Apolipoprotein E genotype affects innate susceptibility to Listeria monocytogenes infection in aged male mice

• Published in: Infection and immunity Vol. 91; no. 9; p. e0025123
• Main Authors: Cho, Jooyoung, Alexander, Katie L, Ferrell, Jessica L, Johnson, Lance A, Estus, Steven, D'Orazio, Sarah E F
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 14.09.2023
• Subjects: Animals; Apolipoprotein E2; Apolipoprotein E3; Apolipoprotein E4; Apolipoproteins E - genetics; Cytokines; Female; Genotype; Host Response and Inflammation; Humans; Listeria monocytogenes; Listeriosis; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; lipid transport; foodborne listeriosis; TNFα; macrophages
• ISSN: 0019-9567; 1098-5522; 1098-5522
• DOI: 10.1128/iai.00251-23

Apolipoprotein E (ApoE) is a lipid transport protein that is hypothesized to suppress proinflammatory cytokine production, particularly after stimulation with Toll-like receptor (TLR) ligands such as lipopolysaccharide (LPS). Studies using transgenic ApoE human replacement mice (APOE) expressing one of three different allelic variants suggest that there is a hierarchy in terms of responsiveness to proinflammatory stimuli such as APOE4/E4 > APOE3/E3 > APOE2/E2. In this study, we test the hypothesis that genotype can also predict susceptibility to infection with the facultative intracellular gram-positive bacterium . We found that bone-marrow-derived macrophages isolated from aged APOE4/E4 mice expressed elevated levels of nitric oxide synthase 2 and were highly resistant to infection with compared to APOE3/E3 and APOE2/E2 mice. However, we did not find statistically significant differences in cytokine or chemokine output from either macrophages or whole splenocytes isolated from APOE2/E2, APOE3/E3, or APOE4/E4 mice following infection. , overall susceptibility to foodborne listeriosis also did not differ by genotype in either young (2 mo old) or aged (15 mo old) C57BL/6 mice. However, we observed a sex-dependent susceptibility to infection in aged APOE2/E2 male mice and a sex-dependent resistance to infection in aged APOE4/E4 male mice that was not present in female mice. Thus, these results suggest that genotype does not play an important role in innate resistance to infection with but may be linked to sex-dependent changes that occur during immune senescence.