LL-37 disrupts the Kaposi's sarcoma-associated herpesvirus envelope and inhibits infection in oral epithelial cells.
Brice. David C DC; Toth. Zsolt Z; Diamond. Gill G
Key Findings
- LL-37 reduces KSHV infection of oral epithelial cells in a dose‑ and structure‑dependent way
- The peptide works by disrupting the viral envelope, blocking entry
- The antiviral action is due to direct interaction with the virus, not changes to the host cells
Practical Outcomes
- Boosting LL-37 levels in the mouth—through vitamin D, certain probiotics, or future topical formulations—might help protect against oral KSHV infection, but human studies are needed before any concrete protocol can be recommended.
Summary
LL-37, a natural antimicrobial peptide, can break apart the outer shell of Kaposi's sarcoma‑associated herpesvirus, stopping the virus from infecting mouth‑lining cells in lab tests. The effect comes from the peptide acting directly on the virus, not on the human cells.
Abstract
Oral epithelial cells (OECs) represent the first line of defense against viruses that are spread via saliva, including Kaposi's sarcoma-associated herpesvirus (KSHV). Infection of humans by KSHV and viral pathogenesis begins by infecting OECs. One method OECs use to limit viral infections in the oral cavity is the production of antimicrobial peptides (AMPs), or host defense peptides (HDPs). However, no studies have investigated the antiviral activities of any HDP against KSHV. The goal of this study was to determine the antiviral activity of one HDP, LL-37, against KSHV in the context of infecting OECs. Our results show that LL-37 significantly decreased KSHV's ability to infect OECs in both a structure- and dose-dependent manner. However, this activity does not stem from affecting OECs, but instead the virions themselves. We found that LL-37 exerts its antiviral activity against KSHV by disrupting the viral envelope, which can inhibit viral entry into OECs. Our data suggest that LL-37 exhibits a marked antiviral activity against KSHV during infection of oral epithelial cells, which can play an important role in host defense against oral KSHV infection. Thus, we propose that inducing LL-37 expression endogenously in oral epithelial cells, or potentially introducing as a therapy, may help restrict oral KSHV infection and ultimately KSHV-associated diseases.
Study Information
pubmed
2018
2018-08-02T00:00:00.000Z
10.1016/j.antiviral.2018.07.025
43
79