TY - JOUR
T1 - Biomolecular modifications in the sacfry of Mogurnda adspersa in response to copper stress
AU - Shakya, Manisha
AU - Holland, Aleicia
AU - Klein, Annaleise R.
AU - Rees, Gavin N.
AU - Laird, Jamie
AU - McCallum, Jeffrey C.
AU - Ryan, Chris G.
AU - Silvester, Ewen
N1 - Funding Information:
This work was supported by La Trobe University Postgraduate Research Scholarship (LTUPRS), a La Trobe University Full Fee Research Scholarship (LTUFFRS) and PhD Top-Up scholarship supported by the Murray Darling Basin Joint Governments in association with the Murray-Darling Freshwater Research Centre (MDFRC/CFE). The authors acknowledge the facilities and scientific and technical assistance of Monash Histology Platform, Department of Anatomy and Developmental Biology, Monash University for assistance in the preparation of M. adspersa sections. This research was undertaken (in-part) on the Infrared Microspectroscopy Beamline at the Australian Synchrotron, Victoria, Australia. The assistance of Shimadzu Australasia (Chris Bowen and Rudi Hollander) in developing the LCMS analytical methods used here is greatly appreciated.
Funding Information:
This work was supported by La Trobe University Postgraduate Research Scholarship (LTUPRS), a La Trobe University Full Fee Research Scholarship (LTUFFRS) and PhD Top-Up scholarship supported by the Murray Darling Basin Joint Governments in association with the Murray-Darling Freshwater Research Centre (MDFRC/CFE). The authors acknowledge the facilities and scientific and technical assistance of Monash Histology Platform, Department of Anatomy and Developmental Biology, Monash University for assistance in the preparation of M. adspersa sections. This research was undertaken (in-part) on the Infrared Microspectroscopy Beamline at the Australian Synchrotron, Victoria, Australia. The assistance of Shimadzu Australasia (Chris Bowen and Rudi Hollander) in developing the LCMS analytical methods used here is greatly appreciated.
Publisher Copyright:
© 2022 Published by Elsevier B.V.
PY - 2022/7
Y1 - 2022/7
N2 - Copper (Cu) is one of the most harmful contaminants in fresh-water systems. Fish larvae such as sacfry are particularly vulnerable to metals such as copper (Cu) due to a less-developed excretory organ system and permeable skin that can absorb metals directly from the water. However, the sublethal effects of metals on this life stage are not well understood. This study assessed the sublethal toxicity of Cu on purple-spotted gudgeon sacfry (PSG, Mogurnda adspersa). For this purpose, 96 h Cu toxicity bioassays were performed and toxic effects of Cu on PSG were measured at different levels of biological organization, from the individual (loss of equilibrium, wet weight), to tissue (chemical changes in retinal tissue composition) and molecular responses (whole body amino acid (AA) profiles). The EC10 and EC50 (ECx: effect concentration that affected X% of test organisms) were found to be 12 (9 – 15) µg Cu L−1 and 22 (19 – 24) µg Cu L−1, respectively. Copper stress caused a decrease in total amino acid content and changed the AA profile of PSG compared to the controls. Proton-induced X-ray emission (PIXE) mapping techniques showed accumulation of Cu in the retinal tissues disturbing the distribution of other elements such as zinc, sulfur, phosphorus and potassium. Fourier-transform infrared (FTIR) microspectroscopy of control and Cu treated eye tissues revealed a change in protein secondary structure in retinal tissues in response to Cu accumulation, as well as decreased levels of the molecular retinal, consistent with the degradation of rhodopsin, a key protein in the visual sensory system. This is the first study to demonstrate the multi-level responses of PSG arising from exposure to environmentally realistic Cu concentrations and suggests that AA profiling can serve as a useful tool to assess the impacts of metals on fresh-water organisms.
AB - Copper (Cu) is one of the most harmful contaminants in fresh-water systems. Fish larvae such as sacfry are particularly vulnerable to metals such as copper (Cu) due to a less-developed excretory organ system and permeable skin that can absorb metals directly from the water. However, the sublethal effects of metals on this life stage are not well understood. This study assessed the sublethal toxicity of Cu on purple-spotted gudgeon sacfry (PSG, Mogurnda adspersa). For this purpose, 96 h Cu toxicity bioassays were performed and toxic effects of Cu on PSG were measured at different levels of biological organization, from the individual (loss of equilibrium, wet weight), to tissue (chemical changes in retinal tissue composition) and molecular responses (whole body amino acid (AA) profiles). The EC10 and EC50 (ECx: effect concentration that affected X% of test organisms) were found to be 12 (9 – 15) µg Cu L−1 and 22 (19 – 24) µg Cu L−1, respectively. Copper stress caused a decrease in total amino acid content and changed the AA profile of PSG compared to the controls. Proton-induced X-ray emission (PIXE) mapping techniques showed accumulation of Cu in the retinal tissues disturbing the distribution of other elements such as zinc, sulfur, phosphorus and potassium. Fourier-transform infrared (FTIR) microspectroscopy of control and Cu treated eye tissues revealed a change in protein secondary structure in retinal tissues in response to Cu accumulation, as well as decreased levels of the molecular retinal, consistent with the degradation of rhodopsin, a key protein in the visual sensory system. This is the first study to demonstrate the multi-level responses of PSG arising from exposure to environmentally realistic Cu concentrations and suggests that AA profiling can serve as a useful tool to assess the impacts of metals on fresh-water organisms.
KW - Amino acid
KW - Copper
KW - FTIR microspectroscopy
KW - PIXE
KW - Purple-spotted Gudgeon
KW - Retinal
KW - Sacfry
KW - Toxicity
UR - http://www.scopus.com/inward/record.url?scp=85130414449&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85130414449&partnerID=8YFLogxK
U2 - 10.1016/j.aquatox.2022.106179
DO - 10.1016/j.aquatox.2022.106179
M3 - Article
C2 - 35576718
AN - SCOPUS:85130414449
SN - 0166-445X
VL - 248
JO - Aquatic Toxicology
JF - Aquatic Toxicology
M1 - 106179
ER -