Roman Biek

Prof. Roman Biek

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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1 February 2008 in Current Biology
Verified
Journal Article
Closed access
SKSophie Köndgen
Sophie Köndgen
HKHjalmar Kühl
Hjalmar Kühl
PNPaul K. N'Goran
Paul K. N'Goran
PWPeter D. Walsh
Peter D. Walsh
SSSvenja Schenk
Svenja Schenk
FLFabian H. Leendertz
Fabian H. Leendertz

28 May 2002 in Conservation Biology
Verified
Journal Article
Closed access
PDF file
RBRoman Biek
Roman Biek
CFChris Funk
Chris Funk
BMBryce A. Maxell
Bryce A. Maxell
LML. Scott Mills
L. Scott Mills

1 May 2014 in Trends in Ecology & Evolution
Verified
Journal Article
Open access
MVMafalda Viana
Mafalda Viana
RMRebecca Mancy
Rebecca Mancy
RBRoman Biek
Roman Biek
SCSarah Cleaveland
Sarah Cleaveland
PCPaul C. Cross
Paul C. Cross
DHDaniel T. Haydon
Daniel T. Haydon
Many pathogens persist in multihost systems, making the identification of infection reservoirs crucial for devising effective interventions. Here, we present a conceptual framework for classifying patterns of incidence and prevalence, and review recent scientific advances that allow us to study and manage reservoirs simultaneously. We argue that interventions can have a crucial role in enriching our mechanistic understanding of how reservoirs function and should be embedded as quasi-experimental studies in adaptive management frameworks. Single approaches to the study of reservoirs are unlikely to generate conclusive insights whereas the formal integration of data and methodologies, involving interventions, pathogen genetics, and contemporary surveillance techniques, promises to open up new opportunities to advance understanding of complex multihost systems.

1 June 2015 in Trends in Ecology & Evolution
Verified
Journal Article
Closed access
RBRoman Biek
Roman Biek
OPOliver G. Pybus
Oliver G. Pybus
JLJames O. Lloyd-Smith
James O. Lloyd-Smith
XDXavier Didelot
Xavier Didelot

5 October 2016 in PLOS Neglected Tropical Diseases
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Journal Article
Open access
PDF file
CDClaire Donald
Claire Donald
BBBenjamin Brennan
Benjamin Brennan
SCStephanie L. Cumberworth
Stephanie L. Cumberworth
VRVeronica V. Rezelj
Veronica V. Rezelj
JCJordan Clark
Jordan Clark
AKAlain Kohl
Alain Kohl
The outbreak of Zika virus (ZIKV) in the Americas has transformed a previously obscure mosquito-transmitted arbovirus of the Flaviviridae family into a major public health concern. Little is currently known about the evolution and biology of ZIKV and the factors that contribute to the associated pathogenesis. Determining genomic sequences of clinical viral isolates and characterization of elements within these are an important prerequisite to advance our understanding of viral replicative processes and virus-host interactions. We obtained a ZIKV isolate from a patient who presented with classical ZIKV-associated symptoms, and used high throughput sequencing and other molecular biology approaches to determine its full genome sequence, including non-coding regions. Genome regions were characterized and compared to the sequences of other isolates where available. Furthermore, we identified a subgenomic flavivirus RNA (sfRNA) in ZIKV-infected cells that has antagonist activity against RIG-I induced type I interferon induction, with a lesser effect on MDA-5 mediated action. The full-length genome sequence including non-coding regions of a South American ZIKV isolate from a patient with classical symptoms will support efforts to develop genetic tools for this virus. Detection of sfRNA that counteracts interferon responses is likely to be important for further understanding of pathogenesis and virus-host interactions. The current ZIKV outbreak is a major public health concern in the Americas. To further understand the virus, and to develop tools and potentially vaccines, more information on the virus strains circulating in the Americas is required. Here we describe the full-length sequence of a ZIKV isolate from a patient with classical symptoms, including the complete non-coding regions which are missing from many currently available sequences, and put these in context. Moreover, we also demonstrate the production of an RNA molecule derived from the 3’ untranslated region that counteracts interferon responses and may therefore be important for understanding the pathogenesis of ZIKV infection.

8 May 2007 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
PDF file
RBRoman Biek
Roman Biek
JHJ. Caroline Henderson
J. Caroline Henderson
LWLance A. Waller
Lance A. Waller
CRCharles E. Rupprecht
Charles E. Rupprecht
LRLeslie A. Real
Leslie A. Real
Emerging pathogens potentially undergo rapid evolution while expanding in population size and geographic range during the course of invasion, yet it is generally difficult to demonstrate how these processes interact. Our analysis of a 30-yr data set covering a large-scale rabies virus outbreak among North American raccoons reveals the long lasting effect of the initial infection wave in determining how viral populations are genetically structured in space. We further find that coalescent-based estimates derived from the genetic data yielded an amazingly accurate reconstruction of the known spatial and demographic dynamics of the virus over time. Our study demonstrates the combined evolutionary and population dynamic processes characterizing the spread of pathogen after its introduction into a fully susceptible host population. Furthermore, the results provide important insights regarding the spatial scale of rabies persistence and validate the use of coalescent approaches for uncovering even relatively complex population histories. Such approaches will be of increasing relevance for understanding the epidemiology of emerging zoonotic diseases in a landscape context.