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1.
Avian Pathol ; 53(4): 257-263, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38353105

ABSTRACT

The aim of the present study was to monitor the dynamics and to measure the safety and efficacy of a live, attenuated, thermosensitive Mycoplasma anserisalpingitidis vaccine candidate, namely MA271, in geese breeder flocks under field conditions. Two rearing flocks were vaccinated with MA271 at 4 weeks of age and boosted at 24 weeks of age by cloaca inoculation (1 ml) and eye-dropping (60 µl). The geese then were transported to multi-aged breeding farms. Two breeding flocks served as controls. Colonization of the cloaca by MA271 showed 75% maximum prevalence between 4 and 6 weeks after the first vaccination. Then the prevalence decreased to 25% until the cooler, humid fall months which coincided with the booster vaccination. Boosting raised cloacal colonization to 100%. No clinical signs were observed in the vaccinated birds. After transportation to five multi-aged breeding farms, the wild-type strain appeared as well as MA271 in three flocks. In one flock, the wild-type strain completely displaced MA271, while in one flock only MA271 was detected. Only wild-type strains were detected in the control flocks; however, due to an HPAI outbreak, both flocks were exterminated before the end of the study. Based on the available data, the median percentage of infertile eggs was 3.7-5.1% in the MA271 vaccinated flocks, and 7.7% in the non-vaccinated flock. In conclusion, MA271 can colonize the cloaca of geese under field conditions. MA271 proved to be safe and presumably protects against M. anserisalpingitidis-induced reproduction losses.


Subject(s)
Bacterial Vaccines , Geese , Mycoplasma Infections , Poultry Diseases , Vaccines, Attenuated , Animals , Poultry Diseases/prevention & control , Poultry Diseases/microbiology , Mycoplasma Infections/veterinary , Mycoplasma Infections/prevention & control , Vaccines, Attenuated/immunology , Vaccines, Attenuated/administration & dosage , Bacterial Vaccines/immunology , Vaccination/veterinary , Cloaca/microbiology , Mycoplasma/immunology , Female , Farms
2.
Environ Monit Assess ; 195(2): 299, 2023 Jan 14.
Article in English | MEDLINE | ID: mdl-36640219

ABSTRACT

Use of medicinal herbs is now gaining popularity especially among the low-income people because it is cheap, readily available and its "seeming" lack of side effects. However, environmental pollution is a potential threat to its continued use. This study examines the effect of air pollution on the soil and consequently on the medicinal herbs grown on such soils. Soil and four medicinal herbs, Chromolaena odorata, Vernonia amygdalina, Carica papaya and Ocimum gratissimum, commonly used in the south western part of Nigeria either as purely medicinal herbs, soup vegetables or both were carefully harvested from Fasina, a polluted area, and Moro, a relatively unpolluted area, all in Ile-Ife, Nigeria. Samples were prepared following standard practice and analysed for nickel, chromium, cadmium and lead using atomic absorption spectroscopy (AAS). The results showed that elemental concentrations at the two locations were within the permissible limit for both soil and herbs, the statistical test also established no significant difference between the two locations. However, toxic metals concentrations (chromium, cadmium and lead) were found higher at the polluted site while that of the essential metal, nickel, was higher at the unpolluted site. Of the four metals, cadmium has the highest transfer ratio (0.39 and 0.34) while lead has the least (0.21 and 0.25) for Moro and Fasina sites respectively. Similarly, Chromolaena odorata has the highest transfer ratio (0.34) while Carica papaya has the least (0.28). In conclusion, gradual build-up of the toxic metals at the polluted site is evident and may eventually contaminate the herbs.


Subject(s)
Metals, Heavy , Plants, Medicinal , Soil Pollutants , Humans , Metals, Heavy/analysis , Iron/analysis , Nickel/analysis , Cadmium/analysis , Plants, Medicinal/chemistry , Nigeria , Soil/chemistry , Environmental Monitoring , Soil Pollutants/analysis , Environmental Pollution/analysis , Chromium/analysis
3.
Acta Vet Hung ; 68(1): 105-111, 2020 03.
Article in English | MEDLINE | ID: mdl-32384062

ABSTRACT

An epizootic caused by a new orthobunyavirus called Schmallenberg virus (SBV) was recognised in European ruminants in 2011 and 2012. The re-emergence of the infection was reported in several countries in the subsequent years. Although the main clinical sign of SBV infection is abortion, the impact of SBV in natural cases of abortion in domestic ruminants had not been systematically examined before this study. The aim of the study was to investigate the role of SBV infection and to compare it to the importance of other causes of abortion by examining 537 natural cases of abortion that had occurred between 2011 and 2017 in Hungary. The cause of abortion was determined in 165 (31%) cases. An infectious cause was proved in 88 (16%) cases. SBV infection was found only in a total of four cases (0.8%) using real-time polymerase chain reaction. Three of them proved to be inapparent SBV infection, and one case was attributed to SBV-induced abortion by detecting non-purulent encephalitis and SBV nucleoprotein by immunohistochemistry in a brain tissue sample. According to the results, SBV played a minor role in natural cases of domestic ruminant abortion in Hungary during the 7-year period following the first SBV outbreak in 2011.


Subject(s)
Abortion, Veterinary/epidemiology , Bunyaviridae Infections/veterinary , Cattle Diseases/epidemiology , Goat Diseases/epidemiology , Orthobunyavirus/physiology , Sheep Diseases/epidemiology , Abortion, Veterinary/classification , Abortion, Veterinary/virology , Animals , Bunyaviridae Infections/complications , Bunyaviridae Infections/epidemiology , Bunyaviridae Infections/virology , Cattle , Cattle Diseases/virology , Female , Goat Diseases/virology , Goats , Hungary/epidemiology , Incidence , Real-Time Polymerase Chain Reaction , Sheep , Sheep Diseases/virology , Sheep, Domestic
4.
Acta Vet Hung ; 67(1): 140-150, 2019 03.
Article in English | MEDLINE | ID: mdl-30922088

ABSTRACT

Enteric viral diseases of swine are one of the most frequent disorders causing huge economic losses in pork production. After the reappearance of an emerging enteropathogen, porcine epidemic diarrhoea virus (PEDV) in Hungary in 2016, an extensive survey was initiated in an attempt to identify diarrhoea-related porcine viruses, including adeno-, astro-, boca-, calici-, circo-, corona-, kobu-, rota- and Torque teno viruses. A total of 384 faecal samples collected during a twoyear period from diarrhoeic and asymptomatic pigs of various ages in 17 farms were screened by conventional and real-time PCR methods. Half of the samples contained at least one examined virus with the dominance of kobuvirus (55.1%) followed by bocaviruses (33.2%) and rotavirus groups A and C together (20.9%), while coronaviruses including PEDV were not found in this set of samples. Statistical analysis showed a highly significant difference (P < 0.0001) in the frequency of single infections compared to mixed ones with the exception of weaned pigs, in which group additionally most viruses were detected. The results of this study suggest that the complexity of this disease may vary with age, which makes the prevention of diarrhoea a challenge, especially in weaned pigs.


Subject(s)
Aging , Diarrhea/veterinary , Swine Diseases/virology , Animals , Diarrhea/epidemiology , Diarrhea/virology , Feces/virology , Hungary/epidemiology , Swine , Swine Diseases/epidemiology
5.
Acta Vet Hung ; 67(2): 307-313, 2019 06.
Article in English | MEDLINE | ID: mdl-31238732

ABSTRACT

Porcine epidemic diarrhoea virus (PEDV) is an emerging enteropathogen, causing great economic losses in the pig industry. After many years of quiescence, PEDV was detected in Hungary in 2016 with a recombination in its S gene. In order to determine the extent of this change, an attempt was made to isolate the recombinant PEDV. This study was extended with a variety of samples collected from three separate farms with newly identified PEDV in 2018. The recombinant PEDV from 2016 was isolated successfully along with three viruses from 2018, and one isolate from the new cases was used for whole genome determination. Whole genome sequence alignment revealed the highest identity with recombinant Hungarian and Slovenian PEDV within the low-pathogenic European viruses. This suggests that these recombinant PEDV are circulating in this area and may spread to other parts of the continent.


Subject(s)
Porcine epidemic diarrhea virus/classification , Porcine epidemic diarrhea virus/isolation & purification , Animals , Coronavirus Infections/veterinary , Coronavirus Infections/virology , Genome, Viral , Hungary , Phylogeny , Porcine epidemic diarrhea virus/genetics , Swine , Swine Diseases/virology
6.
Emerg Infect Dis ; 24(12): 2270-2283, 2018 12.
Article in English | MEDLINE | ID: mdl-30457528

ABSTRACT

We analyzed the highly pathogenic avian influenza (HPAI) H5 epizootic of 2016-17 in Europe by epidemiologic and genetic characteristics and compared it with 2 previous epizootics caused by the same H5 Guangdong lineage. The 2016-17 epizootic was the largest in Europe by number of countries and farms affected and greatest diversity of wild birds infected. We observed significant differences among the 3 epizootics regarding region affected, epidemic curve, seasonality, and outbreak duration, making it difficult to predict future HPAI epizootics. However, we know that in 2005-06 and 2016-17 the initial peak of wild bird detections preceded the peak of poultry outbreaks within Europe. Phylogenetic analysis of 2016-17 viruses indicates 2 main pathways into Europe. Our findings highlight the need for global surveillance of viral changes to inform disease preparedness, detection, and control.


Subject(s)
Influenza A virus/classification , Influenza in Birds/epidemiology , Influenza in Birds/virology , Animals , Animals, Wild , Birds , Disease Outbreaks , Europe/epidemiology , Genome, Viral , Geography, Medical , History, 21st Century , Influenza A virus/pathogenicity , Influenza in Birds/history , Influenza in Birds/transmission , Morbidity , Mortality , Phylogeny , Poultry Diseases/epidemiology , Poultry Diseases/virology , Spatio-Temporal Analysis , Zoonoses
7.
Arch Virol ; 163(8): 2219-2224, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29623433

ABSTRACT

Here, we present a comprehensive analysis of the H5N8/H5N5 highly pathogenic avian influenza (HPAI) virus strains detected in the Czech Republic during an outbreak in 2017. Network analysis of the H5 Hemagglutinin (HA) from 99% of the outbreak localities suggested that the diversity of the Czech H5N8/H5N5 viruses was influenced by two basic forces: local microevolution and independent incursions. The geographical occurrence of the central node H5 HA sequences revealed three eco-regions, which apparently played an important role in the origin and further spread of the local H5N8/HPAI variants across the country. A plausible explanation for the observed pattern of diversity is also provided.


Subject(s)
Evolution, Molecular , Hemagglutinin Glycoproteins, Influenza Virus/genetics , Influenza A Virus, H5N8 Subtype/genetics , Influenza A virus/genetics , Influenza in Birds/virology , Animals , Birds/classification , Birds/virology , Czech Republic/epidemiology , Disease Outbreaks , Genetic Variation , Influenza A Virus, H5N8 Subtype/classification , Influenza A Virus, H5N8 Subtype/isolation & purification , Influenza A Virus, H5N8 Subtype/pathogenicity , Influenza A virus/classification , Influenza A virus/isolation & purification , Influenza A virus/pathogenicity , Influenza in Birds/epidemiology , Phylogeny , Virulence
8.
Acta Vet Hung ; 65(2): 253-261, 2017 06.
Article in English | MEDLINE | ID: mdl-28605965

ABSTRACT

Porcine epidemic diarrhoea virus (PEDV) can cause a severe enteric disease affecting pigs of all ages. In January 2016, diarrhoea with occasional vomiting was observed in a small pig farm in Hungary. All animals became affected, while mortality (of up to 30%) was only seen in piglets. Samples from different age groups and the carcass of a piglet were examined by various methods including pathology, bacteriology and molecular biology. PEDV was confirmed by PCR and its whole genome sequence was determined. The sequence PEDV HUN/5031/2016 showed high identity with recently reported European viruses. Differences were found mostly in the S gene, where recombination was detected with a newly identified and already recombinant swine enteric coronavirus (Se-CoV) from Italy. The present report describes the first porcine epidemic diarrhoea outbreak in Hungary after many years and gives an insight into the genetics of the Hungarian PEDV.


Subject(s)
Coronavirus Infections/veterinary , Porcine epidemic diarrhea virus/genetics , Swine Diseases/virology , Animals , Coronavirus Infections/epidemiology , Coronavirus Infections/virology , Disease Outbreaks/veterinary , Hungary/epidemiology , Phylogeny , Reassortant Viruses , Swine , Swine Diseases/epidemiology
9.
Acta Vet Hung ; 65(4): 517-530, 2017 12.
Article in English | MEDLINE | ID: mdl-29256279

ABSTRACT

One of the main obstacles in freshwater aquaculture is the parasitic ciliate Ichthyophthirius multifiliis (Ich), the causative agent of white spot disease. The use of immunostimulants as feed additives may be a promising approach to control Ich infection. In the present study, we tested the prophylactic effect of orally administered ß-1,3/1,6-glucan and propolis extract E50 against Ich infection in common carp. In total, 122 fish were separated into three experimental groups fed with a control, 3% ß-glucan and 1% propolis diet for 40 consecutive days, respectively. On day 40, 16 fish per group were individually exposed to Ich theronts and the number of trophonts was counted 5 days post exposure. Relative gene expression of interleukin 1-ß (IL-1-ß) in common carp liver was examined by qPCR. Compared to control, the mean infection intensity was lower in the ß-glucan- and propolis-fed groups; however, the difference was not statistically significant. The relative expression of IL-1-ß significantly decreased in the propolis-fed group at day 10. In the ß-glucan-fed group, a significant IL-1-ß decrease was detected at day 15 compared to control. Although the Ich infection intensity was slightly decreased in both treated groups, and IL-1-ß was moderately down-regulated in the liver of common carp, our results suggest that the applied feeding regime is insufficient to prevent Ich outbreaks in common carp.


Subject(s)
Adjuvants, Immunologic/administration & dosage , Carps , Ciliophora Infections/veterinary , Ciliophora , Dietary Supplements , Fish Diseases/parasitology , Animals , Ciliophora/genetics , Ciliophora/isolation & purification , Ciliophora Infections/parasitology , Ciliophora Infections/prevention & control , RNA/genetics
10.
J Virol ; 89(19): 9920-31, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26202246

ABSTRACT

UNLABELLED: The emergence in humans of the A(H1N1)pdm09 influenza virus, a complex reassortant virus of swine origin, highlighted the importance of worldwide influenza virus surveillance in swine. To date, large-scale surveillance studies have been reported for southern China and North America, but such data have not yet been described for Europe. We report the first large-scale genomic characterization of 290 swine influenza viruses collected from 14 European countries between 2009 and 2013. A total of 23 distinct genotypes were identified, with the 7 most common comprising 82% of the incidence. Contrasting epidemiological dynamics were observed for two of these genotypes, H1huN2 and H3N2, with the former showing multiple long-lived geographically isolated lineages, while the latter had short-lived geographically diffuse lineages. At least 32 human-swine transmission events have resulted in A(H1N1)pdm09 becoming established at a mean frequency of 8% across European countries. Notably, swine in the United Kingdom have largely had a replacement of the endemic Eurasian avian virus-like ("avian-like") genotypes with A(H1N1)pdm09-derived genotypes. The high number of reassortant genotypes observed in European swine, combined with the identification of a genotype similar to the A(H3N2)v genotype in North America, underlines the importance of continued swine surveillance in Europe for the purposes of maintaining public health. This report further reveals that the emergences and drivers of virus evolution in swine differ at the global level. IMPORTANCE: The influenza A(H1N1)pdm09 virus contains a reassortant genome with segments derived from separate virus lineages that evolved in different regions of the world. In particular, its neuraminidase and matrix segments were derived from the Eurasian avian virus-like ("avian-like") lineage that emerged in European swine in the 1970s. However, while large-scale genomic characterization of swine has been reported for southern China and North America, no equivalent study has yet been reported for Europe. Surveillance of swine herds across Europe between 2009 and 2013 revealed that the A(H1N1)pdm09 virus is established in European swine, increasing the number of circulating lineages in the region and increasing the possibility of the emergence of a genotype with human pandemic potential. It also has implications for veterinary health, making prevention through vaccination more challenging. The identification of a genotype similar to the A(H3N2)v genotype, causing zoonoses at North American agricultural fairs, underlines the importance of continued genomic characterization in European swine.


Subject(s)
Influenza A virus/genetics , Orthomyxoviridae Infections/veterinary , Sus scrofa/virology , Swine Diseases/epidemiology , Swine Diseases/virology , Animals , Epidemiological Monitoring/veterinary , Europe/epidemiology , Evolution, Molecular , Genotype , Humans , Influenza A Virus, H1N1 Subtype/genetics , Influenza A Virus, H1N1 Subtype/isolation & purification , Influenza A Virus, H1N2 Subtype/genetics , Influenza A Virus, H1N2 Subtype/isolation & purification , Influenza A Virus, H3N2 Subtype/genetics , Influenza A Virus, H3N2 Subtype/isolation & purification , Influenza A virus/isolation & purification , Influenza, Human/epidemiology , Influenza, Human/virology , Molecular Epidemiology , Orthomyxoviridae Infections/epidemiology , Orthomyxoviridae Infections/virology , Phylogeny , Reassortant Viruses/genetics , Swine
11.
Euro Surveill ; 21(49)2016 Dec 08.
Article in English | MEDLINE | ID: mdl-27983512

ABSTRACT

Introduction of highly pathogenic avian influenza (HPAI) virus A(H5N8) into Europe prompted animal and human health experts to implement protective measures to prevent transmission to humans. We describe the situation in 2016 and list public health measures and recommendations in place. We summarise critical interfaces identified during the A(H5N1) and A(H5N8) outbreaks in 2014/15. Rapid exchange of information between the animal and human health sectors is critical for a timely, effective and efficient response.


Subject(s)
Disease Outbreaks/prevention & control , Influenza A Virus, H5N8 Subtype/isolation & purification , Influenza A Virus, H5N8 Subtype/pathogenicity , Influenza in Birds/virology , Influenza, Human/virology , Zoonoses/prevention & control , Animals , Birds , Europe/epidemiology , Humans , Influenza A Virus, H5N1 Subtype/isolation & purification , Influenza A Virus, H5N1 Subtype/pathogenicity , Influenza in Birds/epidemiology , Influenza in Birds/transmission , Influenza, Human/epidemiology , Influenza, Human/transmission , Population Surveillance , Poultry , Poultry Diseases/epidemiology , Public Health , Virulence , Zoonoses/transmission , Zoonoses/virology
12.
Orv Hetil ; 157(40): 1579-1586, 2016 Oct.
Article in Hungarian | MEDLINE | ID: mdl-27690621

ABSTRACT

Several trematodes that parasitize vertebrate animals utilize swimming aquatic larvae to infect the host percutaneously. The most important ones among these parasites are the blood-flukes of birds and mammals comprising species that are also zoonotic. Within this latter group are species that cause the bilharziasis or schistosomiasis of inhabitants of the tropical countries, and other trematode species that are able to penetrate human skin, but do not develop to an adult form of the worm in the body. In temperate climates this latter type of infection occurs mainly in the form of an unpleasant inflammation of the skin and is often called "swimmer's itch". In most of these cases, the origin of the larvae remains unexplored, the source of the infection is neglected by the medical or veterinarian practitioners. Herein we report for the first time in Hungary that the cause of such dermatitis was the cercariae of Schistosoma turkestanicum, which infected red deer (Cervus elaphus) in this country. The local name of this pristine disease is "water mange" and it occurs only in one of the floodplains of the Danube. On the basis of informal communication this symptom seems to be rather regular among people who do fishing or have a bath in the habitat of the blood-fluke. In the case of adequate anamnesis it is worth examining the origin of the cercarial dermatitis which may give cross-reactions with human schistosomiasis during serological tests. Orv. Hetil., 2016, 157(40), 1579-1586.


Subject(s)
DNA, Helminth/isolation & purification , Dermatitis/parasitology , Schistosoma/isolation & purification , Schistosomiasis/diagnosis , Skin Diseases, Parasitic/diagnosis , Adult , Animals , Humans , Hungary , Schistosomiasis/parasitology , Skin Diseases, Parasitic/parasitology , Swimming
13.
J Clin Microbiol ; 53(5): 1582-7, 2015 May.
Article in English | MEDLINE | ID: mdl-25740770

ABSTRACT

Accurate identification of mycobacterial species and subspecies is essential to evaluate their significance and to perform epidemiological studies. The subspecies of Mycobacterium avium have different attributes but coincide in their zoonotic potential. Our knowledge about M. avium subsp. silvaticum is limited, since its identification is uncertain. Mycobacterium avium subsp. avium and M. avium subsp. silvaticum can be discriminated from each other based only on phenotypic characteristics, as they have almost identical genome sequences. Here we describe the development of a diagnostic method which enables the molecular identification of M. avium subsp. silvaticum and discrimination from M. avium subsp. avium based on genomic differences in a duplex high-resolution melt and M. avium subsp. silvaticum-specific mismatch real-time PCR. The developed assay was tested on reference strains and 199 field isolates, which were analyzed by phenotypic methods previously. This assay not only identified all 63 M. avium subsp. silvaticum and 138 M. avium subsp. avium strains correctly but also enabled the detection of mixed M. avium subsp. avium-M. avium subsp. silvaticum cultures. This is the first time that such a large panel of strains has been analyzed, and we also report the first isolation of M. avium subsp. silvaticum from red fox, red deer, wild boar, cattle, and badger. This assay is reliable, rapid, simple, inexpensive, and robust. It eliminates the long-existing problem of ambiguous phenotypic identification and opens up the possibility for detailed and comprehensive strain studies.


Subject(s)
DNA, Bacterial/genetics , Genotyping Techniques/methods , Microbiological Techniques/methods , Molecular Diagnostic Techniques/methods , Mycobacterium avium/classification , Mycobacterium avium/genetics , Tuberculosis/veterinary , Animals , Animals, Domestic , Base Pair Mismatch , Birds , Costs and Cost Analysis , Mammals , Mycobacterium avium/isolation & purification , Real-Time Polymerase Chain Reaction/methods , Reproducibility of Results , Time Factors , Transition Temperature , Tuberculosis/diagnosis , Tuberculosis/microbiology
14.
Arch Virol ; 160(5): 1279-83, 2015 May.
Article in English | MEDLINE | ID: mdl-25643818

ABSTRACT

In the early summer of 2014, mass mortality of sichel (Pelecus cultratus) was observed in Lake Balaton, Hungary. Histological examination revealed degenerative changes within the tubular epithelium, mainly in the distal tubules and collecting ducts in the kidneys and multifocal vacuolisation in the brain stem and cerebellum. Routine molecular investigations showed the presence of the DNA of an unknown alloherpesvirus in some specimens. Subsequently, three genes of the putative herpesviral genome (DNA polymerase, terminase, and helicase) were amplified and partially sequenced. A phylogenetic tree reconstruction based on the concatenated sequence of these three conserved genes implied that the virus belongs to the genus Cyprinivirus within the family Alloherpesviridae. The sequences of the sichel herpesvirus differ markedly from those of the cypriniviruses CyHV-1, CyHV-2 and CyHV-3, putatively representing a fifth species in the genus.


Subject(s)
Cyprinidae/virology , Fish Diseases/epidemiology , Fish Diseases/virology , Herpesviridae Infections/veterinary , Herpesviridae/classification , Herpesviridae/isolation & purification , Animal Structures/virology , Animals , Cluster Analysis , DNA, Viral/chemistry , DNA, Viral/genetics , Fish Diseases/mortality , Fish Diseases/pathology , Herpesviridae/genetics , Herpesviridae Infections/epidemiology , Herpesviridae Infections/mortality , Herpesviridae Infections/pathology , Histocytochemistry , Hungary/epidemiology , Microscopy , Molecular Sequence Data , Phylogeny , Sequence Analysis, DNA , Sequence Homology , Viral Proteins/genetics
15.
Arch Virol ; 160(2): 417-22, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25361819

ABSTRACT

Here, we report the isolation of a type 1 porcine reproductive and respiratory syndrome virus (PRRSV) strain from a clinical outbreak of severe respiratory problems and high fever. Next-generation sequencing was used to determine the complete genome sequence of the isolate (9625/2012). The virus belongs to a new branch within subtype 1, clade D, and shows the highest similarity to PRRSV Olot/1991 and to the Amervac vaccine strain. Mutation analysis of 9625/2012 revealed no evidence of recombination but did show a high proportion of amino acid substitutions in the putative neutralizing epitopes, suggesting an important role of selective immune pressure in the evolution of PRRSV 9625/2012.


Subject(s)
Disease Outbreaks/veterinary , Genome, Viral/genetics , Porcine Reproductive and Respiratory Syndrome/epidemiology , Porcine respiratory and reproductive syndrome virus/genetics , Amino Acid Sequence , Amino Acid Substitution , Animals , Base Sequence , Coinfection , High-Throughput Nucleotide Sequencing , Hungary/epidemiology , Molecular Sequence Data , Mutation , Mycoplasma hyopneumoniae , Pneumonia of Swine, Mycoplasmal/pathology , Pneumonia of Swine, Mycoplasmal/virology , Porcine Reproductive and Respiratory Syndrome/pathology , Porcine Reproductive and Respiratory Syndrome/virology , Porcine respiratory and reproductive syndrome virus/classification , Porcine respiratory and reproductive syndrome virus/isolation & purification , RNA, Viral/genetics , Sequence Alignment , Sequence Analysis, RNA/veterinary , Swine
16.
BMC Vet Res ; 11: 147, 2015 Jul 11.
Article in English | MEDLINE | ID: mdl-26163135

ABSTRACT

BACKGROUND: Brucella microti was first isolated from common vole (Microtus arvalis) in the Czech Republic in Central Europe in 2007. As B. microti is the only Brucella species known to live in soil, its distribution, ecology, zoonotic potential, and genomic organization is of particular interest. The present paper is the first to report the isolation of B. microti from a wild boar (Sus scrofa), which is also the first isolation of this bacterial species in Hungary. RESULTS: The B. microti isolate was cultured, after enrichment in Brucella-selective broth, from the submandibular lymph node of a female wild boar that was taken by hunters in Hungary near the Austrian border in September 2014. Histological and immunohistological examinations of the lymph node sections with B. abortus-, B. suis- and B. canis-specific sera gave negative results. The isolate did not require CO2 for growth, was oxidase, catalase, and urease positive, H2S negative, grew well in the presence of 20 µg/ml basic fuchsin and thionin, and had brownish pigmentation after three days of incubation. It gave strong positive agglutination with anti-A and anti-M but had a negative reaction with anti-R monospecific sera. The API 20 NE test identified it as Ochrobactrum anthropi with 99.9% identity, and it showed B. microti-specific banding pattern in the Bruce- and Suis-ladder multiplex PCR systems. Whole genome re-sequencing identified 30 SNPs in orthologous loci when compared to the B. microti reference genome available in GenBank, and the MLVA analysis yielded a unique profile. CONCLUSIONS: Given that the female wild boar did not develop any clinical disease, we hypothesize that this host species only harboured the bacterium, serving as a possible reservoir capable of maintaining and spreading this pathogen. The infectious source could have been either a rodent, a carcass that had been eaten or infection occurred via the boar rooting in soil. The low number of discovered SNPs suggests an unexpectedly high level of genetic homogeneity in this Brucella species.


Subject(s)
Brucella/classification , Brucellosis/veterinary , Sus scrofa/microbiology , Animals , Brucella/isolation & purification , Brucellosis/epidemiology , Brucellosis/microbiology , Female , Hungary/epidemiology
17.
Acta Vet Hung ; 63(2): 215-22, 2015 Jun.
Article in English | MEDLINE | ID: mdl-26051260

ABSTRACT

Porcine circovirus type 2 (PCV2) associated reproductive disease was diagnosed in a herd containing only gilts. A single case of abortion occurred and no other disorder was evident in the herd. PCV2 antigen and/or DNA were detected in two aborted fetuses. One of the fetuses, revealing both PCV2 DNA and antigen, presented multinucleated giant cells, severe vascular lesions (intramural oedema, fibrinoid necrosis, mild lympho-histiocytic vasculitis, fibrin thrombi) and mild non-suppurative inflammation in the lungs. Other abortifacient infections were not found. This is the only report of PCV2-induced abortion in Hungary since 1999, when PCV2-associated disease was first discovered in the country.

18.
J Virol ; 87(9): 4938-51, 2013 May.
Article in English | MEDLINE | ID: mdl-23408635

ABSTRACT

Poxvirus infections have been found in 230 species of wild and domestic birds worldwide in both terrestrial and marine environments. This ubiquity raises the question of how infection has been transmitted and globally dispersed. We present a comprehensive global phylogeny of 111 novel poxvirus isolates in addition to all available sequences from GenBank. Phylogenetic analysis of the Avipoxvirus genus has traditionally relied on one gene region (4b core protein). In this study we expanded the analyses to include a second locus (DNA polymerase gene), allowing for a more robust phylogenetic framework, finer genetic resolution within specific groups, and the detection of potential recombination. Our phylogenetic results reveal several major features of avipoxvirus evolution and ecology and propose an updated avipoxvirus taxonomy, including three novel subclades. The characterization of poxviruses from 57 species of birds in this study extends the current knowledge of their host range and provides the first evidence of the phylogenetic effect of genetic recombination of avipoxviruses. The repeated occurrence of avian family or order-specific grouping within certain clades (e.g., starling poxvirus, falcon poxvirus, raptor poxvirus, etc.) indicates a marked role of host adaptation, while the sharing of poxvirus species within prey-predator systems emphasizes the capacity for cross-species infection and limited host adaptation. Our study provides a broad and comprehensive phylogenetic analysis of the Avipoxvirus genus, an ecologically and environmentally important viral group, to formulate a genome sequencing strategy that will clarify avipoxvirus taxonomy.


Subject(s)
Avipoxvirus/classification , Avipoxvirus/isolation & purification , Bird Diseases/virology , Phylogeny , Poxviridae Infections/veterinary , Animals , Avipoxvirus/genetics , Avipoxvirus/physiology , Birds , Host Specificity , Molecular Sequence Data , Poxviridae Infections/virology , Recombination, Genetic
19.
Arch Virol ; 159(1): 153-8, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23921622

ABSTRACT

In this study, we sequenced the whole genome of a reovirus isolated from a green bush viper (Atheris squamigera). The bush viper reovirus shared several features with other orthoreoviruses, including its genome organization. In phylogenetic analysis, this strain was monophyletic with Broome virus and baboon orthoreovirus, indicating that these viruses might have originated from a common ancestor. These new molecular data supplement previous information based mainly on biological properties of reptilian reoviruses, confirming their taxonomic position and broadening our knowledge of the evolution of members of the genus Orthoreovirus.


Subject(s)
Evolution, Molecular , Genome, Viral , Mammals/virology , Orthoreovirus/genetics , Viperidae/virology , Animals , Genome Size , Molecular Sequence Data , Orthoreovirus/classification , Orthoreovirus/isolation & purification , Phylogeny , Viral Proteins/genetics
20.
Avian Pathol ; 43(4): 379-86, 2014.
Article in English | MEDLINE | ID: mdl-24992264

ABSTRACT

Duck circovirus, duck hepatitis A virus 1, goose parvovirus and goose haemorrhagic polyomavirus are economically damaging pathogens of waterfowl, and replicate poorly or not at all in established cell lines. AGE1.CR, AGE1.CR.pIX and AGE1.CS cell lines, originating from the Muscovy duck, were tested for their suitability to isolate and identify these viruses. Immunofluorescence (IF) and quantitative polymerase chain reaction investigations verified that all cell lines are permissive for all four viruses; however, AGE1.CR.pIX proved to be the most productive and most sensitive for viral infection. IF experiments revealed that the time of one infectious cycle is approximately 12 to 14 h in the AGE1.CR.pIX cells in the case of the three DNA viruses, while it is 10 to 12 h for DHAV-1. Specific viral infectivity and the limit of detection by IF varied between 55 and 1484 copies, depending on the viruses and cell lines. Despite the high sensitivity of the cell lines for viruses, their viral productivity remained relatively low for the investigated field isolates. However, optimization of virus infection and/or the adaptation of the viruses to the cells can raise viral productivity and can make these cell lines suitable for vaccine development and production.


Subject(s)
Circoviridae Infections/veterinary , Circovirus/growth & development , Ducks , Poultry Diseases/virology , Animals , Anseriformes , Cell Line , Circoviridae Infections/pathology , Circoviridae Infections/virology , Circovirus/genetics , Circovirus/immunology , DNA, Viral/genetics , Liver/virology , Poultry Diseases/pathology , Spleen/virology , Virus Replication
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