Bouterige S, Robert R, Bouchara J P, Marot-Leblond A, Molinero V, Senet J M
Groupe d'Etude des Interactions Hôte-Parasite, Laboratoire de Parasitologie-Mycologie, Faculté de Pharmacie, France.
Appl Environ Microbiol. 2000 Aug;66(8):3277-82. doi: 10.1128/AEM.66.8.3277-3282.2000.
Sunflower downy mildew, caused by the fungus Plasmopara halstedii, is a potentially devastating disease. We produced two monoclonal antibodies (MAbs) (12C9 and 18E2) by immunizing mice with a partially purified extract of P. halstedii race 1. Both MAbs detected in enzyme-linked immunosorbent assay (ELISA) all races of P. halstedii present in France. No cross-reactions were observed with Plasmopara viticola or with other fungi commonly associated with sunflowers. Both MAbs recognized the same three fungal antigens with molecular masses of 68, 140, and 192 kDa. However, the epitopes on the fungal antigens were distinct and repetitive. Seed homogenates from infected plants were incubated in wells coated with MAb 18E2. This resulted in the trapping of P. halstedii antigens that were identified with biotinylated MAb 12C9. No reactions were seen with seed homogenates from healthy plants. Thus, our results suggest that these MAbs might be used to develop a sandwich ELISA detection system for P. halstedii in infected seeds.
由真菌哈氏霜霉(Plasmopara halstedii)引起的向日葵霜霉病是一种具有潜在毁灭性的病害。我们用哈氏霜霉1号生理小种的部分纯化提取物免疫小鼠,制备了两种单克隆抗体(MAb)(12C9和18E2)。两种单克隆抗体在酶联免疫吸附测定(ELISA)中均能检测出法国存在的所有哈氏霜霉生理小种。未观察到与葡萄生单轴霉(Plasmopara viticola)或其他常见的与向日葵相关的真菌发生交叉反应。两种单克隆抗体识别相同的三种分子量分别为68、140和192 kDa的真菌抗原。然而,真菌抗原上的表位是不同且重复的。将感染植株的种子匀浆在包被有单克隆抗体18E2的孔中孵育。这导致捕获了用生物素化单克隆抗体12C9鉴定的哈氏霜霉抗原。未观察到健康植株种子匀浆有反应。因此,我们的结果表明,这些单克隆抗体可用于开发一种夹心ELISA检测系统,用于检测感染种子中的哈氏霜霉。