Comparative analysis of loop‐mediated isothermal amplification combined with microfluidic chip technology and q‐PCR in the detection of clinical infectious pathogens

Background Rapid diagnosis of infectious pathogens at an early stage is crucial to stabilize the patient's condition, reduce medical costs, and shorten hospital stays. Currently, some point‐of‐care tests have their own shortcomings. Therefore, we built a microfluidic chip based on loop‐mediated isothermal amplification to can quickly and sensitively detect infectious pathogens. Methods We extracted the DNA of S. aureus , MRSA , Shigella and Klebsiella pneumoniae . Then, the DNA samples were diluted by 10‐fold and examined by two methods: LAMP‐microfluidic chip and q‐PCR, the sensitivity of whom was also compared. In addition, the specificity of the two was also examined by detecting the target bacteria and other microorganisms using the same methods. Finally, we extracted and tested the DNA of clinically infected humoral samples to determine the coincidence rate between the two methods and the bacterial culture method. Results For S. aureus , MRSA , Shigella , and Klebsiella pneumoniae , the detection limits of the chip were 2.25 × 10 3 copies/μl, 5.32 × 10 3 copies/μl, 2.89 × 10 3 copies/μl, 6.53 × 10 2 copies/μl, and the detection limits of q‐PCR were 2.25 × 10 2 copies/μl, 5.32 × 10 1 copies/μl, 2.89 × 10 2 copies/μl, 6.53 × 10 1 copies/μl, respectively. In terms of detection specificity, neither method cross‐reacted with other strains. For the detection of infectious humoral samples, the total coincidence rate between the q‐PCR and bacterial culture method was 85.7%, 95%, 95%, and 95.5%, and the total coincidence rate between the chip and bacterial culture method was 81%, 95%, 90%, and 86.4%, respectively. Conclusion LAMP‐microfluidic chip provides a simple, sensitive, specific, convenient, and rapid pathogen detection method for clinically infected humoral samples without relying on expensive equipment or technical personnels.