Equine infectious anaemia (EIA, also known as swamp fever) is a viral disease of horses transmitted by blood-feeding insects and caused by a Lentivirus (RNA virus) of the Retroviridae family (Orthoretrovirinae subfamily). It is not transmissible to humans.
The disease can affect all equidae, thus including not only horses but also donkeys, mules and hinnies. The disease is transmitted through contact with infected blood, and thus generally by blood-feeding insects (horse flies and deer flies), which act as mechanical vectors only. The main vectors include the stable fly (Stomoxys calcitrans) and various species of horse fly from the Tabanus spp. and Hybomitra spp. genuses. Transmission peaks in the summer and autumn, when these insects are most active. Transmission can also be iatrogenic, through the use of contaminated veterinary needles and instruments or transfusion of blood from infected animals.
The virus persists in the leukocytes of infected animals for life. Animals showing signs of the disease are more likely to transmit it, as they have a higher viral titre than animals with an inapparent infection. Equine infectious anaemia virus (EIAV) can also be transmitted through the placenta from an infected mother to her fetus, or through her milk in the first months of life. In animals under six months old born from infected mothers, serological positivity may be due to the presence of colostral antibodies.
Equine infectious anaemia is prevalent worldwide. It has been reported in America (Brazil, Canada, Colombia, Paraguay), Asia (Japan, Malaysia, Mongolia), Europe (Belgium, France, Germany, Great Britain, Greece, Hungary, Ireland, Italy, Romania) and Australia.
Figure 1. Worldwide distribution of equine infectious anaemia
After infection the virus spreads through the horse's body, causing damage to the immune system. The pathogenesis is not yet fully clear. In the early stages, the virus reproduces in monocytes/macrophages, thus avoiding the humoral immune response. Over a few weeks a high titre of immune complexes builds up. These settle on the glomerular membranes and small vessels of other tissues, causing glomerulonephritis and vascular damage. Complement and neutrophil activation also causes vascular damage as well as platelet aggregation, intravascular coagulation and circulatory disorders. The anaemia is due to the fact that the viral antigens may be soluble and be released in the blood, adhering to the red blood cells. Specific antibodies then bind to the red blood cells, activating the complement and triggering haemolysis. This is known as immune-mediated haemolytic anaemia. In the bone marrow, the virus can cause reduced erythropoiesis as well as affecting plasma iron turnover.
The time between contagion and manifestation of signs (incubation period) is normally 10-20 days. However, it can vary from just a few days to 90 days. In experimental conditions, seroconversion has been detected by agar gel immunodiffusion (AGID) 45 days after infection. In natural conditions, up to 157 days may pass between infection and detection of circulating antibodies. The course of the disease may be acute, chronic, or subclinical, with no clinical signs:
The main lesions include enlargement of the spleen, liver, and lymph nodes (especially the abdominal lymph nodes). The mucosa may be pale and there may be emaciation in chronic cases. There may also be oedema, widespread petechial haemorrhages of the internal organs (spleen and kidneys), haemorrhages, and thromboses.
Equine infectious anaemia can be diagnosed through serological tests. Infected animals remain carriers and serologically positive for their entire life. The most common diagnostic tests are Coggins AGID and immunoenzymatic tests (ELISA), performed according to the OIE manual (OIE Terrestrial Manual, Equine Infectious Anaemia. Chapter 2.5.6 2008). Coggins test is the official test used for surveillance in Italy and is the test recommended by the OIE for international trade in equidae. Both methods (Coggins and ELISA) provide accurate diagnosis of infection in horses, but can give false negatives in the early stages, where there is a low antibody titre, or more rarely in the acute form, when the circulating virus is capable of neutralising the antibodies in the blood. Polymerase chain reaction (PCR) is used to detect proviral EIAV DNA and for confirmation of serological tests, testing of foals born from infected mothers, and control of seropositive animals.
Differential diagnosis is performed against other diseases presenting with fever, oedema, and anaemia:
As no vaccines are currently available, the disease is controlled by preventive measures, based essentially on serological testing and isolation of positive animals.
Regular treatment to reduce the population of insect vectors in stables and stalls and good hygiene in the use of veterinary instruments are essential measures to limit exposure to infection.
Like all enveloped viruses, EIAV is rapidly inactivated by the most common disinfectants.