Evidence map›Paper›PMID 35582482›Full record

ArticleJournal of veterinary research2022

A New Enzyme-linked Immunosorbent Assay for Serological Diagnosis of Seal Parapoxvirus Infection in Marine Mammals.

Yassien Badr, Md Matiur Rahman, Yoshito Ohno, Keita Ishijima, Ken Maeda, Kaoru Kohyama, Yuji O Kamatari, Kaori Shimizu, Ayaka Okada, Yasuo Inoshima

Open access · goldAbstract read
In one paragraph

Article in Journal of veterinary research, 2022. 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
1.2field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Seroepidemiological survey of sealpox virus infection in marine mammals.The Journal of veterinary medical science · 2026
    Article
  2. Article
  3. Orf, a Human Parapoxvirus Infection.Advances in experimental medicine and biology · 2024
    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

10 authors at 3 institutions in 3 countries.

Yassien BadrLaboratory of Food and Environmental Hygiene, Cooperative Department of Veterinary Medicine, Damanhour, Egypt.
Md Matiur RahmanLaboratory of Food and Environmental Hygiene, Cooperative Department of Veterinary Medicine, Damanhour, Egypt.
Yoshito OhnoPort of Nagoya Public Aquarium, Minato-ku, Nagoya, Aichi 455-0033, Japan.
Keita IshijimaDepartment of Veterinary Science, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan.
Ken MaedaDepartment of Veterinary Science, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo 162-8640, Japan.
Kaoru KohyamaIzu Mito Sea Paradise, Numazu, Shizuoka 410-0224, Japan.
Yuji O KamatariDivision of Instrumental Analysis, Life Science Research Center, Yamaguchi, Japan.
Kaori ShimizuLaboratory of Food and Environmental Hygiene, Cooperative Department of Veterinary Medicine, Damanhour, Egypt.
Ayaka OkadaLaboratory of Food and Environmental Hygiene, Cooperative Department of Veterinary Medicine, Damanhour, Egypt.
Yasuo InoshimaLaboratory of Food and Environmental Hygiene, Cooperative Department of Veterinary Medicine, Damanhour, Egypt.
Damanhour University · EGNational Institute of Infectious Diseases · JPSylhet Agricultural University · BD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Seal parapoxvirus (SPPV) infection has been reported among pinnipeds in aquaria in Japan; however, its seroprevalence is unknown. Therefore, an enzyme-linked immunosorbent assay (ELISA) was developed for serological diagnosis of SPPV infection. Material and Methods: The gene encoding the major envelope protein of SPPV was cloned into the eukaryotic expression vector pAcGFP1-N1, which encodes the green fluorescence protein (GFP), thereby producing a fusion protein (Env-GFP). Parental and cloned vector DNA was independently transfected into cultured seal cells for the expression of GFP and Env-GFP. The wells of an ELISA plate were coated with either GFP- or Env-GFP-transfected cell lysates. The light absorbance of each serum sample was adjusted by subtracting the absorbance of GFP-coated wells from that of Env-GFP-coated wells. Sera from two spotted seals ( Results: Positive reactions were not observed, except in one preserved sample collected ten years ago from a naturally SPPV-infected spotted seal. Conclusion: The established ELISA could be useful in screening marine mammal sera for anti-SPPV antibodies.

Indexed as

aquariumELISAparapoxviruspinnipedsWestern blotting

Identifiers

PMID35582482
PMCPMC8959681
OpenAlexW4229048578

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.