Gregorio Fernandez de Landa, Daniele Alberoni, Chiara Braglia, Loredana Baffoni, Mateo Fernandez de Landa, Pablo Damian Revainera, Silvina Quintana, Francisco Zumpano, Matias Daniel Maggi, Diana Di Gioia
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This study is focused on the impact of different land uses (natural reserve, agroecosystem, and suburban) on the gut microbiome composition of two South American bumble bees, Bombus pauloensis and Bombus bellicosus. Gut microbial DNA extracted from collected bumble bees was sequenced on the Illumina MiSeq platform and correlated with land use. Nosema ceranae load was analyzed with qPCR and correlated with microbiome data. Significant differences in gut microbiome composition between the two wild bumble bee species were highlighted, with notable variations in α- and β-diversity across study sites. Bombus bellicosus showed a high abundance of Pseudomonas, a genus that includes environmental saprobes, and was found to be the second major taxa populating the gut microbiome, probably indicating the vulnerability of this host to environmental pollution. Pathogen analysis unveils a high prevalence of N. ceranae, with B. bellicosus showing higher susceptibility. Finally, Gilliamella exhibited a negative correlation with N. ceranae, suggesting a potential protective role of this commensal taxon. 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引用次数: 0
摘要
南美洲的熊蜂种类繁多,是生物多样性的重要来源,为自然和农业生态系统提供授粉服务。这些授粉者提供了独特的特定微生物壁龛,其中栖息着大量微生物,如共生体、环境机会性细菌和病原体。最近的研究表明,微生物种群不仅受到营养资源和环境条件的影响,还受到人为压力的影响,这对微生物的功能产生了很大影响。本研究的重点是不同土地利用(自然保护区、农业生态系统和郊区)对两种南美熊蜂(Bombus pauloensis 和 Bombus bellicosus)肠道微生物组组成的影响。从采集的熊蜂中提取的肠道微生物 DNA 在 Illumina MiSeq 平台上进行了测序,并与土地使用情况相关联。用 qPCR 分析了陶瓷鼻疽病毒(Nosema ceranae)的载量,并将其与微生物组数据相关联。两种野生熊蜂的肠道微生物组组成存在显著差异,不同研究地点的α和β多样性差异明显。大黄蜂的假单胞菌(Pseudomonas)含量很高,该菌属包括环境酵母菌,是肠道微生物组的第二大类群,这可能表明该宿主易受环境污染的影响。病原体分析揭示了N. ceranae的高流行率,而B. bellicosus表现出更高的易感性。最后,Gilliamella 与 N. ceranae 呈负相关,表明这种共生类群具有潜在的保护作用。我们的发现强调了在传粉昆虫保护战略中考虑微生物动态的重要性,突出了肠道细菌和病原体在影响大黄蜂健康方面的潜在相互作用。
The Gut Microbiome of Two Wild Bumble Bee Species Native of South America: Bombus pauloensis and Bombus bellicosus.
South America is populated by a wide range of bumble bee species that represent an important source of biodiversity, supporting pollination services in natural and agricultural ecosystems. These pollinators provide unique specific microbial niches, populated by a wide number of microorganisms such as symbionts, environmental opportunistic bacteria, and pathogens. Recently, it was demonstrated how microbial populations are shaped by trophic resources and environmental conditions but also by anthropogenic pressure, which strongly affects microbes' functionality. This study is focused on the impact of different land uses (natural reserve, agroecosystem, and suburban) on the gut microbiome composition of two South American bumble bees, Bombus pauloensis and Bombus bellicosus. Gut microbial DNA extracted from collected bumble bees was sequenced on the Illumina MiSeq platform and correlated with land use. Nosema ceranae load was analyzed with qPCR and correlated with microbiome data. Significant differences in gut microbiome composition between the two wild bumble bee species were highlighted, with notable variations in α- and β-diversity across study sites. Bombus bellicosus showed a high abundance of Pseudomonas, a genus that includes environmental saprobes, and was found to be the second major taxa populating the gut microbiome, probably indicating the vulnerability of this host to environmental pollution. Pathogen analysis unveils a high prevalence of N. ceranae, with B. bellicosus showing higher susceptibility. Finally, Gilliamella exhibited a negative correlation with N. ceranae, suggesting a potential protective role of this commensal taxon. Our findings underscore the importance of considering microbial dynamics in pollinator conservation strategies, highlighting potential interactions between gut bacteria and pathogens in shaping bumble bee health.
期刊介绍:
The journal Microbial Ecology was founded more than 50 years ago by Dr. Ralph Mitchell, Gordon McKay Professor of Applied Biology at Harvard University in Cambridge, MA. The journal has evolved to become a premier location for the presentation of manuscripts that represent advances in the field of microbial ecology. The journal has become a dedicated international forum for the presentation of high-quality scientific investigations of how microorganisms interact with their environment, with each other and with their hosts. Microbial Ecology offers articles of original research in full paper and note formats, as well as brief reviews and topical position papers.