Tilapia (Oreochromis niloticus) vitellogenins: development of homologous and heterologous ELISAs and analysis of vitellogenin pathway through the ovarian follicle
Identifieur interne : 000D04 ( Main/Merge ); précédent : 000D03; suivant : 000D05Tilapia (Oreochromis niloticus) vitellogenins: development of homologous and heterologous ELISAs and analysis of vitellogenin pathway through the ovarian follicle
Auteurs : Pap Ndiaye [Sénégal] ; Jean Forgue [France] ; Valérie Lamothe [France] ; Chantal Cauty [France] ; Philippe Tacon [France] ; Pierrette Lafon [France] ; Blandine Davail [France] ; Alexis Fostier [France] ; Françoise Le Menn [France] ; Jesús Nú Ez [France]Source :
- Journal of Experimental Zoology Part A: Comparative Experimental Biology [ 1548-8969 ] ; 2006-07-01.
Abstract
Vitellogenin (VTG) of Oreochromis niloticus was again purified, due to the conflicting results found in the literature. Three purification processes have been used: electrophoresis and electro‐elution, double chromatography (gel filtration and ion‐exchange chromatography) and single ion‐exchange chromatography. Using SDS‐PAGE we confirmed in all cases the presence of two polypeptidic forms of plasma VTG of 130 kDa (VTG1) and 170 kDa (VTG2). We raised polyclonal antibodies against each VTG form and we demonstrated the complete cross‐reactivity of each antibody with both forms of VTG by Enzyme Immuno‐Assay (EIA) and Western blots. The homologous ELISAs developed exhibited a detection limit of 6 ng.ml−1, equivalent to 60 ng.ml−1 of plasma VTG and allowed us to quantify the total plasma VTG of O. niloticus with high specificity and sensitivity. Using photonic and electron immunomicroscopy, we followed the pathway of VTG into the ovarian follicle (OF) demonstrating that VTG enters the oocyte at stage 3 of OF development, at the same time as cortical alveoli and lipid globules appear. Heterologous ELISAs performed on other cichlid species allowed us to quantify plasma VTG in Oreochromis aureus and Sarotherodon melanotheron and to detect it in Hemichromis fasciatus, Hemichromis bimaculatus and Tilapia zillii, constituting a reliable tool for monitoring the presence of xeno‐estrogens in the environment of these fish species. J. Exp. Zool. 305A, 2006. © 2006 Wiley‐Liss, Inc.
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DOI: 10.1002/jez.a.290
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ISTEX:93A5A5BE4EA64A2C273135E47EB93F1F05942A13Le document en format XML
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<front><div type="abstract" xml:lang="en">Vitellogenin (VTG) of Oreochromis niloticus was again purified, due to the conflicting results found in the literature. Three purification processes have been used: electrophoresis and electro‐elution, double chromatography (gel filtration and ion‐exchange chromatography) and single ion‐exchange chromatography. Using SDS‐PAGE we confirmed in all cases the presence of two polypeptidic forms of plasma VTG of 130 kDa (VTG1) and 170 kDa (VTG2). We raised polyclonal antibodies against each VTG form and we demonstrated the complete cross‐reactivity of each antibody with both forms of VTG by Enzyme Immuno‐Assay (EIA) and Western blots. The homologous ELISAs developed exhibited a detection limit of 6 ng.ml−1, equivalent to 60 ng.ml−1 of plasma VTG and allowed us to quantify the total plasma VTG of O. niloticus with high specificity and sensitivity. Using photonic and electron immunomicroscopy, we followed the pathway of VTG into the ovarian follicle (OF) demonstrating that VTG enters the oocyte at stage 3 of OF development, at the same time as cortical alveoli and lipid globules appear. Heterologous ELISAs performed on other cichlid species allowed us to quantify plasma VTG in Oreochromis aureus and Sarotherodon melanotheron and to detect it in Hemichromis fasciatus, Hemichromis bimaculatus and Tilapia zillii, constituting a reliable tool for monitoring the presence of xeno‐estrogens in the environment of these fish species. J. Exp. Zool. 305A, 2006. © 2006 Wiley‐Liss, Inc.</div>
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