scholarly journals Human herpesvirus type 1 and type 2 disrupt mitochondrial dynamics in human keratinocytes

2018 ◽  
Vol 163 (10) ◽  
pp. 2663-2673 ◽  
Author(s):  
Marcin Chodkowski ◽  
Izabela Serafińska ◽  
Joanna Brzezicka ◽  
Anna Golke ◽  
Anna Słońska ◽  
...  
2019 ◽  
Vol 25 (6) ◽  
pp. 765-782 ◽  
Author(s):  
Joanna Cymerys ◽  
Marcin Chodkowski ◽  
Anna Słońska ◽  
Małgorzata Krzyżowska ◽  
Marcin W. Bańbura

Author(s):  
Marcia Helena Braga Catroxo ◽  
Ana Maria Cristina Rebello Pinto da Fonseca Martins ◽  
Eliana Monteforte CassaroVillalobos ◽  
Liliane Milanelo ◽  
Marcia Helena Braga Catroxo ◽  
...  

Human herpesvirus type 1 (HSV-1), a Alphaherpesvirinae, has a broad range of cross-species infectivity with considerable variation in expression and disease severity among different hosts. Infection in humans, results in mild disease characterized by mucocutaneous lesions. In some species of nonhuman primates, however, the infection can be lethal. Transmission occurs through food contaminated by humans with labial herpes, offered to monkeys, constituting an important anthropozoonosis. In this study, we describe the occurrence of two outbreaks of encephalitis caused by HSV-1, occurring in the State of São Paulo, Brazil. The first outbreak affected a Brown howler monkey and three marmosets. The Brown howler monkey had tongue ulcers and enteritis and the marmosets were found dead without presenting clinical symptomatology. The second outbreak affected ten marmosets that were found dead suddenly in the enclosure without presenting symptoms or clinical signs. Organ fragments were processed for transmission electron microscopy, histopathology and inoculation in cell culture techniques. Ballooning degeneration, foci of monolymphocytic inflammatory reaction, corpuscle of eosinophilic inclusion, monolymphocytic meningitis and desquamative monolymphocytic enterocolitis, were the main lesions observed by histopathology. By the negative staining technique, enveloped and non-enveloped, herpesvirus particles were found, measuring 120-200 nm in diameter in all samples of organ fragments. The presence of aggregates formed by antigenantibody complex, characterized the positive result obtained in the immunoelectron microscopy technique for HSV-1. Using the immunocytochemistry technique, the antigen-antibody interaction was strongly enhanced by the colloidal gold particles over the herpesvirus, confirming the presence of HSV-1. Intranuclear incomplete particles measuring 80-100 nm in diameter and complete or enveloped scattered in the cytoplasm, were visualized in ultrathin sections of liver and cell culture measuring 140 nm of diameter. Immature particles budding from cell membranes were also observed. In viral isolation in VERO cells, typical cytopathic effect was observed in brain samples.


AIDS Care ◽  
2017 ◽  
Vol 30 (3) ◽  
pp. 378-382 ◽  
Author(s):  
Lyana Rodrigues Pinto Lima ◽  
Luis Eduardo Barros Costa Fernandes ◽  
Daniel A. M. Villela ◽  
Mariza Gonçalves Morgado ◽  
José Henrique Pilotto ◽  
...  

Author(s):  
Anna Słońska ◽  
Joanna Cymerys ◽  
Marcin Chodkowski ◽  
Piotr Bąska ◽  
Małgorzata Krzyżowska ◽  
...  

AbstractHerpesviruses are capable of infecting not only neurons, where they establish latent infection, but also astrocytes. Since astrocytes are important for the functioning of the central nervous system (CNS), their infection may lead to serious neurological disorders. Thus, in the present study we investigated the ability of human herpesvirus type 2 (HHV-2) to infect primary murine astrocytes in vitro and the effect of infection on their mitochondrial network and actin cytoskeleton. In immunofluorescence assays, antibodies against HHV-2 antigens and glial fibrillary acidic protein (GFAP) were used to confirm that the infected cells are indeed astrocytes. Real-time PCR analysis showed a high level of HHV-2 replication in astrocytes, particularly at 168 h postinfection, confirming that a productive infection had occurred. Analysis of mitochondrial morphology showed that, starting from the first stage of infection, HHV-2 caused fragmentation of the mitochondrial network and formation of punctate and tubular structures that colocalized with virus particles. Furthermore, during the late stages of infection, the infection affected the actin cytoskeleton and induced formation of actin-based cellular projections, which were probably associated with enhanced intracellular spread of the virus. These results suggest that the observed changes in the mitochondrial network and actin cytoskeleton in productively infected astrocytes are required for effective replication and viral spread in a primary culture of astrocytes. Moreover, we speculate that, in response to injury such as HHV-2 infection, murine astrocytes cultured in vitro undergo transformation, defined in vivo as reactive astrocytosis.


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