Evidence map›Paper›PMID 38817667›Full record

ArticleVirus evolution2024

Selection of viral variants with enhanced transmission and reduced neutralization susceptibility alongside lateral introductions may explain the persistence of porcine reproductive and respiratory syndrome virus in vaccinated breeding herds.

Hepzibar Clilverd, Yanli Li, Gerard Martín-Valls, Laia Aguirre, Marga Martín, Martí Cortey, Enric Mateu

Abstract read
In one paragraph

Article in Virus evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

7 authors.

Hepzibar ClilverdDepartment of Animal Health and Anatomy, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 08193, Spain.ORCID https://orcid.org/0000-0002-4309-7506
Yanli LiDepartment of Animal Health and Anatomy, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 08193, Spain.
Gerard Martín-VallsDepartment of Animal Health and Anatomy, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 08193, Spain.
Laia AguirreDepartment of Animal Health and Anatomy, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 08193, Spain.
Marga MartínDepartment of Animal Health and Anatomy, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 08193, Spain.
Martí CorteyDepartment of Animal Health and Anatomy, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 08193, Spain.ORCID https://orcid.org/0000-0003-1126-3423
Enric MateuDepartment of Animal Health and Anatomy, Universitat Autònoma de Barcelona, Cerdanyola del Vallès 08193, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigates the long-term evolutionary dynamics of porcine reproductive and respiratory syndrome virus (PRRSV-1) in an endemically infected and vaccinated pig herd. Over a one year and a half period, piglets from seven farrowing batches in a 300-sow PRRSV-vaccinated farm were monitored from birth to nine weeks of age by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Eighty-five PRRSV-positive samples were subjected to whole genome sequencing (Illumina Miseq), and 251 samples to open reading frame 5 (ORF5) sequencing. Farm-specific PRRSV variants' impact on anti-PRRSV antibodies was evaluated using enzyme-linked immunosorbent and neutralizing antibody assays. The replication kinetics and cytokine inhibition capabilities (IFN-α and TNF-α) of these variants were assessed in porcine alveolar macrophages. The study revealed fluctuating PRRSV-1 incidences in farrowing units and nurseries, attributed to two key evolutionary events: an escape variant emergence and a lateral introduction of a new strain. Initially, strain 1 variant α was swiftly replaced within weeks by variant 1β (99.5 per cent genomic similarity), with twenty-five amino acid mutations, primarily in nsp1α, GP2, GP3, and GP5, including an additional glycosylation site and a deletion downstream the neutralization epitope of GP5. This shift to 1β correlated with increased incidence in nurseries and higher viral loads, with sera from 1α-exposed animals showing reduced neutralization against 1β. Consistently for

Indexed as

endemicpersistencePRRSVvaccinationviral evolution

Identifiers

PMID38817667
PMCPMC11137674

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Registered trials

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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.