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1.
PLoS One ; 4(6): e6020, 2009 Jun 23.
Article in English | MEDLINE | ID: mdl-19547701

ABSTRACT

BACKGROUND: Intracellular pathogens have developed elaborate strategies for silent infection of preferred host cells. Chlamydia pneumoniae is a common pathogen in acute infections of the respiratory tract (e.g. pneumonia) and associated with chronic lung sequelae in adults and children. Within the lung, alveolar macrophages and polymorph nuclear neutrophils (PMN) are the first line of defense against bacteria, but also preferred host phagocytes of chlamydiae. METHODOLOGY/PRINCIPAL FINDINGS: We could show that C. pneumoniae easily infect and hide inside neutrophil granulocytes until these cells become apoptotic and are subsequently taken up by macrophages. C. pneumoniae infection of macrophages via apoptotic PMN results in enhanced replicative activity of chlamydiae when compared to direct infection of macrophages, which results in persistence of the pathogen. Inhibition of the apoptotic recognition of C. pneumoniae infected PMN using PS- masking Annexin A5 significantly lowered the transmission of chlamydial infection to macrophages. Transfer of apoptotic C. pneumoniae infected PMN to macrophages resulted in an increased TGF-ss production, whereas direct infection of macrophages with chlamydiae was characterized by an enhanced TNF-alpha response. CONCLUSIONS/SIGNIFICANCE: Taken together, our data suggest that C. pneumoniae uses neutrophil granulocytes to be silently taken up by long-lived macrophages, which allows for efficient propagation and immune protection within the human host.


Subject(s)
Apoptosis , Chlamydophila pneumoniae/physiology , Chlamydophila pneumoniae/pathogenicity , Macrophages, Alveolar/microbiology , Macrophages, Alveolar/pathology , Neutrophils/metabolism , Cell Line/microbiology , Cell Separation , Cytokines/biosynthesis , Flow Cytometry , Granulocytes/microbiology , Humans , Macrophages/metabolism , Macrophages, Alveolar/metabolism , Models, Biological , Neutrophils/cytology , Reverse Transcriptase Polymerase Chain Reaction
2.
Infect Immun ; 75(12): 5993-6007, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17709416

ABSTRACT

Day-old chicks are very susceptible to infections with Salmonella enterica subspecies. The gut mucosa is the initial site of host invasion and provides the first line of defense against the bacteria. To study the potential of different S. enterica serovars to invade the gut mucosa and trigger an immune response, day-old chicks were infected orally with Salmonella enterica serovar Enteritidis, S. enterica serovar Typhimurium, S. enterica serovar Hadar, or S. enterica serovar Infantis, respectively. The localization of Salmonella organisms in gut mucosa and the number of immune cells in cecum were determined by immunohistochemistry in the period between 4 h and 9 days after infection. Using quantitative real-time reverse transcription (RT)-PCR, mRNA expression of various cytokines, chemokines, and inducible nitric oxide synthase (iNOS) was examined in cecum. As a result, all S. enterica serovars were able to infect epithelial cells and the lamina propria. Notably, serovar Enteritidis showed the highest invasiveness of lamina propria tissue, whereas serovars Typhimurium and Hadar displayed moderate invasiveness and serovar Infantis hardly any invasion capabilities. Only a limited number of bacteria of all serovars were found within intestinal macrophages. Elevated numbers of granulocytes, CD8+ cells, and TCR1+ cells and mRNA expression rates for interleukin 12 (IL-12), IL-18, tumor necrosis factor alpha factor, and iNOS in cecum correlated well with the invasiveness of serovars in the lamina propria. In contrast, changes in numbers of TCR2+ and CD4+ cells and IL-2 mRNA expression seemed to be more dependent on infection of epithelial cells. The data indicate that the capability of Salmonella serovars to enter the cecal mucosa and invade lower regions affects both the level and character of the immune response in tissue.


Subject(s)
Cecum/immunology , Poultry Diseases/immunology , Salmonella Infections, Animal/immunology , Salmonella enterica/immunology , Animals , Apoptosis Regulatory Proteins/metabolism , Cecum/microbiology , Cecum/pathology , Chemokines/biosynthesis , Chemokines/genetics , Chemokines/immunology , Chickens , Cytokines/biosynthesis , Cytokines/genetics , Cytokines/immunology , Immunohistochemistry , Macrophages/immunology , Microscopy, Confocal/methods , Nitric Oxide Synthase Type II/genetics , Nitric Oxide Synthase Type II/immunology , Nitric Oxide Synthase Type II/metabolism , Poultry Diseases/blood , Poultry Diseases/microbiology , Salmonella Infections, Animal/blood , Salmonella Vaccines/immunology , Salmonella enterica/pathogenicity , Spleen/immunology , Spleen/microbiology
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