野外异地诊断:调查鸣禽水库中蜱传细菌传染性的方法

Jens Zarka , Dieter Heylen , Hein Sprong , Manoj Fonville , Joris Elst , Erik Matthysen
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引用次数: 0

摘要

预测自然系统中感染的持续性和传播的一个关键因素是贮存宿主维持感染并将其传播给其他人的能力。众所周知,在物种内部、物种之间以及不同时期,这种能力会有很大的差异,但在野外,对后一部分差异的了解往往较少。鲍瑞氏菌是人类莱姆病的病原体之一,通过硬蜱 Ixodes ricinus 在鸟类宿主中传播。在欧洲,大山雀是已知的 B. garinii 的储库。对于像B. garinii这样的蜱媒病原体,可以使用异种诊断法来测量传染性或宿主到媒介的传播,即用无病原体的媒介喂养宿主,然后对吸血媒介进行病原体检测。在这里,我们描述并评估了一种量化野生大山雀(Parus major)个体对蜱传病原体感染性的方法,包括捕获和重新捕获目标个体。在重新捕获有足够保障的情况下,该方法也有可能应用于其他物种。我们在初次感染后两到三天(即蜱虫完全进食之前)成功地重新捕获了大部分受感染的大山雀,并获得了足够数量的蓖麻蜱幼蜱,随后使用新开发的蓖麻蜱特异性实时 PCR 检测法对这些蓖麻蜱幼蜱进行了 B. garinii 检测。与冬季相比,繁殖季节从鸟类身上发现的蜱虫幼虫数量更多。我们的新型 B. garinii-qPCR 性能良好,大大减少了所需的 Sanger 测序量。初步结果表明,鸟类的传染性既有季节性差异,也有个体差异;要想进一步了解留鸟对 B. garinii 流行病学的贡献,还需要揭示这种异质性。
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Xenodiagnosis in the wild: A methodology to investigate infectiousness for tick-borne bacteria in a songbird reservoir

A crucial factor to predict the persistence and spread of infections in natural systems is the capacity of reservoir hosts to maintain the infection and transmit it to others. This is known to greatly vary within and between species and through time, although the latter part of the variation is often less well understood in the wild. Borrelia garinii is one of the causal agents of Lyme disease in humans and is transmitted among avian hosts by the hard tick Ixodes ricinus. Great tits are known to be a reservoir in Europe for B. garinii. For tick-borne pathogens like B. garinii, infectiousness or host-to-vector transmission can be measured using xenodiagnosis where pathogen-free vectors are fed on a host, and the blood-fed vectors are subsequently tested for the pathogen. Here we describe and evaluate a methodology to quantify infectiousness for tick-borne pathogens in individual wild great tits (Parus major), involving captures and recaptures of targeted individuals. The methodology can potentially be applied to other species where recapturing is sufficiently guaranteed. We successfully recaptured most of the infested great tits two to three days after initial infestation (i.e. just before ticks have fully fed) with sufficient numbers of I. ricinus larval ticks, which were subsequently screened for B. garinii using a newly developed B. garinii-specific real-time PCR assay. Higher larval tick numbers were recovered from birds during the breeding seasons than during the winter months. Our novel B. garinii-qPCR performed well, and greatly reduced the amount of Sanger sequencing needed. Preliminary results suggest both seasonal and individual variation in infectiousness; heterogeneity that needs to be unravelled to further understand the contribution of resident birds to the epidemiology of B. garinii.

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