Genome-wide comparison reveals great inter- and intraspecies variability in B pseudomallei and B mallei pathogens

被引:9
|
作者
Monastyrskaya, G
Fushan, A
Abaev, I
Filyukova, O
Kostina, M
Pecherskih, E
Sverdlov, E
机构
[1] Russian Acad Sci, MM Shemyakin & Yu A Ovchinnikov Inst Bioorgan Che, Lab Struct & Funct Human Genes, Moscow 117997, Russia
[2] State Ctr Appl Microbiol, Obolensk, Russia
关键词
Burkholderia pseudomallei; Burkholderia mallei; subtractive hybridization;
D O I
10.1016/j.resmic.2004.05.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Burkholderia mallei and B. pseudomallei, closely related Gram-negative bacteria, are causative agents of serious infectious diseases of humans and animals: glanders and melioidosis, respectively. Despite numerous studies of these pathogens, the detailed mechanism of their pathogenesis is still unknown. The problem is even more complicated due to natural variability of B. pseudomallei and B. mallei strains, the understanding of which is a prerequisite for rational design of tools for diagnostics, prophylaxis and therapy of the diseases. Using a subtractive hybridization technique, we compared the genomes of B. pseudomallei C-141 and B. mallei C-5 strains. A subtracted library of DNA fragments specific for B. pseudomallei C-141 and absent from B. mallei C-5 was obtained and analyzed. A variety of differences have been detected and mapped on the recently sequenced genome of B. pseudomallei K96243. A comparative sequence analysis also revealed considerable genomic differences between B. pseudomallei C-141 and B. mallei ATCC 23344 strains sequenced at The Institute for Genomic Research (TIGR). We also observed significant genomic differences between B. pseudomallei C-141 and B. pseudomallei K96243. Some of the differential DNA fragments displayed similarity to different mobile elements which have not yet been described for B. pseudomallei, whereas the others matched various prophage components, components of active transport systems, different enzymes and transcription regulators. A substantial proportion of the differential clones had no database matches either at the nucleotide or protein level. The results provide evidence for great genome-wide variability of B. pseudomallei, further confirmed by Southern blot analysis of various B. pseudomallei strains. The data obtained can be useful for future development of efficient diagnostic tools allowing rapid identification of species, strains and isolates of B. mallei and B. pseudomallei. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:781 / 793
页数:13
相关论文
共 50 条
  • [1] Burkholderia mallei and Burkholderia pseudomallei Genome-wide Analysis: Two Bacterial Pathogens of Astonishingly Complex Genomes
    Diniz, M. C.
    Farias, K. M.
    Pacheco, A. C. L. P.
    Viana, D. A.
    Araujo-Filho, R.
    Lima, A. P. S.
    Costa, R. B.
    Oliveira, D. M.
    BRAZILIAN JOURNAL OF HYGIENE AND ANIMAL SANITY, 2008, 2 (01): : 1 - 34
  • [2] Genome-wide Translocation Sequencing Reveals Mechanisms of Chromosome Breaks and Rearrangements in B Cells
    Chiarle, Roberto
    Zhang, Yu
    Frock, Richard L.
    Lewis, Susanna M.
    Molinie, Benoit
    Ho, Yu-Jui
    Myers, Darienne R.
    Choi, Vivian W.
    Compagno, Mara
    Malkin, Daniel J.
    Neuberg, Donna
    Monti, Stefano
    Giallourakis, Cosmas C.
    Gostissa, Monica
    Alt, Frederick W.
    CELL, 2011, 147 (01) : 107 - 119
  • [3] Genome-Wide Expression Profiling Reveals S100B as Biomarker for Invasive Aspergillosis
    Dix, Andreas
    Czakai, Kristin
    Springer, Jan
    Fliesser, Mirjam
    Bonin, Michael
    Guthke, Reinhard
    Schmitt, Anna L.
    Einsele, Hermann
    Linde, Joerg
    Loeffler, Juergen
    FRONTIERS IN MICROBIOLOGY, 2016, 7
  • [4] Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways
    Nair, Rajan P.
    Duffin, Kristina Callis
    Helms, Cynthia
    Ding, Jun
    Stuart, Philip E.
    Goldgar, David
    Gudjonsson, Johann E.
    Li, Yun
    Tejasvi, Trilokraj
    Feng, Bing-Jian
    Ruether, Andreas
    Schreiber, Stefan
    Weichenthal, Michael
    Gladman, Dafna
    Rahman, Proton
    Schrodi, Steven J.
    Prahalad, Sampath
    Guthery, Stephen L.
    Fischer, Judith
    Liao, Wilson
    Kwok, Pui-Yan
    Menter, Alan
    Lathrop, G. Mark
    Awise, Carol
    Begovich, Ann B.
    Voorhees, John J.
    Elder, James T.
    Krueger, Gerald G.
    Bowcock, Anne M.
    Abecasis, Goncalo R.
    NATURE GENETICS, 2009, 41 (02) : 199 - 204
  • [5] Genome-Wide Analysis Reveals Frequent Inactivating Mutations of Acetyltransferase Genes In B-Cell Lymphoma
    Pasqualucci, Laura
    Dominguez-Sola, David
    Chiarenza, Annalisa
    Fabbri, Giulia
    Grunn, Adina
    Trifonov, Vladimir
    Kasper, Lawryn H.
    Lerach, Stephanie
    Jing, Ma
    Rossi, Davide
    Mullighan, Charles
    Gaidano, Gianluca
    Rabadan, Raul
    Brindle, Paul K.
    Dalla-Favera, Riccardo
    BLOOD, 2010, 116 (21) : 211 - 211
  • [6] Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways
    Rajan P Nair
    Kristina Callis Duffin
    Cynthia Helms
    Jun Ding
    Philip E Stuart
    David Goldgar
    Johann E Gudjonsson
    Yun Li
    Trilokraj Tejasvi
    Bing-Jian Feng
    Andreas Ruether
    Stefan Schreiber
    Michael Weichenthal
    Dafna Gladman
    Proton Rahman
    Steven J Schrodi
    Sampath Prahalad
    Stephen L Guthery
    Judith Fischer
    Wilson Liao
    Pui-Yan Kwok
    Alan Menter
    G Mark Lathrop
    Carol A Wise
    Ann B Begovich
    John J Voorhees
    James T Elder
    Gerald G Krueger
    Anne M Bowcock
    Gonçalo R Abecasis
    Nature Genetics, 2009, 41 : 199 - 204
  • [7] Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line
    Solomon, Lauren A.
    Li, Stephen K. H.
    Piskorz, Jan
    Xu, Li S.
    DeKoter, Rodney P.
    CANCER RESEARCH, 2015, 75
  • [8] Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line
    Lauren A Solomon
    Stephen KH Li
    Jan Piskorz
    Li S Xu
    Rodney P DeKoter
    BMC Genomics, 16
  • [9] Genome-wide comparison of PU.1 and Spi-B binding sites in a mouse B lymphoma cell line
    Solomon, Lauren A.
    Li, Stephen K. H.
    Piskorz, Jan
    Xu, Li S.
    DeKoter, Rodney P.
    BMC GENOMICS, 2015, 16
  • [10] Genome-wide expression profiling of B lymphocytes reveals IL4R increase in allergic asthma
    Pascual, Marien
    Roa, Sergio
    Garcia-Sanchez, Asuncion
    Sanz, Catalina
    Hernandez-Hernandez, Laura
    Greally, John M.
    Lorente, Felix
    Davila, Ignacio
    Isidoro-Garcia, Maria
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2014, 134 (04) : 972 - 975