Reevaluation of a Suspected Cronobacter sakazakii Outbreak in Mexico

Emily E Jackson1, Julio Parra Flores2, Eduardo Fernández-Escartín3

  • 1School of Science and Technology, Nottingham Trent University, Clifton Lane, Nottingham, NG11 8NS, UK.

Insights

This study reevaluates a 2010 infant illness outbreak, finding Enterobacter spp., not Cronobacter sakazakii, likely contaminated powdered infant formula (PIF). Accurate diagnostics are crucial for preventing infant infections from contaminated PIF.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Food Safety

Background:

  • In 2010, two infants fell ill, initially attributed to Cronobacter sakazakii in powdered infant formula (PIF).
  • Initial investigations involved phenotyping, PCR, and pulsed-field gel electrophoresis (PFGE).

Purpose of the Study:

  • To re-characterize microbial isolates from a 2010 infant illness outbreak using advanced genomic techniques.
  • To reassess the causative agent and source of the infant infections, focusing on PIF contamination.

Main Methods:

  • Multilocus sequence typing (MLST) and whole genome sequencing (WGS) of clinical, environmental, and PIF isolates.
  • Pulsed-field gel electrophoresis (PFGE) for strain comparison.

Main Results:

  • MLST identified PIF and environmental isolates as Cronobacter sakazakii sequence type 297, but these predated the outbreak.
  • Genotypic analysis revealed patient isolates were Enterobacter hormaechei and Enterobacter spp., matching PFGE profiles from unopened PIF tins.
  • Enterobacter hormaechei was found only in the infants, not in PIF.

Conclusions:

  • The initial identification of Cronobacter sakazakii was likely incorrect, highlighting the need for accurate diagnostic assays in outbreak investigations.
  • Enterobacter spp. transmission from contaminated PIF to infants is a potential cause of illness, possibly representing novel infant infections.
  • This reevaluation underscores the critical importance of precise microbial identification for accurate source attribution and public health response.

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