Evidence map›Paper›PMID 27739035›Full record

ArticleJournal of neurovirology2017

HSV-1 clinical isolates with unique in vivo and in vitro phenotypes and insight into genomic differences.

Robert J Danaher, Derrick E Fouts, Agnes P Chan, Yongwook Choi, Jessica DePew, Jamison M McCorrison, Karen E Nelson, Chunmei Wang, Craig S Miller

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neurovirology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Genome-wide engineering of an infectious clone of herpes simplex virus type 1 using synthetic genomics assembly methods.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
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 2 institutions in 1 country.

Robert J DanaherDepartment of Oral Health Practice, Division of Oral Medicine, Center for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, KY, USA. rjdana0@uky.edu.
Derrick E FoutsDepartment of Genomic Medicine, J. Craig Venter Institute (JCVI), Rockville, MD, USA.
Agnes P ChanDepartment of Genomic Medicine, J. Craig Venter Institute (JCVI), Rockville, MD, USA.
Yongwook ChoiDepartment of Genomic Medicine, J. Craig Venter Institute (JCVI), Rockville, MD, USA.
Jessica DePewDepartment of Genomic Medicine, J. Craig Venter Institute (JCVI), Rockville, MD, USA.
Jamison M McCorrisonDepartment of Genomic Medicine, J. Craig Venter Institute (JCVI), Rockville, MD, USA.
Karen E NelsonDepartment of Genomic Medicine, J. Craig Venter Institute (JCVI), Rockville, MD, USA.
Chunmei WangDepartment of Oral Health Practice, Division of Oral Medicine, Center for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, KY, USA.
Craig S MillerDepartment of Oral Health Practice, Division of Oral Medicine, Center for Oral Health Research, College of Dentistry, University of Kentucky, Lexington, KY, USA.
J. Craig Venter Institute · USUniversity of Kentucky · US

Funding

UKY DENTAL COBRE: POLYBACTERIAL PERIODONTITIS: N-3 PUFA AND ANTIOXIDANTSP20RR020145 · NCRR · UNIVERSITY OF KENTUCKY · PI EBERSOLE, JEFFREY L · 2004 to 2011
$18.3M
Construction Of A Reference Sequence Data Set For The Human Microbiome ProjectU54AI084844 · NIAID · J. CRAIG VENTER INSTITUTE, INC. · PI NELSON, KAREN E. · 2009 to 2012
$10.3M
NIAID NIH HHS U54 AI084844
6 · The paper itself

Abstract

Strain-specific factors contribute in significant but undefined ways to the variable incidence of herpes simplex virus (HSV) recrudescence. Studies that investigate these strain-specific factors are needed. Here, we used qPCR, in vitro assays, and genomic sequencing to identify important relationships between in vitro and clinical phenotypes of unique HSV-1 clinical isolates. Nine HSV-1 isolates from individuals displaying varying reactivation patterns were studied. Isolates associated with frequent recurrent herpes labialis (RHL) (1) displayed higher rates of viral shedding in the oral cavity than those associated with rare RHL and (2) tended to replicate more efficiently at 33 °C than 39 °C. HSV-1 isolates also displayed a more stable phenotype during propagation in U2OS cells than in Vero cells. Draft genome sequences of four isolates and one variant spanning 95.6 to 97.2 % of the genome were achieved, and whole-genome alignment demonstrated that the majority of these isolates clustered with known North American/European isolates. These findings revealed procedures that could help identify unique genotypes and phenotypes associated with HSV-1 isolates, which can be important for determining viral factors critical for regulating HSV-1 reactivation.

Indexed as

Genome, ViralGenotypePhenotypePhylogenyPolymorphism, Single NucleotideAdultAgedAnimalsBase SequenceCell Line, TumorChlorocebus aethiopsFemaleHerpes SimplexHerpesvirus 1, HumanHigh-Throughput Nucleotide SequencingHumansGenetic variationGenomeHerpes virus 1Human/isolation and purificationPhylogenyRecurrenceViralVirus replication

Identifiers

PMID27739035
OpenAlexW2531398180

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.