Evidence map›Paper›PMID 25469535›Full record

ArticleAIDS research and human retroviruses2015

Japanese external quality assessment program to standardize HIV-1 drug-resistance testing (JEQS2010 program) using in vitro transcribed RNA as reference material.

Shigeru Yoshida, Junko Hattori, Masakazu Matsuda, Kiyomi Okada, Yukumasa Kazuyama, Osamu Hashimoto, Shiro Ibe, Shin-ichi Fujisawa, Hitoshi Chiba, Masashi Tatsumi and 2 more

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Article in AIDS research and human retroviruses, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Shigeru Yoshida1 Faculty of Health Sciences, Hokkaido University , Sapporo, Japan .
Junko Hattori
Masakazu Matsuda
Kiyomi Okada
Yukumasa Kazuyama
Osamu Hashimoto
Shiro Ibe
Shin-ichi Fujisawa
Hitoshi Chiba
Masashi Tatsumi
Shingo Kato
Wataru Sugiura

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To design appropriate antiretroviral therapy regimens and avoid the emergence of human immunodeficiency virus (HIV)-1 variants with reduced susceptibility to antiretroviral drugs, genotypic drug-resistance testing (HIV genotyping) is strongly recommended. To monitor the quality of HIV genotyping in Japan, we performed an external quality assessment (EQA), named the Japanese external quality assessment program, to standardize HIV genotyping (JEQS). To accurately evaluate the quality of HIV genotyping, we employed as reference material (RM) a well-characterized sample, in vitro transcribed RNA (trRNA) that includes the HIV gag-pol sequence, and created a JEQS2010 panel consisting of three single variant and three mixed trRNA samples. All 11 participating laboratories showed high concordance rates (>96%) for the single variant samples. Eight laboratories also showed good rates of detecting minor variants, but three laboratories failed to detect the variants comprising one-half of the sample. These three laboratories used a common primer that had four internal mismatches to the minor trRNA clone. This program showed the usefulness of trRNA as RM, the high quality of HIV genotyping, and extensive interlaboratory variation in the ability to detect minor variants. These results suggest that improving the quality of HIV genotyping in Japan requires regularly implementing the EQA program and improving the HIV genotyping protocol in each laboratory.

Indexed as

Drug Resistance, ViralGenotyping TechniquesHIV-1HIV InfectionsHumansJapanLaboratory Proficiency TestingMicrobial Sensitivity Tests

Identifiers

PMID25469535
PMCPMC4347889

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.