Evidence map›Paper›PMID 35205129›Full record

ArticleBiology2022

Side-by-Side Comparison of Post-Entry Quarantine and High Throughput Sequencing Methods for Virus and Viroid Diagnosis.

Marie-Emilie A Gauthier, Ruvini V Lelwala, Candace E Elliott, Craig Windell, Sonia Fiorito, Adrian Dinsdale, Mark Whattam, Julie Pattemore, Roberto A Barrero

Abstract read
In one paragraph

Article in Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

9 authors.

Marie-Emilie A GauthiereResearch, Research Infrastructure, Academic Division, Queensland University of Technology, Brisbane, QLD 4001, Australia.ORCID 0000-0002-5256-9165
Ruvini V LelwalaeResearch, Research Infrastructure, Academic Division, Queensland University of Technology, Brisbane, QLD 4001, Australia.
Candace E ElliottScience and Surveillance Group, Post Entry Quarantine, Department of Agriculture, Water and the Environment, Mickleham, VIC 3064, Australia.
Craig WindelleResearch, Research Infrastructure, Academic Division, Queensland University of Technology, Brisbane, QLD 4001, Australia.
Sonia FioritoPlant Innovation Centre, Post Entry Quarantine, Department of Agriculture, Water and the Environment, Mickleham, VIC 3064, Australia.
Adrian DinsdalePlant Innovation Centre, Post Entry Quarantine, Department of Agriculture, Water and the Environment, Mickleham, VIC 3064, Australia.
Mark WhattamPlant Innovation Centre, Post Entry Quarantine, Department of Agriculture, Water and the Environment, Mickleham, VIC 3064, Australia.
Julie PattemoreScience and Surveillance Group, Post Entry Quarantine, Department of Agriculture, Water and the Environment, Mickleham, VIC 3064, Australia.
Roberto A BarreroeResearch, Research Infrastructure, Academic Division, Queensland University of Technology, Brisbane, QLD 4001, Australia.ORCID 0000-0002-7735-665X

Funding

Hort Innovation MT18005
6 · The paper itself

Abstract

Rapid and safe access to new plant genetic stocks is crucial for primary plant industries to remain profitable, sustainable, and internationally competitive. Imported plant species may spend several years in Post Entry Quarantine (PEQ) facilities, undergoing pathogen testing which can impact the ability of plant industries to quickly adapt to new global market opportunities by accessing new varieties. Advances in high throughput sequencing (HTS) technologies provide new opportunities for a broad range of fields, including phytosanitary diagnostics. In this study, we compare the performance of two HTS methods (RNA-Seq and sRNA-Seq) with that of existing PEQ molecular assays in detecting and identifying viruses and viroids from various plant commodities. To analyze the data, we tested several bioinformatics tools which rely on different approaches, including direct-read, de novo, and reference-guided assembly. We implemented VirusReport, a new portable, scalable, and reproducible nextflow pipeline that analyses sRNA datasets to detect and identify viruses and viroids. We raise awareness of the need to evaluate cross-sample contamination when analyzing HTS data routinely and of using methods to mitigate index cross-talk. Overall, our results suggest that sRNA analyzed using VirReport provides opportunities to improve quarantine testing at PEQ by detecting all regulated exotic viruses from imported plants in a single assay.

Indexed as

high throughput sequencingphytosanitary diagnostic assayplant siRNAplant virus and viroid detectionpost-entry quarantine facility

Identifiers

PMID35205129
PMCPMC8868628

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.