ABSTRACT
The replicative success of vaccinia virus (VACV) depends on its ability to subvert host functions. Poxviruses multiplication and maturation are closely associated with the endoplasmic reticulum (ER) and its membranes. This organelle responds to disturbances caused by the accumulation of misfolded proteins, leading to processing of these proteins or even programmed cell death through the unfolded protein response (UPR). Several studies show that different viruses can activate UPR pathway components and negatively modulate others. Here, we investigate the effects of infections by zoonotic VACV strains from Brazil, Guarani P1 virus (GP1V) and Passatempo virus (PSTV), in the activation of UPR pathway sensors. We observed translocation of ATF6 to the nucleus as well as transcriptional increase after GP1V, PSTV, and reference strain Western Reserve (WR) infection. XBP1 processing appears to be negatively modulated after VACV infection; however, inhibition of the inositol-requiring enzyme 1 (IRE1) kinase domain led to a reduction in plaque sizes for these viruses. The absence of PKR-like endoplasmic reticulum kinase (PERK) has an impact on the plaque phenotype of GP1V, PSTV viruses, as well as for the prototypical strain WR. These results indicate that the VACV manipulates the three arms of the UPR path differently to ensure replicative success.
Subject(s)
Unfolded Protein Response , Vaccinia virus , Endoplasmic Reticulum Stress/physiology , Endoplasmic Reticulum/metabolism , DNA ReplicationABSTRACT
BACKGROUND: Cell responses to different stress inducers are efficient mechanisms that prevent and fight the accumulation of harmful macromolecules in the cells and also reinforce the defenses of the host against pathogens. Vaccinia virus (VACV) is an enveloped, DNA virus, belonging to the Poxviridae family. Members of this family have evolved numerous strategies to manipulate host responses to stress controlling cell survival and enhancing their replicative success. In this study, we investigated the activation of the response signaling to malformed proteins (UPR) by the VACV virulent strain-Western Reserve (WR)-or the non-virulent strain-Modified Vaccinia Ankara (MVA). METHODS: Through RT-PCR RFLP and qPCR assays, we detected negative regulation of XBP1 mRNA processing in VACV-infected cells. On the other hand, through assays of reporter genes for the ATF6 component, we observed its translocation to the nucleus of infected cells and a robust increase in its transcriptional activity, which seems to be important for virus replication. WR strain single-cycle viral multiplication curves in ATF6α-knockout MEFs showed reduced viral yield. RESULTS: We observed that VACV WR and MVA strains modulate the UPR pathway, triggering the expression of endoplasmic reticulum chaperones through ATF6α signaling while preventing IRE1α-XBP1 activation. CONCLUSIONS: The ATF6α sensor is robustly activated during infection while the IRE1α-XBP1 branch is down-regulated.
Subject(s)
Transcription Factors , Vaccinia virus , Transcription Factors/genetics , Vaccinia virus/genetics , Endoribonucleases , Protein Serine-Threonine Kinases , Endoplasmic Reticulum Stress , Unfolded Protein ResponseABSTRACT
RESUMO A recente detecção de material genético (RNA) do novo coronavírus em amostras de fezes e no esgoto aponta para a possibilidade de se identificar a circulação do vírus e até mesmo estimar o número de pessoas infectadas em determinada região pelo monitoramento sistemático do esgoto, configurando-se em importante ferramenta epidemiológica de testagem massiva indireta, incluindo portadores sintomáticos e assintomáticos. Nesse sentido, concebeu-se um projeto para a detecção e a quantificação do novo coronavírus em amostras de esgoto coletadas em 15 sub-bacias de esgotamento sanitário dos ribeirões Arrudas e Onça, visando entender a dinâmica de circulação e a prevalência do vírus nas regiões investigadas. Tais sub-bacias esgotam os efluentes gerados por uma população da ordem de 1,5 milhão de pessoas no município de Belo Horizonte e parte de Contagem. O plano de amostragem contemplou 17 pontos (15 sub-bacias + afluente às 2 estações de tratamento de esgoto) de monitoramento semanal, com coletas compostas durante todo o período da manhã. A detecção e a quantificação do RNA viral efetuaram-se em laboratório por meio de ensaios de RT-qPCR. Os resultados obtidos em quatro semanas de monitoramento (semanas epidemiológicas 21 a 24) mostraram um incremento da ocorrência do vírus, atingindo 100% das regiões investigadas na semana epidemiológica 24. A estimativa da população infectada pelo novo coronavírus pelo monitoramento do esgoto em Belo Horizonte apresentou tendência de crescimento exponencial, sendo até 20 vezes maior do que o número de casos confirmados acumulados. Quanto à circulação do vírus, as concentrações do RNA viral têm se mostrado bastante variáveis nas regiões monitoradas, com maiores porcentagens de população infectada estimada ao norte e nordeste da capital mineira.
ABSTRACT The recent detection of SARS-CoV-2 RNA in stool and sewage samples highlights the possibility of mapping the circulation of the virus and even estimating the number of infected people through the systematic monitoring of sewage in a specific region. Therefore, this is an important epidemiological tool for large-scale indirect testing, including symptomatic and asymptomatic carriers. This project was conceived for the detection and quantification of the SARS-CoV-2 in sewage samples collected in 15 watersheds of the Arrudas and Onça streams, aiming to understand the dynamics of spread and the prevalence of the virus in these regions/watersheds. These sub-basins exhaust the effluents generated by a population of approximately 1.5 million people in the municipality of Belo Horizonte and part of Contagem. Weekly composite samples were collected during the morning periods in seventeen monitoring points (15 water sheds + influent to 2 sewage treatment plants). RNA detection and quantification were performed in the laboratory using RT-qPCR. The results obtained in four weeks of monitoring (epidemiological weeks 21 to 24) showed an increase in the occurrence of the virus, reaching 100% of the monitored regions investigated in epidemiological week 24. The infected population, estimated by sewage monitoring in Belo Horizonte, showed exponential growth, being up to 20 times higher than those of accumulated confirmed cases. As for the dynamics of virus spread, RNA concentrations have shown to be quite variable in the monitored regions with higher percentages of the estimated infected population in the northern and north-eastern portions of Belo Horizonte.
