2017
Cryo-EM study of slow bee paralysis virus at low pH reveals iflavirus genome release mechanism
KALYNYCH, Sergei, Tibor FÜZIK, Antonin PRIDAL, Joachim DE MIRANDA, Pavel PLEVKA et. al.Základní údaje
Originální název
Cryo-EM study of slow bee paralysis virus at low pH reveals iflavirus genome release mechanism
Autoři
KALYNYCH, Sergei (124 Kanada, domácí), Tibor FÜZIK (703 Slovensko, domácí), Antonin PRIDAL (203 Česká republika), Joachim DE MIRANDA (752 Švédsko) a Pavel PLEVKA (203 Česká republika, garant, domácí)
Vydání
Proceedings of the National Academy of Sciences of the United States of America, WASHINGTON, National Academy of Sciences, 2017, 0027-8424
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10600 1.6 Biological sciences
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 9.504
Kód RIV
RIV/00216224:14740/17:00096214
Organizační jednotka
Středoevropský technologický institut
UT WoS
000392095800054
Klíčová slova anglicky
electron microscopy; uncoating; honeybee; structure; virus
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 23. 2. 2018 12:31, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
Viruses from the family Iflaviridae are insect pathogens. Many of them, including slow bee paralysis virus (SBPV), cause lethal diseases in honeybees and bumblebees, resulting in agricultural losses. Iflaviruses have nonenveloped icosahedral virions containing single-stranded RNA genomes. However, their genome release mechanism is unknown. Here, we show that low pH promotes SBPV genome release, indicating that the virus may use endosomes to enter host cells. We used cryo-EM to study a heterogeneous population of SBPV virions at pH 5.5. We determined the structures of SBPV particles before and after genome release to resolutions of 3.3 and 3.4 angstrom, respectively. The capsids of SBPV virions in low pH are not expanded. Thus, SBPV does not appear to form "altered" particles with pores in their capsids before genome release, as is the case in many related picornaviruses. The egress of the genome from SBPV virions is associated with a loss of interpentamer contacts mediated by N-terminal arms of VP2 capsid proteins, which result in the expansion of the capsid. Pores that are 7 angstrom an diameter form around icosahedral threefold symmetry axes. We speculate that they serve as channels for the genome release. Our findings provide an atomic-level characterization of the genome release mechanism of iflaviruses.
Návaznosti
LM2010005, projekt VaV |
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LM2015043, projekt VaV |
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LQ1601, projekt VaV |
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