Ludvigsen Jane, Porcellato Davide, L'Abée-Lund Trine M, Amdam Gro V, Rudi Knut
Faculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Ås, Norway.
Department of Food Safety and Infection Biology, Norwegian University of Life Sciences, Oslo, Norway.
Mol Ecol. 2017 Dec;26(23):6590-6607. doi: 10.1111/mec.14392. Epub 2017 Nov 23.
How long-term antibiotic treatment affects host bacterial associations is still largely unknown. The honeybee-gut microbiota has a simple composition, so we used this gut community to investigate how long-term antibiotic treatment affects host-associated microbiota. We investigated the phylogenetic relatedness, genomic content (GC percentage, genome size, number of genes and CRISPR) and antibiotic-resistant genes (ARG) for strains from two abundant members of the honeybee core gut microbiota (Gilliamella apicola and Snodgrassella alvi). Domesticated honeybees are subjected to geographically different management policies, so we used two research apiaries, representing different antibiotic treatment regimens in their apiculture: low antibiotic usage (Norway) and high antibiotic usage (Arizona, USA). We applied whole-genome shotgun sequencing on 48 G. apicola and 22 S. alvi. We identified three predominating subgroups of G. apicola in honeybees from both Norway and Arizona. For G. apicola, genetic content substantially varied between subgroups and distance similarity calculations showed similarity discrepancy between subgroups. Functional differences between subgroups, such as pectin-degrading enzymes (G. apicola), were also identified. In addition, we identified horizontal gene transfer (HGT) of transposon (Tn10)-associated tetracycline resistance (Tet B) across the G. apicola subgroups in the Arizonan honeybees, using interspace polymorphisms in the Tet B determinant. Our results support that honeybee-gut symbiont subgroups can resist long-term antibiotic treatment and maintain functionality through acquisition of geographically distinct antibiotic-resistant genes by HGT.
长期抗生素治疗如何影响宿主与细菌的关联在很大程度上仍然未知。蜜蜂肠道微生物群的组成简单,因此我们利用这个肠道群落来研究长期抗生素治疗如何影响宿主相关微生物群。我们调查了蜜蜂核心肠道微生物群的两个丰富成员(蜜蜂吉氏菌和阿尔维氏斯诺德格拉斯菌)菌株的系统发育相关性、基因组内容(GC百分比、基因组大小、基因数量和CRISPR)以及抗生素抗性基因(ARG)。家养蜜蜂受到地理上不同的管理政策影响,因此我们使用了两个研究蜂场,它们在养蜂业中代表不同的抗生素治疗方案:低抗生素使用量(挪威)和高抗生素使用量(美国亚利桑那州)。我们对48株蜜蜂吉氏菌和22株阿尔维氏斯诺德格拉斯菌进行了全基因组鸟枪法测序。我们在来自挪威和亚利桑那州的蜜蜂中鉴定出了蜜蜂吉氏菌的三个主要亚群。对于蜜蜂吉氏菌,亚群之间的遗传内容有很大差异,距离相似性计算显示亚群之间存在相似性差异。我们还鉴定了亚群之间的功能差异,例如果胶降解酶(蜜蜂吉氏菌)。此外,我们利用四环素抗性(Tet B)决定簇中的间隔多态性,在亚利桑那州蜜蜂的蜜蜂吉氏菌亚群中鉴定出了转座子(Tn10)相关的四环素抗性(Tet B)的水平基因转移(HGT)。我们的结果支持蜜蜂肠道共生菌亚群可以抵抗长期抗生素治疗,并通过水平基因转移获得地理上不同的抗生素抗性基因来维持功能。