Su Jiayuan, Jin Chanchan, Wu Haizhen, Fei Jilan, Li Na, Guo Yaqiong, Feng Yaoyu, Xiao Lihua
State Key Laboratory of Bioreactor Engineering, School of Resources and Environmental Engineering, East China University of Science and Technology, Shanghai, China.
School of Biotechnology, East China University of Science and Technology, Shanghai, China.
Front Microbiol. 2019 May 29;10:1177. doi: 10.3389/fmicb.2019.01177. eCollection 2019.
and share highly similar proteomes, with merely ~3% divergence in overall nucleotide sequences. -specific MEDLE family is one of the major differences in gene content between the two species. Comparative genomic analysis indicated that MEDLE family may contribute to differences in host range among spp. Previous studies have suggested that CpMEDLE-1 encoded by and CpMEDLE-2 encoded by are potentially involved in the invasion of . In this study, we expressed in the -specific member of the MEDLE protein family, ChMEDLE-1 encoded by and two -specific members, CpMEDLE-3 encoded by and CpMEDLE-5 encoded by . Quantitative PCR, immunofluorescence staining and neutralization assay were conducted to assess their biologic characteristics. The expression of the gene was high during 12-48 h of the culture, while the expression of was the highest at 2 h. ChMEDLE-1 and CpMEDLE-3 proteins were mostly located in the anterior and mid-anterior region of sporozoites and merozoites, whereas CpMEDLE-5 was expressed over the entire surface of these invasive stages. Polyclonal antibodies against MEDLE proteins had different neutralization efficiency, reaching approximately 50% for ChMEDLE-1 and 60% for CpMEDLE-3, but only 20% for CpMEDLE-5. The differences in protein and gene expression and neutralizing capacity indicated the MEDLE proteins may have different roles during invasion and growth.
并且拥有高度相似的蛋白质组,总体核苷酸序列仅有约3%的差异。特定的MEDLE家族是这两个物种在基因含量上的主要差异之一。比较基因组分析表明,MEDLE家族可能导致不同物种宿主范围的差异。先前的研究表明,由[物种1]编码的CpMEDLE-1和由[物种2]编码的CpMEDLE-2可能参与了[病原体名称]的入侵。在本研究中,我们在[宿主名称]中表达了MEDLE蛋白家族的特定物种成员,即由[物种3]编码的ChMEDLE-1以及两个[物种2]特异性成员,由[物种2]编码的CpMEDLE-3和由[物种2]编码的CpMEDLE-5。进行了定量PCR、免疫荧光染色和[病原体名称]中和试验以评估它们的生物学特性。[病原体名称]基因在[宿主名称]培养的12至48小时内表达较高,而[另一种基因名称]在2小时时表达最高。ChMEDLE-1和CpMEDLE-3蛋白主要位于子孢子和裂殖子的前部和中前部区域,而CpMEDLE-5在这些侵入阶段的整个表面表达。针对MEDLE蛋白的多克隆抗体具有不同程度的中和效率,ChMEDLE-1约为50%,CpMEDLE-3约为60%,但CpMEDLE-5仅为20%。蛋白质和基因表达以及中和能力的差异表明MEDLE蛋白在[病原体名称]入侵和生长过程中可能具有不同作用。