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Forschungsstelle
BLV
Projektnummer
1.10.13
Projekttitel
Identifizierung von Sequenzsignaturen zur Bestimmung der Virulenz von Viren der Klassischen Schweinepest
Projekttitel Englisch
Towards a sequence-based diagnostic procedure to evaluate the virulence of classical swine fever viruses

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Erfasste Texte


KategorieText
Schlüsselwörter
(Deutsch)
Virus der klassischen Schweinepest; KSPV; klassische Schweinepest; Pestivirus; Virulenzmarker
Schlüsselwörter
(Englisch)

classical swine fever virus; CSFV; classical swine fever; pestivirus; virulence; pathogenicity; virulence determinants

Kurzbeschreibung
(Deutsch)

Die klassische Schweinepest (KSP) stellt eine ständige Gefahr für die Schweineproduktion dar, nicht zuletzt auch wegen der Erweiterung der Europäischen Union auf Länder, in denen das Virus noch vorkommt. Im Wildschwein – dem natürlichen Wirt – zirkuliert das KSP Virus (KSPV) meistens ohne offensichtliche Symptome.

Im Hausschwein hingegen weisen KSPV Isolate unterschiedliche Virulenz auf. Für die Überwachung von KSP sind vor allem die schwach virulenten Viren problematisch, weil sie nur schwer und oft spät erkannt werden. Deshalb muss ein Diagnostiklabor so rasch wie möglich nach Identifizierung eines neuen KSPV Wildschweinisolates bestimmen können, wie sich dieses Virus im Hausschwein verhalten wird, damit entsprechende Überwachungsmaßnahmen getroffen werden können. Das Ziel dieses Forschungsprojektes ist es daher, virale genetische Determinanten für Virulenz zu identifizieren. Eine Grundlage für diese Arbeit sind Zellkultursysteme, die vor kurzem in unserem Labor entwickelt wurden, um KSPV Virulenz unabhängig von Tierversuchen zu definieren. Die Korrelation von Virulenz mit genetischen Markern wird eine rasche Diagnose ermöglichen, die erlauben wird, angemessene KSP-Überwachungsmaßnahmen zu veranlassen. Virulenzspezifische Sequenzinformationen können auch zur Verfeinerung von KSPV Monitoring und Epidemiologie beitragen.

Kurzbeschreibung
(Englisch)
Classical swine fever represents a constant threat for the pig farming, especially with the extension of the European community to countries in which the virus is still present. In wild boar – the natural reservoir – CSF virus (CSFV) can circulate without inducing apparent disease, while in domestic pigs the virus can manifest various degrees of virulence. Low virulent strains are especially challenging for disease surveillance. Therefore it is essential for a diagnostic laboratory to determine how an emerging wild boar isolate will manifest in domestic pigs. To this end, the present project is aimed at defining viral genomic signatures for virulence, taking advantage of recent advances in defining virulence using porcine cell culture systems as alternative for infection of pigs. This knowledge will provide means of rapid informative diagnostic procedures and appropriate CSF surveillance and control measures to be applied. Virulence-specific sequence information will also contribute to refine CSFV monitoring and epidemiology.
Projektziele
(Deutsch)
In Switzerland, the last classical swine fever (CSF) outbreak in domestic pigs occurred in 1993 (Hofmann
and Bossy, 1998), and the virus was reported for the last time in wild boar in 1999 (Hofmann et al., 1999).
Re-emergence of CSF virus (CSFV) however represents a constant threat for the Swiss pig farming. Indeed,
the OIE regularly registers new cases of classical swine fever (CSF) worldwide including Europe. In Bulgaria,
Slovakia, Hungary and Russia the virus still circulates and results in clinical disease (for the current disease
situation, see http://www.oie.int/wahis/public.php?page=home). The wild boar – the natural CSFV reservoir –
represents the major problem for disease control. Also, the extension of the European community to eastern
European countries along with reduced controls at the borders elevate the risk of re-introducing the disease
in Switzerland through import of contaminated wild boar or pork meat products. A CSFV outbreak in the domestic
pig would generate significant economic losses and restrictions in meat trade. In wild boar, the disease
often remains unapparent and is only detected through an increased mortality rate in the wild boar
population. However, in domestic pigs as well as in wild boar (if animals are monitored closely), a CSFV
isolate can manifest various degrees of virulence, from avirulent to highly virulent. Low and moderately virulent
strains result in a mild, atypical, often chronic disease, and induce a protective immunity. This contrasts
with highly virulent strains that cause acute to peracute symptoms consisting of high fever, diarrhoea, lameness
and haemorrhages. Such disease rapidly progresses within the herd with a high mortality rate, irrespective
of the age and weight of the infected pigs (van Oirschot, 1988).
Infection with low virulent strains is the most challenging situation for disease surveillance and control. The
mild symptoms resemble those of various other, partly common diseases such as porcine multisystemic
wasting syndrome (PMWS). Especially in disease-free periods as it has been the case in Switzerland for the
past decade, the awareness for CSFV among field veterinarians is low. Therefore, if CSFV is found in wild
boar or in domestic pigs, information on its virulence is crucial for guiding the surveillance measures and
supporting disease awareness:

a) The presence of low virulent strains in wild boar will require a comprehensive serological
surveillance to be implemented, due to the lack of distinct disease sign, while in domestic pigs a
thorough analysis of any animals with suspect clinical symptoms is mandatory.
b) If a highly virulent strain starts to circulate, infection of domestic pigs and wild boars is likely to be
rapidly detected, due essentially to the severity of the symptoms and the high infection and mortality
rate.
Thus, the diagnostic laboratory must rapidly provide information on the virulence of an emerging wild boar
isolate. Genetic correlates with virulence are missing, despite extensive sequence information available for
various CSFV isolates. Such knowledge would allow a rapid diagnostic procedures to be applied, providing
essential knowledge to support monitoring and molecular epidemiology of CSFV. It would improve disease
preparedness of veterinarians in the field, and allow appropriate surveillance programs and control measures
to be implemented.
Publikationen / Ergebnisse
(Deutsch)
Publikationen / Ergebnisse
(Englisch)

Eymann-Häni, R.; Leifer, I.; McCullough, KC.; Summerfield, A.; Ruggli, N.; 2011. Classical swine fever virus             propagation in vitro circumventing heparan sulfate-adaptation. J. Virol. Methods. 176:85-95

Leifer, I.; Hoeper, D.; Blome, S.; Beer, M.; Ruggli, N.; 2011. Clustering of classical swine fever virus isolates by codon pair bias. BMC Res. Notes 4:521

Töpfer, A.; Höper, D.; Blome, S.; Beer, M. Beerenwinkel, N.; Ruggli, N.;Leifer, I. (2013). Sequencing approach to analyze the role of quasispecies for classical swine fever. Virology 438 14–19.

Leifer, I.; Ruggli, N.; Blome, S. (2013). Approaches to define the viral genetic basis of classical swine fever virus virulence. Virology 438, 51–55. 

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