The PE/PPE multigene family codes for virulence factors and is a possible source of mycobacterial antigenic variation: Perhaps more?

被引:119
作者
Akhter, Yusuf [1 ]
Ehebauer, Matthias T. [1 ]
Mukhopadhyay, Sangita [2 ]
Hasnain, Seyed E. [3 ,4 ,5 ]
机构
[1] DESY, European Mol Biol Lab Hamburg, D-22603 Hamburg, Germany
[2] Ctr DNA Fingerprinting & Diagnost, Hyderabad 500076, Andhra Pradesh, India
[3] Indian Inst Technol Delhi, Sch Biol Sci, New Delhi 110016, India
[4] Univ Hyderabad Campus, Inst Life Sci, Hyderabad 500046, Andhra Pradesh, India
[5] Inst Liver & Biliary Sci, New Delhi, India
关键词
Mycobacterium tuberculosis; PE/PPE; Antigenic variation; Virulence factor; CULTURE FILTRATE PROTEIN; PE-PGRS PROTEINS; IMMUNE-RESPONSE; TUBERCULOSIS GENES; SECRETION SYSTEM; TUBERCLE-BACILLI; PPE PROTEINS; BOVIS BCG; IFN-GAMMA; IDENTIFICATION;
D O I
10.1016/j.biochi.2011.09.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The PE/PPE multigene family codes for approximately 10% of the Mycobacterium tuberculosis proteome and is encoded by 176 open reading frames. These proteins possess, and have been named after, the conserved proline-glutamate (PE) or proline-proline-glutamate (PPE) motifs at their N-terminus. Their genes have a conserved structure and repeat motifs that could be a potential source of antigenic variation in M. tuberculosis. PE/PPE genes are scattered throughout the genome and PE/PPE pairs are usually encoded in bicistronic operons although this is not universally so. This gene family has evolved by specific gene duplication events. PE/PPE proteins are either secreted or localized to the cell surface. Several are thought to be virulence factors, which participate in evasion of the host immune response. This review summarizes the current knowledge about the gene family in order to better understand its biological function. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:110 / 116
页数:7
相关论文
共 94 条
  • [61] The PPE18 of Mycobacterium tuberculosis Interacts with TLR2 and Activates IL-10 Induction in Macrophage
    Nair, Shiny
    Ramaswamy, Poongothai A.
    Ghosh, Sudip
    Joshi, Dhananjay C.
    Pathak, Niteen
    Siddiqui, Imran
    Sharma, Pawan
    Hasnain, Seyed E.
    Mande, Shekhar C.
    Mukhopadhyay, Sangita
    [J]. JOURNAL OF IMMUNOLOGY, 2009, 183 (10) : 6269 - 6281
  • [62] A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection
    Newport, MJ
    Huxley, CM
    Huston, S
    Hawrylowicz, CM
    Oostra, BA
    Williamson, R
    Levin, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (26) : 1941 - 1949
  • [63] Mycobacterium tuberculosis inhibits MHC class II antigen processing in murine bone marrow macrophages
    Noss, EH
    Harding, CV
    Boom, WH
    [J]. CELLULAR IMMUNOLOGY, 2000, 201 (01) : 63 - 74
  • [64] ORME IM, 1987, J IMMUNOL, V138, P293
  • [65] The use of gene clusters to infer functional coupling
    Overbeek, R
    Fonstein, M
    D'Souza, M
    Pusch, GD
    Maltsev, N
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) : 2896 - 2901
  • [66] omputational identification of beta-barrel outer-membrane proteins in Mycobacterium tuberculosis predicted proteomes as putative vaccine candidates
    Pajon, R.
    Yero, D.
    Lage, A.
    Llanes, A.
    Borroto, C. J.
    [J]. TUBERCULOSIS, 2006, 86 (3-4) : 290 - 302
  • [67] CHARACTERIZATION OF THE HIGHLY ABUNDANT POLYMORPHIC GC-RICH-REPETITIVE SEQUENCE (PGRS) PRESENT IN MYCOBACTERIUM-TUBERCULOSIS
    POULET, S
    COLE, ST
    [J]. ARCHIVES OF MICROBIOLOGY, 1995, 163 (02) : 87 - 95
  • [68] Computational prediction and experimental verification of novel IdeR binding sites in the upstream sequences of Mycobacterium tuberculosis open reading frames
    Prakash, P
    Yellaboina, S
    Ranjan, A
    Hasnain, SE
    [J]. BIOINFORMATICS, 2005, 21 (10) : 2161 - 2166
  • [69] PROCTOR RA, 1982, BLOOD, V59, P681
  • [70] Loss of RD1 contributed to the attenuation of the live tuberculosis vaccines Mycobacterium bovis BCG and Mycobacterium microti
    Pym, AS
    Brodin, P
    Brosch, R
    Huerre, M
    Cole, ST
    [J]. MOLECULAR MICROBIOLOGY, 2002, 46 (03) : 709 - 717