Published February 11, 2011 | Version v1
Journal article

Autophagy is involved in anti-viral activity of pentagalloylglucose (PGG) against Herpes simplex virus type 1 infection in vitro

  • 1. Biomedicine Research and Development Center of Jinan University, Guangzhou, Guangdong 510632 (China)
  • 2. Laboratory of Frontier Science, Tokyo Metropolitan Institute of Medical Science, Bunkyo-ku, Tokyo 113-8613 (Japan)
  • 3. Institute of Tissue Transplantation and Immunology, College of Life Science and Technology, Jinan University, Guangzhou 510632 (China)
  • 4. Division of Molecular Pharmacology of Infectious agents, Department of Molecular Microbiology and Immunology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8521 (Japan)
  • 5. Kunming Institute of Botany, the Chinese Academy of Sciences, Yunnan, Kunming 650204 (China)

Description

Research highlights: → We showed PGG has anti-viral activity against Herpes simplex virus type 1 (HSV-1) and can induce autophgy. → Autophagy may be a novel and important mechanism mediating PGG anti-viral activities. → Inhibition of mTOR pathway is an important mechanism of induction of autophagy by PGG. -- Abstract: Pentagalloylglucose (PGG) is a natural polyphenolic compound with broad-spectrum anti-viral activity, however, the mechanisms underlying anti-viral activity remain undefined. In this study, we investigated the effects of PGG on anti-viral activity against Herpes simplex virus type 1 (HSV-1) associated with autophagy. We found that the PGG anti-HSV-1 activity was impaired significantly in MEF-atg7-/- cells (autophagy-defective cells) derived from an atg7-/- knockout mouse. Transmission electron microscopy revealed that PGG-induced autophagosomes engulfed HSV-1 virions. The mTOR signaling pathway, an essential pathway for the regulation of autophagy, was found to be suppressed following PGG treatment. Data presented in this report demonstrated for the first time that autophagy induced following PGG treatment contributed to its anti-HSV activity in vitro.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2011.01.006

Additional details

Identifiers

DOI
10.1016/j.bbrc.2011.01.006;
PII
S0006-291X(11)00012-X;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
405
Journal Issue
2
Journal Page Range
p. 186-191
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45025695
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
HERPES SIMPLEX; IN VITRO; INHIBITION; KNOCK-OUT REACTIONS; MICE; TRANSMISSION ELECTRON MICROSCOPY; VIRUSES
Descriptors DEC
ANIMALS; DIRECT REACTIONS; DISEASES; ELECTRON MICROSCOPY; INFECTIOUS DISEASES; MAMMALS; MICROORGANISMS; MICROSCOPY; NUCLEAR REACTIONS; PARASITES; RODENTS; SKIN DISEASES; VERTEBRATES; VIRAL DISEASES

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.