Comparison of propidium monoazide with ethidium monoazide for differentiation of live vs. dead bacteria by selective removal of DNA from dead cells

被引:843
作者
Nocker, Andreas
Cheung, Ching-Ying
Camper, Anne K.
机构
[1] Montana State Univ, Ctr Biofilm Engn, Bozeman, MT 59717 USA
[2] Biotium Inc, Hayward, CA 94545 USA
[3] Montana State Univ, Dept Civil Engn, Bozeman, MT 59717 USA
关键词
differentiation live vs. dead; bacterial pathogens; quantitative PCR;
D O I
10.1016/j.mimet.2006.04.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The differentiation between live and dead bacterial cells presents an important challenge in many microbiological applications. Due to the persistence of DNA in the environment after cells have lost viability, DNA-based detection methods cannot differentiate whether positive signals originate from live or dead bacterial targets. We present here a novel chemical, propidium monoazide (PMA), that (like propidium iodide) is highly selective in penetrating only into 'dead' bacterial cells with compromised membrane integrity but not into live cells with intact cell membranes/cell walls. Upon intercalation in the DNA of dead cells, the photo-inducible azide group allows PMA to be covalently cross-linked by exposure to bright light. This process renders the DNA insoluble and results in its loss during subsequent genomic DNA extraction. Subjecting a bacterial population comprised of both live and dead cells to PMA treatment thus results in selective removal of DNA from dead cells. We provide evidence that this chemical can be applied to a wide range of species across the bacterial kingdom presenting a major advantage over ethdium monoazide (EMA). The general application of EMA is hampered by the fact that the chemical can also penetrate live cells of some bacterial species. Transport pumps actively export EMA out of metabolically active cells, but the remaining EMA level can lead to substantial loss of DNA. The higher charge of PMA might be the reason for the higher impermeability through intact cell membranes, thus avoiding DNA loss. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:310 / 320
页数:11
相关论文
共 19 条
[1]  
COFFMAN GL, 1982, J BIOL CHEM, V257, P13205
[2]  
DETRAGLIA MC, 1978, J BIOL CHEM, V253, P1846
[3]  
HIXON SC, 1975, J MOL BIOL, V92, P319, DOI 10.1016/0022-2836(75)90231-4
[4]   STAINING OF ESCHERICHIA-COLI FOR FLOW-CYTOMETRY - INFLUX AND EFFLUX OF ETHIDIUM-BROMIDE [J].
JERNAES, MW ;
STEEN, HB .
CYTOMETRY, 1994, 17 (04) :302-309
[5]   POLYMERASE CHAIN-REACTION DETECTION OF NONVIABLE BACTERIAL PATHOGENS [J].
JOSEPHSON, KL ;
GERBA, CP ;
PEPPER, IL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (10) :3513-3515
[6]   Viability and activity in readily culturable bacteria: a review and discussion of the practical issues [J].
Kell, DB ;
Kaprelyants, AS ;
Weichart, DH ;
Harwood, CR ;
Barer, MR .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 1998, 73 (02) :169-187
[7]   EFFECT OF STRESS TREATMENTS ON THE DETECTION OF LISTERIA-MONOCYTOGENES AND ENTEROTOXIGENIC ESCHERICHIA-COLI BY THE POLYMERASE CHAIN-REACTION [J].
MASTERS, CI ;
SHALLCROSS, JA ;
MACKEY, BM .
JOURNAL OF APPLIED BACTERIOLOGY, 1994, 77 (01) :73-79
[8]   The relationship of host range, physiology, and genotype to virulence on cantaloupe in Pseudomonas syringae from cantaloupe blight epidemics in France [J].
Morris, CE ;
Glaux, C ;
Latour, X ;
Gardan, L ;
Samson, R ;
Pitrat, M .
PHYTOPATHOLOGY, 2000, 90 (06) :636-646
[9]   Assessment of bacterial viability status by flow cytometry and single cell sorting [J].
Nebe-von Caron, G ;
Stephens, P ;
Badley, RA .
JOURNAL OF APPLIED MICROBIOLOGY, 1998, 84 (06) :988-998
[10]   Analysis of bacterial function by multi-colour fluorescence flow cytometry and single cell sorting [J].
Nebe-von-Caron, G ;
Stephens, PJ ;
Hewitt, CJ ;
Powell, JR ;
Badley, RA .
JOURNAL OF MICROBIOLOGICAL METHODS, 2000, 42 (01) :97-114