Transcriptional activity of the host-interaction locus and a putative pilin gene of Bdellovibrio bacteriovorus in the predatory life cycle

被引:23
作者
Schwudke, D
Bernhardt, A
Beck, S
Madela, K
Linscheid, MW
Appel, B
Strauch, E
机构
[1] Humboldt Univ, Dept Chem, D-12489 Berlin, Germany
[2] Robert Koch Inst, Project Grp Biol Safety, D-13353 Berlin, Germany
关键词
D O I
10.1007/s00284-005-0030-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bdellovibrio bacteriovorus is a predatory bacterium that grows and replicates within the periplasm of a large variety of Gram-negative bacteria. So far, the host-interaction locus (hit locus) is the only genetic locus that is implicated in the obligate predatory lifestyle. Sequence analysis revealed that upstream of the hit locus, the genomic regions of the two obligate predatory B. bacteriovorus-type strains HD100 and HD114 encode genes for pilus formation. As pili might be involved in the invasion process, the transcriptional activity of the hit locus and of a putative pilin gene (flp1) of the pilus cluster were studied in synchronized cultures of B. bacteriovorus with Escherichia coli K-12 as prey bacteria. Stages of the life cycle were monitored with scanning electronic microscopy and transcriptional analyses were performed by quantitative reverse transcription polymerase chain reaction. Our study revealed an increased expression level of the putative hit and flp1 genes in the attack phase of B. bacteriovorus, whereas the transcriptional activity significantly decreased during the intracellular replication phase.
引用
收藏
页码:310 / 316
页数:7
相关论文
共 15 条
[1]   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
[2]   Bdellovibrio bacteriovorus strains produce a novel major outer membrane protein during predacious growth in the periplasm of prey bacteria [J].
Beck, S ;
Schwudke, D ;
Strauch, E ;
Appel, B ;
Linscheid, M .
JOURNAL OF BACTERIOLOGY, 2004, 186 (09) :2766-2773
[3]   IDENTIFICATION OF A BDELLOVIBRIO-BACTERIOVORUS GENETIC-LOCUS, HIT, ASSOCIATED WITH THE HOST-INDEPENDENT PHENOTYPE [J].
COTTER, TW ;
THOMASHOW, MF .
JOURNAL OF BACTERIOLOGY, 1992, 174 (19) :6018-6024
[4]   Prey range characterization, ribotyping, and diversity of soil and rhizosphere Bdellovibrio spp. isolated on phytopathogenic bacteria [J].
Jurkevitch, E ;
Minz, D ;
Ramati, B ;
Barel, G .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (06) :2365-2371
[5]   Genes for tight adherence of Actinobacillus actinomycetemcomitans:: from plaque to plague to pond scum [J].
Kachlany, SC ;
Planet, PJ ;
DeSalle, R ;
Fine, DH ;
Figurski, DH .
TRENDS IN MICROBIOLOGY, 2001, 9 (09) :429-437
[6]   flp-1, the first representative of a new pilin gene subfamily, is required for non-specific adherence of Actinobacillus actinomycetemcomitans [J].
Kachlany, SC ;
Planet, PJ ;
DeSalle, R ;
Fine, DH ;
Figurski, DH ;
Kaplan, JB .
MOLECULAR MICROBIOLOGY, 2001, 40 (03) :542-554
[7]   A novel assay to monitor predator-prey interactions for Bdellovibrio bacteriovorus 109 J reveals a role for methyl-accepting chemotaxis proteins in predation [J].
Lambert, C ;
Smith, MCM ;
Sockett, RE .
ENVIRONMENTAL MICROBIOLOGY, 2003, 5 (02) :127-132
[8]   Developmentally regulated protein synthesis during intraperiplasmic growth of Bdellovibrio bacteriovorus 109J [J].
McCann, PP ;
Solimeo, HT ;
Cusick, F ;
Panunti, B ;
McCullen, C .
CANADIAN JOURNAL OF MICROBIOLOGY, 1998, 44 (01) :50-55
[9]   A predator unmasked:: Life cycle of Bdellovibrio bacteriovorus from a genomic perspective [J].
Rendulic, S ;
Jagtap, P ;
Rosinus, A ;
Eppinger, M ;
Baar, C ;
Lanz, C ;
Keller, H ;
Lambert, C ;
Evans, KJ ;
Goesmann, A ;
Meyer, F ;
Sockett, RE ;
Schuster, SC .
SCIENCE, 2004, 303 (5658) :689-692
[10]   Taxonomic studies of predatory bdellovibrios based on 165 rRNA analysis, ribotyping and the hit locus and characterization of isolates from the gut of animals [J].
Schwudke, D ;
Strauch, E ;
Krueger, M ;
Appel, B .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 2001, 24 (03) :385-394