Abstract

Insect transmission is obligatory for persistently transmitted viruses because the vector insect is the only means of virus spread in nature. The insect midgut is the first major barrier limiting virus acquisition, but the mechanisms by which viruses are able to cross the cell membrane and then infect the midgut epithelial cells of the insect have not been elucidated completely. Here, we found that the outer capsid or nucleocapsid protein (NP) of three viruses can interact and colocalize with sugar transporter 6 that is highly expressed in the midgut of Laodelphax striatellus (LsST6). In contrast, LsST6 did not interact with the NP of rice grassy stunt virus, which cannot be transmitted by the same planthopper. LsST6 not only altered the cellular location of viral proteins and then colocalized with them in the cell membrane, but also mediated the entry of rice stripe virus (RSV) particles into Spodoptera frugiperda 9 (Sf9) cells that expressed the heterologous gene LsST6. We further showed that RSV particles initially bound to the cell membrane of midgut epithelial cells where it colocalized with LsST6, and then invaded the cytoplasm. When LsST6 expression was knocked down, viral titre, acquisition percentage and transmission efficiency of the treated insect decreased significantly, but virus replication was not affected. This work thus uncovered a strategy by which LsST6 mediates viral entry into midgut epithelial cells and leads to successful transmission by the insect vector.

Highlights

  • Many viruses persistently transmitted by arthropods cause serious diseases in plants, animals and humans

  • Studies on the insect midgut, the first barrier for virus transmission, and its interactions with viruses and parasites are fundamental to understanding the transmission mechanism in vector insects and the epidemics caused by the vectored pathogen

  • Virus invasion of midgut epithelial cells is mediated by sugar transporter 6 in its insect vector

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Summary

Introduction

Many viruses persistently transmitted by arthropods cause serious diseases in plants, animals and humans. Plant viruses transmitted in a persistent propagative manner and animal arboviruses follow a similar circulative route within their insect vectors. After they are acquired from plant sap or blood ingested by the insect, the virions must first cross the cell membrane of the midgut epithelial cells where the viral particles multiply [11]. They must leave the midgut to disseminate to other tissues including the salivary glands, from where they can be transmitted to new hosts [12]. Arboviruses must overcome multiple barriers, including the infection and dissemination barriers of the midgut, salivary gland escape barrier, and transovarial barrier [13, 14]

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