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Propagation of this virus depended on VP2 being supplied\n                    <jats:italic>in trans<\/jats:italic>\n                    , indicating that this virus could infect only once. Our findings help to elucidate the functions of VP2 in the virus lifecycle and to develop other caliciviral vectors for recombinant attenuated live enteric virus vaccines or therapeutics tools.\n                  <\/jats:p>","DOI":"10.1128\/jvi.01261-23","type":"journal-article","created":{"date-parts":[[2024,1,16]],"date-time":"2024-01-16T09:00:34Z","timestamp":1705395634000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":10,"title":["Production of infectious reporter murine norovirus by VP2\n                    <i>trans<\/i>\n                    -complementation"],"prefix":"10.1128","volume":"98","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4614-6481","authenticated-orcid":false,"given":"Ryoka","family":"Ishiyama","sequence":"first","affiliation":[{"name":"Department of Infection Control and Immunology, Laboratory of Viral Infection, \u014cmura Satoshi Memorial Institute &amp; Graduate School of Infection 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