Presence Of Herpesvirus Research Articles

Surveying Bat-Hosted Adenoviruses and Herpesviruses: A Comprehensive Analysis

Bats have gained cumulative attention as potential reservoirs for viruses, being crucial to increase our ability to predict viral prevalence and transmissions, as well as support the possible management of future zoonotic episodes. Following the PRISMA standard systematic review protocols, we conducted a comprehensive search worldwide for scientific papers dealing with bat-hosted viruses of the Adenoviridae and Herpesviridae families. The search was completed using the Scopus, CABI, and SciELO, databases of bat-associated viruses of these two families as well as the Google Scholar search engine. Our search comprised a total of 2656 scientific papers. After a thorough review and screening of the papers, we selected for our study a total of 90 papers published between 1996 and 2022. We found marked taxonomic and spatial biases, the most studied bats being predominantly vespertilionids, rhinolophids, phyllostomids, and pteropodids, whereas other families (e.g., Natalidae, Noctilionidae, and Furipteridae) are still lacking information. The most studied areas are southern and east Asia, although there are large areas (north Africa, the Middle East, and all the way to central or northern Asia) still overlooked. Out of the total number of papers, as many as 55 identified bat-hosted Adenovirus (AdV) and 54 papers identified Herpesvirus (HSV). Our revision reveals the presence of AdVs in a total of 97 bat species from 42 genera and 11 families. The presence of HSVs is reported also in 109 bat species from 45 genera and 10 families. Although both AdVs and HSVs in general show a clear host specificity and parallel evolution with their hosts, these results also point to the potential of these viruses to cross, in some cases, species barriers.

Herpesvirus reactivation in respiratory tract is associated with increased mortality of severe pneumonia patients and their respiratory microbiome dysbiosis.

Severe pneumonia (SP) is a respiratory tract disease that seriously threatens human health. The herpesvirus detected in patients, especially with severe and immunodeficient diseases, is gradually attracting the attention of clinical doctors. However, little is known about the effect of herpesvirus on the prognosis of SP patients and the pulmonary microbial community. Here, we retrospectively analyzed respiratory samples from 45 SP patients detected by metagenomic next-generation sequencing (mNGS). A total of five types of herpesviruses were detected, with Human alphaherpesvirus 1 (HHV-1) in 19 patients, Human betaherpesvirus 5 (CMV) in 7 patients, Human betaherpesvirus 7 (HHV-7) in 6 patients, Human alphaherpesvirus 2 (HHV-2) in 5 patients, and Human gammaherpesvirus 4 (EBV) in 4 patients. Further analysis showed that the mortality of the herpesvirus-positive group was significantly higher than that of the negative group. The results also showed that HHV-1 was significantly associated with the prognosis of SP patients, while the other herpesviruses did not have a significant difference in patient mortality. A comparison of the microbial community characteristics of SP patients showed a significant difference in beta-diversity between herpesvirus-positive and negative groups. Species difference analysis showed that the herpesvirus-positive group was related to more conditional pathogens, such as Pneumocystis jirovecii and Burkholderia cepacia. In summary, our results suggest that the presence of herpesvirus is associated with the mortality of SP patients. Furthermore, enrichment of conditional pathogens in the respiratory tract of herpesvirus-positive SP patients may be a potential reason for the increased mortality.

Herpesvirus Infection in a Breeding Population of Two Coexisting Strix Owls.

Simple SummaryAlthough infection with herpesvirus in owls has commonly been described as a highly lethal disease, there is very little information about the presence of herpesvirus and its potential impact in living owls in wild populations. Our study detected herpesvirus in a breeding population of Ural owls, which showed no clinical signs of illness nor productivity deviances (i.e., in clutch and brood size). Herpesvirus was detected in Ural owl adults and chicks, but not in a young tawny owl (despite the fact that they were in same nest and in persistent contact). Furthermore, herpesviruses were also detected in yellow-necked mice as both owls’ main prey. However, comparison of the herpesviruses detected showed that different herpesviruses are present in the owls and mice. The results of this study show that herpesvirus may be present in a Ural owl breeding population without any consequences on health and breeding performance. However, in the case of tawny owls, it seems that they are not susceptible to infection, which could be related to their polymorphism. It seems that small rodents are not a source of herpesvirus infection in owls and that the probable herpesvirus transmission pathway takes place intraspecifically, mostly from adults to young.Birds are a frequent host of a large variety of herpesviruses, and infections in them may go unnoticed or may result in fatal disease. In wild breeding populations of owls, there is very limited information about the presence, impact, and potential transmission of herpesvirus. The herpesvirus partial DNA polymerase gene was detected using polymerase chain reaction in oropharyngeal swabs of 16 out of 170 owls examined that were captured in or near nest boxes. Herpesvirus was detected in Ural owls (Strix uralensis), in both adults and young, but not in tawny owls (Strix aluco). In yellow-necked mice (Apodemus flavicollis), as the main prey of tawny owls and Ural owls in the area, herpesvirus was detected in the organs of 2 out of 40 mice captured at the same locations as the owls. Phylogenetic analysis showed that the herpesvirus sequences detected in the Ural owls differed from the herpesvirus sequences detected in the yellow-necked mice. The results indicate that herpesvirus infection exists in the breeding wild Ural owl population. However, herpesvirus-infected owls did not show any clinical or productivity deviances and, based on a phylogenetic comparison of detected herpesvirus sequences and sequences obtained from Genbank database, it seems that mice and other rodents are not the source of owl infections. The most probable transmission pathway is intraspecific, especially from adults to their chicks, but the origin of herpesvirus in owls remains to be investigated.

Prevalence of herpes virus in chronic periodontitis patients with and without type 2 diabetes mellitus: A clinico-microbiological study.

Background:Unfavorable modifications of tooth and its surrounding structures result in periodontal complications. Viruses, in specific herpes virus, are known to increase disease severity in periodontal patients. Periodontitis is known to be more established in type 2 diabetes mellitus (DM2) patients. Hence, the detection of the viral load, its effect on the prevalence of periodontitis and the glycemic control status of patients are to be evidenced. The study aimed to reveal the association of herpes virus with periodontal parameters and its prevalence in DM2 patients.Materials and Methods:The cross-sectional study involved a total of 120 patients falling into three groups; Group I (healthy), Group II (periodontitis without DM2) and Group III (periodontitis with DM2) were subjected for sampling. Subgingival samples of periodontitis patients were tested for clinical parameters, and DNA extraction was performed. The presence of herpes virus (Epstein–Barr virus [EBV-1] and human Cytomegalovirus [HCMV]) was detected using multiplex polymerase chain reaction primers. Glycemic status of patients was recorded as glycosylated hemoglobin and scored accordingly. Chi-square test was performed to analyze the association between the categorical variables, and t-test/Mann–Whitney U-test/analysis of variance/Kruskal–Wallis test was used for continuous data.Results:Significant levels of EBV-1 were detected in Group III (n = 21, 52.5%), followed by Group II (n = 16, 40%) and Group I (n = 2, 5%) (P < 0.0001). HCMV was not detected. A significant association of EBV-1 to periodontal site-specific parameters was observed in Group II patients (P < 0.05). EBV-1 was predominant with poor glycemic status patients.Conclusion:This study revealed that the incidence of herpes virus infection in periodontal patients was higher in diabetic patients and the examined patients were prone to EBV-1 infections.

Risk of a three-year ischemic stroke recurrence and its independent predictors in patients with a confirmed manifestationof viral infection

Objective — to assess the risk of the manifest viral infection impact on the three‑year frequency of the recurrent stroke and to determine its independent predictors.Methods and subjects. From 2014 to 2019 70 patients with ischemic stroke with viral infection manifestation during 2 weeks before hospitalization were examined. The presence of viral infection was confirmed by a polymerase chain reaction (main group). A total of 220 patients without viral manifestation were included in the comparison group, who were compared with the main group by stroke severity, average age and gender. The severity of neurological deficiency was assessed by the NIHSS scale. The pathogenetic subtype of stroke was determined according to TOAST criteria.Results. Over the three‑year period, the three‑year cumulative rate of stroke recurrence was higher in main group patients — 17.4 % (non‑recurring survival 82.6 ± 4.58 %) than in comparison group — 12.1 % (non‑recurring survival 87.9 ± 2.2 %), p = 0.240. In the case of at least 2 types of viruses genomes presence in the blood, the frequency of recurrence has increased to 22.8 % (probability of non‑recurring survival 77.2 6.05 %), in comparison group — 12.1 % (probabilityofnon‑recurringsurvival 87.9 2 %), p = 0.0470. In the case of HSV1 determination, the risk of a stroke reccurence in the main group comparing to comparison group patients increased by 2.16 times: BP = 2.16; 95 % CI: 1.15 — 4.04 (p = 0.0154); HSV2 : 1.69: BP = 1.69; 95 % CI: 0.76 — 3.77 (p = 0.1983); HNV6 : 2.49: BP = 2.49; 95 % CI: 1.05 — 4.56 (p = 0.0356); CMV: 2.82: BP = 2.82; 95 % CI: 1.34 — 5.95 (p = 0.0065); EBV: 2.67 times: BP = 2.67; 95 % CI: 1.26 — 5.68 (p = 0.0106); Influenza virus: 2.64 times: BP = 2.64; 95 % CI: 1.17 — 5.95 (p = 0.0188). HSV1 (B coefficient = 4.52), CMV (B coefficient = 3.63), Influenza virus (B coefficient = 4.11), and Intima‑media thickness (B coefficient = 10.77), constant — 20.57 were determined as independent prognostic factors of a three‑year stroke recurrence in patients with viral manifestation. The predictive value of the model is high with an area of the figure under the ROC curve = 0.971, 95 % CI: 0.900 — 0.966 and model sensitivity — 100.0 %, 95 % CI: 71.5 — 100.0 % and specificity — 83.1 % (95 % CI: 71.0 — 91.6 %).Conclusions. The risk of a stroke recurrence with viral manifestation and the presence of herpes virus and influenza virus genome significantly increases in 1.89 times when two or more types of viruses are present and is 22.8 % to GP (12.1 %). The presence of HSV1, CMV DNA, influenza RNA, and Intima‑media thickness in the patient are the independent prognostic factors of a three‑year stroke recurrance in patients with viral manifestation according to the developed mathematical model using the step‑by‑step multivariant binary logistic regression.

A 20‐year experience of ocular herpes virus detection using immunofluorescence and polymerase chain reaction

BackgroundTo detect the presence of herpes virus in corneal scrapings/corneal grafts of suspected herpetic keratitis patients attending the outpatient department/casualty of the Dr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi for the past 20 years with immunofluorescence assay and to analyse the efficacy of polymerase chain reaction over immunofluorescence for routine laboratory diagnosis in some of the specimens.MethodsCorneal scrapings and corneal grafts were collected by the ophthalmologists from 1,926 suspected herpetic keratitis patients between 1996 and 2015, among whom 1,863 patients were processed with immunofluorescence assay and 302 patients were processed with polymerase chain reaction assay for the detection of herpes virus. Of the 302 patients, clinical specimens from 239 patients were analysed by both polymerase chain reaction and immunofluorescence assay.ResultsOf the 1,863 suspected herpetic keratitis patients diagnosed with immunofluorescence assay, 277 (14.9 per cent) were found positive for herpes simplex virus 1 antigen. Similarly, of the 302 suspected herpetic keratitis patients diagnosed by polymerase chain reaction, 70 (23.2 per cent) were found positive for herpes simplex virus DNA. Of the 239 patients diagnosed by both polymerase chain reaction and immunofluorescence assay, 35 (14.6 per cent) were found positive with immunofluorescence assay, 59 (24.7 per cent) were found positive with polymerase chain reaction, 30 (12.5 per cent) were positive with both immunofluorescence and polymerase chain reaction assay.ConclusionEfficacy and accuracy of the polymerase chain reaction assay was greater compared to the immunofluorescence assay for detection of herpes virus in corneal scrapings/corneal grafts of suspected herpetic keratitis patients. Although the immunofluorescence assay is a rapid test for the detection of herpes virus in suspected herpetic keratitis patients, a combination of polymerase chain reaction with immunofluorescence assay will provide higher reliable and accurate results.

Cytokine Levels and Human Herpesviruses in Saliva from Clinical Periodontal Healthy Subjects with Peri-Implantitis: A Case-Control Study.

This study evaluated the presence of cytokines (IL-1β, IL-2, IL-4, IL-6, MCP-1, MIP-1α, MIP-1β, and TNF-α) and human herpesvirus (HSV1, HSV2, EBV, CMV, VZV, HHV6, HHV7, and HHV8) in saliva samples taken from subjects with and without peri-implantitis. Forty-two periodontally healthy subjects were divided according to peri-implant condition: healthy and peri-implantitis groups. The clinical parameters as probing depth, clinical attachment level, plaque index, gingival bleeding, bleeding on probing, and suppuration were evaluated. For cytokine detection, multiplex analysis was performed, and PCR assay was used to identify herpesviruses. No significant differences were found in cytokine levels between groups (p > 0.05). The presence of herpesvirus was 1.97-fold higher in patients with peri-implantitis (odds ratio, CI 0.52–7.49). The association of the presence or absence of herpesvirus with the salivary markers was statistically significant for MIP-1β (p = 0.0087) and TNF-α (p = 0.0437) only in the peri-implantitis group. The presence of herpesviruses in patients with peri-implantitis suggests the development of a proinflammatory environment, which is characterized by increased expression of MIP-1β and TNF-α in saliva.

Presence of herpesvírus in diseased fishes

Herpesviruses that infect fishes belong to the Herpesvirales order and Alloherpesvirus family. In these species, the different types of herpesvirus can cause tumors, adenocarcinoma and skin lesions. This study aims detect to presence of herpesvirus in fishes from commercial, recreation or experimental creations of the States of Sao Paulo and Minas Gerais, Brazil. Organ fragments and lesions of 53 fish species coming of mortality cases were forwarded at Biological Institute for examination by transmission electron microscopy by research of etiological agent. By transmission electron microscopy through negative staining technique, were observed herpes virus-like particles in 46 fishes and through embedding resin technique, in ultrathin sections were visualized herpes virus immature particles, measuring 90-110nm in diameter, located in the nuclei and complete particles measuring 160nm. In the histopathology technique, lesions associated with the virus as corpuscles inclusion, papillomas, and dermal lesions and in the gills were observed in 27 fishes. The evaluated techniques of TEM and the histopathology were effective for the rapid detection of herpesvirus in the examined samples.

The blood DNA virome in 8,000 humans.

The characterization of the blood virome is important for the safety of blood-derived transfusion products, and for the identification of emerging pathogens. We explored non-human sequence data from whole-genome sequencing of blood from 8,240 individuals, none of whom were ascertained for any infectious disease. Viral sequences were extracted from the pool of sequence reads that did not map to the human reference genome. Analyses sifted through close to 1 Petabyte of sequence data and performed 0.5 trillion similarity searches. With a lower bound for identification of 2 viral genomes/100,000 cells, we mapped sequences to 94 different viruses, including sequences from 19 human DNA viruses, proviruses and RNA viruses (herpesviruses, anelloviruses, papillomaviruses, three polyomaviruses, adenovirus, HIV, HTLV, hepatitis B, hepatitis C, parvovirus B19, and influenza virus) in 42% of the study participants. Of possible relevance to transfusion medicine, we identified Merkel cell polyomavirus in 49 individuals, papillomavirus in blood of 13 individuals, parvovirus B19 in 6 individuals, and the presence of herpesvirus 8 in 3 individuals. The presence of DNA sequences from two RNA viruses was unexpected: Hepatitis C virus is revealing of an integration event, while the influenza virus sequence resulted from immunization with a DNA vaccine. Age, sex and ancestry contributed significantly to the prevalence of infection. The remaining 75 viruses mostly reflect extensive contamination of commercial reagents and from the environment. These technical problems represent a major challenge for the identification of novel human pathogens. Increasing availability of human whole-genome sequences will contribute substantial amounts of data on the composition of the normal and pathogenic human blood virome. Distinguishing contaminants from real human viruses is challenging.

An Immunohistochemical Study of the Myenteric Plexus in Idiopathic Achalasia

Achalasia is a primary esophageal motor disorder characterized by degenerative changes of the myenteric plexus. The pathophysiologic abnormalities may be the final result of several intermeshing mechanisms, and more than one single factor may cause the motor abnormalities. To report our experience in investigating the myenteric plexus of achalasia patients undergoing esophagomyotomy. Tissue samples from 12 patients undergoing Heller myotomy for achalasia were evaluated and compared with esophageal tissue specimens from 7 controls. Enteric neurons and interstitial cells of Cajal (ICC) were assessed by immunohistochemical methods, and the presence of vasoactive intestinal polypeptide ergic fibers and of CD3 lymphocytes. The possible presence of herpesvirus was also assessed by immunohistochemistry, whereas that of papillomavirus was assessed by in-situ hybridization. Compared with controls, achalasia patients displayed a significant decrease of both enteric neurons and ICC. Immunoreactivity for vasoactive intestinal polypeptide was completely absent in each patient. CD3 staining disclosed myenteric plexitis in 5 (42%) patients; no control patient had plexitis. All patients were completely negative for the presence of both herpes simplex virus and human papillomavirus. The enteric nervous system of the lower esophageal sphincter area is impaired in patients with "idiopathic achalasia," and the abnormalities involve ICC and neurons in many patients. The triggering factors for these abnormalities are, however, still unknown.

Presence of herpesvirus in striped dolphins stranded during the cetacean morbillivirus epizootic along the Mediterranean Spanish coast in 2007

A screening for herpesvirus (HV) was carried out using a tissue bank obtained from the cetacean morbillivirus (CeMV) mortality episode that occurred along the Mediterranean Spanish coast in 2007. A total of 14 cetaceans, including six long-finned pilot whales and eight striped dolphins, were studied using histopathology and molecular analysis to detect HV and CeMV. In five of the eight dolphins (62.5%) infected with CeMV, eight novel HV sequences were also detected. No HV lesions were found in any of the coinfected dolphins, which may indicate that HV did not contribute to the mortality in the CeMV outbreak. This is the first report of HV infection in any cetacean from the Mediterranean Sea.

Expression of the simian epstein‐barr virus‐encoded latent membrane protein‐1 in malignant lymphomas of SIV‐infected rhesus macaques

During the course of simian immunodeficiency virus (SIV) infection, nearly 15% of rhesus macaques (Macaca mulatta) and up to 40% of cynomolgus macaques (Macaca fascicularis) developed SIV-associated non-Hodgkin's lymphomas. Most of these malignant lymphomas harbored lymphocryptoviruses, which are closely related to the human Epstein-Barr virus (EBV; Herpesvirus M. mulatta and Herpesvirus M. fascicularis). To characterize the oncogenic role of simian EBV infection for lymphomagenesis during SIV infection, expression of the EBV-encoded latent membrane protein-1 (LMP-1) was analyzed in malignant lymphomas of SIV-infected rhesus macaques. Nine seropositive rhesus macaques suffering from B-cell lymphomas during the late phase of SIV infection were euthanized. Latency stages of EBV infection within malignant lymphomas and simian EBV-infected lymphoblastoid cell lines (LCL8664, H50) were characterized by analyzing expression of the EBV-encoded nuclear antigens EBNA-1, EBNA-2, and small RNAs EBER1/2. In parallel, the presence of viral LMP-1 transcripts was assessed by reverse transcription-polymerase chain reaction (RT-PCR) and in situ hybridization. Results were compared with findings in AIDS-associated malignant lymphomas in two patients infected with human immunodeficiency virus (HIV)-1. Rhesus macaques developed high-grade B-cell lymphomas of the centroblastic (five of nine), immunoblastic (two of nine), centroblastic-centrocytic (one of nine), and Burkitt-like (one of nine) subtypes within 18-29 months postinfection with SIV(mac)251/32H. The presence of Herpesvirus M. mulatta was detected in eight of nine cases. Transcription of the viral oncogene LMP-1 could be demonstrated within the simian EBV-infected cell lines as well as in four of nine SIV-associated malignant lymphomas. These four cases and both of the HIV-1-related non-Hodgkin's lymphomas expressed the full spectrum of latent EBV gene products (LMP-1, EBER1/2, EBNA-1, EBNA-2) and were thus classified as latency type III stages of EBV infection. Simian EBV infection was demonstrated in 90% of lymphomas in SIV-infected rhesus macaques. Analysis of LMP-1 expression suggests an important role for this viral oncogene in the pathogenesis of both SIV and HIV-1-associated malignant lymphomas.

Herpesvirus-like DNA sequences detected in endemic, classic, iatrogenic and epidemic Kaposi's sarcoma (KS) biopsies

The identification of Kaposi's sarcoma (KS) clusters in sub-equatorial Africa (endemic KS, AKS) and the high frequency of KS in sexually transmitted AIDS (epidemic KS, EKS), have previously suggested a role for infectious agents in the etiopathogenesis of KS. The recent identification of herpesvirus (HHV)-like DNA sequences in one case of EKS and their detection in > 90% of all tested EKS, prompted us to determine the prevalence of these viral sequences in all types of KS, such as AKS, EKS, classic KS (CKS) and iatrogenic KS (IKS). The presence of herpesvirus(HHV)-like DNA sequences has been examined in 61 KS skin tumors obtained from Greece, Italy, USA, Uganda and Kenya. All KS types (100%) were positive by polymerase chain reaction (PCR) and Southern-blot analysis, while 5 out of 6 (83%) and 4 out of 7 (57%) uninvolved autologous skin biopsies from AKS and CKS patients, respectively, were positive for HHV-like sequences. All samples from non-KS patients were negative, i.e. 17 human biopsies from healthy individuals or patients affected by other pathologies, 5 human cell lines and 15 peripheral blood mononuclear cells (PBMC) from HIV-positive subjects. These results suggest that HHV-like sequences play a major role in the pathogenesis of this neoplasm.

Replication of Marek's disease virus in chicken feather tips containing vaccinal turkey herpesvirus DNA

The presence of herpesvirus of turkeys (HVT) DNA in the feather tips of chickens vaccinated with HVT was assessed by dot blot hybridisation with a probe specific for HVT and lacking homology to MDV DNA. Only small amounts of HVT DNA were detected in the feather tips of chickens that were vaccinated or left in contact with HVT vaccinated chickens. However when chickens were challenged with virulent MDV, HVT DNA was detected in the feather tips of vaccinated chickens and the largest amount was detected 35 days after vaccination. HVT DNA was recovered in significantly higher quantities from some of the MDV-infected chickens than from those infected by contact. This suggests that MDV infection may provide helper functions for HVT. MDV DNA was identified in the feather tips of MDV-challenged chickens from 25 to 45 days after challenge. Thus, immunisation of chickens with HVT did not prevent the replication of MDV in the feather tips but only diminished it.

The role of herpes simplex virus secreted glycoproteins in herpetic keratitis

We have demonstrated that, in herpetic stromal disease, the clinical manifestation of the disease depends on the presence of herpes virus (HSV) antigens in the stromal layer. In the work reported here, we have shown that the three major groups of HSV glycoproteins were secreted by F, Shealy, E-43, and RE strains, and that glycoprotein C was the major constituent of the secreted proteins. The amount of each glycoprotein secreted varied with the virus strain and the cell line used (VERO, HEp-2, SIRC or RK-13). The stromal disease-producing viruses (RE and Shealy) secreted larger amounts of glycoproteins than the epithelial disease-producing viruses (F and E-43). Our data indicated that there was a correlation between the appearance of stromal or epithelial disease and the amount of glycoproteins secreted. In addition, the manifestations of virus-induced stromal disease were reproduced by the injection of these secreted glycoproteins into the rabbit cornea. We think that the presence of these glycoproteins in the stromal layer at the time of virus growth in the epithelium is an important factor in the induction of herpetic stromal disease.

Diagnostic électro clinique des encéphalites herpétiques

Summary A restrospective study of 16 cases of necrotizing encephalitis, in which the presence of herpes virus was definitely confirmed by culture and/or electron microscopy, demonstrated the major diagnostic value of the E.E.G. in this disease. As well as indicating the site of the primary focus, 14 out of the 16 cases showed evidence of periodic paroxystic activity with fairly typical temporal and spatial characteristics, which can establish the diagnosis when a clinical picture of acute encephalitis and a cytological reaction in the CSF are associated. Other presumptive or affirmative diagnostic criteria are discussed, and the importance of taking a biopsy is underlined. Therapeutic measures (chemotherapy and/or neurosurgery) are briefly outlined.