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Novel antiviral activity of chemokines

Journal Article · · Virology
 [1];  [2];  [1];  [1];  [1];  [1];  [1];  [3];  [2];  [1]
  1. Department of Microbiology, Kinki University School of Medicine, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka 589-8511 (Japan)
  2. Department of Ophthalmology, Kinki University School of Medicine, Osaka (Japan)
  3. Department of Biotechnological Science, Kinki University, Wakayama (Japan)
Antimicrobial peptides are a diverse family of small, mostly cationic polypeptides that kill bacteria, fungi and even some enveloped viruses, while chemokines are a group of mostly cationic small proteins that induce directed migration of leukocytes through interactions with a group of seven transmembrane G protein-coupled receptors. Recent studies have shown that antimicrobial peptides and chemokines have substantially overlapping functions. Thus, while some antimicrobial peptides are chemotactic for leukocytes, some chemokines can kill a wide range of bacteria and fungi. Here, we examined a possible direct antiviral activity of chemokines against an enveloped virus HSV-1. Among 22 human chemokines examined, chemokines such as MIP-1{alpha}/CCL3, MIP-1{beta}/CCL4 and RANTES/CCL5 showed a significant direct antiviral activity against HSV-1. It is intriguing that these chemokines are mostly known to be highly expressed by effector CD8{sup +} T cells. The chemokines with a significant anti-HSV-1 activity commonly bound to HSV-1 virions via envelope glycoprotein gB. Electron microscopy revealed that the chemokines with a significant anti-HSV-1 activity were commonly capable of generating pores in the envelope of HSV-1. Thus, some chemokines have a significant direct antiviral activity against HSV-1 in vitro and may have a potential role in host defense against HSV-1 as a direct antiviral agent.
OSTI ID:
20850530
Journal Information:
Virology, Journal Name: Virology Journal Issue: 2 Vol. 350; ISSN VIRLAX; ISSN 0042-6822
Country of Publication:
United States
Language:
English