Evidence map›Paper›PMID 16207954›Full record

ArticleJournal of clinical microbiology2005

Use of time-saving flow cytometry for rapid determination of resistance of human cytomegalovirus to ganciclovir.

Gyu-Cheol Lee, Dong-Gun Lee, Su-Mi Choi, Jin-Hong Yoo, Sun-Hee Park, Jung-Hyun Choi, Woo-Sung Min, Ok-Hee Cho, Chan-Hee Lee, Wan-Shik Shin

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In one paragraph

Article in Journal of clinical microbiology, 2005. 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
0.6field-weighted citation impact, top 28% 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, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Antiviral drug resistance of human cytomegalovirus.Clinical microbiology reviews · 2010
    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 3 institutions in 1 country.

Gyu-Cheol LeeClinical Research Institute, St. Mary's Hospital, The Catholic University of Korea, College of Medicine, 150-713 Seoul, Korea.
Dong-Gun Lee
Su-Mi Choi
Jin-Hong Yoo
Sun-Hee Park
Jung-Hyun Choi
Woo-Sung Min
Ok-Hee Cho
Chan-Hee Lee
Wan-Shik Shin
Seoul St. Mary's Hospital · KRCatholic University of Korea · KRChungbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are two ways to assess the susceptibility of human cytomegalovirus (HCMV) to ganciclovir (GCV): one is a genotypic test that detects resistance-related mutations and the other is a phenotypic test that actually assesses susceptibility. The advantages of genotyping the UL 97 gene are its rapidity and accuracy. However, to detect novel mutations or mutations affecting the UL 54 DNA polymerase, a phenotypic test such as the plaque reduction assay (PRA) is also required. To avoid the shortcomings of PRA such as its time-consuming nature and labor-intensiveness, we developed a time-saving fluorescence-activated cell sorting (TS-FACS) technique. We obtained a GCV 50% inhibitory concentration (IC(50)) from five clinical isolates and an HCMV laboratory strain (AD169) and compared the results with those from the PRA. The laboratory strain and three clinical isolates were sensitive to GCV. Although there was a minor discrepancy in the case of one of the three isolates, the GCV IC(50) values obtained by TS-FACS analysis correlated well with the results of the PRA. The remaining two isolates were resistant to GCV; one was GCV resistant due to the mutation M 460 V, and the GCV IC(50) results obtained by TS-FACS analysis and by PRA were also comparable. The advantages of TS-FACS analysis are the shorter time required, the possibility of automation, and its comparability to PRA, considered the gold standard. Thus, TS-FACS analysis may be useful as an alternative to PRA in the clinic.

Indexed as

Drug Resistance, ViralAmino Acid SequenceAntiviral AgentsCytomegalovirusCytomegalovirus InfectionsFlow CytometryGanciclovirGenotypeHumansMicrobial Sensitivity TestsMolecular Sequence DataMutationPhenotypePhosphotransferases (Alcohol Group Acceptor)Sequence Analysis, DNATime FactorsAntiviral AgentsGanciclovirganciclovir kinasePhosphotransferases (Alcohol Group Acceptor)

Identifiers

PMID16207954
PMCPMC1248522
OpenAlexW2130064368

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.