Retrospective Analysis of the SARS-CoV-2 Infection Profile in COVID-19 Positive Patients in Vitoria da Conquista, Northeast Brazil.
Anna Carolina S DantasHellen B M OliveiraCamila P GomesDaniele L AlvesPriscilla D B InfanteRosimara de J A CaititéHegger M FritschMarina S CuccoLucas S C SilvaCaline N T OliveiraRafaela de S BittencourtAline Teixeira AmorimAna Luisa P NascimentoFrancely A G C MarinhoDanielle S de MedeirosMárcio Galvão Guimarães de OliveiraSostenes MistroFabricio F de MeloTaiana T S PereiraAna M S GuimarãesJorge TimenetskyPablo Maciel B MoreiraSandra Helena P de OliveiraLuiz Carlos Junior AlcantaraMarta GiovanettiLuciane A SantosVagner FonsecaFernanda Khouri BarretoGuilherme B CamposLucas M MarquesPublished in: Viruses (2022)
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is responsible for causing Coronavirus Disease-2019 (COVID-19), a heterogeneous clinical condition that manifests varying symptom severity according to the demographic profile of the studied population. While many studies have focused on the spread of COVID-19 in large urban centers in Brazil, few have evaluated medium or small cities in the Northeast region. The aims of this study were: (i) to identify risk factors for mortality from SARS-CoV-2 infection, (ii) to evaluate the gene expression patterns of key immune response pathways using nasopharyngeal swabs of COVID-19 patients, and (iii) to identify the circulating SARS-CoV-2 variants in the residents of a medium-sized city in Northeast Brazil. A total of 783 patients infected with SARS-CoV-2 between May 2020 and August 2021 were included in this study. Clinical-epidemiological data from patients who died and those who survived were compared. Patients were also retrospectively divided into three groups based on disease severity: asymptomatic, mild, and moderate/severe. Samples were added to a qPCR array for analyses of 84 genes involved with immune response pathways and sequenced using the Oxford Nanopore MinION technology. Having pre-existing comorbidity; being male; having cardiovascular disease, diabetes, and/or chronic obstructive pulmonary disease; and PCR cycle threshold (Ct) values under 22 were identified as risk factors for mortality. Analysis of the expression profiles of inflammatory pathway genes showed that the greater the infection severity, the greater the activation of inflammatory pathways, triggering the cytokine storm and downregulating anti-inflammatory pathways. Viral genome analysis revealed the circulation of multiple lineages, such as B.1, B.1.1.28, Alpha, and Gamma, suggesting that multiple introduction events had occurred over time. This study's findings help identify the specific strains and increase our understanding of the true state of local health. In addition, our data demonstrate that epidemiological and genomic surveillance together can help formulate public health strategies to guide governmental actions.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- public health
- end stage renal disease
- immune response
- cardiovascular disease
- gene expression
- chronic obstructive pulmonary disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- prognostic factors
- type diabetes
- computed tomography
- magnetic resonance imaging
- mental health
- escherichia coli
- cardiovascular events
- skeletal muscle
- metabolic syndrome
- toll like receptor
- coronary artery disease
- genome wide
- dna methylation
- magnetic resonance
- machine learning
- air pollution
- artificial intelligence
- dendritic cells
- contrast enhanced
- early onset
- human health
- patient reported outcomes
- big data
- health information
- cardiovascular risk factors
- patient reported
- image quality
- glycemic control