Evidence map›Paper›PMID 35056549›Full record

ArticleMicroorganisms2022

Genotyping and Molecular Diagnosis of Hepatitis A Virus in Human Clinical Samples Using Multiplex PCR-Based Next-Generation Sequencing.

Geum-Young Lee, Won-Keun Kim, Seungchan Cho, Kyungmin Park, Jongwoo Kim, Seung-Ho Lee, Jingyeong Lee, Young-Sun Lee, Ji Hoon Kim, Kwan Soo Byun and 1 more

Abstract read
In one paragraph

Article in Microorganisms, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Geum-Young LeeDepartment of Microbiology, Korea University College of Medicine, Seoul 02842, Korea.
Won-Keun KimDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon 24252, Korea.ORCID 0000-0003-3178-8569
Seungchan ChoDepartment of Microbiology, Korea University College of Medicine, Seoul 02842, Korea.
Kyungmin ParkDepartment of Microbiology, Korea University College of Medicine, Seoul 02842, Korea.ORCID 0000-0002-2132-0674
Jongwoo KimDepartment of Microbiology, Korea University College of Medicine, Seoul 02842, Korea.
Seung-Ho LeeDepartment of Microbiology, Korea University College of Medicine, Seoul 02842, Korea.ORCID 0000-0002-7840-422X
Jingyeong LeeDepartment of Microbiology, Korea University College of Medicine, Seoul 02842, Korea.
Young-Sun LeeDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University Medical Center, Seoul 08308, Korea.ORCID 0000-0001-6396-0859
Ji Hoon KimDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University Medical Center, Seoul 08308, Korea.ORCID 0000-0003-3924-0434
Kwan Soo ByunDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University Medical Center, Seoul 08308, Korea.
Jin-Won SongDepartment of Microbiology, Korea University College of Medicine, Seoul 02842, Korea.ORCID 0000-0003-0796-8332

Funding

Institute of Biomedical Science and Food Safety K2108991Korea Institute of Marine Science & Technology Promotion 21210466
6 · The paper itself

Abstract

Hepatitis A virus (HAV) is a serious threat to public health worldwide. We used multiplex polymerase chain reaction (PCR)-based next-generation sequencing (NGS) to derive information on viral genetic diversity and conduct precise phylogenetic analysis. Four HAV genome sequences were obtained using multiplex PCR-based NGS. HAV whole-genome sequence of one sample was obtained by conventional Sanger sequencing. The HAV strains demonstrated a geographic cluster with sub-genotype IA strains in the Republic of Korea. The phylogenetic pattern of HAV viral protein (VP) 3 region showed no phylogenetic conflict between the whole-genome and partial-genome sequences. The VP3 region in serum and stool samples showed sensitive detection of HAV with differences of quantification that did not exceed <10 copies/μL than the consensus VP4 region using quantitative PCR (qPCR). In conclusion, multiplex PCR-based NGS was implemented to define HAV genotypes using nearly whole-genome sequences obtained directly from hepatitis A patients. The VP3 region might be a potential candidate for tracking the genotypic origin of emerging HAV outbreaks. VP3-specific qPCR was developed for the molecular diagnosis of HAV infection. This study may be useful to predict for the disease management and subsequent development of hepatitis A infection at high risk of severe illness.

Indexed as

genotypic analysishepatitis A virusmultiplex polymerase chain reactionnext-generation sequencingphylogenetic analysis

Identifiers

PMID35056549
PMCPMC8779169

What OpenQuestion holds

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Registered trials

None linked

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.