Visual detection of Coxsackievirus A6 using a reverse transcription polymerase spiral reaction method
Visual detection of Coxsackievirus A6 using a reverse transcription polymerase spiral reaction method

Visual detection of Coxsackievirus A6 using a reverse transcription polymerase spiral reaction method

Front Cell Infect Microbiol. 2025 May 13;15:1563495. doi: 10.3389/fcimb.2025.1563495. eCollection 2025.

ABSTRACT

Coxsackievirus A6 (CVA6) ranks as a primary enterovirus associated with hand-foot-mouth disease (HFMD) and herpangina (HA). Given its significant role in these diseases, there is an urgent need for an efficient identification method. This study presents a novel visual approach based on the reverse transcription polymerase spiral reaction (RT-PSR) for the rapid detection of CVA6. We designed an RT-PSR assay that targets and amplifies a segment of the VP1 gene. Hydroxy naphthol blue (HNB) is incorporated as the detection agent in this assay. To evaluate the performance of the RT-PSR assay, we analyzed 142 clinical throat swab samples. The results were benchmarked against those obtained using quantitative reverse transcription – polymerase chain reaction (qRT – PCR). The RT-PSR assay operates at 65°C for 60 minutes and exhibits a detection limit of 10 copies/μL. When tested against other viruses, it consistently yielded negative results, demonstrating its high specificity. Moreover, the RT – PSR assay showed excellent agreement with a commercial qRT – PCR kit. In conclusion, by using HNB as an indicator, the RT – PSR assay emerges as a straightforward and highly sensitive method for detecting CVA6 in symptomatic throat samples. This approach holds great potential for improving the diagnosis and surveillance of CVA6 – related diseases.

PMID:40433657 | PMC:PMC12106450 | DOI:10.3389/fcimb.2025.1563495