Evidence map›Paper›PMID 40598372›Full record

ArticleIrish veterinary journal2025

Effects of serial passaging of field isolates of Bangladeshi PPR virus in Vero cells on the fusion protein.

Md Saiful Islam Siddiqui, Anja Globig, Md Mushfiqur Rahman, Md Rafiqul Islam, Emdadul Haque Chowdhury

Abstract read
In one paragraph

Article in Irish veterinary journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

5 authors.

Md Saiful Islam SiddiquiDepartment of Anatomy & Histology, Faculty of Veterinary, Animal & Biomedical Sciences, Sylhet Agricultural University, Sylhet, 3100, Bangladesh. msisiddiqui2000@yahoo.com.ORCID http://orcid.org/0000-0003-4995-1782
Anja GlobigFriedrich Loffler Institut, Federal Research Institute for Animal Health, Südufer 10, Greifswald, Insel Riems, D-17493, Germany.
Md Mushfiqur RahmanOffice of the Director General, Public Private Partnership, Prime Minister Office, Government of Peoples Republic of Bangladesh, Dhaka, Bangladesh.
Md Rafiqul IslamDepartment of Pathology, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh, 2202, Bangladesh.
Emdadul Haque ChowdhuryDepartment of Pathology, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh, 2202, Bangladesh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesFusion (F) protein is crucial for facilitating viral entry into host cells and contributes to the virulence of Morbilliviruses. Serial passaging of the Peste Des Petits Ruminants virus (PPRV) in nonnative hosts can lead to mutations that potentially reduce pathogenicity. Hence, this study aimed to investigate the effects of serial passaging of a Bangladeshi strain of PPR virus in Vero cells on the Fusion protein and pathogenicity MATERIALS AND

methodsPPR viruses were initially isolated from natural PPR outbreaks, confirmed through reverse transcriptase polymerase chain reaction (RT‒PCR), passaged to the 9th passage in Vero cells, sequenced, and preserved in a previous study. The 9th passage virus from the repository was utilized as the viral inoculant for further passaging in Vero cells, and the 60th passage was completed. The presence of PPR viral RNA was confirmed in tissue culture fluid (TCF) by RT‒PCR at different passage numbers. TCF at the 60th passage was sequenced and used for immunogenicity studies via live animal experiments, and subsequent immunity was measured via cELISA.

resultsComparative analysis of the sequences from the 9th and 60th passages, along with other sequences, revealed substitutions of 14 nucleotides (nts) and 4 amino acids (aa) within the leucine zipper structure of the fusion protein. Notably, live animal experiments demonstrated the occurrence of protective immunity.

conclusionThis study suggests that amino acid substitution and genetic divergence may positively affect viral virulence, highlighting their importance in the development of a potent vaccine.

Indexed as

Cell cultureContinual passagingFusion proteinNucleotide sequenceVirus

Identifiers

PMID40598372
PMCPMC12210771

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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.