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Biochemically aberrant Salmonella enteritidis ser. newington from human sources in Connecticut

Insights

This study identified a unique lactose-fermenting Salmonella enteritidis ser. newington strain that did not produce hydrogen sulfide. This finding has implications for laboratory identification of Salmonella infections.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Bacteriology

Background:

  • Salmonella enteritidis ser. newington is a common bacterial pathogen.
  • Lactose-fermenting Salmonella strains are rare and can be difficult to identify using standard biochemical tests.
  • Hydrogen sulfide (H2S) production is a key characteristic used in Salmonella identification.

Purpose of the Study:

  • To characterize a novel lactose-fermenting, xylose-negative Salmonella enteritidis ser. newington strain.
  • To investigate the biochemical properties, including H2S production and lactose fermentation, of this unusual isolate.
  • To assess the potential for genetic transfer of the lactose-fermenting trait.

Main Methods:

  • Isolation and biochemical characterization of three bacterial strains from patients.
  • Serological testing and antibiogram analysis.
  • Evaluation of H2S production on various agar media (e.g., Salmonella-Shigella agar, triple sugar iron agar, Kligler iron agar, lysine iron agar, XLD agar).
  • Investigation of lactose (lac+) character transfer frequencies.

Main Results:

  • Three identical isolates of Salmonella enteritidis ser. newington were recovered, exhibiting lactose fermentation and xylose negativity.
  • Failure to detect hydrogen sulfide production on several standard media, with H2S production observed on lysine iron agar and XLD agar.
  • A correlation between fermentable carbohydrate concentration and H2S production (pH effect) was noted.
  • Low frequency (below 10^-6) of direct lac+ character transfer was observed.

Conclusions:

  • A distinct variant of Salmonella enteritidis ser. newington with altered H2S production and lactose-fermenting capabilities was identified.
  • Standard biochemical media may not reliably detect this strain due to suppressed H2S production.
  • Recommendations are provided for improved laboratory recognition of similar Salmonella strains to aid in accurate diagnosis and public health surveillance.

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