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Volume 32 Issue 3
June 2017
    Citation: Waqas Ahmad, Yingying Li, Yidi Guo, Xinyu Wang, Ming Duan, Zhenhong Guan, Zengshan Liu, Maolin Zhang. Rabies virus co-localizes with early (Rab5) and late (Rab7) endosomal proteins in neuronal and SH-SY5Y cells .VIROLOGICA SINICA, 2017, 32(3) : 207-215.  http://dx.doi.org/10.1007/s12250-017-3968-9
    shu

    Rabies virus co-localizes with early (Rab5) and late (Rab7) endosomal proteins in neuronal and SH-SY5Y cells

    Rabies virus colocalizes with endosomal proteins

    cstr: 32224.14.s12250-017-3968-9
    • 1.

      Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun 130062, China

    • 2.

      Section of Epidemiology and Public Health, College of Veterinary and Animal Sciences, Jhang 35200, Pakistan

    • Corresponding author: Maolin Zhang, zhrei98@163.com, ORCID: 0000-0001-9217-3643
    • Received Date: 04 March 2017
      Accepted Date: 09 May 2017
      Published Date: 16 June 2017
      Available online: 01 June 2017
    • Rabies virus (RABV) is a highly neurotropic virus that follows clathrin-mediated endocytosis and pH-dependent pathway for trafficking and invasion into endothelial cells.Early (Rab5,EEA1) and late (Rab7,LAMP1) endosomal proteins play critical roles in endosomal sorting,maturity and targeting various molecular cargoes,but their precise functions in the early stage of RABV neuronal infection remain elusive.In this study,the relationship between enigmatic entry of RABV with these endosomal proteins into neuronal and SH-SY5Y cells was investigated. Immunofluorescence,TCID50 titers,electron microscopy and western blotting were carried out to determine the molecular interaction of the nucleoprotein (N) of RABV with early or late endosomal proteins in these cell lines.The expression of N was also determined by down-regulating Rab5 and Rab7 in both cell lines through RNA interference.The results were indicative that N proficiently colocalized with Rab5/EEA1 and Rab7/LAMP1 in both cell lines at 24 and 48 h post-infection,while N titers significantly decreased in early infection of RABV.Down-regulation of Rab5 and Rab7 did not inhibit N expression,but it prevented productive infection via blocking the normal trafficking of RABV in a low pH environment.Ultrathin sections of cells studied by electron microscope also verified the close association of RABV with Rab5 and Rab7 in neurons.From the data it was concluded that primary entry of RABV strongly correlates with the kinetics of Rab-proteins present on early and late vesicles,which provides helpful clues to explain the early events of RABV in nerve cells.
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      Rabies virus co-localizes with early (Rab5) and late (Rab7) endosomal proteins in neuronal and SH-SY5Y cells

        Corresponding author: Maolin Zhang, zhrei98@163.com
      • 1. Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun 130062, China
      • 2. Section of Epidemiology and Public Health, College of Veterinary and Animal Sciences, Jhang 35200, Pakistan
      • Received Date: 04 March 2017
      • Accepted Date: 09 May 2017
      • Published Date: 16 June 2017

      Abstract: Rabies virus (RABV) is a highly neurotropic virus that follows clathrin-mediated endocytosis and pH-dependent pathway for trafficking and invasion into endothelial cells.Early (Rab5,EEA1) and late (Rab7,LAMP1) endosomal proteins play critical roles in endosomal sorting,maturity and targeting various molecular cargoes,but their precise functions in the early stage of RABV neuronal infection remain elusive.In this study,the relationship between enigmatic entry of RABV with these endosomal proteins into neuronal and SH-SY5Y cells was investigated. Immunofluorescence,TCID50 titers,electron microscopy and western blotting were carried out to determine the molecular interaction of the nucleoprotein (N) of RABV with early or late endosomal proteins in these cell lines.The expression of N was also determined by down-regulating Rab5 and Rab7 in both cell lines through RNA interference.The results were indicative that N proficiently colocalized with Rab5/EEA1 and Rab7/LAMP1 in both cell lines at 24 and 48 h post-infection,while N titers significantly decreased in early infection of RABV.Down-regulation of Rab5 and Rab7 did not inhibit N expression,but it prevented productive infection via blocking the normal trafficking of RABV in a low pH environment.Ultrathin sections of cells studied by electron microscope also verified the close association of RABV with Rab5 and Rab7 in neurons.From the data it was concluded that primary entry of RABV strongly correlates with the kinetics of Rab-proteins present on early and late vesicles,which provides helpful clues to explain the early events of RABV in nerve cells.

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