Evidence map›Paper›PMID 18614915›Full record

ArticleJournal of acquired immune deficiency syndromes (1999)2008

Optimization of the oligonucleotide ligation assay, a rapid and inexpensive test for detection of HIV-1 drug resistance mutations, for non-North American variants.

Ingrid A Beck, Claudia Crowell, Robin Kittoe, Helba Bredell, Molefe Machaba, Carolyn Willamson, Wouter Janssens, Sabelle Jallow, Guido van der Groen, Yiming Shao and 7 more

Open access · greenAbstract read
In one paragraph

Article in Journal of acquired immune deficiency syndromes (1999), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 43 citations in OpenAlex.

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  4. A comparison of 3 regimens to prevent nevirapine resistance mutations in HIV-infected pregnant women receiving a single intrapartum dose of nevirapine.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2012
    Trial
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  9. Rapid Near Point-of-Care Assay forAIDS research and human retroviruses · 2021
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  17. Observational
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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

17 authors at 8 institutions in 7 countries.

Ingrid A BeckDivision of Infectious Diseases and Virology, University of Washington, Seattle, WA, USA.
Claudia Crowell
Robin Kittoe
Helba Bredell
Molefe Machaba
Carolyn Willamson
Wouter Janssens
Sabelle Jallow
Guido van der Groen
Yiming Shao
Mini Jacob
N M Samuel
Ivette Lorenzana de Rivera
Nicole Ngo-Giang-Huong
Sharon Cassol
George Alemnji
Lisa M Frenkel
University of Washington · USInstituut voor Tropische Geneeskunde · BETamil Nadu Dr. M.G.R. Medical University · INUniversité de Yaoundé I · CMUniversity of Cape Town · ZAUniversity of Pretoria · ZANational Autonomous University of Honduras · HNNational Center for AIDS/STD Control and Prevention,China CDC · CN

Funding

International Maternal Pediatric Adolescent AIDS Clinical Trials (IMPAACT) GroupU01AI068632 · NIAID · SOCIAL AND SCIENTIFIC SYSTEMS, INC. · PI JACKSON, J BROOKS · 2006 to 2010
$109.7M
University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI Grace C. John-Stewart · 1988 to 2026
$104.9M
Reservoirs of drug-resistant HIV-1R01AI058723 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI FRENKEL, LISA M · 2005 to 2009
$2.0M
NIAID NIH HHS P30 AI027757NIAID NIH HHS P30 AI27757NIAID NIH HHS R01 AI058723NIAID NIH HHS U01 AI068632
6 · The paper itself

Abstract

objectiveWe evaluated the feasibility of the oligonucleotide ligation assay (OLA), a specific, sensitive, and economical ligase-based point mutation assay designed to detect HIV-1 drug-resistance mutations at 12 codons of HIV-1 subtype B pol, for potential use in resource-poor settings.

methodsSpecimens from HIV-1-infected individuals collected by 7 international laboratories, including subtypes A, B, C, D, F, G, J, and recombinants AE and AG, were tested by the OLA developed for HIV-1 subtype B. Common polymorphisms that interfered with reactivity of the OLA were identified and modified probes designed and evaluated.

results92.5% (2,410) of 2,604 codons in specimens from 217 individuals were successfully genotyped by the subtype B OLA. A high rate (range 8.3%-31.2%) of indeterminate results (negative OLA reaction for both mutant and wild type) was observed for 5 codons. Modified probes at reverse transcriptase codons 151 and 184 and protease codon 90 increased the rate of valid OLA to 96.1%.

conclusionsThe OLA designed for HIV-1 subtype B genotyped most pol codons in non-B subtypes from Asia and Africa but was improved by addition of several modified probes. International laboratories experienced in molecular techniques were able to perform the OLA.

Indexed as

Anti-HIV AgentsCodonDNA, ComplementaryDNA LigasesDrug Resistance, ViralFeasibility StudiesGenes, polHIV-1HIV InfectionsHIV ProteaseHumansMolecular Sequence DataOligonucleotide ProbesOligonucleotidesPoint MutationPolymerase Chain ReactionAnti-HIV AgentsCodonDNA, ComplementaryDNA LigasesHIV ProteaseOligonucleotide ProbesOligonucleotidesRNA-Directed DNA Polymerase

Identifiers

PMID18614915
PMCPMC2583356
OpenAlexW2020355960

What OpenQuestion holds

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LicenceTDM
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.