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Published on: April 18, 2019
Polymyxin E-1 (colistin sulphate) (neuro-)intoxication in young ostriches ( Struthio camelus spp.)
Insights
Colistin (polymyxin E) is toxic to young ostriches, causing rapid mortality and neurotoxicity even at moderate doses. Parenteral administration of polymyxin E exceeding 5mg/kg is unsafe for ostriches.
Area of Science:
- Veterinary Toxicology
- Pharmacology
- Avian Medicine
Background:
- Colistin (polymyxin E) is a potent bactericidal antibiotic against Gram-negative bacilli.
- Parenteral administration of polymyxins carries a narrow safety margin, risking neurotoxicity and nephrotoxicity.
Purpose of the Study:
- To evaluate the safety and toxicity of colistin sulphate in young ostriches.
- To determine a safe dosage for parenteral administration of polymyxin E in ostriches.
Main Methods:
- Subcutaneous injection of 39.5mg/kg body weight colistin sulphate in young ostriches.
- Observation of clinical signs, mortality, and postmortem/histological examination.
Main Results:
- Rapid mortality (1-3 hours) observed after subcutaneous injection.
- Clinical signs included apathy, lethargy, and hypotonia, indicative of neurotoxicity.
- Histological findings revealed severe acute edema in the epicardium and intestinal serosa, brain vessel congestion, and cardiac abnormalities.
Conclusions:
- A subcutaneous dose of 39.5mg/kg colistin sulphate is lethal to young ostriches.
- Parenteral administration of polymyxin E at doses greater than 5mg/kg is considered unsafe for ostriches.
- Neurotoxicity and cardiotoxicity are significant concerns with parenteral colistin use in this species.
Abstract:
Colistin (polymyxin E) is a cyclic polypeptide with a potent bactericidal action against most gramnegative bacilli. When used parenterally, polymyxins should be given with great care as they have a very small safety range, and easily induce neurotoxicity and nephrotoxicity. A dose of 39.5mg/kg body weight colistin sulphate injected subcutaneously induced rapid (within 1 to 3 h) mortality in young ostriches. Clinical signs of apathy, lethargy and hypotonia indicative of neurotoxicity of the compound were observed. At postmortem, vascular congestion of brain vessels was seen while, on histology, severe acute oedema was present in the epicardium and the intestinal serosa. Congestion of villi, swelling and vacuolization of the plexus ofAuerbach, as well as intermuscular and perivascular oedema of the heart, were also observed. In view of our observations in ostriches and in other species studied, a dose of >5mg/kg body weight polymyxin E is not considered safe for parenteral administration in ostriches.
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