Evidence map›Paper›PMID 40045076›Full record

ArticleBiotechnology letters2025

Multiplicity of infection and culture medium on the SARS-CoV-2 virus like-particles production by baculovirus/insect system.

Luis Giovani de Oliveira Guardalini, Felipe Moura Dias, Samanta Omae Camalhonte, Jaci Leme, Thaissa Consoni Bernardino, Felipe Soares Sposito, Eduardo Dias, Renato Mancini Astray, Aldo Tonso, Soraia Attie Calil Jorge and 1 more

Abstract read
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In one paragraph

Article in Biotechnology letters, 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

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

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

11 authors.

Luis Giovani de Oliveira GuardaliniLaboratório de Biotecnologia Viral, Instituto Butantan, Av Vital Brasil 1500, São Paulo, SP, CEP 05503-900, Brazil.
Felipe Moura DiasLaboratório de Biotecnologia Viral, Instituto Butantan, Av Vital Brasil 1500, São Paulo, SP, CEP 05503-900, Brazil.
Samanta Omae CamalhonteLaboratório de Biotecnologia Viral, Instituto Butantan, Av Vital Brasil 1500, São Paulo, SP, CEP 05503-900, Brazil.
Jaci LemeLaboratório de Biotecnologia Viral, Instituto Butantan, Av Vital Brasil 1500, São Paulo, SP, CEP 05503-900, Brazil.
Thaissa Consoni BernardinoLaboratório de Biotecnologia Viral, Instituto Butantan, Av Vital Brasil 1500, São Paulo, SP, CEP 05503-900, Brazil.
Felipe Soares SpositoMerck Life Science & Electronics, Alameda Xingu, 350-7° Andar, Alphaville Industrial, Barueri, SP, CEP 06455-911, Brazil.
Eduardo DiasMerck Life Science & Electronics, Alameda Xingu, 350-7° Andar, Alphaville Industrial, Barueri, SP, CEP 06455-911, Brazil.
Renato Mancini AstrayLaboratório Multipropósito, Instituto Butantan, Av. Vital Brasil 1500, São Paulo, SP, CEP 05503-900, Brazil.
Aldo TonsoLaboratório de Células Animais, Departamento de Engenharia Química, Escola Politécnica, Universidade de São Paulo, Av. Prof. Luciano Gualberto, travessa do Politécnico, 380, São Paulo, SP, 05508-010, Brazil.
Soraia Attie Calil JorgeLaboratório de Biotecnologia Viral, Instituto Butantan, Av Vital Brasil 1500, São Paulo, SP, CEP 05503-900, Brazil.
Eutimio Gustavo Fernández NúñezLaboratório de Engenharia de Bioprocessos. Escola de Artes, Ciências e Humanidades (EACH), Universidade de São Paulo, Rua Arlindo Béttio, 1000, São Paulo, SP, CEP 03828-000, Brazil. egfnunez@usp.br.ORCID http://orcid.org/0000-0002-2800-392X

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 20/05264-0Fundação de Amparo à Pesquisa do Estado de São Paulo 21/14451-0Fundação de Amparo à Pesquisa do Estado de São Paulo 22/02713-3Universidade de São Paulo PUB-EACH 83-1
6 · The paper itself

Abstract

This work aimed to assess the SARS-CoV-2 structural proteins' expression and virus-like particles (VLP) production by Baculovirus/Insect cell platform using two levels of Multiplicity of Infection (MOI), and two culture media, one of them a serum-free medium and the other one chemically defined. Two SARS-CoV-2 VLP were obtained from Sf9 cells coinfection using in both cases, three monocistronic recombinant baculoviruses holding the genes of Nucleocapsid (N; MOI = 2 or 0.2), Membrane (M; MOI = 1 or 0.1), and Envelope (E; MOI = 1 or 0.1) viral proteins, and the fourth one was changed between a baculovirus bearing Spike protein (S; MOI = 3 or 0.3) or receptor-binding domain (RBD; MOI = 3 or 0.3) genes of SARS-CoV-2. Similar performance was verified for both culture media in SARS-CoV-2 VLP production bearing four structural virus proteins or RBD domain. The SARS-CoV-2 structural proteins' expression was comparable at different MOIs (tenfold) as well as SARS-CoV-2 VLP size (around 100 nm). The increase in specific death rates over the coinfection phase was confirmed in relatively high MOI assays. This finding was related to an exponential virus titer profile for high MOIs over the entire infection phase, meanwhile, a viral peak was observed at low MOIs, confirming a secondary infection. The SARS-CoV-2 VLP improved production carrying immunogenic S protein was confirmed concerning others holding RBD. However, the protein composition of produced VLP should be studied further to assess the VLP homogeneity when different culture media and MOIs are used.

Indexed as

BaculoviridaeCulture MediaSARS-CoV-2Vaccines, Virus-Like ParticleAnimalsCOVID-19HumansInsectaSf9 CellsSpike Glycoprotein, CoronavirusSpodopteraViral Structural ProteinsCulture MediaSpike Glycoprotein, CoronavirusVaccines, Virus-Like ParticleViral Structural ProteinsChemically defined culture mediumCOVID-19SARS-CoV-2Serum-free culture mediumStirred tank bioreactorVaccineVirus-like particles

Identifiers

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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.