wildlife and zoo assay data sheet
African swine fever
Ultrasensitive detection of African swine fever virus by real
swine fever (ASF) is a highly contagious, generalized disease of
pigs caused by a DNA virus formerly classified as an iridovirus
(Iridoviridae) but recently re-classified into a newly created
family of viruses called Asfarviridae - a name derived from
"African Swine Fever And Related Viruses.” Within that family it
has been allocated to the Genus Asfivirus of which it is the
only member. Different strains of ASF virus exhibit varying
virulence. The virus is very resistant to inactivation, and can
persist up to one month in contaminated pens, in meat up to 15
weeks and in processed hams up to 6 months.
concentrations of ASF virus are shed in secretions and
excretions from acutely infected pigs. Because the virus
survives well in the environment and in meat, its spread can
occur via contaminated livestock pens or by feeding contaminated
garbage. The virus also spreads through pig to pig contact,
ticks and other biting insect vectors, contaminated injection
needles or mechanically by humans and equipment.
pigs usually have an incubation period of 5-15 days before the
disease may manifest itself in a number of forms:
Peracute - pigs
are found moribund with death following rapidly.
Acute - high
fever (up to 42C.) after 1-2 days anorexia and recumbency, skin
blotching, diarrhea and abortion. Mortality close to 100% within
- fluctuating or continuous fever for up to 20 days, with milder
Chronic - transient recurring fever with
stunting and emaciation. Possible pneumonia, lameness, skin
lesions, and secondary infections.
pigs may remain chronically infected and excrete the virus for 6
weeks after infection. Contaminated pens and garbage feeding,
particularly with material from international airports or
seaports, are documented methods of spread due to the resistance
of the virus to inactivation.
Swine Fever is clinically, and upon necropsy, very similar to
Hog Cholera (also known as "Classical Swine Fever"). Laboratory
tests are required to differentiate the two diseases.
diagnosis and culture identification have been used to detect
ASF but they are generally slow and not very specific. Molecular
detection by PCR can provide rapid, specific and sensitive
results (McKillen et al., 2007).
Help confirm the disease causing agent
Identify ASF virus carriers
Help ensure that animal colonies and populations are free of
Early prevention of spread of the virus among animals
Minimize human exposure to the virus
Safety monitoring of biological products that derive
McKillen, J., Hjertner, B., Millar, A., McNeilly, F., Belák, S.,
Adair, B. and Allan, G. (2007) Molecular beacon real-time PCR
detection of swine viruses. J Virol
Specimen requirements: 0.2 ml whole blood in EDTA (purple top) or ACD (yellow top)
tube, or 0.2 ml feces, or rectal swab, or 0.2 ml fresh, frozen
or fixed tissue.
if advice is needed to determine an appropriate specimen type
for a specific diagnostic application. For specimen
types not listed here, please contact Zoologix to confirm
specimen acceptability and shipping instructions.
specimen types, if there will be a delay in shipping, or during
very warm weather, refrigerate specimens until shipped and ship
with a cold pack unless more stringent shipping requirements are
specified. Frozen specimens should be shipped so as to remain
frozen in transit. See shipping
instructions for more information.
2 business days
Qualitative real time PCR