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Herpesvirus and neurological manifestations in patients with severe coronavirus disease

Authors :
Vanessa Cristine de Souza, Carneiro
Soniza Vieira, Alves-Leon
Dmitry José de Santana, Sarmento
Wagner Luis da Costa Nunes Pimentel, Coelho
Otacilio da Cruz, Moreira
Andreza Lemos, Salvio
Carlos Henrique Ferreira, Ramos
Carlos Henrique Ferreira, Ramos Filho
Carla Augusta Barreto, Marques
João Paulo, da Costa Gonçalves
Luciane Almeida Amado, Leon
Vanessa Salete, de Paula
Publication Year :
2022
Publisher :
Research Square Platform LLC, 2022.

Abstract

Background Certain clinical manifestations of coronavirus disease (COVID-19) mimic those associated with human herpesvirus (HHV) infection. In this study, we estimated the prevalence of herpesvirus in patients with COVID-19 and determined if coinfection is associated with poorer outcomes and neurological symptoms. Methods We analyzed samples of 53 patients diagnosed with COVID-19. The samples were evaluated for the presence of alphaherpesviruses, betaherpesviruses, and gammaherpesviruses, and the viral loads were quantified using quantitative polymerase chain reaction (qPCR) method. Results Among the patients, in 79.2% had detection at least one type of herpesvirus. HHV-6 (47.2%), cytomegalovirus (43.3%), and HHV-7 (39.6%) showed the highest detection rates. Patients with a high severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) load were more likely to show herpes simplex virus 1 detection (p = 0.037). Among patients coinfected with SARS-CoV-2 and HHVs, 26.4% showed central nervous system-associated neurological symptoms and herpetic manifestations. A statistically significant association was observed between neurological changes and HHV-6 detection (p = 0.034). Conclusions The findings showed a high prevalence of herpesvirus in patients with COVID-19. Furthermore, even though SARS-CoV-2 and HHV coinfection was not associated with poorer outcomes, the findings demonstrated the association between neurological symptoms and HHV-6 detection.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....c9ebd539264576e83bb6957671ccea0d