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1.
Annu Int Conf IEEE Eng Med Biol Soc ; 2016: 5705-5708, 2016 Aug.
Article in English | MEDLINE | ID: mdl-28269550

ABSTRACT

Electrode and cap concepts for continuous and ubiquitous monitoring of brain activity will open up new fields of application and contribute to increased use of electroencephalography (EEG) in clinical routine, neurosciences, brain-computer-interfacing and out-of-the-lab monitoring. However, mobile and unobtrusive applications are currently hindered by the lack of applicable convenient and reliable electrode and cap systems. We propose a novel modular electrode concept based on a flexible polymer substrate, coated with electrically conductive metallic films. The overall concept enables design adaptation to different head regions and cap designs. We describe the single modules of the system and investigate the influence of electrode pin number, coating material and adduction force on electrode-skin impedance and perceived wearing comfort. Our results contribute to rapid and comfortable multichannel dry EEG.


Subject(s)
Electroencephalography/instrumentation , Equipment Design , Electric Conductivity , Electrodes , Humans , Metals , Polymers
2.
Epidemiol Infect ; 142(6): 1155-66, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24007822

ABSTRACT

SUMMARY: In Germany, active bat rabies surveillance was conducted between 1993 and 2012. A total of 4546 oropharyngeal swab samples from 18 bat species were screened for the presence of EBLV-1- , EBLV-2- and BBLV-specific RNA. Overall, 0·15% of oropharyngeal swab samples tested EBLV-1 positive, with the majority originating from Eptesicus serotinus. Interestingly, out of seven RT-PCR-positive oropharyngeal swabs subjected to virus isolation, viable virus was isolated from a single serotine bat (E. serotinus). Additionally, about 1226 blood samples were tested serologically, and varying virus neutralizing antibody titres were found in at least eight different bat species. The detection of viral RNA and seroconversion in repeatedly sampled serotine bats indicates long-term circulation of the virus in a particular bat colony. The limitations of random-based active bat rabies surveillance over passive bat rabies surveillance and its possible application of targeted approaches for future research activities on bat lyssavirus dynamics and maintenance are discussed.


Subject(s)
Chiroptera , Rabies/veterinary , Animals , Antibodies, Neutralizing/blood , Antibodies, Viral/blood , Germany/epidemiology , Population Surveillance , RNA, Viral/genetics , Rabies/epidemiology , Reverse Transcriptase Polymerase Chain Reaction , Species Specificity
3.
Avian Dis ; 53(4): 578-84, 2009 Dec.
Article in English | MEDLINE | ID: mdl-20095160

ABSTRACT

Between 2003 and 2008, more than 600 white stork (Ciconia ciconia) nestlings in the German federal state of Brandenburg were ringed and examined for influenza A viruses. With the spread of highly pathogenic avian influenza virus (HPAIV) of subtype H5N1 among wild birds in Germany in spring 2006, dead wild birds, including 88 white storks, were tested for infection with HPAIV. Furthermore, fresh fecal samples were examined by RT-PCR to monitor the occurrence of HPAIV in adult storks. While the monitoring of nestlings and adult white storks failed to yield evidence of influenza A virus infections in these birds, two storks found dead in April 2006 in the same location tested positive for HPAIV H5N1. Sequence analysis revealed that the virus isolated from one of the storks belonged to clade 2.2, which was commonly found in wild birds in the north of Germany and other European countries during the epidemic in 2006. Despite these two cases, white storks seemed to serve as neither a vector nor as a reservoir for HPAIV in Germany. The risk of white storks transmitting HPAIV to domestic poultry and humans is low.


Subject(s)
Birds , Influenza A virus/isolation & purification , Influenza in Birds/epidemiology , Animals , Disease Reservoirs , Disease Vectors , Feces/virology , Female , Germany/epidemiology , Influenza A virus/classification , Influenza A virus/pathogenicity , Influenza in Birds/pathology , Influenza in Birds/virology , Male , Virulence
4.
Article in English | MEDLINE | ID: mdl-16629720

ABSTRACT

Wild birds are considered a potential reservoir or a carrier of viral diseases and may therefore play a role in the epidemiology of economically important or zoonotic diseases. In 2001 and 2002, a survey with special emphasis on virus isolation in migrating waders and some other birds were conducted. In one of the most important inland resting sites for migratory waterfowl, tracheal and cloacal swabs were collected from 465 waders representing 19 different species, and 165 other birds that were not captured on purpose. A total of 42 avian viruses were isolated, 34 of these were identified as paramyxoviruses (PMVs). The majority of isolates came from waders and wild ducks, and were characterized as PMV-1. In contrast, PMV-4 was found in wild ducks only, PMV-6 was mainly detected in wader species. Four avian influenza viruses (AIVs), belonging to H4 and H3 haemagglutinin subtype, were isolated from wild duck species. Furthermore, four reo-like viruses were isolated from one particular wader species for the first time. The majority of virus positive birds were <1 year old and did not show any clinical symptoms. There was no evidence for the presence of West Nile virus in these birds. These results confirm that the restricted resting sites in Western Europe must be considered as important locations for the intra- and interspecies transmission of avian viruses.


Subject(s)
Bird Diseases/epidemiology , Bird Diseases/virology , Birds/virology , Animal Migration , Animals , Animals, Wild/virology , Bird Diseases/transmission , Cloaca/virology , Disease Reservoirs/veterinary , Germany/epidemiology , Influenza A virus/isolation & purification , Influenza in Birds/epidemiology , Influenza in Birds/transmission , Influenza in Birds/virology , Paramyxoviridae/isolation & purification , Trachea/virology
5.
Am J Obstet Gynecol ; 185(3): 716-24, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11568803

ABSTRACT

OBJECTIVE: We propose that elucidation of the pathophysiology of preterm labor can be achieved with genome-scale analyses of differential gene expression. STUDY DESIGN: CD-1 mice on day 14.5 of a 19- to 20-day gestation were assigned to one of 4 treatment groups modeling different clinical conditions (n = 5 per group): group A, infection with labor (intrauterine injection of 10(10) heat-killed Escherichia coli, which causes delivery within an average of 20 hours); group B, infection without labor (intrauterine injection of 10(7) heat-killed E coli, which leads to normal delivery at term); group C, labor without infection (ovariectomy, which causes delivery within an average of 27 hours); and group D, no infection and no labor (intrauterine injection of vehicle). Total pooled myometrial RNA was prepared 3.5 hours after surgery for groups A, B, and D and 5 hours after surgery for group C. The relative expression of 4963 genes was assayed in these pools by using DNA microarrays. Transcripts specifically involved in infection-induced labor were identified by subtracting from the list of differentially regulated genes in group A those with common expression in groups B and C. RESULTS: In group A 68 differentially expressed transcripts (>or=2-fold upregulation or downregulation) were identified. Among these are 39 characterized genes. Fourteen (45%) are involved in inflammatory responses, 7 (18%) are involved in growth-differentiation-oncogenesis, and 3 (8%) are involved in apoptosis. Subtraction identified 13 gene products most likely to be important for bacterially induced labor, as opposed to labor without infection or bacterial exposure without labor. CONCLUSION: This study demonstrates the potential of the subtractive DNA microarray technique to identify transcripts important specifically for bacterially induced preterm labor.


Subject(s)
Gene Expression , Obstetric Labor, Premature/genetics , Animals , Apoptosis/physiology , Bacterial Infections/complications , Female , Inflammation/complications , Mice , Mice, Inbred Strains , Neoplasms/complications , Obstetric Labor, Premature/etiology , Oligonucleotide Array Sequence Analysis , Pregnancy , Pregnancy Complications/physiopathology , Pregnancy Complications, Infectious/physiopathology , Transcription, Genetic
6.
Avian Dis ; 43(2): 315-9, 1999.
Article in English | MEDLINE | ID: mdl-10396646

ABSTRACT

The sightings and migration patterns of 65 bean (Anser fabalis) and 65 white-fronted geese (Anser albifrons) are reported. In the past, these geese were serologically screened for the occurrence of Newcastle disease virus (NDV) and other avian viral diseases by Hlinak et al. (3). Of the 130 birds originally tagged and serologically screened in 1991, 53 birds were resighted between 1991 and 1996. Most of the sightings were reported from main wintering and resting sites in Germany and The Netherlands. It is noteworthy that 19 of the 53 birds sighted had serologic evidence that they had been exposed to NDV before the time of marking in 1991. Although the origin of these infections in bean geese and white-fronted geese is still unknown, the sightings reported in this study indicate that, once infected, wild geese may be involved in the dissemination and spread of avian viral diseases, specifically Newcastle disease. The migration patterns of the wild geese provided further evidence that the main resting and wintering areas of migratory waterfowl are likely to be important for the inter- and intraspecies transmission of avian diseases, thereby representing risk areas for the poultry industry.


Subject(s)
Bird Diseases/epidemiology , Disease Outbreaks/veterinary , Newcastle Disease/epidemiology , Poultry Diseases/epidemiology , Animals , Bird Diseases/transmission , Disease Transmission, Infectious , Geese , Germany/epidemiology , Netherlands/epidemiology , Newcastle Disease/transmission , Poultry Diseases/transmission
7.
J Wildl Dis ; 34(3): 479-86, 1998 Jul.
Article in English | MEDLINE | ID: mdl-9706557

ABSTRACT

Sera from wild geese were tested for antibodies to selected viral pathogens at a resting site for wild waterfowl in Germany. Serum samples from both bean geese (Anser fabalis) and white-fronted geese (Anser albifrons) collected in October 1991 were examined using serological methods licensed for routine diagnosis in domestic poultry. Of 130 sera tested, antibodies to several infectious agents were found including Newcastle disease virus (45%), goose parvovirus (48%), avian reovirus (29%), and avian adenovirus or egg drop syndrome 76 virus (6%). Antibodies against duck hepatitis virus were not detected. Differences in seroprevalences were not detected between the two geese species. While role and significance of wild geese in the epidemiology of avian diseases remains to be determined, it is possible that they could be of some importance as reservoirs and carriers of certain viral diseases of domestic poultry.


Subject(s)
Animals, Wild , Antibodies, Viral/blood , Bird Diseases/epidemiology , Geese , Virus Diseases/veterinary , Animals , Aviadenovirus/immunology , Disease Reservoirs , Enzyme-Linked Immunosorbent Assay/veterinary , Germany/epidemiology , Hemagglutination Inhibition Tests/veterinary , Hepatitis Virus, Duck/immunology , Neutralization Tests/veterinary , Newcastle disease virus/immunology , Parvovirus/immunology , Prevalence , Reoviridae/immunology , Virus Diseases/epidemiology
8.
Nature ; 387(6628): 49-55, 1997 May 01.
Article in English | MEDLINE | ID: mdl-9139821

ABSTRACT

Normal mammalian growth and development are highly dependent on the regulation of the expression and activity of the Myc family of transcription factors. Mxi1-mediated inhibition of Myc activities requires interaction with mammalian Sin3A or Sin3B proteins, which have been purported to act as scaffolds for additional co-repressor factors. The identification of two such Sin3-associated factors, the nuclear receptor co-repressor (N-CoR) and histone deacetylase (HD1), provides a basis for Mxi1/Sin3-induced transcriptional repression and tumour suppression.


Subject(s)
Gene Expression Regulation , Histone Deacetylases/physiology , Nuclear Proteins/physiology , Repressor Proteins/physiology , Saccharomyces cerevisiae Proteins , Transcription Factors/physiology , 3T3 Cells , Animals , Basic Helix-Loop-Helix Transcription Factors , DNA-Binding Proteins/physiology , Fungal Proteins/physiology , Genes, myc , Humans , Mice , Nuclear Receptor Co-Repressor 1 , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Saccharomyces cerevisiae/genetics , Transcription, Genetic , Tumor Suppressor Proteins
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