151-161.
26. Martins R.J.E., Boaventura R.A.R. Uptake and release of zinc by aquatic bryophytes (Fontinalis antipyretica L. ex. Hedw.). Water Research 2002, 36:5005-5012.
27. Gimbert F., Mench M., Coeurdassier M., Badot P.M., de Vaufleury A. Kinetic and dynamic aspects of soil-plant-snail transfer of cadmium in the field. Environmental Pollution 2008, 152:736-745.
28. Sergeant K., Spiess N., Renaut J., Wilhelm E., Hausman J.F. One dry summer: a leaf proteome study on the response of oak to drought exposure. Journal of Proteomics 2011, 74:1385-1395.
29. Regier N., Baerlocher L., Münsterkötter M., Farinelli L., Cosio C. Analysis of the Elodea nuttallii transcriptome in response to mercury and cadmium pollution: development of sensitive tools for rapid ecotoxicological testing. Environmental Science & Technology 2013, 47:8825-8834.
30. Regier N., Streb S., Cocozza C., Schaub M., Cherubini P., Zeeman S.C., Frey B. Drought tolerance of two black poplar (Populus nigra L.) clones: contribution of carbohydrates and oxidative stress defence. Plant, Cell & Environment 2009, 32:1724-1736.
31. Beauchamp C., Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Analytical Biochemistry 1971, 44:276-287.
32. Ripoll J.J., Roeder A.H.K., Ditta G.S., Yanofsky M.F. A novel role for the floral homeotic gene APETALA2 during Arabidopsis fruit development. Development 2011, 138:5167-5176.
33. Simon O., Boudou A. Direct and trophic contamination of the herbivorous carp Ctenophatyngodon idella by inorganic mercury and methylmercury. Ecotoxicology and Environmental Safety 2001, 50:48-59.
34. Mendum M.L., Gupta S.C., Goldsbrough P.B. Effect of glutathione on phytochelatin synthesis in tomato cells. Plant Physiology 1990, 93:484-488.
35. 2 and other new extractants. Water, Air, & Soil Pollution 2011, 215:561-572.
36. Sobanska M.A. Wild boar hair (Sus scrofa) as a non-invasive indicator of mercury pollution. Science of the Total Environment 2005, 339:81-88.
37. Pérez-Llamazares A., Galbán-Malagón C.J., Aboal J.R., Ángel Fernández J., Carballeira A. Evaluation of cations and chelating agents as extracellular extractants for Cu, Pb, V and Zn in the sequential elution technique applied to the terrestrial moss Pseudoscleropodium purum. Ecotoxicology and Environmental Safety 2010, 73:507-514.
38. Nicolardi V., Cai G., Parrotta L., Puglia M., Bianchi L., Bini L., Gaggi C. The adaptive response of lichens to mercury exposure involves changes in the photosynthetic machinery. Environmental Pollution 2012, 160:1-10.
39. Sarry J.E., Kuhn L., Ducruix C., Lafaye A., Junot C., Hugouvieux V., Jourdain A., Bastien O., Fievet J.B., Vailhen D., Amekraz B., Moulin C., Ezan E., Garin J., Bourguignon J. The early responses of Arabidopsis thaliana cells to cadmium exposure explored by protein and metabolite profiling analyses. Proteomics 2006, 6:2180-2198.
40. Park J., Song W.Y., Ko D., Eom Y., Hansen T.H., Schiller M., Lee T.G., Martinoia E., Lee Y. The phytochelatin transporters AtABCC1 and AtABCC2 mediate tolerance to cadmium and mercury. The Plant Journal 2012, 69:278-288.
41. Clemens S. Toxic metal accumulation, responses to exposure and mechanisms of tolerance in plants. Biochimie 2006, 88:1707-1719.
42. Chen L.Q., Yang L.M., Wang Q.Q. In vivo phytochelatins and Hg-phytochelatin complexes in Hg-stressed Brassica chinensis L. Metallomics 2009, 1:101-106.
43. Carrasco-Gil S., Alvarez-Fernandez A., Sobrino-Plata J., Millan R., Carpena-Ruiz R.O., Leduc D.L., Andrews J.C., Abadia J., Hernandez L.E. Complexation of Hg with phytochelatins is important for plant Hg tolerance. Plant Cell and Environment 2011, 34:778-791.
44. Vander Mijnsbrugge K., Beeckman H., De Rycke R., Van Montagu M., Engler G., Boerjan W. Phenylcoumaran benzylic ether reductase, a prominent poplar xylem protein, is strongly associated with phenylpropanoid biosynthesis in lignifying cells. Planta 2000, 211:502-509.
45. Ahsan N., Nakamura T., Komatsu S. Differential responses of microsomal proteins and metabolites in two contrasting cadmium (Cd)-accumulating soybean cultivars under Cd stress. Amino Acids 2012, 42:317-327.
46. Carrasco-Gil S., Siebner H., LeDuc D.L., Webb S.M., Millán R., Andrews J.C., Hernández L.E. Mercury localization and speciation in plants grown hydroponically or in a natural environment. Environmental Science & Technology 2013, 47:3082-3090.
47. Cosio C., Vollenweider P., Keller C. Localization and effects of cadmium in leaves of a cadmium-tolerant willow (Salix viminalis L.) I. Macrolocalization and phytotoxic effects of cadmium. Environmental and Experimental Botany 2006, 58:64-74.
48. Vollenweider P., Cosio C., Gunthardt-Goerg M.S., Keller C. Localization and effects of cadmium in leaves of a cadmium-tolerant willow (Salix viminalis L.) Part II Microlocalization and cellular effects of cadmium. Environmental and Experimental Botany 2006, 58:25-40.
49. Cosio C., Martinoia E., Keller C. Hyperaccumulation of cadmium and zinc in Thlaspi caerulescens and Arabidopsis halleri at the leaf cellular level. Plant Physiology 2004, 134:716-725.
50. Pechanova O., Hsu C.Y., Adams J.P., Pechan T., Vandervelde L., Drnevich J., Jawdy S., Adeli A., Suttle J.C., Lawrence A.M., Tschaplinski T.J., Seguin A., Yuceer C. Apoplast proteome reveals that extracellular matrix contributes to multistress response in poplar. BMC Genomics 2010, 11.
51. Cosio C., Dunand C. Specific functions of individual class III peroxidase genes. Journal of Experimental Botany 2009, 60:391-408.
52. Mason R.P., Reinfelder J.R., Morel F.M.M. Uptake, toxicity, and trophic transfer of mercury in a coastal diatom. Environmental Science & Technology 1996, 30:1835-1845.
53. Lawson N.M., Mason R.P. Accumulation of mercury in estuarine food chains. Biogeochemistry 1998, 40:235-247.