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Cryptosporidium species and subtypes in animals inhabiting drinking water catchments in three states across Australia

机译:澳大利亚三个州居住在饮水区的动物的隐孢子虫种类和亚型

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As part of long-term monitoring of Cryptosporidium in water catchments serving Western Australia, New South Wales (Sydney) and Queensland, Australia, we characterised Cryptosporidium in a total of 5774 faecal samples from 17 known host species and 7 unknown bird samples, in 11 water catchment areas over a period of 30 months (July 2013 to December 2015). All samples were initially screened for Cryptosporidium spp. at the 18S rRNA locus using a quantitative PCR (qPCR). Positives samples were then typed by sequence analysis of an 825 bp fragment of the 18S gene and subtyped at the glycoprotein 60 (gp60) locus (832 bp). The overall prevalence of Cryptosporidium across the various hosts sampled was 18.3% (1054/5774; 95% CI, 17.3-19.3). Of these, 873 samples produced clean Sanger sequencing chromatograms, and the remaining 181 samples, which initially produced chromatograms suggesting the presence of multiple different sequences, were re-analysed by Next- Generation Sequencing (NGS) to resolve the presence of Cryptosporidium and the species composition of potential mixed infections. The overall prevalence of confirmed mixed infection was 1.7% (98/5774), and in the remaining 83 samples, NGS only detected one species of Cryptosporidium. Of the 17 Cryptosporidium species and four genotypes detected (Sanger sequencing combined with NGS), 13 are capable of infecting humans; C parvum, C hominis, C ubiquitum, C cuniculus, C meleagridis, C canis, C. fells, C muris, C suis, C scrofarum, C bovis, C erinacei and C fayeri. Oocyst numbers per gram of faeces (g(-1)) were also determined using qPCR, with medians varying from 6021-61,064 across the three states. The significant findings were the detection of C hominis in cattle and kangaroo faeces and the high prevalence of C parvum in cattle. In addition, two novel C fayeri subtypes (1VaA11G3T1 and 1VgA10G1T1R1) and one novel C meleagridis subtype (IIIeA18G2R1) were identified. This is also the first report of C. erinacei in Australia. Future work to monitor the prevalence of Cryptosporidium species and subtypes in animals in these catchments is warranted. (C) 2018 Elsevier Ltd. All rights reserved.
机译:作为对西澳大利亚州,新南威尔士州(悉尼)和澳大利亚昆士兰州的水域中的隐孢子虫进行长期监测的一部分,我们在11个已知宿主物种和7个未知鸟类样品的总共5774份粪便样品中鉴定了隐孢子虫的特征30个月(2013年7月至2015年12月)内的集水区。最初筛选所有样品的隐孢子虫属。使用定量PCR(qPCR)在18S rRNA基因座上进行检测。然后通过对18S基因的825 bp片段进行序列分析来对阳性样品进行分型,并在糖蛋白60(gp60)位点(832 bp)处进行亚型分析。在所有采样的宿主中,隐孢子虫的总体患病率为18.3%(1054/5774; 95%CI,17.3-19.3)。在这些样品中,有873个样品产生了纯净的Sanger测序色谱图,其余181个最初产生色谱图的样品表明存在多个不同的序列,通过下一代测序(NGS)进行了重新分析,以解决隐孢子虫和该物种的存在。潜在的混合感染的组成。确诊混合感染的总体患病率为1.7%(98/5774),在其余的83个样本中,NGS仅检测到一种隐孢子虫。在检测到的17种隐孢子虫物种和四种基因型中(桑格测序与NGS结合使用),有13种能够感染人类。 C小花,Chominis,C遍在,C小球,C meleagridis,C canis,C.falls,C muris,C suis,C scrofarum,C bovis,C erinacei和C fayeri。还使用qPCR确定了每克粪便的卵囊数(g(-1)),这三个州的中位数在6021-61,064之间变化。重大发现是在牛和袋鼠粪便中检测到了人鞭毛杆菌,并且牛中的C小病毒感染率很高。此外,鉴定了两个新颖的C fayeri亚型(1VaA11G3T1和1VgA10G1T1R1)和一个新颖的C meleagridis亚型(IIIeA18G2R1)。这也是澳大利亚C. erinacei的首次报道。今后有必要监测这些流域动物中隐孢子虫种类和亚型的流行。 (C)2018 Elsevier Ltd.保留所有权利。

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