Abstract

The induction of cellular stress response systems, heat shock protein hsp70/Hsp70 and multixenobiotic transporter abcb1, by cadmium chloride (CdCl2) was explored in amphipod species with different stress adaptation strategies from the Lake Baikal area. Based on the lethal concentrations (LC) of CdCl2, the sensitivities of the different species to CdCl2 were ranked (24 hr LC50 in mg/L CdCl2 (mean/95% confidence interval)): Gammarus lacustris (1.7/1.3–2.4) < Eulimnogammarus cyaneus (2.9/2.1–4.0) < Eulimnogammarus verrucosus (5.7/3.8–8.7) < Eulimnogammarus vittatus (18.1/12.4–26.6). Conjugated dienes, indicating lipid peroxidation, were significantly increased after 24 hr exposures to 5 mg/L CdCl2 only in the more CdCl2-sensitive species G. lacustris and E. cyaneus. Upon treatment with 0.54 to 5.8 mg/L CdCl2 for 1, 6 and 24 hrs, hsp70 transcript levels were generally more increased after the longer exposure times and in the more CdCl2-sensitive species. Relating the CdCl2 exposure concentrations to LCx values revealed that across the species the increases of hsp70 transcript levels were comparatively low (up to 2.6-fold) at CdCl2 concentrations ≤LC50. Relative hsp70 transcript levels were maximally increased in E. cyaneus by 5 mg/L CdCl2 (n}{}hat {=}LC70) at 24 hrs (9.1-fold increase above the respective control). When G. lacustris was exposed to 5 mg/L CdCl2 (n}{}hat {=}LC90) for 24 hrs, the increase in hsp70 was in comparison to E. cyaneus considerably less pronounced (3.0-fold increase in hsp70 levels relative to control). Upon exposure of amphipods to 5 mg/L CdCl2, increases in Hsp70 protein levels compared to untreated controls were highest in E. cyaneus at 1 and 6 hrs (5 mg/L CdCl2 n}{}hat {=} LC70) and in E. verrucosus at 24 hrs (5 mg/L CdCl2 n}{}hat {=} LC45). Thus, when the fold increases in Hsp70 protein levels in the different amphipod species were related to the respective species-specific LCx values a similar bell-shaped trend as for hsp70 transcript levels was seen across the species. Transcript levels of abcb1 in CdCl2exposed individuals of the different amphipod species varied up to 4.7-fold in relation to the respective controls. In contrast to hsp70/Hsp70, abcb1 transcripts in CdCl2 exposed individuals of the different amphipod species did not indicate similar levels of induction of abcb1 at equal LCx levels across the species. Induction of hsp70 and abcb1 genes and Hsp70 proteins by CdCl2 in the lethal concentration range shows that these cellular responses are rather insensitive to CdCl2 stress in the examined amphipod species. Furthermore, the increase of expression of these cellular defense systems at such high stress levels suggests that induction of these genes is not related to the maintenance of normal metabolism but to mitigation of the effects of severe toxic stress.

Highlights

  • Cadmium is a non-essential heavy metal entering the environment via various anthropogenic and natural sources

  • Exposure to cadmium was found to lead to an increase in the levels of transcripts of proteins encoded by the cellular stress response genes hsp70 (Blechinger et al, 2002; Da Silva Cantinha et al, 2017; Eufemia & Epel, 2000; Haap & Köhler, 2009; Jung & Lee, 2012; Kim et al, 2014; Lee et al, 2006; Mlambo et al, 2010; Piano, Valbonesi & Fabbri, 2004; Schill, Görlitz & Köhler, 2003; Singer, Zimmermann & Sures, 2005; Werner & Nagel, 1997) and abcb1 (Eufemia & Epel, 2000; Ivanina & Sokolova, 2008; Zucchi et al, 2010) in a range of aquatic organisms

  • The range of LCx values calculated from CdCl2 concentration—lethality relationships varied over an order of magnitude across the species

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Summary

Introduction

Cadmium is a non-essential heavy metal entering the environment via various anthropogenic and natural sources. It causes poisoning in humans and wildlife at low concentrations (Pinot et al, 2000). Toxic cadmium effects have often been related with increased levels of reactive oxygen species (ROS) and reactive nitrogen species (RNS) that cause damage of biological macromolecules such as proteins (Nemmiche, 2017). Induction of the hsp and abcb genes by cadmium can be related to the increased abundance of damaged cellular macromolecules, such as cellular membrane fragments or misfolded proteins (Beyersmann & Hechtenberg, 1997; Thévenod et al, 2000). Increased hsp and abcb transcript levels are seen here as indication for cellular stress caused by cadmium

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