Evidence map›Paper›PMID 37112945›Full record

ArticleViruses2023

A Multiplexed, Tiled PCR Method for Rapid Whole-Genome Sequencing of Infectious Spleen and Kidney Necrosis Virus (ISKNV) in Tilapia.

Shayma Alathari, Dominique L Chaput, Luis M Bolaños, Andrew Joseph, Victoria L N Jackson, David Verner-Jeffreys, Richard Paley, Charles R Tyler, Ben Temperton

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Shayma AlathariDepartment of Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK.ORCID 0000-0003-2745-3045
Dominique L ChaputDepartment of Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK.ORCID 0000-0002-9736-2619
Luis M BolañosDepartment of Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK.
Andrew JosephCentre for Environment, Fisheries and Aquaculture Science (Cefas), The Nothe, Barrack Road, Weymouth DT4 8UB, UK.ORCID 0000-0001-5717-3170
Victoria L N JacksonDepartment of Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK.
David Verner-JeffreysCentre for Environment, Fisheries and Aquaculture Science (Cefas), The Nothe, Barrack Road, Weymouth DT4 8UB, UK.
Richard PaleyCentre for Environment, Fisheries and Aquaculture Science (Cefas), The Nothe, Barrack Road, Weymouth DT4 8UB, UK.ORCID 0000-0003-2288-6300
Charles R TylerDepartment of Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK.
Ben TempertonDepartment of Biosciences, University of Exeter, Stocker Road, Exeter EX4 4QD, UK.ORCID 0000-0002-3667-8302
University of Exeter · GBCentre for Environment, Fisheries and Aquaculture Science · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tilapia farming is one of the most important sectors in aquaculture worldwide and of major importance to global food security. Infectious spleen and kidney necrosis virus (ISKNV) has been identified as an agent of high morbidity and mortality, threatening tilapia aquaculture. ISKNV was detected in Lake Volta, Ghana, in September 2018 and spread rapidly, with mortality rates between 60 and 90% and losses of more than 10 tonnes of fish per day. Understanding the spread and evolution of viral pathogens is important for control strategies. Here, we developed a tiled-PCR sequencing approach for the whole-genome sequencing of ISKNV, using long read sequencing to enable field-based, real-time genomic surveillance. This work represents the first use of tiled-PCR for whole genome recovery of viruses in aquaculture, with the longest genome target (>110 kb dsDNA) to date. Our protocol was applied to field samples collected from the ISKNV outbreaks from four intensive tilapia cage culture systems across Lake Volta, between October 2018 and May 2022. Despite the low mutation rate of dsDNA viruses, 20 single nucleotide polymorphisms accumulated during the sampling period. Droplet digital PCR identified a minimum requirement of template in a sample to recover 50% of an ISKNV genome at 275 femtograms (2410 viral templates per 5 µL sequencing reaction). Overall, tiled-PCR sequencing of ISKNV provides an informative tool to assist in disease control in aquaculture.

Indexed as

DNA Virus InfectionsFish DiseasesIridoviridaeTilapiaAnimalsMultiplex Polymerase Chain ReactionaquacultureArtic-NetworkISKNVlong-read sequencingOreochromis niloticus

Identifiers

PMID37112945
PMCPMC10145788
OpenAlexW4365514834

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.