Translocation of macromolecules between cells is a major area of biomedical interest. In bacteria, the intercellular transfer of macromolecules is commonly orchestrated by surface organelles termed type IV secretion systems. Many bacterial species use type IV systems to deliver DNA substrates within or across species, genus, or even kingdom boundaries through a process termed conjugation. Conjugative DNA transfer contributes to genome plasticity over evolutionary time, and the spread of antibiotic resistance genes and other virulence traits on a more immediate time scale. Many medically-important bacterial pathogens also use type IV systems to deliver effector proteins to eukaryotic target cells during infection processes. The VirB/VirD4 system of Agrobacterium tumefaciens serves as important model for detailed mechanistic studies of type IV machine function. This system, assembled from subunits VirB1 - VirB11 and VirD4, translocates DNA and proteins to phylogenetically-diverse bacterial and eukaryotic target cells by a mechanism dependent on direct cell-to-cell contact. The overall goal of work in this laboratory is to describe in complete molecular terms the VirB/VirD4 machine biogenesis pathway, the basis for substrate recognition and transfer across the cell envelope, and the nature of the VirB/VirD4 machine - target cell contact. Recent studies identified three novel features of VirB10 that focus our attention on this channel subunit: i) it spans the entire Gram-negative cell envelope, a novel property among all described bacterial proteins, ii) it forms an ?-helical pore at the outer membrane, only the second described ?-helical outer membrane pore protein, and iii) it undergoes an ATP-mediated structural transition required for substrate translocation across the outer membrane. We hypothesize that VirB10 forms a structural scaffold across the entire cell envelope for assembly of two structures, the VirB/VirD4 translocation channel and the extracellular T pilus, the latter being important for establishment of target cell contact. We propose to: (A) define the architecture, assembly dynamics, and function of the ?-helical outer membrane pore with respect to substrate transfer and pilus biogenesis, (B) define how VirB10 contributes to channel function through biochemical and structural characterization of VirB10-containing machine subassemblies, and (C) elucidate how the VirB10 transmembrane domain and the VirB4 ATPase located at the inner membrane contribute to pilus biogenesis. Studies of type IV secretion are essential for at least two reasons. First, these are widely used machines among most if not all prokaryotic cells and yet their mechanisms of action remain poorly understood. Second, type IV secretion is a major contributor to the proliferation of antibiotic resistance as well as successful infection by many bacterial pathogens;these systems are therefore excellent targets for therapies aimed at suppressing disease progression.

Public Health Relevance

This project investigates the structure and function of a bacterial type IV secretion system. These systems are widely used by many medically important pathogens for transfer of antibiotic resistance or other virulence traits, as well as effector proteins to human target cells. These systems represent novel targets for therapeutics directed to blocking antibiotic resistance spread and bacterial disease progression.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM048746-19
Application #
8217260
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Ainsztein, Alexandra M
Project Start
1993-01-01
Project End
2014-12-31
Budget Start
2012-01-01
Budget End
2012-12-31
Support Year
19
Fiscal Year
2012
Total Cost
$416,034
Indirect Cost
$137,070
Name
University of Texas Health Science Center Houston
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
800771594
City
Houston
State
TX
Country
United States
Zip Code
77225
Christie, Peter J (2016) The Mosaic Type IV Secretion Systems. EcoSal Plus 7:
Bhatty, Minny; Camacho, Martha I; Gonzalez-Rivera, Christian et al. (2016) PrgU: A Suppressor of Sex Pheromone Toxicity in Enterococcus faecalis. Mol Microbiol :
Gonzalez-Rivera, Christian; Bhatty, Minny; Christie, Peter J (2016) Mechanism and Function of Type IV Secretion During Infection of the Human Host. Microbiol Spectr 4:
Bhatty, Minny; Cruz, Melissa R; Frank, Kristi L et al. (2015) Enterococcus faecalis pCF10-encoded surface proteins PrgA, PrgB (aggregation substance) and PrgC contribute to plasmid transfer, biofilm formation and virulence. Mol Microbiol 95:660-77
Christie, Peter J; Gordon, Jay E (2014) The Agrobacterium Ti Plasmids. Microbiol Spectr 2:
Maindola, Priyank; Raina, Rahul; Goyal, Parveen et al. (2014) Multiple enzymatic activities of ParB/Srx superfamily mediate sexual conflict among conjugative plasmids. Nat Commun 5:5322
Christie, Peter J; Whitaker, Neal; González-Rivera, Christian (2014) Mechanism and structure of the bacterial type IV secretion systems. Biochim Biophys Acta 1843:1578-91
Trokter, Martina; Felisberto-Rodrigues, Catarina; Christie, Peter J et al. (2014) Recent advances in the structural and molecular biology of type IV secretion systems. Curr Opin Struct Biol 27:16-23
Bhatty, Minny; Laverde Gomez, Jenny A; Christie, Peter J (2013) The expanding bacterial type IV secretion lexicon. Res Microbiol 164:620-39
Garza, Isaac; Christie, Peter J (2013) A putative transmembrane leucine zipper of agrobacterium VirB10 is essential for t-pilus biogenesis but not type IV secretion. J Bacteriol 195:3022-34

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