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Developing therapeutic tools relies on a better understanding of their multiplication cycle. For these viruses, the genome replication and transcription activities most\u2010often segregate in membrane\u2010less environments called inclusion bodies (IBs) or viral factories. These \u201corganelles\u201d usually locate far from the cell surface from where new virions are released, and \u2010ssRNA viruses do not encode for transport factors. The efficient trafficking of the genome progeny toward the cell surface is most often ensured by mechanisms co\u2010opting the cellular machineries.<\/jats:p>\n                    <jats:p>In this review, for each \u2010ssRNA viral family, we cover the methods employed to characterize these host\u2010virus interactions, the strategies used by the viruses to promote the virus genome transport, and the current gaps in the literature. Finally, we highlight how Rab11 has emerged as a target of choice for the intracellular transport of \u2010ssRNA virus genomes.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/boc.202200059","type":"journal-article","created":{"date-parts":[[2022,10,3]],"date-time":"2022-10-03T21:34:48Z","timestamp":1664832888000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":12,"title":["Ribonucleoprotein transport in Negative Strand RNA viruses"],"prefix":"10.1111","volume":"115","author":[{"given":"C\u00e9dric","family":"Diot","sequence":"first","affiliation":[{"name":"Universit\u00e9 Paris\u2010Saclay \u2013 Universit\u00e9 de Versailles St. Quentin UMR 1173 (2I) INSERM  Montigny\u2010le\u2010Bretonneux France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gina","family":"Cosentino","sequence":"additional","affiliation":[{"name":"Universit\u00e9 Paris\u2010Saclay \u2013 Universit\u00e9 de Versailles St. 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