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Classical swine fever
David Paton
AETIOLOGY
• Family: Flaviviridae
• Genus: Pestivirus
• Single serotype, 3 major genotypes, 3-4 subgroups
• Generally low environmental persistence (days -weeks)
• Stable at pH 5 – 10
• Survives in animal products
GEOGRAPHIC DISTRIBUTION
OIE WAHID 6-monthly FMD incidence, Jul-Dec 2013
Eradicated from North America in 1976
REGIONAL CSF INCIDENCE2005-2014
Not reported since 2005 Reported since 2005 Last year of report
Aruba Brazil 2005
Belize Cuba 2014
Barbados Dominican Republic 2010
Cayman Islands Ecuador 2014
Costa Rica El Salvador 2008
French Guiana Guatemala 2013
Guyana Haiti 2014
Jamaica Honduras 2007
Suriname Mexico 2009
Trinidad and Tobago Nicaragua 2008
Peru 2014
Venezuela 2005
http://www.oie.int/wahis_2/public/wahid.php/Diseaseinformation/Diseasetimelines
PATHOGENESIS – VIRUS LIFE CYCLE
• Affects domestic pigs and wild boar
• Mild, virulent and chronic forms
• Age related susceptibility• Virus entry:
– Oronasal - tonsil as 1st target– Other mucosa or damaged skin– Transplacental
• Incubation period:– 2-14 days
• Virus shedding:– Can precede clinical signs and
continue until death– Most secretions and excretions
(saliva, nasal and ocular discharges, urine, faeces)
Primary replication in tonsil and regional
lymph nodes
Viraemia
Secondary replication(lymphoid tissues,
endothelia and parenchymatous
organs)
Delayed immune response
Virus shedding Clinical signs
Death, chronic disease or recovery
Incu
bation p
eriod
Late
nt
period
Exposure
PATHOLOGY
• Immunopathological disease
• Leukopenia and thrombocytopenia
• Tonsillitis, swollen lymph nodes, splenicinfarcts
• Haemorrhages – skin, epiglottis, bladder, lymph nodes, kidneys
• Button ulcers in caecum and colon
CLINICAL SIGNS• Depression, fever, anorexia
• Mild strains: rather non-specific signs
• Virulent strains: conjunctivitis, constipation, diarrhoea, inco-ordination, skin hyperaemia and haemorrhage, death in 5-25 days
• Chronic strains: initial improvement before relapse and death within 3 months
• Death after 10-20 days or up to 3 months in chronic cases
• Prenatal infection can lead to fetal death, fetalabnormalities and delayed onset signs after birth
CONJUNCTIVITIS
ERYTHEMA
Images from: http://www.afrivip.org/sites/default/files/CSF/diagnosis.html
Enlarged haemorrhagic lymph node Splenic infarcts
LYMPHOID LESIONS
Swine influenza
PDNS
PRRS
DIFFERENTIAL DIAGNOSIS
PMWS
ROUTES OF SPREAD
• Pig to pig horizontally
• Pig to pig vertically and via semen
• Pig meat eaten by pigs (swill)
• Indirect over long distances (lorries)
• Indirect over short distances (farmers, vets, animals, shared equipment, etc)
• Wild boar
19%
43%
11%
27%Purchase of infectedanimals
Transport vehicles
Human contacts
Neighbourhood infection(cases within 1km of asource caused by ??birds/flies)
ROUTES OF INFECTION BEFORE FIRST CASE CONFIRMED Netherlands 1997/8
17%
9%
13%11%
7%
1%
33%
9%
Purchase of infected animals
Transport vehicles
Human contacts
Rendering trucks
AI and infected semen
Slurry
Neighbourhood
Unknown
ROUTES OF INFECTION AFTER PROTECTION AND SURVEILLANCE ZONES IMPLEMENTED
Netherlands 1997/8
0
0.01
0.02
0.03
0.04
0.05
0.06
0.07
Live pigs frominf herd
Lorry on inffarm same
day
Person on inffarm same
day
AI from infcentre
500m vicinityfarm - 1wk
500-100mvicinity farm -
1wk
1000-2000mvicinity farm -
1wk
Probability of transmission
Probability of transmission
Rate of inter-herd transmission of classical swine fever virus by different types of contact during the 1997–8 epidemic in The Netherlands. Stegeman et al, 2002
CHALLENGES FOR EARLY DETECTION
• Low virulence of many virus strains
• Takes time before sufficient pigs affected
• Fevers difficult to measure
• If visit tracings too early do not recognise disease
• Random virological testing of all is impractical
• Serology - takes too long for antibodies to develop
• Value of individual clinical diagnoses and post mortems
• Clinical – Se 73%, Sp 53%
• PM – Se 72%, Sp 78%
• Elbers et al (2002, 2004)
The Herd Se of clinical diagnosis was 50% at 37 days after virus introduction and reached 90% at 47 days after virus introduction. The estimated herd specificity was 72%. Engel et al (2004)
DIAGNOSIS
• Virus detection (VI, RT-PCR, ELISA, FAT)• Blood and organs are usual samples (tonsil, LNs, spleen,
kidney, distal ileum)• RT-PCR is mainstay and DIVA PCR tests possible
• Serology• Several ELISA configurations – E2, Erns, NS• Some can differentiate antibodies induced by vaccines
and ruminant pestiviruses• VNT as gold standard
• Genetic typing• Helps determine outbreak source
VACCINES
• Cell mediated and/or humoral immunity can protect
• Modified live vaccine• Various attenuated strains, e.g. “C” strain• Highly effective and can be used in oral baits• Marker versions developed
• Subunit• E2 recombinant protein• Good DIVA capability
• Novel vaccines• Viral vectors – e.g. Adeno, pox, pseudorabies• Modified genomes – e.g. swaps with other pestiviruses• DNA• Peptide
CONTROL PRINCIPLES
• EU policy is stamping out
– Early detection of cases
– Movement restrictions to prevent spread
– Slaughter of affected herds
– Tracings of contacts
– Possible pre-emptive slaughter
– Emergency vaccination only
2/5/00 9/5/00
248 pigs 220 pigs
A B D F
SF
2000/2
SF2000/04
SF2000/01
N1
N2
N3
N4
SF2000/05
N5N6 N7
SF2000/03
16/5/00
225 pigs
23/5/00
271 pigs
30/5/00
287 pigs
11/7/00
236 pigs
18/7/00 25/7/00 1/8/00
210 pigs 226 pigs 258
pigsF1
F2
F3
F4
F5
F6
F7 F8 F9
F10 F11F11
G
20/6/00
222 pigs
TRACING FROM UK INDEX CASE, 2000
Infected Premises
supply farms
nursery farms
finisher farms
date pigs supplied
number of pigs supplied
11/7/00
232 pigs
27/6/00
244 pigs
20/6/00
222 pigs
13/6/00
279 pigs
6/6/00
245 pigs
CHALLENGES FOR CSF CONTROL
• High density pig keeping
• Animal movements
• Infection of wild boar
• Globalised trading
• Swill and scrap feeding
ACKNOWLEDGEMENTS
Photographs collated from multiple sources including:
• VLA-Weybridge archives
• UK 2000 CSF outbreaks
• Trevor Drew, AHPA, UK
• John Mackinnon, Stowe Vet Group, UK
http://www.afrivip.org/sites/default/files/CSF/diagnosis.html
Disease information from OIE WAHID:
EFSA Review 2009:
http://www.efsa.europa.eu/en/scdocs/doc/6e.pdf
http://www.oie.int/wahis_2/public/wahid.php/Diseaseinformation/Diseasetimelines