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Updated: Jun 30, 2026

Detection of Helicobacter pylori Infection and Antibiotic Resistance via Stool Quantitative Polymerase Chain Reaction Analysis
Published on: May 16, 2025
Rapid detection of Helicobacter pylori and its virulence genes by fluorescence-chromogenic double-indicator LAMP
Yanghe Liu1, Sijie Yin2, Shiyue Chen3
1Department of Laboratory Medicine, Nanjing Jiangning Hospital of Chinese Medicine,Nanjing,China; Department of Laboratory Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Abstract:
Helicobacter pylori (H. pylori) is a risk factor of gastrointestinal diseases. Vacuolating cytotoxin A (VacA) is a key component of the pathogenicity of H. pylori for gastric diseases, and detection for virulence genotypes facilitates precise clinical diagnosis and individual treatment. Hence, a more accurate, convenient, and highly sensitive detection method is urgently needed. In this study, we developed a method based on fluorescence-colorimetric dual-indicator loop-mediated isothermal amplification (FC-LAMP), allowing for naked-eye readout, using a constant temperature water bath within 40 min in clinical settings. Such an excellent sensitivity and specificity, and user-friendly operation approach achieved a limit of 10-6 ng/μl for 16 s rRNA detection of H. pylori, and 100 % specificity for 55 clinical gastric fluid samples compared with the immunofluorescence staining (IFS) and quantitative polymerase chain reaction (qPCR) as reference methods. In short, this study offers a new strategy for detection of H. pylori and its virulence genotype in primary hospitals and in limited resources settings, facilitating individualized precision eradication of H. pylori.

