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1.
Avian Dis ; 65(1): 52-58, 2021 03.
Article En | MEDLINE | ID: mdl-34339122

A flock of captive bobwhite quail (Colinus virginianus) experienced loose droppings, depression, and increased mortality starting at 3 wk of age. Necropsy of the affected birds revealed intestines dilated with frothy and tan fluid. Irregular dark brown fissures within the koilin layer of the gizzard were found in 20%-30% of the birds. Histologically, gizzards showed multifocal koilin degeneration or fragmentation, degeneration and necrosis of the subjacent epithelial cells, and infiltration of macrophages, lymphocytes, and heterophils. Necrotic epithelial cells occasionally contained large, smudgy, basophilic intranuclear inclusion bodies with marginated nuclear chromatin. Adenoviral paracrystalline arrays composed of icosahedral virions (60-70 nm diameter) were seen on transmission electron microscopy in the nuclei of epithelial cells in the gizzard mucosa. Adenovirus was isolated from gizzard, liver, intestine, and trachea by inoculation of specific-pathogen-free embryonated chicken eggs. Homogenates of the gizzard, liver, and intestine were positive for the adenovirus hexon gene by PCR. Sequencing of PCR amplicons confirmed the virus as fowl aviadenovirus A. The study isolates showed more than 99% and 97% nucleotide identity with quail bronchitis virus and with aviadenoviruses from gizzard erosion and ulceration (GEU) in broilers, respectively. The viral isolates showed six substitutions (G1T, C174A, A229G, C513A, T579A, and G621C) of which two were nonsynonymous (G1T and A229G), resulting in a change in the translated amino acid as A1S and S77G, respectively. These results indicate that adenoviruses of the same type or species can cause different clinical presentations in quails, e.g., bronchitis or GEU.


Artículo regular­Brote de erosiones y ulceraciones de la molleja asociadas con Aviadenovirus A del pollo en codornices de Virginia en cautiverio (Colinus virginianus). Una parvada de codornices de Virginia en cautiverio (Colinus virginianus) mostró heces acuosas, depresión y aumento de la mortalidad a partir de las tres semanas de edad. La necropsia de las aves afectadas reveló intestinos dilatados con líquido espumoso y marrón. Se encontraron fisuras irregulares de color marrón oscuro dentro de la capa de koilin de la molleja en el 20% al 30% de las aves. Histológicamente, las mollejas mostraron degeneración o fragmentación multifocal de la capa de koilin, degeneración y necrosis de las células epiteliales subyacentes e infiltración de macrófagos, linfocitos y heterófilos. Las células epiteliales necróticas contenían ocasionalmente cuerpos de inclusión intranucleares basófilos grandes, con cromatina nuclear marginada. Se observaron matrices paracristalinas adenovirales compuestas de viriones icosaédricos (60-70 nm de diámetro) en el microscopio electrónico de transmisión en los núcleos de las células epiteliales de la mucosa de la molleja. Se aisló adenovirus de molleja, hígado, intestino y tráquea mediante la inoculación de huevos embrionados de pollo libres de patógenos específicos. Los homogeneizados de la molleja, el hígado y el intestino fueron positivos para el gene del hexon del adenovirus por PCR. La secuenciación de amplicones de PCR confirmó la presencia de Aviadenovirus A del pollo. Los aislamientos del estudio mostraron una identidad mayor del 99% y 97% en la secuencia de nucleótidos con el virus de la bronquitis de codorniz y con aviadenovirus asociado con erosión y ulceración de mollejas (con las siglas en inglés GEU) en pollos de engorde, respectivamente. Los aislados virales mostraron seis sustituciones (G1T, C174A, A229G, C513A, T579A y G621C) de las cuales dos eran no-sinónimas (G1T y A229G), lo que resultó en un cambio en el aminoácido traducido como A1S y S77G, respectivamente. Estos resultados indican que los adenovirus del mismo tipo o especie pueden causar diferentes presentaciones clínicas en codornices, por ejemplo, bronquitis o erosión y ulceración de mollejas.


Adenoviridae Infections/veterinary , Aviadenovirus/physiology , Colinus , Poultry Diseases/epidemiology , Stomach Ulcer/veterinary , Adenoviridae Infections/epidemiology , Adenoviridae Infections/pathology , Adenoviridae Infections/virology , Animals , Gizzard, Avian/pathology , Minnesota/epidemiology , Peptic Ulcer , Poultry Diseases/pathology , Poultry Diseases/virology , Stomach Ulcer/epidemiology , Stomach Ulcer/pathology , Stomach Ulcer/virology
4.
Hum Pathol ; 92: 107-112, 2019 10.
Article En | MEDLINE | ID: mdl-30584892

Primary cytomegalovirus (CMV) infection is rare in immunocompetent hosts and generally asymptomatic. CMV infective gastritis in patients without immunosuppression is very unusual. A 44-year-old man presented with complaints of intermittent epigastric pain. He had no history of organ transplantation, human immunodeficiency virus infection, or immunosuppression of any type. Upper gastrointestinal endoscopy revealed ulcers in the gastric antrum and uplift of the gastric body. Computed tomography scan showed obvious thickening of the gastric wall and enlargement of retroperitoneal lymph nodes, suggesting malignancy. However, the first biopsy only showed ulcerative inflammation, necrosis, and mucosal erosions around the ulcer. Repeat biopsy and histopathological examination showed CMV inclusions in glandular endothelial cells. Immunohistochemistry findings supported the diagnosis of CMV infective gastritis. Symptoms subsided after treatment with intravenous ganciclovir, and the gastric ulceration and surrounding mucosal inflammation decreased. This case report and review of literature is presented to increase awareness regarding this rare disease.


Cytomegalovirus Infections/diagnosis , Gastritis/diagnosis , Stomach Neoplasms/diagnostic imaging , Stomach Ulcer/diagnostic imaging , Adult , Cytomegalovirus Infections/diagnostic imaging , Cytomegalovirus Infections/pathology , Diagnostic Errors , Endoscopy , Gastritis/diagnostic imaging , Gastritis/pathology , Gastritis/virology , Humans , Immunohistochemistry , Male , Stomach Ulcer/pathology , Stomach Ulcer/virology , Tomography, X-Ray Computed
5.
Virus Res ; 242: 30-36, 2017 10 15.
Article En | MEDLINE | ID: mdl-28870469

Horses commonly develop gastric mucosal ulcers, similar to humans, a condition known as equine gastric ulcer syndrome (EGUS) that can lead to poor performance and lost training time and care expenses. Unlike humans, however, an infectious bacterial cause of ulcers has not been conclusively identified. Herpesviruses, while well-established causative agents of diseases such as cold sores, genital lesions, and certain types of cancer, have also been implicated in the development of a subset of gastric ulcers in humans. The presence of equid herpesviruses in the gastrointestinal tract and their potential contribution to EGUS has not been evaluated. Here, we provide the first evidence of equid gammaherpesviruses 2 and 5 (EHV-2 and -5) within the epithelium of the gastric mucosa of horses. These viruses were initially detected by a nested PCR screen of gastric tissue samples obtained from client- and university-owned horses with and without ulcers; however, no association with EGUS was found in this limited sample set. We then validated a highly sensitive in situ hybridization (ISH) assay and used this assay to characterize the distribution of these viruses in necropsy gastric tissue samples from five racehorses. Analyses revealed frequent EHV-2 and EHV-5 co-infections within the gastric mucosal epithelium, regardless of the ulcer status. These results are the first to demonstrate the presence of equid gammaherpesviruses in the gastric mucosa of horses and warrants further investigation to determine the contribution of these viruses to the development of EGUS and/or other gastrointestinal diseases.


Epithelium/virology , Gammaherpesvirinae/isolation & purification , Gastric Mucosa/virology , Herpesviridae Infections/veterinary , Horse Diseases/virology , Stomach Ulcer/veterinary , Animals , Coinfection/veterinary , Coinfection/virology , Gammaherpesvirinae/classification , Gammaherpesvirinae/genetics , Herpesviridae Infections/virology , Horses , Nucleic Acid Hybridization , Polymerase Chain Reaction , Stomach Ulcer/virology
7.
Rev. esp. enferm. dig ; 108(10): 670-672, oct. 2016. ilus
Article Es | IBECS | ID: ibc-156754

La afectación gástrica por el virus varicela-zóster es una entidad clínica poco frecuente, cuya sospecha y diagnóstico precoz es importante para evitar las consecuencias derivadas de su elevada morbimortalidad que en pacientes inmunocomprometidos varía entre un 9% y 41% según las series. A continuación se describen dos casos de afectación gástrica por el virus de la varicela-zóster (VVZ) en dos pacientes con enfermedad hematooncológica. Habitualmente las lesiones gástricas van precedidas de la aparición de lesiones cutáneas pápulo-vesiculares características. Cuando la afectación gástrica es el primer síntoma de la enfermedad se puede producir un retraso en el diagnóstico y tratamiento de esta infección que puede conllevar consecuencias graves para el paciente inmunocomprometido. Es por ello que proponemos que sea una entidad tenida en cuenta en el algoritmo de estudio del paciente inmunocomprometido que presenta dolor abdominal y lesiones endoscópicas de tipo ulceroso (AU)


Gastric involvement with the varicella-zoster virus is an uncommon clinical condition where early suspicion and diagnosis are important to prevent the consequences deriving from its high morbidity and mortality, which in immunocompromised patients oscillate between 9% and 41% according to the various series. Two cases of gastric involvement with the varicella-zoster virus (VZV) in two patients with blood cancer are reported below. Gastric lesions are usually preceded by typical papulovesicular skin lesions. When gastric involvement is the first symptom of the disease its diagnosis and management may be delayed, which may entail severe consequences for immunocompromised patients. It is therefore that we suggest its inclusion in the algorithm for immunocompromised patients with abdominal pain and ulcer-like endoscopic lesions (AU)


Humans , Chickenpox/complications , Herpesvirus 3, Human/pathogenicity , Gastritis/virology , Immunocompromised Host , Stomach Ulcer/virology , Abdominal Pain/etiology , Leukemia/complications , Lymphoma, Non-Hodgkin/complications
8.
Intern Med ; 55(14): 1923-7, 2016.
Article En | MEDLINE | ID: mdl-27432105

Tocilizumab, an anti-human interleukin 6 receptor (IL-6R) monoclonal antibody, is widely used to treat rheumatoid arthritis (RA) and is expected to exhibit clinical efficacy when used to treat other autoimmune diseases. However, a risk of opportunistic infection is occasionally recognized. A 54-year-old woman had received an oral corticosteroid and methotrexate to treat RA. Despite receiving these treatments, she received additional treatment with tocilizumab due to poor control of the disease activity. She presented at our hospital with a high fever and epigastralgia 19 days after receiving this treatment. A laboratory evaluation revealed liver injury and cytomegalovirus (CMV) viremia. Abdominal ultrasonography and computed tomography (CT) revealed hepatosplenomegaly, but no ascites. Upper gastrointestinal endoscopy revealed gastric erosions induced by CMV, which were confirmed immunohistochemically. Hence, we diagnosed the patient with CMV reactivation-induced acute hepatitis and gastric erosions under tocilizumab treatment. She received an anti-cytomegalovirus drug, ganciclovir, for 14 days due to her viremia and impaired general condition, which was suggestive of a severe infection. Her general condition subsequently improved, the liver function test results normalized, and the gastric erosions disappeared. In conclusion, although tocilizumab is very useful for treating certain autoimmune and inflammatory diseases, and will be prescribed more widely in the future, associated CMV infections must be closely monitored, as these can be lethal.


Antibodies, Monoclonal, Humanized/adverse effects , Arthritis, Rheumatoid/drug therapy , Cytomegalovirus Infections/etiology , Antibodies, Monoclonal, Humanized/therapeutic use , Cytomegalovirus Infections/drug therapy , Female , Ganciclovir/therapeutic use , Hepatitis/virology , Humans , Methotrexate/therapeutic use , Middle Aged , Stomach Ulcer/virology
11.
Anal Cell Pathol (Amst) ; 2015: 164840, 2015.
Article En | MEDLINE | ID: mdl-26199856

Background. Helicobacter pylori (HP) infection and nonsteroidal anti-inflammatory drugs (NSAID) use are considered the main risk to develop peptic ulcer disease (PUD). However, PUD also occurs in the absence of HP infection and/or NSAID use. Recently, we have found evidence that Epstein-Barr virus (EBV) reactivation increases the risk to develop premalignant and malignant gastric lesions. Objective. To study a possible association between EBV and PUD. Methods. Antibodies against an EBV reactivation antigen, HP, and the HP virulence factor CagA were measured in sera from 207 Mexican subjects, controls (healthy individuals, n = 129), and PUD patients (n = 78, 58 duodenal and 20 gastric ulcers). Statistical associations were estimated. Results. Duodenal PUD was significantly associated with high anti-EBV IgG titers (p = 0.022, OR = 2.5), while anti-EBV IgA was positively associated with gastric PUD (p = 0.002, OR = 10.1). Conclusions. Our study suggests that EBV reactivation in gastric and duodenal epithelium increases the risk to develop PUD.


Epstein-Barr Virus Infections/complications , Herpesvirus 4, Human/physiology , Peptic Ulcer/complications , Peptic Ulcer/virology , Adult , Antibodies, Viral/immunology , Duodenal Ulcer/complications , Duodenal Ulcer/microbiology , Duodenal Ulcer/virology , Female , Helicobacter Infections/complications , Herpesvirus 4, Human/immunology , Humans , Immunoglobulin G/immunology , Male , Middle Aged , Odds Ratio , Peptic Ulcer/microbiology , Risk Factors , Stomach Ulcer/complications , Stomach Ulcer/microbiology , Stomach Ulcer/virology
12.
J Med Virol ; 87(6): 1041-5, 2015 Jun.
Article En | MEDLINE | ID: mdl-25776966

Human cytomegalovirus-induced lesions resembling malignancies have been described in the gastrointestinal tract and include ulcerated or exophytic large masses. The aim of this study was to review the cases registered in the databases of two academic hospitals and formulate a hypothesis concerning the pathogenic mechanisms responsible for cytomegalovirus-induced pseudotumor development. All the diagnoses of human cytomegalovirus infections of the upper gastrointestinal tract recorded from 1991 to 2013 were reviewed. Cases of mucosal alterations misdiagnosed endoscopically as malignancies were selected. Large ulcers occurring in the stomach (three cases) and an irregular exophytic mass at the gastro-jejunal anastomosis were misdiagnosed endoscopically as malignancies (4 cases out of 53). Histologically, all lesions reflected hyperplastic mucosal changes with a prevalence of epithelial and stroma infected cells, without signs of cell atypia. The hypothesis presented is that the development of human cytomegalovirus-induced pseudotumors may be the morphological expression of chronic mucosa damage underlying long-term infection.


Cytomegalovirus Infections/pathology , Cytomegalovirus/physiology , Gastric Mucosa/pathology , Gastrointestinal Neoplasms/diagnosis , Stomach Ulcer/pathology , Adult , Aged , Antibodies, Viral/blood , Chronic Disease , Cytomegalovirus/immunology , Cytomegalovirus Infections/immunology , Cytomegalovirus Infections/virology , Diagnostic Errors , Female , Gastric Mucosa/ultrastructure , Gastric Mucosa/virology , Gastrointestinal Neoplasms/pathology , Humans , Inclusion Bodies, Viral , Male , Middle Aged , Stomach Ulcer/virology , Time Factors
13.
Vopr Virusol ; 58(3): 46-8, 2013.
Article Ru | MEDLINE | ID: mdl-24006634

The study included 120 patients with pre-cancer conditions of the stomach and 30 patients with gastric cancer stage II-IV. The ELISA method in the blood serum was used to determine the markers of the infection caused by Herpes simplex virus (HSV) types 1 and 2, Cytomegalovirus (CMV), and Epstein-Barr virus (EBV). The majority of the patients exhibited high titers of markers of Herpesvirus mixed infection. These data allow recommending the determination of IgG antibodies to antigens of herpesviruses in patients with the diseases of the stomach and assigning the appropriate antiviral drugs.


Antibodies, Viral/blood , Antigens, Viral/blood , Gastritis/blood , Herpes Simplex/blood , Precancerous Conditions/blood , Stomach Neoplasms/blood , Stomach Ulcer/blood , Antibodies, Viral/immunology , Antigens, Viral/immunology , Biomarkers/blood , Cytomegalovirus/immunology , Cytomegalovirus/isolation & purification , Cytomegalovirus Infections/blood , Cytomegalovirus Infections/complications , Cytomegalovirus Infections/immunology , Cytomegalovirus Infections/virology , Enzyme-Linked Immunosorbent Assay , Epstein-Barr Virus Infections/blood , Epstein-Barr Virus Infections/complications , Epstein-Barr Virus Infections/immunology , Epstein-Barr Virus Infections/virology , Gastritis/complications , Gastritis/immunology , Gastritis/virology , Herpes Simplex/complications , Herpes Simplex/immunology , Herpes Simplex/virology , Herpesvirus 1, Human/immunology , Herpesvirus 1, Human/isolation & purification , Herpesvirus 2, Human/immunology , Herpesvirus 2, Human/isolation & purification , Herpesvirus 4, Human/immunology , Herpesvirus 4, Human/isolation & purification , Humans , Immunoglobulin G/blood , Immunoglobulin G/immunology , Precancerous Conditions/complications , Precancerous Conditions/immunology , Precancerous Conditions/virology , Russia , Stomach Neoplasms/complications , Stomach Neoplasms/immunology , Stomach Neoplasms/virology , Stomach Ulcer/complications , Stomach Ulcer/immunology , Stomach Ulcer/virology
15.
World J Gastroenterol ; 19(7): 1143-6, 2013 Feb 21.
Article En | MEDLINE | ID: mdl-23467493

The local injection of triamcinolone acetonide (TA) is effective in preventing pyloric stenosis and deformity following large endoscopic submucosal dissection (ESD). However, because of its long-acting nature, TA can induce long-term local immunosuppression and subsequent adverse events. We report a case of a cytomegalovirus (CMV) ulcer that formed only at the TA local injection site. A 68-year-old man underwent ESD to treat early gastric cancer that formed over the pylorus. The lesion extended to the duodenum, and an artificial ulcer covered more than two-thirds of the circumference of the pylorus. To prevent pyloric stenosis, TA was locally injected into the ulcer floor. On day 12, a deeper ulcer 10 mm in diameter was discovered in the center of the post-ESD ulcer. Biopsies revealed large cells with intranuclear inclusion bodies, which stained positive for the anti-CMV antibody. Local TA injections are useful, however, CMV ulcer might occur as adverse events.


Cytomegalovirus Infections/virology , Immunocompromised Host , Immunosuppressive Agents/adverse effects , Pyloric Stenosis/prevention & control , Steroids/adverse effects , Stomach Ulcer/virology , Triamcinolone Acetonide/adverse effects , Aged , Biopsy , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/immunology , Gastroscopy , Humans , Immunosuppressive Agents/administration & dosage , Injections , Male , Risk Factors , Steroids/administration & dosage , Stomach Ulcer/diagnosis , Stomach Ulcer/immunology , Time Factors , Triamcinolone Acetonide/administration & dosage , Wound Healing
16.
Pediatrics ; 130(5): e1377-81, 2012 Nov.
Article En | MEDLINE | ID: mdl-23045567

We report on an 18-year-old man with common variable immunodeficiency presenting with abdominal pain and vomiting due to gastric ulcers caused by reactivation of varicella-zoster virus (VZV). Endoscopy revealed multiple ulcers in the gastric antrum. Fever and rash developed the next day. Skin biopsy showed multinucleated cells with intranuclear inclusions highly suggestive of VZV infection, and high-dose intravenous acyclovir was started. VZV was detected on direct immunofluorescence from skin biopsy and polymerase chain reaction from endoscopic biopsy. His course was complicated by encephalopathy, pancreatitis, hepatitis, renal impairment, and hyponatremia. After 3 weeks of antiviral therapy, he gradually improved. Skin lesions cleared within a week. He remained well on follow-up 1 year later. Disseminated zoster presenting as gastric ulcers in the absence of the classic rash is unusual but has been reported in immunosuppressed patients with a history of bone marrow and stem cell transplant. We report this rare presentation in a patient with common variable immunodeficiency and highlight the importance of considering zoster as a cause for severe abdominal pain and of seeking endoscopic diagnosis to facilitate early therapy and reduced mortality risk.


Herpes Zoster/complications , Stomach Ulcer/virology , Adolescent , Humans , Male
17.
Oncol Rep ; 28(5): 1653-8, 2012 Nov.
Article En | MEDLINE | ID: mdl-22948745

Hepatitis B virus (HBV) infects many individuals globally each year. Researchers usually focus on the relationship between HBV and liver diseases. In this study, we investigated the effects of HBV infection on gastric mucosa. We detected the levels of HBX protein and mRNA in specimens from sixty-four chronic hepatitis B patients (CHB) with gastric ulcers. We confirmed that HBX could aggravate gastric ulcers according to clinicopathological parameters. In addition, we constructed the pcDNA3.1-HBX plasmid and transfected it into GES-1, a gastric mucosal cell line. The results indicated that HBX could induce apoptosis and G1 arrest in GES-1 cells. Insights into the mechanism of HBX action in GES-1 cells were obtained using western blot analysis.


Gastric Mucosa/cytology , Gastric Mucosa/virology , Stomach Ulcer/virology , Trans-Activators/genetics , Trans-Activators/metabolism , Apoptosis , Cell Line , Female , G1 Phase Cell Cycle Checkpoints , Gastric Mucosa/metabolism , Hepatitis B/complications , Hepatitis B/virology , Hepatitis B virus , Humans , JNK Mitogen-Activated Protein Kinases/metabolism , MAP Kinase Signaling System , Male , Middle Aged , RNA, Messenger/analysis , RNA, Messenger/genetics , Stomach Ulcer/complications , Stomach Ulcer/genetics , Trans-Activators/analysis , Viral Regulatory and Accessory Proteins
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