Department of Biochemistry, Faculty of Science, Mahidol University, Rama VI Rd., Bangkok, 10400, Thailand.
Center for Excellence in Shrimp Molecular Biology and Biotechnology (Centex Shrimp), Faculty of Science, Mahidol University, Rama VI Rd., Bangkok, 10400, Thailand.
Sci Rep. 2024 Feb 28;14(1):4830. doi: 10.1038/s41598-024-55400-2.
The microsporidian Enterocytozoon hepatopenaei (EHP) is a major threat to shrimp health worldwide. Severe EHP infections in shrimp cause growth retardation and increase susceptibility to opportunistic infections. EHP produces spores with a chitin wall that enables them to survive prolonged environmental exposure. Previous studies showed that polar tube extrusion is a prerequisite for EHP infection, such that inhibiting extrusion should prevent infection. Using a proteomic approach, polar tube protein 2 of EHP (EhPTP2) was found abundantly in protein extracts obtained from extruded spores. Using an immunofluorescent antibody against EhPTP2 for immunohistochemistry, extruded spores were found in the shrimp hepatopancreas (HP) and intestine, but not in the stomach. We hypothesized that presence of EhPTP2 might be required for successful EHP spore extrusion. To test this hypothesis, we injected EhPTP2-specific double-stranded RNA (dsRNA) and found that it significantly diminished EHP copy numbers in infected shrimp. This indicated reduced amplification of EHP-infected cells in the HP by spores released from previously infected cells. In addition, injection of the dsRNA into EHP-infected shrimp prior to their use in cohabitation with naïve shrimp significantly (p < 0.05) reduced the rate of EHP transmission to naïve shrimp. The results revealed that EhPTP2 plays a crucial role in the life cycle of EHP and that dsRNA targeting EHP mRNA can effectively reach the parasite developing in host cells. This approach is a model for future investigations to identify critical genes for EHP survival and spread as potential targets for preventative and therapeutic measures in shrimp.
微孢子虫 Enterocytozoon hepatopenaei (EHP) 是全球虾类健康的主要威胁。虾类中严重的 EHP 感染会导致生长迟缓,并增加对机会性感染的易感性。EHP 产生具有几丁质壁的孢子,使其能够在长时间的环境暴露中存活。先前的研究表明,极生管挤出是 EHP 感染的前提条件,因此抑制挤出应该可以防止感染。使用蛋白质组学方法,发现 EHP 的极生管蛋白 2 (EhPTP2) 在从挤出的孢子中获得的蛋白质提取物中大量存在。使用针对 EhPTP2 的免疫荧光抗体进行免疫组织化学染色,发现挤出的孢子存在于虾的肝胰腺 (HP) 和肠道中,但不存在于胃中。我们假设 EhPTP2 的存在可能是 EHP 孢子成功挤出所必需的。为了验证这一假设,我们注射了 EhPTP2 特异性双链 RNA(dsRNA),发现它显著降低了感染虾中的 EHP 拷贝数。这表明从先前感染的细胞释放的孢子使 HP 中感染 EHP 的细胞扩增减少。此外,在将 dsRNA 注射到感染 EHP 的虾中之前,将其与未感染的虾一起饲养,可显著(p<0.05)降低 EHP 向未感染虾的传播率。结果表明,EhPTP2 在 EHP 的生命周期中起着至关重要的作用,并且靶向 EHP mRNA 的 dsRNA 可以有效地到达宿主细胞中发育的寄生虫。这种方法为未来的研究提供了一个模型,以确定 EHP 生存和传播的关键基因,作为虾类预防和治疗措施的潜在靶点。