Protective efficacy of a sulfated sialyl lipid (NMSO3) against human rotavirus-induced diarrhea in a mouse model

被引:22
作者
Takahashi, K
Ohashi, K
Abe, Y
Mori, S
Taniguchi, K
Ebina, T
Nakagomi, O
Terada, M
机构
[1] Fukushima Med Univ, Sch Med, Dept Microbiol, Fukushima 9601295, Japan
[2] Fujita Hlth Univ, Sch Med, Dept Virol & Parasitol, Aichi, Japan
[3] Miyagi Canc Ctr Res Inst, Div Immunol, Natori, Miyagi, Japan
[4] Akita Univ, Dept Microbiol, Akita 010, Japan
[5] Nissin Food Prod Co Ltd, Cent Res Inst, Shiga, Japan
关键词
D O I
10.1128/AAC.46.2.420-424.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antiviral activity of sulfated sialyl lipid (NMSO3) against human rotavirus (RV) was examined in vitro and in vivo. NMSO3 inhibited the replication of four major serotypes (G1 to G4) of human rotavirus with a low 50% effective concentration of 1 to 5 mug/ml and 50% cytotoxic concentration of 153 mug/ml when determined by plaque assays with MA104 cells. Exposure of NMSO3 to HCl (pH 2.0) for 30 min exhibited no loss of anti-RV activity. Time-of-addition experiments revealed that NMSO3 inhibited the adsorption of four serotypes of RV to MA104 cells. Furthermore, an assay of virus binding with radiolabeled RVs revealed that NMSO3 inhibited the binding of virus to MA104 cells, suggesting that NMSO3 may bind to VP4 and/or VP7. Prophylactic oral administration of NMSO3 (10 mug three times per day, 4 days) to fire suckling mice starting 30 min before inoculation of MO strain (3 x 10(6) PFU/mouse) prevented the development of diarrhea. Four of five mice showed no stool or brown formed stool, and only one mouse showed brown soft stool, while water treatment caused watery diarrhea in all five mice. The mean titer of antibody to RV in mice which received NMSO3 at 10 mug three times per day for 4 days was significantly lower than that of untreated, infected mice. NMSO3 is a promising candidate for the prophylactic treatment of human RVs.
引用
收藏
页码:420 / 424
页数:5
相关论文
共 20 条
[1]  
CHAKRAVARTI A, 1992, J DIARRHOEAL DIS RES, V10, P21
[2]   DETERMINANTS OF ROTAVIRUS STABILITY AND DENSITY DURING CSCL PURIFICATION [J].
CHEN, DY ;
RAMIG, RF .
VIROLOGY, 1992, 186 (01) :228-237
[3]   An in vitro study of theaflavins extracted from black tea to neutralize bovine rotavirus and bovine coronavirus infections [J].
Clark, KJ ;
Grant, PG ;
Sarr, AB ;
Belakere, JR ;
Swaggerty, CL ;
Phillips, TD ;
Woode, GN .
VETERINARY MICROBIOLOGY, 1998, 63 (2-4) :147-157
[4]   GASTROENTERITIS IN SUCKLING MICE CAUSED BY HUMAN ROTAVIRUS CAN BE PREVENTED WITH EGG-YOLK IMMUNOGLOBULIN (IGY) AND TREATED WITH A PROTEIN-BOUND POLYSACCHARIDE PREPARATION (PSK) [J].
EBINA, T ;
TSUKADA, K ;
UMEZU, K ;
NOSE, M ;
TSUDA, K ;
HATTA, H ;
KIM, M ;
YAMAMOTO, T .
MICROBIOLOGY AND IMMUNOLOGY, 1990, 34 (07) :617-629
[5]   PROTEASE INHIBITORS PREVENT THE DEVELOPMENT OF HUMAN ROTAVIRUS-INDUCED DIARRHEA IN SUCKLING MICE [J].
EBINA, T ;
TSUKADA, K .
MICROBIOLOGY AND IMMUNOLOGY, 1991, 35 (07) :583-588
[6]   ROTAVIRUS VACCINES - SUCCESS BY REASSORTMENT [J].
GLASS, RI ;
GENTSCH, J ;
SMITH, JC .
SCIENCE, 1994, 265 (5177) :1389-1391
[7]   DIARRHEA IN MICE INFECTED WITH A HUMAN ROTAVIRUS [J].
GOUVEA, VS ;
ALENCAR, AA ;
BARTH, OM ;
DECASTRO, L ;
FIALHO, AM ;
ARAUJO, HP ;
MAJEROWICZ, S ;
PEREIRA, HG .
JOURNAL OF GENERAL VIROLOGY, 1986, 67 :577-581
[8]   Antiviral activity of NMSO3 against adenovirus in vitro [J].
Kaneko, H ;
Kato, K ;
Mori, S ;
Shigeta, S .
ANTIVIRAL RESEARCH, 2001, 52 (03) :281-288
[9]  
Kapikian AZ, 1996, ARCH VIROL, P7
[10]   Synthesis and biological evaluation of N-acetylneuraminic acid-based rotavirus inhibitors [J].
Kiefel, MJ ;
Beisner, B ;
Bennett, S ;
Holmes, ID ;
vonItzstein, M .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (06) :1314-1320