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.

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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