Article

SipA activation of caspase-3 is a decisive mediator of host cell survival at early stages of Salmonella enterica serovar Typhimurium infection

Details

Citation

McIntosh A, Meikle LM, Ormsby MJ, McCormick BA, Christie JM, Brewer JM, Roberts M & Wall DM (2017) SipA activation of caspase-3 is a decisive mediator of host cell survival at early stages of Salmonella enterica serovar Typhimurium infection. Infection and Immunity, 85 (9), Art. No.: e00393-17. https://doi.org/10.1128/IAI.00393-17

Abstract
Salmonella invasion protein A (SipA) is a dual-function effector protein that plays roles in both actin polymerization and caspase-3 activation in intestinal epithelial cells. To date its function in other cell types has remained largely unknown despite its expression in multiple cell types and its extracellular secretion during infection. Here we show that in macrophages SipA induces increased caspase-3 activation early in infection. This activation required a threshold level of SipA linked to multiplicity of infection and may be a limiting factor controlling bacterial numbers in infected macrophages. In polymorphonuclear leukocytes, SipA or other Salmonella pathogenicity island 1 effectors had no effect on induction of caspase-3 activation either alone or in the presence of whole bacteria. Tagging of SipA with the small fluorescent phiLOV tag, which can pass through the type three secretion system, allowed visualization and quantification of caspase-3 activation by SipA-phiLOV in macrophages. Additionally, SipA-phiLOV activation of caspase-3 could be tracked in the intestine through multiphoton laser scanning microscopy in an ex vivo intestinal model. This allowed visualization of areas where the intestinal epithelium had been compromised and demonstrated the potential use of this fluorescent tag for in vivo tracking of individual effectors.

Keywords
Caspase-3; Caspases; Hostpathogen interactions; Imaging; Immune cells; Microscopy; Salmonella; SipA

Journal
Infection and Immunity: Volume 85, Issue 9

StatusPublished
FundersBiotechnology and Biological Sciences Research Council
Publication date30/09/2017
Publication date online19/06/2017
Date accepted by journal02/06/2017
URLhttp://hdl.handle.net/1893/33656
PublisherAmerican Society for Microbiology
ISSN0019-9567
eISSN1098-5522

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