Papillomavirus microbicidal activities of high-molecular-weight cellulose sulfate, dextran sulfate, and polystyrene sulfonate

被引:88
作者
Christensen, ND
Reed, CA
Culp, TD
Hermonat, PL
Howett, MK
Anderson, RA
Zaneveld, LJD
机构
[1] Penn State Univ, Milton S Hershey Med Ctr, Jake Gittlen Canc Res Inst, Hershey, PA 17033 USA
[2] Penn State Univ, Milton S Hershey Med Ctr, Dept Pathol, Hershey, PA 17033 USA
[3] Penn State Univ, Milton S Hershey Med Ctr, Dept Microbiol & Immunol, Hershey, PA 17033 USA
[4] Univ Arkansas, Sch Med, Dept Obstet Gynecol, Little Rock, AR 72205 USA
[5] Rush Presbyterian St Lukes Med Ctr, Sect Obstet Gynecol Res, Chicago, IL 60612 USA
关键词
D O I
10.1128/AAC.45.12.3427-3432.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The high-molecular-weight sulfated or sulfonated polysaccharides or polymers cellulose sulfate, dextran sulfate, and polystyrene sulfonate were tested for microbicidal activity against bovine papillomavirus type 1 (BPV-1) and human papillomavirus type 11 (HPV-11) and type 40 (HPV-40). In vitro assays included the BPV-1-induced focus-forming assay and transient infection of human A431 cells with HPVs. The compounds were tested for microbicidal activity directly by preincubation with virus prior to addition to cell cultures and indirectly by addition of virus to compound-treated cells and to virus-coated cells to test inactivation of the virus after virus-cell binding. The data indicated that all three compounds showed direct microbicidal activity with 50% effective concentrations between 10 to 100 mug/ml. These concentrations were nontoxic to cell cultures for both assays. When a clone of C127 cells was tested for microbicidal activity, approximately 10-fold-less compound was required to achieve a 50% reduction in BPV-1-induced foci than for the uncloned parental C127 cells. Pretreatment of cells with compound prior to addition of virus also demonstrated strong microbicidal activity with dextran sulfate and polystyrene sulfonate, but cellulose sulfate required several orders of magnitude more compound for virus inactivation. Polystyrene sulfonate prevented subsequent infection of HPV-11 after virus-cell binding, and this inactivation was observed up to 4 h after addition of virus. These data indicate that the polysulfated and polysulfonated compounds may be useful nontoxic microbicidal compounds that are active against a variety of sexually transmitted disease agents including papillomaviruses.
引用
收藏
页码:3427 / 3432
页数:6
相关论文
共 29 条
[1]  
Anderson RA, 2000, J ANDROL, V21, P862
[2]   MONOCLONAL ANTIBODY-MEDIATED NEUTRALIZATION OF INFECTIOUS HUMAN PAPILLOMAVIRUS TYPE-11 [J].
CHRISTENSEN, ND ;
KREIDER, JW ;
CLADEL, NM ;
PATRICK, SD ;
WELSH, PA .
JOURNAL OF VIROLOGY, 1990, 64 (11) :5678-5681
[3]   POSTATTACHMENT NEUTRALIZATION OF PAPILLOMAVIRUSES BY MONOCLONAL AND POLYCLONAL ANTIBODIES [J].
CHRISTENSEN, ND ;
CLADEL, NM ;
REED, CA .
VIROLOGY, 1995, 207 (01) :136-142
[4]   2 NEWLY IDENTIFIED HUMAN PAPILLOMAVIRUS TYPES (HPV-40 AND 57) ISOLATED FROM MUCOSAL LESIONS [J].
DEVILLIERS, EM ;
HIRSCHBEHNAM, A ;
VONKNEBELDOEBERITZ, C ;
NEUMANN, C ;
ZURHAUSEN, H .
VIROLOGY, 1989, 171 (01) :248-253
[5]   A QUANTITATIVE INVITRO FOCUS ASSAY FOR BOVINE PAPILLOMA-VIRUS [J].
DVORETZKY, I ;
SHOBER, R ;
CHATTOPADHYAY, SK ;
LOWY, DR .
VIROLOGY, 1980, 103 (02) :369-375
[6]   Identification of the alpha(6) integrin as a candidate receptor for papillomaviruses [J].
Evander, M ;
Frazer, IH ;
Payne, E ;
Qi, YM ;
Hengst, K ;
McMillan, NAJ .
JOURNAL OF VIROLOGY, 1997, 71 (03) :2449-2456
[7]   The promise of public/private sector collaboration in the development of vaginal microbicides [J].
Gabelnick, HL ;
Harper, MJK .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 1999, 67 :S31-S38
[8]   Human papillomavirus infection requires cell surface heparan sulfate [J].
Giroglou, T ;
Florin, L ;
Schäfer, F ;
Streeck, RE ;
Sapp, M .
JOURNAL OF VIROLOGY, 2001, 75 (03) :1565-1570
[9]   THE SPERMICIDE NONOXYNOL-9 DOES NOT INACTIVATE PAPILLOMAVIRUS [J].
HERMONAT, PL ;
DANIEL, RW ;
SHAH, KV .
SEXUALLY TRANSMITTED DISEASES, 1992, 19 (04) :203-205
[10]   Sulfated carbohydrate compounds prevent microbial adherence by sexually transmitted disease pathogens [J].
Herold, BC ;
Siston, A ;
Bremer, J ;
Kirkpatrick, R ;
Wilbanks, G ;
Fugedi, P ;
Peto, C ;
Cooper, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (12) :2776-2780