Reporter Coxsackievirus A5 Expressing iLOV Fluorescent Protein or Luciferase Used for Rapid Neutralizing Assay in Cells and Living Imaging in Mice.
Wei-Ping JinChen WangJie WuJing GuoSheng-Li MengZe-Jun WangDai-Guan YuShuo ShenPublished in: Viruses (2023)
Coxsackievirus A5 (CV-A5) is a re-emerging enterovirus that causes hand, foot, and mouth disease in children under five years of age. CV-A5-M14-611 is a mouse-adapted strain that can infect orally and lead to the death of 14-day-old mice. Here, recombinants based on CV-A5-M14-611 were constructed carrying three reporter genes in different lengths. Smaller fluorescent marker proteins, light, oxygen, voltage sensing (iLOV), and nano luciferase (Nluc) were proven to be able to express efficiently in vitro. However, the recombinant with the largest insertion of the red fluorescence protein gene (DsRed) was not rescued. The construction strategy of reporter viruses was to insert the foreign genes between the C-terminus of VP1 and the N-terminus of 2A genes and to add a 2A protease cleavage domain at both ends of the insertions. The iLOV-tagged or Nluc-tagged recombinants, CV-A5-iLOV or CV-A5-Nluc, exhibited a high capacity for viral replication, genetic stability in cells and pathogenicity in mice. They were used to establish a rapid, inexpensive and convenient neutralizing antibody assay and greatly facilitated virus neutralizing antibody titration. Living imaging was performed on mice with CV-A5-Nluc, which exhibited specific bioluminescence in virus-disseminated organs, while fluorescence induced by CV-A5-iLOV was weakly detected. The reporter-gene-tagged CV-A5 can be used to study the infection and mechanisms of CV-A5 pathogenicity in a mouse model. They can also be used to establish rapid and sensitive assays for detecting neutralizing antibodies.
Keyphrases
- genome wide
- crispr cas
- induced apoptosis
- high fat diet induced
- mouse model
- genome wide identification
- dengue virus
- high throughput
- high resolution
- cell cycle arrest
- young adults
- sars cov
- endoplasmic reticulum stress
- adipose tissue
- dna methylation
- living cells
- staphylococcus aureus
- oxidative stress
- cell death
- transcription factor
- escherichia coli
- wastewater treatment
- cystic fibrosis
- gene expression
- signaling pathway
- cell proliferation
- energy transfer
- amino acid
- pseudomonas aeruginosa
- pi k akt
- aedes aegypti