Paper-based luminescence bioassay method embedding a sequence of enzymatic reactions to detect sulfonamide groups

J Antibiot (Tokyo). 2018 Nov;71(12):1044-1047. doi: 10.1038/s41429-018-0094-3. Epub 2018 Aug 23.

Abstract

Sulfonamide residue in foodstuffs and the environment is a serious global concern for their contribution to the occurrence of antibiotic-resistant bacteria, especially in developing countries. Here, we describe a novel, simple, and low-cost bioassay for sulfonamides, which has high potential versatility for use in low-resource settings. The bioassay method is based on a purpose-built luminescent assay reaction that detects sulfonamide groups. The luminescent assay reaction comprises dihydropteroate synthase, a target enzyme of sulfonamides, and luminescent pyrophosphate detection reagent, which triggers a sequence of biomolecular reactions that convert sulfonamides to emit luminescence. The novel assay detected at least six different sulfonamides with an estimated limit of detection of <25 ng ml-1 in a solution-phase assay using a microplate reader. More importantly, the luminescent assay reaction functioned even after spotting and freeze-drying on a wax pattern-printed paper platform. The paper-embedded luminescent assay reaction showed response signals to sulfadiazine within 30 min at a limit of detection similar to that of the solution-phase assay using a microplate reader. The signal could be recorded using a digital camera in the dark and required no other laboratory infrastructure, freeing the assay from the constraints of a well-fitted laboratory.

MeSH terms

  • Biological Assay / methods*
  • Dihydropteroate Synthase / metabolism
  • Diphosphates / chemistry
  • Luminescent Measurements / methods
  • Sulfonamides / analysis*

Substances

  • Diphosphates
  • Sulfonamides
  • Dihydropteroate Synthase