The structure of enteric human adenovirus 41-A leading cause of diarrhea in children

被引:44
作者
Rafie, K. [1 ,2 ,3 ]
Lenman, A. [4 ,5 ]
Fuchs, J. [6 ]
Rajan, A. [4 ,7 ]
Arnberg, N. [4 ]
Carlson, L-A [1 ,2 ,3 ]
机构
[1] Umea Univ, Dept Med Biochem & Biophys, Umea, Sweden
[2] Umea Univ, Wallenberg Ctr Mol Med, Umea, Sweden
[3] Umea Univ, Mol Infect Med Sweden, Umea, Sweden
[4] Umea Univ, Sect Virol, Dept Clin Microbiol, Umea, Sweden
[5] Ctr Expt & Clin Infect Res, TWINCORE, Inst Expt Virol, Hannover, Germany
[6] Univ Gothenburg, Prote Core Facil, Sahlgrenska Acad, Gothenburg, Sweden
[7] Univ Gothenburg, Inst Biomed, Dept Med Biochem & Cell Biol, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
CRYO-EM; CRYSTAL-STRUCTURE; 3-DIMENSIONAL STRUCTURE; PHYLOGENETIC ANALYSIS; FIBER PROTEIN; BINDING; REVEALS; RECONSTRUCTION; ORGANIZATION; REPLICATION;
D O I
10.1126/sciadv.abe0974
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
Human adenovirus (HAdV) types F40 and F41 are a prominent cause of diarrhea and diarrhea-associated mortality in young children worldwide. These enteric HAdVs differ notably in tissue tropism and pathogenicity from respiratory and ocular adenoviruses, but the structural basis for this divergence has been unknown. Here, we present the first structure of an enteric HAdV-HAdV-F41-determined by cryo-electron microscopy to a resolution of 3.8 angstrom. The structure reveals extensive alterations to the virion exterior as compared to nonenteric HAdVs, including a unique arrangement of capsid protein IX. The structure also provides new insights into conserved aspects of HAdV architecture such as a proposed location of core protein V, which links the viral DNA to the capsid, and assembly-induced conformational changes in the penton base protein. Our findings provide the structural basis for adaptation of enteric HAdVs to a fundamentally different tissue tropism.
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页数:12
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