ArticleWorld journal of microbiology & biotechnology2024
A label-free DNAzyme-based colorimetric sensor for the detection of Leptospira interrogans.
Article in World journal of microbiology & biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- A Label-Free Graphene Quantum Dot-Based Fluorescent Aptasensor for Rapid and Sensitive Detection of Leptospira interrogans.Journal of fluorescence · 2026Article
- Leptospirosis in Southeast Asia: Investigating Seroprevalence, Transmission Patterns, and Diagnostic Challenges.Tropical medicine and infectious disease · 2026Review
- Review
- Isolation of DNA aptamers by Tripartite-hybrid-high throughput SELEX (Tripartite-hybrid-HT SELEX) for the detection of pathogenic Leptospira.World journal of microbiology & biotechnology · 2025Article
- DNAzyme-based colorimetric biosensor for rapid detection of Shigella flexneri.Scientific reports · 2025Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
Leptospirosis is a neglected zoonosis caused by a pathogenic spirochete Leptospira. Diagnosis of leptospirosis in the early stage is difficult and can be easily confused with other infections. The existing detection methods are considered chronophagous and labor-intensive. Leptospira survives in the kidney tubules of reservoir animals such as rodents and shed into the environment through their urine. In this study, we developed an Aptamer-DNAzyme-based biosensor for detecting pathogenic Leptospira in environmental water samples. The cell-specific aptamer with an extensive affinity binds to the cell surface proteins to detect the Leptospira interrogans. The DNAzyme that mimics as a peroxidase enzyme, acts as a transducing agent in the colorimetric reaction positively conditioned by the presence of L. interrogans. The Leptospira-specific aptamer coupled with DNAzyme is coated onto carbon nanotubes, to provide a cost-effective nanomaterial-based detection platform. L. interrogans contamination in the samples is detected with a color change of a peroxidase substrate, ABTS. The dissociation constant of the aptazyme was found to be 356.6 nM. The aptazyme system was able to detect up to 119 CFU/mL of L. interrogans exhibiting a high range of selectivity towards the pathogenic spirochete. This simple detection methodology makes the system promising for the environmental monitoring of L. interrogans.
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Registered trials
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