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      Coxiella burnetii, the Agent of Q Fever, Replicates within Trophoblasts and Induces a Unique Transcriptional Response

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          Abstract

          Q fever is a zoonosis caused by Coxiella burnetii, an obligate intracellular bacterium typically found in myeloid cells. The infection is a source of severe obstetrical complications in humans and cattle and can undergo chronic evolution in a minority of pregnant women. Because C. burnetii is found in the placentas of aborted fetuses, we investigated the possibility that it could infect trophoblasts. Here, we show that C. burnetii infected and replicated in BeWo trophoblasts within phagolysosomes. Using pangenomic microarrays, we found that C. burnetii induced a specific transcriptomic program. This program was associated with the modulation of inflammatory responses that were shared with inflammatory agonists, such as TNF, and more specific responses involving genes related to pregnancy development, including EGR-1 and NDGR1. In addition, C. burnetii stimulated gene networks organized around the IL-6 and IL-13 pathways, which both modulate STAT3. Taken together, these results revealed that trophoblasts represent a protective niche for C. burnetii. The activation program induced by C. burnetii in trophoblasts may allow bacterial replication but seems unable to interfere with the development of normal pregnancy. Such pathophysiologocal processes should require the activation of immune placental cells associated with trophoblasts.

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          Most cited references55

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          Macrophage polarization in bacterial infections.

          Converging studies have shown that M1 and M2 macrophages are functionally polarized in response to microorganisms and host mediators. Gene expression profiling of macrophages reveals that various Gram-negative and Gram-positive bacteria induce the transcriptional activity of a "common host response," which includes genes belonging to the M1 program. However, excessive or prolonged M1 polarization can lead to tissue injury and contribute to pathogenesis. The so-called M2 macrophages play a critical role in the resolution of inflammation by producing anti-inflammatory mediators. These M2 cells cover a continuum of cells with different phenotypic and functional properties. In addition, some bacterial pathogens induce specific M2 programs in macrophages. In this review, we discuss the relevance of macrophage polarization in three domains of infectious diseases: resistance to infection, infectious pathogenesis, and chronic evolution of infectious diseases.
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              Natural history and pathophysiology of Q fever.

              Q fever is a zoonosis caused by Coxiella burnetii. Infection with C burnetii can be acute or chronic, and exhibits a wide spectrum of clinical manifestations. The extreme infectivity of the bacterium results in large outbreaks and makes it a potential bioweapon. In the past decade, the complete genome sequencing of C burnetii, the exploration of bacterial interactions with the host, and the description of the natural history of the disease in human beings and in experimental models have all added to our knowledge about this fascinating disease. Advances in understanding the pathophysiology and natural history of Q fever are reviewed.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2010
                14 December 2010
                : 5
                : 12
                : e15315
                Affiliations
                [1 ]Unité de Recherche sur les Maladies Infectieuses Tropicales et Emergentes, CNRS-IRD UMR 6236, IFR 48, Université de la Méditerranée, Marseille, France
                [2 ]IMTSSA, Transcriptomic Platform, Parc du Pharo, Marseille, France
                [3 ]Centre d'Immunologie de Marseille-Luminy, Université de la Méditerranée, UMR 6546, Marseille, France
                [4 ]INSERM Unité 895, Equipe 6, C3M, Microbial Toxins in Host Pathogen Interactions, Nice, France
                Institut de Pharmacologie et de Biologie Structurale, France
                Author notes

                Conceived and designed the experiments: EG CC JLM. Performed the experiments: ABA EG YLP CL SPS EL. Analyzed the data: ABA EG YLP CL FB. Contributed reagents/materials/analysis tools: SPS EL FB. Wrote the paper: ABA EG CC JLM.

                Article
                PONE-D-10-01486
                10.1371/journal.pone.0015315
                3001886
                21179488
                b5e2d1c2-556d-499b-be5e-2b2a65d97fa3
                Ben Amara et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 2 September 2010
                : 8 November 2010
                Page count
                Pages: 10
                Categories
                Research Article
                Biology
                Computational Biology
                Microarrays
                Regulatory Networks
                Signaling Networks
                Microbiology
                Bacterial Pathogens
                Gram Negative
                Immunity
                Immune Defense
                Microbial Pathogens
                Proteomics
                Spectrometric Identification of Proteins
                Medicine
                Infectious Diseases
                Bacterial Diseases
                Q-Fever
                Obstetrics and Gynecology
                Pregnancy
                Pregnancy Complications

                Uncategorized
                Uncategorized

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