土地利用强度对德国中部蜱类伯氏疏螺旋体流行率和基因多样性的影响。

IF 3.5 2区 医学 Q1 PARASITOLOGY
Suscha Nicolina Lassen, Christian Imholt, Max Müller, Nina Król, Leonard Gothe, Lara Maria Inge Heyse, Martin Pfeffer, Anna Obiegala
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引用次数: 0

摘要

背景:蜱是人畜共患病原体的重要传播媒介,其中欧洲最丰富和最主要的媒介是莱姆病病原伯氏疏螺旋体(Borrelia burgdorferi, s.l)。媒介和水库宿主都依赖于生境结构,而生境结构受土地利用强度的人为影响。本研究旨在分析德国中部不同土地利用梯度草原和森林蜱中伯氏疏螺旋体的流行情况及其基因多样性。方法:采用标记法在25个草原和25个森林采集蜱虫,采用实时聚合酶链反应法检测伯氏疏螺旋体。采用多位点序列分型对阳性样本进行分析,确定了准确的伯氏疏螺旋体基因种和序列型。结果:收集到的1896只蜱中,疏螺旋体呈阳性210只(11.08%);雌蜱和雄蜱的患病率相同(48/156;30.77%),若虫的患病率较低(118/1152;10.24%)。草地采集的蓖麻伊蚊感染率为29.36%,明显高于林地采集的6.43%。草地和林地的土地利用强度与蜱感染伯氏疏螺旋体呈正相关。此外,捕食性和小型兽类的相对丰度指数对蓖麻螨若虫中疏螺旋体的流行率有正向影响。对184份样本进行多位点序列分型。最常见的基因种是阿氏疏螺旋体(65.76%),其次是加里氏疏螺旋体(17.93%)、瓦莱西疏螺旋体(13.59%)和严格的伯氏疏螺旋体(2.72%)。此外,检测到59个已知序列类型和41个新序列类型。结论:具有人畜共患潜力的伯氏疏螺旋体基因型表现出不同的宿主适应性,这似乎促进了种内病原体的高度多样性。我们的研究结果支持稀释假说,因为它们表明保护原生森林和物种多样性可能支持疏螺旋体的生物多样性,同时降低其总体流行率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Land use intensity has an impact on Borrelia burgdorferi sensu lato prevalence and genodiversity in ticks from Central Germany.

Land use intensity has an impact on Borrelia burgdorferi sensu lato prevalence and genodiversity in ticks from Central Germany.

Land use intensity has an impact on Borrelia burgdorferi sensu lato prevalence and genodiversity in ticks from Central Germany.

Land use intensity has an impact on Borrelia burgdorferi sensu lato prevalence and genodiversity in ticks from Central Germany.

Background: Ticks are important vectors of zoonotic pathogens, with Ixodes ricinus being the most abundant and main vector in Europe of Borrelia burgdorferi sensu lato (s.l.), the causative agent of Lyme borreliosis. Both vector and reservoir hosts are dependent on habitat structure, which is anthropogenically influenced by land use intensity. This study aimed to analyse the prevalence of B. burgdorferi s.l. and their genodiversity in ticks along a land use gradient in grassland and forest in Central Germany.

Methods: Ticks were collected from 25 grassland and 25 forest sites by using the flagging method and tested for Borrelia  spp. using real-time polymerase chain reaction. Positive samples were further analysed by using multi-locus sequence typing to identify the exact B. burgdorferi s.l. genospecies and sequence types. To analyse the prevalence of Borrelia and the density of I. ricinus, confidence intervals, generalized linear mixed models, linear models, generalized linear models (Tweedie distribution), model selection (delta Akaike information criterion corrected for small sample size < 2), relative abundance index and the Shannon index were used.

Results: In total, 210 of the 1896 ticks collected tested positive for Borrelia (11.08%). The prevalence in I. ricinus ticks was identical in females (48/156; 30.77%) and males (44/143; 30.77%) and lower in nymphs (118/1152; 10.24%). Ixodes ricinus collected from grassland were significantly more frequently infected (29.36%) than those from woodland (6.43%). A positive correlation between land use intensity and the infection rate of ticks with B. burgdorferi s.l. was found in both grassland and woodland. Furthermore, the relative abundance index of predatory and small mammals had a positive effect on Borrelia spp. prevalence in I. ricinus nymphs. Multilocus sequence typing was performed for 184 samples. The most frequently found genospecies was Borrelia afzelii (65.76%), followed by Borrelia garinii (17.93%), Borrelia valaisiana (13.59%), and Borrelia burgdorferi sensu stricto (2.72%). Furthermore, 59 known and 41 new sequence types were detected.

Conclusions: Borrelia burgdorferi s.l. genotypes with zoonotic potential show variable host adaptation, which seems to promote high intraspecific pathogen diversity. The results of our study support the dilution hypothesis as they show that conserving native forests and species diversity may support the biodiversity of Borrelia spp. while reducing their overall prevalence.

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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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