Detection of bacterial and protozoan pathogens in individual bats and their ectoparasites using high-throughput microfluidic real-time PCR

Author:

Corduneanu Alexandra12ORCID,Zając Zbigniew3,Kulisz Joanna3,Wozniak Aneta3,Foucault-Simonin Angélique4,Moutailler Sara4,Wu-Chuang Alejandra4,Peter Áron25,Sándor Attila D.256,Cabezas-Cruz Alejandro4ORCID

Affiliation:

1. Department of Animal Breeding and Animal Production, University of Agricultural Sciences and Veterinary Medicine , Cluj-Napoca, Romania

2. Department of Parasitology and Parasitic Diseases, University of Agricultural Sciences and Veterinary Medicine , Cluj-Napoca, Romania

3. Department of Biology and Parasitology, Medical University of Lublin , Lublin, Poland

4. ANSES, INRAE, Ecole Nationale Vétérinaire d’Alfort, UMR BIPAR, Laboratoire de Santé Animale , Maisons-Alfort, France

5. Department of Parasitology and Zoology, University of Veterinary Medicine , Budapest, Hungary

6. ELKH-ÁTE Climate Change: New Blood-sucking Parasites and Vector-borne Pathogens Research Group , Budapest, Hungary

Abstract

ABSTRACT Among the most studied mammals in terms of their role in the spread of various pathogens with possible zoonotic effects are bats. These are animals with a very complex lifestyle, diet, and behavior. They are able to fly long distances, thus maintaining and spreading the pathogens they may be carrying. These pathogens also include vector-borne parasites and bacteria that can be spread by ectoparasites such as ticks and bat flies. In the present study, high-throughput screening was performed and we detected three bacterial pathogens: Bartonella spp., Neoehrlichia mikurensis and Mycoplasma spp., and a protozoan parasite: Theileria spp. in paired samples from bats (blood and ectoparasites). In the samples from the bat-arthropod pairs, we were able to detect Bartonella spp. and Mycoplasma spp. which also showed a high phylogenetic diversity, demonstrating the importance of these mammals and the arthropods associated with them in maintaining the spread of pathogens. Previous studies have also reported the presence of these pathogens, with one exception, Neoehrlichia mikurensis , for which phylogenetic analysis revealed less genetic divergence. High-throughput screening can detect more bacteria and parasites at once, reduce screening costs, and improve knowledge of bats as reservoirs of vector-borne pathogens. IMPORTANCE The increasing number of zoonotic pathogens is evident through extensive studies and expanded animal research. Bats, known for their role as reservoirs for various viruses, continue to be significant. However, new findings highlight the emergence of Bartonella spp., such as the human-infecting B. mayotimonensis from bats. Other pathogens like N. mikurensis , Mycoplasma spp., and Theileria spp. found in bat blood and ectoparasites raise concerns, as their impact remains uncertain. These discoveries underscore the urgency for heightened vigilance and proactive measures to understand and monitor zoonotic pathogens. By deepening our knowledge and collaboration, we can mitigate these risks, safeguarding human and animal well-being.

Funder

Agence Nationale de la Recherche

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology

Reference139 articles.

1. A Molecular Phylogeny for Bats Illuminates Biogeography and the Fossil Record

2. Dietz C von Helversen O . 2004. Illustrated identification key to the bats of Europe

3. Dietz C , von Helversen O , Nill D , Lina PH , Hutson AM . 2009. Bats of Britain, Europe and northwest Africa. A & C Black London.

4. Bats as ‘special’ reservoirs for emerging zoonotic pathogens

5. Detection of novel coronaviruses in bats in Myanmar

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Molecular survey of hemoplasmas and Coxiella burnetii in vampire bats from northern Brazil;Comparative Immunology, Microbiology and Infectious Diseases;2024-03

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3