Evidence map›Paper›PMID 29077212›Full record

ArticleJournal of medical virology2018

Genetic variability human respiratory syncytial virus subgroups A and B in Turkey during six successive epidemic seasons, 2009-2015.

Fatma Bayrakdar, Can Naci Kocabas, Ayse Basak Altas, H Gokhan Kavuncuoglu, Yasemin Cosgun, Emine Dibek Mısırlıoglu, Ihsan Durmaz, Gulay Korukluoglu, Aykut Ozkul

Open access · bronzeAbstract read
In one paragraph

Article in Journal of medical virology, 2018. 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
0.5field-weighted citation impact, top 31% 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, 5 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

9 authors at 3 institutions in 2 countries.

Fatma BayrakdarVirology Reference and Research Laboratory, Public Health Institutions of Turkey, Ankara, Turkey.ORCID 0000-0001-7531-5080
Can Naci KocabasPediatric Immunology and Allergy Unit, Faculty of Medicine, Mugla Sitki Koçman Universty, Muğla, Turkey.
Ayse Basak AltasVirology Reference and Research Laboratory, Public Health Institutions of Turkey, Ankara, Turkey.
H Gokhan KavuncuogluVirology Reference and Research Laboratory, Public Health Institutions of Turkey, Ankara, Turkey.
Yasemin CosgunVirology Reference and Research Laboratory, Public Health Institutions of Turkey, Ankara, Turkey.
Emine Dibek MısırlıogluDepartment of Pediatric Allergy and Immunology, Ankara Children's Hematology Oncology Training and Research Hospital, Ankara, Turkey.
Ihsan DurmazVirology Reference and Research Laboratory, Public Health Institutions of Turkey, Ankara, Turkey.
Gulay KorukluogluVirology Reference and Research Laboratory, Public Health Institutions of Turkey, Ankara, Turkey.
Aykut OzkulFaculty of Veterinary Medicine, Department of Virology, Ankara University, Ankara, Turkey.
Ministry of Health · TRAnkara University · TRMuğla University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human respiratory syncytial virus (HRSV) is most important viral respiratory pathogen of acute lower respiratory tract infections in infants and young children worldwide. The circulating pattern and genetic characteristics in the HRSV attachment glycoprotein gene were investigated in Turkey during six consecutive seasons from 2009 to 2015. HRSVA was dominant in the all epidemic seasons except 2011-2012 season. Partial sequences of the HVR2 region of the G gene of 479 HRSVA and 135 HRSVB were obtained. Most Turkish strains belonged to NA1, ON1, and BA9, which were the predominant genotypes circulating worldwide. Although three novel genotypes, TR-A, TR-BA1, and TR-BA2, were identified, they were not predominant. Clinical data were available for 69 HRSV-positive patients who were monitored due to acute lower respiratory tract illness. There were no significant differences in the clinical diagnosis, hospitalization rates, laboratory findings and treatment observed between the HRSVA and HRSVB groups, and co-infections in this study. The major population afflicted by HRSV infections included infants and children between 13 and 24 months of age. We detected that the CB1, GB5, and THB strains clustered in the same branch with a bootstrap value of 100%. CB-B and BA12 strains clustered in the same branch with a bootstrap value of 65%. The BA11 genotype was clustered in the BA9 genotype in our study. The present study may contribute on the molecular epidemiology of HRSV in Turkey and provide data for HRSV strains circulating in local communities and other regions worldwide.

Indexed as

EpidemicsGenetic VariationGenotypeAdolescentAdultAgedChildChild, PreschoolFemaleHumansInfantMaleMiddle AgedNasopharynxPhylogenyRespiratory Syncytial Virus, Humanattachment protein GG glycoprotein, Respiratory syncytial virusRNA, ViralViral Envelope ProteinsViral Fusion Proteinsacute respiratory tract illnessG genehuman respiratory syncytial virusnovel genotypesTurkey

Identifiers

PMID29077212
PMCPMC7166824
OpenAlexW2765812094

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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.