Characterization of type IV pili in the life cycle of the predator bacterium Bdellovibrio

被引:43
作者
Mahmoud, Khaled K. [1 ]
Koval, Susan F. [1 ]
机构
[1] Univ Western Ontario, Dept Microbiol & Immunol, London, ON N6A 5C1, Canada
来源
MICROBIOLOGY-SGM | 2010年 / 156卷
基金
加拿大自然科学与工程研究理事会;
关键词
INTRAPERIPLASMIC GROWTH; NEISSERIA-MENINGITIDIS; BACTERIOVORUS; 109J; RECEPTOR-BINDING; BIOGENESIS; CHEMOTAXIS; ARCHITECTURE; RETRACTION; EXPRESSION; DIVERSITY;
D O I
10.1099/mic.0.036137-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bdellovibrio and like organisms (BALOs) are obligate prokaryotic predators of other Gram-negative bacteria. Bdellovibrio bacteriovorus is the most studied organism among BALOs. It has a periplasmic life cycle with two major stages: a motile, non-replicative stage spent searching for prey (the attack phase) and a stage spent inside the periplasm of the Gram-negative prey cell (the growth phase) after forming an osmotically stable body termed the bdelloplast. Within Bdellovibrio, there are also strains exhibiting an epibiotic life cycle. The genome sequence of the type strain B. bacteriovorus HD100(T) revealed the presence of multiple dispersed pil genes encoding type IV pili. Type IV pili in other bacteria are involved in adherence to and invasion of host cells and therefore can be considered to play a role in invasion of prey cells by Bdellovibrio. In this study, genes involved in producing type IV pili were identified in the periplasmic strain B. bacteriovorus 109J and an epibiotic Bdellovibrio sp. strain JSS. The presence of fibres on attack-phase cells was confirmed by examining negative stains of cells fixed with 10% buffered formalin. Fibres were at the non-flagellated pole on approximately 25% of attack-phase cells. To confirm that these fibres were type IV pili, a truncated form of PilA lacking the first 35 amino acids was designed to facilitate purification of the protein. The truncated PilA fused to a His-tag was overexpressed in Escherichia coli BL21(DE3) plysS. The fusion protein, accumulated in the insoluble fraction, was purified under denaturing conditions and used to produce polyclonal antisera. Immunoelectron microscopy showed that polar fibres present on the cell surface of the predator were composed of PilA, the major subunit of type IV pili. Immunofluorescence microscopy showed the presence of pilin on attack-phase cells of B. bacteriovorus 109J during attachment to prey cells and just after penetration, inside the bdelloplast. Antibodies against PilA delayed and inhibited predation in co-cultures of Bdellovibrio. This study confirms that type IV pill play a role in invasion of prey cells by Bdellovibrio.
引用
收藏
页码:1040 / 1051
页数:12
相关论文
共 53 条
[1]   STRUCTURAL PROPERTIES AND FEATURES OF PARASITIC BDELLOVIBRIO-BACTERIOVORUS [J].
ABRAM, D ;
DAVIS, BK .
JOURNAL OF BACTERIOLOGY, 1970, 104 (02) :948-&
[2]   Functional dissection of a conserved motif within the pilus retraction protein PilT [J].
Aukema, KG ;
Kron, EM ;
Herdendorf, TJ ;
Forest, KT .
JOURNAL OF BACTERIOLOGY, 2005, 187 (02) :611-618
[3]   Analysis of phenotypic diversity among host-independent mutants of Bdellovibrio bacteriovorus 109J [J].
Barel, G ;
Jurkevitch, E .
ARCHIVES OF MICROBIOLOGY, 2001, 176 (03) :211-216
[4]   Cooperative retraction of bundled type IV pili enables nanonewton force generation [J].
Biais, Nicolas ;
Ladoux, Benoit ;
Higashi, Dustin ;
So, Magdalene ;
Sheetz, Michael .
PLOS BIOLOGY, 2008, 6 (04) :907-913
[5]   Three-dimensional imaging of the highly bent architecture of Bdellovibrio bacteriovorus by using cryo-electron tomography [J].
Borgnia, Mario J. ;
Subramaniam, Sriram ;
Milne, Jacqueline L. S. .
JOURNAL OF BACTERIOLOGY, 2008, 190 (07) :2588-2596
[6]   ADSORPTION OF PSEUDOMONAS-AERUGINOSA PILUS-DEPENDENT BACTERIOPHAGES TO A HOST MUTANT WITH NONRETRACTILE PILI [J].
BRADLEY, DE .
VIROLOGY, 1974, 58 (01) :149-163
[7]   ELECTRON MICROSCOPIC OBSERVATIONS ON PENETRATION OF BDELLOVIBRIO BACTERIOVORUS INTO GRAM-NEGATIVE BACTERIAL HOSTS [J].
BURNHAM, JC ;
HASHIMOTO, T ;
CONTI, SF .
JOURNAL OF BACTERIOLOGY, 1968, 96 (04) :1366-+
[8]   Type IV pilus biogenesis in Neisseria meningitidis:: PilW is involved in a step occurring after pilus assembly, essential for fibre stability and function [J].
Carbonnelle, E ;
Hélaine, S ;
Prouvensier, L ;
Nassif, X ;
Pelicic, V .
MOLECULAR MICROBIOLOGY, 2005, 55 (01) :54-64
[9]   A systematic genetic analysis in Neisseria meningitidis defines the Pil proteins required for assembly, functionality, stabilization and export of type IV pili [J].
Carbonnelle, Etienne ;
Helaine, Sophie ;
Nassif, Xavier ;
Pelicic, Vladimir .
MOLECULAR MICROBIOLOGY, 2006, 61 (06) :1510-1522
[10]   Analysis of the PilQ secretin from Neisseria meningitidis by transmission electron microscopy reveals a dodecameric quaternary structure [J].
Collins, RF ;
Davidsen, L ;
Derrick, JP ;
Ford, RC ;
Tonjum, T .
JOURNAL OF BACTERIOLOGY, 2001, 183 (13) :3825-3832