Picornaviruses are small, about 300 angstroms in diameter, and are comprised of an icosahedral protein coat and a single-stranded positive sense RNA genome.

Poliovirus infection occurs by the fecal-oral route, when the host ingests the virus, which replicates in the alimentary tract. The virus is then shed in the feces. Most polio infections are asymptomatic. In about 5 percent of cases, the virus replicates in other tissues. Paralytic poliomyelitis occurs in less than 1 percent of cases.

Viral entry

Poliovirus infection begins with the virus binds to the receptor CD155 on the host cell surface. CD155 is an immunoglobulin-like receptor also known as poliovirus receptor. Upon binding, an irreversible conformational change occurs to the viral particle. The mechanism by which the virus enters the cell is believed to be receptor-mediated endocytosis, after which the viral RNA is released into the cellular cytoplasm.

Polio has a positive sense RNA viral genome. That means it can be directly translated into protein by the host cell. The viral proteins of poliovirus are:

• 3D(pol)--an RNA dependent RNA polymerase
• 2A(pro) 3C(pro)/3CD(pro)--proteases that cleave the viral polypeptide
• VPg (3B)--binds viral RNA and is required for synthesis of RNA
• 2BC, 2B,2C, 3AB, 3A, 3B--protein complex needed for viral replication
• VP0--cleaved into VP1 and VP3, and VP2 and VP4, the proteins of the viral capsid

Journal of Antivirals & Antiretrovirals is using Editorial Manager System for quality in review process. Editorial Manager is an online manuscript submission, review and tracking systems used by most of the best open access journals. Review processing is performed by the editorial board members of journal or outside experts; at least two independent reviewers approval followed by editor's approval is required for acceptance of any citable manuscript.

Send your manuscript at www.longdom.org/submissions/antivirals-antiretrovirals.html or as an e-mail attachment to our Editorial Office at manuscripts@longdom.org

Picornaviruses are small, about 300 angstroms in diameter, and are comprised of an icosahedral protein coat and a single-stranded positive sense RNA genome.

Poliovirus infection occurs by the fecal-oral route, when the host ingests the virus, which replicates in the alimentary tract. The virus is then shed in the feces. Most polio infections are asymptomatic. In about 5 percent of cases, the virus replicates in other tissues. Paralytic poliomyelitis occurs in less than 1 percent of cases.

Viral entry

Poliovirus infection begins with the virus binds to the receptor CD155 on the host cell surface. CD155 is an immunoglobulin-like receptor also known as poliovirus receptor. Upon binding, an irreversible conformational change occurs to the viral particle. The mechanism by which the virus enters the cell is believed to be receptor-mediated endocytosis, after which the viral RNA is released into the cellular cytoplasm.

Polio has a positive sense RNA viral genome. That means it can be directly translated into protein by the host cell. The viral proteins of poliovirus are:

• 3D(pol)--an RNA dependent RNA polymerase
• 2A(pro) 3C(pro)/3CD(pro)--proteases that cleave the viral polypeptide
• VPg (3B)--binds viral RNA and is required for synthesis of RNA
• 2BC, 2B,2C, 3AB, 3A, 3B--protein complex needed for viral replication
• VP0--cleaved into VP1 and VP3, and VP2 and VP4, the proteins of the viral capsid

Journal of Antivirals & Antiretrovirals is using Editorial Manager System for quality in review process. Editorial Manager is an online manuscript submission, review and tracking systems used by most of the best open access journals. Review processing is performed by the editorial board members of journal or outside experts; at least two independent reviewers approval followed by editor's approval is required for acceptance of any citable manuscript.

Send your manuscript at www.longdom.org/submissions/antivirals-antiretrovirals.html or as an e-mail attachment to our Editorial Office at manuscripts@longdom.org