Genetic classification of severe early childhood caries by use of subtracted DNA fragments from Streptococcus mutans

被引:10
作者
Saxena, Deepak [1 ]
Caufield, Page W. [2 ,4 ]
Li, Yihong [1 ]
Brown, Stuart [4 ]
Song, Jinmei [2 ]
Norman, Robert [3 ]
机构
[1] NYU, Coll Dent, Dept Basic Sci & Craniofacial Biol, New York, NY 10010 USA
[2] NYU, Coll Dent, Dept Cariol & Comprehens Care, New York, NY 10010 USA
[3] NYU, Coll Dent, Dept Epidemiol & Hlth Promot, New York, NY 10010 USA
[4] NYU, Sch Med, New York, NY 10010 USA
关键词
D O I
10.1128/JCM.01000-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Streptococcus mutans is one of several members of the oral indigenous biota linked with severe early childhood caries (S-ECC). Because most humans harbor S. mutans, but not all manifest disease, it has been proposed that the strains of S. mutans associated with S-ECC are genetically distinct from those found in caries-free (CF) children. The objective of this study was to identify common DNA fragments from S. mutans present in S-ECC but not in CF children. Using suppressive subtractive hybridization, we found a number of DNA fragments (biomarkers) present in 88 to 95% of the S-ECC S. mutans strains but not in CF S. mutans strains. We then applied machine learning techniques including support vector machines and neural networks to identify the biomarkers with the most predictive power for disease status, achieving a 92% accurate classification of the strains as either S-ECC or CF associated. The presence of these gene fragments in 90 to 100% of the 26 S-ECC isolates tested suggested their possible functional role in the pathogenesis of S. mutans associated with dental caries.
引用
收藏
页码:2868 / 2873
页数:6
相关论文
共 52 条
[31]   SURVEY OF EXTRACHROMOSOMAL GENE POOL OF STREPTOCOCCUS-MUTANS [J].
MACRINA, FL ;
REIDER, JL ;
VIRGILI, SS ;
KOPECKO, DJ .
INFECTION AND IMMUNITY, 1977, 17 (01) :215-226
[32]   Genes for the majority of group A streptococcal virulence factors and extracellular surface proteins do not confer an increased propensity to cause invasive disease [J].
McMillan, David J. ;
Beiko, R. G. ;
Geffers, R. ;
Buer, Jan ;
Schouls, L. M. ;
Vlaminckx, B. J. M. ;
Wannet, W. J. B. ;
Sriprakash, K. S. ;
Chhatwal, G. S. .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (07) :884-891
[33]   TRANSFORMATION OF STREPTOCOCCUS-MUTANS WITH CHROMOSOMAL AND SHUTTLE PLASMID (PYA629) DNAS [J].
MURCHISON, HH ;
BARRETT, JF ;
CARDINEAU, GA ;
CURTISS, R .
INFECTION AND IMMUNITY, 1986, 54 (02) :273-282
[34]  
Qi FX, 1999, APPL ENVIRON MICROB, V65, P3880
[35]   The group I strain of Streptococcus mutans, UA140, produces both the lantibiotic mutacin I and a nonlantibiotic bacteriocin, mutacin IV [J].
Qi, FX ;
Chen, P ;
Caufield, PW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (01) :15-21
[36]   Purification and biochemical characterization of mutacin I from the group I strain of Streptococcus mutans, CH43, and genetic analysis of mutacin I biosynthesis genes [J].
Qi, FX ;
Chen, P ;
Caufield, PW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (08) :3221-3229
[37]   Identification of nucleotide sequences for the specific and rapid detection of Yersinia pestis [J].
Radnedge, L ;
Gamez-Chin, S ;
McCready, PM ;
Worsham, PL ;
Andersen, GL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (08) :3759-3762
[38]   Support Vector Machine-based method for predicting subcellular localization of mycobacterial proteins using evolutionary information and motifs [J].
Rashid, Mamoon ;
Saha, Sudipto ;
Raghava, Gajendra P. S. .
BMC BIOINFORMATICS, 2007, 8
[39]   Chromosomal insertions and deletions in Streptococcus mutans [J].
Robinson, WG ;
Old, LA ;
Shah, DSH ;
Russell, RRB .
CARIES RESEARCH, 2003, 37 (02) :148-156
[40]   Identification by subtractive hybridization of a novel insertion sequence specific for virulent strains of Porphyromonas gingivalis [J].
Sawada, K ;
Kokeguchi, S ;
Hongyo, H ;
Sawada, S ;
Miyamoto, M ;
Maeda, H ;
Nishimura, F ;
Takashiba, S ;
Murayama, Y .
INFECTION AND IMMUNITY, 1999, 67 (11) :5621-5625