Architectural adaptation and protein expression patterns of Salmonella enterica serovar Enteritidis biofilms under laminar flow conditions

被引:31
作者
Mangalappalli-Illathu, Anil K. [1 ]
Lawrence, John R. [2 ]
Swerhone, George D. W. [2 ]
Korber, Darren R. [1 ]
机构
[1] Univ Saskatchewan, Dept Appl Microbiol & Food Sci, Saskatoon, SK S7N 5A8, Canada
[2] Environm Canada, Saskatoon, SK S7N 3H5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Salmonella enteritidis; biofilms; Laminar flow; architecture; adaptation; protein expression;
D O I
10.1016/j.ijfoodmicro.2007.12.021
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Salmonella enterica serovar Enteritidis is a significant biofilm-forming pathogen. The influence of a 10-fold difference in nutrient laminar flow velocity on the dynamics of Salmonello Enteritidis biofilm Formation and protein expression profiles were compared in order to ascertain how flow velocity influenced biofilm structure and function. Low-flow (0.007 cm s(-1)) biofilms consisted of diffusely-arranged microcolonies which grew until merging by similar to 72 h. High-flow (0.07 cm s(-1)) biofilms were significantly thicker (36 +/- 3 mu m (arithmetic mean standard error; n=225) versus 16 +/- 2 mu m Cor low-flow biofilms at 120 h) and consisted of large bacterial Mounds interspersed by water channels. Lectin-binding analysis of biofilm exopolymers revealed a significantly higher (P<0.05) proportion of N-acetylgalactosamine (GalNAc) in low-flow biofilms (55.2%), relative to only 1.2% in high-flow biofilms. Alternatively, the proportions of alpha-L-fucose and N-acetylglycosamine (GlcNAc2)-N-acetylneuraminic acid (NeuNAc) polymer-conjugates were significantly higher (P<0.05) in high-flow biofilms (69.1% and 29.6%, respectively) than low-flow biofilms (33.1% and 11.7%, respectively). Despite an apparent flow rate-based physiologic effect on biofilm structure and exopolymer composition, no major shift in whole-cell protein expression patterns was seen between 168 h-old low-flow and high-flow biofilms, and notably did not include any response involving the stress response proteins, DnaK, SodB, and Tpx. Proteins involved in degradation and energy metabolism (PduA, GapA, GpmA, Pgk, and RpiA), RNA and protein biosynthesis (Tsf, TufA, and RpoZ), cell processes (Crr, MalE, and PtsH), and adaptation (GrcA), and some hypothetical proteins (YcbL and YnaF) became up-regulated in both biofilm systems relative to a 168 h-old planktonic cell control. Our results indicate that Salmonella Enteritidis biofilms altered their structure and extracellular glycoconjugate composition in response to flow and this response is Suggested to be significant in the survival of this pathogen as biofilms. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 120
页数:12
相关论文
共 49 条
[1]   BIOLOGICALLY-ACTIVE SURFACES - PROCESSES GOVERNING THE FORMATION AND PERSISTENCE OF BIOFILMS [J].
BRYERS, JD .
BIOTECHNOLOGY PROGRESS, 1987, 3 (02) :57-68
[2]   IMAGING OF BACTERIAL-CELLS BY FLUORESCENCE EXCLUSION USING SCANNING CONFOCAL LASER MICROSCOPY [J].
CALDWELL, DE ;
KORBER, DR ;
LAWRENCE, JR .
JOURNAL OF MICROBIOLOGICAL METHODS, 1992, 15 (04) :249-261
[3]   GLYOXYLATE BYPASS OPERON OF ESCHERICHIA-COLI - CLONING AND DETERMINATION OF THE FUNCTIONAL MAP [J].
CHUNG, T ;
KLUMPP, DJ ;
LAPORTE, DC .
JOURNAL OF BACTERIOLOGY, 1988, 170 (01) :386-392
[4]   Microbial biofilms: from ecology to molecular genetics [J].
Davey, ME ;
O'toole, GA .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2000, 64 (04) :847-+
[5]   Biofilms: Microbial life on surfaces [J].
Donlan, RM .
EMERGING INFECTIOUS DISEASES, 2002, 8 (09) :881-890
[6]  
*FDA, 2004, FACT SHEET FDA PROP
[7]  
Frenzen P. D., 1999, FoodReview, V22, P10
[8]   Oxygen tension and nutrient starvation are major signals that regulate agfD promoter activity and expression of the multicellular morphotype in Salmonella typhimurium [J].
Gerstel, U ;
Römling, U .
ENVIRONMENTAL MICROBIOLOGY, 2001, 3 (10) :638-648
[9]   Characterization of starvation-induced dispersion in Pseudomonas putida biofilms [J].
Gjermansen, M ;
Ragas, P ;
Sternberg, C ;
Molin, S ;
Tolker-Nielsen, T .
ENVIRONMENTAL MICROBIOLOGY, 2005, 7 (06) :894-906
[10]  
Guerin P J, 2006, Euro Surveill, V11, P61