A filtration based technique for simultaneous SEM and TEM sample preparation for the rapid detection of pathogens.

Viruses

Viral Diseases Division, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB R3E 3P6, Canada.

Published: September 2014

AI Article Synopsis

  • Diagnostic electron microscopy allows comprehensive observation of microorganisms in samples without prior knowledge of their identity.
  • The traditional method involves applying a sample droplet to a support film for negative staining, with a detection sensitivity of about 1 million viruses per mL.
  • The new filtration method improves sensitivity, enabling detection of viruses at concentrations as low as 102 viruses per mL, outperforming conventional methods by detecting as few as 5,000 particles per sample.

Article Abstract

Diagnostic electron microscopy for infectious diseases has the advantage that "everything" in the specimen can be observed, without a priori knowledge of the likely identity of the microorganisms present in the sample. The classical specimen preparation method used employs a droplet of sample, which allows particles to adsorb to a support film, and is subsequently negative stained. This "grid on drop" procedure has a sensitivity range of approximately 106 viruses per mL if no enrichment procedures are used. In the current investigation we present a novel use of filtration that allows us to detect viruses at concentrations as low as 102 viruses per mL. We present here methods based on filtration, in which total virus, and not virus concentration, is the limiting factor for detection. We show that filtration is more sensitive than conventional negative staining and can detect as few as 5 × 103 particles per sample.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189033PMC
http://dx.doi.org/10.3390/v6093458DOI Listing

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