Visualizing virus assembly intermediates inside marine cyanobacteria

被引:96
作者
Dai, Wei [1 ]
Fu, Caroline [1 ]
Raytcheva, Desislava [2 ,3 ]
Flanagan, John [1 ]
Khant, Htet A. [1 ]
Liu, Xiangan [1 ]
Rochat, Ryan H. [1 ,4 ]
Haase-Pettingell, Cameron [2 ]
Piret, Jacqueline [3 ]
Ludtke, Steve J. [1 ,4 ]
Nagayama, Kuniaki [5 ]
Schmid, Michael F. [1 ,4 ]
King, Jonathan A. [2 ]
Chiu, Wah [1 ,4 ]
机构
[1] Baylor Coll Med, Verna & Marrs Mclean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
[4] Baylor Coll Med, Program Struct & Computat Biol & Mol Biophys, Houston, TX 77030 USA
[5] Natl Inst Nat Sci, Natl Inst Physiol Sci, Okazaki, Aichi 4448787, Japan
基金
美国国家卫生研究院;
关键词
ELECTRON CRYOTOMOGRAPHY; CRYOELECTRON MICROSCOPY; BACTERIOPHAGE EPSILON15; RESOLUTION; PROCHLOROCOCCUS; CARBOXYSOMES; ORGANIZATION; ARCHITECTURE; TOMOGRAPHY; REVEAL;
D O I
10.1038/nature12604
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
Cyanobacteria are photosynthetic organisms responsible for similar to 25% of organic carbon fixation on the Earth. These bacteria began to convert solar energy and carbon dioxide into bioenergy and oxygen more than two billion years ago. Cyanophages, which infect these bacteria, have an important role in regulating the marine ecosystem by controlling cyanobacteria community organization and mediating lateral gene transfer. Here we visualize the maturation process of cyanophage Syn5 inside its host cell, Synechococcus, using Zernike phase contrast electron cryo-tomography (cryoET)(1,2). This imaging modality yields dramatic enhancement of image contrast over conventional cryoET and thus facilitates the direct identification of subcellular components, including thylakoid membranes, carboxysomes and polyribosomes, as well as phages, inside the congested cytosol of the infected cell. By correlating the structural features and relative abundance of viral progeny within cells at different stages of infection, we identify distinct Syn5 assembly intermediates. Our results indicate that the procapsid releases scaffolding proteins and expands its volume at an early stage of genome packaging. Later in the assembly process, we detected full particles with a tail either with or without an additional horn. The morphogenetic pathway we describe here is highly conserved and was probably established long before that of double-stranded DNA viruses infecting more complex organisms.
引用
收藏
页码:707 / +
页数:8
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