Antivirulence Genes: Insights into Pathogen Evolution through Gene Loss

被引:93
作者
Bliven, Kimberly A. [1 ]
Maurelli, Anthony T. [1 ]
机构
[1] Uniformed Serv Univ Hlth Sci, F Edward Hebert Sch Med, Dept Microbiol & Immunol, Bethesda, MD 20814 USA
关键词
ENTEROINVASIVE-ESCHERICHIA-COLI; COMPLETE GENOME SEQUENCE; YERSINIA-PESTIS; SALMONELLA-ENTERICA; SHIGELLA-FLEXNERI; FRANCISELLA-TULARENSIS; CONVERGENT EVOLUTION; BACTERIAL PATHOGENS; III SECRETION; BLACK-HOLES;
D O I
10.1128/IAI.00740-12
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The emergence of new pathogens and the exploitation of novel pathogenic niches by bacteria typically require the horizontal transfer of virulence factors and subsequent adaptation-a "fine-tuning" process-for the successful incorporation of these factors into the microbe's genome. The function of newly acquired virulence factors may be hindered by the expression of genes already present in the bacterium. Occasionally, certain genes must be inactivated or deleted for full expression of the pathogen phenotype to occur. These genes are known as antivirulence genes (AVGs). Originally identified in Shigella, AVGs have improved our understanding of pathogen evolution and provided a novel approach to drug and vaccine development. In this review, we revisit the AVG definition and update the list of known AVGs, which now includes genes from pathogens such as Salmonella, Yersinia pestis, and the virulent Francisella tularensis subspecies. AVGs encompass a wide variety of different roles within the microbe, including genes involved in metabolism, biofilm synthesis, lipopolysaccharide modification, and host vasoconstriction. More recently, the use of one of these AVGs (lpxL) as a potential vaccine candidate highlights the practical application of studying AVG inactivation in microbial pathogens.
引用
收藏
页码:4061 / 4070
页数:10
相关论文
共 57 条
  • [1] Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis
    Achtman, M
    Zurth, K
    Morelli, C
    Torrea, G
    Guiyoule, A
    Carniel, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) : 14043 - 14048
  • [2] Sequencing, expression and biochemical characterization of the Porphyromonas gingivalis pepO gene encoding a protein homologous to human endothelin-converting enzyme
    Awano, S
    Ansai, T
    Mochizuki, H
    Yu, WX
    Tanzawa, K
    Turner, AJ
    Takehara, T
    [J]. FEBS LETTERS, 1999, 460 (01) : 139 - 144
  • [3] Leucine-Responsive Regulatory Protein (Lrp) Acts as a Virulence Repressor in Salmonella enterica Serovar Typhimurium
    Baek, Chang-Ho
    Wang, Shifeng
    Roland, Kenneth L.
    Curtiss, Roy, III
    [J]. JOURNAL OF BACTERIOLOGY, 2009, 191 (04) : 1278 - 1292
  • [4] A New Piece of the Shigella Pathogenicity Puzzle: Spermidine Accumulationby Silencing of the speG Gene
    Barbagallo, Marialuisa
    Di Martino, Maria Letizia
    Marcocci, Lucia
    Pietrangeli, Paola
    De Carolis, Elena
    Casalino, Mariassunta
    Colonna, Bianca
    Prosseda, Gianni
    [J]. PLOS ONE, 2011, 6 (11):
  • [5] Bäumler AJ, 1998, INFECT IMMUN, V66, P4579
  • [6] CadC is the preferential target of a convergent evolution driving enteroinvasive Escherichia coli toward a lysine decarboxylase-defective phenotype
    Casalino, M
    Latella, MC
    Prosseda, G
    Colonna, B
    [J]. INFECTION AND IMMUNITY, 2003, 71 (10) : 5472 - 5479
  • [7] Insights into the evolution of Yersinia pestis through whole-genome comparison with Yersinia pseudotuberculosis
    Chain, PSG
    Carniel, E
    Larimer, FW
    Lamerdin, J
    Stoutland, PO
    Regala, WM
    Georgescu, AM
    Vergez, LM
    Land, ML
    Motin, VL
    Brubaker, RR
    Fowler, J
    Hinnebusch, J
    Marceau, M
    Medigue, C
    Simonet, M
    Chenal-Francisque, V
    Souza, B
    Dacheux, D
    Elliott, JM
    Derbise, A
    Hauser, LJ
    Garcia, E
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (38) : 13826 - 13831
  • [8] Massive gene decay in the leprosy bacillus
    Cole, ST
    Eiglmeier, K
    Parkhill, J
    James, KD
    Thomson, NR
    Wheeler, PR
    Honoré, N
    Garnier, T
    Churcher, C
    Harris, D
    Mungall, K
    Basham, D
    Brown, D
    Chillingworth, T
    Connor, R
    Davies, RM
    Devlin, K
    Duthoy, S
    Feltwell, T
    Fraser, A
    Hamlin, N
    Holroyd, S
    Hornsby, T
    Jagels, K
    Lacroix, C
    Maclean, J
    Moule, S
    Murphy, L
    Oliver, K
    Quail, MA
    Rajandream, MA
    Rutherford, KM
    Rutter, S
    Seeger, K
    Simon, S
    Simmonds, M
    Skelton, J
    Squares, R
    Squares, S
    Stevens, K
    Taylor, K
    Whitehead, S
    Woodward, JR
    Barrell, BG
    [J]. NATURE, 2001, 409 (6823) : 1007 - 1011
  • [9] Pathoadaptive mutations that enhance virulence:: Genetic organization of the cadA regions of Shigella spp.
    Day, WA
    Fernández, RE
    Maurelli, AT
    [J]. INFECTION AND IMMUNITY, 2001, 69 (12) : 7471 - 7480
  • [10] Day WA, 2006, EVOLUTION OF MICROBIAL PATHOGENS, P109