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Dive into the research topics where Maria Jenckel is active.

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Featured researches published by Maria Jenckel.


Emerging Infectious Diseases | 2015

Comparison of Porcine Epidemic Diarrhea Viruses from Germany and the United States, 2014

Dennis Hanke; Maria Jenckel; Anja Petrov; Mathias Ritzmann; Julia Stadler; Valerij Akimkin; Sandra Blome; Anne Pohlmann; Horst Schirrmeier; Martin Beer; Dirk Höper

Since 2013, highly virulent porcine epidemic diarrhea virus has caused considerable economic losses in the United States. To determine the relation of US strains to those recently causing disease in Germany, we compared genomes and found that the strain from Germany is closely related to variants in the United States.


The New England Journal of Medicine | 2015

A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis

Bernd Hoffmann; Dennis Tappe; Dirk Höper; Christiane Herden; Annemarie Boldt; Christian Mawrin; Olaf Niederstraßer; Tobias Müller; Maria Jenckel; Elisabeth van der Grinten; Christian Lutter; Björn Abendroth; Jens Peter Teifke; Daniel Cadar; Jonas Schmidt-Chanasit; Rainer G. Ulrich; Martin Beer

Between 2011 and 2013, three breeders of variegated squirrels (Sciurus variegatoides) had encephalitis with similar clinical signs and died 2 to 4 months after onset of the clinical symptoms. With the use of a metagenomic approach that incorporated next-generation sequencing and real-time reverse-transcriptase quantitative polymerase chain reaction (RT-qPCR), the presence of a previously unknown bornavirus was detected in a contact squirrel and in brain samples from the three patients. Phylogenetic analyses showed that this virus, tentatively named variegated squirrel 1 bornavirus (VSBV-1), forms a lineage separate from that of the known bornavirus species. (Funded by the Federal Ministry of Food and Agriculture [Germany] and others.).


Emerging Infectious Diseases | 2014

Novel Bluetongue Virus in Goats, Corsica, France, 2014

Stéphan Zientara; Corinne Sailleau; Cyril Viarouge; Dirck Höper; Martin Beer; Maria Jenckel; Bernd Hoffmann; Aurore Romey; Labib Bakkali-Kassimi; Aurore Fablet; Damien Vitour; Emmanuel Bréard

During 2000–2013, 4 genotypes of bluetongue virus (BTV) were detected in Corsica, France. At the end of 2013, a compulsory BTV-1 vaccination campaign was initiated among domestic ruminants; biological samples from goats were tested as part of a corresponding monitoring program. A BTV strain with nucleotide sequences suggestive of a novel serotype was detected.


Genome Announcements | 2015

Complete Coding Genome Sequence of Putative Novel Bluetongue Virus Serotype 27

Maria Jenckel; Emmanuel Bréard; Claudia Schulz; Corinne Sailleau; Cyril Viarouge; Bernd Hoffmann; Dirk Höper; Martin Beer; Stéphan Zientara

ABSTRACT We announce the complete coding genome sequence of a novel bluetongue virus (BTV) serotype (BTV-n = putative BTV-27) detected in goats in Corsica, France, in 2014. Sequence analysis confirmed the closest relationship between sequences of the novel BTV serotype and BTV-25 and BTV-26, recently discovered in Switzerland and Kuwait, respectively.


Journal of Virology | 2014

Mixed Triple: Allied Viruses in Unique Recent Isolates of Highly Virulent Type 2 Bovine Viral Diarrhea Virus Detected by Deep Sequencing

Maria Jenckel; Dirk Höper; Horst Schirrmeier; Ilona Reimann; Katja V. Goller; Bernd Hoffmann; Martin Beer

ABSTRACT In February 2013, very severe acute clinical symptoms were observed in calves, heifers, and dairy cattle in several farms in North Rhine Westphalia and Lower Saxony, Germany. Deep sequencing revealed the coexistence of three distinct genome variants within recent highly virulent bovine viral diarrhea virus type 2 (BVDV-2) isolates. While the major portion (ca. 95%) of the population harbored a duplication of a 222-nucleotide (nt) segment within the p7-NS2-encoding region, the minority reflected the standard structure of a BVDV-2 genome. Additionally, unusual mutations were found in both variants, within the highly conserved p7 protein and close to the p7-NS2 cleavage site. Using a reverse genetic system with a BVDV-2a strain harboring a similar duplication, it could be demonstrated that during replication, genomes without duplication are generated de novo from genomes with duplication. The major variant with duplication is compulsorily escorted by the minor variant without duplication. RNA secondary structure prediction allowed the analysis of the unique but stable mixture of three BVDV variants and also provided the explanation for their generation. Finally, our results suggest that the variant with duplication plays the major role in the highly virulent phenotype. IMPORTANCE This study emphasizes the importance of full-genome deep sequencing in combination with manual in-depth data analysis for the investigation of viruses in basic research and diagnostics. Here we investigated recent highly virulent bovine viral diarrhea virus isolates from a 2013 series of outbreaks. We discovered a unique special feature of the viral genome, an unstable duplication of 222 nucleotides which is eventually deleted by viral polymerase activity, leading to an unexpectedly mixed population of viral genomes for all investigated isolates. Our study is of high importance to the field because we demonstrate that these insertion/deletion events allow another level of genome plasticity of plus-strand RNA viruses, in addition to the well-known polymerase-induced single nucleotide variations which are generally considered the main basis for viral adaptation and evolution.


Journal of Virology | 2015

Out of the Reservoir: Phenotypic and Genotypic Characterization of a Novel Cowpox Virus Isolated from a Common Vole

Donata Hoffmann; Annika Franke; Maria Jenckel; Aistė Tamošiūnaitė; Julia Schluckebier; Harald Granzow; Bernd Hoffmann; Stefan Fischer; Rainer G. Ulrich; Dirk Höper; Katja V. Goller; Nikolaus Osterrieder; Martin Beer

ABSTRACT The incidence of human cowpox virus (CPXV) infections has increased significantly in recent years. Serological surveys have suggested wild rodents as the main CPXV reservoir. We characterized a CPXV isolated during a large-scale screening from a feral common vole. A comparison of the full-length DNA sequence of this CPXV strain with a highly virulent pet rat CPXV isolate showed a sequence identity of 96%, including a large additional open reading frame (ORF) of about 6,000 nucleotides which is absent in the reference CPXV strain Brighton Red. Electron microscopy analysis demonstrated that the vole isolate, in contrast to the rat strain, forms A-type inclusion (ATI) bodies with incorporated virions, consistent with the presence of complete ati and p4c genes. Experimental infections showed that the vole CPXV strain caused only mild clinical symptoms in its natural host, while all rats developed severe respiratory symptoms followed by a systemic rash. In contrast, common voles infected with a high dose of the rat CPXV showed severe signs of respiratory disease but no skin lesions, whereas infection with a low dose led to virus excretion with only mild clinical signs. We concluded that the common vole is susceptible to infection with different CPXV strains. The spectrum ranges from well-adapted viruses causing limited clinical symptoms to highly virulent strains causing severe respiratory symptoms. In addition, the low pathogenicity of the vole isolate in its eponymous host suggests a role of common voles as a major CPXV reservoir, and future research will focus on the correlation between viral genotype and phenotype/pathotype in accidental and reservoir species. IMPORTANCE We report on the first detection and isolation of CPXV from a putative reservoir host, which enables comparative analyses to understand the infection cycle of these zoonotic orthopox viruses and the relevant genes involved. In vitro studies, including whole-genome sequencing as well as in vivo experiments using the Wistar rat model and the vole reservoir host allowed us to establish links between genomic sequences and the in vivo properties (virulence) of the novel vole isolate in comparison to those of a recent zoonotic CPXV isolated from pet rats in 2009. Furthermore, the role of genes present only in a reservoir isolate can now be further analyzed. These studies therefore allow unique insights and conclusions about the role of the rodent reservoir in CPXV epidemiology and transmission and about the zoonotic threat that these viruses represent.


Viruses | 2017

Classification of Cowpox Viruses into Several Distinct Clades and Identification of a Novel Lineage

Annika Franke; Florian Pfaff; Maria Jenckel; Bernd Hoffmann; Dirk Höper; Markus Antwerpen; Hermann Meyer; Martin Beer; Donata Hoffmann

Cowpox virus (CPXV) was considered as uniform species within the genus Orthopoxvirus (OPV). Previous phylogenetic analysis indicated that CPXV is polyphyletic and isolates may cluster into different clades with two of these clades showing genetic similarities to either variola (VARV) or vaccinia viruses (VACV). Further analyses were initiated to assess both the genetic diversity and the evolutionary background of circulating CPXVs. Here we report the full-length sequences of 20 CPXV strains isolated from different animal species and humans in Germany. A phylogenetic analysis of altogether 83 full-length OPV genomes confirmed the polyphyletic character of the species CPXV and suggested at least four different clades. The German isolates from this study mainly clustered into two CPXV-like clades, and VARV- and VACV-like strains were not observed. A single strain, isolated from a cotton-top tamarin, clustered distantly from all other CPXVs and might represent a novel and unique evolutionary lineage. The classification of CPXV strains into clades roughly followed their geographic origin, with the highest clade diversity so far observed for Germany. Furthermore, we found evidence for recombination between OPV clades without significant disruption of the observed clustering. In conclusion, this analysis markedly expands the number of available CPXV full-length sequences and confirms the co-circulation of several CPXV clades in Germany, and provides the first data about a new evolutionary CPXV lineage.


Emerging Infectious Diseases | 2017

Variegated Squirrel Bornavirus 1 in Squirrels, Germany and the Netherlands

Kore Schlottau; Maria Jenckel; Judith M. A. van den Brand; Christine Fast; Christiane Herden; Dirk Höper; Timo Homeier-Bachmann; Jens Thielebein; Niels Mensing; Bert Diender; Donata Hoffmann; Rainer G. Ulrich; Thomas C. Mettenleiter; Marion Koopmans; Dennis Tappe; Jonas Schmidt-Chanasit; Chantal Reusken; Martin Beer; Bernd Hoffmann

We screened squirrels in Germany and the Netherlands for the novel zoonotic variegated squirrel bornavirus 1 (VSBV-1). The detection of VSBV-1 in 11 squirrels indicates a considerable risk for transmission to humans handling those animals. Therefore, squirrels in contact with humans should routinely be tested for VSBV-1.


Archives of Virology | 2017

Quasispecies composition and diversity do not reveal any predictors for chronic classical swine fever virus infection

Maria Jenckel; Sandra Blome; Martin Beer; Dirk Höper

Classical swine fever (CSF) can run acute, chronic, and prenatal courses in both domestic pigs and wild boar. Although chronic infections are rare events, their epidemiological impact is very high due to the long-term shedding of virus. So far, little is known about the factors that influence disease course and outcome from either the host or virus’s perspective. To elucidate the viral determinants, we analyzed the role of the viral populations for the development of chronic CSF virus (CSFV) infections. Three different animal trials that had led to both chronic and acute infections were chosen for a detailed analysis by deep sequencing. The three inocula represented sub-genogroups 2.1 and 2.3, and two viruses were wild-type CSFV, one derived from an infectious cDNA clone. These viruses and samples derived from acutely and chronically infected animals were subjected to next-generation sequencing. Subsequently, the derived full-length genomes were compared at both the consensus and the quasispecies level. At consensus level, no differences were observed between the parental viruses and the viruses obtained from chronically infected animals. Despite a considerable level of variability at the quasispecies level, no indications were found for any predictive pattern with regard to the chronicity of the CSFV infections. While there might be no direct marker for chronicity, moderate virulence of some CSFV strains in itself seems to be a crucial prerequisite for the establishment of long-term infections which does not need further genetic adaption. Thus, general host and virus factors need further investigation.


Genome Announcements | 2015

Complete Genome Sequence of Avian Paramyxovirus Strain APMV-6/red-crested pochard/Balkhash/5842/2013 from Kazakhstan

Kobey Karamendin; Aidyn Kydyrmanov; Aigerim Seidalina; Maria Jenckel; Elke Starick; Christian Grund; Saule Asanova; Elizaveta Khan; Klara Daulbayeva; Yermukhammet Kasymbekov; Kainar Zhumatov; Marat Sayatov; Martin Beer; Sasan R. Fereidouni

ABSTRACT An avian paramyxovirus 6 strain was isolated during a wild bird monitoring study in Kazakhstan in 2013. The virus was isolated from a wild duck red-crested pochard (Netta rufina) in southeastern Kazakhstan. Here, we present the complete genome sequence of the virus.

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Bernd Hoffmann

Friedrich Loeffler Institute

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Dirk Höper

Friedrich Loeffler Institute

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Martin Beer

Ludwig Maximilian University of Munich

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Donata Hoffmann

Friedrich Loeffler Institute

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Sandra Blome

Friedrich Loeffler Institute

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Rainer Ulrich

Humboldt State University

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Christine Fast

Friedrich Loeffler Institute

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Dennis Tappe

Bernhard Nocht Institute for Tropical Medicine

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