Diversity of the Ixodes ricinus Microbiome Across Belgian Ecoregions and Its Association with Pathogen and Symbiont Presence.

IF 3.3 3区 生物学 Q2 ECOLOGY
Camille Philippe, Lianet Abuin Denis, Manoj Fonville, Bert Devriendt, François E Dufrasne, Dasiel Obregon, Apolline Maître, Štefánia Skičková, Eric Cox, Hein Sprong, Alejandro Cabezas Cruz, Marcella Mori
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引用次数: 0

Abstract

Ticks are important vectors of zoonotic pathogens, and their presence can be influenced by the composition of the tick microbiome. In turn, this microbiome is shaped by environmental and ecological factors, as demonstrated in several studies conducted under controlled conditions. However, the extent of these influences under natural ecological conditions remains underexplored. In this study, we investigated the diversity of the microbiome and the prevalence of pathogens in Ixodes ricinus nymphs across three distinct Belgian ecoregions: Sandy Loam, Condroz, and Ardennes. Using real-time quantitative PCR (qPCR) and Oxford Nanopore 16S rRNA sequencing, we assessed how geography and pathogen presence influence tick-associated microbial communities. Our results revealed significant regional differences in microbiome composition and pathogen prevalence. Borrelia burgdorferi sensu lato (s.l.) was most prevalent in the Ardennes (9% (7.4-10.9) vs 3.8% (2.8-5.2) in the Condroz and 2.1% (1.4-3.2) in Sandy Loam) while Anaplasma phagocytophilum was more common in the Sandy Loam region (21.1% (18.7-23.8) vs 4% (3-5.4) in the Condroz and 3.2% (2.2-4.4) in the Ardennes). Endosymbionts such as Midichloria mitochondrii and Spiroplasma ixodetis also exhibited distinct geographic distributions. Network analysis identified potential pathogen-microbiota interactions, with certain bacterial taxa showing positive or negative associations with specific pathogens. Moreover, microbiome composition was influenced not only by ecoregion but also by microorganisms such as Rickettsia helvetica, suggesting that its colonization may actively shape microbial community structure, potentially through competition or facilitation mechanisms. Additionally, microbiome network robustness varied across ecoregions, highlighting the role of ecological context in shaping microbial interactions within ticks. These findings underscore the complex interplay between geography, pathogen presence, and microbial diversity in ticks, highlighting the importance of integrating these interactions to inform microbiome-based strategies for vector control and disease prevention.

比利时各生态区蓖麻蜱微生物群的多样性及其与病原体和共生体存在的关系。
蜱是人畜共患病原体的重要传播媒介,其存在受蜱微生物群组成的影响。反过来,这种微生物组是由环境和生态因素塑造的,正如在受控条件下进行的几项研究所证明的那样。然而,这些影响在自然生态条件下的程度仍未得到充分探讨。在这项研究中,我们调查了比利时三个不同生态区(Sandy Loam, Condroz和Ardennes)的蓖麻伊蚊(Ixodes ricinus)的微生物群多样性和病原体流行率。利用实时定量PCR (qPCR)和牛津纳米孔16S rRNA测序,我们评估了地理位置和病原体存在对蜱虫相关微生物群落的影响。我们的研究结果揭示了微生物组组成和病原体流行的显著区域差异。伯氏疏螺旋体(Borrelia burgdorferi senu lato)在阿登地区最常见(9% (7.4-10.9)vs 3.8%(2.8-5.2),沙壤土地区2.1%(1.4-3.2)),而嗜吞噬细胞无形体在沙壤土地区更常见(21.1% (18.7-23.8)vs 4%(3-5.4),阿登地区3.2%(2.2-4.4))。内共生体如线粒体Midichloria和螺原体ixodetis也表现出不同的地理分布。网络分析确定了潜在的病原体-微生物群相互作用,某些细菌分类群与特定病原体表现出正相关或负相关。此外,微生物组组成不仅受到生态区域的影响,还受到helvetica立克次体等微生物的影响,这表明其定植可能通过竞争或促进机制积极塑造微生物群落结构。此外,微生物组网络的稳健性在不同的生态区域有所不同,突出了生态环境在塑造蜱虫内微生物相互作用中的作用。这些发现强调了蜱中地理、病原体存在和微生物多样性之间复杂的相互作用,强调了整合这些相互作用以告知基于微生物组的媒介控制和疾病预防策略的重要性。
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来源期刊
Microbial Ecology
Microbial Ecology 生物-海洋与淡水生物学
CiteScore
6.90
自引率
2.80%
发文量
212
审稿时长
3-8 weeks
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.
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