Extracellular vesicles: Vehicles of en bloc viral transmission

被引:61
作者
Altan-Bonnet, Nihal [1 ]
Perales, Celia [2 ,3 ,4 ]
Domingo, Esteban [3 ,4 ]
机构
[1] NHLBI, Lab Host Pathogen Dynam, Cell Biol & Dev Biol Ctr, NIH, Bldg 10, Bethesda, MD 20892 USA
[2] UAM, Dept Clin Microbiol, IIS Fdn Jimenez Diaz, Av Reyes Catolicas 2, Madrid 28040, Spain
[3] UAM, Ctr Biol Mol Severo Ochoa, CSIC, Campus Cantoblanco, Madrid, Spain
[4] Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Madrid, Spain
基金
美国国家卫生研究院;
关键词
Virus; Transmission; Extracellular vesicle; En bloc; Quasispecies; RNA virus; DNA virus; Fitness; Virulence; Population; Multiplicity of infection; Exosome; Phosphatidylserine; HEPATITIS-C VIRUS; LETHAL MUTAGENESIS; EXOSOMES; RNA; RECEPTOR; PHOSPHATIDYLSERINE; CELLS; INFECTION; MULTIPLICITY; DISEASE;
D O I
10.1016/j.virusres.2019.03.023
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
En Bloc transmission of viruses allow multiple genomes to collectivelly penetrate and initiate infection in the same cell, often resulting in enhanced infectivity. Given the quasispecies (mutant cloud) nature of RNA viruses and many DNA viruses, en bloc transmission of multiple genomes provides different starting points in sequence space to initiate adaptive walks, and has implications for modulation of viral fitness and for the response of viral populations to lethal mutagenesis. Mechanisms that can enable multiple viral genomes to be transported en bloc among hosts has only recently been gaining attention. A growing body of research suggests that extracellular vesicles (EV) are highly prevalent and robust vehicles for en bloc delivery of viral particles and naked infectious genomes among organisms. Both RNA and DNA viruses appear to exploit these vesicles to increase their multiplicity of infection and enhance virulence.
引用
收藏
页码:143 / 149
页数:7
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