Occurrence changes of Escherichia coli (including O157:H7 serotype) in wastewater and sewage sludge by quantitation method of (EMA) real time-PCR

被引:14
作者
Fijalkowski, K. L. [1 ]
Kacprzak, M. J. [1 ]
Rorat, A. [1 ]
机构
[1] Czestochowa Tech Univ, Inst Environm Engn, PL-42200 Czestochowa, Poland
关键词
Wastewater; Sewage sludge; EMA; real time-PCR; Escherichia coli; BACTERIAL PATHOGENS; QUANTIFICATION; COMMUNITIES; WETLANDS; SAMPLES;
D O I
10.1080/19443994.2014.887499
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
There are hundreds of Escherichia coli serotypes and among them enterohaemorrhagic strain E. coli O157:H7 causing gastrointestinal disorders such as: bloody diarrhea, cramping and abdominal pain and the infectious "hemolytic uremic syndrome". Therefore, it's important to develop some rapid and reliable methods of detecting this pathogen in wastewater and sewage sludge. This will allow one to determine the potential risk of infection for humans and animals as far as wastewater and sewage management is concerned. E. coli non- and -O157:H7 gene copies were detected in primary influents and final effluents in winter from municipal wastewater treatment plant. The ethidium monoazide bromide (EMA) application revealed false-positive detection of this bacteria in final effluents. In spring and summer, E. coli gene was not found either in wastewater or in sludge. In autumn, E. coli genes were found in primary influents (20,000 copies of gene/100 mL) and final effluents (2,511 copies of gene/100 mL). High amounts of E. coli O157: H7 gene were detected in both kinds of sludge: waste activated sludge (3,890,451 copies of gene/100 mL) and final sewage sludge (1,819,700 copies of gene/100 mL). We detected the large amount of "free DNA" that is derived from dead cells, which can give false-positive results (overestimation). The use of EMA will make it possible to avoid this inconvenience and allow for effective and appropriate selection of EMA concentration, however, it needs further analysis.
引用
收藏
页码:3965 / 3972
页数:8
相关论文
共 19 条
[1]  
[Anonymous], 2005, Standards methods for the examination of water and wastewater, V21
[2]  
[Anonymous], HLTH RISK AQUIFER RE
[3]   How to become a uropathogen:: Comparative genomic analysis of extraintestinal pathogenic Escherichia coli strains [J].
Brzuszkiewicz, Elzbieta ;
Brueggemann, Holger ;
Liesegang, Heiko ;
Emmerth, Melanie ;
Oeschlaeger, Tobias ;
Nagy, Gabor ;
Albermann, Kaj ;
Wagner, Christian ;
Buchrieser, Carmen ;
Emody, Levente ;
Gottschalk, Gerhard ;
Hackert, Joerg ;
Dobrindt, Ulrich .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (34) :12879-12884
[4]   New perspectives on microbiological water control for wastewater reuse [J].
Campos, C. .
DESALINATION, 2008, 218 (1-3) :34-42
[5]   Development of a quantitative PCR method to differentiate between viable and nonviable bacteria in environmental water samples [J].
Gedalanga, Phillip B. ;
Olson, Betty H. .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2009, 82 (03) :587-596
[6]  
Gerardi M.H., 2005, WASTEWATERS PATHOGEN
[7]  
Heijnen Leo, 2006, Journal of Water and Health, V4, P487, DOI 10.2166/wh.2006.0032
[8]   Multiplex fluorogenic real-time PCR for detection and quantification of Escherichia coli O157:H7 in dairy wastewater wetlands [J].
Ibekwe, AM ;
Watt, PM ;
Grieve, CM ;
Sharma, VK ;
Lyons, SR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (10) :4853-4862
[9]   Contamination of surface and potable water in South Asia by Salmonellae: Culture-independent quantification with molecular beacon real-time PCR [J].
Jyoti, Anurag ;
Ram, Siya ;
Vajpayee, Poornima ;
Singh, Gulshan ;
Dwivedi, Premendra D. ;
Jain, Swatantra K. ;
Shanker, Rishi .
SCIENCE OF THE TOTAL ENVIRONMENT, 2010, 408 (06) :1256-1263
[10]   The comparative mycological analysis of wastewater and sewage sludges from selected wastewater treatment plants [J].
Kacprzak, M ;
Neczaj, E ;
Okoniewska, E .
DESALINATION, 2005, 185 (1-3) :363-370