Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 43 min ago
Peer-reviewedCC BYViruses

An RT–qPCR Assay for Rapid Detection of Coxsackievirus A4

  1. 1Health Inspection Center, (Hangzhou Health Supervision Institution), Hangzhou 310021, China; (X.Q.); (F.C.); (S.C.)

Abstract

Coxsackievirus A4 (CV-A4) is a major cause of hand, foot, and mouth disease and herpangina in children, and has been linked to severe complications. However, current detection methods, including commercial RT-qPCR kits, suffer from false-negative and false-positive results. This study aimed to develop a sensitive and specific TaqMan-based RT-qPCR assay for the rapid detection of CV-A4, targeting the conserved VP1 region covering genotypes A–D and subgenotypes C1–C5, with emphasis on the predominant C2 subgenotype in China. The assay was evaluated using a panel of enteroviruses, influenza virus, adenovirus, and rhinovirus, and compared with two commercial kits using 82 CV-A4-positive and 100 negative clinical specimens. The established assay demonstrated high specificity with no cross-reactivity, a detection limit of 2.1 TCID₅₀ equivalents/mL, and excellent reproducibility (CV ≤ 3.03%). In clinical testing, it achieved a 100% detection rate (82/82) with no false positives within 1.5 h, outperforming the two commercial kits, which showed positive rates of 91.5% and 89.0%, and false-positive rates of 0% and 1%, respectively. These findings indicate that our RT-qPCR assay offers superior sensitivity and specificity for CV-A4 detection, particularly for the C2 subgenotype, and represents a promising tool for laboratory diagnosis and epidemiological surveillance.

Related

  1. Development of a Single Thermal Cycling Multiplex RT-qPCR Assay for Rapid Arbovirus Detection
    Róger J. Costa, Andreas Stocker, Cleyde Marconi +6
    Diagnostics (Basel, Switzerland)Peer-reviewedCC BYFull textGeneral medicineEurope PMC
  2. Hybrid Molecular Lateral Flow Assay Targeting the lipL32 Gene for Rapid and Highly Sensitive Detection of Pathogenic Leptospira
    Syahira Aulia Difa, Widoretno, Farida Dwi Handayani +5
    Tropical medicine and infectious diseasePeer-reviewedCC BYFull textGeneral medicineEurope PMC
  3. Rapid direct-from-urine growth detection to triage culture-negative urine: a prospective diagnostic accuracy study of a two-tube nitrate-reduction and bromothymol blue assay (SIBURI/SIBURI+)
    R. R. Naik, L. S. Naik, P. Naik +2
    medRxivPreprintAll rights reservedFull textGeneral medicinemedRxiv
  4. Development of a multiplex quantitative real-time PCR (qPCR) assay for simultaneous detection of Schistosoma haematobium and high-risk human papillomaviruses
    Emmanuel Timmy Donkoh, Isaac Williams, Rita Nyaaba Akologo +11
    PLOS Neglected Tropical DiseasesPeer-reviewedCC BY 4.0Full textMicrobiologyInfectious diseasePLOS
  5. Rapid simultaneous detection of katG S315T and rpoB S531L mutations for molecular screening of multidrug-resistant tuberculosis using a dual LAMP-lateral flow assay
    Jutturong Ckumdee, Somchai Santiwatanakul, Nakarin Vutipow +1
    Microbiology SpectrumPeer-reviewedCC BY 4.0Full textInfectious diseasePMC
BibTeX
@article{qiu2026rtqpcr,
  title = {{An RT–qPCR Assay for Rapid Detection of Coxsackievirus A4}},
  author = {Xiaofeng Qiu and Feifei Cao and Shi Cheng and Jun Li},
  journal = {Viruses},
  year = {2026},
  month = oct,
  doi = {10.3390/v18101120},
  url = {https://europepmc.org/article/PMC/PMC13709941},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - An RT–qPCR Assay for Rapid Detection of Coxsackievirus A4
AU  - Xiaofeng Qiu
AU  - Feifei Cao
AU  - Shi Cheng
AU  - Jun Li
PY  - 2026
DA  - 2026/10/01
JO  - Viruses
DO  - 10.3390/v18101120
UR  - https://europepmc.org/article/PMC/PMC13709941
AB  - Coxsackievirus A4 (CV-A4) is a major cause of hand, foot, and mouth disease and herpangina in children, and has been linked to severe complications. However, current detection methods, including commercial RT-qPCR kits, suffer from false-negative and false-positive results. This study aimed to develop a sensitive and specific TaqMan-based RT-qPCR assay for the rapid detection of CV-A4, targeting the conserved VP1 region covering genotypes A–D and subgenotypes C1–C5, with emphasis on the predominant C2 subgenotype in China. The assay was evaluated using a panel of enteroviruses, influenza virus, adenovirus, and rhinovirus, and compared with two commercial kits using 82 CV-A4-positive and 100 negative clinical specimens. The established assay demonstrated high specificity with no cross-reactivity, a detection limit of 2.1 TCID₅₀ equivalents/mL, and excellent reproducibility (CV ≤ 3.03%). In clinical testing, it achieved a 100% detection rate (82/82) with no false positives within 1.5 h, outperforming the two commercial kits, which showed positive rates of 91.5% and 89.0%, and false-positive rates of 0% and 1%, respectively. These findings indicate that our RT-qPCR assay offers superior sensitivity and specificity for CV-A4 detection, particularly for the C2 subgenotype, and represents a promising tool for laboratory diagnosis and epidemiological surveillance.
SN  - 1999-4915
ER  -