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首页> 外文期刊>Ticks and tick-borne diseases >Molecular detection and phylogenetic analysis of Anaplasma marginale and Anaplasma centrale amongst transhumant cattle in north-eastern Uganda
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Molecular detection and phylogenetic analysis of Anaplasma marginale and Anaplasma centrale amongst transhumant cattle in north-eastern Uganda

机译:乌干达东北部牛的牛肾上腺素和Anaplasma Centrale的分子检测和系统发育分析

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摘要

There is little molecular data from Anaplasma marginale and Anaplasma centrale isolates from cattle in Uganda. Between November 2013 and January 2014, blood was collected from 240 cattle in 20 randomly-selected herds in two districts of the Karamoja Region in north-eastern Uganda. A duplex quantitative real-time polymerase chain reaction (qPCR) assay was used to detect and determine the prevalence of A. marginale (targeting the msp1 beta gene) and A. centrale (targeting the groEL gene). The qPCR assay revealed that most cattle (82.9%; 95% confidence interval [CI] 78.2-87.7%) were positive for A. marginale DNA, while fewer cattle (12.1%; 95% CI 7.9-16.2%) were positive for A. centrale DNA. A mixed effects logistic regression model showed that the age of cattle was significantly associated with A. centrale infection, while the prevalence of A. marginale varied significantly according to locality. The near full-length 16S ribosomal RNA (16S rRNA) gene and the heat shock protein gene, groEL, for both Anaplasma species were amplified from a selection of samples. The amplicons were cloned and the resulting recombinants sequenced. We found three novel A. marginale 16S rRNA variants, seven A. marginale groEL gene sequence variants and two A. centrale groEL gene sequence variants. Phylogenetic trees were inferred from sequence alignments of the 16S rRNA gene and GroEL amino acid sequences determined here and published sequences using maximum likelihood, Bayesian inference and parsimony methods Phylogenetic analyses classified the 16S rRNA gene and GroEL amino acid sequences into one clade for A. marginale and a separate clade for A. centrale. This study reveals a high prevalence and sequence variability of A. marginale and A. centrale, and is the first report on the phylogenetic characterisation of A. marginale and A. centrale from cattle in Uganda using molecular markers. Sequence variation can be attributed to mobile pastoralism, communal grazing and grazing with wildlife. These data support future epidemiological investigations for bovine anaplasmosis in Uganda.
机译:来自乌干达的牛的Anplasma Marginale和Anaplasma Centrale分离物的分子数据很少。 2013年11月至2014年1月期间,在乌干达东北部喀拉莫省地区的两个地区的240个牛中收集了血液。双工定量实时聚合酶链反应(QPCR)测定检测并确定A. Marginale(靶向MSP1β基因)的患病率和A. Centrale(靶向腹股沟基因)。 QPCR测定显示大多数牛(82.9%; 95%置信区间[CI] 78.2-87.7%)对于A. Marginale DNA呈阳性,而牛较少(12.1%; 95%CI 7.9-16.2%)是阳性的。Centrale DNA。混合效应逻辑回归模型表明,牛的年龄与A. Centrale感染有显着相关,而A. Marginale的患病率根据地方性差异很大。从各种样品中扩增近全长16S核糖体RNA(16s rRNA)基因和热休克蛋白基因,腹股沟,腹股沟族物种。克隆扩增子,并将得到的重组剂测序。我们发现三个新颖的A. Marginale 16s RRNA变体,七个A. Marginale Groel基因序列变体和两个A. Centrale Groel基因序列变体。从这里测定的16S rRNA基因和腹股沟氨基酸序列的序列比对推断出系统发育树,使用最大可能性,贝叶斯推理和分析方法发表了序列,将16S rRNA基因和腹股沟氨基酸序列分类为A. Marginale的一个疏油液和一个单独的A. Centrale。本研究揭示了A. Marginale和A. Centrale的高普遍性和序列变异性,是第一个关于A. Marginale和A的系统发育表征的第一个报告。使用分子标记的牛牛中的牛中的离心机。序列变异可以归因于移动牧场主,共同放牧和用野生动物放牧。这些数据支持乌干达的未来流行病学调查。

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