Yuta ShiroganeMakoto TakedaMasaharu IwasakiNobuhisa IshiguroHiroki TakeuchiYuichiro NakatsuMaino TaharaHídeaki KikutaYusuke Yanagi
ABSTRACT Human metapneumovirus (HMPV) is a major causative agent of severe bronchiolitis and pneumonia. Its fusion (F) protein must be cleaved by host proteases to cause membrane fusion, a critical step for virus infection. By generating Vero cells constitutively expressing the transmembrane serine protease TMPRSS2 and green fluorescent protein-expressing recombinant HMPV, we show that TMPRSS2, which is expressed in the human lung epithelium, cleaves the HMPV F protein efficiently and supports HMPV multiplication. The results indicate that TMPRSS2 is a possible candidate protease involved in the development of lower respiratory tract illness in HMPV-infected patients.
Markku H. VaaralaKatja PorvariSakari KellokumpuAtte P. KyllönenPirkko Vihko
Mariko EsumiMariko IshibashiHiromi YamaguchiSatomi NakajimaYuhi TaiSachiko KikutaMasahiko SugitaniTadatoshi TakayamaMaino TaharaMakoto TakedaTakaji Wakita
Emile VerhulstMichelle De bruynPascale BerckmansYani SimKoen AugustynsIsabel PintelonMaya BergPieter Van WielendaeleAnne‐Marie LambeirYann G.‐J. SterckxInge NelissenIngrid De Meester