Evidence map›Paper›PMID 27722206›Full record

ArticleHeliyon2016

Whole genomic analysis of G2P[4] human Rotaviruses in Mymensingh, north-central Bangladesh.

Satoru Aida, Samsoon Nahar, Shyamal Kumar Paul, Muhammad Akram Hossain, Muhammad Rashidul Kabir, Santana Rani Sarkar, Salma Ahmed, Souvik Ghosh, Noriko Urushibara, Mitsuyo Kawaguchiya and 3 more

Abstract read
In one paragraph

Article in Heliyon, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 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

13 authors.

Satoru AidaDepartment of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.
Samsoon NaharDepartment of Microbiology, Mymensingh Medical College, Mymensingh, Bangladesh.
Shyamal Kumar PaulDepartment of Microbiology, Mymensingh Medical College, Mymensingh, Bangladesh.
Muhammad Akram HossainDepartment of Microbiology, Mymensingh Medical College, Mymensingh, Bangladesh.
Muhammad Rashidul KabirDepartment of Microbiology, Mymensingh Medical College, Mymensingh, Bangladesh.
Santana Rani SarkarDepartment of Microbiology, Mymensingh Medical College, Mymensingh, Bangladesh.
Salma AhmedDepartment of Microbiology, Mymensingh Medical College, Mymensingh, Bangladesh.
Souvik GhoshDepartment of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan; Department of Biomedical Sciences, Ross University School of Veterinary Medicine, St. Kitts, West Indies.
Noriko UrushibaraDepartment of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.
Mitsuyo KawaguchiyaDepartment of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.
Meiji Soe AungDepartment of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.
Ayako SumiDepartment of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.
Nobumichi KobayashiDepartment of Hygiene, Sapporo Medical University School of Medicine, Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rotavirus A (RVA) is a dominant causative agent of acute gastroenteritis in children worldwide. G2P[4] is one of the most common genotypes among human rotavirus (HRV) strains, and has been persistently prevalent in South Asia including Bangladesh. In the present study, whole genome sequences of a total of 16 G2P[4] HRV strains (8 strains each in 2010 and 2013) detected in Mymensingh, north-central Bangladesh were determined. These strains had typical DS-1-like genotype constellation. Most of gene segments from DS-1 genogroup exhibited high level sequence identities to each other (>98%), while slight diversity was observed for VP1, VP3, and NSP4 genes. By phylogenetic analysis, individual RNA segments were classified into one (V) or two-three lineages (V-VI or V-VII). In terms of lineages (sublineages) of 11 gene segments, the 16 Bangladeshi strains could be further classified into four clades (A-D) containing 8 lineage constellations, revealing the presence of three clades (A-C) with three lineage constellations in 2010, and a single clade (D) with four constellations in 2013. Therefore, co-existence of multiple G2P[4] HRV strains with different lineage constellations, and change in clades for the study period were demonstrated. Although amino acids in the antigenic regions on VP7 and VP4 were mostly identical to those of global G2P[4] strains after 2000, VP4 of clade D RVAs in 2013 had alanine and proline at positions 88 and 114, respectively, which are novel substitutions compared with recent global G2P[4] strains. Replacement of lineage constellations associated with unique amino acid changes in the antigenic region in VP4 suggested continuous genetic evolutionary state for emerging new G2P[4] rotavirus strains in Bangladesh.

Indexed as

EvolutionGeneticsMicrobiology

Identifiers

PMID27722206
PMCPMC5047856

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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.