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首页> 外文期刊>The Science of the Total Environment >Tracing enteric pathogen contamination in sub-Saharan African groundwater
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Tracing enteric pathogen contamination in sub-Saharan African groundwater

机译:追踪撒哈拉以南非洲地下水中的肠道病原体污染

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Quantitative PCR (qPCR) can rapidly screen for an array of faecally-derived bacteria, which can be employed as tracers to understand groundwater vulnerability to faecal contamination. A microbial DNA qPCR array was used to examine 45 bacterial targets, potentially relating to enteric pathogens, in 22 groundwater supplies beneath the city of Kabwe, Zambia in both the dry and subsequent wet season. Thermotolerant (faecal) coliforms, sanitary risks, and tryptophan-like fluorescence, an emerging real-time reagentless faecal indicator, were also concurrently investigated. There was evidence for the presence of enteric bacterial contamination, through the detection of species and group specific 16S rRNA gene fragments, in 72% of supplies where sufficient DNA was available for qPCR analysis. DNA from the opportunistic pathogen Citrobacter freundii was most prevalent (69% analysed samples), with Vibrio cholerae also perennially persistent in groundwater (41% analysed samples). DNA from other species such as Bifidobacterium longum and Arcobacter butzleri was more seasonally transient Bacterial DNA markers were most common in shallow hand-dug wells in laterite/saprolite implicating rapid subsurface pathways and vulnerability to pollution at the surface. Boreholes into the underlying dolomites were also contaminated beneath the city highlighting that a laterite/saprolite overburden, as occurs across much of sub-Saharan aquifer, does not adequately protect underlying bedrock groundwater resources. Nevertheless, peri-urban boreholes all tested negative establishing there is limited subsurface lateral transport of enteric bacteria outside the city limits. Themnotolerant coliforms were present in 97% of sites contaminated with enteric bacterial DNA markers. Furthermore, tryptophan-like fluorescence was also demonstrated as an effective indicator and was in excess of 1.4 μg/L in all contaminated sites.
机译:定量PCR(qPCR)可以快速筛选一系列粪便来源的细菌,这些细菌可以用作示踪剂,以了解地下水对粪便污染的脆弱性。在干旱和随后的湿润季节中,使用微生物DNA qPCR阵列检查了赞比亚Kabwe市以下22个地下水源中的45个细菌靶标,这些靶标可能与肠道病原体有关。还同时研究了耐热(粪便)大肠菌群,卫生风险和色氨酸样荧光(一种新兴的实时无试剂粪便指示剂)。通过检测物种和特定于群体的16S rRNA基因片段,有证据表明存在肠道细菌污染,其中72%的供应中有足够的DNA可用于qPCR分析。机会性病原体弗氏柠檬酸杆菌的DNA最普遍(分析样品占69%),霍乱弧菌也常年存在于地下水中(分析样品占41%)。来自其他物种(如长双歧杆菌和布氏杆菌)的DNA在季节上更为短暂。细菌DNA标记最常见于红土/腐泥土的浅手挖孔中,这意味着快速的地下途径和易受表面污染的影响。埋在地下白云岩中的钻孔也受到了城市下方的污染,突显出撒哈拉沙漠以南的大部分含水层中发生的红土/腐泥土覆盖层不能充分保护地下的基岩地下水资源。尽管如此,郊区的所有钻孔都被测试为阴性,这表明肠道细菌在城市范围以外的地下地下横向迁移是有限的。耐肠溶菌大肠菌存在于97%受肠道细菌DNA标记物污染的部位。此外,色氨酸样荧光也被证明是一种有效的指示剂,并且在所有受污染的部位均超过1.4μg/ L。

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