Evidence map›Paper›PMID 29948828›Full record

ReviewJournal of microbiology (Seoul, Korea)2018

Phylogenetic comparison of Epstein-Barr virus genomes.

Su Jin Choi, Seok Won Jung, Sora Huh, Hyosun Cho, Hyojeung Kang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of microbiology (Seoul, Korea), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 26 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

5 authors at 2 institutions in 1 country.

Su Jin ChoiCollege of Pharmacy, Research Institute of Pharmaceutical Sciences and Kyungpook National University Cancer Research Institute, Kyungpook National University, Daegu, 41566, Republic of Korea.
Seok Won JungCollege of Pharmacy, Research Institute of Pharmaceutical Sciences and Kyungpook National University Cancer Research Institute, Kyungpook National University, Daegu, 41566, Republic of Korea.
Sora HuhCollege of Pharmacy, Research Institute of Pharmaceutical Sciences and Kyungpook National University Cancer Research Institute, Kyungpook National University, Daegu, 41566, Republic of Korea.
Hyosun ChoCollege of Pharmacy, Duksung Women's University, Seoul, 01369, Republic of Korea. hyosun1102@duksung.ac.kr.
Hyojeung KangCollege of Pharmacy, Research Institute of Pharmaceutical Sciences and Kyungpook National University Cancer Research Institute, Kyungpook National University, Daegu, 41566, Republic of Korea. hkang72@knu.ac.kr.
Kyungpook National University · KRDuksung Women's University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Technologies used for genome analysis and whole genome sequencing are useful for us to understand genomic characterization and divergence. The Epstein-Barr virus (EBV) is an oncogenic virus that causes diverse diseases such as Burkitt's lymphoma (BL), nasopharyngeal carcinoma (NPC), Hodgkin's lymphoma (HL), and gastric carcinoma (GC). EBV genomes found in these diseases can be classified either by phases of EBV latency (type-I, -II, and -III latency) or types of EBNA2 sequence difference (type-I EBV, type-II EBV or EBV-1, EBV-2). EBV from EBV-transformed lymphoblastoid cell line (LCL) establishes type-III latency, EBV from NPC establishes type-II latency, and EBV from GC establishes type-I latency. However, other important factors play key roles in classifying numerous EBV strains because EBV genomes are highly diverse and not phylogenetically related to types of EBV-associated diseases. Herein, we first reviewed previous studies to describe molecular characteristics of EBV genomes. Then, using comparative and phylogenetic analyses, we phylogenetically analyzed molecular variations of EBV genomes and proteins. The review of previous studies and our phylogenetic analysis showed that EBV genomes and proteins were highly diverse regardless of types of EBV-associated diseases. Other factors should be considered in determining EBV taxonomy. This review will be helpful to understand complicated phylogenetic relationships of EBV genomes.

Indexed as

Genetic VariationGenome, ViralPhylogenyEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHumansViral ProteinsViral ProteinsEpstein-Barr virusgenomic variationsphylogenetic analysis

Identifiers

PMID29948828
OpenAlexW2808126062

What OpenQuestion holds

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Registered trials

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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.