Host cell-free growth of the Q fever bacterium Coxiella burnetii

被引:299
作者
Omsland, Anders [1 ]
Cockrell, Diane C. [1 ]
Howe, Dale [1 ]
Fischer, Elizabeth R. [2 ]
Virtaneva, Kimmo [3 ]
Sturdevant, Daniel E. [3 ]
Porcella, Stephen F. [3 ]
Heinzen, Robert A. [1 ]
机构
[1] NIAID, NIH, Coxiella Pathogenesis Sect, Intracellular Parasites Lab, Hamilton, MT 59840 USA
[2] NIAID, NIH, Electron Microscopy Unit, Hamilton, MT 59840 USA
[3] NIAID, NIH, Genom Unit, Res Technol Sect,Res Technol Branch,Rocky Mt Labs, Hamilton, MT 59840 USA
基金
美国国家卫生研究院;
关键词
axenic growth; metabolism; microaerophile; obligate intracellular pathogen; LEGIONELLA-PNEUMOPHILA; CHOLESTEROL-METABOLISM; GENOME SEQUENCE; CYTOCHROME BD; GUINEA-PIGS; INFECTION; OXYGEN; REQUIREMENTS; MACROPHAGES; VIRULENCE;
D O I
10.1073/pnas.0812074106
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
07 ; 0710 ; 09 ;
摘要
The inability to propagate obligate intracellular pathogens under axenic (host cell-free) culture conditions imposes severe experimental constraints that have negatively impacted progress in understanding pathogen virulence and disease mechanisms. Coxiella burnetii, the causative agent of human Q (Query) fever, is an obligate intracellular bacterial pathogen that replicates exclusively in an acidified, lysosome-like vacuole. To define conditions that support C. burnetii growth, we systematically evaluated the organism's metabolic requirements using expression microarrays, genomic reconstruction, and metabolite typing. This led to development of a complex nutrient medium that supported substantial growth (approximately 3 log(10)) of C. burnetii in a 2.5% oxygen environment. Importantly, axenically grown C. burnetii were highly infectious for Vero cells and exhibited developmental forms characteristic of in vivo grown organisms. Axenic cultivation of C. burnetii will facilitate studies of the organism's pathogenesis and genetics and aid development of Q fever preventatives such as an effective subunit vaccine. Furthermore, the systematic approach used here may be broadly applicable to development of axenic media that support growth of other medically important obligate intracellular pathogens.
引用
收藏
页码:4430 / 4434
页数:5
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