Anti-HSV activity of lactoferrin and lactoferricin is dependent on the presence of heparan sulphate at the cell surface

被引:153
作者
Andersen, JH [1 ]
Jenssen, H [1 ]
Sandvik, K [1 ]
Gutteberg, TJ [1 ]
机构
[1] Univ Tromso Hosp, Dept Med Microbiol, N-9038 Tromso, Norway
关键词
antiviral activity; glycosaminoglycans; Herpes virus;
D O I
10.1002/jmv.20171
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学]; 100705 [微生物与生化药学];
摘要
Lactoferrin (LF) is a multifunctional glycoprotein, which plays an important role in immune regulation and defense mechanisms against bacteria, fungi, and viruses. Lactoferricin (Lfcin) is a potent antimicrobial peptide generated from the N-terminal part of LF by pepsin cleavage. In this study, we investigated the mechanisms of the anti-herpes simplex virus (anti-HSV) activity of LF and Lfcin, The results demonstrated that LF and Lfcin inhibited the entry of HSV into Vero cells. LF had no effect against HSV after the virus had entered the cells, while Lfcin exerted antiviral activity also after the initial binding of the virus to the host cell. The distribution of LF and Lfcin in the cells was investigated by immunogold-labeling and transmission electron microscope (TEM). LF was found mainly at the cell surface in cells expressing heparan sulphate. Lfcin was randomly distributed intracellularly. LF must be present at the cell surface to exert antiviral activity, while Lfcin exert its antiviral activity also when found mainly intracellularly. Both LF and Lfcin were dependent on the presence of heparan sulphate at the cell surface to exert their antiviral activity.
引用
收藏
页码:262 / 271
页数:10
相关论文
共 43 条
[1]
Lactoferrin and lactoferricin inhibit Herpes simplex 1 and 2 infection and exhibit synergy when combined with acyclovir [J].
Andersen, JH ;
Jenssen, H ;
Gutteberg, TJ .
ANTIVIRAL RESEARCH, 2003, 58 (03) :209-215
[2]
Lactoferrin and cyclic lactoferricin inhibit the entry of human cytomegalovirus into human fibroblasts [J].
Andersen, JH ;
Osbakk, SA ;
Vorland, LH ;
Traavik, T ;
Gutteberg, TJ .
ANTIVIRAL RESEARCH, 2001, 51 (02) :141-149
[3]
SEQUENTIAL ISOLATION OF PROTEOGLYCAN SYNTHESIS MUTANTS BY USING HERPES-SIMPLEX VIRUS AS A SELECTIVE AGENT - EVIDENCE FOR A PROTEOGLYCAN-INDEPENDENT VIRUS ENTRY PATHWAY [J].
BANFIELD, BW ;
LEDUC, Y ;
ESFORD, L ;
SCHUBERT, K ;
TUFARO, F .
JOURNAL OF VIROLOGY, 1995, 69 (06) :3290-3298
[4]
IDENTIFICATION OF THE BACTERICIDAL DOMAIN OF LACTOFERRIN [J].
BELLAMY, W ;
TAKASE, M ;
YAMAUCHI, K ;
WAKABAYASHI, H ;
KAWASE, K ;
TOMITA, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1121 (1-2) :130-136
[5]
Lactoferrin binds CpG-containing oligonucleotides and inhibits their immunostimulatory effects on human B cells [J].
Britigan, BE ;
Lewis, TS ;
Waldschmidt, M ;
McCormick, ML ;
Krieg, AM .
JOURNAL OF IMMUNOLOGY, 2001, 167 (05) :2921-2928
[6]
BULLEN JJ, 1979, IMMUNOLOGY, V36, P781
[7]
SINGLE AMINO-ACID SUBSTITUTIONS IN GD OF HERPES-SIMPLEX VIRUS-1 CONFER RESISTANCE TO GD-MEDIATED INTERFERENCE AND CAUSE CELL-TYPE-DEPENDENT ALTERATIONS IN INFECTIVITY [J].
DEAN, HJ ;
TERHUNE, SS ;
SHIEH, MT ;
SUSMARSKI, N ;
SPEAR, PG .
VIROLOGY, 1994, 199 (01) :67-80
[8]
Heparin-interacting sites of bovine lactoferrin are involved in anti-adenovirus activity [J].
Di Biase, AM ;
Pietrantoni, A ;
Tinari, A ;
Siciliano, R ;
Valenti, P ;
Antonini, G ;
Seganti, L ;
Superti, F .
JOURNAL OF MEDICAL VIROLOGY, 2003, 69 (04) :495-502
[9]
The herpes simplex virus gE-gI complex facilitates cell-to-cell spread and binds to components of cell junctions [J].
Dingwell, KS ;
Johnson, DC .
JOURNAL OF VIROLOGY, 1998, 72 (11) :8933-8942