Czerny, Claus-Peter

[["dc.bibliographiccitation.journal","Frontiers in Veterinary Science"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Roller, Marco"],["dc.contributor.author","Hansen, Sören"],["dc.contributor.author","Knauf-Witzens, Tobias"],["dc.contributor.author","Oelemann, Walter M. R."],["dc.contributor.author","Czerny, Claus-Peter"],["dc.contributor.author","Abd El Wahed, Ahmed"],["dc.contributor.author","Goethe, Ralph"],["dc.date.accessioned","2021-04-14T08:30:11Z"],["dc.date.available","2021-04-14T08:30:11Z"],["dc.date.issued","2020"],["dc.description.abstract","Mycobacterium avium subspecies paratuberculosis (MAP) is the causative agent of paratuberculosis (ParaTB or Johne's disease), a contagious, chronic and typically fatal enteric disease of domestic and non-domestic ruminants. Clinically affected animals present wasting and emaciation. However, MAP can also infect non-ruminant animal species with less specific signs. Zoological gardens harbor various populations of diverse animal species, which are managed on limited space at higher than natural densities. Hence, they are predisposed to endemic trans-species pathogen distribution. Information about the incidence and prevalence of MAP infections in zoological gardens and the resulting potential threat to exotic and endangered species are rare. Due to unclear pathogenesis, chronicity of disease as well as the unknown cross-species accuracy of diagnostic tests, diagnosis and surveillance of MAP and ParaTB is challenging. Differentiation between uninfected shedders of ingested bacteria; subclinically infected individuals; and preclinically diseased animals, which may subsequently develop clinical signs after long incubation periods, is crucial for the interpretation of positive test results in animals and the resulting consequences in their management. This review summarizes published data from the current literature on occurrence of MAP infection and disease in susceptible and affected zoo animal species as well as the applied diagnostic methods and measures. Clinical signs indicative for ParaTB, pathological findings and reports on detection, transmission and epidemiology in zoo animals are included. Furthermore, case reports were re-evaluated for incorporation into accepted consistent terminologies and case definitions."],["dc.identifier.doi","10.3389/fvets.2020.572724"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83135"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.publisher","Frontiers Media S.A."],["dc.relation.eissn","2297-1769"],["dc.rights","http://creativecommons.org/licenses/by/4.0/"],["dc.title","Mycobacterium avium Subspecies paratuberculosis Infection in Zoo Animals: A Review of Susceptibility and Disease Process"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1653"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Journal of Dairy Science"],["dc.bibliographiccitation.lastpage","1660"],["dc.bibliographiccitation.volume","96"],["dc.contributor.author","Pilla, Rachel"],["dc.contributor.author","Malvisi, M."],["dc.contributor.author","Snel, G. G. M."],["dc.contributor.author","Schwarz, Daniel"],["dc.contributor.author","Koenig, S."],["dc.contributor.author","Czerny, C-P"],["dc.contributor.author","Piccinini, Renata"],["dc.date.accessioned","2018-11-07T09:27:48Z"],["dc.date.available","2018-11-07T09:27:48Z"],["dc.date.issued","2013"],["dc.description.abstract","Changes in relative cell proportions occurring in diseased mammary glands of dairy cows can be determined using differential cell count (DCC). The present study was carried out in 2 consecutive trials, with 2 goals: (a) to test the consistency of DCC results on subsequent days, and (b) to establish an effective cutoff value for the diagnosis of mastitis. In the first trial, quarter milk and blood samples were taken from 8 healthy cows for 5 consecutive days. Milk samples were tested by somatic cell count (SCC) and bacteriological analysis, and DCC was performed on blood and milk samples by flow cytometer. In the second trial, 16 animals were randomly selected from a different herd and quarter milk samples taken on 3 consecutive milkings. All samples were cyto-bacteriologically analyzed and DCC was performed on the second sampling. In the first trial, mean SCC was 77,770 cells/mL and 4 samples were bacteriologically positive. No fixed or random effect had a significant influence on percentages of individual cell populations or ratios in blood or milk. A cutoff value of 0.495 for logarithmic polymorphonuclear neutrophilic leukocyte:lymphocyte ratio was established. Mean SCC of milk samples collected in the second trial was 543,230 cells/mL, and infection was detected in 53.1% of quarters, mostly caused by Staphylococcus aureus. When the cutoff value was applied to the data along with SCC, sensitivity and specificity of the diagnostic method were 97.3 and 92.3%, respectively."],["dc.identifier.doi","10.3168/jds.2012-6298"],["dc.identifier.isi","000315061700031"],["dc.identifier.pmid","23332851"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/30621"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Inc"],["dc.relation.issn","0022-0302"],["dc.title","Differential cell count as an alternative method to diagnose dairy cow mastitis"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","5033"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Journal of Dairy Science"],["dc.bibliographiccitation.lastpage","5044"],["dc.bibliographiccitation.volume","94"],["dc.contributor.author","Schwarz, Daniel"],["dc.contributor.author","Diesterbeck, Ulrike S"],["dc.contributor.author","Koenig, S."],["dc.contributor.author","Bruegemann, Kerstin"],["dc.contributor.author","Schlez, Karen"],["dc.contributor.author","Zschoeck, Michael"],["dc.contributor.author","Wolter, Wilfried"],["dc.contributor.author","Czerny, C-P"],["dc.date.accessioned","2018-11-07T08:51:19Z"],["dc.date.available","2018-11-07T08:51:19Z"],["dc.date.issued","2011"],["dc.description.abstract","Somatic cell counts (SCC) are generally used as an indicator of udder health. In Germany; a cutoff value of 100,000 cells/mL is currently used to differentiate between healthy and diseased mammary glands. In addition to SCC, differential cell counts (DCC) can be applied for a more detailed evaluation of the udder health status. The aim of this study was to differentiate immune cells in milk of udder quarters classified as healthy based on SCC values of <100,000 cells/mL. Twenty cows were selected and 65 healthy udder quarters were compared with a control group of 15 diseased udder quarters (SCC > 100,000 cells/mL). Cells were isolated from milk of all quarters to measure simultaneously percentages of lymphocytes, macrophages, and polymorphonuclear neutrophilic leukocytes (PMNL) by flow cytometric analysis. The bacteriological status of all 80 quarters was also determined. Differential cell count patterns of milk samples (n = 15) with extreme low SCC values of <= 6,250 cells/mL revealed high lymphocyte proportions of up to 88%. Milk cell populations in samples (n = 42) with SCC values from >6,250 to <= 25,000 cells/mL were also dominated by lymphocytes, whereas DCC patterns of 6 out of 41 milk samples with SCC values from >= 9,000 to <= 46,000 cells/mL indicated already inflammatory reactions based on the predominance of PMNL (56-75%). In 13 of 15 milk samples of the diseased udder quarters (SCC >100,000 cells/mL), PMNL were categorically found as dominant cell population with proportions of >= 49%. Macrophages were the second predominant cell population in almost all samples tested in relation to lymphocytes and PMNL. Farther analysis of the data demonstrated significant differences of the cellular components between udder quarters infected by major pathogens (e.g., Staphylococcus aureus; n = 5) and culture-negative udder quarters (n = 56). Even the percentages of immune cells in milk from quarters infected by minor pathogens (e.g., coagulase-negative staphylococci; n = 19) differed significantly from those in milk of culture-negative quarters. Our flow cytometric analysis of immune cells in milk of udder quarters classified as healthy by SCC <100,000 cells/mL revealed inflammatory reactions based on DCC."],["dc.identifier.doi","10.3168/jds.2011-4348"],["dc.identifier.isi","000295192600028"],["dc.identifier.pmid","21943754"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/21906"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Inc"],["dc.relation.issn","0022-0302"],["dc.title","Flow cytometric differential cell counts in milk for the evaluation of inflammatory reactions in clinically healthy and subclinically infected bovine mammary glands"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","448"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Journal of Dairy Research"],["dc.bibliographiccitation.lastpage","455"],["dc.bibliographiccitation.volume","78"],["dc.contributor.author","Schwarz, Daniel"],["dc.contributor.author","Diesterbeck, Ulrike S."],["dc.contributor.author","Koenig, Sven"],["dc.contributor.author","Bruegemann, Kerstin"],["dc.contributor.author","Schlez, Karen"],["dc.contributor.author","Zschoeck, Michael"],["dc.contributor.author","Wolter, Wilfried"],["dc.contributor.author","Czerny, Claus-Peter"],["dc.date.accessioned","2018-11-07T08:50:13Z"],["dc.date.available","2018-11-07T08:50:13Z"],["dc.date.issued","2011"],["dc.description.abstract","Somatic cell count (SCC) is generally regarded as an indicator of udder health. A cut-off value of 100 x 10(3) cells/ml is currently used in Germany to differentiate between normal and abnormal secretion of quarters. In addition to SCC, differential cell counts (DCC) can be applied for a more detailed analysis of the udder health status. The aim of this study was to differentiate somatic cells in foremilk samples of udder quarters classified as normal secreting by SCC < 100 x 10(3) cells/ml. Twenty cows were selected and 72 normal secreting udder quarters were compared with a control group of six diseased quarters (SCC > 100 x 10(3) cells/ml). In two severely diseased quarters of the control group (SCC of 967 x 10(3) cells/ml and 1824 x 10(3) cells/ml) Escherichia coli and Staphylococcus aureus were detected. DCC patterns of milk samples (n = 25) with very low SCC values of <= 6.25 x 10(3) cells/ml revealed high lymphocyte proportions of up to 92%. Milk cell populations in samples (n = 41) with SCC values of (> 6.25 to <= 25) x 10(3) cells/ml were also dominated by lymphocytes (mean value 47%), whereas DCC patterns of milk from udder quarters (n = 6) with SCC values (> 25 to 4100) x 10(3) cells/ml changed. While in samples (n = 3) with SCC values of (27-33) x 10(3) cells/ml macrophages were predominant (35-40%), three milk samples with (43-45) x 10(3) cells/ml indicated already inflammatory reactions based on the predominance of polymorphonuclear leucocytes (PMN) (54-63%). In milk samples of diseased quarters PMN were categorically found as dominant cell population with proportions of >= 65%. Macrophages were the second predominant cell population in almost all samples tested in relationship to lymphocytes and PMN. To our knowledge, this is the first study evaluating cell populations in low SCC milk in detail. Udder quarters classified as normal secreting by SCC < 100 x 10(3) cells/ml revealed already inflammatory processes based on DCC."],["dc.identifier.doi","10.1017/S0022029911000574"],["dc.identifier.isi","000297106100010"],["dc.identifier.pmid","21843398"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/8759"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/21647"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Cambridge Univ Press"],["dc.relation.issn","0022-0299"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Microscopic differential cell counts in milk for the evaluation of inflammatory reactions in clinically healthy and subclinically infected bovine mammary glands"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","212"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Veterinary Pathology"],["dc.bibliographiccitation.lastpage","218"],["dc.bibliographiccitation.volume","43"],["dc.contributor.author","Mätz-Rensing, K."],["dc.contributor.author","Ellerbrok, H."],["dc.contributor.author","Ehlers, B."],["dc.contributor.author","Pauli, G."],["dc.contributor.author","Floto, A."],["dc.contributor.author","Alex, M."],["dc.contributor.author","Czerny, C.-P."],["dc.contributor.author","Kaup, F.-J."],["dc.date.accessioned","2022-10-06T13:26:19Z"],["dc.date.available","2022-10-06T13:26:19Z"],["dc.date.issued","2016"],["dc.description.abstract","An epizootic infection was observed in a colony of 80 New World monkeys consisting of various species including a group of marmosets and Saguinus species. During the summer and autumn of 2002, 30 animals died of unknown diseases. Six animals were sent to the German Primate Center for investigation of the cause of death. A complete pathologic and histologic investigation was carried out. The animals exhibited erosive-ulcerative lesions of the oral mucous membranes. Advanced stages of the disease were characterised by hemorrhagic lesions on the skin distributed randomly over the body, but principally on the face, scrotal region, soles, and palms. Electron microscopy revealed virus particles with orthopox-like morphology within intracytoplasmic inclusions in epithelial cells. The DNA samples from various tissues were analyzed by use of a set of orthopox virus-specific, real-time polymerase chain reaction assays. Amplification products were sequenced to define the virus more precisely. Sequencing confirmed the presence of an orthopox virus. Sequence data indicated that all six animals were infected with the same virus. Propagation of the virus on Vero cells resulted in a rapidly progressive cytopathogenic effect. Preliminary phylogenetic analyses of two genes revealed closest homology to cowpox viruses. The origin of this poxvirus outbreak remains unexplained, and the strain and genus of the virus need to be determined in detail."],["dc.identifier.doi","10.1354/vp.43-2-212"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/115058"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-602"],["dc.relation.eissn","1544-2217"],["dc.relation.issn","0300-9858"],["dc.relation.orgunit","Deutsches Primatenzentrum"],["dc.title","Fatal Poxvirus Outbreak in a Colony of New World Monkeys"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","211"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","Journal of Medical Primatology"],["dc.bibliographiccitation.lastpage","217"],["dc.bibliographiccitation.volume","46"],["dc.contributor.author","Fechner, Kim"],["dc.contributor.author","Mätz-Rensing, Kerstin"],["dc.contributor.author","Lampe, Karen"],["dc.contributor.author","Kaup, Franz-Josef"],["dc.contributor.author","Czerny, Claus-Peter"],["dc.contributor.author","Schäfer, Jenny"],["dc.date.accessioned","2020-12-10T18:29:00Z"],["dc.date.available","2020-12-10T18:29:00Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1111/jmp.12270"],["dc.identifier.issn","0047-2565"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76490"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.relation.issn","0047-2565"],["dc.title","Detection of Mycobacterium avium subsp. paratuberculosis in non-human primates"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","162"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","DEUTSCHE TIERARZTLICHE WOCHENSCHRIFT"],["dc.bibliographiccitation.lastpage","166"],["dc.bibliographiccitation.volume","115"],["dc.contributor.author","Moorkamp, L."],["dc.contributor.author","Beineke, Andreas"],["dc.contributor.author","Kaim, U."],["dc.contributor.author","Diesterbeck, Ulrike S"],["dc.contributor.author","Urstadt, S."],["dc.contributor.author","Czerny, C.-P"],["dc.contributor.author","Rueberg, H."],["dc.contributor.author","Grosse, Beilage E."],["dc.date.accessioned","2018-11-07T11:16:25Z"],["dc.date.available","2018-11-07T11:16:25Z"],["dc.date.issued","2008"],["dc.description.abstract","Swinepox virus infection results in an acute, mild or subclinical course and is characterised by typical poxvirus skin lesions in affected pigs. Additionally, sporadic vertical swinepox virus transmission leads to congenital generalised infection and subsequent abortion or stillbirth. The present report describes the occurrence of epidermal efflorescences in two piglets after intrauterine natural suipoxvirus infection. No clinical abnormalities of the gilt and littermates as well as in other pigs from this herd were present. One of the affected piglets was stillborn and submitted for necropsy, the other animal was alive at birth, but died 3 days later. Histologically, a proliferative to ulcerative dermatitis with epithelial ballooning degeneration and characteristic intracytoplasmatic inclusion bodies was observed. The pathomorphological and histopathological suspected diagnosis of a poxvirus infection was confirmed by electron microscopy. Furthermore, the agent was identified as suipoxvirus by polymerase chain reaction. As demonstrated here, obvious skin lesions in suipoxvirus infection leads to a suspected diagnosis in newborn piglets on macroscopic examination. However, further post mortem examinations, including electron microscopy as well as molecular techniques are essential for the identification of the aetiology and the exclusion of differential diagnoses. Because the disease only affected two pigs there was only a small economic loss. A valid diagnostic plays an important role in advising farmers and for herd health monitoring."],["dc.identifier.doi","10.2377/0341-6593-115-162"],["dc.identifier.isi","000255153100006"],["dc.identifier.pmid","18500151"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/54586"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","M H Schaper Gmbh Co Kg"],["dc.relation.issn","0341-6593"],["dc.title","Swinepox - skin disease with sporadic occurrence"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","493"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Viruses"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Ahsendorf, Henrike"],["dc.contributor.author","Gan, Li"],["dc.contributor.author","Eltom, Kamal"],["dc.contributor.author","Abd El Wahed, Ahmed"],["dc.contributor.author","Hotop, Sven-Kevin"],["dc.contributor.author","Roper, Rachel"],["dc.contributor.author","Beutling, Ulrike"],["dc.contributor.author","Broenstrup, Mark"],["dc.contributor.author","Stahl-Hennig, Christiane"],["dc.contributor.author","Hoelzle, Ludwig"],["dc.contributor.author","Czerny, Claus-Peter"],["dc.date.accessioned","2019-07-09T11:51:50Z"],["dc.date.available","2019-07-09T11:51:50Z"],["dc.date.issued","2019"],["dc.description.abstract","The vaccinia virus (VACV) A27 protein and its homologs, which are found in a large number of members of the genus Orthopoxvirus (OPXV), are targets of viral neutralization by host antibodies. We have mapped six binding sites (epitopes #1A: aa 32-39, #1B: aa 28-33, #1C: aa 26-31, #1D: 28-34, #4: aa 9-14, and #5: aa 68-71) of A27 specific monoclonal antibodies (mAbs) using peptide arrays. MAbs recognizing epitopes #1A-D and #4 neutralized VACV Elstree in a complement dependent way (50% plaque-reduction: 12.5-200 µg/mL). Fusion of VACV at low pH was blocked through inhibition of epitope #1A. To determine the sequence variability of the six antigenic sites, 391 sequences of A27 protein homologs available were compared. Epitopes #4 and #5 were conserved among most of the OPXVs, while the sequential epitope complex #1A-D was more variable and, therefore, responsible for species-specific epitope characteristics. The accurate and reliable mapping of defined epitopes on immuno-protective proteins such as the A27 of VACV enables phylogenetic studies and insights into OPXV evolution as well as to pave the way to the development of safer vaccines and chemical or biological antivirals."],["dc.identifier.doi","10.3390/v11060493"],["dc.identifier.pmid","31146446"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16205"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/60022"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.subject.ddc","630"],["dc.title","Species-Specific Conservation of Linear Antigenic Sites on Vaccinia Virus A27 Protein Homologs of Orthopoxviruses"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","31"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Zoonoses and Public Health"],["dc.bibliographiccitation.lastpage","37"],["dc.bibliographiccitation.volume","54"],["dc.contributor.author","Schulze, Catharina"],["dc.contributor.author","Alex, M."],["dc.contributor.author","Schirrmeier, H."],["dc.contributor.author","Hlinak, A."],["dc.contributor.author","Engelhardt, Antje"],["dc.contributor.author","Koschinski, B."],["dc.contributor.author","Beyreiss, B."],["dc.contributor.author","Hoffmann, M."],["dc.contributor.author","Czerny, C.-P."],["dc.date.accessioned","2018-11-07T11:07:49Z"],["dc.date.available","2018-11-07T11:07:49Z"],["dc.date.issued","2007"],["dc.description.abstract","A 4-month-old female domestic shorthair cat was infected by a virus of the Poxvirus family. The animal developed a severe pneumonia and generalized ulcerating lesions of the skin. Histologically, typical eosinophilic intracytoplasmic inclusion bodies indicative of an Orthopoxvirus (OPV) infection were present. The lung showed grey-white to haemorrhagic nodular lesions with a central zone of complete necrosis of alveolar and bronchial tissue. Electron microscopy from skin and lung nodules revealed typical square-shaped OPV particles. Cultivation of the virus on chorio-allantoic membranes of embryonated chicken eggs resulted in haemorrhagic plaques. Restriction enzyme analysis, PCR and sequencing of the D8L gene identified the OPV isolate as a typical Cowpox virus. It was transmitted by the cat to a human contact person who developed a local nodular dermatitis at the inoculation site in association with signs of general infection and had an increase of OPV-specific neutralizing antibodies in paired serum samples."],["dc.identifier.doi","10.1111/j.1863-2378.2007.00995.x"],["dc.identifier.isi","000245472400006"],["dc.identifier.pmid","17359444"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/52663"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Blackwell Publishing"],["dc.relation.issn","1863-1959"],["dc.title","Generalized fatal Cowpox virus infection in a cat with transmission to a human contact case"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1007"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Microorganisms"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Okuni, Julius Boniface"],["dc.contributor.author","Hansen, Sören"],["dc.contributor.author","Eltom, Kamal H."],["dc.contributor.author","Eltayeb, ElSagad"],["dc.contributor.author","Amanzada, Ahmad"],["dc.contributor.author","Omega, Joseph Amesa"],["dc.contributor.author","Czerny, Claus Peter"],["dc.contributor.author","Abd El Wahed, Ahmed"],["dc.contributor.author","Ojok, Lonzy"],["dc.date.accessioned","2021-04-14T08:25:03Z"],["dc.date.available","2021-04-14T08:25:03Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.3390/microorganisms8071007"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/81506"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","2076-2607"],["dc.title","Paratuberculosis: A Potential Zoonosis and a Neglected Disease in Africa"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]