Evidence map›Paper›PMID 40778204›Full record

ArticleFrontiers in microbiology2025

A phosphoprotein gene RT-qPCR assay for detecting all lineages of peste des petits ruminants virus.

Jiao Xu, Yonggang Zhao, Huicong Li, Qinghua Wang, Jiarong Yu, Yingli Wang, Jingyue Bao, Zhiliang Wang

Abstract read
In one paragraph

Article in Frontiers in microbiology, 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
  2. Article
  3. Review
  4. Article
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

8 authors.

Jiao XuExotic Herbivore Disease Surveillance and Research Center, China Animal Health and Epidemiology Center, Qingdao, China.
Yonggang ZhaoExotic Herbivore Disease Surveillance and Research Center, China Animal Health and Epidemiology Center, Qingdao, China.
Huicong LiCollege of Veterinary Science, Qingdao Agricultural University, Qingdao, China.
Qinghua WangExotic Herbivore Disease Surveillance and Research Center, China Animal Health and Epidemiology Center, Qingdao, China.
Jiarong YuExotic Herbivore Disease Surveillance and Research Center, China Animal Health and Epidemiology Center, Qingdao, China.
Yingli WangExotic Herbivore Disease Surveillance and Research Center, China Animal Health and Epidemiology Center, Qingdao, China.
Jingyue BaoExotic Herbivore Disease Surveillance and Research Center, China Animal Health and Epidemiology Center, Qingdao, China.
Zhiliang WangExotic Herbivore Disease Surveillance and Research Center, China Animal Health and Epidemiology Center, Qingdao, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peste des petits ruminants (PPR) is a highly contagious disease caused by peste des petits ruminants virus (PPRV). PPRV is classified into four lineages based on the nucleocapsid (N) or fusion (F) genes. We established a TaqMan quantitative real-time reverse transcription polymerase chain reaction (RT-qPCR) assay using a pair of primers and a probe based on the phosphoprotein (P) gene. The assay was assessed for its sensitivity, specificity, and repeatability in the detection of field samples and was compared with the standard detection method. The developed method could detect all lineages of PPRV, with a sensitivity of four copies/μL for lineage II to IV and 40 copies/μL for lineage I. The results of the specificity test indicated that only the different lineages of PPRV could be detected using the developed method, with no cross-reaction observed with other viruses. The coefficients of variation for both intra-assay and inter-assay repeatability tests were all below 1.50%, demonstrating good repeatability. The detection of field samples, including PPRV-positive and PPRV-negative samples, indicated that all samples were detected correctly, showing a high concordance with the standard detection method. The developed method could detect PPRV with a lower cycle threshold value compared to the previously established N gene-based method, especially for weakly positive samples. This RT-qPCR assay provides a valuable tool to facilitate targeted surveillance and rapid differential diagnosis in regions with an active circulation of PPRV, enabling timely epidemiological investigations and strain-specific identification.

Indexed as

diagnosislineageP genePPRVRT-qPCR

Identifiers

PMID40778204
PMCPMC12328439

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.