Evidence map›Paper›PMID 32015044›Full record

ArticleAntimicrobial agents and chemotherapy2020

Hypersusceptibility of Human Cytomegalovirus to Foscarnet Induced by Mutations in Helices K and P of the Viral DNA Polymerase.

Karima Zarrouk, Van Dung Pham, Jocelyne Piret, Rong Shi, Guy Boivin

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2020. 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
–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

2 citing papers in PubMed.

  1. Article
  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

5 authors.

Karima ZarroukResearch Center in Infectious Diseases, CHU de Québec-Laval University, Quebec City, Quebec, Canada.
Van Dung PhamDepartment of Biochemistry, Microbiology, and Bioinformatics, PROTEO, Laval University, Quebec City, Quebec, Canada.
Jocelyne PiretResearch Center in Infectious Diseases, CHU de Québec-Laval University, Quebec City, Quebec, Canada.
Rong ShiDepartment of Biochemistry, Microbiology, and Bioinformatics, PROTEO, Laval University, Quebec City, Quebec, Canada.
Guy BoivinResearch Center in Infectious Diseases, CHU de Québec-Laval University, Quebec City, Quebec, Canada Guy.Boivin@crchudequebec.ulaval.ca.

Funding

CIHR 148361
6 · The paper itself

Abstract

Herein, we phenotypically and enzymatically characterize the theoretical mutation Q579I in helix K and the already described clinical mutation K805Q in helix P of cytomegalovirus DNA polymerase for susceptibility to foscarnet. Q579I and K805Q recombinant viruses were hypersusceptible to foscarnet (respective mean 50% effective concentrations [EC

Indexed as

Antiviral AgentsCytomegalovirusCytomegalovirus InfectionsDNA-Directed DNA PolymeraseDNA, ViralDrug Resistance, ViralFoscarnetHumansModels, MolecularMutationAntiviral AgentsDNA-Directed DNA PolymeraseDNA, ViralFoscarnetDNA polymerasefoscarnethuman cytomegalovirushypersusceptibilitymolecular modelingresistance

Identifiers

PMID32015044
PMCPMC7179328

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.