Evidence map›Paper›PMID 23687576›Full record

ArticleJournal of the Pediatric Infectious Diseases Society2012

Longitudinal Characterization of Herpes Simplex Virus (HSV) Isolates Acquired From Different Sites in an Immune-Compromised Child: A New HSV Thymidine Kinase Mutation Associated With Resistance.

Andrew H Karaba, Laura K Cohen, Taly Glaubach, Sarah J Kopp, Jennifer L Reichek, Hawke H Yoon, Xiaotian T Zheng, William J Muller

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the Pediatric Infectious Diseases Society, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. New strategies against drug resistance to herpes simplex virus.International journal of oral science · 2016
    Review
  2. 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

8 authors at 2 institutions in 1 country.

Andrew H KarabaDepartments of Microbiology-Immunology.
Laura K CohenPediatrics, and.
Taly GlaubachPediatrics, and.
Sarah J KoppDepartments of Microbiology-Immunology Pediatrics, and.
Jennifer L ReichekPediatrics, and.
Hawke H YoonOphthalmology, Northwestern University Feinberg School of Medicine.
Xiaotian T ZhengDepartment of Pathology and Laboratory Medicine; Children's Memorial Hospital, Chicago, Illinois.
William J MullerPediatrics, and.
Pediatrics and Genetics · USLurie Children's Hospital · US

Funding

Herpes Simplex Virus Entry Receptors in Immune Memory and Newborn InfectionK08AI089942 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MULLER, WILLIAM JOSEPH · 2010 to 2012
$387k
NIAID NIH HHS K08 AI089942
6 · The paper itself

Abstract

backgroundHerpes simplex virus resistance to acyclovir is well described in immune-compromised patients. Management of prolonged infection and recurrences in such patients may be problematic.

methodsA patient with neuroblastoma developed likely primary herpes gingivostomatitis shortly after starting a course of chemotherapy, with spread to the eye during treatment with acyclovir. Viral isolates were serially obtained from separate sites after treatment was begun and tested for susceptibility to acyclovir and foscarnet by plaque reduction and plating efficiency assays. The thymidine kinase and DNA polymerase genes from each isolate were sequenced.

resultsInitial isolates from a throat swab, an oral lesion, and conjunctiva were resistant to acyclovir within 13 days of treatment. Subsequent isolates while on foscarnet were initially acyclovir-susceptible, but reactivation of an acyclovir-resistant isolate was subsequently documented while on acyclovir suppression. Genotypic analysis identified a previously unreported UL23 mutation in some resistant isolates. None of the amino acid changes identified in UL30 were associated with resistance.

conclusionsPhenotypic and genotypic antiviral resistance of herpes simplex isolates may vary from different compartments and over time in individual immune-compromised hosts, highlighting the importance of obtaining cultures from all sites. Phenotypic resistance testing should be considered for isolates obtained from at-risk patients not responding to first-line therapy. Empiric combination treatment with multiple antivirals could be considered in some situations.

Identifiers

PMID23687576
PMCPMC3656553
OpenAlexW2168357009

What OpenQuestion holds

Textmetadata
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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.