Evidence map›Paper›PMID 33434663›Full record

ArticleInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2021

Development of a quantitative one-step multiplex RT-qPCR assay for the detection of SARS-CoV-2 in a biological matrix.

Jackson Alves da Silva Queiroz, Rita de Cássia Pontello Rampazzo, Edivá Basílio da Silva Filho, Gabriella Sgorlon Oliveira, Suyane da Costa Oliveira, Luan Felipo Botelho Souza, Soraya Dos Santos Pereira, Moreno Magalhães de Souza Rodrigues, Adriana Cristina Salvador Maia, Cicileia Correia da Silva and 11 more

Open access · goldAbstract read
In one paragraph

Article in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

21 authors at 4 institutions in 1 country.

Jackson Alves da Silva QueirozFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil; Programa de Pós Graduação em Biologia Experimental, Fundação Universidade Federal de Rondônia- PGBIOEXP/UNIR, Porto Velho, Rondônia, Brazil.
Rita de Cássia Pontello RampazzoInstituto de Biologia Molecular do Paraná - IBMP, Curitiba, Paraná, Brazil.
Edivá Basílio da Silva FilhoFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil; Programa de Pós Graduação em Biologia Experimental, Fundação Universidade Federal de Rondônia- PGBIOEXP/UNIR, Porto Velho, Rondônia, Brazil.
Gabriella Sgorlon OliveiraFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil.
Suyane da Costa OliveiraFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil.
Luan Felipo Botelho SouzaLaboratório Central de Saúde Pública do Estado de Rondônia - LACEN/RO, Porto Velho, Rondônia, Brazil.
Soraya Dos Santos PereiraFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil; Programa de Pós Graduação em Biologia Experimental, Fundação Universidade Federal de Rondônia- PGBIOEXP/UNIR, Porto Velho, Rondônia, Brazil.
Moreno Magalhães de Souza RodriguesFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil.
Adriana Cristina Salvador MaiaLaboratório Central de Saúde Pública do Estado de Rondônia - LACEN/RO, Porto Velho, Rondônia, Brazil.
Cicileia Correia da SilvaLaboratório Central de Saúde Pública do Estado de Rondônia - LACEN/RO, Porto Velho, Rondônia, Brazil.
Aline Linhares Ferreira de Melo MendonçaLaboratório Central de Saúde Pública do Estado de Rondônia - LACEN/RO, Porto Velho, Rondônia, Brazil.
Celina Aparecida Bertoni LugtenburgLaboratório Central de Saúde Pública do Estado de Rondônia - LACEN/RO, Porto Velho, Rondônia, Brazil.
Francisco de Assis Araújo AguiarLaboratório Central de Saúde Pública do Estado de Rondônia - LACEN/RO, Porto Velho, Rondônia, Brazil.
Rosiane de Souza Soares RodriguesLaboratório Central de Saúde Pública do Estado de Rondônia - LACEN/RO, Porto Velho, Rondônia, Brazil.
Caio Henrique Nemeth SantosSecretaria de Estado de Finanças de Rondônia - SEFIN RO, Porto Velho, Rondônia, Brazil.
Alice Paula Di Sabatino GuimarãesFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil.
Fernando Rodrigues MáximoSecretaria de Estado da Saúde de Rondônia - SESAU, Porto Velho, Rondônia, Brasil.
Alcione de Oliveira Dos SantosFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil.
Marco Aurélio KriegerInstituto Carlos Chagas Fundação Oswaldo Cruz, FIOCRUZ-PR, Curitiba, Paraná, Brazil.
Juan Miguel Villalobos SalcedoFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil.
Deusilene Souza Vieira Dall'AcquaFundação Oswaldo Cruz, FIOCRUZ, Unidade Rondônia, Porto Velho, Rondônia, Brazil; Programa de Pós Graduação em Biologia Experimental, Fundação Universidade Federal de Rondônia- PGBIOEXP/UNIR, Porto Velho, Rondônia, Brazil. Electronic address: deusilene.vieira@fiocruz.br.
Universidade Federal de Rondônia · BRFundação Oswaldo Cruz · BRFundação Carlos Chagas · BRInstituto de Biologia Molecular do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCoronavirus disease-2019 (COVID-19) is a disease caused by Severe Acute Respiratory Syndrome Virus 2 (SARS-CoV-2) that emerged in China in late 2019. The rapid viral spread has made the disease a public health emergency of worldwide concern. The gold standard for diagnosing SARS-CoV-2 is reverse transcription followed by qualitative real-time polymerase chain reaction (RT-qPCR); however, the role of viral load quantification has not been thoroughly investigated yet.

objectiveThe aim of this study was to develop a high-precision quantitative one-step RT-qPCR reaction using the association of the viral target and the human target in the same reaction.

methodsThe assay standardization involved the absolute quantification method, with serial dilutions of a plasmid with the N gene in a biological matrix to build a standard curve. RESULTS AND DISCUSSION: The results demonstrated the possibility of quantifying as few as 2.5 copies/reaction and an analysis of 244 patients with known results selected by cross-section that revealed 100% agreement with a qualitative RT-qPCR assay registered by Anvisa. In this population, it was possible to quantify patients with between 2.59 and 3.5 × 10

conclusionThis assay can be a useful tool for a proper patient management, because the level and duration of viral replication are important factors to assess the risk of transmission and to guide decisions regarding the isolation and release of patients; an accurate diagnosis is critical information, whereas the current COVID-19 pandemic represents the biggest current global health problem.

Indexed as

AdolescentAdultAgedAged, 80 and overChildChild, PreschoolCOVID-19COVID-19 Nucleic Acid TestingFemaleHumansInfantMaleMiddle AgedMultiplex Polymerase Chain ReactionReal-Time Polymerase Chain ReactionReference Standards

Identifiers

PMID33434663
PMCPMC7831874
OpenAlexW3119736736

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.