Evidence map›Paper›PMID 25968238›Full record

ArticleJournal of clinical laboratory analysis2016

Accurate Detection of Hepatitis B Virus G1896A Mutant by Developed Taqman-ARMS Followed a Strict Control System.

Renfei Lu, Jianguo Shao, Min Zhou, Hongping Zhang, Yueping Wu

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2016. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Renfei LuDepartment of Laboratory, The Third People's Hospital of Nantong, Nantong, Jiangsu, P. R., China.
Jianguo ShaoDepartment of Laboratory, The Third People's Hospital of Nantong, Nantong, Jiangsu, P. R., China.
Min ZhouNantong Center for Disease Control and Prevention, Nantong, Jiangsu, P. R., China.
Hongping ZhangNantong Center for Disease Control and Prevention, Nantong, Jiangsu, P. R., China.
Yueping WuDepartment of Laboratory, The Third People's Hospital of Nantong, Nantong, Jiangsu, P. R., China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatitis B virus (HBV) G1896A mutation was associated with HBeAg seronegativity and hepatitis B related acute-on-chronic liver failure. In this study, we developed Taqman amplification refractory mutation system (Taqman-ARMS) and established a strict control system to detect HBV G1896A mutant.

methodsHBV viral DNA was isolated from 60 patient serum samples, and full-length HBV genome was cloned. Then, Taqman-ARMS was used to detect HBV G1896A mutant.

resultsThe assay has the sensitivity of 1E+3 IU/ml G1896A template, and 0.1% weak population virus with G1896A could be found in mixtures. Total of all 60 clinical samples random collected were detected by Taqman-ARMS, the results were consistent with those by DNA sequencing.

conclusionThe proposed Taqman-ARMS real-time PCR method for the detection of G1896A mutation of HBV was rapid, simple, sensitive, specific, and applicable in the clinical setting.

Indexed as

Hepatitis B virusHumansMutationReal-Time Polymerase Chain ReactionSensitivity and SpecificityG1896A mutationHBVTaqman-ARMS

Identifiers

PMID25968238
PMCPMC6807175

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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.