Pathogens and symbionts in ticks: prevalence of Anaplasma phagocytophilum (Ehrlichia sp.), Wolbachia sp., Rickettsia sp., and Babesia sp. in Southern Germany

Kathrin Hartelt , Rainer Oehme , Henning Frank , Stefan O. Brockmann , Dieter Hassler , Peter Kimmig
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引用次数: 159

Abstract

Tick-transmitted diseases like tick-borne encephalitis and Lyme borreliosis have been well known in Germany for decades. Ongoing research now gives an additional focus to a broad range of other bacteria and parasites in ticks like Anaplasma phagocytophilum, former Ehrlichia sp., Rickettsia sp. and Babesia sp. Knowledge about the prevalence of these infectious agents in ticks is an important prerequisite for risk assessment of human diseases. Therefore nymphs and adult Ixodes ricinus ticks were collected and examined for Anaplasma phagocytophilum (n = 5424 ticks), Rickettsia sp. (n = 1187), and Babesia sp. (n - 3113). For the detection of Anaplasma phagocytophilum, DNA from the 16S rDNA gene was amplified by nested PCR and hybridized with a DIG-labeled oligonucleotide probe. The examination of Rickettsia sp. was performed by single PCR. A partial sequence of the citrate synthase gene was amplified. As a target for the detection of Babesia sp., DNA from the 18S rDNA gene was amplified, also by single PCR. All positive PCR products were sequenced to control specificity.

Anaplasma phagocytophilum was detected by PCR in n = 103 (1.9%) out of 5,424 examined ticks from 11 investigation areas. However, not all positive PCR products hybridized using DIG-labeled oligonucleotide probe. Thus, the result of sequencing indicated that only 1.0% (n = 54) belonged to Anaplasma phagocytophilum and nearly half of these PCR products (0.9%) were identified as Wolbachia sp.

Rickettsia sp. in Ixodes ricinus ticks from 3 areas were found in n = 105 (8.9%) out of 1,187 ticks examined (range from 13.3% to 5.6%). Sequencing showed Rickettsia helvetica exclusively. In about 2.6% of Rickettsia-positive ticks, double infection with Anaplasma phagocytophilum was found.

Babesia sp. was detected in n = 31 (1.0%) out of 3,113 ticks examined, which originated from 4 different areas. By sequencing, n = 28 (90.0%) were identified as Babesia divergens. Three of all Babesia — positive ticks were identified as harboring Babesia microti.

The detection of Anaplasma phagocytophilum, Rickettsia sp. and Babesia sp. demonstrates their possible role as a source of human infection in Germany.

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蜱中的病原体和共生体:德国南部嗜吞噬细胞无形体(埃利希氏体)、沃尔巴克氏体、立克次体和巴贝斯虫的流行
蜱传疾病,如蜱传脑炎和莱姆病,在德国已经众所周知了几十年。目前正在进行的研究将更多的重点放在蜱虫中其他广泛的细菌和寄生虫上,如嗜吞噬细胞无原体、前埃利希氏体、立克次体和巴贝斯虫。了解这些传染性病原体在蜱虫中的流行情况是评估人类疾病风险的重要先决条件。为此,采集蓖麻蜱若虫和成虫,检测嗜吞噬细胞无形体(5424只)、立克次体(1187只)和巴贝斯虫(3113只)。为了检测嗜吞噬细胞无原体,采用巢式PCR扩增16S rDNA基因DNA,并与dig标记的寡核苷酸探针杂交。立克次体检测采用单PCR法。扩增了柠檬酸合酶基因的部分序列。作为检测巴贝斯虫的靶点,从18S rDNA基因中扩增出DNA,同样采用单次PCR。所有阳性PCR产物测序以控制特异性。11个调查地区5424只蜱中,PCR检出嗜吞噬细胞无原体103只(1.9%)。然而,并不是所有阳性PCR产物都使用digi标记的寡核苷酸探针进行杂交。因此,测序结果显示,只有1.0% (n = 54)属于嗜吞噬细胞无原体,近一半(0.9%)的PCR产物被鉴定为沃尔巴克氏体,来自3个地区的1187只蜱(13.3% ~ 5.6%)中,有105只蜱(8.9%)检出立克次体。测序仅显示helvetica立克次体。在约2.6%的立克次体阳性蜱中,发现有嗜吞噬细胞无原体双重感染。3113只蜱中检出巴贝斯虫31只(1.0%),来自4个不同地区。通过测序,鉴定出分化巴贝斯虫28例(90.0%)。所有巴贝斯虫阳性蜱中有3只被鉴定为携带微小巴贝斯虫。吞噬细胞无原体、立克次体和巴贝斯虫的检测表明它们可能是德国人类感染的一个来源。
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