Evidence map›Paper›PMID 32046345›Full record

ArticleInternational journal of environmental research and public health2020

Genetic Diversity and Phylogenetic Analysis of Human Bocavirus 2 in Pediatric Patients with Acute Gastroenteritis in Taiwan.

Marco Yung-Cheng Lin, Hsiu-Chuan Chan, Hsin Chi, Shu-Chun Chiu, Zaiga Nora-Krukle, Santa Rasa-Dzelzkaleja, Anda Vilmane, Modra Murovska, Jih-Hui Lin, Hsin-Fu Liu

Open access · goldAbstract read
In one paragraph

Article in International journal of environmental research and public health, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

5 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 5 institutions in 2 countries.

Marco Yung-Cheng LinDepartment of Medical Research, MacKay Memorial Hospital, Taipei 10449, Taiwan.
Hsiu-Chuan ChanLipid Science and Aging Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Hsin ChiDepartment of Pediatrics, MacKay Children's Hospital and MacKay Memorial Hospital, Taipei 10449, Taiwan.
Shu-Chun ChiuCenter of Diagnostics and Vaccine Development, Centers for Disease Control, Taipei 11561, Taiwan.
Zaiga Nora-KrukleInstitute of Microbiology and Virology, Riga Stradins University, LV-1067 Riga, Latvia.
Santa Rasa-DzelzkalejaInstitute of Microbiology and Virology, Riga Stradins University, LV-1067 Riga, Latvia.
Anda VilmaneInstitute of Microbiology and Virology, Riga Stradins University, LV-1067 Riga, Latvia.
Modra MurovskaInstitute of Microbiology and Virology, Riga Stradins University, LV-1067 Riga, Latvia.
Jih-Hui LinCenter of Diagnostics and Vaccine Development, Centers for Disease Control, Taipei 11561, Taiwan.
Hsin-Fu LiuDepartment of Medical Research, MacKay Memorial Hospital, Taipei 10449, Taiwan.
Riga Stradiņš University · LVMackay Memorial Hospital · TWNational Taiwan Ocean University · TWDevelopment Center for Biotechnology · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human bocavirus (HBoV) is a causative agent of respiratory and gastrointestinal diseases worldwide. Four HBoV species (HBoV1-4) have been identified so far. Although a previous report has documented the HBoV association with acute gastroenteritis (AGE) in Taiwan, their epidemiology, genetic diversity, and phylogenetic relationships remain unclear. In this study, we focused on an investigation of these unsolved issues, which will help to reveal molecular epidemiology and phylogeny of the circulating HBoV2 in Taiwan. A total of 176 stool samples were collected from children with AGE for this study. PCR amplification and sequencing on the VP1 gene region were used to identify species. Phylogenetic analysis was conducted by maximum-likelihood and neighbor-joining methods. Selection pressure was also estimated to obtain HBoV evolutionary information. Our results showed the prevalence of HBoV in AGE children was 8.5%, of which HBoV1 was the predominant species (6.3%), followed by HBoV2 (2.3%). Phylogenetic analysis showed those Taiwanese HBoV2 strains have significant genetic variability and can be divided into two clusters. One belongs to HBoV2 genotype A and the other forms an independent unclassified cluster. The nucleotide distance between that independent cluster and the known HBoV2 genotypes was more than 5%, suggesting a new HBoV2 genotype. No positive selection site was found and the virus was under purifying selection. This is the first report to reveal HBoV2 genetic diversity and phylogenetic relationships among AGE children in Taiwan. We find that HBoV2 may have been introduced into the country by multiple origins, and a potential new HBoV2 genotype is proposed.

Indexed as

Genetic VariationPhylogenyAcute DiseaseChildChild, PreschoolFecesFemaleGastroenteritisGenotypeHuman bocavirusHumansInfantMaleMolecular EpidemiologyParvoviridae InfectionsPrevalenceacute gastroenteritisgenotypehuman bocavirus 2phylogenetic analysis

Identifiers

PMID32046345
PMCPMC7037009
OpenAlexW3005473678

What OpenQuestion holds

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LicenceCC BY
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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.