College of Food Science and Nutritional Engineering, China Agricultural University, Beijing, 100083, China.
Key Laboratory for Bee Genetics and Breeding, Jilin Provincial Institute of Apicultural Sciences, Jilin, 132000, China.
Microbiome. 2022 May 3;10(1):69. doi: 10.1186/s40168-022-01268-1.
The spread of antibiotic resistance genes (ARGs) has been of global concern as one of the greatest environmental threats. The gut microbiome of animals has been found to be a large reservoir of ARGs, which is also an indicator of the environmental antibiotic spectrum. The conserved microbiota makes the honeybee a tractable and confined ecosystem for studying the maintenance and transfer of ARGs across gut bacteria. Although it has been found that honeybee gut bacteria harbor diverse sets of ARGs, the influences of environmental variables and the mechanism driving their distribution remain unclear.
We characterized the gut resistome of two closely related honeybee species, Apis cerana and Apis mellifera, domesticated in 14 geographic locations across China. The composition of the ARGs was more associated with host species rather than with geographical distribution, and A. mellifera had a higher content of ARGs in the gut. There was a moderate geographic pattern of resistome distribution, and several core ARG groups were found to be prevalent among A. cerana samples. These shared genes were mainly carried by the honeybee-specific gut members Gilliamella and Snodgrassella. Transferrable ARGs were frequently detected in honeybee guts, and the load was much higher in A. mellifera samples. Genomic loci of the bee gut symbionts containing a streptomycin resistance gene cluster were nearly identical to those of the broad-host-range IncQ plasmid, a proficient DNA delivery system in the environment. By in vitro conjugation experiments, we confirmed that the mobilizable plasmids could be transferred between honeybee gut symbionts by conjugation. Moreover, "satellite plasmids" with fragmented genes were identified in the integrated regions of different symbionts from multiple areas.
Our study illustrates that the gut microbiota of different honeybee hosts varied in their antibiotic resistance structure, highlighting the role of the bee microbiome as a potential bioindicator and disseminator of antibiotic resistance. The difference in domestication history is highly influential in the structuring of the bee gut resistome. Notably, the evolution of plasmid-mediated antibiotic resistance is likely to promote the probability of its persistence and dissemination. Video Abstract.
抗生素耐药基因(ARGs)的传播是全球关注的最大环境威胁之一。动物的肠道微生物群已被发现是 ARGs 的一个巨大储存库,也是环境抗生素谱的一个指标。保守的微生物群落使蜜蜂成为研究肠道细菌中 ARGs 维持和转移的一个易于处理和受限的生态系统。尽管已经发现蜜蜂肠道细菌携带了多种 ARGs,但环境变量的影响及其分布的驱动机制仍不清楚。
我们对在中国 14 个地理地点驯化的两种密切相关的蜜蜂物种——中华蜜蜂和西方蜜蜂的肠道抗药性进行了特征描述。ARGs 的组成更多地与宿主物种有关,而与地理位置关系不大,并且西方蜜蜂的肠道中 ARGs 含量更高。抗药性组分布存在中等程度的地理模式,并且在中华蜜蜂样本中发现了几个核心 ARG 组普遍存在。这些共享基因主要由蜜蜂特有的肠道成员 Gilliamella 和 Snodgrassella 携带。可转移的 ARGs 在蜜蜂肠道中频繁检测到,并且在西方蜜蜂样本中的负荷要高得多。含有链霉素抗性基因簇的蜜蜂肠道共生菌的基因组基因座与广泛宿主范围的 IncQ 质粒几乎相同,这是环境中一种有效的 DNA 传递系统。通过体外接合实验,我们证实可移动质粒可以通过接合在蜜蜂肠道共生菌之间转移。此外,在来自多个地区的不同共生体的整合区域中,还鉴定出了具有断裂基因的“卫星质粒”。
我们的研究表明,不同蜜蜂宿主的肠道微生物群在抗生素耐药结构上存在差异,这突出了蜜蜂微生物组作为抗生素耐药性的潜在生物标志物和传播者的作用。驯化历史的差异对蜜蜂肠道抗药性的结构有很大的影响。值得注意的是,质粒介导的抗生素耐药性的进化可能会促进其持久性和传播的可能性。