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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.
Abstract:
In 2010, two infants became ill at a hospital in Mexico. Subsequently, a range of clinical, environmental, and powdered and rehydrated infant formula isolates were identified by using a combination of phenotyping and PCR probes. The strains were clustered according to pulsed-field gel electrophoresis. The causative agent was reported as Cronobacter sakazakii, with powdered infant formula (PIF) identified as the likely source of the infections. This new study further characterized the isolates from this outbreak by using multilocus sequence typing and whole genome sequencing of selected strains. Though four PIF isolates and one hospital environmental isolate were identified as C. sakazakii sequence type 297 by multilocus sequence typing, they were isolated 6 months prior to the outbreak. Genotypic analyses of patient isolates identified them as Enterobacter hormaechei and Enterobacter spp. The pulsed-field gel electrophoresis profile of the Enterobacter spp. isolates matched those of isolates from previously unopened tins of PIF. E. hormaechei was only isolated from the two infants and not PIF. The reevaluation of this outbreak highlights the need for accurate detection and identification assays, particularly during outbreak investigations in which incorrect identifications may mislead the investigation and attribution of the source. Though the species responsible for the symptoms could not be determined, this outbreak demonstrated the possible transmission of Enterobacter spp. from PIF to infants. These are possibly the first reported cases of Enterobacter spp. infection of infants from bacterial-contaminated PIF.
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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