A comparative study of the microbiomes of the ticks Rhipicephalus microplus and Hyalomma anatolicum.

IF 2.3 2区 医学 Q2 PARASITOLOGY Parasite Pub Date : 2024-01-01 Epub Date: 2024-11-28 DOI:10.1051/parasite/2024074
Adeel Mumtaz Abbasi, Shiza Nasir, Amna Arshad Bajwa, Haroon Akbar, Muhammad Muddassir Ali, Muhammad Imran Rashid
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Abstract

Hyalomma anatolicum and Rhipicephalus microplus are tick species that are important vectors of numerous pathogens affecting both humans and livestock. Endosymbionts, such as Coxiella-like endosymbionts (CLE), Francisella-like endosymbionts (FLE), and Candidatus Midichloria, play a crucial role in the physiology and vector competence of these ticks. In this study, we investigated the microbial composition of H. anatolicum and R. microplus from four geographically distinct regions of Pakistan to assess whether environmental differences influence their microbiomes. We analyzed the ticks' gut microbiome targeting the V3-V4 hypervariable region of 16S rRNA for Illumina 16S metagenome NGS sequencing and processed overall 144 ticks. Analysis of gut bacterial composition resulted in observation of 1200 R. microplus and 968 H. anatolicum unique amplicon sequencing variants (ASVs). Relative abundance, Alpha diversity (Shannon, Faith's phylogenetic distance) and beta diversity metrics (Bray-Curtis, Jaccard and UniFrac) were analyzed and revealed that H. anatolicum ticks have significantly unique and diverse microbial communities with Acinetobacter indicus and Francisella-like endosymbionts dominating as opposed to Candidatus Midichloria. Rhipicephalus microplus exhibited results consistent with the previous studies with no major changes in microbiome including Coxiella-like endosymbionts as the major contributor. These findings suggest that geographical and environmental factors play a significant role in shaping the tick microbiome, with potential consequences for disease transmission and tick survivability. Further research is needed to elucidate the functional roles of these microbial shifts and their impact on public health and livestock in affected regions.

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微头蜱和鸭眼蜱微生物组的比较研究。
猪眼透明瘤和微型鼻头蜱是影响人类和牲畜的许多病原体的重要媒介。Coxiella-like内共生体(CLE)、Francisella-like内共生体(FLE)和Midichloria Candidatus在蜱的生理和媒介能力中起着至关重要的作用。在这项研究中,我们研究了来自巴基斯坦四个地理上不同地区的H. anatolicum和R. microplus的微生物组成,以评估环境差异是否会影响它们的微生物组。我们针对16S rRNA的V3-V4高变区对蜱的肠道微生物组进行了Illumina 16S宏基因组NGS测序,共处理了144只蜱。通过对肠道细菌组成的分析,观察到1200个微弧菌和968个安纳托利菌独特扩增子测序变异(asv)。通过对相对丰度、α多样性(Shannon, Faith’s系统发育距离)和β多样性指标(bry - curtis, Jaccard和UniFrac)的分析,发现H. anatolicum蜱的微生物群落具有显著的独特性和多样性,其中不动杆菌(Acinetobacter indicus)和Francisella-like内共生菌占主导地位,而Midichloria则占主导地位。微加Rhipicephalus microplus的结果与以往的研究结果一致,微生物组没有发生重大变化,其中coxiella样内共生体是主要贡献者。这些发现表明,地理和环境因素在形成蜱微生物组方面发挥着重要作用,对疾病传播和蜱的生存能力具有潜在影响。需要进一步的研究来阐明这些微生物转移的功能作用及其对受影响地区公共卫生和牲畜的影响。
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来源期刊
Parasite
Parasite 医学-寄生虫学
CiteScore
5.50
自引率
6.90%
发文量
49
审稿时长
3 months
期刊介绍: Parasite is an international open-access, peer-reviewed, online journal publishing high quality papers on all aspects of human and animal parasitology. Reviews, articles and short notes may be submitted. Fields include, but are not limited to: general, medical and veterinary parasitology; morphology, including ultrastructure; parasite systematics, including entomology, acarology, helminthology and protistology, and molecular analyses; molecular biology and biochemistry; immunology of parasitic diseases; host-parasite relationships; ecology and life history of parasites; epidemiology; therapeutics; new diagnostic tools. All papers in Parasite are published in English. Manuscripts should have a broad interest and must not have been published or submitted elsewhere. No limit is imposed on the length of manuscripts, but they should be concisely written. Papers of limited interest such as case reports, epidemiological studies in punctual areas, isolated new geographical records, and systematic descriptions of single species will generally not be accepted, but might be considered if the authors succeed in demonstrating their interest.
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