Enterovirus D68 receptor requirements unveiled by haploid genetics

被引:95
作者
Baggen, Jim [1 ]
Thibaut, Hendrik Jan [1 ]
Staring, Jacqueline [2 ]
Jae, Lucas T. [2 ]
Liu, Yue [3 ]
Guo, Hongbo [1 ]
Slager, Jasper J. [1 ]
de Bruin, Jost W. [1 ]
van Vliet, Arno L. W. [1 ]
Blomen, Vincent A. [2 ]
Overduin, Pieter [4 ]
Sheng, Ju [3 ]
de Haan , Cornelis A. M. [1 ]
de Vries, Erik [1 ]
Meijer, Adam [4 ]
Rossmann, Michael G. [3 ]
Brummelkamp, Thijn R. [2 ,5 ]
van Kuppeveld, Frank J. M. [1 ]
机构
[1] Univ Utrecht, Fac Vet Med, Div Virol, Dept Immunol & Infect Dis, NL-3584 CL Utrecht, Netherlands
[2] Netherlands Canc Inst, Div Biochem, NL-1006 BE Amsterdam, Netherlands
[3] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[4] Natl Inst Publ Hlth & Environm, Div Virol, Ctr Infect Dis Res Diagnost & Screening, NL-3720 BA Bilthoven, Netherlands
[5] Canc Genom Ctr, NL-3584 CG Utrecht, Netherlands
基金
欧洲研究理事会; 美国国家卫生研究院;
关键词
enterovirus D68; haploid genetic screen; receptor; sialic acid; VIRUS ENTRY REQUIRES; HUMAN-CELLS; BINDING; RHINOVIRUS; INFECTION; EMERGENCE; SEROTYPE; SCREENS; PROTEIN;
D O I
10.1073/pnas.1524498113
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
Enterovirus D68 (EV-D68) is an emerging pathogen that can cause severe respiratory disease and is associated with cases of paralysis, especially among children. Heretofore, information on host factor requirements for EV-D68 infection is scarce. Haploid genetic screening is a powerful tool to reveal factors involved in the entry of pathogens. We performed a genome-wide haploid screen with the EV-D68 prototype Fermon strain to obtain a comprehensive overview of cellular factors supporting EV-D68 infection. We identified and confirmed several genes involved in sialic acid (Sia) biosynthesis, transport, and conjugation to be essential for infection. Moreover, by using knockout cell lines and gene reconstitution, we showed that both alpha 2,6- and alpha 2,3-linked Sia can be used as functional cellular EV-D68 receptors. Importantly, the screen did not reveal a specific protein receptor, suggesting that EV-D68 can use multiple redundant sialylated receptors. Upon testing recent clinical strains, we identified strains that showed a similar Sia dependency, whereas others could infect cells lacking surface Sia, indicating they can use an alternative, nonsialylated receptor. Nevertheless, these Sia-independent strains were still able to bind Sia on human erythrocytes, raising the possibility that these viruses can use multiple receptors. Sequence comparison of Sia-dependent and Sia-independent EV-D68 strains showed that many changes occurred near the canyon that might allow alternative receptor binding. Collectively, our findings provide insights into the identity of the EV-D68 receptor and suggest the possible existence of Sia-independent viruses, which are essential for understanding tropism and disease.
引用
收藏
页码:1399 / 1404
页数:6
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