Polymicrobial periodontal pathogen transcriptomes in calvarial bone and soft tissue

被引:10
作者
Bakthavatchalu, V. [2 ]
Meka, A. [1 ]
Mans, J. J. [3 ]
Sathishkumar, S. [2 ]
Lopez, M. C. [4 ]
Bhattacharyya, I. [5 ]
Boyce, B. F. [6 ]
Baker, H. V. [4 ]
Lamont, R. J. [7 ]
Ebersole, J. L. [2 ]
Kesavalu, L. [1 ,3 ]
机构
[1] Univ Florida, Coll Dent, Dept Periodontol, Gainesville, FL 32610 USA
[2] Univ Kentucky, Coll Dent, Ctr Oral Hlth Res, Lexington, KY USA
[3] Univ Florida, Coll Med, Dept Oral Biol, Gainesville, FL 32610 USA
[4] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, Gainesville, FL 32610 USA
[5] Univ Florida, Coll Dent, Dept Oral & Maxillofacial Diagnost Sci, Gainesville, FL 32610 USA
[6] Univ Rochester, Med Ctr, Dept Pathol & Lab Med, Rochester, NY 14642 USA
[7] Univ Louisville, Ctr Oral Hlth & Syst Dis, Louisville, KY 40292 USA
关键词
calvarial bone tissue; gene expression; microarray; polymicrobial infection; Porphyromonas gingivalis; Tannerella forsythia; Treponema denticola; PORPHYROMONAS-GINGIVALIS; TANNERELLA-FORSYTHIA; TREPONEMA-DENTICOLA; IN-VIVO; EXPRESSION; INFECTION; RESPONSES; RESORPTION; INDUCTION; INVASION;
D O I
10.1111/j.2041-1014.2011.00619.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia are consistently associated with adult periodontitis. This study sought to document the host transcriptome to a P. gingivalis, T. denticola, and T. forsythia challenge as a polymicrobial infection using a murine calvarial model of acute inflammation and bone resorption. Mice were infected with P. gingivalis, T. denticola, and T. forsythia over the calvaria, after which the soft tissues and calvarial bones were excised. A Murine GeneChip (R) array analysis of transcript profiles showed that 6997 genes were differentially expressed in calvarial bones (P < 0.05) and 1544 genes were differentially transcribed in the inflamed tissues after the polymicrobial infection. Of these genes, 4476 and 1035 genes in the infected bone and tissues were differentially expressed by upregulation. Biological pathways significantly impacted by the polymicrobial infection in calvarial bone included leukocyte transendothelial migration (LTM), cell adhesion molecules, adherens junction, major histocompatibility complex antigen, extracellular matrix-receptor interaction, and antigen processing and presentation resulting in inflammatory/cytokine/chemokine transcripts stimulation in bone and soft tissue. Intense inflammation and increased activated osteoclasts were observed in calvarias compared with sham-infected controls. Quantitative real-time RT-PCR analysis confirmed that the mRNA level of selected genes corresponded with the microarray expression. The polymicrobial infection regulated several LTM and extracellular membrane pathway genes in a manner distinct from mono-infection with P. gingivalis, T. denticola, or T. forsythia. To our knowledge, this is the first definition of the polymicrobially induced transcriptome in calvarial bone and soft tissue in response to periodontal pathogens.
引用
收藏
页码:303 / 320
页数:18
相关论文
共 44 条
  • [31] Rapid sequence divergence in mammalian β-defensins by adaptive evolution
    Maxwell, AI
    Morrison, GM
    Dorin, JR
    [J]. MOLECULAR IMMUNOLOGY, 2003, 40 (07) : 413 - 421
  • [32] Porphyromonas gingivalis infection-induced tissue and bone transcriptional profiles
    Meka, A.
    Bakthavatchalu, V.
    Sathishkumar, S.
    Lopez, M. C.
    Verma, R. K.
    Wallet, S. M.
    Bhattacharyya, I.
    Boyce, B. F.
    Handfield, M.
    Lamont, R. J.
    Baker, H. V.
    Ebersole, J. L.
    Kesavalu, L.
    [J]. MOLECULAR ORAL MICROBIOLOGY, 2010, 25 (01) : 61 - 74
  • [33] Adenosine A2A receptor inactivation increases survival in polymicrobial sepsis
    Nemeth, Zoltan H.
    Csoka, Balazs
    Wilmanski, Jeanette
    Xu, DaZhong
    Lu, Qi
    Ledent, Catherine
    Deitch, Edwin A.
    Pacher, Pal
    Spolarics, Zoltan
    Hasko, Gyorgy
    [J]. JOURNAL OF IMMUNOLOGY, 2006, 176 (09) : 5616 - 5626
  • [34] Microbial etiology of periodontitis
    Nishihara, T
    Koseki, T
    [J]. PERIODONTOLOGY 2000, 2004, 36 : 14 - 26
  • [35] Gingival Transcriptome Patterns During Induction and Resolution of Experimental Gingivitis in Humans
    Offenbacher, Steven
    Barros, Silvana P.
    Paquette, David W.
    Winston, J. Leslie
    Biesbrock, Aaron R.
    Thomason, Ryan G.
    Gibb, Roger D.
    Fulmer, Andy W.
    Tiesman, Jay P.
    Juhlin, Kenton D.
    Wang, Shuo L.
    Reichling, Tim D.
    Chen, Ker-Sang
    Ho, Begonia
    [J]. JOURNAL OF PERIODONTOLOGY, 2009, 80 (12) : 1963 - 1982
  • [36] Subgingival bacterial colonization profiles correlate with gingival tissue gene expression
    Papapanou, Panos N.
    Behle, Jan H.
    Kebschull, Moritz
    Celenti, Romanita
    Wolf, Dana L.
    Handfield, Martin
    Pavlidis, Paul
    Demmer, Ryan T.
    [J]. BMC MICROBIOLOGY, 2009, 9
  • [37] Small proline-rich protein 1A is a gp130 pathway- and stress-inducible cardioprotective protein
    Pradervand, S
    Yasukawa, H
    Muller, OG
    Kjekshus, H
    Nakamura, T
    St Amand, TR
    Yajima, T
    Matsumura, K
    Duplain, H
    Iwatate, M
    Woodard, S
    Pedrazzini, T
    Ross, J
    Firsov, D
    Rossier, BC
    Hoshijima, M
    Chien, KR
    [J]. EMBO JOURNAL, 2004, 23 (22) : 4517 - 4525
  • [38] Periodontal microbial ecology
    Socransky, SS
    Haffajee, AD
    [J]. PERIODONTOLOGY 2000, 2005, 38 : 135 - 187
  • [39] Microbial complexes in subgingival plaque
    Socransky, SS
    Haffajee, AD
    Cugini, MA
    Smith, C
    Kent, RL
    [J]. JOURNAL OF CLINICAL PERIODONTOLOGY, 1998, 25 (02) : 134 - 144
  • [40] Absence of leukotriene B4 receptor 1 confers resistance to airway hyperresponsiveness and Th2-type immune responses
    Terawaki, K
    Yokomizo, T
    Nagase, T
    Toda, A
    Taniguchi, M
    Hashizume, K
    Yagi, T
    Shimizu, T
    [J]. JOURNAL OF IMMUNOLOGY, 2005, 175 (07) : 4217 - 4225