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Isolation and identification of compounds from Kalanchoe pinnata having human alphaherpesvirus and vaccinia virus antiviral activity.

Authors :
Cryer M
Lane K
Greer M
Cates R
Burt S
Andrus M
Zou J
Rogers P
Hansen MD
Burgado J
Panayampalli SS
Day CW
Smee DF
Johnson BF
Source :
Pharmaceutical biology [Pharm Biol] 2017 Dec; Vol. 55 (1), pp. 1586-1591.
Publication Year :
2017

Abstract

Context: Kalanchoe pinnata (Lam.) Pers. (Crassulaceae) is a succulent plant that is known for its traditional antivirus and antibacterial usage.<br />Objective: This work examines two compounds identified from the K. pinnata plant for their antivirus activity against human alphaherpesvirus (HHV) 1 and 2 and vaccinia virus (VACV).<br />Materials and Methods: Compounds KPB-100 and KPB-200 were isolated using HPLC and were identified using NMR and MS. Both compounds were tested in plaque reduction assay of HHV-2 wild type (WT) and VACV. Both compounds were then tested in virus spread inhibition and virus yield reduction (VYR) assays of VACV. KPB-100 was further tested in viral cytopathic effect (CPE) inhibition assay of HHV-2 TK-mutant and VYR assay of HHV-1 WT.<br />Results: KPB-100 and KPB-200 inhibited HHV-2 at IC <subscript>50</subscript> values of 2.5 and 2.9 μg/mL, respectively, and VACV at IC <subscript>50</subscript> values of 3.1 and 7.4 μg/mL, respectively, in plaque reduction assays. In virus spread inhibition assay of VACV KPB-100 and KPB-200 yielded IC <subscript>50</subscript> values of 1.63 and 13.2 μg/mL, respectively, and KPB-100 showed a nearly 2-log reduction in virus in VYR assay of VACV at 20 μg/mL. Finally, KPB-100 inhibited HHV-2 TK- at an IC <subscript>50</subscript> value of 4.5 μg/mL in CPE inhibition assay and HHV-1 at an IC <subscript>90</subscript> of 3.0 μg/mL in VYR assay.<br />Discussion and Conclusion: Both compounds are promising targets for synthetic optimization and in vivo study. KPB-100 in particular showed strong inhibition of all viruses tested.

Details

Language :
English
ISSN :
1744-5116
Volume :
55
Issue :
1
Database :
MEDLINE
Journal :
Pharmaceutical biology
Publication Type :
Academic Journal
Accession number :
28395583
Full Text :
https://doi.org/10.1080/13880209.2017.1310907