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Salmonella enterica  serovars Choleraesuis and Typhimurium are among the non-typhoid  Salmonella  serovars that are important zoonotic pathogens. In clinical observation,  S.  Typhimurium typically causes diarrheal diseases; however,  S.  Choleraesuis shows high predilection to cause bacteremia. The mechanism why  S.  Choleraesuis is more invasive to humans remains unknown. In this study, we compared the  S.  Typhimurium LT2 and  S.  Choleraesuis SC-B67 proteomes through stable isotope labeling of amino acid in cell culture (SILAC). In SILAC, the expression of many virulence proteins in two type III secretion systems (T3SSs) were significantly higher in  S.  Choleraesuis than in  S.  Typhimurium. Similar differences were also found at the transcriptional level. Compared to  S.  Typhimurium,  S.  Choleraesuis showed a higher penetration level to Caco-2 (>100-fold) and MDCK (>10-fold) monolayers. In mice after oral challenge, the invasion of spleen and liver was also higher in  S.  Choleraesuis than in  S.  Typhimurium. The transcription of  hilD  in  S.  Choleraesuis was increased in physiological (1 mM) or high (10 mM) concentrations of Mg 2+ , but not in low (8 μM) concentration. We conclude that  S.  Choleraesuis showed hyperinvasiveness in cellular as well as mouse models due to hyperexpression of T3SS genes.

Hyperinvasiveness of Salmonella enterica serovar Choleraesuis linked to hyperexpression of type III secretion systems in vitro