Maitre Apolline, Kratou Myriam, Cano-Argüelles Ana Laura, Porcelli Stefania, Abuin-Denis Lianet, Piloto-Sardiñas Elianne, Mateos-Hernández Lourdes, Obregon Dasiel, Tonk-Rügen Miray, Abdelali Salma Kaoutar, Moutailler Sara, Cabezas-Cruz Alejandro
ANSES, INRAE, Ecole Nationale Vétérinaire d'Alfort, UMR BIPAR, Laboratoire de Santé Animale, Maisons-Alfort, France.
INRAE, UR 0045 Laboratoire de Recherches sur le Développement de l'Elevage (SELMET-LRDE), Corte, France.
Int J Microbiol. 2025 Jun 21;2025:7747795. doi: 10.1155/ijm/7747795. eCollection 2025.
Ticks, particularly , are significant vectors of pathogens such as spp. and tick-borne encephalitis virus (TBEV), which cause Lyme borreliosis (LB) and tick-borne encephalitis (TBE), respectively. Understanding how these pathogens interact within the tick microbiome is essential for developing vector control strategies. This study investigates the impact of and TBEV, as well as their coinfection, on the microbiota composition and structure of nymphs. Using a network-based approach, we analyzed the microbial communities of ticks exposed to infected or coinfected mice. DNA extracted from newly molted nymphs was sequenced for the bacterial 16S rRNA gene, and microbial diversity metrics (alpha and beta diversity) were calculated. Our results showed that TBEV infection increased microbiome diversity compared to the uninfected and groups. Co-occurrence network analyses revealed that while microbial structures remained consistent across conditions, TBEV-infected networks exhibited higher robustness to perturbations, indicating a stabilizing effect on the tick microbiome. Furthermore, the hierarchical position and associations of varied significantly depending on the infection scenario, highlighting its adaptive role within the tick microbiota. The study demonstrates that pathogen presence alters tick microbial dynamics, with TBEV enhancing stability, suggesting virus-mediated modifications of the microbiome. These findings advance our understanding of pathogen-tick-microbiome interactions and provide insights into the ecological mechanisms underlying pathogen coexistence within ticks. This research underscores the importance of microbial networks in ticks and offers new perspectives for targeted approaches in managing tick-borne diseases.
蜱虫,尤其是[具体种类未提及],是诸如[具体病原体种类未提及]属和蜱传脑炎病毒(TBEV)等病原体的重要传播媒介,它们分别导致莱姆病(LB)和蜱传脑炎(TBE)。了解这些病原体如何在蜱虫微生物组内相互作用对于制定病媒控制策略至关重要。本研究调查了[具体病原体未提及]和TBEV及其共同感染对[具体蜱虫种类未提及]若虫微生物群组成和结构的影响。使用基于网络的方法,我们分析了暴露于感染或共同感染小鼠的蜱虫的微生物群落。从新蜕皮的若虫中提取的DNA对细菌16S rRNA基因进行测序,并计算微生物多样性指标(α和β多样性)。我们的结果表明,与未感染和[具体病原体未提及]组相比,TBEV感染增加了微生物组多样性。共现网络分析表明,虽然微生物结构在不同条件下保持一致,但TBEV感染的网络对扰动表现出更高的稳健性,表明对蜱虫微生物组有稳定作用。此外,[具体病原体未提及]的层次位置和关联根据感染情况有显著差异,突出了其在蜱虫微生物群中的适应性作用。该研究表明病原体的存在会改变蜱虫微生物动态,TBEV增强了稳定性,表明病毒介导了微生物组的修饰。这些发现推进了我们对病原体-蜱虫-微生物组相互作用的理解,并为蜱虫体内病原体共存的生态机制提供了见解。这项研究强调了蜱虫中微生物网络的重要性,并为管理蜱传疾病的靶向方法提供了新的视角。