Modulation of OMV Production by the Lysis Module of the DLP12 Defective Prophage of Escherichia coli K12

被引:14
|
作者
Pasqua, Martina [1 ]
Zennaro, Alessandro [1 ]
Trirocco, Rita [1 ]
Fanelli, Giulia [1 ]
Micheli, Gioacchino [2 ]
Grossi, Milena [1 ]
Colonna, Bianca [1 ]
Prosseda, Gianni [1 ]
机构
[1] Sapienza Univ Roma, Dipartimento Biol & Biotecnol C Darwin, Ist Pasteur Italia, Via Sardi 70, I-00185 Rome, Italy
[2] Consiglio Nazl Ric CNR, Ist Biol & Patol Mol, Ple Aldo Moro 5, I-00185 Rome, Italy
关键词
OMV; cryptic prophage; lysis module; cell wall; phage domestication;
D O I
10.3390/microorganisms9020369
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Outer membrane vesicles (OMVs) are nanostructures mostly produced by blebbing of the outer membrane in Gram negative bacteria. They contain biologically active proteins and perform a variety of processes. OMV production is also a typical response to events inducing stress in the bacterial envelope. In these cases, hypervesiculation is regarded as a strategy to avoid the dangerous accumulation of undesired products within the periplasm. Several housekeeping genes influence the biogenesis of OMVs, including those correlated with peptidoglycan and cell wall dynamics. In this work, we have investigated the relationship between OMV production and the lysis module of the E. coli DLP12 cryptic prophage. This module is an operon encoding a holin, an endolysin and two spannins, and is known to be involved in cell wall maintenance. We find that deleting the lysis module increases OMV production, suggesting that during evolution this operon has been domesticated to regulate vesiculation, likely through the elimination of non-recyclable peptidoglycan fragments. We also show that the expression of the lysis module is negatively regulated by environmental stress stimuli as high osmolarity, low pH and low temperature. Our data further highlight how defective prophages finely contribute to bacterial host fitness.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 50 条
  • [11] Termination troubles in Escherichia coli K12
    Dreyfus, Marc
    Heurgue-Hamard, Valerie
    MOLECULAR MICROBIOLOGY, 2011, 79 (02) : 288 - 291
  • [12] ON MECHANISM OF CONJUGATION IN ESCHERICHIA COLI K12
    BRESLER, SE
    LANZOV, VA
    LUKJANIE.AA
    MOLECULAR AND GENERAL GENETICS, 1968, 102 (04): : 269 - &
  • [13] MUTATIONS OF F EPISOME IN ESCHERICHIA COLI K12 .I. DEFECTIVE MUTANTS
    CUZIN, F
    JACOB, F
    ANNALES DE L INSTITUT PASTEUR, 1967, 112 (01): : 1 - &
  • [14] ISOLATION AND CHARACTERIZATION OF DELETIONS IN BACTERIOPHAGE-LAMBDA RESIDING AS PROPHAGE IN ESCHERICHIA-COLI K12
    CASTELLAZZI, M
    BRACHET, P
    EISEN, H
    MOLECULAR AND GENERAL GENETICS, 1972, 117 (03): : 211 - +
  • [15] THYMINELESS INDUCTION IN ESCHERICHIA COLI K12(LAMBDA)
    KORN, D
    WEISSBACH, A
    BIOCHIMICA ET BIOPHYSICA ACTA, 1962, 61 (05) : 775 - &
  • [16] Modelling fim Expression in Escherichia Coli K12
    de Vries, Patrick
    Johnson, Colin G.
    Blomfield, Ian C.
    COMPUTATIONAL SYSTEMS-BIOLOGY AND BIOINFORMATICS, 2010, 115 : 14 - +
  • [17] TOLC LOCUS IN ESCHERICHIA-COLI K12
    WHITNEY, EN
    GENETICS, 1971, 67 (01) : 39 - +
  • [18] MOLYBDENUM UPTAKE IN ESCHERICHIA-COLI K12
    CORCUERA, GL
    BASTIDAS, M
    DUBOURDIEU, M
    JOURNAL OF GENERAL MICROBIOLOGY, 1993, 139 : 1869 - 1875
  • [19] DEOXYRIBOSIDE SENSITIVE MUTANT OF ESCHERICHIA COLI K12
    OKADA, T
    TORII, H
    KUNO, S
    JAPANESE JOURNAL OF GENETICS, 1968, 43 (06): : 436 - +
  • [20] FORMATION OF HFR STRAINS IN ESCHERICHIA COLI K12
    BRODA, P
    GENETICAL RESEARCH, 1967, 9 (01) : 35 - &