ABSTRACT
Necrolytic acral erythema is a distinct erythema that has been described as an extrahepatic manifestation of hepatitis C virus infection. Most reported cases have been in Africa, especially Egypt. We report the first case (to the best of our knowledge) of necrolytic acral erythema in a Chinese patient with HCV and HBV coinfection. We aim to increase awareness for recognizing this condition in the Chinese population.
Subject(s)
Coinfection/complications , Erythema/pathology , Erythema/virology , Hepatitis B/complications , Hepatitis C/complications , Adult , China , Coinfection/pathology , Extremities/pathology , Hepatitis B/pathology , Hepatitis C/pathology , Humans , Male , Necrosis/virologyABSTRACT
Abstract: Necrolytic acral erythema is a distinct erythema that has been described as an extrahepatic manifestation of hepatitis C virus infection. Most reported cases have been in Africa, especially Egypt. We report the first case (to the best of our knowledge) of necrolytic acral erythema in a Chinese patient with HCV and HBV coinfection. We aim to increase awareness for recognizing this condition in the Chinese population.
Subject(s)
Humans , Male , Adult , Hepatitis C/complications , Erythema/pathology , Erythema/virology , Coinfection/complications , Hepatitis B/complications , China , Hepatitis C/pathology , Extremities/pathology , Coinfection/pathology , Hepatitis B/pathology , Necrosis/virologyABSTRACT
Respiratory syncytial virus (RSV) is a major cause of diseases of the respiratory tract in young children and babies, being mainly associated with bronchiolitis. RSV infection occurs primarily in pulmonary epithelial cells and, once infection is established, an immune response is triggered and neutrophils are recruited. In this study, we investigated the mechanisms underlying NET production induced by RSV. We show that RSV induced the classical ROS-dependent NETosis in human neutrophils and that RSV was trapped in DNA lattices coated with NE and MPO. NETosis induction by RSV was dependent on signaling by PI3K/AKT, ERK and p38 MAPK and required histone citrullination by PAD-4. In addition, RIPK1, RIPK3 and MLKL were essential to RSV-induced NETosis. MLKL was also necessary to neutrophil necrosis triggered by the virus, likely promoting membrane-disrupting pores, leading to neutrophil lysis and NET extrusion. Finally, we found that RSV infection of alveolar epithelial cells or lung fibroblasts triggers NET-DNA release by neutrophils, indicating that neutrophils can identify RSV-infected cells and respond to them by releasing NETs. The identification of the mechanisms responsible to mediate RSV-induced NETosis may prove valuable to the design of new therapeutic approaches to treat the inflammatory consequences of RSV bronchiolitis in young children.
Subject(s)
Extracellular Traps/metabolism , Necrosis/metabolism , Neutrophils/metabolism , Protein-Arginine Deiminases/metabolism , Reactive Oxygen Species/metabolism , Respiratory Syncytial Virus Infections/metabolism , Respiratory Syncytial Virus, Human/pathogenicity , Adult , Alveolar Epithelial Cells/metabolism , Alveolar Epithelial Cells/virology , Animals , Apoptosis/physiology , Bronchiolitis/metabolism , Bronchiolitis/virology , Cell Line , Chlorocebus aethiops , Extracellular Traps/virology , Female , Humans , Lung/metabolism , Lung/virology , Male , Necrosis/virology , Neutrophils/virology , Phosphatidylinositol 3-Kinases/metabolism , Protein-Arginine Deiminase Type 4 , Respiratory Syncytial Virus Infections/virology , Signal Transduction/physiology , Vero CellsABSTRACT
Oncolytic viruses have the ability to infect tumor cells and leave healthy cells intact. In this study, bovine herpesvirus 1 (BHV1; Los Angeles, Cooper, and SV56/90 strains) and bovine herpesvirus 5 (BHV5; SV507/99 and GU9457818 strains) were used to infect two neuronal tumor cell lineages: neuro2a (mouse neuroblastoma cells) and C6 (rat glial cells). BHV1 and BHV5 strains infected both cell lines and positively correlated with viral antigen detection (p < 0.005). When neuro2a cells were infected by Los Angeles, SV507/99, and GU9457818 strains, 40 % of infected cells were under early apoptosis and necroptosis pathways. Infected C6 cells were >40 % in necroptosis phase when infected by BHV5 (GU9457818 strain). Blocking caspase activation did not interfere with cell death. However, when necroptosis was blocked, 60-80 % of both infected cells with either virus switched to early apoptosis pathway with no interference with virus replication. Moreover, reactive oxygen species production and mitochondrial membrane dysfunction were detected at high levels in both infected cell lines. In spite of apoptosis and necroptosis blockage, tumor necrosis factor alpha (TNFA) and virus transcription were positively correlated for all viral strains studied. Thus, these results contribute to the characterization of BHV1 and BHV5 as potential oncolytic viruses for non-human cells. Nonetheless, the mechanisms underlying their oncolytic activity in human cells are still to be determined.
Subject(s)
Apoptosis/genetics , Herpesvirus 1, Bovine/growth & development , Herpesvirus 5, Bovine/growth & development , Necrosis/virology , Neuroglia/virology , Neurons/virology , Animals , Antigens, Viral/genetics , Cattle , Cell Line, Tumor , Gene Expression , Herpesvirus 1, Bovine/genetics , Herpesvirus 5, Bovine/genetics , Host-Pathogen Interactions , Humans , Mice , Mitochondria/metabolism , Mitochondria/virology , Necrosis/genetics , Necrosis/pathology , Neuroglia/metabolism , Neuroglia/pathology , Neurons/metabolism , Neurons/pathology , Oncolytic Viruses/genetics , Oncolytic Viruses/growth & development , Organ Specificity , Oxidative Stress , Rats , Reactive Oxygen Species/metabolism , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/metabolism , Virus ReplicationABSTRACT
Hydroa vacciniforme-like lymphoma is a recently recognized cutaneous T-cell lymphoma associated with Epstein-Barr virus. The disease is observed in children of Latin American or Asian ethnicity. The authors report the clinical, histopathological, and immunophenotypical features of 9 new Mexican patients (M:F = 2:1; mean age, 14.5 years; median age, 13.3 years; age range, 4-27 years), expanding on previous observations of this elusive disease. The most common clinical aspects were persistent facial edema with necroses and pitted scars. Histopathological analyses revealed variably dense lymphoid infiltrates with common angiodestructive features. Neoplastic cells expressed CD3 and cytotoxic markers in all cases and were constantly positive for Epstein-Barr virus (EBER-1). Expression of other markers was variable. Follow-up data revealed that all patients died within 6 months or less, thus showing a very aggressive course with poor prognosis.
Subject(s)
Edema/pathology , Epstein-Barr Virus Infections/complications , Face/pathology , Facial Neoplasms/pathology , Hydroa Vacciniforme/pathology , Lymphoma, T-Cell, Cutaneous/pathology , Adolescent , Adult , CD3 Complex/analysis , Child , Child, Preschool , Cicatrix/pathology , Cicatrix/virology , Edema/virology , Extremities/pathology , Facial Neoplasms/chemistry , Facial Neoplasms/virology , Female , Humans , Hydroa Vacciniforme/virology , Immunohistochemistry , Lymphoma, T-Cell, Cutaneous/chemistry , Lymphoma, T-Cell, Cutaneous/virology , Male , Mexico , Necrosis/pathology , Necrosis/virology , Prognosis , Torso/pathology , Young AdultABSTRACT
PURPOSE: To evaluate and compare the efficacy of rapamycin used topically in a mouse model of herpetic stromal keratitis. METHODS: The corneas were infected with herpes simplex virus type-1 strain KOS. Animals were divided into: control (CG), rapamycin (RAPA), cyclosporine (CsA), and dexamethasone (DEXA). The evolution of the disease was assessed clinically and histologically. RESULTS: On day 10 postinfection (pi), the RAPA group showed only a significantly lower angiogenic development than the CG. On day 14 pi, the treated groups had significantly lower scores for angiogenesis and necrosis than the CG. Also, on day 14 pi, the RAPA and DEXA groups showed significantly lower histopathological scores compared to the CG. CONCLUSIONS: The topical application of 0.05% rapamycin showed greater efficacy than 0.5% cyclosporine and similar efficacy to 0.1% dexamethasone to minimize the immuno-inflammatory process. Also, rapamycin showed early inhibition of the formation of new vessels.
Subject(s)
Antiviral Agents/therapeutic use , Keratitis, Herpetic/drug therapy , Sirolimus/therapeutic use , Administration, Ophthalmic , Animals , Corneal Stroma/drug effects , Corneal Stroma/pathology , Corneal Stroma/virology , Cyclosporine/therapeutic use , Dexamethasone/therapeutic use , Herpesvirus 1, Human/drug effects , Keratitis, Herpetic/pathology , Keratitis, Herpetic/virology , Mice , Mice, Inbred BALB C , Necrosis/drug therapy , Necrosis/virology , Neovascularization, Pathologic/drug therapy , Neovascularization, Pathologic/pathology , Neovascularization, Pathologic/virology , Severity of Illness Index , Sirolimus/administration & dosage , Treatment OutcomeABSTRACT
Cytomegalovirus (CMV) infection is usually asymptomatic in immunocompetent patients. A mononucleosis-like syndrome may develop in some patients. Various organ involvements (eg: encephalitis, meningitis, retinitis, myocarditis, pneumonia, hepatitis, enterocolitis, neuritis), which rarely occur in immunocompetent patients, have also been reported. Cutaneous necrotizing vasculitis caused by CMV infection has been reported very rarely in the literature. Here, a case with a very rare clinical form of CMV infection, presenting with persistent fever and livedo reticularis on the extremities and cutaneous necrotizing vasculitis of the toes, is described, and the relevant literature is reviewed. This case report aims to highlight the possibility of CMV infection to be a cause of cutaneous necrotizing vasculitis.
Subject(s)
Adolescent , Female , Humans , Cytomegalovirus Infections/pathology , Toes/pathology , Vasculitis/pathology , Biopsy , Necrosis/pathology , Necrosis/virology , Toes/virology , Vasculitis/virologyABSTRACT
Cytomegalovirus (CMV) infection is usually asymptomatic in immunocompetent patients. A mononucleosis-like syndrome may develop in some patients. Various organ involvements (e.g.: encephalitis, meningitis, retinitis, myocarditis, pneumonia, hepatitis, enterocolitis, neuritis), which rarely occur in immunocompetent patients, have also been reported. Cutaneous necrotizing vasculitis caused by CMV infection has been reported very rarely in the literature. Here, a case with a very rare clinical form of CMV infection, presenting with persistent fever and livedo reticularis on the extremities and cutaneous necrotizing vasculitis of the toes, is described, and the relevant literature is reviewed. This case report aims to highlight the possibility of CMV infection to be a cause of cutaneous necrotizing vasculitis.
Subject(s)
Cytomegalovirus Infections/pathology , Toes/pathology , Vasculitis/pathology , Adolescent , Biopsy , Female , Humans , Necrosis/pathology , Necrosis/virology , Toes/virology , Vasculitis/virologyABSTRACT
This report describes the naturally occurring atypical neuropathological manifestation of systemic canine distemper virus (CDV) infection in two 16-day-old Pit Bull pups. CDV-induced changes affected the gray and white matter of the forebrain while sparing the hindbrain. Histologically, there was necrosis with destruction of the nervous parenchyma due to an influx of inflammatory and reactive cells associated with eosinophilic intranuclear inclusion bodies within glial cells. Positive immunoreactivity against CDV antigens was predominantly observed within astrocytes and neurons. RT-PCR was used to amplify CDV-specific amplicons from brain fragments. These findings suggest the participation of CDV in the etiopathogenesis of these lesions.
Subject(s)
Distemper Virus, Canine , Distemper/virology , Encephalitis/veterinary , Necrosis/veterinary , Animals , Antigens, Viral , Central Nervous System/pathology , Central Nervous System/virology , Dogs , Encephalitis/pathology , Encephalitis/virology , Necrosis/pathology , Necrosis/virologyABSTRACT
Viral and bacterial associations appear to be implicated in the development of periodontal infections. Little information is available describing the periodontopathic agents in root canals with necrotic pulp. In this study, the occurrence and the combinations among herpes simplex virus type 1 (HSV-1) and Dialister pneumosintes, Tannerella forsythia, and Treponema denticola in patients with chronic periodontitis and necrotic pulp were evaluated. Clinical samples from healthy subjects and patients with periodontal or pulp infections were analyzed using a nested polymerase chain reaction PCR to detect HSV and PCR to detect the 3 periodontal bacteria. The presence of Tannerella forsythia and Treponema denticola was observed in healthy, periodontitis, and necrotic pulp patients. HSV was observed in periodontitis and necrotic pulp patients, and no healthy subject harbored D. pneumosintes or HSV. The occurrence of Tannerella forsythia was not statistically significant in patients with necrotic pulp (P = 0.704). Periodontal bacteria were observed varying from 10.3% to 20.7% in periodontitis and necrotic pulp patients. The presence of Treponema denticola - HSV association was predominant in patients showing necrotic pulp (24.1%); however, HSV alone was observed in one patient with periodontitis and in another patient with necrotic pulp. The presence of double association among bacteria or bacteria - HSV could indicate a role in both periodontitis and necrotic pulp, and Tannerella forsythia - Treponema denticola - HSV and Tannerella forsythia - D. pneumosintes - Treponema denticola - HSV associations might be important in periodontitis.
Subject(s)
Dental Pulp , Gram-Negative Bacteria/isolation & purification , Gram-Negative Bacterial Infections/epidemiology , Herpes Simplex/epidemiology , Herpesvirus 1, Human/isolation & purification , Periodontitis , Adolescent , Adult , Bacteroidetes/genetics , Bacteroidetes/isolation & purification , Chronic Disease , Dental Pulp/microbiology , Dental Pulp/pathology , Dental Pulp/virology , Female , Gram-Negative Bacteria/classification , Gram-Negative Bacteria/genetics , Gram-Negative Bacterial Infections/microbiology , Herpes Simplex/virology , Herpesvirus 1, Human/genetics , Humans , Male , Middle Aged , Necrosis/epidemiology , Necrosis/microbiology , Necrosis/virology , Periodontitis/epidemiology , Periodontitis/microbiology , Periodontitis/virology , Polymerase Chain Reaction , Treponema denticola/genetics , Treponema denticola/isolation & purification , Veillonellaceae/genetics , Veillonellaceae/isolation & purificationABSTRACT
An Anticarsia gemmatalis multiple nucleopolyhedrovirus (AgMNPV) mutant, vApAg, induces apoptosis in a cell culture derived from Anticarsia gemmatalis (UFL-AG-286), reducing viral progeny. We have investigated apoptosis induction in vivo by vApAg in A. gemmatalis larvae and its correlation to infectivity reduction. LC(50), LD(50), LT(50) and the mean time to death of larvae were determined for vApAg and AgMNPV. Apoptosis was accessed for hemocytes of infected larvae using light and transmission electron microscopy. All types of hemocytes can be infected by vApAg. After 12h post-infection (h p.i.), typical cellular modifications associated to nucleopolyhedrovirus infection were observed. Apoptosis becomes evident after 24h p.i., and massive after 72h p.i. Necrosis of infected cells was also observed. Despite cell death, hemocytes produced budded viruses and polyhedra. Pl and gh1-type hemocytes presented phagocytic activity. Agarose gel electrophoresis revealed fragmentation of hemocytes DNA at late times post-infection. The LC(50) and LD(50) were between five- and six-fold higher for vApAg. The LT(50) and the mean time to death were higher for vApAg in a same treatment or for a similar mortality induced by AgMNPV. These results show correlation of apoptosis and the reduced infectivity of vApAg in A. gemmatalis larvae.