Temperate phages TP901-1 and φLC3, belonging to the P335 species, apparently use different pathways for DNA injection in Lactococcus lactis subsp cremoris 3107

被引:19
作者
Breum, Solvej Ostergaard
Neve, Horst
Heller, Knut J.
Vogensen, Finn K.
机构
[1] Univ Copenhagen, Fac Life Sci, Dept Food Sci, DK-1958 Frederiksberg, Denmark
[2] Ctr Adv Food Studies, Frederiksberg, Denmark
[3] Fed Res Ctr Nutr & Food, Inst Microbiol, Kiel, Germany
[4] Tech Univ Denmark, Natl Food Inst, Dept Microbiol & Risk Assessment, DK-1790 Copenhagen, Denmark
关键词
Lactococcus lactis; phage P335 species; DNA injection; phage adsorption; TP901-1;
D O I
10.1111/j.1574-6968.2007.00928.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Five mutants of Lactococcus lactis subsp. cremoris 3107 resistant to phage TP901-1 were obtained after treatment with ethyl methanesulfonate. Two of the mutants were also resistant to phage phi LC3. The remaining three mutants were as sensitive as 3107. Mutants E46 and E100 did not adsorb the two phages. Mutants E119, E121 and E126 adsorbed phage phi LC3 as well as 3107 but phage TP901-1 with significantly reduced efficiency. All, except E46, could be lysogenized with phage TP901-BC1034, a derivative of TP901-1 harboring an erythromycin-resistance marker. However, the lysogenization frequency was 10(3)-10(4) fold higher for 3107 than for the mutants. Mitomycin C induction of lysogenized mutants 3107 indicated that phage propagation was not affected in these four mutants. Electron microscopy and analysis of total DNA of infected cells showed that DNA was liberated from the phage particle during infection of strain 3107 with TP901-1 and that intracellular phage DNA replication occurred. This was not the case for mutants E121 and E126. This strongly suggests that some step starting with triggering DNA release and ending with DNA injection is impaired during infection with TP901-1. As such impairment was not seen when infecting E119, E121 and E126 with phi LC3, we conclude that TP901-1 and phi LC3 either are differently triggered by their receptor or utilize different pathways of injection.
引用
收藏
页码:156 / 164
页数:9
相关论文
共 38 条
[1]  
[Anonymous], 1989, Molecular Cloning
[2]   High-conductance channel induced by the interaction of phage lambda with its receptor maltoporin [J].
Berrier, C ;
Bonhivers, M ;
Letellier, L ;
Ghazi, A .
FEBS LETTERS, 2000, 476 (03) :129-133
[3]   Complete genome sequence of the Lactococcus lactis temperate phage φLC3:: comparative analysis of φLC3 and its relatives in lactococci and streptococci [J].
Blatny, JM ;
Godager, L ;
Lunde, M ;
Nes, IF .
VIROLOGY, 2004, 318 (01) :231-244
[4]  
BRAUN V, 1989, J GEN MICROBIOL, V135, P2551
[5]   Analysis of the complete DNA sequence of the temperate bacteriophage TP901-1: Evolution, structure, and genome organization of lactococcal bacteriophages [J].
Brondsted, L ;
Ostergaard, S ;
Pedersen, M ;
Hammer, K ;
Vogensen, FK .
VIROLOGY, 2001, 283 (01) :93-109
[6]   CHARACTERIZATION OF THE LACTOCOCCAL TEMPERATE PHAGE TP901-1 AND ITS SITE-SPECIFIC INTEGRATION [J].
CHRISTIANSEN, B ;
JOHNSEN, MG ;
STENBY, E ;
VOGENSEN, FK ;
HAMMER, K .
JOURNAL OF BACTERIOLOGY, 1994, 176 (04) :1069-1076
[7]   Biodiversity and classification of lactococcal phages [J].
Deveau, Helene ;
Labrie, Simon J. ;
Chopin, Marie-Christine ;
Moineau, Sylvain .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (06) :4338-4346
[8]   Detection of lactococcal 936-species bacteriophages in whey by magnetic capture hybridization PCR targeting a variable region of receptor-binding protein genes [J].
Dupont, K ;
Vogensen, FK ;
Josephsen, J .
JOURNAL OF APPLIED MICROBIOLOGY, 2005, 98 (04) :1001-1009
[9]   Identification of the receptor-binding protein in 936-species lactococcal bacteriophages [J].
Dupont, K ;
Vogensen, FK ;
Neve, H ;
Bresciani, J ;
Josephsen, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) :5818-5824
[10]   Identification of Lactococcus lactis genes required for bacteriophage adsorption [J].
Dupont, K ;
Janzen, T ;
Vogensen, FK ;
Josephsen, J ;
Stuer-Lauridsen, B .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) :5825-5832