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Ellipsometric-based novel DNA biosensor for label-free, real-time detection of Bordetella parapertussis
S Rafique1, M Idrees2, H Bokhari2
1Department of Physics, Air University, PAF Complex, E-9, Islamabad, 44000, Pakistan. saima.rafique@mail.au.edu.pk.
Abstract:
Pertussis (or whooping cough) is a contagious disease mainly affecting infants and children and predominantly caused by Bordetella pertussis followed by Bordetella parapertussis. B. parapertussis causes a milder cough but usually symptomatically appears like B. pertussis infection. Thus the epidemiology of illness caused by B. parapertussis is not well understood. In this study, a sensitive and specific method for the rapid diagnosis of B. parapertussis is presented. The covalent immobilization of thiol-terminated DNA oligonucleotides (ss DNA SAM) on a silicon surface by disulfide bond formation is investigated with atomic force microscopy (AFM) and ellipsometry. The measurements indicated an average layer thickness of 5 ± 0.84 nm for 2 μg/μl concentration and 24 h incubation time. This thickness changed to 8.4 ± 0.92 nm for the same concentration (2 μg/μl) by altering the incubation time to 48 h. Ellipsometric data recorded before and after hybridization of B. parapertussis revealed an increase in mean grain area from 91 nm2 to 227 nm2 and a change in the refractive index from 1.489 to 1.648 for 2 μg/μl B. parapertussis, respectively. This change in the refractive index was used to evaluate the amount of adsorbed molecules and their density. The results showed that the density of adsorbed molecules increased from 0.2 to 0.97 g/cm3 after B. parapertussis attachment, respectively. To confirm the hybridization of B. parapertussis to ss DNA SAM, the ds DNA SAM was denatured and the ss DNA SAM surface was reproduced with an average height variation of 6.42 ± 0.75 nm. This showed the stability of the DNA film that can be tuned by varying the concentration and incubation time, thus providing a robust method for the label-free detection of B. parapertussis other than routinely used PCR detection.
Insights
A new method uses DNA on silicon surfaces to rapidly detect Bordetella parapertussis, a cause of whooping cough. This technique offers a sensitive, label-free alternative to PCR for diagnosing B. parapertussis infections.
Area of Science:
- Microbiology
- Nanotechnology
- Biomedical Engineering
Background:
- Pertussis (whooping cough) is primarily caused by Bordetella pertussis and Bordetella parapertussis.
- Bordetella parapertussis infections often present with milder symptoms, leading to underdiagnosis and poorly understood epidemiology.
- There is a need for sensitive and specific diagnostic methods for B. parapertussis.
Purpose of the Study:
- To develop and characterize a novel method for the rapid, label-free detection of Bordetella parapertussis.
- To investigate the covalent immobilization of DNA on silicon surfaces for biosensing applications.
- To optimize DNA immobilization parameters for enhanced B. parapertussis detection.
Main Methods:
- Utilized atomic force microscopy (AFM) and ellipsometry to analyze DNA oligonucleotide immobilization on silicon surfaces.
- Investigated the effect of DNA concentration and incubation time on layer thickness and surface properties.
- Assessed B. parapertussis hybridization by measuring changes in grain area and refractive index after attachment.
Main Results:
- Optimized DNA immobilization achieved layer thicknesses of 5 ± 0.84 nm (24h) and 8.4 ± 0.92 nm (48h).
- B. parapertussis hybridization significantly increased mean grain area (91 to 227 nm²) and refractive index (1.489 to 1.648).
- Adsorbed molecule density increased from 0.2 to 0.97 g/cm³, demonstrating successful and quantifiable B. parapertussis attachment.
Conclusions:
- A robust, label-free method for detecting B. parapertussis was successfully developed using DNA-functionalized silicon surfaces.
- The DNA film stability and detection sensitivity can be tuned by adjusting concentration and incubation time.
- This approach offers a promising alternative to traditional PCR for rapid B. parapertussis diagnosis.
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