| Nature of the disease |
| Transmissible gastro-enteritis (TGE) is an
acute highly contagious disease of pigs caused by virus from the
Coronaviridae family, Coronavirus genus. The disease is
characterised by profuse diarrhoea and vomiting. There is high morbidity
and mortality in piglets.
Recently a respiratory variant of the TGE virus (TGEV), known as the porcine respitratory coronavirus (PRCV) emerged in Europe, causing interference in the diagnosis of TGE. |
| Classification |
| OIE List B disease |
| Susceptible species |
| Clinical disease only occurs in pigs. Cats, dogs and foxes have been described as potential carrier but without clinical signs of the disease. |
| Distribution |
| TGE is present in much of Europe, the Americas
(North, South and Central), Asia (including China, Japan and Korea), South
East Asia, and parts of West Africa. TGE is suspected in some countries of
the region but few surveys were conducted (absent from French Polynesia, New Caledonia,
Solomon Islands, Wallis and Futuna).
As a result of the development of the blocking ELISA test (which differentiates between TGEV and PRCV) the prevalence of TGE has dramatically decreased in many Western European countries and the prevalence of PRCV has proportionally increased. |
| Clinical signs |
| When introduced into a susceptible herd, TGE
spreads rapidly. Pigs less than two weeks are the most severely
affected.
Clinical symptoms include:
|
| Post-mortem findings |
Gross lesions are confined to the
gastro-intestinal tract, except for the dehydration:
|
| Differential diagnosis |
The following should be considered:
|
| Specimens required for diagnosis |
| Virus identification can be done by isolation
from tissue culture, fluorescent antibody test, ELISA and PCR. Samples include faeces from carcass,
particularly loops of affected small intestine. The loops should be
tied-off to retain the contents and kept chilled at 4°C. For immunological
methods the best samples are sacrificed piglets (less than 1 week) at the
beginning of the disease.
Blood samples (20 ml) should be collected from pigs in the acute and convalescent stages of the disease for serology. Techniques include virus neutralisation, indirect ELISA and competitive ELISA. These tests can be used to demonstrate a free status for trade purpose. In addition the blocking ELISA test allows differentiation between TGEV and PRCV. |
| Transmission |
| Outbreaks of TGE usually start following the
introduction of infected pigs. Sub-clinically infected animals can be a
source of infection and recovered pigs often become carriers
and can shed the virus for 2-3 weeks in their faeces. Large amounts
of virus are excreted in the faeces of infected animals.
The exact mechanisms of transmission of the disease are still unclear; the proposed means are:
In Northern countries the disease is clearly related to winter outbreaks, probably because of the sensibility of the virus to warm temperatures. Therefore it is likely that under tropical conditions, the role of fomites would be less important. |
| Risk of introduction |
| The greatest risk of introducing TGE is through
the importation of pigs from endemically infected countries.
Fresh or frozen pigmeat imports from infected countries could represent a potential source as the virus is stable in cold temperatures. The OIE has recommendations on the trade of semen and embryo although there is no formal evidence that these materials are at risk. |
| Control / vaccines |
| Vaccination of pregnant sows has been under
investigation but commercial vaccines are not yet available. Commercial
oral and injectable attenuated virus vaccines appear to be better at
boosting immunity, rather than inducing a primary immune response.
Treatment of TGE should consist in alleviating dehydration and starvation. To reduce risk of spread, only introduce animals from serologically negative herds and sterilize swills. If an outbreak occurs, good hygiene practices can help reducing the impact of the disease. It appears to be difficult to eradicate the disease. One approach consists of preventing contamination of newborn piglets by isolation. The other approach aims to minimize the duration of the disease by exposing all the pregnant sows to the disease to develop transplacental immunity of farrows. |
| References |
|