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Molecular analysis of microbial communities identified in different developmental stages of Ixodes scapularis ticks from Westchester and Dutchess Counties, New York

机译:来自纽约州威彻斯特和荷兰郡的in肩x不同发育阶段鉴定的微生物群落的分子分析

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Ixodes scapularis ticks play an important role in the transmission of a wide variety of pathogens between various mammalian species, including humans. Pathogens transmitted by ticks include Borrelia, Anaplasma and Babesia. Although ticks may harbour both pathogenic and non-pathogenic microflora, little is known about how the diversity of the microflora within ticks may influence the transmission of pathogens. To begin addressing this question, we examined the composition of bacterial communities present in Ixodes scapularis collected from Westchester and Dutchess Counties, New York State, at different developmental and nutritional stages. Genetic fingerprints of bacterial populations were generated by temporal temperature gradient gel electrophoresis (TTGE) separation of individual polymerase chain reaction (PCR)-amplified 16S rRNA gene fragments, followed by DNA sequence analysis for bacterial identification. The fingerprints of the TTGE bands were grouped into five clusters. The most abundant DNA sequence found in all the samples was Rickettsia, followed by Pseudomonas and Borrelia. Ralstonia, Anaplasma, Enterobacterias, Moraxella, Rhodococcus and uncultured proteobacterium were present as well. We also determined the prevalence of Anaplasma phagocytophilum and Borrelia burgdorferi by PCR and DNA sequence analysis. Statistical analyses indicated significant variations in the bacterial communities depending on tick developmental stage and degree of engorgement. We suggest that these two elements affect microbial diversity within the tick and may in turn influence pathogen transmission to humans and animals after tick bite.
机译:肩cap虫在包括人类在内的各种哺乳动物物种之间传播多种病原体中起着重要作用。壁虱传播的病原体包括疏螺旋体,无浆膜和巴贝斯虫。尽管tick可能同时包含致病性和非致病性微生物区系,但人们对tick内部的微生物区系多样性如何影响病原体的传播知之甚少。为了开始解决这个问题,我们研究了在纽约州威彻斯特和荷兰郡的不同发育和营养阶段收集的肩I虾中细菌群落的组成。细菌种群的遗传指纹图谱是通过瞬时温度梯度凝胶电泳(TTGE)分离单个聚合酶链反应(PCR)扩增的16S rRNA基因片段而产生的,然后进行DNA序列分析以鉴定细菌。 TTGE谱带的指纹分为五个簇。在所有样品中发现的最丰富的DNA序列是立克次体,其次是假单胞菌和疏螺旋体。还存在Ralstonia,无形体,肠杆菌,莫拉氏菌,红球菌和未培养的变形杆菌。我们还通过PCR和DNA序列分析确定了嗜噬细胞无形体和伯氏疏螺旋体的患病率。统计分析表明,取决于tick的发育阶段和充血程度,细菌群落的显着变化。我们建议这两个因素影响the内部的微生物多样性,并可能进而影响pathogen咬后病原体向人和动物的传播。

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