Evidence map›Paper›PMID 26751207›Full record

Observational studyPloS one2016

Simplified Paper Format for Detecting HIV Drug Resistance in Clinical Specimens by Oligonucleotide Ligation.

Nuttada Panpradist, Ingrid A Beck, Michael H Chung, James N Kiarie, Lisa M Frenkel, Barry R Lutz

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

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  12. Rapid Near Point-of-Care Assay forAIDS research and human retroviruses · 2021
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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

6 authors at 2 institutions in 2 countries.

Nuttada PanpradistDepartment of Bioengineering, University of Washington, Seattle, Washington, United States of America.
Ingrid A BeckSeattle Children's Research Institute, Seattle, Washington, United States of America.
Michael H ChungDepartment of Internal Medicine, University of Washington, Seattle, Washington, United States of America.
James N KiarieDepartments of Obstetrics and Gynecology, University of Nairobi, Nairobi, Kenya.
Lisa M FrenkelDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.
Barry R LutzDepartment of Bioengineering, University of Washington, Seattle, Washington, United States of America.
University of Washington · USUniversity of Nairobi · KE

Funding

A rapid point-of-treatment diagnostic assay for HIV-resistance to 1st-line ARTR01AI110375 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI FRENKEL, LISA M · 2014 to 2018
$2.3M
Reservoirs of drug-resistant HIV-1R01AI058723 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI FRENKEL, LISA M · 2005 to 2009
$2.0M
NIAID NIH HHS 1R01AI110375-01NIAID NIH HHS R01 AI058723NIAID NIH HHS R01-AI058723NIAID NIH HHS R01 AI110375
6 · The paper itself

Abstract

Human immunodeficiency virus (HIV) is a chronic infection that can be managed by antiretroviral treatment (ART). However, periods of suboptimal viral suppression during lifelong ART can select for HIV drug resistant (DR) variants. Transmission of drug resistant virus can lessen or abrogate ART efficacy. Therefore, testing of individuals for drug resistance prior to initiation of treatment is recommended to ensure effective ART. Sensitive and inexpensive HIV genotyping methods are needed in low-resource settings where most HIV infections occur. The oligonucleotide ligation assay (OLA) is a sensitive point mutation assay for detection of drug resistance mutations in HIV pol. The current OLA involves four main steps from sample to analysis: (1) lysis and/or nucleic acid extraction, (2) amplification of HIV RNA or DNA, (3) ligation of oligonucleotide probes designed to detect single nucleotide mutations that confer HIV drug resistance, and (4) analysis via oligonucleotide surface capture, denaturation, and detection (CDD). The relative complexity of these steps has limited its adoption in resource-limited laboratories. Here we describe a simplification of the 2.5-hour plate-format CDD to a 45-minute paper-format CDD that eliminates the need for a plate reader. Analysis of mutations at four HIV-1 DR codons (K103N, Y181C, M184V, and G190A) in 26 blood specimens showed a strong correlation of the ratios of mutant signal to total signal between the paper CDD and the plate CDD. The assay described makes the OLA easier to perform in low resource laboratories.

Indexed as

Genotyping TechniquesMolecular Diagnostic TechniquesPoint MutationAnti-HIV AgentsDried Blood Spot TestingDrug Resistance, ViralGenotypeHIV-1HIV InfectionsHumansKenyaLigase Chain ReactionOligonucleotide ProbesPaperpol Gene Products, Human Immunodeficiency VirusRetrospective StudiesAnti-HIV AgentsOligonucleotide Probespol Gene Products, Human Immunodeficiency Virus

Identifiers

PMID26751207
PMCPMC4713472
OpenAlexW2236447343

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.