Phage release from biofilm and planktonic Staphylococcus aureus cells

被引:61
作者
Resch, A
Fehrenbacher, B
Eisele, K
Schaller, M
Götz, F
机构
[1] Univ Tubingen, Dept Dermatol, D-72076 Tubingen, Germany
[2] Univ Tubingen, Dept Membrane Physiol, D-72076 Tubingen, Germany
关键词
bacteriophages; biofilm; lysogeny; phage release; electron microscopy;
D O I
10.1016/j.femsle.2005.08.048
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The ability of pathogenic staphylococci to form biofilms facilitates colonization and the development of chronic infections. Therapy is hampered by the high tolerance of biofilms towards antibiotic treatment and the immune system. We found evidence that lysogenic Staphylococcus aureus cells in a biofilm and in planktonic cultures spontaneously release phages into their surroundings. Phages were detected over a much longer period in biofilm cultures than in planktonic supernatants because the latter were degraded by secreted proteases. Phage release in planktonic and biofilm cultures was artificially increased by adding mitomycin C. Two morphologically distinct phages in the S. aureus strain used in this work were observed by electron microscopy. We postulate that phage-release is a frequent event in biofilms. The resulting lysis of cells in a biofilm might promote the persistence and survival of the remaining cells, as they gain a nutrient reservoir from their dead and lysed neighboring cells. This might therefore be an early differentiation and apoptotic mechanism. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 96
页数:8
相关论文
共 43 条
[1]  
ACKERMANN HW, 1975, PATHOL BIOL, V23, P247
[2]  
[Anonymous], [No title captured]
[3]   PHYSICAL MAPPING OF THE BGLI, BGLII, PSTI AND ECORI RESTRICTION FRAGMENTS OF STAPHYLOCOCCAL PHAGE PHI11 DNA [J].
BACHI, B .
MOLECULAR & GENERAL GENETICS, 1980, 180 (02) :391-398
[4]   Global gene expression in Staphylococcus aureus biofilms [J].
Beenken, KE ;
Dunman, PM ;
McAleese, F ;
Macapagal, D ;
Murphy, E ;
Projan, SJ ;
Blevins, JS ;
Smeltzer, MS .
JOURNAL OF BACTERIOLOGY, 2004, 186 (14) :4665-4684
[5]   GENETIC-TRANSFORMATION IN STAPHYLOCOCCUS-AUREUS - ISOLATION AND CHARACTERIZATION OF A COMPETENCE-CONFERRING FACTOR FROM BACTERIOPHAGE-80-ALPHA LYSATES [J].
BIRMINGHAM, VA ;
PATTEE, PA .
JOURNAL OF BACTERIOLOGY, 1981, 148 (01) :301-307
[6]   MORPHOLOGY AND PHYSICAL PROPERTIES OF STAPHYLOCOCCUS BACTERIOPHAGE P11-M15 [J].
BROWN, DT ;
BURLINGHAM, BT ;
BROWN, NC .
JOURNAL OF VIROLOGY, 1972, 9 (04) :664-+
[7]   RESISTANCE OF BACTERIAL BIOFILMS TO ANTIBIOTICS - A GROWTH-RATE RELATED EFFECT [J].
BROWN, MRW ;
ALLISON, DG ;
GILBERT, P .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1988, 22 (06) :777-780
[8]   Phages and the evolution of bacterial pathogens:: From genomic rearrangements to lysogenic conversion [J].
Brüssow, H ;
Canchaya, C ;
Hardt, WD .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2004, 68 (03) :560-+
[9]   NOVEL ORGANIZATION OF THE SITE-SPECIFIC INTEGRATION AND EXCISION RECOMBINATION FUNCTIONS OF THE STAPHYLOCOCCUS-AUREUS SEROTYPE-F VIRULENCE-CONVERTING PHAGES PHI-13 AND PHI-42 [J].
CARROLL, D ;
KEHOE, MA ;
CAVANAGH, D ;
COLEMAN, DC .
MOLECULAR MICROBIOLOGY, 1995, 16 (05) :877-893
[10]  
COLEMAN DC, 1989, J GEN MICROBIOL, V135, P1679