{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T18:59:11Z","timestamp":1785437951588,"version":"3.56.0"},"reference-count":58,"publisher":"American Society for Microbiology","issue":"2","license":[{"start":{"date-parts":[[2026,2,17]],"date-time":"2026-02-17T00:00:00Z","timestamp":1771286400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,2,17]],"date-time":"2026-02-17T00:00:00Z","timestamp":1771286400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["31870155"],"award-info":[{"award-number":["31870155"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Virol"],"published-print":{"date-parts":[[2026,2,17]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      Autographa californica multiple nucleopolyhedrovirus (AcMNPV) E18 (AC143, ODV-E18) is an envelope protein common to both occlusion-derived virions (ODVs) and budded virions (BVs). The\n                      <jats:italic toggle=\"yes\">e18<\/jats:italic>\n                      gene has been demonstrated to be essential for generating infectious BVs. However, its functional role in virion morphogenesis remains unclear. In this study, we constructed an\n                      <jats:italic toggle=\"yes\">e18<\/jats:italic>\n                      knockout virus and an\n                      <jats:italic toggle=\"yes\">e18<\/jats:italic>\n                      repair virus to investigate the effects of\n                      <jats:italic toggle=\"yes\">e18<\/jats:italic>\n                      deletion on virion morphogenesis. Our data indicated that\n                      <jats:italic toggle=\"yes\">e18<\/jats:italic>\n                      is required for normal intranuclear microvesicle (IMV) formation and accumulation, for intranuclear envelopment and nuclear egress of nucleocapsids, as well as for embedding of ODVs into occlusion bodies (OBs) and BV production. Additionally, we created and characterized a series of recombinant viruses with truncated\n                      <jats:italic toggle=\"yes\">e18<\/jats:italic>\n                      of varying lengths to identify domains involved in nuclear translocation and virion morphogenesis. We identified two low-complexity domains (LCDs) in E18, in addition to a known transmembrane domain (TM). The AA30-34 sequence within the TM was found to be essential, but not sufficient for nuclear translocation. However, an \u03b1-helix structure encompassing the TM domain proved adequate to mediate a fusion protein\u2019s trafficking into the nucleus in the context of additional viral factors. Furthermore, we discovered that the TM was required for the accumulation of IMVs, while both the TM and LCD 1 were necessary for intranuclear envelopment, nuclear egress of nucleocapsids, and the embedding of ODVs into OBs; LCD 2 influenced the processing of IMVs and ODV formation. Both the TM and the two LCDs were essential for BV production.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        The envelope protein E18 is a conserved component common to both ODV and BV virion types of baculoviruses, yet its functional role in virion morphogenesis remains unclear. This study investigated the\n                        <jats:italic toggle=\"yes\">e18<\/jats:italic>\n                        gene of Autographa californica multiple nucleopolyhedrovirus, determining that it is essential for normal IMV formation and accumulation, intranuclear envelopment and nuclear egress of nucleocapsids, as well as for the embedding of ODVs into occlusion bodies and BV production. The functional roles of the single TM domain and two LCD domains within E18 during virion morphogenesis were identified. Furthermore, it was found that an \u03b1-helix structure encompassing the TM domain is sufficient to facilitate the trafficking of a fusion protein into the nucleus in the context of other viral factors, with AA30-34 being critical for the nuclear import of E18.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/jvi.01338-25","type":"journal-article","created":{"date-parts":[[2026,1,6]],"date-time":"2026-01-06T14:00:41Z","timestamp":1767708041000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Autographa californica multiple nucleopolyhedrovirus\n                    <i>e18<\/i>\n                    is essential for the formation of normal intranuclear membrane microvesicles and intranuclear envelopment and nuclear egress of nucleocapsids"],"prefix":"10.1128","volume":"100","author":[{"given":"Lingqian","family":"Wang","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03x1jna21","id-type":"ROR","asserted-by":"publisher"}],"name":"Hubei Key Laboratory of Genetic Regulation and Integrative Biology, College of Life Sciences, Central China Normal University","place":["Wuhan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaowei","family":"Zhou","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03x1jna21","id-type":"ROR","asserted-by":"publisher"}],"name":"Hubei Key Laboratory of Genetic Regulation and Integrative Biology, College of Life Sciences, Central China Normal University","place":["Wuhan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiyu","family":"Zhao","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03x1jna21","id-type":"ROR","asserted-by":"publisher"}],"name":"Hubei Key Laboratory of Genetic Regulation and Integrative Biology, College of Life Sciences, Central China Normal University","place":["Wuhan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaotao","family":"Zeng","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03x1jna21","id-type":"ROR","asserted-by":"publisher"}],"name":"Hubei Key Laboratory of Genetic Regulation and Integrative Biology, College of Life Sciences, Central China Normal University","place":["Wuhan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0002-3287-7117","authenticated-orcid":true,"given":"Lu-Lin","family":"Li","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03x1jna21","id-type":"ROR","asserted-by":"publisher"}],"name":"Hubei Key Laboratory of Genetic Regulation and Integrative Biology, College of Life Sciences, Central China Normal University","place":["Wuhan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_3_2_2","volume-title":"Baculovirus molecular biology","author":"Rohrmann GF","year":"2019","unstructured":"Rohrmann GF. 2019. 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