| Literature DB >> 33561699 |
Miyuki Kimura1, Kazutaka Egawa2, Tatsuhiko Ozawa3, Hiroyuki Kishi3, Masayuki Shimojima4, Satoshi Taniguchi4, Shuetsu Fukushi4, Hikaru Fujii5, Hiroshi Yamada1, Long Tan1, Kaori Sano6, Harutaka Katano6, Tadaki Suzuki6, Shigeru Morikawa7, Masayuki Saijo4, Hideki Tani8.
Abstract
The heartland virus (HRTV) is a novel phlebovirus that causes severe infections in the USA and closely related to the severe fever thrombocytopenia syndrome virus (SFTSV), a causative agent for SFTS in Asia. The entry mechanisms of HRTV remain unclear. Here, we developed the pseudotyped vesicular stomatitis virus bearing the HRTV glycoprotein (GP) (HRTVpv), and the antigenicity and the entry mechanisms of HRTV were analyzed. HRTVpv was neutralized by anti-SFTSV Gc antibody, but not the anti-SFTSV Gn antibodies. Entry of HRTVpv to cells was inhibited by bafilomycin A1 and dynasore, and but it was enhanced in cells overexpressed with C-type lectins. Production of infectious HRTVpv and SFTSVpv was reduced by Nn-DNJ, α-glucosidase inhibitor. The entry of HRTV occurs via pH- and dynamin-dependent endocytosis. Furthermore, Nn-DNJ may be a possible therapeutic agent against HRTV and SFTSV.Entities:
Keywords: Antigenicity; Glycoprotein; Heartland virus (HRTV); Host cell entry; Pseudotyped virus; Severe fever thrombocytopenia syndrome virus (SFTSV)
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Year: 2020 PMID: 33561699 DOI: 10.1016/j.virol.2020.10.006
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616