Exposure to Alexandrium spp. impairs the development of Green-lipped mussel (Perna canaliculus) embryos and larvae

被引:4
|
作者
Greenhough, Hannah [1 ,2 ]
Vignier, Julien [1 ]
Peychers, Carol [1 ]
Smith, Kirsty F. [1 ]
Kenny, Nathan J. [2 ]
Rolton, Anne [1 ]
机构
[1] Cawthron Inst, 98 Halifax St East, Nelson 7010, New Zealand
[2] Univ Otago, Dept Biochem Te Tari Matu Koiora, Dunedin, New Zealand
关键词
Harmful algal blooms (HAB); Alexandrium pacificum; Bivalves; Early life stages; Bioactive extracellular compounds (BEC); Paralytic shellfish toxins (PST); DINOFLAGELLATE HETEROCAPSA-CIRCULARISQUAMA; RED TIDE DINOFLAGELLATE; KARENIA-BREVIS; SHELLFISH AQUACULTURE; CRASSOSTREA-VIRGINICA; EASTERN OYSTER; CLIMATE-CHANGE; TAMARENSE; TOXINS; DIATOM;
D O I
10.1016/j.hal.2023.102465
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
The green-lipped mussel (GLM) Perna canaliculus is an economically, ecologically, and culturally important species in Aotearoa New Zealand. Since 2011, harmful algal blooms (HABs) of Alexandrium spp. have occurred annually in the Marlborough Sounds, the largest GLM aquaculture region in New Zealand. Across a similar timeframe, there has been a severe reduction in wild spat (juvenile mussel) catch. This research investigated the effects of Alexandrium pacificum (which produces paralytic shellfish toxins; PSTs) and A. minutum (a non-producer of PSTs) on the development of four GLM larval life stages (gametes, embryos, D-stage and settlement). Early life stages of GLM were exposed to environmentally relevant concentrations of Alexandrium spp. as whole cell, lysate and filtrate treatments. A 48-h exposure of embryos to whole A. pacificum cells at 500 cells mL-1 caused lysis of embryos, severe abnormalities, and reduced development through to veliger (D-stage) larvae by 85%. GLM growth was impaired at cell concentrations as low as 250 cells mL-1 during a 4-day exposure of D-stage larvae to both Alexandrium spp. Exposure of GLM to both whole and lysed treatments of Alexandrium spp. at 500 cells mL-1 resulted in halved larval growth rates (2.00 & mu;m day-1 vs 4.48 & mu;m day-1 in the control) and growth remained impeded during a 4-day recovery period. Both A. pacificum and A. minutum were found to negatively impact D-larvae. Both whole-cell and lysed-cell treatments of A. pacificum had similar negative effects, suggesting that Alexandrium spp. toxicity to D-larvae is independent of PSTs. Additionally, cell membrane-free treatments of A. pacificum had no negative effects on embryo development, indicating that cell surface-associated bioactive compounds may be responsible for the observed negative effects during this early life stage. Conversely, non-PST-producing A. minutum was toxic to D-stage larvae but not to embryos; larval growth was reduced following a brief 1 h exposure of sperm to cell membrane-free treatments of A. pacificum. No effects were recorded in GLM larvae exposed during settlement, highlighting the potential for differences in susceptibility of early life stages to Alexandrium spp. exposure and the influence of exposure durations. In the wild, blooms of Alexandrium spp. can persist for several months, reaching cell densities higher than those investigated in the present study, and as such may be detrimental to the vulnerable early life stages of GLM.
引用
收藏
页数:10
相关论文
共 50 条
  • [11] Effects of stock origin and environment on growth and reproduction of the green-lipped mussel Perna canaliculus
    Ren, Jeffrey S.
    Fox, Stephen P.
    Howard-Williams, Clive
    Zhang, Jihong
    Schiel, David R.
    AQUACULTURE, 2019, 505 : 502 - 509
  • [12] ALLOMETRY AND GROWTH OF THE GREEN-LIPPED MUSSEL PERNA-CANALICULUS IN NEW-ZEALAND
    HICKMAN, RW
    MARINE BIOLOGY, 1979, 51 (04) : 311 - 327
  • [13] The role of ethylenediaminetetraacetic acid in green-lipped mussel (Perna canaliculus) embryo development: A biochemical and morphological characterization
    Gale, Samantha L.
    Burritt, David J.
    Adams, Serean L.
    AQUACULTURE, 2016, 463 : 22 - 27
  • [14] Waterborne cadmium impacts immunocytotoxic and cytogenotoxic endpoints in green-lipped mussel, Perna canaliculus
    Chandurvelan, Rathishri
    Marsden, Islay D.
    Gaw, Sally
    Glover, Chris N.
    AQUATIC TOXICOLOGY, 2013, 142 : 283 - 293
  • [15] Isolation and structural characterization of bioactive glycosaminoglycans from the green-lipped mussel Perna canaliculus
    Mubuchi, Ayumu
    Katsumoto, Shoo
    Tsuboi, Makoto
    Ishikawa, Hideaki
    Nomura, Yoshihiro
    Higashi, Kyohei
    Miyata, Shinji
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2022, 612 : 50 - 56
  • [16] The influence of green-lipped mussel powder (perna canaliculus) on alleviating arthritic signs in dogs
    Bui, LM
    Pawlowski, K
    Bierer, TL
    FASEB JOURNAL, 2000, 14 (04): : A218 - A218
  • [17] Systematic review of the nutritional supplement Perna Canaliculus (green-lipped mussel) in the treatment of osteoarthritis
    Brien, S.
    Prescott, P.
    Coghlan, B.
    Bashir, N.
    Lewith, G.
    QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2008, 101 (03) : 167 - 179
  • [18] A METHOD FOR THE DETECTION AND IDENTIFICATION OF HUMAN ENTEROVIRUSES IN THE GREEN-LIPPED MUSSEL PERNA-CANALICULUS
    LEWIS, GD
    AUSTIN, FJ
    LOUTIT, MW
    NEW ZEALAND JOURNAL OF SCIENCE, 1982, 25 (04): : 367 - 370
  • [19] CONDITION CYCLE OF THE GREEN-LIPPED MUSSEL PERNA-CANALICULUS IN NEW-ZEALAND
    HICKMAN, RW
    ILLINGWORTH, J
    MARINE BIOLOGY, 1980, 60 (01) : 27 - 38
  • [20] Paternal heat exposure affects progeny larval development in green-lipped mussels Perna canaliculus
    Kozal, Logan C.
    Hofmann, Gretchen E.
    Hawes, Nicola A.
    Ragg, Norman L. C.
    AQUACULTURE ENVIRONMENT INTERACTIONS, 2024, 16 : 43 - 57