MdsABC-Mediated Pathway for Pathogenicity in Salmonella enterica Serovar Typhimurium

• Published in: Infection and immunity Vol. 83; no. 11; pp. 4266 - 4276
• Main Authors: Song, Saemee, Lee, Boeun, Yeom, Ji-Hyun, Hwang, Soonhye, Kang, Ilnam, Cho, Jang-Cheon, Ha, Nam-Chul, Bae, Jeehyeon, Lee, Kangseok, Kim, Yong-Hak
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.11.2015
• Subjects: Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Gene Expression Regulation, Bacterial; Humans; Macrophages - metabolism; Macrophages - microbiology; Membrane Transport Proteins - genetics; Membrane Transport Proteins - metabolism; Molecular Pathogenesis; Salmonella enterica; Salmonella Infections - microbiology; Salmonella typhimurium; Salmonella typhimurium - genetics; Salmonella typhimurium - metabolism; Salmonella typhimurium - pathogenicity; Virulence
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/iai.00653-15

MdsABC is a Salmonella-specific tripartite efflux pump that has been implicated in the virulence of Salmonella enterica serovar Typhimurium; however, little is known about the virulence factors associated with this pump. We observed MdsABC expression-dependent alterations in the degree of resistance to extracellular oxidative stress and macrophage-mediated killing. Thin-layer chromatography and tandem mass spectrometry analyses revealed that overexpression of MdsABC led to increased secretion of 1-palmitoyl-2-stearoyl-phosphatidylserine (PSPS), affecting the ability of the bacteria to invade and survive in host cells. Overexpression of MdsABC and external addition of PSPS similarly rendered the mdsABC deletion strain resistant to diamide. Diagonal gel analysis showed that PSPS treatment reduced the diamide-mediated formation of disulfide bonds, particularly in the membrane fraction of the bacteria. Salmonella infection of macrophages induced the upregulation of MdsABC expression and led to an increase of intracellular bacterial number and host cell death, similar to the effects of MdsABC overexpression and PSPS pretreatment on the mdsABC deletion strain. Our study shows that MdsABC mediates a previously uncharacterized pathway that involves PSPS as a key factor for the survival and virulence of S. Typhimurium in phagocytic cells.