突尼斯蜱虫中卢西塔尼亚包柔氏菌的检测和基因鉴定

Rachid Selmi , Khaoula Abdi , Hanène Belkahia , Meriem Ben Abdallah , Aymen Mamlouk , Myriam Kratou , Mourad Ben Said , Lilia Messadi
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摘要

方法本研究旨在确定从突尼斯北部采集的共存蓖麻蜱和inopinatus蜱中的勃氏杆菌的流行率和系统发育。2020 年冬季,研究人员在突尼斯北部的贝哈省(Beja gouvernorate)采用拖蜱法收集了 100 只蜱虫。进行了针对 B. burgdorferi s.l. 23S rRNA 基因的实时 PCR 检测。使用引物 FlaF/FlaR 对阳性 DNA 样品进行传统 PCR 检测,检测波氏杆菌鞭毛蛋白(la)基因的 457 bp 片段。对鉴定出的包柔氏菌分离物进行了部分序列分析,以确定包柔氏菌的种属并评估其系统发育位置。不同种类和性别的蜱虫感染率差异不大(p > 0.05)。有趣的是,这项研究强调,在突尼斯北部,I. inopinatus 和 I. ricinus 在同一地理区域共存。此外,突尼斯首次在I. inopinatus蜱虫体内检测到了B.所发现的 B. lusitaniae 细菌与之前在地中海地区发现的菌株相似,但与只从塞尔维亚、罗马尼亚和波兰等东欧和中欧国家分离出来的菌株不同。本研究强调了 B. burgdorferi s.l. 在 I. ricinus/I. inopinatus 蜱虫中的流行情况,并首次在突尼斯 I. inopinatus 蜱虫中发现了 B. lusitaniae。这可能有助于了解 Ixodes ticks 的生态学、自然感染以及鲍瑞氏杆菌在该国的传播动态。
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Detection and genetic identification of Borrelia lusitaniae in questing Ixodes inopiatus tick from Tunisia

Background

Until now, there has been limited information on the prevalence and the phylogeny of Borrelia burgdorferi sensu lato in Ixodes ticks in Tunisia, particularly in Ixodes inopinatus.

Methods

The present study aimed to determine the prevalence and the phylogeny of B. burgdorferi s.l., in coexisted I. ricinus and I. inopinatus ticks collected from Northern Tunisia. One hundred questig ticks were collected during winter 2020 by tick-dragging method in Beja gouvernorate located in the north of Tunisia. Real-time PCR panel targeting B. burgdorferi s.l. 23S rRNA gene were performed. Positive DNA samples were subjected to conventional PCRs targeting 457 bp fragment of the Borrelia sp. flagellin (fla) gene using primers FlaF/FlaR. The identified Borrelia sp. isolate underwent partial sequence analysis to determine genospecies and evaluate their phylogenetic position.

Results

The study revealed a prevalence rate of 28% (28/100) for B. burgdorferi sensu lato in the Ixodes ticks. The prevalence rates across tick species and genders did not show significant variations (p > 0.05). Interestingly, the study underlines the coexistence of I. inopinatus and I. ricinus sharing the same geographic areas in Northern Tunisia. Furthermore, DNA of B. lusitaniae was detected in I. inopinatus ticks for the first time in Tunisia. Revealed B. lusitaniae bacterium is similar to previously identified strains in Mediterranean region, but distinct from those isolated exclusively from countries of Eastern and Central Europe, such as Serbia, Romania, and Poland. This study highlights the prevalence of B. burgdorferi s.l. in I. ricinus/I. inopinatus ticks, and reveals B. lusitaniae in I. inopinatus ticks for the first time in Tunisia.

Conclusion

These findings suggest the involvement of I. inopinatus as a potential vector of this pathogenic genospeciess in Tunisia. This may help understanding the ecology of Ixodes ticks, the natural infection and the transmission dynamics of Borrelia species in this country.

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