Institute of Entomology and Molecular Biology, College of Life Science, Chong Qing Normal University, Chong Qing 401331, China.
Exp Parasitol. 2012 Feb;130(2):116-25. doi: 10.1016/j.exppara.2011.12.001. Epub 2011 Dec 20.
Entomopathogenic nematode Heterorhabditis bacteriophora Az29 and Az36 isolates with different virulence against Popillia unipuncta and soil survival time were isolated from the Azorean archipelago (Portugal) and used for the study. RAPD analysis revealed a very low-level of genetic diversity (GD(axenic Az36 isolate)(axenic Az29 isolate)=0.2338±0.0541) between axenic Az29 and Az36 isolates, and a relative low-level of diversity (GD(Az36 isolate)(Az29 isolate)=0.3366±0.0471) between Az29 and Az36 isolates. To unravel the molecular differences, a suppressive subtractive hybridization library was constructed from the parasitic stage. Assembling 150 high quality ESTs produced 70 singletons and 17 contigs. BLAST analysis revealed that 48 ESTs showed significant similarity to known protein and 39 ESTs had no significant hits in the database, perhaps representing novel genes. Functional annotation revealed some of these genes to be involved in metabolism, cellular process and signaling, information storage and processing, stress response and host-parasite interactions. Genes with a role in the parasitism process were identified including lectin, metalloprotease, enolase, chitinase, surface-associated antigen, and as well as genes (aquaporin, Hsp70A, Hsp10 and Hsp20) essential for stresses tolerance. The work described here provides the molecular data necessary for investigating the fundamental molecular aspects of host-parasite interactions. Future investigations should be focused on determining the molecular mechanism of those genes in entomopathogenic nematode life cycle.
从亚速尔群岛(葡萄牙)分离到具有不同毒力的昆虫病原线虫 Heterorhabditis bacteriophora Az29 和 Az36 分离株,并用于研究。RAPD 分析显示,无菌 Az29 和 Az36 分离株之间遗传多样性水平非常低(GD(axenic Az36 isolate)(axenic Az29 isolate)=0.2338±0.0541),而 Az29 和 Az36 分离株之间的遗传多样性水平相对较低(GD(Az36 isolate)(Az29 isolate)=0.3366±0.0471)。为了揭示分子差异,从寄生阶段构建了一个抑制性消减杂交文库。组装 150 个高质量 ESTs 产生了 70 个单基因和 17 个基因簇。BLAST 分析表明,48 个 ESTs 与已知蛋白具有显著相似性,39 个 ESTs 在数据库中没有显著匹配,可能代表新基因。功能注释显示,这些基因中的一些参与代谢、细胞过程和信号转导、信息存储和处理、应激反应和宿主-寄生虫相互作用。鉴定出一些在寄生过程中起作用的基因,包括凝集素、金属蛋白酶、烯醇酶、几丁质酶、表面相关抗原,以及对压力耐受至关重要的基因(水通道蛋白、Hsp70A、Hsp10 和 Hsp20)。这里描述的工作为研究宿主-寄生虫相互作用的基本分子方面提供了必要的分子数据。未来的研究应集中于确定这些基因在昆虫病原线虫生活史中的分子机制。