Žugelj Alenka, Papić Bojan, Zdovc Irena, Zajc Urška, Golob Majda, Avberšek Jana, Kušar Darja
Unit Maribor-Ptuj, Veterinary Faculty, National Veterinary Institute, University of Ljubljana, Šentiljska Cesta 109, SI-2000 Maribor, Slovenia.
Veterinary Faculty, Institute of Microbiology and Parasitology, University of Ljubljana, Gerbičeva 60, SI-1000 Ljubljana, Slovenia.
Insects. 2021 Apr 19;12(4):362. doi: 10.3390/insects12040362.
is the causative agent of American foulbrood (AFB), a fatal disease of honeybee brood. Here, we obtained 506 isolates originating from honey or brood samples and from different geographic regions of Slovenia in the period 2017-2019. In the first part of the study, we conducted ERIC-PCR typing to assess the frequency of ERIC types in Slovenia. Capillary electrophoresis was used for the analysis of ERIC patterns, revealing good separation efficiency and enabling easy lane-to-lane comparisons. ERIC II was the predominant type (70.2%), followed by ERIC I (29.8%); two slightly altered ERIC I banding patterns were observed but were not considered relevant for the discrimination of ERIC types. No evident spatiotemporal clustering of ERIC types was observed. To assess the clonality of the outbreak-related ERIC I isolates, 59 isolates of this type underwent whole-genome sequencing (WGS). Whole-genome multilocus sequence typing (wgMLST) revealed seven ERIC I-ST2 outbreak clusters (≤35 allele differences) with the median intra-outbreak diversity ranging from 7 to 27 allele differences. In all seven clusters, the transmission of outbreak clone within a 3-km radius (AFB zone) was observed, which could be explained by the activity of honeybees. In three clusters, the transmission of the outbreak clone between geographically distant apiaries was revealed, which could be explained by the activities of beekeepers such as migratory beekeeping and trading of bee colonies. The present findings reinforce the importance of beekeeping activities in the transmission of . WGS should be used as a reference typing method for the detection of transmission clusters.
是美洲幼虫腐臭病(AFB)的病原体,这是一种蜜蜂幼虫的致命疾病。在此,我们获得了506株分离株,这些分离株来自2017 - 2019年期间斯洛文尼亚不同地理区域的蜂蜜或幼虫样本。在研究的第一部分,我们进行了ERIC - PCR分型,以评估斯洛文尼亚ERIC类型的频率。毛细管电泳用于分析ERIC模式,显示出良好的分离效率,并便于进行泳道间的比较。ERIC II是主要类型(70.2%),其次是ERIC I(29.8%);观察到两种略有改变的ERIC I条带模式,但认为它们与ERIC类型的区分无关。未观察到ERIC类型有明显的时空聚集。为了评估与疫情相关的ERIC I分离株的克隆性,对该类型的59株分离株进行了全基因组测序(WGS)。全基因组多位点序列分型(wgMLST)揭示了7个ERIC I - ST2疫情簇(等位基因差异≤35),疫情内的中位多样性范围为7至27个等位基因差异。在所有7个簇中,观察到疫情克隆在3公里半径内(AFB区域)传播,这可以用蜜蜂的活动来解释。在3个簇中,揭示了疫情克隆在地理上相距遥远的蜂场之间传播,这可以用养蜂人的活动如转地养蜂和蜂群交易来解释。目前的研究结果强化了养蜂活动在传播中的重要性。WGS应用作检测传播簇的参考分型方法。