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INFECTIOUS LARYNGOTRACHEITIS Infectiöse Laryngotrachitis Infekční laryngotracheitida Infectious Laryngotracheitis • viral respiratory disease affects chicken. • first report in USA in 1924 • It is recognise worldwide. • Serious disease outbreaks occur periodically when strains of infectious laryngotrachitis viru (ILTV) spread from persistently infected flocks to nonvaccinated birds. Infectious Laryngotracheitis Cause Family Herpesviridae Subfamily Alfaherpesvirinae Gallid herpesvirus 1 (Iltovirus =ILT-like virus) Field strains may show considerable variaton in virulence. Infectious Laryngotracheitis Host Naturally infect only domestic fowl and occasionally pheasants. All age of fowl are susceptible, the disease is most commonly seen in field in birds 3-9 months old. In general males are more susceptible then females and heavier breeds more susceptible than light ones. Disease my be exacerbated concurrent infection with variety of others patogens such ND, infectious bronchitis and fowl pox viruses, and Haemophillus paragalinarum and Mycoplasma gallisepticum. Infectious Laryngotracheitis Spread Virus enters the bird in infective droplets or mucus via the upper respiratory tract and cunjunctiva. It is shed mainly in exudates from nares, oropharynx, trachea and conjunctiva an is transmitted in aerosol or expectorant form (blood or mucus). The virus remains in latent form in the trigeminal ganglia in brain. Source of infection living infected bird, fomite mechanical cariers – personnel, wild birds Infectious Laryngotracheitis Clinical sings period of incubation 6-12 days possible peracute acute or mild or asymptomatic infection Infectious Laryngotracheitis Peracute form • Sudden acuted dyspnoe with severe coughing and expectoration of mucus, blood stained exudate or blood clots. • Spreading of disease is very fast • High morbidity 70% of affected birds may die, mortality more then 50% Infectious Laryngotracheitis Peracute form Lesions – haemorrhagic tracheitis in which the trachea contains blood cast throughout the whole or part of its length or is filled with blood-stained mucus – respiratory obstruction Infectious Laryngotracheitis Acute form – clinical sings • Dyspnoe, but with not as sudden in onset • Breathe with a wide-open beak • Moist rales can be heard • Nasal discharge and conjunctivitis with frothy exsudate • morbidity is high, mortality 10 - 30% • Drop in egg production – loss 60 % Lesion – mukoid exsudate with or without blood in trachea – Caseous diphteric exsudate – Obstructive plugs in laryng and syring Infectious Laryngotracheitis Mild form Clinical sings • moist rales, slight coughing and head shaking • nasal exudate, conjunctivitis Asymptomatic form • without clinical sings and its presence in small flock may go undetected Infectious Laryngotracheitis Others patological findings • in peracute and acute forms very good body condition of dead birds • atrophy of ovary • congestion of lungs • thickening of air sac walls Infectious Laryngotracheitis Diagnostic methods: • histological examination of trachea • virus detection • antibody detection Infectious Laryngotracheitis Histological findings in trachea • inflamatory response and necrosis with or without haemorrhage • diagnostical sings – presence of intranuclear inclusion bodies Cowdry type A in some epithelial cells • are present only for a few days before desquamation of epithelial cells Infectious Laryngotracheitis Virus detection/isolation • embryonated eggs or cell cultures • samples – exudate, epithelial scrapings or tracheal swabs • Inoculation on chorioallanoic membrane (CAM)1012 day-old eggs – positive findings – production of posck on CAM • on monolayer of chick embryo liver cell cultures – positive findings – syncytium formation after several days Infectious Laryngotracheitis Rapid methods - Immunofluorescence or immunoperoxidase staining of tracheal sections - antigen capture ELISA - electron microscopy – negative staining - DNA hybridization techniques - PCR Infectious Laryngotracheitis Serology Aim– detection of antibodies to ILTV in chicken serum Methods AGID – agar gel imunodiffusion Virus neutralisation – gold standard (time consuming) Indirect immunofluorescence – serum to fixed cell cultures ELISA – ease testing of large numbers of sera with commercial kits - system of choice for flock testing Infectious Laryngotracheitis Vaccination Live vaccine in area with no-high risk in age between 3 and 18 weeks repeated vaccination past 2-3 weeks Methods - eye drop vaccination, coarse spray, inclusion in the drinking water Disadvantage - Possibility of latent infection, in first occurence is better destock completely and clean and disinfect