Claudia Bachofen

Dr. Claudia Bachofen

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
4 March 2010 in Veterinary Research
Verified
Journal Article
Open access
PDF file
EPErnst Peterhans
Ernst Peterhans
CBClaudia Bachofen
Claudia Bachofen
HSHanspeter Stalder
Hanspeter Stalder
MSMatthias Schweizer
Matthias Schweizer
Bovine viral diarrhea virus (BVDV), a Flaviviridae pestivirus, is arguably one of the most widespread cattle pathogens worldwide. Each of its two genotypes has two biotypes, non-cytopathic (ncp) and cytopathic (cp). Only the ncp biotype of BVDV may establish persistent infection in the fetus when infecting a dam early in gestation, a time point which predates maturity of the adaptive immune system. Such fetuses may develop and be born healthy but remain infected for life. Due to this early initiation of fetal infection and to the expression of interferon antagonistic proteins, persistently infected (PI) animals remain immunotolerant to the infecting viral strain. Although only accounting for some 1% of all animals in regions where BVDV is endemic, PI animals ensure the viral persistence in the host population. These animals may, however, develop the fatal mucosal disease, which is characterized by widespread lesions in the gastrointestinal tract. Cp BVD virus, in addition to the persisting ncp biotype, can be isolated from such animals. The cp viruses are characterized by unrestrained genome replication, and their emergence from the persisting ncp ones is due to mutations that are unique in each virus analyzed. They include recombinations with host cell mRNA, gene translocations and duplications, and point mutations. Cytopathic BVD viruses fail to establish chains of infection and are unable to cause persistent infection. Hence, these viruses illustrate a case of “viral emergence to extinction” – irrelevant for BVDV evolution, but fatal for the PI host.

1 November 2005 in Preventive Veterinary Medicine
Verified
Journal Article
Closed access
HSH.P. Stalder
H.P. Stalder
PMPh. Meier
Ph. Meier
GPG. Pfaffen
G. Pfaffen
CCClaudio Wageck Canal
Claudio Wageck Canal
JRJ. Rüfenacht
J. Rüfenacht
EPE. Peterhans
E. Peterhans

1 May 2021 in Journal of Clinical Virology
Verified
Journal Article
Open access
JVJutte J. C. De Vries
Jutte J. C. De Vries
JBJulianne R. Brown
Julianne R. Brown
NCNatacha Couto
Natacha Couto
MBMartin Beer
Martin Beer
PMPhilippe Le Mercier
Philippe Le Mercier
FLF. Xavier Lopez-Labrador
F. Xavier Lopez-Labrador
Metagenomic next-generation sequencing (mNGS) is an untargeted technique for determination of microbial DNA/RNA sequences in a variety of sample types from patients with infectious syndromes. mNGS is still in its early stages of broader translation into clinical applications. To further support the development, implementation, optimization and standardization of mNGS procedures for virus diagnostics, the European Society for Clinical Virology (ESCV) Network on Next-Generation Sequencing (ENNGS) has been established. The aim of ENNGS is to bring together professionals involved in mNGS for viral diagnostics to share methodologies and experiences, and to develop application guidelines. Following the ENNGS publication Recommendations for the introduction of mNGS in clinical virology, part I: wet lab procedure in this journal, the current manuscript aims to provide practical recommendations for the bioinformatic analysis of mNGS data and reporting of results to clinicians.

1 August 2021 in Journal of Clinical Virology
Verified
Journal Article
Open access
JVJutte J. C. De Vries
Jutte J. C. De Vries
JBJulianne R. Brown
Julianne R. Brown
NFNicole Fischer
Nicole Fischer
ISIgor Sidorov
Igor Sidorov
SMSofia Morfopoulou
Sofia Morfopoulou
ECEric C.J. Claas
Eric C.J. Claas
Metagenomic sequencing is increasingly being used in clinical settings for difficult to diagnose cases. The performance of viral metagenomic protocols relies to a large extent on the bioinformatic analysis. In this study, the European Society for Clinical Virology (ESCV) Network on NGS (ENNGS) initiated a benchmark of metagenomic pipelines currently used in clinical virological laboratories. Metagenomic datasets from 13 clinical samples from patients with encephalitis or viral respiratory infections characterized by PCR were selected. The datasets were analyzed with 13 different pipelines currently used in virological diagnostic laboratories of participating ENNGS members. The pipelines and classification tools were: Centrifuge, DAMIAN, DIAMOND, DNASTAR, FEVIR, Genome Detective, Jovian, MetaMIC, MetaMix, One Codex, RIEMS, VirMet, and Taxonomer. Performance, characteristics, clinical use, and user-friendliness of these pipelines were analyzed. Overall, viral pathogens with high loads were detected by all the evaluated metagenomic pipelines. In contrast, lower abundance pathogens and mixed infections were only detected by 3/13 pipelines, namely DNASTAR, FEVIR, and MetaMix. Overall sensitivity ranged from 80% (10/13) to 100% (13/13 datasets). Overall positive predictive value ranged from 71-100%. The majority of the pipelines classified sequences based on nucleotide similarity (8/13), only a minority used amino acid similarity, and 6 of the 13 pipelines assembled sequences de novo. No clear differences in performance were detected that correlated with these classification approaches. Read counts of target viruses varied between the pipelines over a range of 2-3 log, indicating differences in limit of detection. A wide variety of viral metagenomic pipelines is currently used in the participating clinical diagnostic laboratories. Detection of low abundant viral pathogens and mixed infections remains a challenge, implicating the need for standardization and validation of metagenomic analysis for clinical diagnostic use. Future studies should address the selective effects due to the choice of different reference viral databases.

1 September 2008 in Veterinary Microbiology
Verified
Journal Article
Closed access
CBClaudia Bachofen
Claudia Bachofen
HSHanspeter Stalder
Hanspeter Stalder
UBUeli Braun
Ueli Braun
MHMonika Hilbe
Monika Hilbe
FEFelix Ehrensperger
Felix Ehrensperger
EPErnst Peterhans
Ernst Peterhans

1 January 2013 in Veterinary Research
Verified
Journal Article
Open access
PDF file
CBClaudia Bachofen
Claudia Bachofen
HVHans-Rudolf Vogt
Hans-Rudolf Vogt
HSHanspeter Stalder
Hanspeter Stalder
TMTanja Mathys
Tanja Mathys
RZReto Zanoni
Reto Zanoni
EPErnst Peterhans
Ernst Peterhans
Bovine viral diarrhoea virus (BVDV) is an economically important pathogen of cattle worldwide. Infection of a pregnant animal may lead to persistent infection of the foetus and birth of a persistently infected (PI) calf that sheds the virus throughout its life. However, BVD viruses are not strictly species specific. BVDV has been isolated from many domesticated and wild ruminants. This is of practical importance as virus reservoirs in non-bovine hosts may hamper BVDV control in cattle. A goat given as a social companion to a BVDV PI calf gave birth to a PI goat kid. In order to test if goat to goat infections were possible, seronegative pregnant goats were exposed to the PI goat. In parallel, seronegative pregnant goats were kept together with the PI calf. Only the goat to goat transmission resulted in the birth of a next generation of BVDV PI kids whereas all goats kept together with the PI calf aborted. To our knowledge, this is the first report which shows that a PI goat cannot only transmit BVD virus to other goats but that such transmission may indeed lead to the birth of a second generation of PI goats. Genetic analyses indicated that establishment in the new host species may be associated with step-wise adaptations in the viral genome. Thus, goats have the potential to be a reservoir for BVDV. However, the PI goats showed growth retardation and anaemia and their survival under natural conditions remains questionable.