Distribution of Porphyromonas gingivalis fimA and mfa1 fimbrial genotypes in subgingival plaques

被引:14
作者
Nagano, Keiji [1 ]
Hasegawa, Yoshiaki [1 ]
Iijima, Yura [1 ]
Kikuchi, Takeshi [2 ]
Mitani, Akio [2 ]
机构
[1] Aichi Gakuin Univ, Sch Dent, Dept Microbiol, Nagoya, Aichi, Japan
[2] Aichi Gakuin Univ, Sch Dent, Dept Periodontol, Nagoya, Aichi, Japan
来源
PEERJ | 2018年 / 6卷
关键词
Fimbriae; Porphyromonas gingivalis; FimA; Genotype; Periodontitis; Mfa1; INFLAMED SURFACE-AREA; PERIODONTAL-DISEASE; BACTEROIDES-GINGIVALIS; CAPSULAR SEROTYPES; EPITHELIAL-CELLS; PREVALENCE; MECHANISMS; MICROBIOTA; PROTEIN; PURIFICATION;
D O I
10.7717/peerj.5581
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Strains of periodontal disease-associated bacterium Porphyromonas gingivalis have different pathogenicity, which can be attributed to clonal genetic diversity. P. gingivalis typically expresses two types of fimbriae, FimA and Mfa1, which comprise six (I, Ib, II, III, IV, and V) and two (mfa(53) and mfa(70)) genotypes, respectively. This study was conducted to investigate the distribution of the two fimbrial genotypes of P. gingivalis in clinical specimens. Methods: Subgingival plaques were collected from 100 participants during periodontal maintenance therapy and examined for P. gingivalis fimbrial genotypes by direct polymerase chain reaction and/or DNA sequencing. We also analyzed the relationship between fimbrial genotypes and clinical parameters of periodontitis recorded at the first medical examination. Results: Both fimbrial types could be detected in 63 out of 100 samples; among them, fimA genotype II was found in 33 samples (52.4%), in which the mfa(70) genotype was 1.75 times more prevalent than mfa(53). The total detection rate of fimA genotypes I and Ib was 38.1%; in these samples, the two mfa1 genotypes were observed at a comparable frequency. In two samples positive for fimA III (3.2%), only mfa53 was detected, whereas in four samples positive for fimA IV (6.3%), the two mfa1 genotypes were equally represented, and none of fimA V-positive samples defined the mfa1 genotype. No associations were found between clinical parameters and fimbrial subtype combinations. Discussion: Both P. gingivalis fimbrial types were detected at various ratios in subgingival plaques, and a tendency for fimA and mfa1 genotype combinations was observed. However, there was no association between P. gingivalis fimbrial genotypes and periodontitis severity.
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页数:12
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