Author: Kumar, Satyendra; Arankalle, Vidya A.
Title: Intracranial Administration of P Gene siRNA Protects Mice from Lethal Chandipura Virus Encephalitis Document date: 2010_1_7
ID: 1mzq227n_60
Snippet: For the siRNA dosing yielding optimum protection (2 doses, 24hr apart) additional parameters were evaluated. Daily monitoring of CHPV titers in the brain by real time one step RT-PCR (Fig 8) clearly showed 4logs reduction in mice treated with P-2 siRNA when compared to ncsiRNA treated controls. Histopathological analysis demonstrated that P-2 siRNA treated mice brains did not exhibit common features of viral encephalitis seen exclusively in the c.....
Document: For the siRNA dosing yielding optimum protection (2 doses, 24hr apart) additional parameters were evaluated. Daily monitoring of CHPV titers in the brain by real time one step RT-PCR (Fig 8) clearly showed 4logs reduction in mice treated with P-2 siRNA when compared to ncsiRNA treated controls. Histopathological analysis demonstrated that P-2 siRNA treated mice brains did not exhibit common features of viral encephalitis seen exclusively in the control group (Fig 9) . In order to prove that Figure 9 . Histopathology of mice brain treated with P-2 siRNA. Hematoxylin and eosin-stained vertical brain sections from control mice treated with ncsiRNA and infected with CHPV (a, b) and P-2 siRNA treated mice on 5 th day PI (c, d) at indicated magnifications. doi:10.1371/journal.pone.0008615.g009 the protection offered was indeed due to siRNA, we screened sera of survived mice at 7, 14 and 21 days after infection for the presence of anti-CHP-IgG antibodies. Absence of such antibodies demonstrated limited / no viral replication leading to no development of humoral response (Data not shown).
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