RATIONALE: Staphylococcus aureus is a major pathogen complicating postsurgical care. OBJECTIVES: To test the effect of sterile laparotomy (LAP) on pulmonary clearance of S. aureus in a murine model. METHODS: Control and LAP mice were infected intranasally with 10(8) cfu of S. aureus. Microbial clearance, pulmonary leukocyte recruitment, and cytokine profiles were compared between the groups. Antibody neutralization or cytokine gene knockout mice were used to evaluate the role of cytokines. MEASUREMENTS AND MAIN RESULTS: Laparotomy resulted in a 10-fold increase in S. aureus lung colony-forming units on Days 2 and 3 postinfection. Both groups cleared the infection by Day 4. No defect in leukocyte recruitment into the lungs was observed in infected LAP animals; however, an increase in the number of Mac-3-positive cells and a significant decrease of cells with high surface expression of Fc-gammaR suggest suboptimal activation of leukocytes in the lungs of infected LAP animals. Infected LAP mice had decreased expression of interferon (IFN)-gamma and increased expression of mRNA for IL-13 in the lungs on Day 1 postinfection and decreased levels of IL-6, keratinocyte-derived chemokine (KC), and macrophage inflammatory protein-2 (MIP-2) in bronchoalveolar lavage at Day 2 postinfection. Neutralization of IFN-gamma mimicked the effect of LAP with impaired clearance on Day 2. CONCLUSIONS: Sterile LAP induced temporary deactivation of innate immune responses to pulmonary S. aureus challenge. Impaired microbial clearance was accompanied by altered cytokine expression and suboptimal activation of pulmonary leukocytes. Lack of early IFN-gamma induction in the infected lungs of LAP animals is a likely mechanism contributing to the observed phenotype.
RATIONALE: Staphylococcus aureus is a major pathogen complicating postsurgical care. OBJECTIVES: To test the effect of sterile laparotomy (LAP) on pulmonary clearance of S. aureus in a murine model. METHODS: Control and LAP mice were infected intranasally with 10(8) cfu of S. aureus. Microbial clearance, pulmonary leukocyte recruitment, and cytokine profiles were compared between the groups. Antibody neutralization or cytokine gene knockout mice were used to evaluate the role of cytokines. MEASUREMENTS AND MAIN RESULTS: Laparotomy resulted in a 10-fold increase in S. aureus lung colony-forming units on Days 2 and 3 postinfection. Both groups cleared the infection by Day 4. No defect in leukocyte recruitment into the lungs was observed in infected LAP animals; however, an increase in the number of Mac-3-positive cells and a significant decrease of cells with high surface expression of Fc-gammaR suggest suboptimal activation of leukocytes in the lungs of infected LAP animals. Infected LAP mice had decreased expression of interferon (IFN)-gamma and increased expression of mRNA for IL-13 in the lungs on Day 1 postinfection and decreased levels of IL-6, keratinocyte-derived chemokine (KC), and macrophage inflammatory protein-2 (MIP-2) in bronchoalveolar lavage at Day 2 postinfection. Neutralization of IFN-gamma mimicked the effect of LAP with impaired clearance on Day 2. CONCLUSIONS: Sterile LAP induced temporary deactivation of innate immune responses to pulmonary S. aureus challenge. Impaired microbial clearance was accompanied by altered cytokine expression and suboptimal activation of pulmonary leukocytes. Lack of early IFN-gamma induction in the infected lungs of LAP animals is a likely mechanism contributing to the observed phenotype.
Authors: Mohammed Awad; Mohamed Yosri; Marwa M Abdel-Aziz; Ahmed M Younis; Nagwa M Sidkey Journal: Biol Trace Elem Res Date: 2021-01-02 Impact factor: 3.738
Authors: Kathryn E Barletta; R Elaine Cagnina; Kori L Wallace; Susan I Ramos; Borna Mehrad; Joel Linden Journal: J Immunol Methods Date: 2011-10-02 Impact factor: 2.303
Authors: Agnieszka Rynda-Apple; Ann Harmsen; Anfin S Erickson; Kyle Larson; Rachelle V Morton; Laura E Richert; Allen G Harmsen Journal: Eur J Immunol Date: 2014-09-01 Impact factor: 5.532
Authors: Lei Sun; Ren-Feng Guo; Michael W Newstead; Theodore J Standiford; Demetrio R Macariola; Thomas P Shanley Journal: Am J Respir Cell Mol Biol Date: 2008-12-18 Impact factor: 6.914
Authors: Agnieszka Rynda-Apple; Erin Dobrinen; Mark McAlpine; Amanda Read; Ann Harmsen; Laura E Richert; Matthew Calverley; Kyler Pallister; Jovanka Voyich; James A Wiley; Ben Johnson; Mark Young; Trevor Douglas; Allen G Harmsen Journal: Am J Pathol Date: 2012-05-26 Impact factor: 4.307