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10.1016/j.celrep.2017.02.014

http://scihub22266oqcxt.onion/10.1016/j.celrep.2017.02.014
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C5340982!5340982!28249158
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suck abstract from ncbi


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pmid28249158      Cell+Rep 2017 ; 18 (9): 2113-23
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  • Ultrastructural Characterization of Zika Virus Replication Factories #MMPMID28249158
  • Cortese M; Goellner S; Acosta EG; Neufeldt CJ; Oleksiuk O; Lampe M; Haselmann U; Funaya C; Schieber N; Ronchi P; Schorb M; Pruunsild P; Schwab Y; Chatel-Chaix L; Ruggieri A; Bartenschlager R
  • Cell Rep 2017[Feb]; 18 (9): 2113-23 PMID28249158show ga
  • A global concern has emerged with the pandemic spread of Zika virus (ZIKV) infections that can cause severe neurological symptoms in adults and newborns. ZIKV is a positive-strand RNA virus replicating in virus-induced membranous replication factories (RFs). Here we used various imaging techniques to investigate the ultrastructural details of ZIKV RFs and their relationship with host cell organelles. Analyses of human hepatic cells and neural progenitor cells infected with ZIKV revealed endoplasmic reticulum (ER) membrane invaginations containing pore-like openings toward the cytosol, reminiscent to RFs in Dengue virus-infected cells. Both the MR766 African strain and the H/PF/2013 Asian strain, the latter linked to neurological diseases, induce RFs of similar architecture. Importantly, ZIKV infection causes a drastic reorganization of microtubules and intermediate filaments forming cage-like structures surrounding the viral RF. Consistently, ZIKV replication is suppressed by cytoskeleton-targeting drugs. Thus, ZIKV RFs are tightly linked to rearrangements of the host cell cytoskeleton.
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