Evidence map›Paper›PMID 40671821›Full record

ArticleFrontiers in veterinary science2025

A novel L1C.5 RFLP-1-4-4 recombinant porcine reproductive and respiratory syndrome virus between wild-type virus and a modified-live virus vaccine is highly pathogenic to piglets.

Xue Gao, Jun Zhou, Runmin Kang, Haohao Lu, Shuo Feng, Yiwen Pei, Jie Liu, Zhidong Zhang, Long Zhou

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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.

Xue GaoKey Laboratory of Veterinary Medicine in Universities of Sichuan Province, College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu, China.
Jun ZhouSichuan Boce Testing Technology Co., Ltd., Chengdu, China.
Runmin KangSichuan Provincial Key Laboratory of Animal Breeding and Genetics, Sichuan Animal Science Academy, Chengdu, Sichuan, China.
Haohao LuKey Laboratory of Veterinary Medicine in Universities of Sichuan Province, College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu, China.
Shuo FengKey Laboratory of Veterinary Medicine in Universities of Sichuan Province, College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu, China.
Yiwen PeiKey Laboratory of Veterinary Medicine in Universities of Sichuan Province, College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu, China.
Jie LiuKey Laboratory of Veterinary Medicine in Universities of Sichuan Province, College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu, China.
Zhidong ZhangKey Laboratory of Veterinary Medicine in Universities of Sichuan Province, College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu, China.
Long ZhouKey Laboratory of Veterinary Medicine in Universities of Sichuan Province, College of Animal and Veterinary Sciences, Southwest Minzu University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Porcine reproductive and respiratory syndrome (PRRS) is a severe viral disease in pigs caused by porcine reproductive and respiratory syndrome virus (PRRSV). It poses a severe threat to the global swine breeding industry. Recently, the emergence of PRRSV lineage 1C.5 in the United States and China with the RFLP 1-4-4 pattern has raised worldwide attention; however, there are few studies on the genome and pathogenic characteristics of the L1C.5 RFLP 1-4-4 PRRSV in China. In this study, a novel PRRSV-2 variant, designated GX2024, was isolated from a RespPRRS MLV-vaccinated piglet in China using Marc-145 cells and porcine alveolar macrophages (PAMs). The complete viral genome was further determined and analyzed. Phylogenetic analysis of its ORF5 gene showed that GX2024 belonged to PRRSV-2 L1C.5 (RFLP-1-4-4) group, whereas the complete genome sequence clustered into L8E (JXA1-like) group and it contains a discontinuous 131-aa deletion in NSP2 when compared to the NADC30 strain. Notably, recombination analyses indicated that GX2024 is a multiple recombinant virus from two wild-type PRRSVs L1C.5 (NADC30-like) and L8E (JXA1-like), and a RespPRRS MLV vaccine (L5A) strain. To tested the pathogenicity of GX2024, nine four-week-old piglets were divided into two groups (GX2024-challenge group,

Indexed as

highly pathogenicL1C RFLP-1-4-4MLVporcine reproductive and respiratory syndrome virusrecombination

Identifiers

PMID40671821
PMCPMC12263378

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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.