Development of Colorimetric and Fluorometric Loop-Mediated Isothermal Amplification (LAMP) Assays for the Point-of-Care Molecular Diagnosis of Blastocystis spp.
Zedan, R.; Tombuloglu, H.; El-Badry, A. A.
Show abstract
Blastocystis species (spp.) is a genetically diverse protozoan parasite found in the digestive tract of animals and humans. Current clinical diagnosis relies heavily on wet mount microscopy, a method with known limitations, as well as molecular techniques like PCR, nested-PCR, and RT-PCR. However, neither microscopy nor PCR-based approaches are a perfect standard method due to their limitations, such as low accuracy, high equipment cost, and the need for well-trained personnel. Loop-mediated isothermal amplification (LAMP) technique offers the advantage of eliminating these limitations. Therefore, this study aimed to develop rapid and accurate fluorometric LAMP (fLAMP) and colorimetric LAMP (cLAMP) assays. We collected a total of 197 stool samples from both asymptomatic individuals and patients with gastrointestinal conditions. The performance of the LAMP assays was evaluated and compared against a standard RT-PCR assay. Results showed that both LAMP assays provided rapid detection of Blastocystis spp. in 20.0 to 29.2 minutes. The cLAMP assay demonstrated a sensitivity of 95.77%, a specificity of 85.00%, and an accuracy of 90.97%. The fLAMP assay exhibited a sensitivity of 91.43%, a specificity of 93.26%, and an accuracy of 92.27%. The limit-of-detection (LoD) of the fLAMP and cLAMP assays was 5x10-6 ng/{micro}L, which corresponds to 5 fg/{micro}L. The cLAMP assay offers a distinct advantage with its simplified visual result interpretation via a naked-eye color change, eliminating the need for complex instruments. This makes the cLAMP assay suitable for point-of-care testing (PoCT). These characteristics, combined with the femtogram-level detection capability of both assays, make the assays suitable for testing samples containing low DNA copy numbers. This is the first study to develop and elucidate the performance of two LAMP-based assays for the diagnosis of Blastocystis spp. The cLAMP assay exhibits potential to be used for PoCT, particularly in resource-limited settings. Their speed, accuracy, and analytical sensitivity hold promise for improving the diagnosis of Blastocystis spp. infections in patients with gastrointestinal symptoms.
Matching journals
The top 9 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Rapid detection of Pecan Root-Knot Nematode, Meloidogyne partityla, in laboratory and field conditions using loop-mediated isothermal amplification 97%
- A Novel Dual Probe-based Method for Mutation Detection using Isothermal Amplification 95%
- Probing Loop-Mediated Isothermal Amplification (LAMP) targeting two gene-fragments of rose rosette virus 95%
Similar papers in this journal
- RT-LAMP-CRISPR-Cas13a technology as a promising diagnostic tool for the SARS-CoV-2 virus 96%
- Optimal processing of tongue swab samples for Mycobacterium tuberculosis detection by the Xpert MTB/RIF Ultra assay 94%
- Evaluation of flow cytometry for cell count and detection of bacteria in biological fluids. 94%
Similar papers in this journal
- Performance of microbiological tests for tuberculosis diagnostic according to the type of respiratory specimen: a 10-year retrospective study 93%
- Wide application of minimally processed saliva on multiple RT-PCR kits for SARS-CoV-2 detection in Indonesia 93%
- Multiple Cross Displacement Amplification Coupled with Gold Nanoparticles-Based Lateral Flow Biosensor for Detection of the Mobilized Colistin Resistance Gene mcr-1 92%
Similar papers in this journal
- Optimization and validation of a quadruplex real-time PCR assay for the diagnosis of diphtheria 94%
- False-positive detection of Group B Streptococcus (GBS) in chromogenic media due to presence of Enterococcus faecalis in High Vaginal Swabs 94%
- Validation of a Single-step, Single-tube Reverse Transcription-Loop-Mediated Isothermal Amplification Assay for Rapid Detection of SARS-CoV-2 RNA 94%
Similar papers in this journal
- A broad-based probe-free qPCR assay for detection and discrimination of three human herpes viruses 95%
- A one-step real-time RT-PCR assay for simultaneous typing of SARS-CoV-2 mutations associated with the E484K and N501Y spike protein amino-acid substitutions 94%
- Comparison of three TaqMan Real-Time Reverse Transcription-PCR assays in detecting SARS-CoV-2 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.