Evidence map›Paper›PMID 23308179›Full record

ArticlePloS one2013

Development of two murine antibodies against Neospora caninum using phage display technology and application on the detection of N. caninum.

Jinhua Dong, Takahiro Otsuki, Tatsuya Kato, Tetsuya Kohsaka, Kazunori Ike, Enoch Y Park

Abstract read
In one paragraph

Article in PloS one, 2013. 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.

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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

6 authors.

Jinhua DongLaboratory of Biotechnology, Graduate School of Science and Technology, Shizuoka University, Shizuoka, Japan.
Takahiro Otsuki
Tatsuya Kato
Tetsuya Kohsaka
Kazunori Ike
Enoch Y Park

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neosporosis, caused by an intracellular parasite, Neospora caninum, is an infectious disease primarily of cattle and dogs. It occurs worldwide and causes huge damages to dairy farms. In this study, we immunized mice with recombinant surface-associated protein 1 of N. caninum (rNcSAG1) and developed two novel monoclonal antibodies, A10 and H3, against NcSAG1 using phage-display technology. Both clones bound to purified rNcSAG1 and the half maximal inhibitory concentrations of A10 and H3 are 50 and 72 nM of rNcSAG1, respectively. In immunofluorescence assays, both A10 and H3 Fabs bound to N. caninum parasites. Direct detection of N. caninum parasites was developed firstly using an enzyme-linked immunosorbent assay (ELISA) with A10 and H3. Binding of A10 and H3 antibodies to rNcSAG1 was also inhibited by some certain anti-N. caninum antibodies in the neosporosis-positive cattle sera, suggesting they might bind to the same epitopes of NcSAG1 with those anti-N. caninum antibodies of bovine. These antibodies were demonstrated to have a potential for monitoring the N. caninum parasites in a dairy farm, which may lead to protect livestock from parasite-infection.

Indexed as

Enzyme-Linked Immunosorbent AssayAnimalsAntibodies, MonoclonalAntibodies, ProtozoanAntigens, ProtozoanCattleCell Surface Display TechniquesCoccidiosisDogsImmunizationMiceMice, Inbred BALB CNeosporaProtozoan ProteinsAntibodies, MonoclonalAntibodies, ProtozoanAntigens, ProtozoanProtozoan Proteins

Identifiers

PMID23308179
PMCPMC3540087

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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.