Sequential detection of Salmonella typhimurium and Bacillus anthracis spores using magnetoelastic biosensors

S Huang1, H Yang, R S Lakshmanan

  • 1Materials Engineering, Auburn University, Auburn, AL 36849, USA. huangsh@auburn.edu

Insights

This study developed phage-based magnetoelastic (ME) biosensors for simultaneous pathogen detection. The novel biosensors accurately identified specific bacteria and spores with high selectivity, paving the way for multi-pathogen diagnostics.

Area of Science:

  • Biosensing and Nanotechnology
  • Microbiology and Immunology
  • Materials Science

Background:

  • Magnetoelastic (ME) biosensors offer a label-free detection method.
  • Phage display technology enables specific pathogen recognition.
  • Simultaneous detection of multiple pathogens remains a challenge.

Purpose of the Study:

  • To develop and evaluate multiple phage-based ME biosensors for simultaneous detection of different pathogens.
  • To assess the specificity and selectivity of the developed biosensors.
  • To establish a foundation for a multi-pathogen detection system.

Main Methods:

  • Immobilization of specific phages (E2 for S. typhimurium, JRB7 for B. anthracis) and BSA onto ME resonators.
  • Sequential introduction of target pathogens to a system with multiple, individually monitored sensors.
  • Measurement of resonance frequency shifts in response to analyte binding.
  • Scanning electron microscopy for visual verification of analyte-biosensor interaction.

Main Results:

  • Each phage-coated sensor specifically responded to its cognate pathogen, indicated by a decrease in resonance frequency.
  • BSA blocking effectively prevented non-specific binding, confirmed by a stable reference sensor.
  • Simultaneous monitoring of multiple sensors demonstrated selective detection of S. typhimurium and B. anthracis spores.

Conclusions:

  • Multiple phage-based ME biosensors can be simultaneously monitored for selective detection of specific pathogenic species.
  • BSA blocking is crucial for eliminating non-specific binding in ME biosensor systems.
  • This work represents a significant first step towards a multiplexed pathogen detection platform.