Evidence map›Paper›PMID 41754512›Full record

ArticleViruses2026

Optimized Propagation and Purification Protocols for Large-Scale Production of Rhinovirus C.

Jason Kaiya, Mark K Devries, James E Gern, Yury A Bochkov

Abstract read
In one paragraph

Article in Viruses, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Jason KaiyaDepartment of Pediatrics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53792, USA.
Mark K DevriesDepartment of Pediatrics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53792, USA.
James E GernDepartment of Pediatrics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53792, USA.ORCID 0000-0002-6667-4708
Yury A BochkovDepartment of Pediatrics, School of Medicine and Public Health, University of Wisconsin, Madison, WI 53792, USA.ORCID 0000-0003-2618-4496

Funding

Mechanisms of Enhanced Neutralizing Antibody Responses to Rhinovirus CR01AI148707 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI BOCHKOV, YURY A · 2020 to 2024
$3.9M
NIAID NIH HHS R01 AI148707NIH HHS 1U19AI181979-01NIH HHS R01AI148707
6 · The paper itself

Abstract

backgroundRhinovirus C (RV-C) is one of three species of rhinoviruses (RVs), which cause the common cold, preschool wheezing illnesses and exacerbations of asthma. RV-C types are more virulent, especially in children, but progress in developing treatments is limited by difficulties in generating high-titer virus preparations. The goals of this study were to optimize methods for large-scale production and purification of RV-C to facilitate structure and immune response studies.

methodsWe optimized protocols for the propagation and purification of RV-C15a, a clinical isolate adapted to HeLa-E8 cells stably expressing virus receptor CDHR3. We compared virus yields in adherent and suspension cultures, evaluated the effects of calcium supplementation and infection timing, and tested multiple purification strategies, including ultracentrifugation, dialysis, and lipase treatment.

resultsRV-C15a yields were significantly lower in suspension vs. adherent cultures despite comparable virus binding and entry, suggesting post-entry replication limitations in suspended cells. In adherent cultures, infecting soon after cell seeding and calcium supplementation reduced the time of virus production and modestly improved virus progeny yields. Surface CDHR3 expression declined over time, potentially restricting viral spread. Among purification methods, lipase treatment of infected cell lysates followed by ultracentrifugation produced highly pure and concentrated virus preparations suitable for structural and immunological applications, with high yields.

conclusionsWe present a robust system for large-scale RV-C15a production in adherent HeLa-E8 cells and recommend a lipase-based purification method as a rapid and effective approach for producing high-quality viral preparations. These advances will support structural studies and accelerate the development of RV-C-targeted therapeutics and vaccines.

Indexed as

RhinovirusVirus CultivationCadherin Related ProteinsEnterovirusHeLa CellsHumansMembrane ProteinsPicornaviralesVirus ReplicationCadherin Related ProteinsCDHR3 protein, humanMembrane Proteinscadherin-related family member 3propagationpurificationrhinovirus C

Identifiers

PMID41754512
PMCPMC12945259

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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.