ABSTRACT
OBJECTIVE: We aimed at determining the effectiveness of mechanical thrombectomy (MT) in patients with major vessel occlusion and infected with COVID-19, evaluating its clinical outcome and comparing it with non-COVID patients. PATIENTS AND METHODS: During the pandemic, 729 patients who underwent MT in stroke centers due to Acute Ischemic Stroke (AIS) with large vessel occlusion were evaluated. This study included 40 patients with a confirmed COVID-19 diagnosis by a positive PCR test between March 11, 2020, and December 31, 2020. These patients were compared to 409 patients who underwent MT due to major vessel occlusion between March 11, 2019, and December 31, 2019. RESULTS: Of the patients with AIS who are infected with COVID-19, 62.5% were males, and all patients have a median age of 63.5 ± 14.4 years. The median NIHSS score of the COVID-19 group was significantly higher than that of the non-COVID-19 groups. Dissection was significantly more in the COVID-19 group. The mortality rates at 3 months were higher in the COVID-19 groups compared to non-COVID-19 groups. CONCLUSIONS: This study revealed an increased frequency of dissection in patients with COVID-19. COVID-19-related ischemic strokes are associated with worse functional outcomes and higher mortality rates than non-COVID-19 ischemic strokes.
Subject(s)
Brain Ischemia , COVID-19 , Ischemic Stroke , Stroke , Aged , Brain Ischemia/complications , COVID-19 Testing , Female , Humans , Ischemic Stroke/epidemiology , Ischemic Stroke/surgery , Male , Middle Aged , Pandemics , Prognosis , Retrospective Studies , Stroke/complications , Thrombectomy/adverse effects , Treatment OutcomeABSTRACT
Toscana virus (TOSV) is a prominent arthropod-borne viral agent of human central nervous system infections occurring in the Mediterranean region. The main transmission route to susceptible individuals involves sandflies as vectors. Despite several reports revealing widespread TOSV activity in Turkey, vectors remained unidentified. A sandfly field survey was carried out in five provinces in Central, Southeast and Mediterranean Anatolia in 2017 to identify TOSV and related sandfly-borne phleboviruses and Leishmania parasites, with evidence for circulation in the region. A total of 7136 sandfly specimens, collected via standard methods, were evaluated in 163 pools. TOSV was detected in 11 pools (6.7%), comprising Phlebotomus major sensu lato, Sergentomyia dentata and Phlebotomus papatasi species. TOSV partial L and S segment sequences were characterized, that phylogenetically clustered with local and global genotype A strains. An amino acid substitution outside the conserved motifs of the viral polymerase, also present in previous TOSV sequences in endemic regions, was observed. Leishmania tropica was detected in a single pool of Ph. sergentii (0.6%). This is the first report of TOSV in sandflies from Turkey, and this study further provides evidence for additional sandfly species with the potential to transmit TOSV.
Subject(s)
Phlebotomus , Sandfly fever Naples virus , Animals , Bunyaviridae Infections/transmission , Humans , Insect Vectors/parasitology , Insect Vectors/virology , Leishmania tropica/isolation & purification , Leishmaniasis, Cutaneous/transmission , Phlebotomus/classification , Phlebotomus/parasitology , Phlebotomus/virology , Phylogeny , Psychodidae/classification , Psychodidae/parasitology , Psychodidae/virology , RNA, Viral , Sandfly fever Naples virus/genetics , Sandfly fever Naples virus/isolation & purification , Turkey/epidemiology , Vector Borne Diseases/parasitology , Vector Borne Diseases/transmission , Vector Borne Diseases/virologyABSTRACT
OBJECTIVE AND IMPORTANCE: Cerebral vasculitis (CV) is a rare described complication of rheumatoid arthritis (RA). Although the most frequent neurological manifestations of RA are peripheral neuropathy and cervical spinal cord compression due to subluxation of the cervical vertebrae, CV can be seen especially in patients with seropositive and long-standing RA. CLINICAL PRESENTATION: We report two cases of CV associated with RA. Both patients had no extraarticular manifestations and RA clinics were under control. Our first case is a 30-years-old woman with seropositive RA for 15âyears who had suddenly onset left facial and upper extremity weakness. In magnetic resonance imaging (MRI) DWI, hyperintensity in frontotemporal region due to acute ischaemia was detected. The new lacuner acute ischaemic lesions in right precentral gyrus, bilateral frontoparietal and corpus callosal region were detected in the control MRI. The cerebral MR angiography and transcranial doppler findings were consistent with CV. The patient responded favourably to pulse methylprednisolone and oral azathiopurine treatments. The second patient is a 52-year-old man who had been RA for 29âyears. He admitted to our neurology clinic with speech difficulty and right upper extremity minimal weakness. Magnetic resonance imaging DWI showed left parietooccipital acute ischaemia which was progressed within a week and a new right parietooccipital ischaemia was added. His cerebral MR angiography and cerebral angiography were concordant with CV. The cyclophosphamide therapy was started since the cerebral ischaemia was progressed during pulse methylprednisolone and he responded well to this therapy. CONCLUSION: CV due to RA is an uncommon serious complication which can be life-threatening. Therefore clinicians should be aware of the possibility of CV especially in progressive strokes in RA.
Subject(s)
Arthritis, Rheumatoid/complications , Vasculitis, Central Nervous System/diagnosis , Adult , Anti-Inflammatory Agents/therapeutic use , Female , Humans , Magnetic Resonance Angiography , Male , Methylprednisolone/therapeutic use , Middle Aged , Vasculitis, Central Nervous System/complications , Vasculitis, Central Nervous System/drug therapyABSTRACT
Toscana virus (TOSV), West Nile virus (WNV) and tickborne encephalitis virus (TBEV) are among major viral pathogens causing febrile disease and meningitis/encephalitis. The impact of these viruses was investigated at a referral centre in Ankara Province, Central Anatolia in 2012, where previous reports suggested virus circulation but with scarce information on clinical cases and vector activity. Serum and/or cerebrospinal fluid samples from 94 individuals were evaluated, in addition to field-collected arthropod specimens that included 767 sandflies and 239 mosquitoes. Viral nucleic acids in clinical samples and arthropods were sought via specific and generic nested/real-time PCRs, and antibody responses in clinical samples were investigated via commercial indirect immunofluorescence tests (IIFTs) and virus neutralization. A WNV antigen assay was also employed for mosquitoes. WNV neuroinvasive disease has been identified in a 63-year-old male via RNA detection, and the WNV strain was characterized as lineage 1. TOSV infections were diagnosed in six individuals (6.3%) via RNA or IgM detection. Partial sequences in a 23-year-old female, presented with fever and transient pancytopenia, were characterized as TOSV genotype A. Febrile disease with arthralgia and/or peripheral cranial nerve involvement was noted in cases with TOSV infections. Previous WNV and TOSV exposures have been observed in 5.3% and 2.1% of the subjects, respectively. No confirmed TBEV exposure could be identified. Morphological identification of the field-collected mosquitoes revealed Culex pipiens sensu lato (74.4%), Anopheles maculipennis (20.9%), An. claviger (2.1%) and others. Sandfly species were determined as Phlebotomus papatasi (36.2%), P. halepensis (27.3%), P. major s. l. (19.3%), P. sergenti (8.9%), P. perfiliewi (4.4%), P. simici (2.6%) and others. Viral infections in arthropods could not be demonstrated. TOSV genotype A and WNV lineage 1 activity have been demonstrated as well as serologically proven exposure in patients. Presence of sandfly and mosquito species capable of virus transmission has also been revealed.
Subject(s)
Bunyaviridae Infections/blood , Bunyaviridae Infections/cerebrospinal fluid , Sandfly fever Naples virus , West Nile Fever/blood , West Nile Fever/cerebrospinal fluid , Adult , Animals , Culicidae/virology , Female , Genotype , Humans , Immunoglobulin G/blood , Immunoglobulin G/cerebrospinal fluid , Immunoglobulin M/blood , Immunoglobulin M/cerebrospinal fluid , Insect Vectors/virology , Male , Middle Aged , Psychodidae/virology , RNA, Viral/blood , RNA, Viral/cerebrospinal fluid , RNA, Viral/genetics , Real-Time Polymerase Chain Reaction , Sandfly fever Naples virus/genetics , Sandfly fever Naples virus/isolation & purification , Sequence Analysis , Turkey , West Nile virus/genetics , West Nile virus/isolation & purification , Young Adult , Zoonoses/blood , Zoonoses/cerebrospinal fluid , Zoonoses/virologyABSTRACT
The objective of this study was to identify the impact of West Nile virus (WNV) and Toscana virus (TOSV) in febrile diseases of unknown aetiology in Eastern Thrace, Turkey; this study was conducted during August-October 2012, and included 18 clinical cases and 296 blood donors for local serosurveillance. Antibodies were determined via commercial assays and further tested for specificity via neutralization assays (NA). Viral RNAs were sought via specific and/or generic primers. WNV infections were diagnosed in seven patients (38.8%), detected via RNA+IgM in four, RNA in one and IgM and low avidity IgG in two cases. The most common symptom was fever (>38°C), followed by headache, malaise/fatigue, myalgia/arthralgia, muscle stiffness/lower back pain, anorexia, nausea/vomiting, diarrhoea, supraorbital/retrobulbar pain and abdominal pain. Neurological symptoms were noted in one individual. WNV strains in RNA-detectable patients were characterized as lineage 1. TOSV RNA or IgM were identified in two individuals with confirmed WNV infections and in one patient without evidence of WNV exposure. The clinical and laboratory findings in individuals with WNV/TOSV co-infection were comparable to those in WNV-induced disease. The TOSV strain in the patient with detectable viral RNA was characterized as genotype A. In local blood donors, seroreactivity for specific WNV and TOSV immunoglobulins was observed in 1.7% (5/296) and 14.4% (26/180), respectively. These findings indicate the emergence of WNV and TOSV-associated diseases in Eastern Thrace. WNV/TOSV co-infections were documented for the first time.
Subject(s)
Bunyaviridae Infections/complications , Bunyaviridae Infections/epidemiology , Coinfection/epidemiology , Coinfection/virology , West Nile Fever/complications , West Nile Fever/epidemiology , Adult , Aged , Antibodies, Viral/blood , Bunyaviridae Infections/pathology , Bunyaviridae Infections/virology , Coinfection/pathology , Female , Humans , Male , Molecular Sequence Data , RNA, Viral/genetics , Sandfly fever Naples virus/genetics , Sandfly fever Naples virus/immunology , Sandfly fever Naples virus/isolation & purification , Sequence Analysis, DNA , Turkey/epidemiology , West Nile Fever/pathology , West Nile Fever/virology , West Nile virus/genetics , West Nile virus/immunology , West Nile virus/isolation & purification , Young AdultABSTRACT
We hypothesized, allergic reactions of the tonsillar mucosa may cause secondary lymphoid hypertrophy in children. To evaluate this, we compared tonsil sizes and skin prick test results. Children of ages 6-12 years were divided into two groups according to the results of the skin prick tests (SPT), as atopic and non-atopic groups. All tonsil sizes were evaluated by the same observer using the Brodsky L. Scala. No statistically meaningful difference was found between the tonsil sizes of the atopic and the non-atopic groups of children. No statistically meaningful correlation was found between tonsil sizes and allergen sensitivity degrees. Even though some highly allergic children were observed to have large tonsils, it was not statistically meaningful. Since no correlation is found between SPT and tonsil sizes, allergy may not be an etiologic factor of tonsillar hypertrophy in children.
ABSTRACT
In 2010, 47 human cases of West Nile virus (WNV)infection, including 12 laboratory-confirmed and 35 probable cases, were identified in Turkey. These were the first cases detected during routine surveillance.The patients were from 15 provinces, mainly located in the western part of the country. Incidence was 0.19/100,000 with a maximum of 1.39 in Sakarya province.Forty of the total 47 cases showed neuroinvasive manifestation. Median age was 58 years with a range of four to 86. Ten of the patients died. Enhanced surveillance in humans and animals and mosquito control measures were implemented. The WNV infections were included in the national notifiable diseases list as of April 2011. In 2011, three probable and two confirmed cases of WNV infection were diagnosed in provinces where infections had been detected in the previous year, supporting a lower activity than 2010. However,detection of WNV infections in humans in 2010 and 2011 consecutively, may indicate that WNV has become endemic in the western part of Turkey. Field epidemiological studies were undertaken to understand more about the nature of infection in Turkey.
Subject(s)
Communicable Diseases, Emerging/epidemiology , Population Surveillance , West Nile Fever/epidemiology , West Nile virus/immunology , Adolescent , Adult , Aged , Aged, 80 and over , Algorithms , Animals , Child , Child, Preschool , Clinical Laboratory Techniques , Disease Notification/standards , Encephalitis/diagnosis , Encephalitis/etiology , Endemic Diseases/statistics & numerical data , Hospitalization/statistics & numerical data , Hospitalization/trends , Humans , Infection Control , Insect Vectors , Middle Aged , Mosquito Control , Risk Factors , Seroepidemiologic Studies , Travel , Turkey/epidemiology , West Nile Fever/diagnosis , West Nile Fever/microbiologyABSTRACT
Toscana virus (TOSV), a sandfly fever virus serotype of medical and public health importance, is a major pathogen involved in aseptic meningtis occurring in Mediterranean countries and poses a threat to the residents as well as travellers. Limited data on TOSV activity are present from Turkey despite being located in the endemic zone. We aimed to identify TOSV exposure in 1115 healthy blood donors at the Hacettepe University Hospital Blood Bank in Ankara, Turkey, using commercial indirect fluorescence assays (IFAs) and virus neutralization test (VNT) for antibody detection and specificity confirmation. A total of 199 samples (17.8%) were positive for anti-TOSV that include IgG reactivity in 10.4%, IgM reactivity in 8.2% and IgM + IgG reactivity in 0.7% of the sera. Anti-TOSV specificity could be confirmed via VNT in 56% of the IgG- and 43.6% of the IgM-positive sera, making up a total of 58 samples (5.2%). Risk factors associated with TOSV IgG reactivity were male gender, residing in rural areas, frequent sighting of mosquitoes/sandflies and working outdoors. TOSV-specific antibody prevalence increased significantly with age. Evidence of exposure to other sandfly fever viruses was noted. These data reveal that mild or asymptomatic infections with TOSV are frequent in central and northern Anatolia. TOSV exposure has also been identified in residents of 9 provinces in southern/southeastern Anatolia for the first time.
Subject(s)
Antibodies, Viral/blood , Bunyaviridae Infections/epidemiology , Psychodidae/virology , Sandfly fever Naples virus/immunology , Adolescent , Adult , Animals , Blood Donors , Bunyaviridae Infections/immunology , Female , Humans , Male , Middle Aged , Public Health , Risk Factors , Rural Population , Sandfly fever Naples virus/isolation & purification , Seroepidemiologic Studies , Sex Factors , Turkey/epidemiology , Young AdultABSTRACT
BACKGROUND: Norovirus (NoV) is recognised as one of the most common causes of foodborne infections. Contaminated shellfish, food, water and hospitals are well documented sources of the virus. OBJECTIVE: NoV in diarrheic children has not previously been investigated in Istanbul, Turkey, hence the aim of this study was to detect and investigate the frequency and phylogeny of human NoV genogroups I and II in children with acute gastroenteritis. STUDY DESIGN: 238 stool samples were collected from diarrheic children from 2 hospitals (Cerrahpasa Medical School and Haseki) in Istanbul and analysed by ELISA, RT-PCR and real-time RT-PCR using both SYBR Green and probe-based assays for human NoV. Primers targeting the RNA-polymerase gene were used for RT-PCR to allow DNA sequencing of Turkish NoV strains and phylogenetic analysis to be performed. RESULTS: NoV GII was detected in 36 (15.1%) of 238 samples by SYBR Green real-time RT-PCR, 10.9% by a probe-based real-time RT-PCR and 10.5% by ELISA (Ridascreen). Genogroup II (GII) the Turkish NoVs clustered with including GII4 (72.2%), GII16 (5.5%), GIIb (16.7%) and GIIe (5.5%). Two variants of GII4 (GII4-2006b and GII4-2008), GII16 and recombinant noroviruses (GIIb and GIIe) were identified. CONCLUSION: This study shows a high frequency and genetic diversity of NoV GII infections in children with acute gastroenteritis in Istanbul, Turkey.
Subject(s)
Caliciviridae Infections/epidemiology , Gastroenteritis/epidemiology , Genetic Variation , Norovirus/classification , Norovirus/isolation & purification , Phylogeny , Adolescent , Caliciviridae Infections/virology , Child , Child, Preschool , Diarrhea/virology , Enzyme-Linked Immunosorbent Assay , Feces/virology , Female , Gastroenteritis/virology , Genotype , Humans , Infant , Male , Norovirus/genetics , Prevalence , RNA, Viral/genetics , Reverse Transcriptase Polymerase Chain Reaction , Turkey/epidemiologyABSTRACT
We investigated bovine coronavirus (BCoV) as an etiological agent in cattle with clinical respiratory and digestive signs using 147 feces and 199 nasal swab samples. A total of 18 test samples (16 feces and 2 nasal swap samples) were detected positive by ELISA and/or RT-PCR targeting the BCoV N gene. The partial S1 gene regions of BCoVs (An-4 and An-11) detected in feces samples from two herd-mate dairy calves were compared. Virological and serological results indicated that BCoVs are widespread in Turkey and are likely etiological agents in diarrhea cases in calves.
Subject(s)
Cattle Diseases/epidemiology , Coronavirus Infections/veterinary , Coronavirus, Bovine/genetics , Spike Glycoprotein, Coronavirus/genetics , Animals , Cattle , Cattle Diseases/virology , Coronavirus Infections/epidemiology , Coronavirus Infections/virology , Coronavirus, Bovine/isolation & purification , Coronavirus, Bovine/metabolism , Enzyme-Linked Immunosorbent Assay/veterinary , Feces/virology , Molecular Sequence Data , Nose/virology , Phylogeny , Sequence Analysis, DNA/veterinary , Spike Glycoprotein, Coronavirus/metabolism , Turkey/epidemiologyABSTRACT
PURPOSE: To investigate the effects of vitamin C and N-acetylcysteine (NAC) against cyclophosphamide (CP) -induced genotoxic damage in exfoliated bladder cells of mice by micronucleus (MN) assay. METHODS: For each experimental step, 6-8 Swiss albino balb/c male mice were used. CP was used as positive control. Vitamin C (10, 30 and 60 mg/kg) and CP (51.6 mg/kg) were administered intraperitoneally to the experimental animals. Vitamin C was administered twice, one dose 24 h prior to the CP administration and the second dose simultaneously with the CP. NAC (200, 400 and 800 mg/kg) was administered by gavage for 7 consecutive days before the injection of CP. Distilled water and normal saline as negative controls I and II were used, respectively. Ten days after CP treatment, the mice were sacrificed and bladders were isolated and cut, and exfoliated cells were scraped from the bladder walls. Air-dried smears were stained by Feulgen reaction. MN frequencies were scored in 1000 epithelial cells per animal and defined as MN per thousand (per thousand). RESULTS: Three doses of vitamin C (10, 30 and 60 mg/ kg) showed a significant inhibitory effect on MN frequencies in mouse bladder cells when compared with those of positive control group (p <0.05). Dose-dependent inhibitory effect of vitamin C was observed only between the doses of 10 and 60 mg/kg (p <0.05). Histopathological changes that depended on CP- induced inflammatory infiltration and haemorrhage in mucosa propria were not observed in all 3 vitamin C doses. Three doses of NAC (200, 400 and 800 mg/kg) inhibited the CP-induced genotoxicity (p <0.05), however, the antigenotoxic effect of NAC was not dose-dependent. Histopathological changes that depended on CP-induced inflammatory infiltration and haemorrhage in mucosa propria were not observed in 200 and 400 mg/kg NAC dosage. The extent of desquamation in bladder was similar in all 3 doses of NAC when compared with the positive control group. CONCLUSION: Our study indicated that vitamin C and NAC reduced the CP-induced MN frequencies in target (bladder) cells of mice by 41-71% in all cases. The modifying effects of vitamin C and NAC against CP-induced genotoxic damage may be due to their antioxidant, nucleophilic properties and to the ability to act as precursors of glutathione.
Subject(s)
Acetylcysteine/pharmacology , Ascorbic Acid/pharmacology , Cyclophosphamide/toxicity , Micronuclei, Chromosome-Defective/drug effects , Urinary Bladder/drug effects , Urinary Bladder/pathology , Animals , Antineoplastic Agents, Alkylating/toxicity , Antioxidants/pharmacology , Hemorrhage/chemically induced , Hemorrhage/pathology , Hemorrhage/prevention & control , Inflammation/chemically induced , Inflammation/pathology , Inflammation/prevention & control , Male , Mice , Mice, Inbred BALB C , Micronucleus TestsABSTRACT
Blood samples from sheep and/or goats from eight small ruminant flocks in the Turkish provinces of Aydin and Burdur were tested for the presence of Pestiviruses using an antigen-capture ELISA. From clinically affected animals, pathological and immunohistochemical findings were recorded. Post mortem examination of a virus-positive lamb showing abnormal fleece and paralysis of the hind legs revealed nonsuppurative meningoencephalomyelitis with hypomyelinogenesis. By immunohistochemistry Pestivirus antigen was detected in all parts of the brain including cerebellum, cerebral hemispheres and midbrain. Two Pestivirus isolates from a sheep and a goat kid, respectively, were isolated from samples that were positive in the antigen-capture ELISA. Genetic typing using the 5'-NTR (288bp) and N(pro) (738bp) showed that both were Border disease virus (BDV) isolates. By phylogenetic analysis, they formed a cluster clearly separated from the known clusters BDV-1 to BDV-6 and might therefore represent a new subgroup (BDV-7?). This is the first report confirming the occurrence and partial characterisation of BDV infection in small ruminants in Turkey.
Subject(s)
Border Disease/epidemiology , Border disease virus/pathogenicity , Animals , Antibodies, Viral/immunology , Antigens, Viral/analysis , Antigens, Viral/blood , Border disease virus/classification , Border disease virus/genetics , Cerebrum/virology , Genotype , Geography , Goat Diseases/blood , Goat Diseases/epidemiology , Goat Diseases/virology , Goats/virology , Hindlimb/virology , Pestivirus/genetics , Pestivirus/isolation & purification , Reverse Transcriptase Polymerase Chain Reaction , Sheep , Sheep Diseases/blood , Sheep Diseases/epidemiology , Sheep Diseases/virology , Turkey/epidemiologyABSTRACT
Concurrent infection with peste des petits ruminants virus (PPRV) and pestivirus was diagnosed in stillborn twin lambs. With the flock history, the findings of epidermal syncytial cells and necrotizing bronchitis/bronchiolitis prompted testing for PPRV infection, and PPRV antigen was detected by immunohistochemistry (IHC) in the skin, lungs, kidneys, rumen, and thymus. Macroscopic anomalies that were typical of border disease included scoliosis, brachygnathism, prognathism, arthrogryposis, hydranencephaly, cerebellar hypoplasia, and hairy fleece; pestiviral antigen was detected by IHC in the brain, liver, lungs, and kidneys. Tissues from both lambs were positive by reverse transcriptase-polymerase chain reaction (RT-PCR) for PPRV and pestivirus. To the authors' knowledge, PPR has not been reported previously as a congenital infection or in combination with pestiviral infection.
Subject(s)
Peste-des-Petits-Ruminants/virology , Peste-des-petits-ruminants virus/isolation & purification , Pestivirus Infections/veterinary , Pestivirus/isolation & purification , Sheep Diseases/virology , Animals , Animals, Newborn , Fatal Outcome , Female , Immunohistochemistry/veterinary , Peste-des-Petits-Ruminants/congenital , Peste-des-petits-ruminants virus/genetics , Pestivirus/genetics , Pestivirus Infections/congenital , Pestivirus Infections/virology , Pregnancy , RNA, Viral/chemistry , RNA, Viral/genetics , Reverse Transcriptase Polymerase Chain Reaction/veterinary , SheepABSTRACT
In this study, natural cycling of BoHV-1 infection was investigated in two groups of dairy cattle containing 2120 head. Group 1 comprised 127 animals and they were monitored for BoHV-1 infection virologically and serologically in six consecutive sampling periods. It consisted of naive heifers between 6 and 8 months of age, while in group 2, age, sex and the BoHV-1 serostatus of the animals were disregarded. The animals in group 1 were found to have seroconverted at the second sampling. Results of the serological study showed slight antibody response after natural BoHV-1 infection in the herd and neutralizing titres fell below protective levels in the 6-8 months after the peak. During the 2-year study period, one recurrence was detected after primary infection. Virus isolation studies revealed a cytopathic effect indicative of BoHV-1 in two nasal swabs taken during the fifth sampling period from animals with mild upper respiratory tract symptoms. As the study was carried out under natural conditions, it is not known whether the viruses isolated were from recurrences or re-infections. Data from cross-neutralization tests with herd isolates showed higher antibody response than those with the reference virus. The dynamics of BoHV-1 in both groups were found to be statistically similar.
Subject(s)
Disease Outbreaks/veterinary , Herpesvirus 1, Bovine/isolation & purification , Infectious Bovine Rhinotracheitis/epidemiology , Infectious Bovine Rhinotracheitis/virology , Animals , Antibodies, Viral/blood , Cattle , DNA, Viral/chemistry , DNA, Viral/genetics , Dairying , Female , Herpesvirus 1, Bovine/genetics , Longitudinal Studies , Male , Neutralization Tests , Polymerase Chain Reaction/veterinary , Seroepidemiologic StudiesSubject(s)
Diarrhea/veterinary , Dog Diseases/epidemiology , Dog Diseases/virology , Virus Diseases/veterinary , Animals , Animals, Newborn , Coronavirus, Canine/genetics , Coronavirus, Canine/isolation & purification , DNA Primers , Diarrhea/epidemiology , Diarrhea/virology , Distemper Virus, Canine/genetics , Distemper Virus, Canine/isolation & purification , Dog Diseases/etiology , Dogs , Parvovirus, Canine/genetics , Parvovirus, Canine/isolation & purification , RNA, Viral/analysis , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Rotavirus/genetics , Rotavirus/isolation & purification , Turkey/epidemiology , Virus Diseases/epidemiology , Virus Diseases/virologyABSTRACT
The present study describes pathologic and virologic findings in 15 sheep and 6 goats that died of natural peste des petits ruminants virus infection in Turkey. Pathologic findings included erosive-ulcerative stomatitis, fibrino-necrotic tracheitis, bronchointerstitial pneumonia, multifocal coagulation necroses in the liver, and severe lymphocytolysis in lymphoid tissues. Syncytial cells were conspicuous, especially in the oral mucosa, pulmonary alveoli, liver, and lymphoid tissues. In addition to the typical tissue distribution, eosinophilic intracytoplasmic and/or intranuclear inclusions were observed in epithelial cells lining the renal pelvis and abomasal mucosa. Immunolabeling of the viral antigen was observed in the kidney, brain, rumen, abomasum, heart, and myocytes of the tongue besides its more typical locations. In this study, we report and describe in detail the first peste des petits ruminants endemic in Kirikkale Province, Central Anatolia of Turkey. In conclusion, these previously unreported pathologic findings in natural peste des petits ruminants virus infection establish a basis for resemblance to other morbillivirus infections, such as canine distemper and distemper of sea mammals. Reverse transcriptase-polymerase chain reaction analyses indicated that the 448-bp genome fragment was amplified in 18 cases (18/21, 85.7 %). Phylogenetic analysis showed that viruses belong to lineage 4 in the peste des petits ruminants virus common phylogenetic tree.
Subject(s)
Goat Diseases/pathology , Peste-des-Petits-Ruminants/pathology , Sheep Diseases/pathology , Animals , Goats , Ileum/pathology , Kidney/pathology , Liver/pathology , Mouth Mucosa/pathology , Myocardium/pathology , Peste-des-petits-ruminants virus/genetics , Phylogeny , Sheep , Tongue/pathology , Trachea/pathologyABSTRACT
Poxvirus epidemics occur almost every year and cause significant economic losses for small-scale animal producers in Turkey. In this study, the causative agent of the most recent epidemic in Central Anatolia was detected in clinical samples using electron microscopy (EM) and amplified using an in house polymerase chain reaction procedure for the first time. Additionally, the aetiological agent was isolated from a sheep and identified using EM and PCR.
Subject(s)
Capripoxvirus/classification , Capripoxvirus/isolation & purification , Disease Outbreaks/veterinary , Poxviridae Infections/veterinary , Sheep Diseases/virology , Animals , Capripoxvirus/genetics , Poxviridae Infections/epidemiology , Poxviridae Infections/virology , Sheep Diseases/epidemiology , Turkey/epidemiologyABSTRACT
In this study, the sera collected from a variety of mammalian species (ass-mules, cat, cattle, dog, horse, human and sheep) in 10 representative provinces of Turkey, were surveyed for the presence of neutralizing antibodies to West Nile virus (WNV). Overall, 1 of 40 (2.5%) ass-mules, 4 of 100 (4%) cattle, 43 of 114 (37.7%) dogs, 35 of 259 (13.5%) horses, 18 of 88 (20.4%) humans and 1 of 100 (1%) sheep, tested positive for WNV-neutralizing antibodies. The results indicate that a wide range of mammals are exposed to a West Nile-related virus and this could contribute to the long-term survival of this virus in the absence of overt disease.
Subject(s)
Animals, Domestic/virology , Antibodies, Viral/blood , West Nile virus/isolation & purification , Animals , Cats/virology , Cattle/virology , Disease Reservoirs/veterinary , Dogs/virology , Equidae/virology , Humans , Seroepidemiologic Studies , Sheep/virology , TurkeyABSTRACT
Apoptosis seems to play an important role in the pathogenic profile of bovine herpesvirus 1 (BHV-1) infection. Nitric oxide (NO) is also important as a signal molecule. In this study, apoptosis was selectively induced in HEp-2 cells in the early stage [1-3 h postinfection (PI)] of BHV-1 multiplication, and this apoptotic process was realised through the caspase-8, and partially through the caspase-3, pathway. BHV-1 infection inhibited staurosporine- (SS-) induced apoptosis only if the SS was added at 6 h PI. The results of this study showed that the 'NO-apoptosis' relation was realised through the caspase-8 pathway ('outer membrane receptor' pathway) at a later stage of infection in apoptosis induced by BHV-1 + SS. Our previous report (Yazici et al., 2004) and this study together showed that BHV-1 might induce and inhibit cell-type-specific pathways of apoptosis.