Lalawmpuii K, Lalrinkima H
Selesih, Aizawl, Mizoram India College of Veterinary Sciences and Animal Husbandry, Central Agricultural University.
J Parasit Dis. 2023 Jun;47(2):203-214. doi: 10.1007/s12639-023-01567-w. Epub 2023 Jan 23.
Screening of vaccine or drug target in parasitic helminth is hindered by lack of robust tool for functional studies of parasite protein which account for the availability of only a few anti-helminthic vaccines, diagnostic assay and slower pace of development of an anthelmintic drug. With the piling up of parasite transcriptomic and genomic data, in silico screening for possible vaccine/drug target could be validated by functional characterization of proteins by RNA interference or CRISPR/Cas9. These reverse genetic engineering tools have opened up a better avenue and opportunity for screening parasitic proteins in vitro as well as in vivo. RNA interference provides a technique for silencing targeted mRNA transcript for understanding a gene function in helminth as evidence by work in . Recent genetic engineering tool, CRISPR/Cas9 allows knock-out/deletion of the desired gene in parasitic helminths and the other provision it provides in terms of gene knock-in/insertion in parasite genome is still to be explored in future. This manuscript discussed the work that has been carried out on RNAi and CRISPR/Cas9 for functional studies of helminth parasitic proteins.
由于缺乏用于寄生虫蛋白质功能研究的强大工具,寄生虫疫苗或药物靶点的筛选受到阻碍,这导致抗蠕虫疫苗数量有限、诊断检测方法不足以及驱虫药物研发速度较慢。随着寄生虫转录组学和基因组数据的不断积累,通过RNA干扰或CRISPR/Cas9对蛋白质进行功能表征,可以验证计算机筛选出的潜在疫苗/药物靶点。这些反向基因工程工具为体外和体内筛选寄生虫蛋白质开辟了更好的途径和机会。RNA干扰提供了一种沉默靶向mRNA转录本的技术,以了解蠕虫中的基因功能, 中的工作已证明了这一点。最新的基因工程工具CRISPR/Cas9能够敲除/删除寄生蠕虫中所需的基因,而其在寄生虫基因组中进行基因敲入/插入方面的其他作用仍有待未来探索。本文讨论了利用RNA干扰和CRISPR/Cas9对蠕虫寄生蛋白质进行功能研究的相关工作。