Evidence map›Paper›PMID 28738914›Full record

ArticleEpidemiology and infection2017

Characterization of group B coxsackieviruses isolated from non-polio acute flaccid paralysis patients in Pakistan: vital assessment before polio eradication.

M Angez, S Shaukat, R Zahra, M M Alam, S Sharif, A Khurshid, Y Arshad, M Suleman, G Mujtaba, S S Z Zaidi

Open access · bronzeAbstract read
In one paragraph

Article in Epidemiology and infection, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Coxsackievirus B1 resulting acute flaccid myelitis with entire spinal cord lesion: a case report.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Article
  3. Article
  4. Acute Flaccid Paralysis and Enteroviral Infections.Current infectious disease reports · 2018
    Review
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 2 institutions in 1 country.

M AngezDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
S ShaukatDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
R ZahraDepartment of Microbiology,Faculty of Biological Sciences,Quaid-i-Azam University,Islamabad-45320,Pakistan.
M M AlamDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
S SharifDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
A KhurshidDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
Y ArshadDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
M SulemanDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
G MujtabaDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
S S Z ZaidiDepartment of Virology,National Institute of Health,Chak Shahzad,Park Road,Islamabad-45500,Pakistan.
National Institute of Health · PKQuaid-i-Azam University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pakistan is at the verge of polio eradication but isolation of non-polio enteroviruses (NPEVs) from acute flaccid paralysis (AFP) cases may result in serious or even fatal outcome. Many enteroviruses share similar symptoms and epidemiology as is the case with poliovirus and coxsackievirus (CV). The present study was designed to genetically characterize coxsackievirus B (CV-B) serotypes isolated from non-polio acute flaccid paralytic children, as well as to understand their probable role in paralysis. A total of 63 (20·1%) out of 313 stool samples during 2013 were found positive for NPEVs in rhabdomyosarcoma cells. Only 24 (38·0%) NPEVs were typed as CV-B by microneutralization assay and were further characterized by sequencing of the viral protein 1 (VP1) gene. Molecular phylogenetic analyses classified the study strains into six coxsackievirus B serotypes (coxsackievirus B1 to B6) with their respective prototype strains with evidence of epidemiological linkage and distinct clusters. Moreover, four major differences were found within the amino acid sequences of BC-loop in VP1 of CV-B strains. In conclusion, this study presented the molecular evolutionary genetic overview and distinct phylogenetic pattern of CV-B isolates from AFP cases in Pakistan, and explored the possible link between CV-B infections and AFP cases. Furthermore, our data reveal that these viruses might contribute to the incidence of paralysis in population and there is need of time to establish an enterovirus surveillance system for better understanding of epidemiological and virological characteristics of NPEV infections associated with AFP cases in the country.

Indexed as

Capsid ProteinsChildChild, PreschoolCoxsackievirus InfectionsDisease EradicationEnterovirus B, HumanFecesFemaleHumansInfantMalePakistanParalysisPhylogenyPoliomyelitisSequence Analysis, RNACapsid Proteinsechovirus 9 capsid protein vp1Acute flaccid paralysiscoxsackievirus Benterovirusmolecular epidemiologyPakistan

Identifiers

PMID28738914
PMCPMC9148784
OpenAlexW2737869306

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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.