Necrotrophic growth of Legionella pneumophila

被引:93
作者
Temmerman, R. [1 ]
Vervaeren, H. [1 ]
Noseda, B. [1 ]
Boon, N. [1 ]
Verstraete, W. [1 ]
机构
[1] Univ Ghent, Lab Microbial Ecol & Technol, B-9000 Ghent, Belgium
关键词
D O I
10.1128/AEM.00070-06
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study examined whether Legionella pneumophila is able to thrive on heat-killed microbial cells (necrotrophy) present in biofilms or heat-treated water systems. Quantification by means of plate counting, real-time PCR, and flow cytometry demonstrated necrotrophic growth of L. pneuntophila in water after 96 h, when at least 100 dead cells are available to one L. pneumophila cell. Compared to the starting concentration of L. pneumophila, the maximum observed necrotrophic growth was 1.89 log units for real-time PCR and 1.49 log units for plate counting. The average growth was 1.57 +/- 0.32 log units (n = 5) for real-time PCR and 1.14 +/- 0.35 log units (n = 5) for plate counting. Viability staining and flow cytometry showed that the fraction of living cells in the L. pneumophila population rose from the initial 54% to 82% after 96 h. Growth was measured on heat-killed Pseudomonas putida, Escherichia coli, Acanthamoeba castellanii, Saccharomyces boulardii, and a biofilm sample. Gram-positive organisms did not result in significant growth of L. pneumophila, probably due to their robust cell wall structure. Although necrotrophy showed lower growth yields compared to replication within protozoan hosts, these findings indicate that it may be of major importance in the environmental persistence of L. pneumophila. Techniques aimed at the elimination of protozoa or biofilm from water systems will not necessarily result in a subsequent removal of L. pneumophila unless the formation of dead microbial cells is minimized.
引用
收藏
页码:4323 / 4328
页数:6
相关论文
共 33 条
[21]  
Surman S, 2002, LEGIONELLA, P86
[22]   Culture-independent analysis of probiotic products by denaturing gradient gel electrophoresis [J].
Temmerman, R ;
Scheirlinck, I ;
Huys, G ;
Swings, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (01) :220-226
[23]   GROWTH OF LEGIONELLA-PNEUMOPHILA IN ASSOCIATION WITH BLUE-GREEN-ALGAE (CYANOBACTERIA) [J].
TISON, DL ;
POPE, DH ;
CHERRY, WB ;
FLIERMANS, CB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1980, 39 (02) :456-459
[24]  
TOBIN JOH, 1980, LANCET, V2, P118
[25]   Dynamics of living and dead bacterial cells within a mixed-species biofilm during toluene degradation in a biotrickling filter [J].
Tresse, O ;
Lescob, S ;
Rho, D .
JOURNAL OF APPLIED MICROBIOLOGY, 2003, 94 (05) :849-855
[26]   Biofilm formation and multiplication of Legionella in a model warm water system with pipes of copper, stainless steel and cross-linked polyethylene [J].
van der Kooij, D ;
Veenendaal, HR ;
Scheffer, WJH .
WATER RESEARCH, 2005, 39 (13) :2789-2798
[27]   Elucidation and control of biofilm formation processes in water treatment and distribution using the unified biofilm approach [J].
van der Kooij, D ;
Vrouwenvelder, JS ;
Veenendaal, HR .
WATER SCIENCE AND TECHNOLOGY, 2003, 47 (05) :83-90
[28]  
VERVAEREN H, UNPUB
[29]   EFFECT OF NON-LEGIONELLACEAE BACTERIA ON THE MULTIPLICATION OF LEGIONELLA-PNEUMOPHILA IN POTABLE WATER [J].
WADOWSKY, RM ;
YEE, RB .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1985, 49 (05) :1206-1210
[30]   Cell death in Pseudomonas aeruginosa biofilm development [J].
Webb, JS ;
Thompson, LS ;
James, S ;
Charlton, T ;
Tolker-Nielsen, T ;
Koch, B ;
Givskov, M ;
Kjelleberg, S .
JOURNAL OF BACTERIOLOGY, 2003, 185 (15) :4585-4592