Chen Jie, Geng Lina, Long Mengxian, Li Tian, Li Zhi, Yang Donglin, Ma Chao, Wu Haijing, Ma Zhengang, Li Chunfeng, Pan Guoqing, Zhou Zeyang
State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, China.
Parasitology. 2013 Sep;140(11):1394-402. doi: 10.1017/S0031182013000875. Epub 2013 Aug 7.
The spore wall of Nosema bombycis plays an important role in microsporidian pathogenesis. Protein fractions from germinated spore coats were analysed by two-dimensional polyacrylamide gel electrophoresis and MALDI-TOF/TOF mass spectrometry. Three protein spots were identified as the hypothetical spore wall protein NbHSWP12. A BAR-2 domain (e-value: 1.35e-03) was identified in the protein, and an N-terminal protein-heparin interaction motif, a potential N-glycosylation site, and 16 phosphorylation sites primarily activated by protein kinase C were also predicted. The sequence analysis suggested that Nbhswp12 and its homologous genes are widely distributed among microsporidia. Additionally, Nbhswp12 gene homologues share similar sequence features. An indirect immunofluorescence analysis showed that NbHSWP12 localized to the spore wall, and thus we renamed it spore wall protein 12 (NbSWP12). Moreover, NbSWP12 could adhere to deproteinized N. bombycis chitin coats that were obtained by hot alkaline treatment. This novel N. bombycis spore wall protein may function in a structural capacity to facilitate microsporidial spore maintenance.
家蚕微孢子虫的孢子壁在微孢子虫致病过程中起重要作用。通过二维聚丙烯酰胺凝胶电泳和基质辅助激光解吸电离飞行时间串联质谱(MALDI-TOF/TOF)对萌发孢子壁的蛋白质组分进行分析。三个蛋白点被鉴定为假定的孢子壁蛋白NbHSWP12。在该蛋白中鉴定出一个BAR-2结构域(期望值:1.35e-03),还预测了一个N端蛋白-肝素相互作用基序、一个潜在的N-糖基化位点以及16个主要由蛋白激酶C激活的磷酸化位点。序列分析表明,Nbhswp12及其同源基因在微孢子虫中广泛分布。此外,Nbhswp12基因同源物具有相似的序列特征。间接免疫荧光分析表明,NbHSWP12定位于孢子壁,因此我们将其重新命名为孢子壁蛋白12(NbSWP12)。此外,NbSWP12可以黏附于通过热碱处理获得的去蛋白化家蚕微孢子虫几丁质外壳。这种新型的家蚕微孢子虫孢子壁蛋白可能在结构上发挥作用,以促进微孢子虫孢子的维持。