Neutrophils from Both Susceptible and Resistant Mice Efficiently Kill Opsonized Listeria monocytogenes

• Published in: Infection and immunity Vol. 86; no. 4
• Main Authors: Pitts, Michelle G, Combs, Travis A, D'Orazio, Sarah E F
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.04.2018
• Subjects: Animals; Biomarkers; Disease Resistance - immunology; Disease Susceptibility - immunology; Host Response and Inflammation; Immunity, Innate; Listeria monocytogenes - immunology; Listeriosis - immunology; Listeriosis - metabolism; Listeriosis - microbiology; Liver - immunology; Liver - metabolism; Liver - microbiology; Liver - pathology; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Microbial Viability - immunology; Neutrophil Infiltration - immunology; Neutrophils - immunology; Neutrophils - metabolism; Neutrophils - microbiology; Oxidation-Reduction; Phagocytosis - immunology; Reactive Oxygen Species - metabolism; Respiratory Burst - immunology; Species Specificity; innate immunity; C57BL/6 mice; liver; reactive oxygen species; BALB/cBy/J mice
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.00085-18

Inbred mouse strains differ in their susceptibility to infection with the facultative intracellular bacterium , largely due to delayed or deficient innate immune responses. Previous antibody depletion studies suggested that neutrophils (polymorphonuclear leukocytes [PMN]) were particularly important for clearance in the liver, but the ability of PMN from susceptible and resistant mice to directly kill has not been examined. In this study, we showed that PMN infiltrated the livers of BALB/c/By/J (BALB/c) and C57BL/6 (B6) mice in similar numbers and that both cell types readily migrated toward leukotriene B4 in an chemotaxis assay. However, CFU burdens in the liver were significantly higher in BALB/c mice than in other strains, suggesting that PMN in the BALB/c liver might not be able to clear as efficiently as B6 PMN. Unprimed PMN harvested from either BALB/c or B6 bone marrow killed directly , and pretreatment with autologous serum significantly enhanced killing efficiency for both. were internalized within 10 min and rapidly triggered intracellular production of reactive oxygen species in a dose-dependent manner. However, PMN from gp91 -deficient mice also readily killed , which suggested that nonoxidative killing mechanisms may be sufficient for bacterial clearance. Together, these results indicate that there is not an intrinsic defect in the ability of PMN from susceptible BALB/c mice to kill and further suggest that if PMN function is impaired in BALB/c mice, it is likely due to locally produced modulating factors present in the liver during infection.