Automatic milking

Workpackage 5: Prevention of antibiotic residues

Background

Antibiotic residues are unwanted in products for human consumption and may cause problems during dairy processing. When milk is found to be positive for (bacterial) growth inhibitors, i.e. contains antibiotic components, farmers in several countries are severely penalised. An important measure of prevention is the withdrawal time of milk after a cow has been treated (most frequently against mastitis) with antibiotics, either intramammary or systemically. Each antibiotic formula has a specific withdrawal time, based upon the maximum residue level. However, under practical circumstances the excretion period of antibiotic residues may differ from the withdrawal period indicated. This being the case with conventional milking systems with more or less regular milking intervals, there is a complete lack of information on the adequacy of the indicated withdrawal periods in a situation with more frequent milking and with irregular intervals as in automatic milking.

Objectives

The excretion characteristics of antibiotic residues in milk after treatment of healthy cows milked with different milking frequencies and intervals will be determined under experimental conditions. Additionally, the excretion of antibiotic residues will be studied in cows with naturally occurring clinical mastitis and milked in an automatic milking system. The detection of residues will be based on maximum residue limits fixed by EU-regulations for health protection of consumers. Results will lead to recommendations for management of antibiotic treatment of cows in automatic milking systems.

Subpackage 1: Investigation of excretion of antibiotic residues in milk under experimental conditions. 

Methodology and study materials

The excretion of antibiotic residues in milk will be determined in cows with different milking frequencies and intervals. Four different commercially available antibiotic formulas for treatment of mastitis will be selected according to their use in European countries, mode of application and application in body compartments. Three groups of cows will be treated per formula. Each group consists of 5 cows with comparable milk production level, number and stage of lactation. The control group will be milked at ordinary milking times (milking intervals 10 and 14 h). Two experimental groups will be milked with higher milking frequency (three times daily/milking interval 8 h) and with irregular milking intervals, respectively. If prolonged excretion is suspected milking intervals will be adapted for the following experiments. Milk will be sampled at every milking during a period exceeding the withholding period for at least two days. Existing microbiological (e.g. brilliant black reduction-test) and/or immunological (e.g. radioimmunoassay)/chemico-physical (HPLC) methods will be applied for qualitative and quantitative/semi-quantitative detection of antibiotic residues at MRL-level.

Subpackage 2: Excretion of antibiotic residues in milk when using an automatic milking system. 

Methodology and study materials

Excretion characteristics of antibiotic residues in clinically diseased cows milked by an automatic milking system will be determined. Cows with naturally occurring mastitis will be treated with antibiotics and milked automatically in the system. Milk samples of every milking will be collected by an automatic sampling device provided by partner 10 and stored frozen until determination of antibiotic residues. Detection of antibiotic residues will be correlated with data on milking frequencies and milk yield obtained by the system.

Deliverables

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