Detail
Článek
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Evaluation of different techniques for identification of human papillomavirus types of low prevalence

I Sabol, M Salakova, J Smahelova, M Pawlita, M Schmitt, NM Gasperov, M Grce, R Tachezy

. 2008 ; 46 (5) : 1606-1613.

Jazyk angličtina Země Spojené státy americké

Typ dokumentu srovnávací studie, hodnotící studie, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc13033254

Grantová podpora
NR8852 MZ0 CEP - Centrální evidence projektů

Digitální knihovna NLK
Plný text - Článek
Zdroj

E-zdroje NLK Online Plný text

Free Medical Journals od 1975 do Před 6 měsíci
Freely Accessible Science Journals od 1995 do Před 6 měsíci
PubMed Central od 1975 do Před 6 měsíci
Europe PubMed Central od 1975 do Před 6 měsíci
Open Access Digital Library od 1975-01-01
Open Access Digital Library od 1975-01-01

Human papillomaviruses (HPVs) have been recognized as etiologic factors in a variety of diseases. Due to the large number of HPV types, methods for HPV genotyping are difficult to standardize. Despite this fact, several methods exist, and some of them are available commercially. In this study, we evaluated the Roche Diagnostics linear array (LA) HPV genotyping assay, the Innogenetics INNO-LiPA (line probe assay [LiPA]), and two noncommercial reverse line blot (RLB) assays based on either primers GP5+ and GP6+ (GP) or newly designed broad-spectrum primers BSGP5+ and BSGP6+ (BS). The reliabilities of these assays were tested with a wide spectrum of HPV types less prevalent in cervical samples. This is the first study to compare the performance of the most widely used HPV genotyping methods with selected samples positive for low-prevalence HPV types. We focused on interassay agreement, both overall and type specific, in cases with single and/or multiple HPV infections. Interassay agreement was moderate in cases of single HPV infections and poor in cases of multiple HPV infections. The LA and the BS-based RLB assays found a higher rate of cases positive for multiple HPV types than LiPA and the GP-based RLB assay. The weakest capability in detecting multiple HPV infections was observed for LiPA. The use of only one assay in epidemiological and clinical studies might lead to biased conclusions. Therefore, a universally evaluated and agreed upon HPV typing assay or a combination of current assays is needed for possible clinical applications, and knowledge of their limitations is advised.

Bibliografie atd.

Literatura

000      
00000naa a2200000 a 4500
001      
bmc13033254
003      
CZ-PrNML
005      
20131022123916.0
007      
ta
008      
131015s2008 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1128/JCM.02328-07 $2 doi
035    __
$a (PubMed)18322064
040    __
$a ABA008 $d ABA008 $e AACR2 $b cze
041    0_
$a eng
044    __
$a xxu
100    1_
$a Sabol, Ivan $u Division of Molecular Medicine, Rudjer Boskovic Institute, Zagreb, Croatia
245    10
$a Evaluation of different techniques for identification of human papillomavirus types of low prevalence / $c I Sabol, M Salakova, J Smahelova, M Pawlita, M Schmitt, NM Gasperov, M Grce, R Tachezy
504    __
$a Literatura
520    9_
$a Human papillomaviruses (HPVs) have been recognized as etiologic factors in a variety of diseases. Due to the large number of HPV types, methods for HPV genotyping are difficult to standardize. Despite this fact, several methods exist, and some of them are available commercially. In this study, we evaluated the Roche Diagnostics linear array (LA) HPV genotyping assay, the Innogenetics INNO-LiPA (line probe assay [LiPA]), and two noncommercial reverse line blot (RLB) assays based on either primers GP5+ and GP6+ (GP) or newly designed broad-spectrum primers BSGP5+ and BSGP6+ (BS). The reliabilities of these assays were tested with a wide spectrum of HPV types less prevalent in cervical samples. This is the first study to compare the performance of the most widely used HPV genotyping methods with selected samples positive for low-prevalence HPV types. We focused on interassay agreement, both overall and type specific, in cases with single and/or multiple HPV infections. Interassay agreement was moderate in cases of single HPV infections and poor in cases of multiple HPV infections. The LA and the BS-based RLB assays found a higher rate of cases positive for multiple HPV types than LiPA and the GP-based RLB assay. The weakest capability in detecting multiple HPV infections was observed for LiPA. The use of only one assay in epidemiological and clinical studies might lead to biased conclusions. Therefore, a universally evaluated and agreed upon HPV typing assay or a combination of current assays is needed for possible clinical applications, and knowledge of their limitations is advised.
590    __
$a bohemika - dle Pubmed
650    02
$a ženské pohlaví $7 D005260
650    02
$a lidé $7 D006801
650    12
$a diagnostické techniky molekulární $x metody $7 D025202
650    02
$a Papillomaviridae $x genetika $x izolace a purifikace $x klasifikace $7 D027383
650    12
$a infekce papilomavirem $x diagnóza $x virologie $7 D030361
650    02
$a senzitivita a specificita $7 D012680
650    12
$a virologie $x metody $7 D014773
655    _2
$a srovnávací studie $7 D003160
655    _2
$a hodnotící studie $7 D023362
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Saláková, Martina $7 xx0086174 $u Department of Experimental Virology, Institute of Hematology and Blood Transfusion, Prague, Czech Republic
700    1_
$a Šmahelová, Jana $7 xx0110565 $u Department of Experimental Virology, Institute of Hematology and Blood Transfusion, Prague, Czech Republic
700    1_
$a Pawlita, Michal
700    1_
$a Schmitt, Markus
700    1_
$a Gašperov, Nina Milutin
700    1_
$a Grce, Magdalena
700    1_
$a Tachezy, Ruth
773    0_
$t Journal of Clinical Microbiology $g Roč. 46, č. 5 (2008), s. 1606-1613 $p J Clin Microbiol $x 0095-1137 $w MED00002592
773    0_
$p J Clin Microbiol $g 46(5):1606-13, 2008 May
910    __
$a ABA008 $b B 1646 $y 3 $z 0
990    __
$a 20131015101247 $b ABA008
991    __
$a 20131022124507 $b ABA008
999    __
$a ok $b bmc $g 997423 $s 831707
BAS    __
$a 3
BMC    __
$a 2008 $b 46 $c 5 $d 1606-1613 $i 0095-1137 $m Journal of clinical microbiology $x MED00002592 $n J Clin Microbiol
GRA    __
$a NR8852 $p MZ0
LZP    __
$a 2013-10/dpbo

Najít záznam

Citační ukazatele

Nahrávání dat...

Možnosti archivace

Nahrávání dat...