InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays

Detalhes bibliográficos
Autor(a) principal: Magalhães, AC
Data de Publicação: 2022
Outros Autores: Ricardo, S, Moreira, AC, Nunes, M, Tavares, M, Pinto, RJ, Gomes, MS, Pereira, L
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/151609
Resumo: The recently emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has forced the scientific community to acquire knowledge in real-time, when total lockdowns and the interruption of flights severely limited access to reagents as the global pandemic became established. This unique reality made researchers aware of the importance of designing efficient in vitro set-ups to evaluate infectious kinetics. Here, we propose a histology-based method to evaluate infection kinetics grounded in cell microarray (CMA) construction, immunocytochemistry and in situ hybridization techniques. We demonstrate that the chip-like organization of the InfectionCMA has several advantages, allowing side-by-side comparisons between diverse cell lines, infection time points, and biomarker expression and cytolocalization evaluation in the same slide. In addition, this methodology has the potential to be easily adapted for drug screening. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
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spelling InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection AssaysCell cycle and apoptosis; Cell microarrays; Human receptors for viruses; Immunocytochemistry; In vitro infectious assays; SARS-CoV-2The recently emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has forced the scientific community to acquire knowledge in real-time, when total lockdowns and the interruption of flights severely limited access to reagents as the global pandemic became established. This unique reality made researchers aware of the importance of designing efficient in vitro set-ups to evaluate infectious kinetics. Here, we propose a histology-based method to evaluate infection kinetics grounded in cell microarray (CMA) construction, immunocytochemistry and in situ hybridization techniques. We demonstrate that the chip-like organization of the InfectionCMA has several advantages, allowing side-by-side comparisons between diverse cell lines, infection time points, and biomarker expression and cytolocalization evaluation in the same slide. In addition, this methodology has the potential to be easily adapted for drug screening. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.MDPI20222022-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/151609eng2076-081710.3390/pathogens11030313Magalhães, ACRicardo, SMoreira, ACNunes, MTavares, MPinto, RJGomes, MSPereira, Linfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T14:03:32Zoai:repositorio-aberto.up.pt:10216/151609Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:53:42.898787Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
title InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
spellingShingle InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
Magalhães, AC
Cell cycle and apoptosis; Cell microarrays; Human receptors for viruses; Immunocytochemistry; In vitro infectious assays; SARS-CoV-2
title_short InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
title_full InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
title_fullStr InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
title_full_unstemmed InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
title_sort InfectionCMA: A Cell MicroArray Approach for Efficient Biomarker Screening in In Vitro Infection Assays
author Magalhães, AC
author_facet Magalhães, AC
Ricardo, S
Moreira, AC
Nunes, M
Tavares, M
Pinto, RJ
Gomes, MS
Pereira, L
author_role author
author2 Ricardo, S
Moreira, AC
Nunes, M
Tavares, M
Pinto, RJ
Gomes, MS
Pereira, L
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Magalhães, AC
Ricardo, S
Moreira, AC
Nunes, M
Tavares, M
Pinto, RJ
Gomes, MS
Pereira, L
dc.subject.por.fl_str_mv Cell cycle and apoptosis; Cell microarrays; Human receptors for viruses; Immunocytochemistry; In vitro infectious assays; SARS-CoV-2
topic Cell cycle and apoptosis; Cell microarrays; Human receptors for viruses; Immunocytochemistry; In vitro infectious assays; SARS-CoV-2
description The recently emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has forced the scientific community to acquire knowledge in real-time, when total lockdowns and the interruption of flights severely limited access to reagents as the global pandemic became established. This unique reality made researchers aware of the importance of designing efficient in vitro set-ups to evaluate infectious kinetics. Here, we propose a histology-based method to evaluate infection kinetics grounded in cell microarray (CMA) construction, immunocytochemistry and in situ hybridization techniques. We demonstrate that the chip-like organization of the InfectionCMA has several advantages, allowing side-by-side comparisons between diverse cell lines, infection time points, and biomarker expression and cytolocalization evaluation in the same slide. In addition, this methodology has the potential to be easily adapted for drug screening. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
publishDate 2022
dc.date.none.fl_str_mv 2022
2022-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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url https://hdl.handle.net/10216/151609
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 2076-0817
10.3390/pathogens11030313
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