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      Vesicle-Cloaked Virus Clusters Are Optimal Units for Inter-organismal Viral Transmission

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          Abstract

          <p class="first" id="P2">In enteric viral infections, such as those with rotavirus and norovirus, individual viral particles shed in stool are considered the optimal units of fecal-oral transmission. We reveal that rotaviruses and noroviruses are also shed in stool as viral clusters enclosed within vesicles that deliver a high inoculum to the receiving host. Cultured cells non-lytically release rotaviruses and noroviruses inside extracellular vesicles. Additionally, stools of infected hosts contain norovirus and rotavirus within vesicles of exosomal or plasma membrane origin. These vesicles remain intact during fecal-oral transmission and thereby transport multiple viral particles collectively to the next host, enhancing both the multiplicity of infection and disease severity. Vesicle-cloaked viruses are non-negligible populations in stool and have a disproportionately larger contribution toinfectivity than free viruses. Our findings indicate that vesicle-cloaked viruses are highly virulent units of fecal-oral transmission and highlight a need for antivirals targeting vesicles and virus clustering. </p><p class="first" id="P3"> <div class="figure-container so-text-align-c"> <img alt="" class="figure" src="/document_file/c49eb3fd-9f75-4a46-84a7-0c6d2dd83512/PubMedCentral/image/nihms-982511-f0001.jpg"/> </div> </p><p id="P4">Freely disseminating standalone viral particles are considered the optimal agents for spreading infection. Santiana et al., discover that enteric viruses are also shed in feces as viral clusters cloaked in vesicles. These virus-containing vesicles are a more potent infectious form that enhances the multiplicity of infection and disease severity. </p>

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          Author and article information

          Journal
          Cell Host & Microbe
          Cell Host & Microbe
          Elsevier BV
          19313128
          August 2018
          August 2018
          : 24
          : 2
          : 208-220.e8
          Article
          10.1016/j.chom.2018.07.006
          6226266
          30092198
          6b5909f6-7114-4e1e-9a81-8fbf9d0b42e1
          © 2018

          https://www.elsevier.com/tdm/userlicense/1.0/

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