Development of a cell-free toehold switch for hepatitis A virus type I on-site detection.
Xiaodan KangChen ZhaoShuting ChenXi ZhangBin XueChenyu LiShang WangXiaobo YangZhiqiang XiaYongchun XuYongliang HuangZhi-Gang QiuChao LiJingfeng WangJian PangZhiqiang ShenPublished in: Analytical methods : advancing methods and applications (2023)
Picornavirus hepatitis A virus (HAV) is a common cause of hepatitis worldwide. It is spread primarily through contaminated food and water or person-to-person contact. HAV I has been identified as the most common type of human HAV infection. Here, we have developed a cell-free toehold switch sensor for HAV I detection. We screened 10 suitable toehold switch sequences using NUPACK software, and the VP1 gene was used as the target gene. The optimal toehold switch sequence was selected by in vivo expression. The best toehold switch concentration was further found to be 20 nM in a cell-free system. 5 nM trigger RNA activated the toehold switch to generate visible green fluorescence. The minimum detection concentration decreased to 1 pM once combined with NASBA. HAV I trigger RNA could be detected accurately with excellent specificity. In addition, the cell-free toehold switch sensor was verified in HAV I entities. The successful construction of the cell-free toehold switch sensor provided a convenient, rapid, and accurate method for HAV I on-site detection, especially in developing countries, without the involvement of expensive facilities and additional professional operators.
Keyphrases
- cell free
- loop mediated isothermal amplification
- circulating tumor
- real time pcr
- label free
- endothelial cells
- poor prognosis
- genome wide
- photodynamic therapy
- copy number
- air pollution
- long non coding rna
- climate change
- risk assessment
- binding protein
- transcription factor
- human health
- genome wide identification
- high density