Périodique
Detection of HIV-1 DNA in needle/syringes, paraphernalia, and washes from shooting galleries in Miami: a preliminary laboratory report
(Dépistage d'ADN infecté par le VIH-1 dans les seringues, les aiguilles, et le matériel d'injection en provenance de salles d'injection à Miami : rapport préliminaire de laboratoire)
Auteur(s) :
SHAH, S. M. ;
SHAPSHAK, P. ;
RIVERS, J. E. ;
STEWART, R. V. ;
WEATHERBY, N. L. ;
XIN, K. Q. ;
PAGE, J. B. ;
CHITWOOD, D. D. ;
MASH, D. C. ;
VLAHOV, D. ;
McCOY, C. B.
Année
1996
Page(s) :
301-306
Langue(s) :
Anglais
Refs biblio. :
35
Domaine :
Drogues illicites / Illicit drugs
Discipline :
MAL (Maladies infectieuses / Infectious diseases)
Thésaurus mots-clés
VIH
;
CONTAMINATION
;
MATERIEL LIE A L'USAGE
;
MATERIEL D'INJECTION
;
SERINGUE
;
DEPISTAGE
;
USAGER
;
VOIE INTRAVEINEUSE
;
INJECTION
;
STRUCTURE DE PROXIMITE
Note générale :
Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology, 1996, 11, (3), 301-306
Résumé :
Shared use of injection equipment (needle/syringes), registering, booting, and backloading are practices among injection drug users (IDUs) that increase the risk for transmission of human immunodeficiency virus type 1 (HIV-1). The sharing of injection paraphernalia (including cookers and cottons) and washwater for rinsing used needle/syringes and dissolving drugs could be potential sources for secondary transmission of HIV-1. Laboratory rinses were made from needle/syringes, cottons, and cookers obtained from shooting galleries, and washwaters were obtained from shooting galleries in Miami. Three rinses were analyzed and antibodies to HIV-1 proteins were detected by using Western blot and HIV-1 DNA was detected by using nested polymerase chain reaction (PCR) specific for the gag and envelope genes of HIV-1. Antibodies to HIV-1 proteins were detected in 12 (52%) of 23 rinses from visibly contaminated needle/syringes, in three (18%) of 17 rinses from cottons, in three (14%) of 21 rinses from cookers, and in one (6%) of 17 washwaters. No antibodies were detected in laboratory rinses from visibly clean needles. Using nested PCR followed by Southern blot confirmation of the amplified targets, HIV-1 gag gene DNA was detected in 16 (84%) of 19 and envelope gene DNA in 17 (85%) of 20 laboratory rinses from visibly contaminated needle/syringes. We detected gag and envelope gene DNA, respectively, in three (27%) and four (36%) of 11 cottons, in six (46%) and seven (54%) of 13 cookers, and in five (38%) of 13 and in 10 (67%) of 15 washwaters from shooting galleries. No HIV-1 DNA was detected in laboratory rinses from visibly clean needles. These results indicate that HIV-1 might be present in contaminated cottons, cookers, and washwaters as well as in contaminated needle/syringes at shooting galleries. Reduction of risks of exposure to HIV-1 among IDUs may require modification of behaviors that are ancillary to the act of injection, such as the use of common cookers, cottons, and washwater. (Review' s abstract)
Affiliation :
Etats-Unis. United States.
Cote :
A01466
Historique