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Comparative Genomics and Description of Putative Virulence Factors of Melissococcus plutonius , the Causative Agent of European Foulbrood Disease in Honey Bees

机译:蜂蜜蜜蜂植物细菌植物植物植物植物腐败因子的比较基因组学与描述,蜂蜜蜜蜂欧洲犯规疾病的致病因子

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In Europe, approximately 84% of cultivated crop species depend on insect pollinators, mainly bees. Apis mellifera (the Western honey bee) is the most important commercial pollinator worldwide. The Gram-positive bacterium Melissococcus plutonius is the causative agent of European foulbrood (EFB), a global honey bee brood disease. In order to detect putative virulence factors, we sequenced and analyzed the genomes of 14 M. plutonius strains, including two reference isolates. The isolates do not show a high diversity in genome size or number of predicted protein-encoding genes, ranging from 2.021 to 2.101 Mbp and 1589 to 1686, respectively. Comparative genomics detected genes that might play a role in EFB pathogenesis and ultimately in the death of the honey bee larvae. These include bacteriocins, bacteria cell surface- and host cell adhesion-associated proteins, an enterococcal polysaccharide antigen, an epsilon toxin, proteolytic enzymes, and capsule-associated proteins. In vivo expression of three putative virulence factors (endo-alpha- N -acetylgalactosaminidase, enhancin and epsilon toxin) was verified using naturally infected larvae. With our strain collection, we show for the first time that genomic differences exist between non-virulent and virulent typical strains, as well as a highly virulent atypical strain, that may contribute to the virulence of M. plutonius . Finally, we also detected a high number of conserved pseudogenes (75 to 156) per genome, which indicates genomic reduction during evolutionary host adaptation.
机译:在欧洲,大约84%的栽培作物种类依赖于昆虫粉粉,主要是蜜蜂。 Apis Mellifera(西部蜂蜜蜜蜂)是全球最重要的商业粉丁师。革兰氏阳性细菌蜜糖培养皿是欧洲犯规(EFB)的致病剂,全球蜂蜜蜂巢疾病。为了检测推定的毒力因子,我们测序并分析了14米培养皿菌株的基因组,包括两个参考分离株。分离株不会在基因组大小或预测蛋白编码基因的数量中显示出高的多样性,范围为2.021至2.101 MBP和1589至1686。比较基因组学检测到可能在EFB发病机制中发挥作用的基因,最终在蜂蜜蜂幼虫的死亡中。这些包括细菌素,细胞表面和宿主细胞粘附相关蛋白,肠球菌多糖抗原,ε毒素,蛋白水解酶和胶囊相关蛋白质。在三种推定的毒力因子(endo-α-乙酰甘油酰胺酶,增强蛋白和ε-毒素)的体内表达中使用天然感染的幼虫验证。通过我们的应变系列,我们首次表明了非毒力和毒力典型菌株的基因组差异,以及高毒性的非典型菌株,这可能有助于培养皿的毒力。最后,我们还检测到每种基因组的大量保守的伪原(75至156),这表明进化宿主适应期间的基因组减少。

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