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Antibiotic use during influenza infection augments lung eosinophils that impair immunity against secondary bacterial pneumonia
Marilia Sanches Santos Rizzo Zuttion, Tanyalak Parimon, Stephanie A. Bora, Changfu Yao, Katherine Lagree, Catherine A. Gao, Richard G. Wunderink, Georgios D. Kitsios, Alison Morris, Yingze Zhang, Bryan J. McVerry, Matthew E. Modes, Alberto M. Marchevsky, Barry R. Stripp, Christopher M. Soto, Ying Wang, Kimberly Merene, Silvia Cho, Blandine L. Victor, Ivan Vujkovic-Cvijin, Suman Gupta, Suzanne L. Cassel, Fayyaz S. Sutterwala, Suzanne Devkota, David M. Underhill, Peter Chen
Marilia Sanches Santos Rizzo Zuttion, Tanyalak Parimon, Stephanie A. Bora, Changfu Yao, Katherine Lagree, Catherine A. Gao, Richard G. Wunderink, Georgios D. Kitsios, Alison Morris, Yingze Zhang, Bryan J. McVerry, Matthew E. Modes, Alberto M. Marchevsky, Barry R. Stripp, Christopher M. Soto, Ying Wang, Kimberly Merene, Silvia Cho, Blandine L. Victor, Ivan Vujkovic-Cvijin, Suman Gupta, Suzanne L. Cassel, Fayyaz S. Sutterwala, Suzanne Devkota, David M. Underhill, Peter Chen
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Research Article Infectious disease Pulmonology

Antibiotic use during influenza infection augments lung eosinophils that impair immunity against secondary bacterial pneumonia

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Abstract

A leading cause of mortality after influenza infection is the development of a secondary bacterial pneumonia. In the absence of a bacterial superinfection, prescribing antibacterial therapies is not indicated but has become a common clinical practice for those presenting with a respiratory viral illness. In a murine model, we found that antibiotic use during influenza infection impaired the lung innate immunologic defenses toward a secondary challenge with methicillin-resistant Staphylococcus aureus (MRSA). Antibiotics augment lung eosinophils, which have inhibitory effects on macrophage function through the release of major basic protein. Moreover, we demonstrated that antibiotic treatment during influenza infection caused a fungal dysbiosis that drove lung eosinophilia and impaired MRSA clearance. Finally, we evaluated 3 cohorts of hospitalized patients and found that eosinophils positively correlated with antibiotic use, systemic inflammation, and worsened outcomes. Altogether, our work demonstrates a detrimental effect of antibiotic treatment during influenza infection that has harmful immunologic consequences via recruitment of eosinophils to the lungs, thereby increasing the risk of developing a secondary bacterial infection.

Authors

Marilia Sanches Santos Rizzo Zuttion, Tanyalak Parimon, Stephanie A. Bora, Changfu Yao, Katherine Lagree, Catherine A. Gao, Richard G. Wunderink, Georgios D. Kitsios, Alison Morris, Yingze Zhang, Bryan J. McVerry, Matthew E. Modes, Alberto M. Marchevsky, Barry R. Stripp, Christopher M. Soto, Ying Wang, Kimberly Merene, Silvia Cho, Blandine L. Victor, Ivan Vujkovic-Cvijin, Suman Gupta, Suzanne L. Cassel, Fayyaz S. Sutterwala, Suzanne Devkota, David M. Underhill, Peter Chen

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Figure 4

Eosinophils suppress macrophage phagocytosis through secretion of MBP-1.

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Eosinophils suppress macrophage phagocytosis through secretion of MBP-1....
(A and B) Macrophages (RAW 264.7 cells) were processed for RNA-Seq. DEGs (see Supplemental Table 3 for entire DEG list) were analyzed with IPA. (A) Macrophages were cultured in conditioned medium from either eosinophils or epithelial cells as a control. Disease and Function Analysis was performed, and nonredundant pathways (|z score| > 2) were visualized. See Supplemental Table 4 for the complete list of pathways. (B) Macrophages were cultured in eosinophil conditioned medium with addition of an isotype or anti–MBP-1 antibody. Disease and Function Analysis was performed, and nonredundant pathways (|z score| > 2) were visualized. See Supplemental Table 4 for the complete list. (C) MRSA was cultured alone, with macrophages, or with macrophages and primary eosinophils for 4 hours and MRSA CFU was calculated. (D) Quantification of MRSA CFU (n = 6). **P < 0.01 by repeated-measures 1-way ANOVA and post hoc analysis. (E) CFU of MRSA cultured for 4 hours alone, with macrophages, or with macrophages and conditioned medium from primary eosinophils (n = 11). **P < 0.01 by repeated-measures 1-way ANOVA and post hoc analysis. (F) CFU of MRSA cultured for 2 hours with macrophages plus addition of control (BSA) or recombinant MBP-1 (n = 4). *P < 0.05 by 2-tailed Student’s t test. (G) Fluorescence intensity over time reflects phagocytosis of pHrodo-labeled S. aureus bioparticles (n = 4). *P < 0.05, **P < 0.01 by repeated-measures 2-way ANOVA. (H and I) Effect of MBP-1 on phagocytosis of S. aureus bioparticles by murine alveolar macrophages in vivo (control, n = 13; MBP-1, n = 15) (H) and in an ex vivo PCLS culture (control, n = 5; MBP-1, n = 4) (I). *P < 0.05 by 2-tailed Student’s t test.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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