section name header

Basics

Outline


BASICS

Definition!!navigator!!

  • Infection of the respiratory tract by the EIV
  • Highly contagious
  • Most economically important contagious respiratory disease of the horse

Pathophysiology!!navigator!!

  • Inhalation of aerosolized virus allows deposition of viral particles throughout respiratory tract
  • Virus enters epithelial cells lining respiratory tract, replicates, and is released into the airways
  • Infected cells undergo apoptosis
  • Rapid spread of virus causes desquamation and denudation of respiratory epithelial cells and clumping of cilia
  • Impaired mucociliary clearance results and may persist for 4 weeks post infection
  • Secondary bacterial infections may occur

Systems Affected!!navigator!!

  • Respiratory
  • Musculoskeletal (rare)
  • Cardiac (rare)

Incidence/Prevalence!!navigator!!

  • Outbreaks occur among large groups of susceptible horses, often young racehorses
  • Age and previous exposure (natural or vaccination) determine prevalence
  • Morbidity can approach 100% in young naive horses

Geographic Distribution!!navigator!!

  • Endemic in North and South America, Europe, the Middle East, and Asia
  • First outbreak in Australia in 2007 (currently EIV free)
  • Not present in New Zealand or Iceland

Signalment!!navigator!!

  • Equidae of all ages are susceptible
  • Young horses (1–3 years) are more commonly affected

Signs!!navigator!!

  • 1–2 day incubation period
  • Fever, anorexia, depression
  • Frequent dry cough
  • Mucoid nasal discharge. May become mucopurulent to purulent if secondary bacterial infection occurs
  • Limb edema
  • Conjunctivitis, epiphora
  • Submandibular lymphadenopathy
  • Muscle stiffness, soreness
  • Clinical signs typically less severe in vaccinated horses

Causes!!navigator!!

  • Caused by an influenza A virus, family Orthomyxoviridae, genus Influenza A virus and Influenza B virus
  • Subtypes identified by surface antigens HA and NA
  • 2 subtypes of the virus exist:
    • A/equine/1 (H7N7)—has not been identified since 1979
    • A/equine/2 (H3N8)—currently identified virus
  • Virus undergoes antigenic drift (minor changes of HA and NA surface proteins) and antigenic shift (major change)
  • 2 antigenically distinct but related influenza A viruses currently co-circulate in America and Europe: Florida clade 1 and Florida clade 2

Risk Factors!!navigator!!

  • Where virus has been reported
  • Age and immunity. Epidemics often occur when young, susceptible horses congregate
  • Spread throughout the world, possibly facilitated by international transport of horses
  • Donkeys are more severely affected

Diagnosis

Outline


DIAGNOSIS

Differential Diagnosis!!navigator!!

  • Infections with EHV-1, EHV-4, EVA, and Streptococcus equi ssp. equi can look similar
  • Influenza typically spreads more rapidly
  • Cough is less commonly observed in animals infected with EHV, EVA, or S. equi
  • The lymphadenopathy seen in cases of S. equi infection is typically more marked

CBC/Biochemistry/Urinalysis!!navigator!!

  • Early lymphopenia and eosinopenia followed by a monocytosis may be seen, although transient
  • Leukocytosis and hyperfibrinogenemia may occur if a secondary bacterial pneumonia develops
  • Increased creatine phosphokinase and aspartate aminotransferase have been rarely reported in horses which develop severe myopathies

Other Laboratory Tests!!navigator!!

  • Diagnosis based on classic clinical signs but can be confirmed by many methods—often needed in vaccinated horses with mild signs
  • Virus isolation of nasopharyngeal swabs—infected, nonvaccinated horses may shed virus for up to 7–10 days. Take within 24–48 h of the development of clinical signs to maximize chances of isolating virus. Place in cool transport medium
  • Antigen capture ELISAs (nasopharyngeal swab) used in diagnosis of human influenza are validated in horses. Rapid turnaround time. Useful in an outbreak situation
  • RT-PCR of nasopharyngeal swabs—rapid, highly sensitive, specific, and widely available; first choice in outbreak control and screening programs for EI
  • Seroconversion—4-fold increase in antibody titer between acute and convalescent samples obtained 10–14 days apart is considered diagnostic. hemagglutinin inhibition, virus neutralization, and single radial hemolysis tests can be used

Imaging!!navigator!!

Ultrasonographic or radiographic evaluation of the thorax can be used to diagnose pneumonia as a sequel.

Pathologic Findings!!navigator!!

  • Foals more likely to die in an outbreak of naive horses than older animals
  • Pregnant mares may abort or deliver stillborn fetus
  • Tracheitis
  • Bronchointerstitial bacterial pneumonia

Treatment

Outline


TREATMENT

Appropriate Health Care!!navigator!!

  • Affected animals should be isolated to prevent spread
  • Most horses will recover from EI infection within 1–3 weeks

Nursing Care!!navigator!!

House in well-ventilated stalls.

Activity!!navigator!!

  • Stall rest or limited exercise until the respiratory epithelium has healed
  • Early return to exercise can delay recovery. May lead to serious long-term and life-threatening complications (myocarditis)

Diet!!navigator!!

Feed palatable feeds with low-dust content.

Client Education!!navigator!!

  • Animals new to a population or potentially exposed horses returning to a group should be isolated for at least several days (ideally 2 weeks). Monitor closely for development of a fever or nasal discharge
  • If an outbreak of influenza or other respiratory disease is suspected, a quarantine should be established. Arrivals and departures from the premise should be prevented
  • Owners should be aware that vaccination of horses does not prevent infection

Medications

Outline


MEDICATIONS

Drugs (S) of Choice!!navigator!!

  • No antiviral drugs are marketed for the treatment of EI
  • Antiviral drugs such as amantadine and rimantadine have been investigated but antivirals are typically not used
  • Treatment is supportive—NSAIDs such as flunixin meglumine (1.1 mg/kg PO, IV every 12 h) or phenylbutazone (2.2–4.4 mg/kg IV, PO every 12 h) can be used to alleviate fever, depression, and muscle soreness
  • Secondary bacterial pneumonia should be treated with antimicrobials based on sensitivity pattern of organisms identified from transtracheal wash. Pending culture results, broad-spectrum antimicrobial combinations targeted at commonly isolated organisms (Streptococcus spp. and Actinobacillus spp.) can be used (such as penicillin, tetracycline, ceftiofur, and gentamicin; trimethoprim–sulfamethoxazole)

Contraindications!!navigator!!

Corticosteroids are immunosuppressive. Recovery from influenza depends largely on an effective immune response. These drugs should not be used.

Precautions!!navigator!!

NSAIDs should be used judiciously in horses that are inappetent and dehydrated owing to the potential development of gastrointestinal and renal toxicity.

Follow-up

Outline


FOLLOW-UP

Patient Monitoring!!navigator!!

Monitoring of vital signs, appetite, and attitude will allow horses that develop secondary sequelae such as bacterial pneumonia to be identified.

Prevention/Avoidance!!navigator!!

  • Biosecurity measures and vaccination are the basis for prevention and control
  • Hand-washing, minimizing horse-to-horse contact, and controlling fomites significantly reduce the risk of disease transmission
  • Several vaccine types are available—all provide short-lived immunity compared with up to 12 months following natural infection
  • Based on current OIE EI vaccine recommendations vaccines should include viral antigens of the currently circulating virus strains, including representatives of the Florida clade 1 and clade 2 lineages (both H3N8)
  • Vaccines available (country dependent) include:
    • Whole inactivated virus vaccines, immuno-stimulating complex adjuvanted vaccines (ISCOM and ISCOM-Matrix), a live attenuated EIV vaccine, and a recombinant poxvirus-vectored vaccine
  • Vaccination can be used in the face of an outbreak—most useful in previously vaccinated animals
  • Foals
    • Schedule will depend on type of vaccine. AAEP guidelines:
      • Inactivated—first dose at 6 months, second dose 3–4 weeks later, third dose at 10–12 months of age
      • Modified live vaccine (intranasal)—first dose at 6–7 months; second dose at 11–12 months of age
      • Canary pox vector vaccine—first dose at 6 months; second dose 5 weeks later
      • ISCOM vaccine—first dose at 6 months; second dose 4 weeks later; third dose 5 months after dose 2
    • Broodmares—booster vaccination 4–6 weeks before foaling (do not use intranasal vaccine due to limited antibody production, limited transfer of passive immunity)
    • Adult horses at low risk—yearly booster
  • Vaccination rules for competition horses vary depending on regulatory body governing the competition.
    • FEI/AAEP:
      • Primary course—2 vaccinations not less than 21 days and not more than 92 days apart
      • Booster vaccination within 7 months of second vaccination
      • Boosters within 6 months + 21 days of previous vaccination
    • UK Thoroughbred racing:
      • Primary course—2 vaccinations not less than 21 days and not more than 92 days apart
      • Booster not less than 150 days and not more than 215 days after second vaccination
      • Yearly booster

Possible Complications!!navigator!!

  • Secondary bacterial infections, causing pneumonia and pleuropneumonia, are potential sequelae. The destruction of the mucociliary apparatus by the virus removes 1 of the major defenses of the respiratory tract
  • Auscultation of the thorax may reveal abnormal lung sounds such as wheezes and crackles in the case of pneumonia, or dull ventral sounds if pleural effusion develops
  • Myocarditis and immune-mediated myositis—rarely reported as a sequela to influenza infection
  • Persistent coughing has been anecdotally reported

Expected Course and Prognosis!!navigator!!

  • Most recover within 1–3 weeks
  • Respiratory tract recovery can take longer, often lost to competition for >3 months
  • The prognosis is excellent if sufficient rest is provided
  • Secondary bacterial pneumonia or pleuropneumonia results in worse prognosis, but most will recover with aggressive treatment and prolonged rest

Miscellaneous

Outline


MISCELLANEOUS

Age-Related Factors!!navigator!!

Foals without maternal antibodies against influenza can develop severe viral pneumonia, prognosis is generally guarded, even with intensive care.

Zoonotic Potential!!navigator!!

EIV has not been shown to infect humans.

Pregnancy/Fertility/Breeding!!navigator!!

  • Pregnant mares that become infected may abort
  • NSAIDs may help prevent abortion in exposed mares

Synonyms!!navigator!!

Equine flu

Abbreviations!!navigator!!

  • AAEP = American Association of Equine Practitioners
  • EHV = equine herpesvirus
  • EI = equine influenza
  • EIV = equine influenza virus
  • ELISA = enzyme-linked immunosorbent assay
  • EVA = equine viral arteritis
  • FEI = Fédération Equestre Internationale
  • HA = hemagglutinin
  • NA = neuraminidase
  • NSAID = nonsteroidal anti-inflammatory drug
  • RT-PCR = reverse transcription–polymerase chain reaction
  • OIE = Office International Epizooties/World Organisation for Animal Health

Internet Resources!!navigator!!

Animal Health Trust. Equiflunet. https://www.aht.org.uk/disease-surveillance/equiflunet

Suggested Reading

Cullinane A, Newton JR. Equine influenza—a global perspective. Vet Microbiol 2013;167:205214.

Landolt GA. Equine influenza virus. Vet Clin North Am Equine Pract 2014;30:507522.

Slater J, Borchers K, Chambers T, et al. Report of the international equine influenza roundtable expert meeting at Le Touquet, Normandy, February 2013. Equine Vet J 2014;46:645650.

Author(s)

Author: Imogen Johns

Consulting Editor: Ashley G. Boyle