ArticleAnnals of translational medicine2022
A virus preservation solution that inactivates the virus while maintaining the virus particle intact.
Article in Annals of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Improving the Thermostability of the Qβ Bacteriophage Coat Protein Through Single-Site Mutation Based on Molecular Dynamics.International journal of molecular sciences · 2026Article
- Evaluations of modes of pooling specimens for COVID-19 screened by quantitative PCR and droplet digital PCR.Scientific reports · 2024Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: The global coronavirus disease 2019 (COVID-19) pandemic has caused immeasurable losses to society. An important part of disease prevention and control is to diagnose infected patients as soon as possible, and nucleic acid detection plays an important role in diagnosing diseases such as COVID-19. Reverse transcription-polymerase chain reaction (RT-PCR) is a common method for the diagnosis of COVID-19 infection, but the false negative rate of covid nucleic acid is currently very high. Methods: In this paper, HEK293T cells and lentivirus were used to verify the effect of virus preservation solution, fluorescence method was used to verify the inactivation effect of virus preservation solution, real-time fluorescence PCR experiment was used to verify that the genetic material in virus particles was not destroyed, and protein gel electrophoresis was used to verify the integrity of virus particles in the preservation solution. Results: In this study, we developed a new virus preservation solution using homogeneous reaction technology that can immediately inactivate the virus within 5 minutes at room temperature and maintain the stability of viral nucleic acid for at least 7 days. Importantly, we found that while our solution differed from existing commercial preservatives that contain guanidinium, analyzing the cycle threshold (Ct) showed that it still maintained virion integrity. Conclusions: These advantages could reduce false negatives and the risk of laboratory exposure to infection. In addition, our solution achieved room temperature preservation, which could aid in the transportation of samples. Therefore, this new sample preservation solution could provide significant benefits to the clinical detection of viruses such as COVID-19.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.