Detection of Paenibacillus larvae spores in honey by conventional PCR and its potential for American foulbrood control

The present study attempted to detect Paenibacillus larvae spores in naturally contaminated honeys by conventional PCR and to determine the sensitivity of the reaction with different primer pairs in order to assess its potential for American foulbrood control. For this purpose, duplicated honey samples were collected from 5 bee colonies with clinical American foulbrood and 5 clinically healthy colonies in the same apiary. The samples were analysed for the presence of Paenibacillus larvae spores by culture method and subsequent PCR detection in bacterial colonies. The PCR performed directly with spore DNA failed in 6 out of the 20 honeys investigated with spore load of 10–46 cfu/g. The established sensitivity of 70% of the reaction in the present study shows that the adequate control of American foulbrood by analysis of honeys for Paenibacillus larvae spore contamination should be done by combination of culture method followed by PCR in bacterial colonies, whose sensitivity was 100%.