Evidence map›Paper›PMID 26923062›Full record

ArticleProtein expression and purification2016

Characterization of an Sf-rhabdovirus-negative Spodoptera frugiperda cell line as an alternative host for recombinant protein production in the baculovirus-insect cell system.

Ajay B Maghodia, Christoph Geisler, Donald L Jarvis

Erratum issuedAbstract read
In one paragraph

Article in Protein expression and purification, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

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  16. CRISPR-Cas9 vectors for genome editing and host engineering in the baculovirus-insect cell system.Proceedings of the National Academy of Sciences of the United States of America · 2017
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Ajay B MaghodiaGlycoBac, LLC, Laramie, WY 82072, USA.
Christoph GeislerGlycoBac, LLC, Laramie, WY 82072, USA.
Donald L JarvisGlycoBac, LLC, Laramie, WY 82072, USA; Department of Molecular Biology, University of Wyoming, Laramie, WY 82071, USA. Electronic address: dljarvis@uwyo.edu.
University of Wyoming · US

Funding

Glycoengineered insect cells for commercial biologics manufacturingR44GM102982 · NIGMS · GLYCOBAC, LLC · PI BLAIR, CAROL D, JARVIS, DONALD L. · 2016 to 2017
$940k
Glycoengineering insect cells for commercial recombinant glycoprotein productionR43GM102982 · NIGMS · GLYCOBAC, LLC · PI GEISLER, CHRISTOPH, JARVIS, DONALD L. · 2013 to 2014
$599k
Glycoengineered baculoviruses for the production of more efficacious influenza vaR43AI112118 · NIAID · GLYCOBAC, LLC · PI MAGHODIA, AJAYKUMAR B. · 2014 to 2014
$225k
NIAID NIH HHS R43 AI112118NIGMS NIH HHS R43 GM102982NIGMS NIH HHS R44 GM102982
6 · The paper itself

Abstract

Cell lines derived from the fall armyworm, Spodoptera frugiperda (Sf), are widely used as hosts for recombinant protein production in the baculovirus-insect cell system (BICS). However, it was recently discovered that these cell lines are contaminated with a virus, now known as Sf-rhabdovirus [1]. The detection of this adventitious agent raised a potential safety issue that could adversely impact the BICS as a commercial recombinant protein production platform. Thus, we examined the properties of Sf-RVN, an Sf-rhabdovirus-negative Sf cell line, as a potential alternative host. Nested RT-PCR assays showed Sf-RVN cells had no detectable Sf-rhabdovirus over the course of 60 passages in continuous culture. The general properties of Sf-RVN cells, including their average growth rates, diameters, morphologies, and viabilities after baculovirus infection, were virtually identical to those of Sf9 cells. Baculovirus-infected Sf-RVN and Sf9 cells produced equivalent levels of three recombinant proteins, including an intracellular prokaryotic protein and two secreted eukaryotic glycoproteins, and provided similar N-glycosylation patterns. In fact, except for the absence of Sf-rhabdovirus, the only difference between Sf-RVN and Sf9 cells was SF-RVN produced higher levels of infectious baculovirus progeny. These results show Sf-RVN cells can be used as improved, alternative hosts to circumvent the potential safety hazard associated with the use of Sf-rhabdovirus-contaminated Sf cells for recombinant protein manufacturing with the BICS.

Indexed as

Cloning, MolecularAnimalsBaculoviridaeErythropoietinGene ExpressionHumansMycoplasmaRecombinant ProteinsRhabdoviridaeSf9 CellsSpodopteraEPO protein, humanErythropoietinRecombinant ProteinsBaculovirusInsect cellsRecombinant protein productionSf-rhabdovirusSf-RVN cells

Identifiers

PMID26923062
PMCPMC4842140
OpenAlexW2288165644

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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.