“TwinDemic" Diagnostic System Rapidly and Simultaneously Detects SARS-CoV-2 and Influenza A Virus
|
By LabMedica International staff writers Posted on 16 Jan 2025 |

The COVID-19 pandemic in 2019 sparked efforts to raise public awareness about pandemics and led to accelerated vaccine development. While these actions effectively reduced viral transmission, they also resulted in unintended consequences, such as a decrease in the spread of other viruses and disruptions in vaccination schedules. However, rapidly mutating pathogens like viruses remain a significant threat, with predictions suggesting future co-infections could lead to "twindemics" or "tripledemics." Reverse Transcriptase-quantitative PCRs (RT-qPCRs) are reliable diagnostic assays, but their reliance on expensive equipment and reagents limits their use in resource-limited settings. This creates a need for a rapid, sensitive, and accurate molecular diagnostic tool capable of detecting multiple viruses at the point-of-care. To address this need, a novel tool has been developed for the simultaneous and rapid detection of SARS-CoV-2 and influenza A virus.
Researchers from Incheon National University (INU, Incheon, South Korea) have developed the TwinDemic Detection (TDD) system, a point-of-care diagnostic tool that uses a novel, non-enzymatic signal amplification method. The TDD system includes a transparent poly (methyl methacrylate) microfluidic chip with hydrogel-based, enzyme-free gene detection sensors, along with a handheld fluorescence reader. These hydrogel chambers are embedded with customized probes designed to detect the target viral pathogens, SARS-CoV-2 and influenza A. The reaction between the target viral DNA and the specific probe amplifies the fluorescence signal. The TDD system is user-friendly, cost-effective, and has a detection limit of 0.46 picomolar (pM) for SARS-CoV-2 and 0.39 pM for influenza A virus. When tested with human nasopharyngeal samples, TDD was shown to simultaneously detect both SARS-CoV-2 and influenza A, demonstrating its potential for rapid on-site testing of a wide range of viruses.
To assess the diagnostic accuracy of the TDD system, 15 nasopharyngeal swabs each from healthy individuals, COVID-19 patients, and those with influenza A were tested. The results, published in Sensors and Actuators B: Chemical, showed that for COVID-19, the TDD system correctly identified positive samples in 93.3% of cases and negative samples in 96.7%. For influenza A, positive and negative samples were correctly identified in 100% and 96.7% of cases, respectively. This study highlights the TDD system as a promising novel diagnostic tool for accurate and rapid simultaneous detection of multiple viruses at the point of care, potentially enabling clinicians to make timely and informed treatment decisions.
"The application of our TDD system can be further expanded by introducing additional channels and sensing hydrogels on the microfluidic chip, as well as integrating highly sensitive nucleic acid amplification systems for simultaneous detection and differentiation of a wider range of viruses," said INU’s Professor Eunjung Kim who led the TDD’s development.
Latest Molecular Diagnostics News
- AI Tool Improves Long-Read Detection of Cancer Mutations
- FDA Clears Molecular Test for Bacterial Vaginosis and Candida Vaginitis
- Blood Gene Expression Fluctuates More Than Expected Over Time
- Genomic Fingerprints Reveal Early Chemotherapy Resistance in Childhood Cancer
- Genomic Test Helps Early Breast Cancer Patients Avoid Chemotherapy
- Residual Disease Test Predicts Merkel Cell Carcinoma Recurrence Earlier Than Antibody Assay
- Portable Rapid Test Aims to Detect Ebola at Point of Care
- New Test Delivers Four Prenatal Genetic Screens from One Blood Sample
- Point-of-Care Molecular Technology Promises Transformative Shift in Oncology
- Multiplex PCR Test Differentiates Four Causes of Ulcerative Skin Lesions
- Blood Test Guides Patient Selection for Radiopharmaceutical Therapy in Prostate Cancer
- New Biomarker Helps Guide Combination Therapy for Treatment-Resistant Breast Cancer
- Blood-Based Gene Expression Test Detects Early Pancreatic Cancer
- Blood-Based Biomarker Panel Outperforms Existing Liver Disease Tests
- Fully Automated Test Advances Hepatitis D Diagnosis and Monitoring
- HPV Assay Gains Expanded CE Mark for Self-Collected Vaginal Samples
Channels
Clinical Chemistry
view channel
Blood Test Enters UK Primary Care Pathway for Earlier Alzheimer’s Diagnosis
Alzheimer’s disease is often first suspected in primary care, yet definitive evaluation frequently depends on specialized imaging or cerebrospinal fluid testing. This creates a persistent gap between disease... Read more
Machine Learning Model Shows Promise for Improving Metanephrine Testing Accuracy
Pheochromocytomas and paragangliomas are rare tumors that form in or near the adrenal glands and cause overproduction of stress hormones. Plasma-free metanephrines are the recommended first-line test,... Read moreHematology
view channel
Age-Specific CBC Reference Intervals Support Pediatric Diagnosis in Vietnam
Complete blood count (CBC) results underpin pediatric evaluation for anemia, infection, inflammation, and platelet disorders. Yet laboratories in Vietnam have largely relied on reference intervals derived... Read more
Spectral Flow Cytometry Assay Enhances MRD Detection in Multiple Myeloma
Minimal residual disease (MRD) monitoring is pivotal in multiple myeloma, where persistent malignant plasma cells drive relapse risk and help guide therapy decisions. In the United States, approximately... Read moreImmunology
view channel
Study Reveals Immune Mechanism Driving Severe COVID-19 Progression
Severe COVID-19 has highlighted gaps in understanding of early antiviral responses, particularly why some patients deteriorate despite timely care. Type I interferons are central to host defense, yet their... Read more
Antibody Profiling Identifies Preclinical Inflammatory Bowel Disease Years Before Diagnosis
Inflammatory bowel disease often develops after a prolonged symptom-free period, complicating timely recognition and clinical intervention. Limited understanding of immune activity during this silent phase... Read more
Ultrasensitive Blood Test Detects Sjögren’s Signature Years Before Diagnosis
Sjögren’s disease is a common autoimmune condition that can be difficult to recognize early, leading to delayed diagnosis and persistent symptom burden. It affects around half a million people in the UK... Read more
New Assays Expand Cytokine Testing for Transplant and Immunocompromised Patients
Eurofins Viracor has introduced three plasma-based assays—CXCL9 (Test Code 33607), CXCL10 (Test Code 33609), and interleukin-18 (IL-18) (Test Code 33611)—expanding its immunology testing menu for transplant... Read moreMicrobiology
view channel
New Sensitive Blood Assay Detects Tuberculosis Antigen Directly in Blood
Tuberculosis continues to be a leading global infectious disease, and diagnosis still hinges on sputum samples that many patients cannot produce early in illness. Delays in confirming Mycobacterium tuberculosis... Read more
High-Throughput Automated Platform to Advance Latent Tuberculosis Testing
Testing for tuberculosis remains a persistent global need, with demand driven by immigration screening, pre-treatment evaluation for immunosuppressive therapies, and public health programs.... Read morePathology
view channel
AI Pathology Tool Predicts Relapse Risk in Stage II Colorectal Cancer
Bowel cancer is Australia’s fourth most commonly diagnosed cancer and the second leading cause of cancer death, while remaining the third most common cancer worldwide. In stage-two disease, determining... Read more
AI Pathology Tool Stratifies Rectal Cancer to Guide Chemoradiotherapy
Choosing intensified regimens for locally advanced rectal cancer is challenging because these therapies can cause serious side effects. Colorectal cancer is the fourth-most fatal cancer in the UK, and... Read more
PD-L1 Assay Guides Pembrolizumab Eligibility in Ovarian, Fallopian Tube, and Peritoneal Cancers
Agilent Technologies’ PD-L1 IHC 22C3 pharmDx (Code SK006) has received European Union certification as a companion diagnostic to aid in identifying patients with epithelial ovarian, fallopian tube, or... Read moreTechnology
view channel
Training Device Improves Accuracy of Pooled Molecular Diagnostics
High-throughput molecular diagnostics have transformed infectious disease detection, but many workflows remain difficult to execute accurately without extensive training. Sample pooling can cut per‑test... Read more
New CE-Certified Software Advances Whole-Genome Cancer Testing
European hospitals are increasingly using comprehensive tumor genomics to guide therapy, but routine whole genome sequencing (WGS) requires validated, regulation-compliant workflows. A newly CE-certified... Read more
National Rare Disease Registry Standardizes Genetic and Clinical Data for Coordinated Care
Rare diseases collectively impose a significant clinical burden despite their individual rarity, often involving multisystem presentations and prolonged diagnostic journeys. Limited specialist expertise... Read moreIndustry
view channelLumiQuick Advances Oxidative Stress Research with Expanded AOXRE Portfolio
LumiQuick Diagnostics, Inc. (Santa Clara, CA, USA) has announced the addition of the AOXRE product line to its portfolio and introduced expanded services to help biotechnology and diagnostic companies... Read more
Collaboration Advances Sputum-Based Diagnostics for Asthma and COPD
Asthma and chronic obstructive pulmonary disease are highly prevalent inflammatory airway conditions, affecting more than 40 million Americans and more than 650 million people worldwide.... Read more








