| Autor: |
Chander, Yogesh, Kumar, Ram, Verma, Assim, Khandelwal, Nitin, Nagori, Himanshu, Singh, Namita, Sharma, Shalini, Pal, Yash, Puvar, Apurvasinh, Pandit, Rameshchandra, Shukla, Nitin, Chavada, Priyank, Tripathi, Bhupendra N, Barua, Sanjay, Kumar, Naveen |
| Předmět: |
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| Zdroj: |
Molecular Biology & Evolution; Sep2022, Vol. 39 Issue 9, p1-16, 16p |
| Abstrakt: |
Host-dependency factors have increasingly been targeted to minimize antiviral drug resistance. In this study, we have demonstrated that inhibition of p38 mitogen-activated protein kinase (a cellular protein) suppresses buffalopox virus (BPXV) protein synthesis by targeting p38-MNK1-eIF4E signaling pathway. In order to provide insights into the evolution of drug resistance, we selected resistant mutants by long-term sequential passages (P; n = 60) in the presence of p38 inhibitor (SB239063). The P60-SB239063 virus exhibited significant resistance to SB239063 as compared to the P60-Control virus. To provide mechanistic insights on the acquisition of resistance by BPXV-P60-SB239063, we generated p38-α and p38-ϒ (isoforms of p38) knockout Vero cells by CRISPR/Cas9-mediated genome editing. It was demonstrated that unlike the wild type (WT) virus which is dependent on p38-α isoform, the resistant virus (BPXV-P60-SB239063) switches over to use p38-ϒ so as to efficiently replicate in the target cells. This is a rare evidence wherein a virus was shown to bypass the dependency on a critical cellular factor under selective pressure of a drug. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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