Proteomics of Porphyromonas gingivalis within a model oral microbial community

被引:81
作者
Kuboniwa, Masae [3 ]
Hendrickson, Erik L. [4 ]
Xia, Qiangwei [2 ,4 ,5 ]
Wang, Tiansong [4 ,5 ]
Xie, Hua [6 ]
Hackett, Murray [4 ]
Lamont, Richard J. [1 ]
机构
[1] Univ Florida, Dept Oral Biol, Gainesville, FL 32610 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Osaka Univ, Dept Prevent Dent, Grad Sch Dent, Osaka, Japan
[4] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[5] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[6] Meharry Med Coll, Sch Dent, Nashville, TN 37208 USA
来源
BMC MICROBIOLOGY | 2009年 / 9卷
关键词
PROTEIN IDENTIFICATION; STREPTOCOCCUS-GORDONII; FUSOBACTERIUM-NUCLEATUM; BIOFILM FORMATION; GENOME SEQUENCE; GENE-EXPRESSION; STRAIN; PLAQUE; PERIODONTOPATHOGENS; COAGGREGATION;
D O I
10.1186/1471-2180-9-98
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Porphyromonas gingivalis is a periodontal pathogen that resides in a complex multispecies microbial biofilm community known as dental plaque. Confocal laser scanning microscopy showed that P. gingivalis can assemble into communities in vitro with Streptococcus gordonii and Fusobacterium nucleatum, common constituents of dental plaque. Whole cell quantitative proteomics, along with mutant construction and analysis, were conducted to investigate how P. gingivalis adapts to this three species community. Results: 1156 P. gingivalis proteins were detected qualitatively during comparison of the three species model community with P. gingivalis incubated alone under the same conditions. Integration of spectral counting and summed signal intensity analyses of the dataset showed that 403 proteins were down-regulated and 89 proteins up-regulated. The proteomics results were inspected manually and an ontology analysis conducted using DAVID. Significant decreases were seen in proteins involved in cell shape and the formation of the cell envelope, as well as thiamine, cobalamin, and pyrimidine synthesis and DNA repair. An overall increase was seen in proteins involved in protein synthesis. HmuR, a TonB dependent outer membrane receptor, was up-regulated in the community and an hmuR deficient mutant was deficient in three species community formation, but was unimpaired in its ability to form mono- or dual-species biofilms. Conclusion: Collectively, these results indicate that P. gingivalis can assemble into a heterotypic community with F. nucleatum and S. gordonii, and that a community lifestyle provides physiologic support for P. gingivalis. Proteins such as HmuR, that are up-regulated, can be necessary for community structure.
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页数:14
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