Evidence map›Paper›PMID 25187888›Full record

ArticleAnnals of laboratory medicine2014

Application of HTB-SiHa cells transfected with a recombinant plasmid for external quality assessment of Chlamydia trachomatis PCR.

Kuo Zhang, Hong Huo, Yu Sun, Lunan Wang, Rui Zhang, Guigao Lin, Jiehong Xie, Qingtao Wang, Jinming Li

Abstract read
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Article in Annals of laboratory medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Kuo ZhangNational Center for Clinical Laboratories, Beijing Hospital, Beijing, China.
Hong HuoDepartment of Clinical Laboratory, Beijing Chaoyang Hospital Affiliated to the Capital University of Medical Sciences, Beijing, China.
Yu SunNational Center for Clinical Laboratories, Beijing Hospital, Beijing, China.
Lunan WangNational Center for Clinical Laboratories, Beijing Hospital, Beijing, China.
Rui ZhangNational Center for Clinical Laboratories, Beijing Hospital, Beijing, China.
Guigao LinNational Center for Clinical Laboratories, Beijing Hospital, Beijing, China.
Jiehong XieNational Center for Clinical Laboratories, Beijing Hospital, Beijing, China.
Qingtao WangDepartment of Clinical Laboratory, Beijing Chaoyang Hospital Affiliated to the Capital University of Medical Sciences, Beijing, China.
Jinming LiNational Center for Clinical Laboratories, Beijing Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe participation of laboratories in external quality assessment (EQA) programs is required for the quality assurance of nucleic acid amplification of Chlamydia trachomatis. This study aimed to construct a new quality control (QC) material applicated in EQA of C. trachomatis PCR.

methodsA QC material-HTB-SiHa cells transfected with a recombinant plasmid containing the cryptic plasmid sequence-was constructed for C. trachomatis PCR detection, and four different panels, each consisting of 4 positive samples with serial dilution of the constructed QC material and 1 negative sample, were distributed by the National Center for Clinical Laboratories among four groups of 275, 268, 317, and 304 participants across China from 2011 through 2012. A total of eight commercial kits were used for C. trachomatis PCR detection in participants.

resultsNine laboratories reported false-positive results (0.9%). As the series dilution increased, the correct reporting of the data sets decreased; the lowest correct rate was 96.3% in the weakest positive samples (10(4) copies/mL). Eight laboratories reported false-positive results, and 42 laboratories reported false-negative results in the EQA detection of C. trachomatis. No significant differences were observed in the detection of the constructed C. trachomatis positive samples (97.9%, 98.5%, 100%, 98.5%; P=0.36) and negative samples (100%, 99.0%, 100%, 99.0%; P=0.764) using four commercial kits commonly used in China.

conclusionsThe results of the EQA study indicated that the constructed material provides a noninfectious, stable control material with sufficient volume for PCR detection of C. trachomatis.

Indexed as

Cell LineChlamydia InfectionsChlamydia trachomatisDNA, BacterialFalse Negative ReactionsHumansLaboratoriesPlasmidsPolymerase Chain ReactionQuality ControlReagent Kits, DiagnosticDNA, BacterialReagent Kits, DiagnosticChlamydia trachomatisEpithelial cellsExternal Quality AssessmentPolymerase chain reactionQuality control

Identifiers

PMID25187888
PMCPMC4151004

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