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评估多形拟杆菌在土壤中存活的能力。

An evaluation of the ability of Dichelobacter nodosus to survive in soil.

机构信息

Department of Large Animal Science, Faculty of Health and Medical Sciences, University of Copenhagen, Grønnegårdsvej 3, DK-1870, Frederiksberg C, Denmark.

出版信息

Acta Vet Scand. 2013 Jan 23;55(1):4. doi: 10.1186/1751-0147-55-4.

DOI:10.1186/1751-0147-55-4
PMID:23343097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3561160/
Abstract

BACKGROUND

Dichelobacter nodosus is the causative agent of footrot in sheep. The survival of the bacterium in soil is of importance for the epidemiology of the disease. The investigation evaluates the survival of D. nodosus in soil with and without added hoof powder stored under different temperatures.

RESULTS

An experimental setup was used with bacteriological culture and real-time polymerase chain reaction (PCR), and the results indicate that the bacteria can survive in soil for longer time than previously expected. The survival time was found to be dependent on temperature and the addition of hoof powder to the soil, with the longest survival time estimated to be 24 days in soil samples with hoof powder stored at 5°C.

CONCLUSION

Our findings indicate that the survival time of D. nodosus and its ability to infect susceptible sheep on pasture under different climatic conditions should be studied further.

摘要

背景

坏死梭杆菌是导致绵羊腐蹄病的病原体。该细菌在土壤中的存活对于疾病的流行病学具有重要意义。本研究评估了在不同温度下,有无添加蹄粉的情况下,土壤中坏死梭杆菌的存活情况。

结果

本研究采用细菌培养和实时聚合酶链反应(PCR)的实验设置,结果表明,与之前的预期相比,细菌在土壤中的存活时间更长。存活时间取决于温度以及向土壤中添加蹄粉,在 5°C 下储存添加蹄粉的土壤样本中,估计最长存活时间为 24 天。

结论

我们的研究结果表明,应进一步研究不同气候条件下,坏死梭杆菌的存活时间及其在牧场感染易感绵羊的能力。

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本文引用的文献

1
Development and comparison of a real-time PCR assay for detection of Dichelobacter nodosus with culturing and conventional PCR: harmonisation between three laboratories.检测双芽巴贝斯虫的实时 PCR 检测方法的建立与比较:三个实验室间的一致性研究(培养法和常规 PCR)。
Acta Vet Scand. 2012 Jan 31;54(1):6. doi: 10.1186/1751-0147-54-6.
2
Development of a sensitive detection method for stressed E. coli O157:H7 in source and finished drinking water by culture-qPCR.通过培养-聚合酶链式反应(qPCR),开发一种用于敏感检测源水和饮用水中应激大肠杆菌 O157:H7 的方法。
Environ Sci Technol. 2011 Mar 15;45(6):2250-6. doi: 10.1021/es103365b. Epub 2011 Feb 22.
3
Persistence of free plasmid DNA in soil monitored by various methods, including a transformation assay.通过各种方法(包括转化测定法)监测土壤中游离质粒 DNA 的持久性。
Appl Environ Microbiol. 1992 Sep;58(9):3012-9. doi: 10.1128/aem.58.9.3012-3019.1992.
4
Current approaches to the management of ovine footrot.绵羊腐蹄病的当前管理方法。
Vet J. 2005 Jan;169(1):28-41. doi: 10.1016/j.tvjl.2004.05.008.
5
Evaluating real-time PCR for the quantification of distinct pathogens and indicator organisms in environmental samples.评估实时荧光定量PCR用于环境样本中不同病原体和指示生物的定量分析。
Water Sci Technol. 2004;50(1):263-70.
6
PCR assay for detection of the E. coli O157:H7 eae-gene and effect of the sample preparation method on PCR detection of heat-killed E. coli O157:H7 in ground beef.用于检测大肠杆菌O157:H7 eae基因的PCR检测方法以及样品制备方法对碎牛肉中热灭活大肠杆菌O157:H7的PCR检测效果
Int J Food Microbiol. 1999 Nov 1;52(1-2):85-95. doi: 10.1016/s0168-1605(99)00132-4.
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Bacterial gene transfer by natural genetic transformation in the environment.环境中自然遗传转化介导的细菌基因转移
Microbiol Rev. 1994 Sep;58(3):563-602. doi: 10.1128/mr.58.3.563-602.1994.