Molecular Survey of Anaplasmataceae Agents, Rickettsia spp., Bartonella spp., and Piroplasmids in Ectoparasites from Cave-Dwelling Bats in Mainland Portugal.

IF 3.3 3区 医学 Q2 MICROBIOLOGY
Gustavo Seron Sanches, Luísa Rodrigues, Estefania Torrejón, Ricardo Bassini-Silva, Ana Cláudia Calchi, Daniel Antônio Braga Lee, Paulo Vitor Cadina Arantes, Eder Barbier, Darci Moraes Barros-Battesti, Gustavo Graciolli, Rosangela Zacarias Machado, Sandra Antunes, Ana Domingos, Marcos Rogério André
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Abstract

Bats and their ectoparasites play a crucial role in understanding the ecology and transmission of vector-borne pathogens, yet these dynamics remain poorly studied in Portugal. This study aimed to investigate the molecular occurrence of vector-borne bacteria (Anaplasma spp., Bartonella spp., Ehrlichia spp., and Rickettsia spp.) and protozoa (Babesia spp. and Theileria spp.) in ectoparasites of cave-dwelling bats. Bats were sampled from two caves in Portugal, and their ectoparasites included wing mites (Spinturnix myoti), ticks (Ixodes simplex), and bat flies (Penicillidia conspicua and Nycteribia schmidlii). Molecular analyses revealed the presence of Bartonella spp. in S. myoti and N. schmidlii. Phylogenetic inference based on the gltA gene positioned the detected genotypes close to those previously reported in bats and Nycteribiidae flies in Europe, Asia, and Africa. Notably, no DNA from Anaplasmataceae, Rickettsia spp., or piroplasmids was detected. The prevalence of S. myoti was high, with all examined bats being infested, showing notable differences in ectoparasite diversity concerning sex and cave-specific location. These findings suggest that host behavior, environmental conditions, and ectoparasite lifecycles play critical roles in shaping pathogen transmission dynamics. This study advances the understanding of bat ectoparasite-pathogen interactions in a region with limited data and highlights the need for continued research to assess the zoonotic potential and ecological impacts of the Bartonella genotypes detected herein.

蝙蝠及其体外寄生虫在了解病媒传播病原体的生态学和传播方面起着至关重要的作用,但葡萄牙对这些动态的研究仍然很少。本研究旨在调查穴居蝙蝠体外寄生虫中病媒传播细菌(阿那普拉斯菌属、巴顿氏菌属、埃立克次体属和立克次体属)和原生动物(巴贝斯菌属和泰勒菌属)的分子发生情况。蝙蝠的体外寄生虫包括翼螨(Spinturnix myoti)、蜱(Ixodes simplex)和蝠蝇(Penicillidia conspicua 和 Nycteribia schmidlii)。分子分析表明,S. myoti 和 N. schmidlii 中存在巴顿氏菌属。基于 gltA 基因的系统发育推断将检测到的基因型定位为与之前在欧洲、亚洲和非洲的蝙蝠和 Nycteribiidae 苍蝇中报告的基因型接近。值得注意的是,没有检测到来自Anaplasmataceae、立克次体属或piroplasmids的DNA。S.myoti的感染率很高,所有受检蝙蝠都受到感染,这表明外寄生虫的多样性在性别和洞穴特定位置方面存在明显差异。这些发现表明,宿主行为、环境条件和外寄生虫的生命周期在形成病原体传播动态方面起着关键作用。这项研究加深了人们对数据有限的地区蝙蝠体外寄生虫与病原体之间相互作用的了解,并强调了继续开展研究以评估本文检测到的巴顿氏菌基因型的人畜共患可能性和生态影响的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pathogens
Pathogens Medicine-Immunology and Allergy
CiteScore
6.40
自引率
8.10%
发文量
1285
审稿时长
17.75 days
期刊介绍: Pathogens (ISSN 2076-0817) publishes reviews, regular research papers and short notes on all aspects of pathogens and pathogen-host interactions. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodical details must be provided for research articles.
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