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

被引:58
作者
Ben Amara, Amira [1 ]
Ghigo, Eric [1 ]
Le Priol, Yannick [2 ]
Lepolard, Catherine [1 ]
Salcedo, Suzana P. [3 ]
Lemichez, Emmanuel [4 ]
Bretelle, Florence [1 ]
Capo, Christian [1 ]
Mege, Jean-Louis [1 ]
机构
[1] Univ Mediterranee, CNRS, IRD UMR 6236, Unite Rech Malad Infect Trop & Emergentes,IFR 48, Marseille, France
[2] IMTSSA, Marseille, France
[3] Univ Mediterranee, Ctr Immunol Marseille Luminy, UMR 6546, Marseille, France
[4] Fac Med Nice, INSERM, Unite 895, Equipe 6,C3M, F-06034 Nice, France
关键词
EXPRESSION; ACTIVATION; MONOCYTES; INFECTION; PREGNANCY; PLACENTA; BRUCELLA; RECEPTOR; CELLS; DIFFERENTIATION;
D O I
10.1371/journal.pone.0015315
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
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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页数:10
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