Null mutation in sspA of Cronobacter sakazakii influences its tolerance to environmental stress

Jie Zhan1,2, Xin Tan1,3, Xiaoyuan Wang1,3,2

  • 1State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi 214122, China.

Insights

Cronobacter sakazakii stress tolerance was studied by examining stringent starvation protein A (SspA). Deleting sspA impacted acid and desiccation tolerance, offering insights into infant formula pathogen survival.

Area of Science:

  • Food microbiology
  • Bacterial stress response
  • Molecular biology

Background:

  • Cronobacter sakazakii is an opportunistic foodborne pathogen linked to infant formula infections.
  • Its pathogenicity may stem from significant stress tolerance, despite manufacturing hurdles.
  • Stringent starvation protein A (SspA) is crucial for E. coli survival under stress.

Purpose of the Study:

  • To investigate the role of SspA in Cronobacter sakazakii BAA894 stress tolerance.
  • To assess the impact of sspA gene knockout on C. sakazakii's resistance to acid, desiccation, and antibiotics.

Main Methods:

  • Created an sspA-knockout mutant of C. sakazakii BAA894.
  • Assessed acid, desiccation, and antibiotic tolerance of the wild type and mutant strains.
  • Performed transcriptome analysis to identify differentially expressed genes in the mutant.

Main Results:

  • The sspA knockout decreased acid tolerance but increased desiccation tolerance in LB medium, while decreasing it in M9 medium.
  • Minimum inhibitory concentrations for several antibiotics differed between the wild type and mutant strains.
  • Transcriptome analysis revealed significant differential gene expression in the mutant, particularly in genes related to metabolism and chemotaxis.

Conclusions:

  • SspA plays a complex role in C. sakazakii BAA894 stress tolerance.
  • The sspA mutation affects acid and desiccation resistance, as well as antibiotic susceptibility.
  • Understanding SspA's function provides insights into C. sakazakii's survival mechanisms in food environments.

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