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Evaluation of an alternative method for the enumeration and confirmation of Clostridium perfringens from untreated water samples including sewage effluent

机译:评价从未处理的水样品(包括污水)中枚举和鉴定产气荚膜梭菌的另一种方法

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摘要

Aims: Clostridium perfringens is recommended as a suitable indicator bacterium for human enteric viruses, Giardia cysts and Cryptosporidium oocysts in finished water and in the assessment and evaluation of water treatment. Several agars and confirmation procedures were evaluated in parallel with the Australian/New Zealand Standard (AS/NZ) Method for the enumeration of Cl. perfringens from treated and untreated sewage samples. Methods and Results: The current AS/NZ method utilizes tryptose sulfite cycloserine agar (TSC), lactose gelatin medium (LG) and nitrate motility medium (NM) at an incubation temperature of 37°C. Sixty treated and untreated sewage samples were used to evaluate TSC agar, membrane Cl. perfringens agar (mCP), Perfringens agar (OPSP) and Perfringens agar with 4-methylumbelliferyl phosphate (OPSP–MUP) for enumeration of Clostridium. An incubation temperature of 44°C for 24 h was used for comparison. Confirmation procedures were also evaluated using 103 isolates and included LG and NM, ortho-nitrophenyl-β-D-galactopyranoside (ONPG) with MUP (ONPG–MUP) and phosphatase reagent (PR). OPSP compared favourably with TSC agar. One false negative result was obtained from each of the LG/NM and ONPG–MUP procedures. No false results were obtained using the PR confirmation procedure. Conclusions: OPSP agar and PR were determined as suitable replacements for the AS/NZ Standard procedure with no interference from spreading organisms. Significance and Impact of the Study: This is a simple and rapid method for isolating and enumerating Cl. perfringens from sewage samples and confirmed results can be reported more quickly due to shorter analytical turnaround times.
机译:目的:建议将产气荚膜梭菌作为人肠道病毒,贾第鞭毛虫囊和隐孢子虫卵囊的合适指示细菌,并用于水处理的评估和评估。与澳大利亚/新西兰标准(AS / NZ)方法同时评估了几种琼脂和确证程序,以计算Cl。从处理过的和未处理过的污水样品中提取香气。方法和结果:当前的AS / NZ方法在37°C的孵育温度下使用亚硫酸胰蛋白亚硫酸环丝氨酸琼脂(TSC),乳糖明胶培养基(LG)和硝酸盐活力培养基(NM)。使用60个处理过的和未处理的污水样品评估TSC琼脂膜Cl。产气荚膜琼脂(mCP),产气荚膜琼脂(OPSP)和产气荚膜琼脂用4-甲基伞形磷酸酯(OPSP–MUP)进行梭菌计数。将44℃的孵育温度24小时用于比较。还使用103个分离株评估了确认程序,包括LG和NM,邻硝基苯基-β-D-吡喃半乳糖苷(ONPG)和MUP(ONPG-MUP)和磷酸酶试剂(PR)。 OPSP优于TSC琼脂。从LG / NM和ONPG-MUP程序中的每一个都获得了一个假阴性结果。使用PR确认程序未获得任何错误结果。结论:OPSP琼脂和PR被确定为AS / NZ标准程序的合适替代品,且不受传播生物的干扰。研究的意义和影响:这是分离和枚举Cl的简单快速的方法。由于更短的分析周转时间,因此可以更快地报告污水样品中的香精气和确认结果。

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