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Development of a quantitative enzyme-linked immunosorbent assay for vitellin in the mysid Neomysis integer (Crustacea: Mysidacea)
Ghekiere, A.; Fenske, M.; Verslycke, T.; Tyler, C.; Janssen, C.R. (2005). Development of a quantitative enzyme-linked immunosorbent assay for vitellin in the mysid Neomysis integer (Crustacea: Mysidacea). Comp. Biochem. Physiol., Part A Physiol. 142(1): 43-49
In: Comparative Biochemistry and Physiology. Part A. Physiology. Pergamon: Oxford. ISSN 1096-4940, more
Peer reviewed article

Available in Authors 
    VLIZ: Open Repository 115441 [ OMA ]

Keywords
    Endocrine glands; Vitellogenesis; Neomysis integer (Leach, 1814) [WoRMS]; Belgium, Zeeschelde, Galgenweel [gazetteer]; Brackish water

Project Top | Authors 
  • Endocrine disruption in the Scheldt Estuary: distribution, exposure and effects, more

Authors  Top 
  • Ghekiere, A., more
  • Fenske, M.
  • Verslycke, T., more
  • Tyler, C.
  • Janssen, C.R., more

Abstract
    Mysid crustaceans have been put forward by several regulatory bodies as suitable test organisms to screen and test the potential effects of environmental endocrine disruptors. Despite the well-established use of mysid reproductive endpoints such as fecundity, egg development time, and time to first brood release in standard toxicity testing, little information exists on the hormonal regulation of these processes. Control of vitellogenesis is being studied intensively because yolk is an excellent model for studying mechanisms of hormonal control, and vitellogenesis can be chemically disrupted. Yolk protein or vitellin is a major source of nourishment during embryonic development of ovigorous egg-laying invertebrates. The accumulation of vitellin during oocyte development is vital for the production of viable offspring. In this context, we developed a competitive enzyme-linked immunosorbent assay (ELISA) for vitellin of the estuarine mysid Neomysis integer. Mysid vitellin was isolated using gel filtration, and the purified vitellin was used to raise polyclonal antibodies. The ELISA was sensitive within a working range of 4 to 500 ng vitellin/mL. Serial dilutions of whole body homogenates from female N. integer and the vitellin standard showed parallel binding curves, validating the specificity of the ELISA. The intra- and interassay coefficients of variation were 8.2% and 13.8%, respectively. Mysid vitellin concentrations were determined from ovigorous females and eggs at different developmental stages. The availability of a quantitative mysid vitellin ELISA should stimulate further studies on the basic biology of this process in mysids. Furthermore, it could provide a means to better understand and predict chemically induced reproductive effects in mysids.

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