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American and European foulbrood (AFB and EFB) are devastating bacterial brood diseases of honey bees (Apis mellifera), which cause colony and economic losses worldwide. The causative agent of AFB, Paenibacillus larvae, are grouped into different ERIC-genotypes (Enterobacterial repetitive intergenic consensus) the two most common of which are ERIC I and ERIC II. In the field, the differentiation between the symptoms of AFB and EFB (caused by Melissococcus plutonius) can be difficult. The differentiation between the ERIC-genotypes in the field based on the symptoms is not possible at all. The differentiation between the ERIC-genotypes of P. larvae during diagnosis can help to understand the spread of the AFB disease. Hence, a tool capable of detection and distinction between the bacterial brood diseases and the P. larvae-genotypes is needed. For the optimal prevention of disease spread, the diagnosis needs to be fast, cheap and reliable.
This study focuses on the development of a diagnostic sandwich ELISA and a lateral flow device (LFD) for the detection and distinction of EFB and AFB, including the differentiation of the two main occurring P. larvae genotypes. The therefore necessary specific monoclonal antibodies (mAbs) were obtained by immunizing mice with M. plutonius or P. larvae strains belonging to either ERC I or ERIC II. The generated mAbs were characterized for their specificity towards the target bacteria and for their cross reactivity towards other bee-associated bacteria. The screening for suitable mAbs resulted in two specific mAbs against M. plutonius, two against P. larvae in general and two against ERIC II. In combination with the anti-P. larvae mAbs, the anti-ERIC II mAbs were used for genotyping.
In order to evaluate the suitability of the mAbs, their antigens were identified. The target antigens of the produced mAbs turned out to be proteins that could be of further interest as they seem to be involved in the pathogenesis and host-pathogen-interaction. The mAbs with the same antigens were used in the sandwich ELISA for testing the cross reactivity and strain detection. Suitable mAb combinations were used for LFD production. The LFDs were then successfully tested against several field isolates of AFB and EFB causing agents and no cross reactivity with bee-associated bacteria was detected. The P. larvae strains used for mAb testing were genotyped to obtain information about the respective genetic variance. In the process atypical P. larvae strains were identified and further characterized using the generated mAbs. The ability of the mAbs to also recognise the atypical strains as well indicates that the mAbs bind to an antigen that is common among different P. larvae strains.
All in all, a fast tool for detection and differentiation of EFB, AFB and the two ERIC-genotypes was developed that has to be further tested for its reliability in the field.